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Foraminifera and Stratigraphy of the Upper Part of the Pierre Shale and Lower Part of the Fox Hills Sandstone () North-Central South Dakota

GEOLOGICAL SURVEY PROFESSIONAL PAPER 611

Foraminifera and Stratigraphy of the Upper Part of the Pierre Shale and Lower Part of the Fox Hills Sandstone (Cretaceous) North-Central South Dakota By JAMES F. MELLO

GEOLOGICAL SURVEY PROFESSIONAL PAPER 611 Description, illustration, and interpretation of the L,ate Cretaceous foraminiferal faunas of parts of the Pierre Shale and Fox Hills Sandstone, and discussion of the stratigraphy of these lithologic units

UNITED STATES GOVERNMENT PRINTING OFFICE, WASHINGTON : 1969 UNITED STATES DEPARTMENT OF THE INTERIOR WALTER J. HIGKEL, Secretary

GEOLOGICAL SURVEY William T. Pecora, Director

Library of Congress catalog-card No. OS 68-365

For sale by the Superintendent of Documents, U.S. Government Printing Office Washington, D.C. 20402 - Price $2.25 (paper cover) CONTENTS

Page Continued Abstract.______1 Paleoecology ______19 Introduction. ______1 Paleogeographic setting______19 Acknowledgments. ______2 Foraminiferal biofacies______21 Field methods.______3 Lower arenaceous biofacies______21 Lithostratigraphy. ______3 Upper arenaceous biofacies__ ___. 22 Earlier investigations.______3 biofacies ______22 Lithology of the Pierre Shale______3 Stratigraphic and areal distribution. 23 Virgin Creek Member of the Pierre Shale._____ 4 Faunal details and origin.______23 Mobridge Member of the Pierre Shale.______4 Environmental interpretations.___-_____-__-___. 25 Elk Butte Member of the Pierre Shale______4 Biologic information.______25 Type sections of the members.______5 Lithologic information.______35 General discussion of the lithologic subdivisions- 5 Recent analogs.______.__----____-__--. 36 Distinctive features of the upper part of the Conclusions.______-_---__------__-_--. 36 Pierre Shale.______6 Paleontology.______---__----_____-___. 37 Methods of correlation.______7 Laboratory methods.______37 Composite stratigraphic sequences ______8 Macrof ossils. ______38 Stratigraphic sequence along the Moreau River. 8 Stratigraphic sequence along the Grand River. _ 9 Ostracodes______39 Relationship of the sequences______11 Classification and of Foraminifera. 39 Biostratigraphy.. ______15 Descriptions of measured sections______102 Regional correlation ______15 References cited______112 Composition of the fauna.______19 __ 117

ILLUSTRATIONS

[Plates 1-11 follow index; plate 12 is in pocket] PLATE 1. Verneuilinoides, Pseudoclavulinaf, Clavulinoides, Trochammina, Oolina, , fLoxostoma, and "." 2. Nuttallinellaf, Pullenia, Biglobigerinella, Rugoglobigerina, and Anomalinoides. 3. , Anomalinoides, and . 4. Bathysiphon, Reophax, , Glomospira, Haplophragmoides, Spiroplectammina, and Gaudryina. 5. Pseudoclavulinaf, Heterostomella, Silicosigmoilina, , Trochammina, and Robulus. 6. Marginulina, Astacolus, Dentalina, and Nodosaria. 7. Rectoglandulina, Citharina, , Frondicularia, , Oolina, Fissurina, Guttulina, and Globulina. 8. Pyrulina, Ramulina, , Bolivinopsis, Rectoguembelina, Bolivinoides, Tappanina, Eouvigerina, and Bulimina. 9. Bulimina, Neobulimina, Bolivina, Loxostoma, Pleurostomella, and Stilostomella. 10. "Gyroidina," Gyroidina, Osangularia, Quadrimorphina, "Discarbis," and Nuttallinellaf. 11. Hoeglundina, Pullenia, Planulina, and Cibicides. 12. Graphic representations of measured sections in the upper part of the Pierre Shale and lower part of the Fox HTTs Sandstone (Cretaceous), north-central South Dakota. in IV CONTENTO Page FIGURE 1. Index map of north-central South Dakota__-____--______-__-_---__------__-----____-______2 2-6. Charts: 2. Ranges of Foraminifera useful in local correlation from the Moreau River composite section.______10 3. Ranges of Foraminifera useful in local correlation from the Grand River composite section.______11 4. Correlation of stratigraphic sections along the Moreau River and environs..______12 5. Correlation of stratigraphic sections along the Grand River and environs______13 6. Foraminiferal biofacies in composite stratigraphic sections along the Moreau and Grand Rivers. _ _ _ 14 7. Lithofacies and paleogeographic maps of the Western United States in Verendrye and Virgin Creek time, Mobridge time, and Fox HLlls time______20 8. Graph showing the number of species in 192 samples from the upper part of the Pierre Shale and lower part of the Fox Hills Sandstone______-_-_._-___-___-----____----___---_____-____.______27 9-12. Graphs showing distribution of families in: 9. Fifty samples from the upper arenaceous biofacies______28 10. Sixty-six samples from the calcareous biofacies______28 11. Fifty-three samples from the calcareous biofacies______29 12. Ten samples from the lower arenaceous biofacies______29 13-14. Charts: 13. Composite stratigraphic ranges of Foraminifera in sections along and near the Moreau River. _ _ _ _ 30 14. Composite stratigraphic ranges of Foraminifera in sections along and near the Grand River______32

TABLES

Page TABLE 1. Gulf Coast stratigraphic distribution (after Cushman, 1946) of Foraminifera found in the upper part cf the Pierre Shale and lower part of the Fox Hills Sandstone..______17 2. Analysis of the number of genera, number of species, planktonic-benthonic ratios, and percentage of arena­ ceous specimens in 67 samples from the upper part of the Pierre Shale representing the three recognized foraminif eral biof acies. ______35 FORAMINIFERA AND STRATIGRAPHY OF THE UPPER PART OF THE PIERRE SHALE AND LOWER PART OF THE FOX HILLS SANDSTONE (CRETACEOUS), NORTH-CENTRAL SOUTH DAKOTA

By JAMES F. MELLO

ABSTRACT Comparison of the 62 species and subspecies that occur in Twenty-two stratigraphic sections along and near the Grand both the upper part of the Pierre Shale and in the Cretaceous and Moreau Rivers in north-central South Dakota depict the deposits of the Gulf Coastal Plain indicates a probable ear'y stratigraphy of the Virgin Creek, Mobridge, and Elk Butte Navarro age. Other comparisons also indicate an earliest Members of the upper part of the Pierre Shale and the lower Maestrichtian or latest Campanian age for the upper part of 74 feet of the Pox Hills Sandstone. The Virgin Creek Member, the Pierre Shale. about 60 feet thick, is noncalcareous fissile shale in all but the Paleoecological interpretations based on familial compositions upper 10 to 15 feet; in the lower 20 feet are numerous thin of the faunas, foraminiferal number, planktonic-benthonic ratios, bentonite beds. The Mobridge Member, between about 200 and and lithologic data indicate that the upper part of the Pierre 225 feet thick, is typically calcareous shale with numerous con­ Shale and the lower part of the Fox Hills sandstone were de­ cretion horizons and a few bentonite beds. The Elk Butte posited in waters less than about 200 feet deep. Deepest water Member, 103 feet thick along the Moreau River and 192 feet conditions prevailed during deposition of the lower part of t^re thick along the Grand River, is noncalcareous shale with very calcareous biofaeies. The water, however, became increasingly few bentonite beds; it becomes very silty in the upper 15 to shallow during deposition of the calcareous and upper arena­ 30 feet. The lower part of the Fox Hills Sandstone is com­ ceous biofaeies. Shallowest conditions prevailed during depo^i- pacted but nonindurated sandy, clayey silt and silty, clayey tion of the upper part of the upper arenaceous biofaeies. Fauiml sand, which in most places lacks bedding. Correlation of in­ comparison at the family level indicates similarities between dividual sections was made by means of bentonite beds and the upper and lower arenaceous biofaeies which may reflect concretion horizons wherever possible. Two relatively thick similar environmental conditions, bentonite beds in the Mobridge Member were used as datum planes. The contacts between the calcareous shale of the Mo­ INTRODUCTION bridge Member and the noncalcareous shales of the Virgin Creek Member below and the Elk Butte Member above are gra- Cretaceous rocks exposed in the Great Plains province dational and are not uniform in stratigraphic position in sec­ of the conterminous United States are admirably suited tions correlated on the basis of bentonites. to broad areal stratigraphic study. The gently dipping One hundred and one species, subspecies, or varieties of Foraminifera from 57 genera and 20 families, including seven strata crop out over wide areas, and light rainfall pre­ new species and 12 taxa which could not be identified to species, vents thick cover. Many good, relatively fresh, are described. Three stratigraphically separate foraminiferal measurable sections occur where streams have cut into biofaeies are recognized: the strata. 1. The lower arenaceous biofaeies in the lower 55 feet of the In north-central South Dakota, the essentially flr.t- Virgin Creek Member. Arenaceous (agglutinated), porcel­ laneous, and siliceous Foraminifera are dominant in num­ lying beds of the Fox Hills Sandstone and the Pierre ber of taxa. Shale are exposed over hundreds of square miles and 2. The calcareous biofaeies in the upper 5 feet of the Virgin in many places are dissected by streams. Few authors Creek Member, throughout the Mobridge Member, and in the have mentioned the commonly abundant Foraminifera lower 55 feet or less of the Elk Butte Member. Calcareous from the upper part of the Pierre Shale, and none has perforate Foraminifera are dominant in both number of taxa and number of specimens. placed these in a detailed stratigraphic frame­ 3. The upper arenaceous biofaeies in the upper part of the Elk work or attempted to determine what paleoecologic Butte Member and the lower 74 feet of the Fox Hills Sand­ information could be inferred from them. There are stone. Arenaceous (agglutinated) Foraminifera are domi­ no papers that deal with the faunas of the lower pr-rt nant in both number of taxa and number of specimens. of the Fox Hills. The calcareous biofaeies gradually changes upward into the upper arenaceous biofaeies, but its boundary with the under­ The first objective of the present study was to measure lying lower arenaceous biofaeies is more abrupt, the change and examine a number of exposures to work out the taking place through a short stratigraphic interval. stratigraphic succession in the upper part of the Pierre 1 FORAMINIFERA, STRATIGRAPHY, PIERRE SHALE, FOX HILLS SANDSTONE, S. DAK.

Shale. Seventy-four sections were measured during this ACKNOWLEDGMENTS study; locations of the 23 most significant sections are The assistance of the following persons and institu­ shown in figure 1. The second objective was the sys­ tions is gratefully acknowledged: tematic sampling of many of the measured sections for Prof. Karl M. Waage of Yale University and the Foraminifera. The purpose here was to obtain micro- U.S. Geological Survey acquainted me with the Upper faunas from known stratigraphic positions for identifi­ Cretaceous deposits of South Dakota, suggested the cation and description and for study of ranges, abund­ problem, and provided a great deal of help and en­ ances, associations, and paleoecologic implications. couragement during the course of research. Prof. A. Lee Four of the 23 sections extend upward into the lower McAlester of Yale University and Dr. Johr Sanders part of the Fox Hills Sandstone. Foraminifera from of Hudson Laboratories gave valuable advice a,nd assist­ these sections were noted, but no detailed stratigraphic ance. I am especially grateful for the help of my col­ study of the Fox Hills was made. league, Miss Ruth Todd, whose knowledge of Foramini­ The present investigation covers much of Gorson and fera was called upon frequently. I am also grateful to Dewey Counties and a very small part of Ziebach Dr. William A. Cobban, Dr. Norman Sohl, and Dr. J. County. Within this area, suitable outcrops are confined Thomas Dutro, all of the U.S. Geological Survey, and to the valleys of the Moreau and Grand Rivers, east- to Mr. Ernesto Sarpi of Columbia University for read­ flowing major tributaries of the Missouri River, to the ing the manuscript and providing numerous useful valleys of their main tributaries, and to some recently criticisms. opened railroad cuts in the vicinity of Wakpala in Photographs of the Foraminifera were made by Mr. Corson County. David Massie of the U.S. Geological Survey; the draw-

EXPLANATION .50 44 Location of measured section

30' -

D E W\ E Y

45°15' -

101°30' 100°30'

10 20 MILES

FIGURE 1. Index map of north-central South Dakota showing approximate locations of measured sections. Location numbers shown here match section numbers shown on plate 12 and in figures 4 and 5. LITHOSTRATIGRAPHY

ings are the work of Mrs. Elinor Stromberg of the U.S. EARLIER INVESTIGATIONS Geological Survey. The extensive Cretaceous deposits of the western in­ Fieldwork and research were supported in part by terior of the United States were first studied by F. B. funds from the Yale University Schuchert Fund, by Meek and F. V. Hayden during the middle of the 19th the Society of the Sigma Xi through two grants from century. The stratigraphic succession was subdivided the Sigma Xi RESA Research Fund, and by the U.S. into five formations (Meek and Hayden, 1856, p. 63). Geological Survey. They later (1861, p. 419) gave the names Dakota Group, Fort Benton Group, Niobrara Division, Fort Pierre FIELD METHODS Group, and Fox Hills beds to formations 1 through 5, Good exposures were found by reference to topo­ respectively. The type area of the Fort Pierre Group graphic maps and aerial photographs and by field re­ lies about 60 miles south of the area investigated for this connaissance. The main factors determining choice of report, near the city of Pierre. slopes to be measured were vertical thickness of the After Meek and Hayden's survey, no detailed strati- exposure, degree of freshness of the surface, and posi­ graphic work was done on the Pierre Shale in this area tion with respect to other measured sections. It was until Searight (1937) subdivided the Pierre into five usually possible to find sections that had sufficient over­ members in central and southeastern South Dakota. lap with nearby sections to make correlation possible. These are, in descending order, the Elk Butte, Mobridge, Because altitude increases gradually to the west, succes­ Virgin Creek, Sully, and Gregory Members. Searight sions of stratigraphically higher sections were found (1937), and others have since renamed and redefined by following the rivers westward; however, both large- several of these members. The last of these revisers was scale and small-scale slumping made altitude a useless Crandell (1950); his subdivisions (1958, fig. 4), in criterion for correlation. The slopes were first trenched descending order, are: Elk Butte Member, Mobridge Member, Virgin Creek Member, Verendrye Member, to a fresh surface from top to bottom along at least DeGrey Member, Crow Creek Member, Gregory Mem­ one vertical line. Measurement was made by hand level ber, and Sharon Springs Member. and steel tape. Color, hardness, calcareous content, and All revisers of Searight's original subdivisions of the silt-sand content of the shale were noted, as were con­ Pierre have recognized the Elk Butte, Mobridge, and cretions, bentonites, and other distinctive horizons. Virgin Creek Members, which are grouped under the Color-chart comparisons were not made because the general designation "upper part of the Pierre Shale" color of the shale varied widely with moisture content. in this paper. However, there have been differences of Lithologic samples, where desired, were taken at each opinion and interpretation regarding the boundaries of hand-level interval (5 ft 9 in.) except where special the Mobridge Member. These differences are discussed circumstances required closer or more widely spaced further on. samples. Every effort was made to secure fresh, uncon- LITHOLOGY OF THE PIERRE SHALE taminated shale for these samples. The term "shale" applied to this unit is somewhat LITHOSTRATIGRAPHY misleading because "The Pierre formation as a whole In the following discussion no attempt is made to give consists of stratified gray, dark gray to black clays and a complete history or lithologic description of the Pierre shale, concretions, marls and , interbedded with Shale. The history of exploration and interpretation of many layers of bentonite" (Petsch, 1946, p. 26). The the Cretaceous rocks of the western interior has been Pierre Shale in the area investigated for this report is typicaly a dark-gray claystone or clay shale (terminol­ summarized by Cobban and Reeside (1952, p. 1014- ogy after Dunbar and Rodgers, 1957, p. 166). The rock 1015) and is described in detail in articles to which they contains only minor amounts of silt and sand except in refer. Therefore, only the major contributions pertain­ the upper part directly below the Fox Hills Sandstone. ing to the stratigraphy and lithology of the upper pait Bedding is very obscure in fresh exposures but is em­ of the Pierre Shale in north-central South Dakota are phasized by weathering. Bedding fissility is evident in discussed here. A brief historical summary is given first; some beds, which typically break down into small chips a lithologic description of the members of the upper part before decomposing into mud. Bentonite layers, concre­ of the Pierre Shale as originally defined and as modified tions, and other distinctive lithologic features are pres­ by other authors follows; and, finally, these members ent at many levels. The rock is not well indurated and and their modifications are discussed in the light of my weathers rapidly to gentle slopes which are havily cov­ .studies. ered with soil, rock fragments of various sizes, or tough FORAMTNIFERA, STRATIGRAPHY, PIERRE SHALE, FOX HILLS SANDSTONE, S. DAK gumbo. Steeper slopes and fresher exposures are main­ to gumbo, and good exposures are few. Where fresh tained near drainage, and on these exposures the rock is rock is observable, it "* * * consists of gray shale commonly a light to medium gray or is lightly stained which weathers rapidly to light gray, leaden gray, and to various shades of brown, maroon, and red. brownish gray gumbo which is arranged in horizontal The upper part of the Pierre Shale in the area in­ bands of varying widths" (p. 37). vestigated was subdivided into the Elk Butte, Mobridge, The small fossiliferous concretions referred to above and Virgin Creek Members by Searight, and the type are sporadically distributed in the lower part of the sections for these members are within this area. In the upper Virgin Creek zone and are buff gray and brown following paragraphs the distinctive lithologic features when fresh but weather to light tan or off v^iite. They of these three members are summarized by using either are typically formed about pelecypods, baculites, crabs, direct quotes or paraphrasings of Searight's (1937, p. and other fossils and are usually perforated with small 35-38,11 16, 50-56) original descriptions of the mem­ holes. bers. MOBRIDGE MEMBER OP THE PIERRE SHALE VIRGIN CHEEK MEMBER OP THE PIERRE SHALE Searight (1937, p. 44) described the Mobridge Mem­ The Virgin Creek Member is defined to include ber as "* * * a succession of highly calcareous shale, "* * * all beds between the Sully Member and the marl, and beds which lies above the gumbo- highly calcareous, chalky beds of the Mobridge Mem­ forming shales of the Virgin Creek Member and below ber. It thus includes the bentonite bearing shales which the noncalcareous shale beds of the Elk Butte Member. lie above the Verendrye zone [Verendrye Member of The member forms a wide buff band on the outcrop Crandell, 1952], with its characteristic iron carbonate between the dark color of the underlying and overlying concretions, and all characteristically noncalcareous beds." The member "* * * consists of medium gray beds to the base of the Mobridge" (p. 35). and medium bluish gray to dark gray shale and chalk" The Virgin Creek Member was divided by Searight and is "* * * everywhere highly calcareous and more into two zones on the basis of lithology. "The lower of or less chalky * * *" (p. 45). len-^es and con­ these [the lower Virgin Creek zone] is composed of cretions of several kinds are present at many horizons in relatively resistant, light to medium gray shale which the Mobridge Member. Fossils do not commonly occur contains a number of thin but conspicuous bentonite in the concretions, but concretionary material is always beds" (p. 36). The shale of the lower Virgin Creek zone present within the living chambers of specimens of is relatively resistant to erosion and usually is stained Baculites. Also present are lenses of calcareous mate­ various shades of rusty brown, maroon, and purple rial that have cone-in-cone structure and tl^at range in on clean exposures. It typically breaks down into chips thickness from a fraction of an inch to several inches. and flakes, which are brittle and harsh to the touch. Bentonite beds are not as numerous in this member as "Thin bentonite beds [14 to iy2 in. thick] are a char­ they are in the lower part of the Virgin Creek Member, acteristics feature of the lower Virgin Creek. Indeed, but several of the bentonites are fairly thick (6 to 16 it is on the basis of numerous thin white bentonite in.) and were used as a means of correlation. Searight streaks across the outcrops that these beds are most did not note any thick bentonites in th?, Mobridge readily distinguished" (p. 36). Concretions, though Member. present in the Virgin Creek Member, are not abundant. ELK BUTTE MEMBER OP THE PIERRT3 SHALE However, a layer of concretions at the type section serves to mark the base of the member. The Elk Butte Member is denned as including "The upper part of the Virgin Creek [the upper "* * * all beds in South Dakota betweer the top of Virgin Creek Zone], especially the lower beds, breaks the Mobridge Member and the base of th°» Fox Hills down to leaden gray gumbo, in many places tinged Formation. It thus includes as its basal bee's those non- with rusty brown. The upper Virgin Creek in many calcareous shales which immediately overlie the cal­ places contains characteristic, small fossiliferous con­ careous * * * shales of the Mobridge Member. The cretions in the lower part and a bed containing large upper limit, which is at the Pierre-Fox Pills contact, limestone concretions, in some cases very fossiliferous, cannot be placed with extreme exactness, even at the in the upper part" (p. 36). "Included in the upper type locality, where the basal Fox Hill? is a mas­ Virgin Creek are those beds of shale which lie above sive sandstone, because the contact is one of grada­ the bentonitic lower Virgin Creek and below the highly tion" (Searight, 1937, p. 50). Lithologically, the mem­ calcareous shale and chalk of the Mobridge Member" ber "* * * consists of very fine-texturnd, medium (p. 37). The upper Virgin Creek shale erodes readily gray shale which is apparently very uniform through- GENERAL DISCUSSION OF THE LITHOLOGIC SUBDIVISIONS out" (p. 51). Commonly on steeper slopes the shale the general lithology and stratigraphy. Specific infor­ initially breaks down into thin, flat chips which weather mation of this sort gathered in the present investiga­ to gumbo. The rock becomes brownish gray as the sand tion will be introduced in order to place it on record. and silt content increases toward the top of the mem­ Second, and more important, are modifications of ber. Layers of concretions are also sporadic in this boundary criteria and means of correlation of the Mo­ member, and near its top there are a few very large (as bridge Member. Although stratigraphers have consist­ much as 3 ft in diameter) limestone concretions. Ben- ently recognized the Virgin Creek, Mobridge, and Ell* tonite beds in the Elk Butte Member are sparse and Butte Members (see Crandell, 1958, fig. 4), there are r- usually less than an inch thick. number of difficulties in determining the boundaries of the Mobridge Member. In the southern part of Soutl TYPE SECTIONS OF THE MEMBERS Dakota, " * * * the lower and upper contacts of the The lower part of the Virgin Creek Member was chalky Morbridge zone are sharp and easily found still well exposed in 1962 at the type section, but the * * V according to Gries (1942, p. 27). But Crandell upper part of this member was not. The perforated con­ (1958, p. 16-17), working in the vicinity of Pierre, cretions described by Searight from the lower part S. Dak., had some difficulty in choosing the contacts of of the upper zone of the Virgin Creek were weather­ the Mobridge Member. He concluded that "The base of ing out of the gumbo-covered slopes at and near the the Mobridge Member thus is here [Pierre area] defined type locality. The concretion layers described by - as the contact between calcareous shale that weathers to right at and near the base of the Virgin Creek Mem­ a grayish-orange ('buff') color and somewhat calcareou^ ber were still visible. shale that weathers gray." Crandell also used color The type section of the Mobridge Member is a series change to define the contact between the Mobridge and of readouts which apparently were fresh when Sea- Elk Butte Members. He stated (1958, p. 18) that "Th*, right measured the section but which are now heavily contact used to delimit the two members is the line of soil covered and poorly exposed. The construction of the division between the grayish-orange-weathering shale of Oahe Dam, near Pierre, has created a lake which had the Mobridge and the gray gumbo-forming beds of tha, covered part, if not all, of the Virgin Creek Member Elk Butte Member." Rothrock (1947), who studied tbs exposed at the type locality of the Mobridge Member Pierre Shale in and around the type area of the Mo­ in 1962. In addition, there seemed to be many slump bridge Member, also was unable to determine consist­ blocks, some quite large, in the vicinity of the 'type sec­ ently the contacts of the Mobridge Member on the basis tion. It is now impossible to determine whether Sea- of the reaction of the shale to acid. Furthermore, lie right's description of the type section included any of apparently recognized no color change that he couH these slump blocks. use to define the contacts because his new criteria fcr The type section of the Elk Butte Member, which member definition did not include color. consists of small exposures along 4 miles of old U.S. Like Rothrock, I have found that first and last occur­ Koute 12, extends from the top of Rattlesnake Butte, rences of calcareous shale vary in stratigraphic position erroneously called Elk Butte by Searight, to a short from section to section and that no color change or distance west of Wakpala. Here again, exposures, which other lithologically or faunally distinct horizons con­ must have been fresh when Searight visited the area, sistently parallel these changes. were heavily covered in 1960. Even the part of the The contacts of the Mobridge Member with the Virgin section that extends up Rattlesnake Butte was too Creek and ,Elk Butte Members in north-central South heavily weathered and talus covered to permit, observa­ Dakota are entirely gradational. The markedly lighter tion of the rock. color that sets off the Mobridge Member from the Elk Butte and Virgin Creek Members to the south is not GENERAL DISCUSSION OF THE LITHOLOGIC SUBDIVISIONS noticeable in the area investigated. In order to delimit Modifications of Searight's (1937) stratigraphic in­ boundaries of the Mobridge Member more precisely, terpretations of the upper part of the Pierre Shale have some authors have chosen bentonite beds and concretion been of two general kinds. One, of lesser significance, horizons as markers. Because of the local extent of such has been the clarification of the local lithology. Those markers, however, they are of no use in defining widely who have studied the sequence in more detail than Sea- recognizable boundaries. No attempt is made here to right, and with different purposes, have naturally un­ establish precise limits of the Mobridge Member, ard covered new facts or have made new interpretations of the boundaries of the member are considered to be inter­ old facts. For the most part these local details sup­ vals of transition between calcareous and noncalcareous plement rather than modify Searight's description of rocks. For purposes of graphic representation, however, 6 FORAMINIFERA, STRATIGRAPHY, PIERRE SHALE, FOX HILLS SANDSTONE, S. DAK. the boundaries of the Mobridge Member are shown as use a framework of key beds, but he failed to present lines that mark the first and last occurrences of signifi­ either measured sections or adequate discussion of his cant thicknesses of calcareous shale. new subdivision boundaries. The criteria or which he In summary, the upper part of the Pierre Shale, al­ based his subdivisions could not be recognized in the though quite) homogeneous in its general character, can course of this study, and, consequently, I could not apply be subdivide^ primarily on the basis of detectable cal­ his subdivisions to the stratigraphic succession. cium carbonate. The calcareous middle part of the rock Hereafter, the terms Virgin Creek, Mobridge, and succession is the Mobridge Member, the Virgin Creek Elk Butte are used only to denote the lower noncalcar- Member being below and the Elk Butte Member above. eous, middle calcareous and upper noncalcareous lith- The contact^ between these members are gradational ologies, respectively, with no precisely defined bound­ and probably not precisely synchronous over the area aries implied. investigated. Although recognition of the Mobridge Member solely based on content is less DISTINCTIVE FEATURES OF THE UPPER PART OF THE PIERRE SHALE precise than Searight (1937) originally intended, the basic distinguishing calcareous character of the Mo­ Generally speaking, the upper pant of the Pierre bridge is retained. In all probability the increased cal­ Shale is lithologically monotonous, but it does contain cium carbonate content of the Mobridge Member reflects many distinctive features which have been referred to an environmental change which resulted either in an by previous workers. Some of these features I have absolute increase in production of calcium carbonate or found useful in correlation. Color of the shale, steepness an increase relative to the rate of sedimentation. If so, of outcrop slope, and size and nature of fr°> particles any contact determined solely on calcium carbonate con­ produced by weathering have all been used by others to tent will be gradational, in the sense that the strati- characterize! various parts of this shale sequence. How­ graphic level at which the calcium carbonate increase ever, these features are largely dependent upon the de­ first becomes noticeable will vary between outcrops and gree of weathering to which the outcrop has been sub­ even within single outcrops. However, local fluctuations jected. Although such features may be charscteristic of of calcium carbonate content may reflect local and atypi­ particular types of shale after a certain amount or kind cal diagenetic or postdiagenetic conditions. of weathering, they are of limited use in st-atigraphic Because only two measured sequences cross the Virgin work. Creek-Verendrye boundary as defined by Searight, little Concretions in the shale exhibit a wide range in size, can be said concerning the nature of this contact. Where color, reaction to acid, and composition. Small, various­ it was observed, there seemed to be no lithologic change ly shaped, white-weathering, very calcareous, not very at all. The boundary between these two members has compact, and commonly perforated concretions with or been termed gradational by Gries (1942, p. 23). without a harder limy core occur in noncalcs.reous shale The boundary between the Elk Butte Member and the at several levels. Crabs and other fossils are sometimes Fox Hills Sandstone was clearly described by Searight found in this type of concretion in the Virgin Creek (1937, p. 50) as gradational, and my own observa­ Member. Larger, ovoid to spherical blue-gray limestone tions confirm this. Several attempts have been made to concretions which also weather white or buff have been define this boundary more precisely by means of "jaro- found at many levels. They are not confined to any par­ site" and other distinctive layers in detailed local strati- ticular type of shale and locally contain fossils. They graphic studies (Waage, 1961, p. 232, 233; Rothrock, may be septariate, and hi many the cracks are filled 1947, p. 5). In this investigation, the contact has been with yellow crystals. Most concretions observed selected at or near a subjectively determined change during this study weather rusty red and are discoidal from silty shale to clayey silt. Again, for purposes of in shape. The interiors of these concretions range from graphic representation, this boundary is shown as a brownish gray and moderately calcareous to brick red sharp line rather than as a gradational interval. and noncalcareous. Reduction in calcareous content g'en- One of the original aims of this investigation was to erally parallels increase in redness in these concretions, delimit the members of the upper part of the Pierre but the existence of calcareous red-cored concretions and Shale more precisely, and it is unfortunate that no sound noncalcareous gray-cored concretions indicates that this criteria for accomplishing this purpose could be found, parallelism is not complete. In several places concre­ especially as the type sections of the Elk Butte, Mo­ tions that are predominantly gray with only a thin red bridge, and Virgin Creek Members lie within the area rind have been traced from fresh exposures onto more investigated. Rothrock (1947) attempted a more precise weathered slopes where the concretions in the same definition of lithologic units in this area by trying to layer are red all the way through. At one place this type METHODS OF CORRELATION of concretion weathered a deep purple and had a pol­ jectively rated, and the shale was designated very, quite, ished surface. In addition to these more common kinds moderately, slightly, or noncalcareous. These evalua­ of concretions, limy internal molds of the living cham­ tions have been illustrated for all sections discussed in bers of baculites, heavy gypsum incrustations around this report by the vertical lines at the right sides of tin pelecypods and ammonites, and small barite concretions stratigraphic columns (pi. 12). Calcareous shale gener­ have been found. ally contains the most abundant and diversified assem - Bentonite beds are common in the lower two-thirds blages of calcareous Foraminifera, and the calcareous of the upper part of the Pierre Shale and are very com­ reaction may be due to the dissolution of the contained mon in the lower one-third. They are typically waxy tests of these fossils or of their recrystallized remains'. yellow or green and have a sharp basal contact and a The scarcity of calcareous-shelled macrofossils and gradational upper contact. Many bentonite beds are macrofossil molds suggests that they did not contribute graded, and in these the silty lower part contains abun­ much calcium carbonate to the shale. Any contributior s dant dark flakes of biotite and clear angular quartz by organisms smaller than Foraminifera, such as coc- grains. Several distinctive materials are frequently colithophores, are not known. associated with the bentonites and sometimes replace The lower part of the Virgin Creek Member has been them. These include thin stringers of vertically fibrous described as siliceous by Rothrock (1947, p. 12), who calcite, bands with cone-in-cone structure, and limestone stated "A short distance south of [the mouth of] the concretions 3 to 12 inches thick. The most common asso­ Moreau [River] this zone [lower part of the Virgin ciate is a powdery yellow mineral, questionably identi­ Creek] becomes siliceous and north of the Moreau as fied as melanterite. The same or a similar mineral occurs far as it could be traced it was entirely siliceous." Radio- in the Fox Hills sandstone and has been called jarosite, laria, which are often found in siliceous shales, were bentonite, and melanterite (Waage, 1961, p. 233). found in samples from two sections of the lower part Melanterite(?) occurs directly above and (or) below of the Virgin Creek Member (fig. 1, loc. 1, 3). The few many bentonites, and the stratigraphic intervals of in­ calcareous Foraminifera in this interval are usualhT dividual bentonite beds are sometimes occupied solely preserved as internal molds in silica or are filled with by 'beds of shale containing considerable amounts of silica. In addition to these occurrences, have melanterite(?). Whether this mineral is an alteration been found through considerable stratigraphic thicl-- product of bentonite or is related to it in some other way nesses of shale at localities 44, 49, and 52 and in tire is not known. It also occurs independently of discrete lower part of the Fox Hills Sandstone at locality 50. bentonite beds as scattered pods and blebs in the shale. Through each of these intervals the few specimens of The vertically fibrous calcite, cone-in-cone structure and calcerous Foraminifera that are present are silicified. limestone concretions also occur independently of dis­ These noncalcareous Radiolaria-bearing shale intervals crete bentonite beds as well as being associated with resemble the lower part of the Virgin Creek Member but them and occupying the stratigraphic positions where differ because they are less fissile and more clayey anrl the bentonites themselves are absent. lack heavy staining. Rubey (1929) discussed in detail During the course of fieldwork an effort was made to the origin of the siliceous Mowry Shale and concluded determine the silt-sand content of the shale at regular that the silica was derived from the alteration of vo1- intervals for each measured section. A small piece of canic ash. He stated (1929, p. 153) that "As a probable fresh shale was crushed between the teeth and the degree method of this derivation, it is suggested that tire of grittiness subjectively assigned to one of five cate­ original ash was unusually siliceous, that it was decom­ gories ; very, quite, moderately, slightly, or iionsilty. The posed by long exposure to sea water, and that silica variations in silt-sand content so determined do not dissolved from it was precipitated by decaying organic appear to bear any consistent relationship to other litho- matter." The exhaustive information on which Rubey logic features and are apparently of only limited lateral based his conclusions for the Mowry Shale is not avail­ extent. Generally speaking, the silt-sand content is low able for the upper part of the Pierre Shale. Howeve^, throughout most of the upper part of the Pierre Shale for the bentonitic shale in the lower part of the Virgin but gradually increases as the Fox Hills sandstone is Creek Member at least, similar conditions may have approached. This increase eventually results in the produced the abundance of silica reflected in the pres­ transition of the shale into the clayey sandy silt of the ervation and composition of the microf auna. basal part of the Fox Hills sandstone. Calcareous content was determined on the outcrop by METHODS OF CORRELATION putting a few drops of 10-percent hydrochloric acid on The sections measured along the Grand and Moreau a fresh chunk of shale. The degree of reaction was sub­ River valleys have been fitted together (figs. 4, 5) to 8 FORAMINIFERA, STRATIGRAPHY, PIERRE SHALE, FOX HILLS SANDSTONE, S. DAK. establish the stratigraphic sequences in these major measured. In the following paragraphs the nature of areas of outcrop. Correlation of local sections is com­ these composite sequences is explained, and pertinent plicated by a considerable amount of slumping that details are noted. involves both large and small bodies of shale. Most sections contain one or more key beds which make cor­ STRATIGRAPHIC SEQUENCE ALONG THE MOREAU relation with other nearby sections possible. The most RIVER useful key beds are bentoiiites, but concretion horizons, Of the sections measured along the Moreau River (see zones of increased or decreased calcareous content, and figs. 1, 4) only sections 1 and 3 extend to the base of other distinctive lithologic features were used as a the Virgin Creek Member. The base of section 1, which check on the correlations based on bentonites and were is within half a mile of the type locality of the member, themselves used for correlations where bentonites were is at the more persistent and lower of two clor^ly spaced absent. Dependence on bentonites for correlation gradu­ concretion horizons, presumably the concretion layer ally increased during the course of fieldwork as it be­ which Searight described as forming the base of the came apparent that they persisted farther laterally than member. Section 1 was correlated with section 3 on the other lithologically distinctive beds. In addition, ben­ basis of the numerous thin bentonites and fissile maroon- tonites are ideally suited for correlation because indi­ to purple-stained shale in the lower parts of both sec­ vidual beds precisely define time planes. Generally tions. Seven thin bentonites occur in the lower 20 feet of speaking, the thickest beds were recognizable over the section 1, and five occur in the lower 20 feet of section widest areas. Beds less than an inch thick locally dis­ 3. In both sections the distinctive staining and fissility appeared between sections only a few miles apart, but gradually disappear above the bentonite interval, and their levels were commonly marked by vertically fibrous in section 3, which extends much higher, the shale calcite, cone-in-cone structures, or beds of shale con­ grades imperceptibly into the overlying nonfissila cal­ taining melanterite( ?). careous shale. The first calcareous shale occurs about Macrofossils are too rare in the upper part of the 58 feet above the base of section 3. The upper limit of Pierre Shale to be useful for local correlation, but their the silicified and siliceous microfauna and the initial regional distribution is better known, and they are use­ increase in the number of species and specimens of cal­ ful for broader scale correlations. The opposite is true careous Foraminifera occur 5 to 10 feet belor7 this level. for Foraminifera. In order to use the Foraminifera The calcareous shale that is more or less persistent most successfully, it was necessary to establish a refer­ throughout the remaining 75 feet of section 3 contains ence stratigraphic sequence by physical means. The 12 bentonite beds. stratigraphic positions of other sections were then in­ Correlation of section 3 with sections 4 and 7 was ferred by comparing their microf aunas with the micro- made based on two of the uppermost and tHckest ben­ faunas of the reference sequence. The assumptions were tonites. In section 7 the upper of these bentonites is that changes which took place in the microf auna at one overlain by 65 feet of calcareous shale containing only locality also took place over a wider area and that these a few thin bentonites. This interval is cr.pped by a changes were synchronous, or nearly so, over this area. prominent and persistent bentonite, referred to here­ Generally speaking, the more species of Foraminifera in after as the "lower key bentonite," which attains a thick­ a sample, the more closely the sample could be related ness of 10 inches in section 7 but is less than 4 inches to samples from other sections. Species that were abun­ thick in section 20 farther to the west. Ovoid, tan- to dant within limited stratigraphic ranges are the most buff-weathering calcareous concretions and more dis- useful for relating sections, and a list of such species coidal rusty-weathering calcareous concretions are com­ and their ranges in the area is given in figures 2 and 3. mon locally above this bentonite, though none were found in section 7. COMPOSITE STRATIGRAPHIC SEQUENCES The shale is mostly calcareous for 54 feet above the Figures 4 and 5 illustrate the composite stratigraphic lower key bentonite, but noncalcareous rust-stained beds sequences along the Moreau and Grand Kivers, respec­ of shale, some of which contain pods and ble^s of melan- tively. It is not considered feasible or necessary to de­ terite(?), are present at various levels. In the sections scribe all 74 sections measured during this investigation. to the west, this interval is capped by a second thick Figures 4 and 5 show the 23 sections from which samples bentonite, referred to hereafter as the "upper key ben­ were examined for . This group of sections tonite," which is 16 inches thick in section 27 but de­ contains the more stratigraphically significant ones creases in thickness to the east. This bentonite layer is FORAMINIFERA, STRATIGRAPHY, PIERRE SHALE, FOX HILLS SANDSTONE, S. DAK. absent in section 7, where its level is occupied by a layer STRATIGRAPHIC SEQUENCE ALONG THE GRAND of shale 3 to 4 feet thick which contains considerable RIVER amounts of melanterite (?). The lowest sections measured along the Grand River Calcareous shale persists for as little as 12 feet to as (see figs. 1, 5) are along a railroad cut in the vicinity much as 49 feet above the upper key bentoniite. The sec­ of Wakpala, S. Dak., and begin in calcareous shale. In tions used in compiling figure 4 show a general thick­ these sections, the lower 15 feet of shale generally con­ ening of this interval to the west, but this situation is tains white to buff-weathering calcareous concretions; fortuitous. Several other sections measured in the in some sections these concretions continue to 80 fee4 vicinity of localities 11 and 20, but not shown in figure above the base. A single bentonite bed 1 to 3 inche^ 1, have more calcareous shale above the upper key ben­ thick, interpreted as correlative with the lower key ben­ toniite than either section 11 or section 20, and one has tonite in the Moreau Eiver sections, is present in th^ more than section 44. The change from calcareous to lower part of the sequence. This single bed occurs 48 noncalcareous shale is gradual and varies in strati- feet above the base of section 41, and farther to th^ graphic position from section to section and even from north, it occurs 39 feet above the base of section 42 and place to place on the same exposure. In several sections, just above the base of section 44. In section 37, a short rusty-weathering discoidal noncalcareous to slightly distance south of section 41, its level is occupied by a calcareous concretions are present through 10 to 30 4- to 6-inch-thick layer of indurated very calcareous feet of shale beginning 14 to 42 feet above the upper key marl 48 feet above the base of the section. The interval bentoniite. Despite its thickness, this concretionary in­ between the lower and upper key bentonites in section terval is not present in all sections. 44 is characterized by a lack of bentonites, few concre­ The shale is noncalcareous from the top of the cal­ tions, generally slight and sporadic calcareousness, and careous shale interval just described to the base of the scattered pods and blebs of melanterite(?). This inter­ Fox Hills Sandstone. It is characterized by fairly nu­ val is capped by a 4- to 12-inch-thick bentonite in siv merous but not very persistent concretion horizons and sections, three of which are illustrated in figure 5. This by a very few thin bentonites. One fairly persistent bed was correlated with the upper key bentonite of th°» bentonite l1/^ to 1% inches thick is present between 60 Moreau Eiver stratigraphic sequence. Calcareous shata and 70 feet above the upper key bentonite in section persists from 4 to 10 feet above this bentonite in all six 27A and in several sections not shown in figure 4. The sections before giving way to noncalcareous shale. contact between the Pierre Shale and the Fox Hills About 192 feet of noncalcareous shale is present be­ Sandstone is considered to be at 103 feet above the top tween the base of the Fox Hills Sandstone and the too of the Mobridge Member in section 27A on the basis of the calcareous shale. Correlation of the sections of a lithologic change from silty shale to clayey silt and which consists only of rocks from this interval was on a color change from brownish-gray shale to grayish- difficult 'because of the lack of marker beds. A few thin brown silt. Both gram size and color changes are grada- bentonite beds, some of which contain small subspherr- tional, and the choice of an exact level for the contact cal bladed barite concretions, occur but do not persist was arbitrary. Correlation between sections 27A and laterally. Section 49, which is correlated with section. 31 is based on the Pierre-Fox Hills contact and must 44 by means of the upper key bentonite, contains a be considered approximate. In section 31 the change 1-inch bentonite 54 feet above the upper key bentonito. from silty shale to clayey silt, which is again grada- This 1-inch bentonite has been correlated with a 14-inch bentonite 9 feet above the base of section 54, but ther°, tional, was used to delimit the contact. As thus cor­ are no supplementary criteria, either from these or ir- related, the concretion horizons in these two sections are tervening sections, to substantiate this correlation. not well matched, presumably because of a lack of Sections 54, 53, and 52, all within half a mile of each lateral persistence. other, were very difficult to correlate. Correlations wei^ The Fox Hills Sandstone in section 31, where 74 feet made by elevation as determined by sighting through of it is exposed, is a clayey silt, containing a few inter- a hand level because none of these sections contains key beds of silty shale and shale. In section 27A, most of horizons which could be recognized confidently in other the 39 feet of exposed Fox Hills is shale; only the lower sections. Silt and sand content rapidly increases, begin- 6y2 feet is clayey silt. This lithology is not typical of ing about 32 feet above the base of section 52, and the lower part of the Fox Hills in more easterly ex­ clayey, sandy silt predominates at 40 feet above the bare posures and must be due to f acies changes within the of the section. The contact between the Pierre Shale and lower part of the Fox Hills, assuming that the Pierre- the Fox Hills Sandstone is arbitrarily placed 40 feet Fox Hills contact recognized here is correct. above the base of this section. 10 FORAMINIFERA, STRATIGRAPHY, PIERRE SHALE, POX HILLS SANDSTONE, S. DAK. About 23 feet of silty noncalcareous shale is exposed About 22 feet of the Fox Hills Sandstone is exposed below the Pierre-Fox Hills contact in section 50 where in section 52, and about 71 feet is exposed in section 50. the contact has been placed just below a concretion hori­ The Fox Hills in these two sections is predominantly zon containing the characteristic basal Fox Hills am­ unstratified sandy, clayey silt. Because detailed study monite Discoscaphites nicolleti. The rock is a silty clay of the stratigraphy of the Fox Hills Sandstone was for about 7 feet above this level before grading into outside the scope of this study, no attempts p,t correla­ siltstone. tion or member subdivision were made.

S '5 r« s K : s r S i C j i E % ; ^ £ < Top of ! ~ 5- - S s, iCJ 0 0 &3 S c c? C3 t.5 =5 C ? >Z cB '< <*5 a5 a :3 t! s^

-- - I 350'- 1 i r0) CD . UJ 300'-

Upper key bentonite 250'~

Lower key .*> bentonite 200'-

s? 1 b D_ i1

DC 150'- £ O

100'-

' L

. t- 50'- tu 'ys Base of > section i rv-

FIGURE 2. Ranges of Foraniinifera useful in local correlation of the upper part of the Pierre Shale and lower part of the Fox Hills Sandstone relative to the composite stratigraphic sequences along the Moreau River. Thickness of the interval between the lower and upper key bentonites is1 the average of the interval's thickness at localities 7, 11, and 13. Thickness of the interval between the upper key bentonite and the top of the Mobridge Member is the average of the interval's thick­ ness at localities 7,11,13, 20, and 27. FORAMINIFERA, STRATIGRAPHY, PIERRE SHALE, FOX HILLS SANDSTONE, S. DAK. 11

RELATIONSHIP OF THE SEQUENCES The calcareous Mobridge shale grades upward into non- The relationship between the generalized strati- calcareous, slightly fissile shale of the Elk Butte Mem­ graphic sections along the valleys of the Grand and ber. Approximately 103 feet of noncalcareous Elk Butte Moreau Rivers is shown in figure 6. In the Moreau shale lies between the highest calcareous shale and tin sequence the lower 58 feet is noncalcareous shale of the base of the Fox Hills Sandstone. Bentonite beds ar-*, Virgin Creek Member. This grades upward into gen­ common in the Virgin Creek and Mobridge Members', erally calcareous and more readily decomposed shale of Two of these, designated the lower and upper key the Mobridge Member that persists for about 218 feet. bentonites, are more widespread and generally thicker

'C ^ 5 S

0 5 a s s ; » 13 . 0 I s 3 S - ^ 3 3 e+H -O c ^3 2 2 i s 1 2 r : s: S = ^ * *l i 2 c 5 3 ; o4 D I I ^ h a, 3 ^. -a 2 3 . i <*H ; H>: ^ e*H 1 ^ 3 3 S 2 0 a g o £ J * ^ S 0 . .£ i = s 1 ' a " c i ; s = £ ^ " i 'i " s a 1 =«3 a -< S 3 3 3 2 .s" a -~ M ft ~ s . i g C t Ss " ~ * S " 0 r - 3 i ~i " c S r - ~ rf - S e : s 3 § 2 ^ ^ S a 3 S s w ^.5 * : | £ s s -^5 JB | f. "g 5 ~t3 1 s « s SS Top oi s s :u u s u S £ | | § C3 ;?&d s? C S 25 oq c ~j C5 c3 o3 C3 ^ EC *5 ' section i c q t ' t- a; fi 350'-

c TO 300'- \i 250'-

XI ._ 200'- - ^ i 0) UJ (O

(/) 150'- V

ix

Upper key 100' bentonite

Member Lower key ' bentonite $Q'_

00 .a o S Base ol section

FIGURE 3. Ranges of Foraminifera useful in local correlation of the upper part of the Pierre Shale and lower part of the Fox Hills Sandstone relative to the composite stratigraphie sequences along the Grand River. Thickness of the interval between the upper key bentonite and the top of the Mobridge Member is the average of the interval's thieknesis at localities 44 and 49. 12 FORAMINIFERA, STRATIGRAPHY, PIERRE SHALE, FOX HILLS SANDSTONE, S. DAK. than the others. These two bentonites were useful for grades upward into the silts and sands of the Fox Hills correlation of both near and distant sections and were sandstone. Bentonite beds are much less common in the used as reference levels for the stratigraphic work. On Grand River sections, but both the upper and lower key a more local scale, other bentonites and laterally per­ bentonites were recognized. sistent features were also utilized for correlation. In the Moreau River sequence, and to a greater extent Calcareous shale of the Mobridge Member occurs at along the Grand River, sections above the upper key the base of the Grand River sequence and persists up­ bentonite were difficult to correlate because of the lack ward for about 93 feet before grading into the non- of persistent bentonites and the general unreliability or calcareous shale of the Elk Butte Member. The non- scarcity of concretion horizons. Foraminifera were of calcareous Elk Butte shale is about 192 feet thick and little help because only a few long-ranging and non-

FEET -50 - 40 - 30 - 20 - 10 -0

Lower key bentonite

Datum Section 3

Base of Mobridge Membe

Datum Base of Virgin Creek Member/ of Pietre Shale

53/i 7% 111/, HORIZONTAL DISTANCE, IN MILES

FIGUBE 4. Correlation chart of stratigraphic sections along the Moreau Biver and environs (see fig. 1 for location of sections). RELATIONSHIP OF THE SEQUENCES 13 diagnostic species are present, particularly in the upper Upland lacking any adequate exposures of Piei^e part of the Elk Butte Member. Shale extends for 21 miles and separates the two closest The upper key bentonite, because of its importance sections in the valleys of the Moreau and Grand Rivers in relating the two stratigraphic sequences, is discussed that include the upper key bentonite (sections 5, and in more detail. This bentonite varies in thickness from 49, figs. 4, 5). The identity of this bentonite along bo+h 0 to 16 inches in the Moreau River valley and occurs in rivers is accepted because it is the highest thick and sections as much as 27 miles apart. It thins considerably persistent bentonite beneath the Fox Hills Sandstone to the southeast and is absent in section 7 where its level and because it is the only thick bentonite in the upper is occupied by a 3- to 4-foot bed of shale heavily inter­ part of the Mobridge Member. In the Moreau River laced with melanterite( ?). In the Grand River valley sections it is usually 10 to 30 feet below the change from this bentonite varies in thickness from 4 to 12 inches and calcareous to overlying noncalcareous shale, and in the occurs in section as much as 18 miles apart. Grand River sections it is 4 to 10 feet below this change.

FEET

- 40 - 30 - 20 - 10 - 0

Top of Mobridge Me of Plerre Shale

Datum Upper key bentonite

key bentonite

V3 X " 7 ^^1/2^' ~ 11 '5 31/2 ' 2 ' 2iA 3% 61/z

HORIZONTAL DISTANCE, IN MILES

FIGURE 5. Correlation chart of stratigraphic sections along the Grand River and environs (see fig. 1 for location of sections). *Indicates section could not be correlated on the basis of lithology or key beds. Foraminiferal ranges indicate section is between 0 and 150 feet below the lower key bentonite. Dashed line indicates partly exposed section. 323-073 O 69 2 14 FORAMINIFERA, STRATIGRAPHY, PIERRE SHALE, FOX HILLS SANDSTONE, S. DAK.

Virgin Creek Member

FIGURE 6. Foraminiferal biofaeies in composite stratigraphic sections of the upper part of the Pierre Shale and lower part of the Fox Hills Sandstone along the valleys of the Moreau (left) and Grand (right) Rivers. REGIONAL CORRELATION

The lowest and highest occurrences of most species of the Gulf Coast where their local ranges are well known. Foraminifera match well between the two stratigraphic Therefore, it is possible to compare the upper part of sequences when they were correlated on the basis of the the Pierre and the lower part of the Fox Hills forminif- upper key bentonite. Thus the f aunal evidence, although eral faunas with those of the Gulf Coast. not conclusive, supported the correlation. Of the 86 species of Foraminifera positively or ten­ Matching of the Grand and Moreau stratigraphic se­ tatively identified from the upper part of the Pierro quences based on the upper key bentonite placed the Shale and the lower part of the Fox Hills Sandstone, 3-inch bentonite of the Grand River stratigraphic se­ seven are new. Sixty-two were reported from the Cre­ quence, which is the thickest and most persistent taceous deposits of the Gulf Coastal Plain as summa­ bentonite between the upper key bentonite and the base rized by Cushman (1946). The remaining 17 specie? of the sequence, in approximately the same stratigraphic either were not noted by Cushman or have not been position as the lower key bentonite of the Moreau se­ definitely identified from the Gulf Coastal Plain. O* quence, and consequently they are considered to be the the 62 species in common, 15 occur only in beds of Na- same bed. varro age, 15 occur only in beds of Taylor and Navarro ages, 19 range from Austin to Navarro age, six occur BIOSTRATIGRAPHY only in beds of Taylor age, five occur only in beds of REGIONAL CORRELATION Austin and Taylor ages, and two occur only in beds of Macrofossils, which are very rare in the upper part Austin age. The stratigraphic occurrences of these spe­ of the Pierre Shale, have traditionally served as the cies in the Gulf Coast deposits are illustrated in table 1. means of regional correlation in the western interior. The correlation chart of Cobban and Reeside (1952) in­ The intensive studies of the of the western dicates that the Navarro-Taylor boundary in the western interior by W. A. Cobban have made them the most interior is well below the base of the Virgin CreeV useful group for correlation within the region and have Member of the Pierre Shale. Therefore, the presence of permitted interregional correlation. The 13 species of Foraminifera in the Pierre faunas which species Bacidites clinolobatus Elias, present in the lower do not range into Navarro age beds in the Gulf Coast, and middle parts of the Mobridge Member, can be re­ according to Cushman (1946), deserves attention. lated to Cobban and Reeside's (1952) zonal scheme. 13 species are listed below: According to Cobban (1958, p. 114), B. clinolobdtus is the immediate descendant of B. grandis Hall and Meek. Species Range B. grandis occurs in beds correlative with beds of prob­ Astacolus cretaceus (Cush­ Reported from beds of man). trichtian age (according to able early Maestrichtian age in Europe and with beds Cobban and Reeside (1952, in the upper one-third of the Navarro Group of the chart lOb), the Maestrichtian Gulf Coast. Clearly, B. clinolobatus represents a slightly includes the late Navarro) in later timespan than does B. grandis. Puerto Rico (Pessagno, 196% The study of Foraminifera in the western interior p. 94). Nodosaria cf. N. aspera Ruess- Reported from the Maestricli- stands in contrast to the study or cephalopods and tian of western Siberia (Gla- some other macrofossil groups in that no systematic zunova and others, 1960, p. attempt has been made to discover the occurrence and 87). distribution of foraminiferal species. Once this is done, Nodosaria proboscidea Reuss_ Most commonly reported from beds of late Taylor age. Ore there is no reason Foraminifera should not be as useful questionable reference to this in regional correlation within the western interior as species from beds of Cana- macrofossils currently are. The planktoiiic Foraminif­ p a n i a n-Maestrichtian are era are considered to be most useful for interregional made by Pessagno (I960) from the Cretaceous of correlation. Unfortunately, the four planktonic species Puerto Rico. found in the upper part of the Pierre Shale were of little Paltmila primitive, Cushman-_ No record higher than latent use in precise correlation because their ranges are long Taylor. or poorly known. Benthonic Foraminifera, predominant Nodosaria gracilitatis Cush­ No record above late Taylor. man. in the upper part of the Pierre and lower part of the Rectogunibelitia minuta Cush­ Apparently only one occur­ Fox Hills, are presently less useful than the planktonics man. rence of this species has been in interregional correlation because of their much less discovered, in beds of Taylor age, though this occurrence finely divided age ranges. However, most of the ben- has been reported three thonic species are present also in Cretaceous deposits of time®. 16 FORAMINIFERA, STRATIGRAPHY, PIERRE SHALE, FOX HILLS SANDSTONE, S. DAK. Species Range kind of scrutiny in order to determine which may be Gaiidryina bentonensis (Car­ Reported by Cushman and Renz considered to be reliable indices of Navarro age. The man). (1946, p. 10) from the upper zone of the Lizard Springs ranges of each of these species in areas other than the Formation of Trinidad, which Gulf Coastal Plain are considered below: they considered to be of latest Range Cretaceous age. Species HeteroJielia pulcJira (Brot- Reported from beds of Mae- Astacolus jarviselliis Mello, Most references are from beds zen). strichtian age in Denmark new name. of Navarro age or equiva­ (Hofker, I956a, p. 77) and lents, but this species has Egypt (Ansary and Fakhr, been reported from beds as 1958, p. 121). old as Coniaciar and San- Robulus taytorensis (Plum- Reported six times from beds of tonian in California (Tru- mer). Taylor or Austin age. jillo, 1960, p. 317). Spiroplectammina laevis (Ro- Reported from late Campanian Cibicides liarperi (Sandidge)- No reports of this species from emer) cretosa Cushman. (equivalent to the early and rocks older than Navarro middle Navarro, according to age. Cobban and Reeside (1952, Neobulitnina navarroana Do. chart 10b)) of Bavaria (Cushman). (Hagn, 1953, p. 9), and from Bulimina reussi Morrow na- Do. the Mt. Laurel and Navesink varroemis Cushman and Formations (of Navarro age, Parker. according to Stephenson and Astacolus navarroanus (Cush­ Do. others (1942, chart 9)) in man). New Jersey (Jennings, 1936, Astacolus dissonus Plummer_ Do. p. 12). Bolivina decurretis (Ehren- Do. Nodosaria fustila Reuss. The few references to this spe­ berg). cies are all from beds of Gaudryina watersi (Cush­ Do. Taylor or Austin age. man). Planulina Tcansasensis Mor­ Most of the references to this Loxostoma gemma ( Cush­ Do. row. species are from the Niobrara man). Formation of the western Osangularia navarrowna Do. interior, with a few reports (Cushman). from beds of equivalent Robulus spissocostatus Cush­ Do. Austin age in Gulf Coastal man. Plain deposits. Bulimina arkadelpMana Cush­ Do. Pleurostomella nitida- Mor­ This species has been reported man and Parker. row. only from the Greenhorn Tappanina costifera (Cush­ Do. Formation of Kansas and the man). Austin Chalk of Texas. Marginulina curvatura Cush­ Reported from the Rumoi coal man. fields, Hokkaido, Japan (Fu- To summarize the occurrence data given above, of the kuta, 1957, p. 12) and from beds containing Foraminif- 13 species which do not occur in beds of Navarro age era of Austin, Taylor, and in the Gulf Coast Cretaceous deposits, five species have Navarro ages. Fukuta did been reported in other areas from beds correlative with not correlate the Ruinoi beds the Navarro, one species has been reported with ques­ ,with either Austin, Taylor or tion from beds correlative with the Navarro, at least two Navarro but ir stead com­ promised by calling them species (Rectogiunbelimi minuta and Pleurostomella probably Campanian. Speci­ nitida) have been reported too few times to assign any mens questionably referred age importance to their occurrence, and five species have to this species by Rompf no previous record of occurrence in beds of Navarro or (1960, p. 33) are from the equivalent age. Of these five species, four are repre­ of Germany. sented by a relatively few specimens in the upper part Lagena sttlcata (Walker and There is no puiblisl ed report of Jacob) semiinterrupta W. this species occurring in beds of the Pierre Shale (Palmula pritiutiva is represented Berry. older than Navarro, but by one specimen) but the fifth species, Plwmlina Tcan- Cushman (194£a, p. 256) sasensis, is one of the more abundant species in the stated that the species oc­ curs in beds of Navarro and upper part of the stratigraphic sequence. Taylor ages. The 15 species present in the upper part of the Pierre Shale which are reported only from beds of Navarro age Of the 15 species present in the upper part of the in the Gulf Coast deposits are deserving of the same Pierre Shale and restricted to beds of Favarro or REGIONAL CORRELATION 17 younger ages in the Gulf Coast deposits, 12 have never In summary, in the upper part of the Pierre Shale been reported from pre-Navarro rocks. There is some there are at least five well-established species whicl doubt whether two other species range lower than have not been reported from beds of Navarro or equiva­ Navarro, and one species has been positively identified lent age, and at least 10 which have not been reported from older rocks. Of the 12 species apparently restricted from beds older than Navarro. This indicates a Navarro to beds of Navarro age, two (Tappanina, cost If era and age for the upper part of the Pierre Shale, in accord Osangularia navarroana} have been reported from only with the macrofossil evidence, based on a balance of a few samples, and thus their ranges cannot be con­ evidence. Perhaps the presence of Taylor species indi­ sidered well known. cates a lower Navarro equivalence for the upper part

TABLE 1. Gulf Coast stratigraphic distribution (after Cushman, 1946) of For aminifera found in the upper part of the Pierre Shale and lower part of the Fox Hills .Sandstone [Synonyms under which Cushman recorded these species are given in parentheses!

Austin age Taylor age Navarro age

MarlBonham OzanForma­ ChalkAnnona BipleyForma­ EctorTongue LowerSehna MarlBurditt AustinChalk GoberTongue LowerTaylor MiddleSelma MarlbrookMarl ChalkSaratoga Neylandville SandNacatoch BluffPrairie MarlCorsicana Arkadelphia Brownstown WolfeCity Chalk Chalk Ow £ Marl 02 JM Chalk Marl Marl Marl tion Sand tion §0 1

Astacolus dissonus (Planularia dissona) ...... X X X .... y Astacolus jarvisellus (Marginulina jarvisi) ...... y Astacolus navarroanus (Marginulina navarroana) ...... X X X y X X y Bulimina reussi navarroensis (including Buliminetta carseyae var. plana)...... X X X X y X X y Gaudryina watersi...... X X X X X X y X X Loxostoma gemma ...... X X "x" X Marginulina cursatura...... X XIXXXX e~' X Osangularia navarroana (PulvinulineUa navarroana) .... X X X Robulus spissocostatus ...... X X X X Tappanina costifera (Bolivinita costifera) ...... Astacolus cretace us (Marginulina cretace a) ...... X X X X X X X X X X X X X X X X X X X X X .... Dentalina catenula ...... X X X X X X Dentalina cf. D. consobrina...... X X >' Dentalina pertinens...... X X Eouvigerina hispida ...... Frondicularia archiatiana ...... X X X X X X X Guttulina trigonula...... X Heterohelix globulosa ( Guembelina globulosa) ...... X X X X X X X X X X HeterostomeMa americana...... X X ---- X X X X X X X -y" Hoeglundina supracretacea (Epistomina caracolla) . X X X X X X .... X Palmula reticulata...... X X X X Pyrulina cylindroides...... X X X X X X X y X X X X X X X X X X X - X X X X X X "x" X X X X X Bulimina kickapooensis...... X X X X X X X "x X .... X ...... Cibicides subcarinatus...... X X X X X X X X X X X X V X X X .y.. Dentalina legumen. -..---.-_--._ X X X X - X .... X X "x" X X X X .... X X X Dentalina solvata...... X X X X X X "x X X xxxxxxxxxxx Globulina lacrima (including range of var. horrida) X X "x" "x" X X X X X X .... X X X X X X X X "x" XX!XXXXXX xxxxxxxx X X X X X X X X X X X X X xixxxxxi xxxxxxxix X X y X X X X X X X Loxostoma plaita ...... X X X X X y X X X X X X X x" X X X X X X Nodosaria affinis ...... X X X X X X X X X X X "x" X X X Palmula rugosa ...... X X X X X X X X ?.'.. Quadrimorphina allomorphinoides (Valvulineria allmnophi- X X X X X X X X X X X X X X X X X Stilostomella pseudoscripta (Ellipsonodosaria pseudoscripta) X X .... X X X X ---- X .... X ...... Nodosaria cf. N. aspera X X X X X X X Palmula primitiva. . X X X X x" X X X X X X X X X X ---_ X X X X X Robulus taylorensis ...... X X X X X X X X X X X X X X X X 18 FORAMINIFERA, STRATIGRAPHY, PIERRE SHALE, FOX HILLS SANDSTONE, S. DAK. of the Pierre Shale than has been suggested by correla­ Species Range tion on the basis of ceplialopods. Lagena sp. aff. L. quudralata The general morphologic simi­ Brady. larity between the Pierre The 17 tentatively or firmly identified species, which specimens and sweimens of are neither new or discussed above because of their lack this Recent species is indi­ of occurrence or confused age data in the Gulf Coast cated by this designation. Cretaceous, may also be considered in discussing the age Ramtilina cf. R. muricatina Name was erected to replace Loeblich and Tappan. the name Ramulina aculeata of the upper part of the Pierre Shale. Wright. R. muricaUna has only been reported from the Species Range , mostly from Bathy siphon brosgei Tap- According to Tappan (1962, p. beds of Taylor age, but with pan (?). 128), this species is present some occurrences of Austin in beds of from to late age, according to Cushman Campanian ages in northern (1948a, p. 257). Alaska. Bolivinoides decoratus Assigned a latest Campanian Glomospira charoides (Jones Reported from beds of Bar- ( Jones) australis EdgelL age by Edgell (1954, p. 71) and Parker). remian to Tertiary age. and apparently an early Haplophragnwides rota Tappan (1962, p. 133, 134) re­ Maestrichtian ag^ by Hilter- Nauss and Haplophrag- ported both these species mann (1963, tatles 1, 2). moides bonanzaensis from beds of Turonian to late Eouvigerina aspera (Mars- Noted once and designated of Stelck and Wall. Campanian age. son) inflata Marie (?). Late Cretaceous age. Spiroplectammina mor- In northern Alaska this species Rugoglobigerina cf. H. rugosa There is taxonomic confusion denensis Wickenden. occurs in beds of (Plummer) ______surrounding this species. No and Campanian ages (Tap- generally accepted age limits pan, 1962, p. 140). have been determined, bait most records are from th.e Verneuilinoides cf. V. per- Reported twice from beds of Campanian and Maestrich­ ple&us (Loeblich). Cenomanian age. tian. It has be?n reported Silicosigmoilina futabaensis The range of this species has from beds a® old as Asa no. not been adequately estab­ i&antonian. lished in Japan, where it Biglobigerinella biforaminata Both the taxonorry and the was first discovered. Fukuta (Hofker) ______range of this species are un­ (1957, p. 10) felt that it is certain. It has most frequent­ probably Campanian. The ly been reported from beds only previous reference of of Maestrichtian age, with specimens to this species out­ one reference to it from the side Japan was made by Maestrichtian - Campanian Trujillo (1960, p. 303), who boundary. recorded it from beds of Con- iacian and Santonian ages in California. Of these 17 taxa, the subspecies Bolivinoides deco­ Trochammina globigerinifor- Reported from beds that range ratus australis is of special interest for correlation be­ mis Cushman. in age at least from the Early cause it is a member of a group of species and subspecies Cretaceous to the latest Late which have been related phylogenetically and which are Cretaceous and probably into the Tertiary. of rather limited geologic range. Its age is considered Trochammina globosa Bolin__ The type reference (Bolin, latest Campanian or early Maestrichtian, and it is the 1956, p. 289) is the only pub­ most precisely defined taxoii, with respect to age, in the lished reference to this entire upper Pierre fauna. It occurs in tv^o samples species; Bolin reported it from beds of questioned from the upper part of the Pierre, one at 5 feet below Cenomanian age. and one immediately below the lower key b^ntonite in Dentalina niobrarensis Loet- Reported twice from the Nio- section 41. terle. brara Formation of Coni- The foraminiferal evidence suggests that the upper acian-Santonian age. part of the Pierre Shale is more likely of early than Rectoglandulina appressa The only reference (Loeblich late Navarro age and that it is close to the Campanian- Loeblich and Tappan. and Tappan, 1955, p. 4) to o *- this species is from the Upper Maestrichtian boundary. Cobban and Keeride (1952, Cretaceous of Arkansas and chart lOb) questionably placed the Campanian- Texas where the species was Maestrichtian boundary within the Mobridgft Member; reported from beds of Seno- nian, early Campanian, and this placement agrees well with the age indicated by Maestrichtian ages. B. decoratus australis. PALEOGEOGRAPHIC SETTING

COMPOSITION OF THE FAUNA PALEOECOLOGY A total of 101 species and subspecies of Foraminifera PALEOOEOGBAPHIC SETTING were found in the upper part of the Pierre Shale and Tourtelot's (1962, p. 10) conception of the regioral lower part of the Fox Hills Sandstone. It was possible paleogeography of the western interior during the time to identify 86 of these, at least tentatively, to the spe­ of deposition of the Pierre Shale is as follow "The cific or subspecific level. Of these 86,17 taxa have arena­ Pierre Shale and equivalent rocks were deposited in ceous (agglutinated) or siliceous tests, and 69 have cal­ and adjacent to a relatively narrow and shallow sea careous tests. Four species (HeteroheUx globidosa, H. extending southward across the present western interior pulchra, Rugoglobigerina cf. R. rugose^ and Biglobig- region of the United States. The sea probably was CCTI- ermetta biforaminata) are planktonic. In addition, sev­ nected at the north with world oceanic waters and at the eral kinds of radiolarians, fish bones and scales, scole- south from time to time with the of the Gulf Coast. codonts, rare spicules, echinoid spines and ophi- The eastern shore area of this sea has not been preserved uroidea ossicles, several genera and species of ostracodes, and the Pierre rocks contain little evidence of its nature. and what appear to be crushed spore cases were recov­ It must have been made up, however, of rocks of Pre- ered from the samples. and Paleozoic age that probably formed a Relatively few genera and species of macrofossils broad nearly stable lowland in the present midconti- were found. Specimens of Baculites occur sporadically nent region. * * * During much of Pierre time * * * the from the base of the section to the level of the lower western shore lay * * * in what is now western Montana, key bentonite. Linguloid , the most numer­ eastern Idaho, central Utah, and perhaps central or ous macrofossils found, occur from 20 feet below the eastern Arizona. Most of the land behind the shore was lower key bentonite into the lower part of the Fox composed of preexisting sedimentary rocks, although Hills Sandstone. Several species of pelecypods and cystalline rocks of age were exposed in gastropods occur in the Mobridge Member. Rare Colorado during Pierre time. Several centers of con­ scaphitid ammonites were found at several levels, most temporaneous volcanic activity are known to have commonly in the Mobridge Member. In addition, the existed near the western shore in west-central Montana." plant fossil "Serpula" wallace?isls Elias, also called the Reeside (1957) gave a detailed account of events oc­ curring in the western interior during the Late Creta­ Indian-bead, and small crabs were found in limited ceous and placed them in a broad regional paleogeo- numbers in the Virgin Creek Member. graphic and tectonic setting. His reconstructions of the In a discussion of the broad f aunal relations of the events affecting the rocks presently under consideration western interior macrofossils, Cobban and Reeside are summarized as follows: The fine-grained sediment (1952, p. 1025) stated: "In general, the faunas [of the composing the Virgin Creek Member was deposited Pierre shale] are similar to those found to the north, while the sea was making its last westward advance, in Canada, and are not matched by closely similar as­ during late Campanian time (fig. TA). Considerable semblages to the south in part of the Taylor Marl and volcanic activity is attested to by the numerous, though the Navarro Group of the Gulf region * * * though generally thin, bentonites which characterize this mem­ enough forms are found to provide a rational corre­ ber. In the early Maestrichtian, a fairly steady eastward lation. Seemingly the Pierre faunas are boreal or retreat of the strand line took place, during which time largely endemic." More than three-fourths of the iden­ the calcareous shales of the Mobridge Member were tified species of Foraminifera from the upper part of deposited (fig. IB). Reeside did not mention the Elk the Pierre Shale are also present in beds of the Austin, Butte Member, but presumably these beds were laid Taylor, and Navarro of the Gulf Coast, an indication down asi the shoreline continued to retreat eastward. that access to the southern seas was available. It may The Fox Hills Sandstone of middle and late Maestrich­ tian age is composed of sediments deposited close to the be possible to determine whether this access was con­ shoreline and represents the culmination of this retreat stant or intermittent by studying the foraminiferal (% 760- faunas in the middle and lower parts of the Pierre. As the shoreline retreated eastward, the northern con­ In either case, the composition of the Pierre macro- nection of the interior sea with world oceanic waters fauna indicates that, although conditions in the west­ was broken. Correlation charts given by Cobban and ern interior were not favorable for most Gulf Coast Reeside (1952) indicate terrestrial conditions in Wyo­ macromvertebrates, they were favorable for Gulf Coast ming and Montana, the probable northern access of the foraminiferal species, at least during the time of depo­ Pierre sea during or immediately after the time of sition of the upper part of the Pierre Shale. Baculites grandis. B. clinolobatus, a direct descendant FORAMINIFERA, STRATIGRAPHY, PIERRE SHALE, FOX HILLS SANDSTONE, S. DAK.

100 0 100 500 MILES I ... I -L 100 0 100 500 KILOMETERS L...I I -I I I I

EXPLANATION

Volcanic mud Sand

T.-Lithofacies and paleogeographic maps (from Reeside, 1957, figs. 19-21). A, Verendrye and Virgin Creek time. FIGURE B, Mobridge time. C, Fox Hills time. FORAMINIFERAL BIOFACIES 21 of B. grandis (Cobban, 1958, p. 114), is found in the LOWER ARENACEOUS BIOFACIES Mobridge Member. Thus, the northward connection was This biofacies has been recognized in two sections probably closed prior to the deposition of this member. (fig. 4, sections 1 and 3) in the Moreau River strati- Closure probably occurred earlier in Canada, perhaps graphic sequence. It characteristically consists of four even before the Virgin Creek Member was deposited. to 10 species, several of which may be represented by On a more local scale, Waage (1961, p. 238) reported numerous specimens. The fauna is composed of at least that "* * * the entire marine sequence of the Fox Hills 50 percent arenaceous species but, as a rule, also contains and at least the upper 250 feet of underlying Pierre fairly abundant specimens of a few calcareous benthonic Shale pass westward within 50 miles (of the longitude species and scarce specimens of one or two planktonic of Dupree, S. Dak.), into a sandy sequency of predomin­ species. The most commonly occurring species in tHs antly brackish- and fresh-water beds." Thus, the shore­ f acies are BatJiysiphon brosgei?, Ammodiscus cretacer-s, line was within 50 to 100 miles west of the area of in­ Haplophragmoides rota, Gaudryina bentonensis, Bu- vestigation during the deposition of the uppermost part limina kickapooens-is, and Oibicides Jiarperi. of the Pierre Shale. The lower arenaceous biofacies is found in the low^r The original extent of the Elk Butte, Mobridge, and 45 to 50 feet of the Virgin Creek Member. The top is Virgin Creek lithologies is unknown. Searight (1937, not a clearly demarcated boundary between two easily p. 35, pi. 7) described the Virgin Creek Member as crop­ distinguishable faunas but rather the level at which a ping out along nearly the entire length of the Missouri marked increase in the number of foraminiferal speci°s River in South Dakota and stated that "It covers wide begins. This increase in species is dependent, for the areas north, south and east of the Black Hills and has most part, on a marked increase in the number of crl- been observed beyond these South Daktota outcrops in careous benthonic species, especially species of the Lag- southwestern North Dakota and in eastern Montana enidae, Buliminidae, and Rotaliidae. There is also a along the crest of the Cedar Creek anticline." Searight large relative increase in the number of arenaceous spe­ did not trace the Mobridge Member westward beyond cies from four or five to eight or nine, but this is only a small percentage of the total increase in number of South Dakota State Highway 63 (this paper, fig. 1) but species. reported (p. 44) that it "* * * extends from a position Concomitant mineralogic and lithologic features near the North Dakota boundary to the southern bound­ help to characterize the lower arenaceous biofacies. ary of South Dakota. * * * The Elk Butte Member has Throughout the entire stratigraphic interval in wlxhh been identified in outcrops extending between southeast­ this biofacies exists there is evidence of the presence of ern Gregory and southwestern Charles Mix Counties [S. free silica in the form of usually very abundant radio- Dak.] on the south, to northeastern Corson County larian tests and siliceous fillings of Foraminifera. Every [S. Dak.] on the north" (Searight, 1937, p. 50). Accord­ specimen of calcareous Foraminifera seen from this ing to Tourtelot (1962, p. 8), these members are pres­ biofacies was filled with silica, but arenaceous speci­ ently recognizable "for some distance along the valleys mens were usually not filled. Lithologically this strati- of the streams entering the Missouri River from the graphic interval, which includes all the lower part of west." the Virgin Creek Member of Searigiit (1937) and part FOBAMINIFERAL BIOFACIES of the upper part of the Virgin Creek Member, is char­ acterized by the presence of numerous thin bentonite The -foraminiferal faunas of the upper part of the layers, especially in the lower part, and by the non- Pierre Shale and lower part of the Fox Hill Sandstone calcareous and relatively erosion-resistant nature of are variable. They change in specific, generic, and the rock. familial composition and in the number of families, The species below occur in the lower, but not the genera, and species from place to place through the upper, arenaceous biofacies; only those species marked stratigraphic column; they define several assemblages by an asterisk occurred in more than one sample: or biofacies that probably reflect local changes in the * Gaudryina bentonensis benthic environment. These biofacies are not associated G. watersi with obvious lithologic f acies. *Silicosigm>oilina futabaensis Three foraminiferal biofacies were recognized in the Robiilus muensteri area investigated. These were the lower arenaceous (the Dentatina legmnen term arenaceous being used to include all noncalcareous Nodosaria proboscidea Foraminifera), upper arenaceous, and calcareous bio­ Palmula cf. P. rugosa facies. Lagena apiculata 22 FORAMINIFERA, STRATIGRAPHY, PIERRE SHALE, FOX HILLS SANDSTONE, S. DAK. Heterolielix gldbulosa, noides cf, V. perplexus. In addition, Reophax sp. and *Gyroidina- girardana Spiroplectammina inordenensis are present in some *"Discorbis" quadrilobus samples from the Grand River stratigraphic sequence. NuttaUinetta? disca Several calcareous benthonic species of Forpminifera Hoeglundma supracretacea occur in various samples, but the most frequently pres­ Rugoglobigerina cf. R. rugosa, ent and abundant is Planulina kansasensis. T e species *Cibicide8 harperi below occur in the upper, but not the lower, arenaceous

UPPER ARENACEOUS BIOFACIES biofacies; only those species marked by an asterisk oc­ curred in more than one sample: The upper arenaceous biofacies occurs throughout much of the Elk Butte Member and is also found in the *Reop7iax, sp., *Verneuilinoides cf. V. perplexus. lower part of the Fox Hills Sandstone. The lower limit *Quinqueloculina, sp., *Trochaiwnina globosa. of this biofacies in the Moreau River stratigraphic sec­ Oolina obeliscata,, Bulimina prolixa, *Neobulimina tion was found only in section 27 A (fig. 4) where navarroana, *Planulina Jcansasensis, Cibicides there is a transition from a predominantly calcareous subcarinatus, Incertae sedis sp. fauna to an overlying predominantly arenaceous fauna The stratigraphic interval containing the upper through about 15 feet of section. The base of the arenaceous biofacies is usually noncalcareous, easily biofacies was arbitrarily placed 36 feet below the base eroded gray shale or clay stone containing a few thin of the Fox Hills Sandstone, in about the middle of the bentonite beds, numerous concretion horizons, and only transition interval. In section 31 (fig. 4) the lowest a few species and scarce specimens of Eadiolaria. sample examined was about 56 feet belowT the base of Throughout most of this interval, the average amount the Fox Hills, but no transition interval was found, the of residue retained on a 200-mesh sieve per unit weight arenaceous species being dominant from the base to the of unwashed rock was the same as for the underlying top of the section. rocks, but within about 50 feet of the top of the Pierre The contact between the calcareous biofacies and the Shale the amount of residue increased. Generally asso­ upper arenaceous biofacies in the Grand River strati- ciated with this increase were increases in tin precent- graphic sequence occupies a transition interval of about ages of muscovite and fossil plant fibers in tin residues. 10 feet. It is present in two of the sections for which CALCAREOUS BIOFACIES faunal data are available (fig. 5, sections 49 and 54). In both sections the boundary was arbitrarily placed The calcareous biofacies lies between, and is grada- in about the middle of the transition interval, about 72 tional with, the upper and lower arenaceous biofacies feet above the upper key bentonite in section 54 and (fig. 6). It is characterized by the presence, in most about 60 feet above the upper key bentonite in section samples, of a rather large number (eight to 36) of cal­ 49. careous, mostly benthonic, species of Foramirifera. The In the Moreau River stratigraphic sequence the upper number of arenaceous species in the samples is slightly key bentonite is about 130 feet below the base of the larger than the mimber in either of the arenr?eous bio­ Fox Hills Sandstone. The top 36 feet or so of this in­ facies. terval is occupied by the upper arenaceous biofacies. In The lower boundary of this biofacies is present only the Grand River stratigraphic sequence the thickness in section 3 (fig. 4) in the Moreau River sections, where from the upper key bentonite to the base of the Fox it lies about 155 feet below the base of the lower key Hills Sandstone is approximately 200 feet, the upper bentonite. The lower boundary was not seen in any of 130 to 140 feet of which is the upper arenaceous bio­ the Grand River sections, none of which extends any facies. The thicknesses of all the intervals cited here lower than 48 feet below the lower key bentonite. The are approximations because of the transitional nature upper boundary is present only at locality 27 A (fig. of the lower boundary of the upper arenaceous biofacies 4) in the Moreau sections, where it occur? about 36 and because the thicknesses given for some strati- feet below the base of the Fox Hills Sandstone. In the graphic intervals are averages. The upper arenaceous Grand River sections the upper boundary is present at biofacies is present throughout the part of the Fox Hills localities 49 and 54 (fig. 5) where it occur? approxi­ Sandstone studied in the outcrop areas of the Grand mately 60 to 75 feet above the upper key bentonite. and Moreau River. The generic and specific compositions of faunas The upper arenaceous biofacies is characterized by within the stratigraphic interval containing the cal­ Haplophragmoides rota (the most abundant and most careous biofacies vary from sample to sample, but the consistently present species), H. bonanzaemis, Bathy- number of species and genera decrease as a general rule siphon brosgei?, Amm.odisous cretaceous, and Vemeuili- from the base to the top. On the familial level, the Lage- FORAMINIFERAL BIOFACIES 23 nidae are more abundant than any other family in the upper arenaceous biofacies from the Grand River the number of species and genera, though not in the sections were similar in faunal composition to the same number of specimens, throughout much of the biof acies. respective biofacies in the Moreau River sections. It Lagenid species are most common in the lower 100 to should be possible to find these three biofacies, in the 150 feet of the biof acies and gradually decrease in num­ order in which tl ey occur in this area, through differ- ber up the section. Other families of importance are ent timespans wit tiin the eastern part of the Pierre and the Aiiomalinidae, represented in the lower part of the Fox Hills outcrop area, though it is likely that there biof acies primarily by Cibicides harperi and C. subcari- will be difference 3 in specific composition and in domi- natiis and in the upper part by Plamdina kansasensis; nant species. the Chilostomellidae, represented by Pullenia ddkoten- FAUNAX DETAILS AND ORIGIN sis; the Epistominidae, represented by Nuttallinellaf disca; the Rotaliidae, represented chiefly by Gyroidina As so far considered, the biofacies are no more than depressa; the Buliminidae, represented chiefly by BuU- empirically defined pieces of a larger faunal complex. mina kickapooensis and Loxostoma plaita; the Hetero- In order to improve understanding of them, it is neces­ helicidae, represented chiefly by Heterohelix globulosa; sary to consider some faunal details and various alter­ and the Textulariidae, represented by Spiroplectam- native explanations for their existence. 'tnina, laevis cretosa. The family Ceratobuliminidae, rep­ One of the more important questions which can be resented by Hoeghmdina suprafretacea, is common in asked with regard to these foraminiferal faunas, anc1 samples from the Moreau River stratigraphic sequence one of the more difficult to answer, is to what degree but rare in the Grand River sequence. The species re­ they represent the remains of actual living communi­ stricted to or most common in the lower part of the ties. Possibilities which must be taken into account in­ calcareous biof acies and generally represented by large clude the addition of specimens of "foreign" species by numbers of specimens are Cibicides harperi, C. subcari- currents, the selective removal of parts of the original iiatiis, Gyroidina. girardana, G. globosa, and Spiroplec- communities by liagenetic or postdiagenetic destruc­ taiwnina laems cretosa. Their counterparts in the upper tion, and the mixing of a number of communities during part of the biofacies are Plamdina kan-sasensis, Buli- sampling. It is more likely that longer ranging specie? mina kickapooensis, Loxostomm plaita, andNeobulimina have been secondarily introduced because they persist navarroana. Samples taken at random were accurately while the genera compositions of the faunas change., placed stratigraphically by a comparison of the con­ presumably because of ecologic changes. But specimen'? tained species with the ranges of these diagnostic spe­ of these long-ranging species are generally as well pre­ cies. The accuracy of this stratigraphic placement is di­ served as the associated specimens, and they are pres­ rectly dependent upon the number of diagnostic species ent in large num :>ers. Both factors seem to contradic* in the sample. Despite the predominance of Lagenidae transportation. T le presence of long-ranging species in in the calcareous biofacies, no lagenid species are con­ the upper part of the Pierre and lower part of the Fox sidered diagnostic because specimens of the various Hills, for lack of contrary evidence, implies that thes^ lagenids are scarce and because there is typically little species were able to survive under a variety of ecologic continuity to the stratigraphic distribution of the spe­ conditions, some of which could not be tolerated by cies within the biofacies. other species. The problem of the selective diagenetn The stratigraphic interval occupied by the calcareous removal of specimens is real, as indicated by the pres­ biofacies is typically a gray, slightly to very calcareous, ence of pyrjtic internal molds of some specimens in a easily eroded shale or claystone which includes both number of samples. The degree to which this biases in­ the upper and lower key bentonites, a few thinner and terpretation of tie original faunal composition cannct less persistent bentonites, and a large number of con­ be determined. ] n. samples containing abundant well- cretion horizons. preserved calcareous specimens, I have assumed destruc­ tion to be relatively unimportant. The usual presence STHATIGHAPHIC AND AREAL DISTRIBUTION of one or more cslcareous species, represented by abur- The three biofacies characterize the vertical formini- dant specimens in the upper arenaceous biofacies and feral succession in the upper part of the Pierre Shale. the scarcity of internal molds indicates that the procers The boundaries between the biofacies are gradational. of selective destruction of calcareous specimens was not Strata containing the lower arenaceous biofacies were the cause of the faunal aspect of this biofacies. How­ not found in any sections along the Grand River, but ever, there is evic ence from some samples that selective the upper two biofacies were found in sections from destruction was o Derative, just as it was in some samples both the Grand and Moreau Rivers. The calcareous and from the calcareous biofacies. Calcareous specimens in I 24 FORAMINIFERA, STRATIGRAPHY, PIERRE SHALE, FOX HILLS SANDSTONE, S. DAK. the lower arenaceous biofacies are always filled with the fauna noticeably. In fact, there may have been no silica, and many specimens have had their original cal­ effect on the living fauna at all but simply accelerated careous tests dissolved away. Selective destruction was destruction of the tests in the sediment. In the shale certainly operative here but apparently was largely off­ above that bentonite, the presence of pyritic internal set by the production of internal molds of silica in many molds of several calcareous species of Foraminifera in­ of the calcareous specimens originally present. -The dicates that a larger fauna may have been living on the usual presence of fairly large numbers of internal molds site than has been preserved. for most, of the calcareous species makes it unlikely that Several sections have hard light-gray to buff highly there originally was a significantly larger representa­ calcareous shale beds a foot to several feet thick. Sev­ tion of calcareous species than has been discovered. eral of these beds were examined for micrcfossils and The three biofacies encompass variations that occur yielded abundant planktonic Foraminifera. In one bed, from sample to sample and between small groups of the coarse fraction was composed almost entirely of spec­ samples. All species are only sporadically present within imens of Heterohelix globulosa and BiglobigerineTla T)i- the limits of their total vertical ranges, a fact indicating foraminata, the latter predominant. It is impossible to that conditions from time to time and from place to say whether the entire calcareous content T^as derived place were unfavorable for either their existence or from the tests of these planktonic . Nevertheless, preservation. Analysis of all the individual variations their tremendous abundance and their presence in much is not attempted, but several more f aunal changes within less spectacular numbers elsewhere indicate that condi­ the calcareous biofacies are deserving of comment. tions favoring their proliferation or preservation were A dramatic faunal change occurs in the vicinity of only rarely achieved; lack of lateral persistence of the lower key bentonite in the Grand River valley. highly calcareous planktonic-rich layers suggests that Sample 10 of section 37 (fig. 5), immediately below the these favorable conditions were extremely local. lower key bentonite, contains 25 species, four of which The siliceous nature of the microf auna in the lower are arenaceous, whereas in sample 12, about 8 feet above 50 feet of the Virgin Creek Member in sections 1 and 3 this bentonite, there are only five species, two of which (fig. 4) and in the shale above the upper key bentonite in are arenaceous. Another section which shows the same sections 44 and 49 (fig. 5) has already been mentioned. set of conditions is section 42 (fig. 5) where 23 species, In sections 1 and 3, radiolarians are preser^ in abund­ two of which are arenaceous, are present immediately ance, and the Foraminifera are few and silicified. In sec­ below the bentonite, and six species, all arenaceous, are tion 44, radiolarians are present, and the S'licified for- present in the next sample 6 feet above it. In section 44 aminiferal fauna is composed of few specimens and spe­ (fig. 5), sample 1A, immediately below this bentonite, cies. In section 49, the foraminiferal fauna is repre­ contains nine species, two of which are arenaceous; sam­ sented by a small number of silicified specimens belong­ ple 1, immediately above the bentonite, contains only ing to a few species, but there are no radiolarians. The one species, and it is arenaceous. Higher in section 44 presence of radiolarians must have been favored by some of the calcareous species present below the ben­ conditions which were only occasionally in effect because tonite reappear, but the fauna never regains the diver­ they are absent in most of the upper part of the Pierre sity present below the bentonite. The group of sections Shale. The release of silica into the sea water as a re­ in which this marked faunal change occurs is in a north- sult of the alteration of volcanic ash, now preserved as south strip of territory in the vicinity of the town of bentonite in the lower part of the Virgin Creek Mem­ Wakpala, S. Dak. (fig. 1). One other section, section ber, may have provided either directly or indirectly for 45 (fig. 5), which lies about 5 miles west of Wakpala the proliferation of these organisms and for the small begins just above the level of the lower key bentonite number of Foraminifera. Alternatively, the number and yet has a diverse fauna of 27 species, three of which are kinds of Foraminifera may have been origir ally greater, arenaceous, at its base. No such marked faunal change but adverse chemical conditions within the sediment occurs in the vicinity of the lower key bentonite in any may have destroyed most specimens. If the release of of the Moreau Kiver sections. Thus the cause or causes silica were responsible for the silicificatior of the For­ of this change operated over a restricted area. What aminifera in sections 44 and 49 and for the presence of relationship the bentonite had to this change is not clear. the radiolarians in section 44, then it can be assumed that It is not likely that the effects of the fall of this single the volcanic ash was disseminated through the shale. layer of ash should have been so drastic or so perma­ Discrete bentonite beds like those in the lower part of nent, especially in view of the fact that considerably the Virgin Creek Member are not present in the inter­ thicker bentonites elsewhere have not appeared to affect vals that contain the silicified fossils in these sections. ENVIRONMENTAL INTERPRETATIONS 25 ENVIRONMENTAL INTERPRETATIONS considerable and leaves little doubt that presence or ab- sense of individual genera does not give precise depth The environmental interpretations of the upper part information. Other authors have considered the dom­ of the Pierre Shale and lower part of the Fox Hills inance of various genera and families at different Sandstone are by no means complete characterizations of depths; some of the information that they presented is the original living environments. Rather, they are the considered later. result of inference and analogy based on the biologic Problems of preservation must also be considered and lithologic evidence found in these deposits and on in interpreting fossil faunas. This subject was ably ex­ pertinent evidence from other areas. The biologic data plored by Johnson (1960), who, by means of models, include information on the composition, abundance, illustrated the many ways in which death assemblages preservation, and the vertical and, to a lesser extent, may be altered or destroyed before they are available horizontal distribution of the foraminiferal faunas. The to the paleontologist for sampling. Alteration of the lithologic data from the upper part of the Pierre in­ character of a foraminiferal faunal assemblage on the clude information on the relative abundance of calcium bottom or below the sediment surface would appear to carbonate and silt-sand, the composition of the coarse be most readily accomplished on the basis of com­ fraction of the shale, and the vertical and, to a lesser ex­ position. Parker and Athearn (1959) recorded dramat­ tent, horizontal nature of the stratigraphic sequence. ic evidence of preferential removal of calcareous tests BIOLOGIC INFORMATION within the upper 1 centimeter of sediment in the marshes of Poponesset Bay, Mass. They noted (1959, Because Foraminifera are abundant fossils commonly p. 338) that calcareous species are represented for the found in the strata invesigated, they are well suited for most part by living specimens: "Very few dead ones use in interpreting paleoecology. Phleger (1960a, p. 102- were observed. This leads to the inference that below 103), in his discussion of depth distribution of Kecent the sediment surface, or perhaps even at the sediment- Foraminif era, stated that the important ecologic factors water interface, the pH is sufficiently low to cause the may be one, all, or some of the following: temperature, dissolution of the tests. If this condition exists in the salinity, food supply, water chemistry, hydrostatic pres­ 'living environment' of the species they must have some sure, turbidity, turbulence, substrate, currents, biologic mechanism to resist the acidity. Since this implies the competition, or disease. Consequently, the depth range expenditure of considerable energy on the part of the of a species is an obtuse and imprecise expression of the organism, it seems more probable that the increase in limits of effectiveness of the numerous ecologic factors acidity occurs immediately below the sediment surface, which actually determine the distribution of the species. probably due to decaying vegetation, and that it is here However, because little information is available on the that the solution of tests occurs." degree or manner in which many factors affect species The presence of pyrite and unoxidized plant frag­ of Foraminifera and because depth is an easily deter- ments in most samples from the upper part of the Pierre minable factor, most foraminiferal ecologists have ex­ Shale and lower part of the Fox Hills Sandstone in­ pressed the distribution of modern species in terms of dicates that reducing conditions prevailed beneath if depth. not above the sediment-water interface during deposi­ The application of modern distributional information tion. Also, the presence of pyritic or siliceous internal to fossil faunas is complicated by two factors: evolution molds of calcareous Foraminifera in a number of sam­ and preservation. If the fossil fauna contains species ples indicates that some process of removal of CaCO3 present in modern oceans, it is customary to infer for was operative. In discussing the changes produced in the fossils an environment similar to that in which the sediments as a result of the activities of micro-organisms, modern representatives live. Only a few species from the ZoBell (1942, p. 131) stated that "Depending upon the upper part of the Pierre Shale have living representa­ numbers and kinds of micro-organisms present, the sub­ tives, so the ecologic conditions to which the majority strate and environmental conditions, [] might of species were adapted cannot be inferred by reference increase the acidity or decrease it." And later, ZoBell to modern faunas. Thus, the present can be a key to the past only 011 the generic or familial level or by means of (1946, p. 503) reported that "The pH of the bottom interpretations which do not depend upon genetic affilia­ deposits ranges from 6.4 to 9.5, most of them falling tions. in the range of pH 7.5 to 9.0," and "The pH of most An examination of the data which Phleger (1960a, sediments was found to increase with depth." Shepard figs 14-36) presented on the depth distribution of mod­ and Moore (1955, fig. 44C) recorded changes in pH ern species off the coasts of the United States and Mex­ in several modern environments along the central Texas ico reveals that the depth distribution of most genera is coast. They found that the pH of marine sediments is 26 FORAMINIFERA, STRATIGRAPHY, PIERRE SHALE, FOX HILLS SANDSTONE, S. DAK. slightly higher than neutral at the surface and increases lies are still represented in Recent seas, but there is a slightly with depth within several short cores. concomitant loss of precision because of the large en­ In discussing the geochemistry of the Pierre Shale, vironmental ranges of most families. Although presence Tourtelot (1962, p. 11) was more positive about the or absence of individual families is of practically no use pH of sediments containing unoxidized organic mat­ in making paleoecologic interpretations, soir^ informa­ ter. He stated that "Bacterial or chemical reduction of tion, even if only suggestive, may be obtained when the sulfate also promoted acidic as well as reducing condi­ familial compositions of many different samples are con­ tions. Some calcium carbonate and other compounds sidered together. In the following family-level analysis were increasingly dissolved and were either cycled back of the upper Pierre-lower Fox Hills foraminiferal to the overlying sea water or were segregated as diagene- faunas, the family designations are chiefly those of Cush- tic concretions in favorable microenvironnients within man (1946). the zone of ." Though this statement may be The Foraminifera in the upper part of the Pierre true in general and possibly explains the absence of Shale and lower part of the Fox Hills sandstone have calcareous Foraminifera in certain parts of the Pierre been placed in. 20 foraminiferal families. T^ e presence section, it cannot be rigorously applied to the calcareous of members of these families varies, of course, from biof acies of the upper part of the Pierre Shale. There, sample to sample. It is possible to analyze this variation abundant calcareous tests have been preserved, an in­ in several ways, the most simple of which is based on dication that this process, if it worked at all, did not go specimen counts for each species in each sample. Because to completion, perhaps because of insufficient amounts abundances were estimated rather than counted in this of organic material. study, these estimated abundances were not used in the Comparison of fossil and Recent foraminiferal analyses, although they were included under the species faunas can be most precisely done on the species level, descriptions. Beginning with the data on presence or but because very few of the species found in this study absence of species in samples, the first step in analyzing persist to the Recent, it was necessary to utilize less the available data was the plotting of the number of precise measures. One such measure was the compari­ species present in each sample against the total number son of the distribution and abundance of fossil genera of samples to determine the more typical faunal sizes. with the same genera in the Recent. Attempts to make This plot, representing 192 samples (fig. 8), shows that this kind of comparison between the genera from the 87 samples contain zero to five species, 50 samples con­ upper part of the Pierre Shale and lower part of the Fox tain six to 10 species, and 55 samples contain more than Hills Sandstone and the same genera in the Gulf of 10 species. Another step in drawing together informa­ Mexico, based on data given by Phleger (1960b) and tion on the distribution of families in these faunas was Lowman (1949), were not very successful. Several of the plotting of familial composition of each sample ex­ the dominant benthonic genera and species (Bulimina amined on 360° pie diagrams. It is not possible to in­ Ttickapooetisis, Pullenia dakotensis, Hoeglundina supra- clude all these diagrams here, so I have separated the cretacea, and Gyroidina depressa), remain dominant faunas into three broad divisions correspording to the through nearly the entire thickness of rock examined, foraminiferal biof acies discussed earlier. The 50 f ossilif- although most other species, including several parti­ erous samples examined from the upper arenaceous bio- cularly common ones (Cibieides harperi, C, siibcarma,- f acies, none of which contains more than 10 species, are tus, Lomostoma plaita, and Planulina kansasensis) , represented in figure 9. The 66 fossiliferour samples of are more confined in vertical range. This pattern and 10 or fewer species examined from the calcareous bio- its poor comparability with the Recent Gulf patterns facies are represented in figure 10. The 53 fossiliferous seem to have two possible explanations. First, the Cre­ samples from this biof acies of more than 10 species are taceous Foraminifera were adapted to conditions in an represented in figure 11, and the 10 fossiliferous samples interior sea that may not have been analogous to con­ from the lower arenaceous biof acies, including one of ditions in the Gulf. Second, the ability of several species more than 10 species, are represented in figure 12. Each to persist through a considerable length of time and to of these figures is a plot of the number of samples in remain dominant throughout suggests that con­ which representatives of the various families occur, and ditions were fairly uniform. Thus, the faunal changes the number of samples in which any family is dominant might indicate smaller scale fluctuations in environ­ is indicated by patterns. Dominance of a family is in ment not comparable with Recent depth patterns. terms of number of species, not number of ptmcimens. Recent and fossil formamini feral comparisons may Examination of the family occurrences in the upper also be made at the familial level. Comparability be­ arenaceous biof acies (fig. 9) reveals that th°, Lituolidae comes better at this level because most Cretaceous fami­ is the family most commonly represented and most ENVIRONMENTAL INTERPRETATIONS 27

20

15

-10 cc LJ CD

^^^ 10 15 20 25 30 35 40 45 NUMBER OF SPECIES

FIGURE 8. Number of species in 192 samples from the upper part of the Pierre Shale and lower part of the Fox Hills Sandstone.

commonly dominant. The arenaceous nature of this bio- modiscidae, Textulariidae, and Verneuilinidae. The las4" facies is reflected in the larger number of arenaceous is the most commonly present arenaceous family. families represented and their greater frequency of The familial pattern for the 10 samples representing represenation. Among the calcareous families, the the lower arenaceous biofacies (fig. 12) is basically like Anomalinidae and Buliminidae are the best represented that from the upper arenaceous biofacies. The arena­ and are occasionally dominant. ceous families are more often represented than are the In the calcareous biofacies, those samples containing calcareous benthonic or planktonic families. The are­ 10 or fewer species (fig. 10) almost always contain naceous families more often present are the Ammodie- species of Buliminidae and are most often dominated by cidae, Lituolidae, and Verneuilinidae. The Buliminidae Buliminidae. Other prominent and occasionally domi­ and Anomalinidae are again the calcareous families nant calcareous families in these faunas are the Ano­ more often represented, as they were in the upper are­ malinidae, Kotaliidae, Chilostomellidae, and - naceous biofacies. Indication of dominance is lacking ic . The Lituolidae is still the most often in figure 12 because in most samples more than three present and most often dominant of the arenaceous f amilies were equally dominant. families, followed closely by the Textulariidae. In sam­ Figures 9-12 show some of the more obvious faum.l ples from the calcareous biofacies that contain 11 or patterns present at the familial level in the foraminif- more species (fig. 11), the average faunal character is eral faunas examined. To a certain degree they aid in markedly changed. The Lagenidae, which is not a dom­ quantifying the foraminiferal biofacies. Because they inant family in smaller faunas from this facies, is the are useful for comparison between Recent and ancient most often dominant family, followed closely by the patterns of family distribution, they facilitate interpre­ Buliminidae. One or the other of these two families is tation of environments. Finally, they are a means of dominant in almost eveiy sample, although the Rotali- comparison between the family-level characteristics of idae, Anomalinidae, and planktonic Heterohelicidae the various biofacies. Before examining analogous Re­ are also present in almost all samples. The large in­ cent and ancient patterns or drawing comparative par­ crease in frequency of occurrence of calcareous ben- allels between facies, it must be emphasized that because thonic and planktonic species and the presence of more these patterns represent rather crude generalizations families overshadow a smaller increase in the frequency the results must be considered only suggestive. of occurrence of arenaceous species and a shift in their The general similarity of pattern between the lower pattern of familial representation. In these samples, the and upper arenaceous biofacies suggests similar ecologic Lituolidae are less commonly present than are the Am- controls. It is not known whether these controls wer?, 28 FORAMINIFERA, STRATIGRAPHY, PIERRE SHALE, FOX HILLS SANDSTONE, S. DAK. 45 55 EXPLANATION

One family dominant 40 - EXPLANATION 50 - 1 Two families dominant One family dominant - 45 ~~ Three families dominant 35 Two families dominant

- Three families dominant 40 30

35 -

25 in UJ a! 30 - - 1 u. 20 O NUMBER roOl - -

15

20 - -

10 - 15 -

10 - | | -

^

fl: 5 - -

n , 1 ( rfl 1 \ I 1 ( 1 .K a II .«"§.*£ ^ ? a^-5 GSS ^^ *5vT ^^

FIGURE 9. Distribution of families in 50 fossiliferous samples from the upper arenaceous biofacies. Families are plotted ^ § ii ^ against the number of samples in which they occur. Height of patterned area indicates the number of samples in which FIGURE 10. Distribution of families in 66 fossilifero'is samples one to three families are dominant. That family containing containing one to 10 species from the calcareous biofacies. the most species in a given sample is considered dominant. See figure 9 for explanation. For samples with two or three families equally dominant, each family is considered one-half or one-third dominant. Where four or more families contain the same number of species, no family is considered dominant. ENVIRONMENTAL INTERPRETATIONS 29

DD 201 EXPLANATION EXPLANATION

One family dominant - One family dominant 50 15 1 Two families dominant Two families dominant - 45 Three families dominant

40 - -

35 - -

y S 30 * *

u- O = -i i § -~ -i DC 5 X ^ "e £ ~ UJ S a § is _S s CO g § £ o _g ^ S> 2 ^ 25 _ _ * & z

FIGURE 12. Distribu ion of families in 10 fossiliferous samples from the lower ! renaceous biofacies. See figure 9 for - 20 explanation.

15 - ditions were in some way different for these faunas, I The transition fro n the lower arenaceous biofacies to the lower part of the calcareous biofacies (fig. 13) is more abrupt than tie transition between the calcareous 10 - \ and upper arenacec us biofacies (figs. 13,14). If the rate of sedimentation was uniform, this asymmetry reflects a more abrupt change of ecologic conditions at the lower 5 - boundary of the c Icareous biofacies than occurred at the upper boundar r, possibly because of a rapid trans­ gression and slow r gression similar to those inferred by Weimer (1960) for the central and western parts of the r> il 1\ 1 I , Cretaceous sea in the western interior. Alternatively, the asymmetry ma^ be a result of slower sedimentation

la, at the lower bound ,ry and may not reflect a more rapid change in ecologic < onditions. I I According to Ph eger (1960a, p. 261), the use of fam- I 1 2s £ ilies in foraminife ral paleoecology is of questionable value. Neverthelesi some of the information on Recent and ancient family level distributions can be related to FIGURE 11. Distribution of families in 53 samples containing the upper part of he Pierre to lower part of the Fox 11 or more species from the calcareous biofacies. See figure 9 Hills distributions Lowman (1949, table 2, p. 1956) for explanation. discussed the Recen depth distribution of Foraminif era in three traverses nto the Gulf of Mexico and sum- marized some of h s data, in part at the family level, related to depth similarities or to depth-independent If the genera and f milies represented in the upper part parameters. The markedly different character of the of the Pierre Shale are related to Lowman's generalized calcareous biofacies pattern suggests that ecologic con- Gulf Coast sequen , both of the arenaceous biofacies 323-073 O 69 3 30 FORAMINIFERA, STRATIGRAPHY, PIERRE SHALE, FOX HILLS SANDSTONE, S. DAK.

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I II 1 I j i" " ' " " " s s = = - s - = £ -j~.2.~-~^.~ H - - * '^ "I o § - = 5 a ~ - c= ~Z ? ^ 5 S Top of 1 - S 5 LJ C Si ^* " 'c c = ia : c h : ~* &, " ft5 *T 5 CC 0 § c- 5 o 5 >-i v3 ^ i U; ^ 1 N 5 c I \a; s5 ft j >-5 CISS a5 o; a Q 3H « c section 350' -

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_Q o 25'- ' Base of section '<"!-.- ENVIRONMENTAL INTERPRETATIONS 33

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? " I '. [J 1 -]^ (\P . JsL JL JnL \>c -\\ . ]J ? 34 FORAMINIFERA, STRATIGRAPHY, PIERRE SHALE, FOX HILLS SANDSTONE, S. DAK. are assignable to his "Bottom living; stagnant ?; brack­ terest because the familial compositions of the faunas ish or marine" environment (based on the dominance are somewhat similar to those of this stud^. They de­ of arenaceous genera, including Haplophragmoides and scribed a shallow-water benthonic foraminiferal bio­ Bathysiphon}. That part of the Pierre calcareous bio- facies composed mainly of arenaceous genera and facies dominated by genera, species, and specimens of species and a deeper benthonic biofacies composed Buliminidae would seem to belong in Lowman's "Upper mainly of specimens of calcareous genera ?,nd species. part of continental slope (inner bathyal)" environment In the deeper benthonic f acies, specimens of Bulimin­ where there is a "Dominance of Buliminidae, especially idae are dominant at one stratigraphic level, and speci­ Uvigerina and Bolivina" The part of the Pierre cal­ mens of Lagenidae, Rotaliidae, and Anomalinidae com­ careous biofacies dominated by genera and species (but bined are dominant at two stratigraphic levels. The not specimens) of Lagenidae would seem to belong in main similarity between the Grayson and the upper part Lowman's "Outer continental shelf (outer neritic)" en­ of the Pierre and lower part of the Fox Hills is that vironment, where there is a "Great abundance of genera in both there are faunas characterized by arenaceous and species; conspicuous number and variety of La­ specimens, by specimens of Buliminidae, and by a more genidae." The approximate depth ranges given by Low- diverse assemblage containing varied forms of Lageni­ man (1949, fig. 12, p. 1952) for these environments are: dae. In both the Grayson and the upper part of the bottom living; stagnant (?) environment, about 0 to 20 Pierre Shale, the assemblages that lie between the feet; outer neritic environment, about 75 to 200 feet; lagenid and arenaceous assemblages in the Gulf of and inner bathyal environment, about 200 to 1,500 feet. Mexico are absent. It should be pointed out that Lowman recognized two Other data on the distribution of Recent foraminif­ other marine environments in the depth range 0 to 75 eral faunas were provided by Phleger (19fOb, p. 280- feet, characterized by groups that are absent or in­ 281), who discussed the general features of the fora­ conspicuous in the upper Pierre and lower Fox Hills miniferal faunas of the Gulf of Mexico. He character­ faunas. Thus, when the familial patterns for the Creta­ ized, in a generalized manner, the funas known from ceous Foraminifera are compared with Lowman's syn­ several environments in terms of number of species, thesis of Recent distributions, it is possible to infer a number of genera, population size, planktonio-benthonic maximum depth of 200 to 1,500 feet and a minimum ratio, percentage of arenaceous forms, and characteris­ depth of 0 to 20 feet for the environment of deposition tic genera. The number of genera and species, the esti­ of the upper part of the Pierre and the lower part of the mated planktonic-benthonic ratios, and the estimated Fox Hills. When a comparison of Lowman's complete percentage of arenaceous specimens present in some sequence of faunas is made with the Cretaceous pat­ samples from all three foraminiferal biofrcies in the terns, however, there is little total agreement. If the in­ upper part of the Pierre Shale were determined for use terpretation that the calcareous and then the upper in comparison with Phleger's data. Intermediate number arenaceous biofacies were deposited under gradually values were given to the estimated abundarces of each shoaling conditions is accepted, one difference is that species in a sample (see species descriptions for original the buliminid-dominated and lagenid-dominated faunas abundance estimates) in order to provide numbers that are in reversed order. To put these faunas in their Re­ could be compared with Phleger's data. Sixty-seven cent order would require deepening water through this samples from the upper part of the Pierre Shale were stratigraphic interval, and this does not seem likely. In analyzed, and the results are given in table 2. The any case, the close stratigraphic relationship between averages for the samples from the upper and lower the buliminid and lagenid faunas suggests that the min­ arenaceous biofacies, despite small differences between imum water depth of 200 feet rather than the maximum them, much more closely resemble each other than they of 1,500 feet is probably closer to being correct. do the samples from the calcareous biofacie" Also, the Albritton, Schell, Hill, and Puryear (1954) dealt differences between the averages for samples of the cal­ with faunas at the family level at least in part com­ careous biofacies that contain one to 10 species and 11 or parable with those of the upper part of the Pierre more species are much less than are the dif erences be­ Shale and lower part of the Fox Hills Sandstone. They tween the calcareous biofacie,s averages as a whole and treated the families on the basis of numbers of speci­ the averages of either of the arenaceous biofacies. The mens, which I have not done, though it is possible to characteristics of the upper and lower arenaceous bio­ make approximate comparisons. These fossil faunas are facies expressed in table 2 are most closely comparable also interpreted in terms of Lowman's Gulf of Mexico with characteristics of faunas that Phleger grouped data. Their paper deals with Foraminifera from the under the designations "Marine Marsh" and "Coastal Lower Cretaceous Grayson Marl of Texas and is of in­ Lagoon" environments, except for the fact that the LITHOLOGIC INFORMATION 35 TABLE 2. Analysis of the number of genera, number of species, mens in a group of upper Pierre-lower Fox Hills planktonic-benthonic ratios, and percentage of arenaceous speci­ mens in 67 samples from the upper part of the Pierre Shale samples. These comparisons indicate: representing the three recognized foraminiferal biofacies a. that the lower and upper arenaceous biofacies [Abundances used in compiling planktonic-benthonic ratios and average percentages are quite similar; of arenaceous specimens are estimates] b. that the calcareous biofacies differs markedly Average Average Average Average from the two arenaceous biofacies. number number planktonic- percentage No. of genera of species benthonic of arena- of 2. Comparison with data on the distribution of Recent per per ratio per ceous sam- sample sample specimens pies Foraminifera in the Gulf of Mexico indicates that per sample the upper Pierre-lower Fox Hills faunas lived it Upper arenaceous bio- waters that probably did not exceed about 200 feet 2.8 3.0 1 00 95. 7 i; Calcareous biofacies 2 __ 7.4 7.7 1:3.9 14. 8 1< 17.3 21 1:8.4 7.1 2; in depth and that the faunas of the arenaceous1 Total calcareous 14.1 16.6 1:6.9 8.8 4( biofacies lived at considerably shoaler depths. Lower arenaceous bio- 6.8 6.8 1:350 67. 5 1( 3. The ecology and inferred paleoecology of linguloid brachiopods suggests that the strata containing 1 This ratio is infinity because no planktonic specimens were found in these samples. 2 Samples of one to 10 species, them (from 20 feet below the lower key bentonite s Samples of 11 or more species. to 37 feet above the base of the Fox Hills sand­ stone) were laid down in warm water of normal salinity at depths not greater than about 100 feet- dominant genera are not the same. The characteristics of the samples from the calcareous biofacies most LITHOLOGIC INFORMATION closely resemble the characteristics of Phleger's "Inner The upper part of the Pierre Shale is typically very Continental Shelf" environment, again except for a dif­ fine grained and homogeneous with no megascopically ference in dominant genera. Phleger (1960b, p. 267), apparent sedimentary structures. A sufficiently high gave a depth range of 0 to 30 fathoms for the inner con­ content of calcium carbonate to cause a visible reactior tinental-shelf environment. with dilute hydrochloric acid is characteristic of the The application of Recent occurrence data to Creta­ middle part of the stratigraphic sequence. Silt and sane1 ceous formainiferal faunas is subject to question. are apparently irregularly distributed through the shale Phleger (1960b, p. 280) prefaced his data with a word and form barely distinguishable discontinuous layerr of caution, and it is known that the planktonic- along which the shale parts. In the upper part of the benthonic ratios given by Phleger do not hold for sequence, near the contact with the Fox Hills Formation, Recent faunas in some places in the Gulf of Maine layers of silty and sandy shale become more commor (Thomas G. Gibson, written commun., 1963). Never­ theless, similarities between the Pierre faunas and those and are thicker. The lower part of the Fox Hills Sand­ stone is typically a clayey sandy silt with more clay ir from the Gulf of Mexico are suggestive, and it is prob­ able, from this line of evidence, that the Foraminifera the lower part and more sand in the upper part. from the upper part of the Pierre Shale and lower part A grain count of the constituents of the coarse­ of the Fox Hills sandstone lived in waters that were grained sediment fraction (0.074 mm and larger) waf not deeper than about 200 feet. made for each sample examined for microfossils. The Linguloid brachiopods, sporadically present in sam­ coarse-grained fraction generally composed only one- ples from 20 feet below the lower key bentonite to 37 fiftieth to one-one hundredth of the original sample, feet above the base of the Fox Hills sandstone, may except for those samples from the upper part of the Elk also be used as environment indicators. Cooper (1937, Butte Member and from the lower part of the Fox Hills' p. 30) reported that Recent linguloid brachiopods live Sandstone, where sand-sized grains were more common. from the tidal zone to depths of about 100 feet, They Quartz, pyrite, clayey calcareous and noncalcareous ag­ are presently found in tropical and warm-temperate gregates, and rusty aggregates of clay and silt were the waters (Allan, 1936, p. 384) and are not tolerant of most common grains found; fewer grains of glauconite, fresh or brackish water for more than a few hours at muscovite, biotite, Foraminifera, carbonized plant frag­ a time (Rudwick, 1965, p. H211). ments, and other materials were also present. Glau­ This attempt to use biologic data in environmental conite, muscovite, and carbonized plant fragments are interpretation has yielded the following results: usually found only in the uppermost part of the Elk 1. Some characteristics of the three foraminiferal bio­ Butte and in the lower part of the Fox Hills. Glauconite facies are elucidated by familial compositions, is almost always associated with quartz grains of ap­ numbers of genera and species, planktonic-ben­ proximately the same size, a fact suggesting that the thonic ratios, and percentages of arenaceous speci­ glauconite was probably not authigenic. The carbonized 36 FORAMINIFERA, STRATIGRAPHY, PIERRE SHALE, FOX HILLS SANDSTONE, S. DAK. plant fragments are never more than 5 percent of the gous to the same changes occurring in the upper arena­ total coarse fraction, and muscovite is generally less ceous biofacies from its top in the lower par* of the Fox than 20 percent. Foraminifera are usually very few in Hills Sandstone downward into the Elke Butte Member samples containing muscovite and carbonized plant of the Pierre Shale. fragments. CONCLUSIONS RECENT ANALOGS The limited areal and stratigraphic nature of this in­ An attempt has been made to find faunal and litho- vestigation precludes definitely relating the environ­ logic similarities between the strata studied for this re­ ments represented to any specific Recent analog. The port and sediments being laid down at present. Because biologic comparisons also do not closely def tie environ­ of inferred shallow-water and relatively nearshore con­ ments. However, the lithologic and biologic data do sug­ ditions during deposition of these strata, comparisons gest that the vertical changes occurring from about the have been made with Recent near-shore and continental- base of the Mobridge Member through the, lower part shelf deposits. Many modern outer-shelf environments of the Fox Hills Sandstone are analogous, in general, are poorly suited for comparison because of the pres­ to the changes that occur from inner continental-shelf ence of anomalous sediments laid down during the low­ depths to nearshore in some areas of Recent deposition. ered sea level of the . Additional observations and inferences can be made on Reports on the nearshore and continental-shelf de­ the more local aspects of the upper part of the Pierre posits of the Mississippi delta (Shepard, 1956; Scruton, and lower part of the Fox Hills environments. 1960), the Texas Gulf Coast (Shepard and Moore, The faunas of the upper arenaceous biofacies lived 1955), the Paria-Trinidad shelf (Koldewijn, 1958), in shallow water. The increasing percentages of fossil the western Guiana shelf (Nota, 1958), and the East plant fibers and muscovite and the decreasing foramini­ China and South China Seas (Niino and Emery, 1961) feral number toward the top of the biofacies indicate an were examined. In each of these areas, grain size de­ increasingly close approach to shore. Increase in the creases seaward, and calcium carbonate content in­ sand-silt content of the strata towards the tcio of the bio­ creases seaward, at least to the point where Pleistocene facies indicates that the sea bottom had come into an deposits begin. In each of these modern areas the num­ environment of higher energy. Recent bracHsh marshes ber of species and specimens of Foraminifera per gram and lagoons discussed by Phleger (1960a, p. 258) sup­ of dry sediment (foraminiferal number) increases off­ port exclusively or predominantly arenaceous faunas, shore, as does the proportion of planktonic specimens. and it is possible, though not likely, that the faunas of Along the western Guiana shelf, a shallow depth zone the upper arenaceous biofacies lived in waters of low­ paralleling the shore contains no Foraminifera, and in ered salinity. Lowered salinity has been suggested as the other areas mentioned above, small foraminiferal the factor responsible for the small predominantly numbers nearshore are usual. This foraminiferal dis­ arenaceous faunas in the beds of the Arctic tribution in a horizontal plane from offshore to near- slope of Alaska (Tappan, 1951, p. 3) and thQ, Cretaceous shore is analogous to the vertical distribution in the Thermopolis Shale (Eicher, 1960, p. 48). strata studied from the base of the calcareous biofacies It is possible that increased turbidity inhibited the to the top of the upper arenaceous biofacies. growth of calcareous Foraminifera or that increased In discussing the marginal deposits of the Mississippi turbulence exposed abandoned tests to the water a suffi­ delta, Shepard (1956, p. 2537) reported the presence of cient number of times to promote complete dissolution. abundant wood fibers and mica and a low foraminiferal Introduction of more organic material from land may number in the foreset deposits. Foraminiferal number have produced toxic conditions which could not be tol­ increases and wood fibers and mica decrease away from erated by most calcareous species, or the anaerobic de­ shore in the lower foreset and bottomset beds. Abundant struction of this material within the sediment may have wood fibers were also reported in the nearshore silty produced acidity which destroyed calcareous tests. Also, pelites on the western Guiana shelf (Nota, 1958, p. 38, the population of arenaceous Foraminifera may have 39), but they are much less common in the offshore pelites. Muscovite and carbonized plant fragments are filled the normal nearshore niche today occupied by the most abundant in the upper part of the upper arena­ calcareous species , , and Buccella. ceous biofacies, and foraminiferal number is low. Both In short, although various authors explained the pres­ muscovite and plant fragments decrease and foramini­ ence of largely or totally arenaceous fossil foraminiferal feral number increases as the Cretaceous section is faunas as probably due to lowered salinity, this does not descended. Thus, changes that occur in these parameters seem to have been the cause of the arenaceous nature of in modern areas from nearshore to offshore are analo­ the foraminiferal faunas in the upper arenaceous bio- PALEONTOLOGY 37

facies, and other possible but unverified explanations strata containing the lower arenaceous biofacies are are suggested. assumed to have been deposited in rather shallow water, The composition of the faunas of the calcareous bio- but the locale of deposition must have been far enough facies indicates that they lived in rather shallow water, offshore not to receive noticeable quantities of plant although deeper than that in which the upper arenace­ fibers and mica. Alternatively, it could be assumed that ous biofacies lived. The scarcity of silt and sand in the these strata were deposited at the same or greater depths enclosing shale indicates that the sea bottom was not than those in which the strata of the calcareous biofacies affected by Strong winnowing currents. The size and di­ accumulated and that faunal similarities between the versity of the faunas suggest that the bottom waters lower and upper arenaceous biofacies are depth-inde­ were well aerated and of normal salinity. pendent or fortuitous. In either case the rapid transition The small predominantly arenaceous foraminiferal from the lower arenaceous to the calcareous biofacies faunas which compose the lower arenaceous biofacies indicates a rather rapid change in environmental con­ present certain difficulties in interpretation. The simi­ ditions. If the first assumption is accepted, this change larities of these faunas with those of the upper arena­ may have been due to deepening, possibly in conjunction ceous biofacies, at least in terms of the comparisons with an advance of the Cretaceous sea. If the second made in this study, suggest similar environments. On assumption is accepted, the change may have been due the other hand, the presence of abundant Radiolaria, the to environmental changes not related to depth. The filling of calcareous specimens with silica, and the nu­ gradual decrease in faunal size and diversity in the merous thin bentonite beds in strata containing the upper part of the calcareous biofacies and the gradual lower 'arenaceous foraminiferal biofacies contrast mark­ transition to the overlying upper arenaceous biofacies edly with the strata containing the upper arenaceous bio­ indicate shallowing through this time interval. The facies where these features are absent. The Radiolaria upper arenaceous biofacies was deposited in increas­ themselves seem not to have occupied a restricted niche ingly shoaling water, as shown by the nature of the because they also occur in the upper arenaceous bio­ fauna and by the sedimentologic and lithologic changes facies, in the Fox Hills Sandstone, and in shales of the that take place upward, culminating in the deposition calcareous biofacies. In this case, they certainly do not of the very nearshore sands and silts of the lower part indicate water of abyssal depth. The undisturbed nature of the Fox Hills Sandstone. of the bentonite beds in the strata of the lower part of the biofacies indicates that bottom-disrupting currents PALEONTOLOGY were not operative. However, the presence of several thin LABORATORY METHODS and laterally persistent bentonite beds in the lower part Samples were usually taken at 5-foot 9-inch intervals, of the Fox Hills Sandstone indicates that lack of dis­ but generally only every other sample was examined ruption is not a criterion of deep water (Fox Hills for microfossils. These samples were processed by the data from Karl M. Waage, written commun., 1963). In following methods: One-quarter pound (113.4 g) of short, no unequivocal lithologic evidence of deposition the largest pieces of rock in each sample were boiled in of the Virgin Creek shale in deeper water has been a weak solution of sodium hexametaphosphate and observed. The upper and lower foraminiferal biofacies water unt.il broken down. The mud was washed through probably had similar living conditions, which may indi­ a 200-mesh sieve (openings of 0.074 mm). The residue cate a shallow depositional depth for the Virgin Creek, was dried, weighed, and bottled. Few samples left a as for the upper part of the Elk Butte Member and residue of more than 2 g, and most left less than 1 g. lower part of the Fox Hills Sandstone. It is not possible, Of this amount approximately 0.1 to 0.15 g, or the on the faunal evidence, to do more than suggest this equivalent of about 6 to 17 g of shale, was examined because similarities of fauna may be due to those of under the microscope. Before any specimens were environment independent of water depth. A brackish- picked, at least 100 randomly encountered grains of water environment is considered unlikely for the upper residue, including fossils, were counted and assigned arenaceous biofacies because linguloid brachiopods, to categories on the basis of mineralogy or other dis­ sporadically present throughout, are not found in tinguishing characteristics. brackish water today and because the diversity of the Magnetic separation of Foraminifera from ferrugi­ benthonic and nektonic molluscan fauna in the upper nous residue was successful for nearly all samples on beds (Fox Hills Sandstone) containing this biofacies which it was tried. This method removed at least 50 is atypical of a brackish-water environment. percent and sometimes as much as 90 percent of the One can postulate a general sequence of events in the ferruginous particles from the residue. The loss of speci­ deposition of the upper part of the Pierre Shale. The mens that were preserved as ferruginous internal molds 38 FORAMINIFERA, STRATIGRAPHY, PIERRE SHALE, FOX HILLS SANDSTONE, S. DAK. or that contained pyrite was more than compensated for Locality by the many-fold concentration of unfilled tests. How­ CalUsta? cf. C. peUucida Meek and Hayden 60 ft above base of section, 21 ft above lower key bentonite. ever, it was impractical to separate either calcareous or Scaphites sp. 76 ft above base of section, 37 ft above arenaceous Foraminifera from a quartz-rich residue by lower key bentonite. this method. 11 Linguloid brachiopods, from sample 3, directly above the After picking, sorting, and mounting the Forami­ upper key bentonite. nifera, estimates of species abundance were recorded. 13 Inoceramus fibrosus (Meek and Hayden) and Scaphites sp. from 85 to 110 ft above base of section, from These were the estimated number of specimens of each 34 to 59 ft above lower key bentonite. species seen in the course of picking the 0.1 to 0.15 gram 20 Lucina? sp. 16 ft above base of section, 29 ft below upper of residue examined. Nine abundance categories were key bentonite. established. The estimates are comparable for most sam­ 27 Scaphitest sp. at base of section, 20 ft belcw the upper key bentonite. ples because in all samples except those from the siltier Linguloid brachiopods, in samples 3, 6, 9, and 10, range upper part of the Elk Butte Member and lower part of from just below to 35 ft above the upper key bentonite. the Fox Hills Sandstone, weight percentages of residues 27A Discoscaphites sp. 108 ft above base of section, 12 feet were comparable. below the base of the Fox Hills Sandstone. Linguloid brachiopods, in samples 2, 3, 5, 6, 7, 11, 12, Category Specimens and symbol 14, 15, 17, 18, 19, and 23, range from 84 ft below to Abundant______>1,000 (A) 32 ft above the base of the Fox Hills Sandstone. Very common.______500-1,000 (VC) 31 Drepanochilus americana (Evans and Shumard), Goniomya Common___.______150-499 (C) americana Meek and Hayden, Discozcaphites sp., Rather common______50-149 (RC) Pteria linguiformis (Evans and Shumard), and Lunatia Rather rare______20-49 (RR) cf. L. concinna (Hall and Meek) top of the section, Rare______10-19 (R) 107 ft above the base of the Fox Hills Sandstone. Veryrare-_----_--_--_-____-._- 4-9 (VR) Linguloid brachiopods, in samples 1, 3, 5; 7(?), and 9, Scarce______2-3 (S) range from 45 ft below to 11 ft below tre base of the Exclusive-_-----_--_-______1 (X) Fox Hills Sandtone. 36 "Serpula" wallacensis Elias of Searight (1937, p. 38), The estimated abundance of each species in the ex­ and Baculites cf. B. grandis Hall and Meek fossils amined residue of each sample in which it occurs is scattered through the section; stratigrapl ic position of the section not precisely known but believed to be given under "Occurrence" following each species de­ 50 to 150 ft below the lower key bentonite. scription. Under "Material" is an estimate of the total 37 Baculites cf. B. clinolobatus Elias and Scaphites sp. fossils number of specimens observed (although not necessarily scattered through the lower 40 ft of the section, from picked), based on the total of the estimated abundances. 0 to 40 ft below the lower key bentonite. 39 Drepanochilus sp. on the basis of the mbrofauna, this MACROFOSSILS short section appears to lie 50 to 100 ft below the lower key bentonite. Listed below are the macrofossils that were collected 41 Baculites cf. B. clinolobatus Elias and Inoceramus sp. and identified and the sections and stratigraphic hori­ fossils occur from base of section to approximately zons from which they came. Identifications were made 45 feet above the base, 5 to 50 ft below the lower key bentonite. chiefly by reference to the classic work on western in­ Linguloid brachiopods, in samples 1, 3, 5, and 7, range terior invertebrates by Meek (1876). No comparative from 32 ft below to directly below the lower key material was studied. bentonite. 49 Linguloid brachiopods, in samples 1, 3, 5,. 7, 9, 11, 13, Locality and 15, range from directly above to 53 ft 10 inches 3 Baculites sp. 41 ft above base of section, 169 ft below above the upper key bentonite. the lower key bentonite. 50 Discoscaphites nicolleti (Morton) 2 to 9 ft above the Ostrea peUucida Meek and Hayden and Inoceramus cf. base of the Fox Hills Sandstone. 7. cripsiit Mantell var. bambini Morton 32 ft above Gervillia sp. 24 to 30 ft above the base of the Fox Hills base of section, 178 ft below lower key bentonite. Sandstone. 4 Inoceramus sp. float. Protocardia sp. 40 ft above the base of the Fox Hills 7 Lucina sp., Nuculana cf. N. bisulcata Meek and Hayden, Sandstone. and hamulid worm tubes 56 ft above base of section, 52 Linguloid brachiopods, in sample 3, 28 ft t years; the more im­ species or subspecies. Also, because no concerted effort portant are based at least in part on test composition was made to collect macrofossils from the Fox Hills and features of morphology that are more difficult to Sandstone, only a few of the many genera and species observe but that are considered to be of basic impor­ present in this formation are listed here. tance. The best documented recent classification is that of Loeblich Tappan, and others (1964). This impressive OSTRACODES work was published too recently to permit application A small suite of ostracodes from the upper part of the to the faunas discussed here. Pierre Shale was submitted to I. G. Sohn of the U.S. Taxonomically, the familial and generic distinctions Geological Survey for identification. Below is a list of are adopted from Cushman, with several exceptions. genera and species identified and the localities from The large number of taxa made it impossible to investi­ which they came. gate the taxonomy of all genera and families, although Locality several genera were analyzed in detail. 3 Cytherella sp. For most species the dimensions of one or a few speci­ Cytheropteron? sp. mens, visually determined to be of average size for the Brachycythere sphenoides (Reuss) Alexander, 1929. Veenia parallelopora (Alexander), 1929. Pierre specimens, were measured as described below. Asciooythere? sp. The measurements are in no way statistical averages; Cytherella, sp. they are meant only to give a general idea of the sizes Paracypris? sp. of the several species. Measurements were made with a Cytheropteron?, one fragment. 7 Cytherella sp. binocular microscope and screw micrometer eyepiece 13 Cytherella sp. at a magnification of X 50. 36 Brachycythere sphenoides (Reuss) Alexander, 1929. 1. On planispiral and low trochospiral specimens: Veenia parallelopora (Alexander), 1929. Loxoconcha?, juvenile. Maximum diameter. The greatest distance be­ Paracypris f, juvenile. tween opposite peripheries measured perpendic­ Cytherella?, fragment. ular to the axis of coiling along a line passing Asciocythere? sp. across the center of the umbilicus or axis of coil­ 37 Cytherura? sp. ing. One end of the line usually terminates at 39 Haptocytheridea? sp. the outer periphery of the final chamber. 41 Loxoconcha?, fragment. Minimum diameter. The least distance between Loxoconcha or Cytheropteron, one poorly preserved cara­ pace. opposite peripheries measured along a line pass­ Brachycythere, one fragment. ing across the center of the umbilicus or axis of Loxoconeha sp. coiling. One end of the line usually terminates Cytherella?, one fragment. at the periphery of the first chamber in the final 52 Cytherella, large juvenile. whorl. Paracypris f sp. Diameter. Measured in the same plane as maxi­ 53 Cytheropteron?, crushed carapace. Monooaratinaf, fragment. mum and minimum diameter along a line pass­ ing through the center of the umbilicus or axir In addition to the ostracodes, Sohn identified ophiu- of coiling and used for species in which there if roid ossicles from locality 36, sample 3, and locality 52, no appreciable difference between diameters. sample 3. Thickness. The greatest distance observed hi the CLASSIFICATION AND TAXONOMY OF FORAMINIFERA horizontal plane which includes the umbilicus or axis of coiling when the specimen is oriented The classification used here is essentially that of with the axis of coiling and apertural face ir Cushman (1948b), although a number of modifications the vertical plane. This is usually a measure of have been adopted. One advantage to this classification the distance across one of the last few chamberr is that most of the work on Foraminifera over the past in the final whorl in planispirally coiled formr 30 years or so has been either in terms of this classifica­ or of the height of the spire in trochospirally tion or its somewhat more simplified earlier versions; coiled forms. 40 FORAMINIFERA, STRATIGRAPHY, PIERRE SHALE, FOX HILLS SANDSTONE, S. DAK.

2. On elongate flattened specimens: in some larger specimens. Quartz grains with a minor Length. Distance along the axis of elongation. amount of cement compose the wall in other Targe speci­ Breadth. Greatest distance in the plane of com­ mens and in some smaller specimens. Series of specimens pression and perpendicular to the axis of elon­ have been found that exhibit all stages between the two gation. extremes. Thickness. Greatest distance perpendicular to the Silt particles are all approximately the same size in plane of compression. each test. Grain size does not appear directly related to 3. On elongate cylindrical specimens, including high- test size; some of the narrowest specimens ar°. composed trochospiral specimens: of very coarse grains, whereas some of the wider and Length. Distance along the axis of elongation. presumably more mature tests are composed of rather Breadth. Greatest distance perpendicular to the fine grains. axis of elongation. Specimens composed entirely of amorphous material 4. On single-chambered specimens: may be as thick walled as coarsely arenaceous specimens, Height. Distance from the aperture to the base though in general they are more delicate and some of the chamber. This is the only dimension in exhibited thin translucent walls. globular tests. The range of variation of the upper Pierre and lower Breadth. Greatest distance in the plane of com­ Fox Hills specimens, coupled with the scarcity of diag­ pression and perpendicular to the axis of height nostic criteria to identify species of this genus, makes it or, in cylindrical forms, the greatest distance difficult to determine the species to which these speci­ perpendicular to the axis of height. mens should be assigned. The more common smoothly Thickness. As defined in (2) above, if the cham­ finished specimens resemble Bathysiphon brosgei Tap- ber is compressed. pan (Tappan, 1957, p. 202, pi. 65, figs. 1-5). The larger Almost all taxa, including those that could not be smooth specimens resemble what Tappan (1962, p. 128) identified to species, are described, with the exception of referred to as B. vitta Nauss. Because of the gradational a few well-known and frequently cited species. All sequence that the upper Pierre and lower Fox Hills identified species and most of those that could not be specimens exhibit, all the specimens are tentatively as­ identified to species are illustrated. Photographs illus­ signed to B. ~brosgei Tappan. All specimens are incom­ trate most species, but drawings are used for the new plete. species and for a few others. Retouching of photographs Occurrence. Bathysiphon brosgei Tappan has pre­ was done by me or by Mrs. Elinor Stromberg under my viously been reported from the Cretaceous of Alaska, direction. where it is found throughout the Colville and Nanu- Family RHIZAMMINIDAE shuk Groups and in the underlying Fort res? Mountain Formation (Tappan, 1957, p, 202; 1962, p. 128); from Genus BATHYSIPHON M. Sars, 1872 shales of Coniaciaii and Saiitonian ages in the Redding Bathysiphon brosgei Tappan? area, Shasta County, Calif.; and from the Holz Shale Plate 4, figure I Member of the Ladd Formation of late Turonian to early Campanian ages in the Santa Ana Mountains, Test single chambered, elongate, cylindrical or com­ Calif. (Trujillo, 1960, p. 302). pressed, with occasional constrictions; compressed speci­ The species occurs at nearly all levels in the upper mens often with a troughlike central depression due to part of the Pierre Shale and lower part of th?, Fox Hills the collapsing of the wall into the central cavity; wall Sandstone. It is usually scarce but occasionally becomes thick in larger specimens, rather thin in some smaller an abundant element in the fauna. specimens, and consists of amorphous noncalcareous ce­ Material. Several hundred specimens v^ere found. ment and silt grains in widely varying proportions, the Locality Sample texture ranging from smooth to very rough; aperture, Locality Sample 5-RR 7------3-X the open end of the tube. Dimensions of average-sized 7-VR 11?-VR specimens: length, about 0.7 mm; breadth, about 0.2 mm 9-R 15-R (crushed). 1-RR 17-RR 3-R 23-X Remarks. The most distinctive characteristic of 5-RR 13 ___ _ 23-X these specimens is the range of variation in wall compo­ 9-RR 20_ 17-VR sition. The proportions of amorphous cement and silt 11-RC 27 6-S 9-RC grains vary considerably. Amorphous material composes 14- RR 16-X 2-RC all the wall in most smaller specimens and virtually all 18-RC 3-VR PALEONTOLOGY 41

Locality Sample Locality Sample Locality Sample Locality Sample 27A. 9-RC 41______10-S 50 .._ 1-VR 52___. .___.___..._ 5?-VR 11?-X 11-VR 3-VR 6-VR 19-X 13-VR 5-VR 53.. .__.______-._. 13?-S 23-VR 42______7-R 7-X 157-S 31- 1-X 9-S 27?-VR 17?-S 5-S 44.__.______1A-VR 297-X 7-X 3-R 31-X 9-VR 12-VR 11-S 19-RR 12?-X 45..__.__.____. 1-X 14-S 49______15-S 16-S 17-X 36_. 1-X 50. 25-X Family AMMODISCIDAE 2-S 27-X 3-S 29-S Genus AMMODISCUS Beuss, 1861 4-S 31-S Ammodiscus cretaceus (Beuss) 5-VR 53. 5-VR 1-VR 7-S 37. Plate 4, figure 3 41. 1-VR 13-S 3-X 54_ 1-S Operculina cretacea Reuss, 1845, Versteinerungen Bohniischen 5-S 5-VR Kreideformation, pt. 1, p. 35, pi. 13, figs. 64, 65. 9-VR 13-X Cornuspira cretacea Reuss, 1860, Akad. Wiss. Wien, Matt.- naturw. Kl. Sitzungsber., v. 40, p. 177, pi. 1, fig. 1. Ammodiscus cretacea (Reuss). Cushman, 1934, Cushman Lab. Foram. Research Contr., v. 10, pt. 2, p. 45. Test planispiral, biconcave, closely and uniformly Family REOPHACIDAE coiled, partially involute; each succeeding whorl covers Genus REOPHAX Montfort, 1808 about one-half the preceding whorl; chamber size in­ creases gradually and uniformly, with many coils, com­ Reophax sp. monly distorted in fossilization; suture distinct, de­ Plate 4, figure 2 pressed ; wall fairly thick, composed completely of non- calcareous cement, surface matte textured, milky white; Test incomplete or distorted in all specimens. The aperture the open end of the chamber, generally flat­ best specimens are rectilinear, uniserial, with globular tened or distorted by crushing. Dimensions of average- partly overlapping chambers; wall composed of moder­ sized specimens: maximum diameter, about 0.5 mrr; ately coarse, angular silt grains, about 30 percent minimum diameter, about 0.4 mm; thickness, about 0.1 cement;/ surface smooth relative to the size of the ograins mm. composing the wall; aperture 'believed to be terminal but Remarks. The specimens included in this specie7, not positively identified in any of the few specimens like those included in Batliysiphon brosgei Tappan? having the final chamber preserved. Dimensions of exhibit a wide range in variation in wall thicknes?. average-sized specimens: length, about 0.7 mm; breadth, Smaller, presumably less mature, specimens have about 0.2 mm. thinner and more translucent walls than the associated Remarks. Although the specimens are typically larger specimens. Most specimens were distorted dur­ crushed and broken, shape of the test and chambers in­ ing compaction of the sediments, and many were flat­ dicates that they are in the genus Reophax. Lack of tened in the plane of coiling. Thinner walled specimens complete specimens and apertural details precludes were flattened relatively more than thicker walled one?. specific identification. The specimens resemble R. Occurrence. This species has been reported from tlie tnimda Tappan and R. arctica Bracly in size, nature of Pierre Shale of South Dakota (Loetterle, 1937, p. 56), the external globular chambers, and coarseness of wall from the Riding Mountain Formation of Saskatchewan composition. They are more closely similar to R. minuta and Manitoba (Wickenden, 1945, p. 50), and from the Tappan than to any other Cretaceous species of this Sentinel Hill Member of the Schrader Bluff Formation genus known to me. in Alaska (Tappan, 1962, p. 130, 131). Cushman (1946, Occurrence. These specimens are found from 66 feet p. 17) recorded it from beds of Austin, Taylor, ani above to 74 feet below the base of the Fox Hills Sand- Navarro ages in Cretaceous deposits of the Gulf Coastrl stone. Plain. Since 1946, the species has been reported from a Material. Fewer than 50 specimens were found. borehole penetrating Upper Cretaceous rocks near Sails - 42 FORAMINIFERA, STRATIGRAPHY, PIERRE SHALE, FOX HILLS SANDSTONE, S. DAK. bury, Md. (Cushman, 1948a, p. 245), and from the Arka- white material, with no foreign particles visible; aper­ delphia Marl in Arkansas (Cushman, 1949, p. 2). In ture formed by the open end of the chamber at the addition to these North American occurrences, Am- basal rim of the spire. Dimensions of average-sized modiscus cretaceus has been reported from the Cretace­ specimens: thickness, about 0.1 mm; diameter, about ous of France, the Netherlands, Germany, Spain, 0.25 mm. All specimens distorted. Poland, and Ireland, and also from Japan and Aus­ Remarks. The specimens differ from Glomospira tralia. charoides var. corona Cushman and Jarvis in lacking Specimens are generally few in any one sample but the "crown" of irregular coils from which the variety occur through the entire measured section. takes its name. They differ from most other specimens Material: Several hundred specimens were found. of G. charoides which I have seen in being completely opaque rather than slightly translucent; as a result, the Locality Locality Sample coiling pattern is not clearly accentuated in the Pierre 1-X 31. 3-VR 3-VR 5-X specimens. 5-RR 7-VR Occurrence: Glomospira charoides var. corona has 7-VR 14-S ben reported from the Pierre Shale of South Dakota 9-S 18-X (Searight, 1938, p. 135; Applin, 1933, p. 219). It has 1-RC 20-X 3-RR 36. 1-S not been recorded from Upper Cretaceous deposits of 5-RR 2-S the Gulf Coast. G. charoides has not previously been 7-VR 3-VR recorded from the United States, to my knowledge, but 9-RR 4-R has been recorded from the Upper Cretaceous of Mexico 11-RR 5-VR (White, 1928, p. 187) and from the Cretaceous of 12-VR 37. 1-VR 14-RC 3-VR Switzerland, Czechoslovakia, Germany, the Nether­ 16-R 5-X lands, Poland, England, and France. 18-R 6-VR In the upper part of the Pierre Shale of north-central 22-R 8-R South Dakota, this species is represented by a few speci­ 4-X 39. 1-X 4-S 41. 1-R mens found 52 to 143 feet below the lower key bentonite 5-VR 3-R in the Moreau River stratigraphic sequence. 9?-VR 5-S Material. About a dozen specimens were found. 17-S 9-S 23-S 11-VR Locality Sample 29?-X 42. 9-R 11-S 20... 24-S 44. 3-VR 14-VR 27... 9-S 52. 7?-X 16-X 27A. 5-S 53_ 3?-X 18-S 7-X 5-X 9-X 11-S 7?-X 17-X 54. 1-X Family LITUOLIDAE 21-VR 5-VR Genus HAPLOPHRAGMOIDES Cushman, 19TO 9-VR Haplophragmoides rota Nauss Genus GLOMOSPIRA Ezehak, 1888 Plate 4, figures 5a, b Glomospira charoides (Jones and Parker) Haplophragmoides rota Nauss, 1947, Jour. Paleontology, v. 21, Plate 4, figures 4a, b no. 4, p. 339, pi. 49, figs. 1,3. Trochammina squamata, var. charoides Jones and Parker, 1860, Geol. Soc. London Quart. Jour., v. 16, p. 304. Test planispiral, compressed, completely involute, Glomospira charoides (Jones and Parker). White, 1928, Jour. with small shallow umbilici; periphery subacu^e, smooth Paleontology, v. 2, no. 3, p. 187, pi. 27, fig. 7. to slightly lobulate; chambers rather indistinct, eight to 10 in the final whorl, slightly if at all inflated; sutures Test small, composed of a proloculus and an undivided unrecognizable except where slightly depressed between tubular chamber which forms a low bell-shaped, inflated chambers, straight to slightly convex toward rounded spire; in most specimens the area enclosed by the aperture; walls moderately coarsely arenaceous, the spire is occupied by a slightly protruding to slightly rather smoothly finished, with relatively little cement, depressed convex lump of shell material; several other silt grains fairly well size sorted; aperture not well pre­ specimens are more discoidal, perhaps because of de­ served, apparently a low silt between the br.se of the formation; wall noncalcareous, composed of milky- apertural face and the underlying chamber; color white PALEONTOLOGY to rust tinted, generally the former. Dimensions of aver­ Locality Sample Locality Sample 5-VR age-sized specimens: maximum diameter, about 1.0 mm; 37 ______6-X 50- 10-VR 7-S minimum diameter, about 0.7 mm; thickness, about 0.2 12-RR 97-R mm. All specimens at least partly distorted. 41 ___-_ _ 3-S 117-R Remarks. Direct comparison of the Pierre and Fox 5-RR 137-S Hill specimens with the holotype and paratypes or Hap- 13-RC 17-VR lophragmoides rota Nauss was not possible. However, 42_.__._._.__.._. 77-C 19-VR 87-C 25-R hypotypes of this species from the Cretaceous of Alaska, 9-RC 27-VR designated by Tappan (1962, p. 134-135), compare 44______--_-_--_- 1A-RC 29-RR well with some of the Pierre specimens in both the well- 17-RR 31-S preserved and deformed states. 3-S 52_ 1-RR 57-S 3-R Nearly all specimens of Haplophragmoides recovered 10-S 57-R in this study were distorted in one way or another. This 197-R 67-S added greatly to the difficulty of assigning the specimens 217-S 53. 5-R to species. As a result, the assignments to H. rota have 45 ---_----__ 17-S 13-RR been much more subjective than for almost every other 37-VR 15-R 49 _ __ _ 137-R 17-RC species; many specimens could only be tentatively as­ 15-R 54. 1-X signed to this species. Furthermore, the distinction be­ 50------1-RR 37-RR tween small specimens of H. rota and average-sized spec­ 3-VR 137-S imens of H. 'bonanzas nsis Stelck and Wall are often not clear cut. H. rota and H. bonanzaensis, at least as Haplophragmoides bonanzaensis Stelck and Wall I have recognized them, may be variants of a single Plate 4, figures 6a, b species. Haplophragmoides bonanzaensis Stelck and Wall, 1954, Research Occurrence. This species was first reported from the Council Alberta Kept. 68, p. 24, pi. 2, fig. 10. Mulga, Grizzly Bear, and Vanesti Tongues of the Belly River Formation in Alberta, Canada (Nauss, 1947, Test planispiral, completely involute, biumbilicato; p. 339). It has since been tentatively identified from beds periphery fairly broad, well rounded, slightly lobulate; of Coniacian and Santonian age in Alberta (Wall, umbilici open, shallow, small; chambers large, distinct, 1960, p. 20) and has been identified from the Seabee and slightly inflated, five to seven in last-formed whorl, Schrader Bluff Formations in Alaska (Tappan, 1962, usually six; sutures distinct, depressed, straight, radial, p. 134-135). occasionally oblique; wall smoothly finished, noncal- Specimens which are here included in Haplophrag- careous, with a rather high proportion of cement en­ moides rota. Nauss occur from 11 feet above the base of closing fine- to medium-grained silt particles; color the Virgin Creek Member to 66 feet above the base of the usually milky white but, ranges to rusty orange; aper­ Fox Hills Sandstone. ture a very low interiomarginal equatorial silt. Dimen­ Material. More than 1,000 specimens were found. sions of average-sized specimens: maximum diameter, Locality Sample Locality Sample 0.2 mm to 0.25 mm; minimum diameter, about 0.2 mm ; 1-. 17-RR 20_ _ 24-VR thickness, about 0.15 mm. 3-VR 27- 10-VR Remarks. The apertures of most specimens are 57-R 27A. 7-RR poorly defined or are not visible at all, but on some 97-R 97-RC 1-C 11?-R specimens the apertural area is clear and undistorted, 37-RC 177-RR and the aperture is a low-arched interiomarginal slit. 57-RC 19-X The specimens compare well with hypotypes of Haplo- 77-R 21-RR 97-RC 23-S phragmwides bonanzaensis from the Upper Cretaceous 31. 1-R of Alaska (Tappan, 1962, p. 134) in terms of siz-% 18-RC 3-RC chamber shape, and chamber number, although preser­ 22-R 5-RR 9-R 7-S vation is quite different. 177-S 9-R Specimens of this species are commonly distorted in 19-X 11-S various planes, as are the specimens of H. rota Nauss 27-C 12-VR with which they are commonly associated. H. bonan- 297-C 147-S zaensis, as differentiated from H. rota in this study, is 307-X 17-VR 337-S 20-VR generally smaller, has a smoother and less arenaceous 44 FORAMINIFERA, STRATIGRAPHY, PIERRE SHALE, FOX HILLS SANDSTONE, S. DAK.

wall, and has fewer chambers in the final whorl. In Family TEXTTTIARIIDAE other respects these species are quite similar, and they Genus SPIROPLECTAMMINA Clishman, may be variants of a single species. Spiroplectammina laevis (Roemer) cretosa Cu^hman Occurrence, Haplophragmoides bonanzaensis Stelck Plate 4, figures 7a-c and Wall was first, reported from the Kaskapau Forma­ tion of Turonian age in Alberta and British Columbia Spiroplectammina laevis (Roemer) var. cretosa, Cnshman, 1932, (Stelck and Wall, 1954, p. 24). It has since been re­ Cuslnnan Lab. Foram. Research Contr., v. 8, pt. 4, p. 87, ported from the Seabee and Schrader Bluff Formations pi. 11, figs. 3a, b. of Turonian to Campanian age in Alaska (Tappan, Test biserial, elongate, about li/2 times as long as 1962, p. 134). broad, compressed; tapers rather rapidly to a sharply This species occurs from 25 feet above the base of rounded initial end, greatest breadth at th?i apertural the Virgin Creek Member to 24 feet above the base of end, thickest at the apertual end through th°, middle of the Fox Hills Sandstone. It becomes a dominant ele­ the test; periphery subacute to acute, lobulate, in some ment, in the fauna only in the upper part, of the sequence specimens dentate; apertural end nearly flat, widest at where it increases in number and where its relative im­ the center and tapers rapidly to the acute peripheries, portance is greatly increased because of reduction in perpendicular to the vertical axis at the midline, be­ size of the fauna as a whole. comes oblique toward the peripheries, apertural face very low and rounded; early coiled part obs cure, small, Material. 100 to 200 specimens were found. involves only the first few chambers, rapidly becomes Locality Sample Locality Sample biserial; chambers distinct, not inflated, long, low, !__--___-______5-R 42. 9-R slightly overlapping; sutures flush or slightly raised, 3______11-R 44. 19-S limbate, gently convex upward, oblique to the axis of 147-R 49. 15-R 22-S 17-RC elongation; wall finely arenaceous, with a variable but 23?-X 19-RR generally high proportion of calcareous cement, not 7______77-S 50. 1-VR usually collapsed; aperture an arched, centrally located, 20_----______-___ 24-VR 3-VR interiomarginal opening extending f o>r one-third to one- 27A_____.______6-R 52. 1-RR 7-RR 3-R fourth the thickness of the test, slightly recessed be­ 21-RR 5-R tween the lateral areas of the apertural face. 31. ._------_ 1-R 53_ 3-X Dimensions of average-size specimens: length, 0.25 to 7-VR 9-RR 0.35 mm; breadth, about 0.25 mm; thickness, 0.1 to 0.15 9-VR 11-C mm. 14-VR 13-RC 36. ______4-R 15-R Remarks. Specimens of this subspecies are often 41. ------1-R 54_ 5-R preserved as pyritic internal molds. They are commonly 11-R associated with a predominantly calcareous-perforate suite of Foramiiiifera. Some specimens, referred to this Haplophragmoid.es sp. subspecies with question, have iioncalcareous walls but Many specimens of Haplophragnwides were too are otherwise very similar to the more common speci­ poorly preserved to permit species identification. The mens with calcareous walls. Nbiicalcareou? specimens localities and samples from 'vliich these specimens came have not been found in samples containing calcareous areenu eiated below. specimens. Diagenetic replacement of calcite by silica may account for this difference, or it may 1)3 due to the Locality Sample Locality Sample substitution of silica by calcite as a cementing agent by 7-VR 3-S 36_ the living . 4-S 5-VR 16-VR 42. 10-C Spiroplectammina nuttalU Lalicker is in general very 35-S 49. 1-S similar to S. laevis cretosa but differs in having a 17-VR 3-S smoother periphery, in being somewhat thicker, and in 9-VR 27__ 7-X lacking raised, strongly limbate sutures. S. knebeli Le- 27A 3-X 9-VR 5-S 52. 7-S Roy is quite a bit wider than the Pierre species, whereas 15-X $. knebeli var. longa Said and Kenawy is more closely PALEONTOLOGY 45 similar but differs in being slightly thicker and in hav­ eries usually irregular in outline, sometimes smooth, ing a smoother surface texture. S. esnaensis LeRoy acute to subacute; apertural end rhomboidal in outline, has a different wall texture and slightly higher cham­ slightly convex, composed of the upper surfaces of the bers. The Pierre specimens differ from the type speci­ last and penultimate chambers which meet at an acute mens of $. laevis cretosa only in having slightly higher angle in the midline of the test; planispiral part com­ chambers. Cushman did not state that the wall of this posed of four to seven chambers in addition to the pro- subspecies is calcareous, but a plesiotype designated by loculus, diameter of the initial end dependent upon the him was tested with dilute hydrochloric acid and was size of the chambers composing the coil; specimens with found to be very calcareous. a coiled part of large diameter increase less rapidly in Occurrence. To my knowledge, Spiroplectammina breadth than specimens with a coiled part of small laevis cretosa has not been reported previously from diameter; size of chambers in the coil apparently rot deposits in the western interior of the United States or directly related to the size of the proloculus; biseral from Canada. Cushman (1946, p. 28) recorded its oc­ part composing most of the test in all but the smallest currence in beds of Austin and Taylor ages in the Gulf specimens, usually composed of four or five pairs of Coastal Plain. It was reported from the Mt. Laurel and chambers, but some specimens have as many as seven Navesink Formations in New Jersey (Jennings, 1936, pairs; chambers oblique to axis of elongation, usually p. 12) and from the Hammond well near Salisbury, Md. not inflated, two to three times broader than high, regu­ (Cushman, 1948a, p. 245). It was also reported from larly increase in size as added, slightly overlapping; in the Upper Cretaceous of France, Japan, Israel, Ireland, all longer specimens the final few pairs of chambers be­ Germany, and Western Australia. come nearly as high as broad; sutures usually flush with In the upper part of the Pierre Shale this subspecies the surface, indistinct, occasionally slightly depressed, occurs from 115 feet below the lower key bentonite to slightly if at all limbate, oblique to the axis of elonga­ 81 feet above the upper key bentonite. tion, straight or slightly convex toward the apertural Material. More than 1,000 specimens were found. end; Wc^ll arenaceous, composed of either calcareous or noncalcareous particles; particle size ranges from rela­ Locality Sample Locality Sample tively coarse grained to fine grained, amount of cement 16-S 27_ 6-S 20-R 7-X variable, finer grained particles and more cement char­ 22-RR 27A 7-VR acteristic of calcareous specimens; aperture a low- 23-S 9-VR arched interiomarginal opening at the midline of the 4-RC 36 test, located in a slight invagination at the base of the 5-RC 2-R 1-RR 3-R low rounded apertural face. 3-R 37 __- _ 1-RR Remarks. The breadths, lengths, and thicknesses of 5-RC 5-RR 13 specimens were measured. The specimens ranged 6-VR 6-VR from 0.23 mm to 0.47 mm in length. The length-to- 7-S 10-RR breadth ratio varied from 1.3:1 to 1.9:1; the length-to- 9-S 39 _ _-_.- 1-RR 11-VR 41.___-__-____.-. 1-RR thickness ratio varied from 2.2:1 to 4.7:1; and the 13-R 3-S breadth-to-thickness ratio varied from 1.7:1 to 2.5:1. 15-RC 5-X Only one definitely megalospheric specimen was found. 16-VR 9-RR Its length-to-breadth ratio was slightly higher (.2.0:1) 17-RR 10-RC than the highest value of this ratio for microspheric 29?-X 117-S 13. 1-VR 13?-S specimens (1.9:1), but the other ratios for this specimen 3-RR 42. _. ___._ . 7-RC were within the ranges shown by the microspheric speci­ 5-R 9-S mens. 9-RR 44-______.___- 19-VR 23-S As can be inferred from the variations described for the measured dimensions, amount and coarseness of Spiroplectammina mordenensis Wickenden arenaceous material, calcareous and noncalcareous na­ Plate 4, figures 8a-d ture of the wall, chamber shape, and initial coiled part, Spiroplectammina mordenensis Wickenden, 1932, Royal the interpretation of the species encompasses specimens Canada Trans. 3d ser., v. 26, sec. 4, p. 86, pi. 1, fig. 4. different from each other in a number of ways. All these Test initially planispiral, later becoming biserial, variations are either present in single specimens or r-re elongate in larger specimens, compressed ; 1*4 to 2 times gradational within suites of specimens, except that the as long as broad, broadest and thickest at apertural end wall is either calcareous or noncalcareous. Features that except in some of the longest specimens ; lateral periph- unite these specimens are the fairly uniform number of 323-073 O 69 4 46 FORAMINIFERA, STRATIGRAPHY, PIERRE SHALE, FOX HILLS SANDSTONE, S. DAK. chambers in the coiled part and the generally small bulimine arrangement; slightly twisted triserial part, number, obliquity, and shape of chambers in the biserial when present, composed of as many as four whorls; part. chambers slightly to moderately inflated, sub^lobular, To my knowledge, the only previously described spe­ rather closely appressed, slightly to moderately over­ cies of Spiroplectcwnmina that includes at least some of lapping, generally increase regularly and moderately the specimens found in the Pierre samples is 8. mwden- in size as added but in some specimens show an unusual ensis Wickenden. These similar specimens seem to be increase in size near the apertural end of the test, often related to specimens showing the described variations at the start of bulimine chamber arrangement; sutures through several suites of morphologically intermediate in early part indistinct, flush or slightly depr^^sed, dis­ specimens. Some of the Pierre specimens resemble S. tinct and depressed between later and larger chambers; gandtana Lalicker, and others resemble 8. gryzbowsMi wall arenaceous, composed of numerous closely fitted Frizzell, but none is considered similar enough to be quartz grains held by a rather small amount of cement; placed in these species. surface moderately rough textured, nonc^.lcareous; Occurrence. Spiroplectammina. iiwrdenensis Wick­ aperture a high-arched opening at the base of the aper­ enden was originally described from the Upper Cretace­ tural face, set in a large indentation of the apertural ous Morden beds of Manitoba, Canada (Wickenden, face, not well preserved on most specimens. Dimensions 1932a, p. 86). It has since been reported from the Senti­ of average-sized specimens: length, about 0.4 mm; nel Hill and Barrow Trail Members of the Schrader breadth, about 0.15 mm. Bluff Formation in Alaska (Tappan, 1962, p. 140) and Remarks. Most of the Pierre specimens are distorted, from the Tuluga Member of the Schrader Bluff Forma­ but several of the better preserved specimens closely tion (Tappan, 1951, p. 5). resemble the holotype and paratypes of Verneuilinoides The Pierre specimens are found in small numbers in perplexus. Distorted specimens correspond very well samples sporadically distributed from 107 feet below the with distorted paratypes (Cushman colln. 44122). lower key bentonite to within 20 feet of the base of the Despite the similarity of some of the Pierre specimens Fox Hills Sandstone. to the type specimens of Verneuilinoides perplexus, as­ Material. Fewer than 150 specimens were found, signment to this species is not positive because of the many of which were not well preserved. bulimine arrangement of chambers in at leas4: a part of nearly all specimens. In addition, the Pierre specimens Locality Sample Locality Sample 3-S 49- 9-RR are more coarsely arenaceous and contain less cement 7-S 11-RR than the types. 9-RR 13-RR Occurrence. Verneuilinoides perplexus (Loeblich) 11-S 15-RR was originally described from the Upper Cretaceous 12-X 17-RR Pepper Shale (Pepper Shale Member of Woodbine For­ 36. 4-R 19-R 37- 1-S 52. 5-S mation) of Texas (Loeblich, 1946, p. 138) and has since 5-S 53. 11-VR been reported from shale of Cenomanian agQ. (Dunve- 12-VR 13-VR ganoceras zone) in Alberta, Canada (Stelck and Wall, 3-X 44. 15-VR 1955, p.60). 10-S 54. 1-X 15-S 3-X This species occurs from 70 feet above the upper key 17-X 5-S bentonite to 24 feet above the base of the Fox Hills 19-VR 13-S Sandstone in the Moreau River sections and from 58 Family VERNEUILINIDAE feet above the upper key bentonite to just below the base of the Fox Hills in the Grand River sections. Genus VERNEUILINOIDES Loeblich. and Tappan, 1949 Material. 100 to 200 specimens were found, most of Verneuilinoides cf. V. perplexus (Loeblich) which were distorted. Plate 1, figures la, b Local Sample Locality Sample VerneuiUna perplexa Loeblieh, 1946, Jour. Paleontology, v. 20, 27A. 7 X 52. 1 RR no. 2, p. 138, pi. 22, figs. 14-16. 21 S 3 RR Yerneuilinoides perplexus (Loeblich). Loeblieh and Tappan, 3L 1 VR 5 RR 1949, Washington Acacl. Sci. Jour., v. 39. no. 3, p. 91. 3 VR 6 VR 9? S 53. 7 S Test elongate, slender to rather rapidly flaring with 20 X 9 S early part of some specimens in a definite slightly 49. 17? R 11 RR twisted triserial arrangement followed by a more buli- 50. 1 RR 13 RR 3 R 15 RR mine arrangement of later chambers; other specimens 5 R 17 RR apparently with all chambers in a strongly twisted or 7 S PALEONTOLOGY 47

Genus GATTDRYINA d'Orbigny, 1839, emend. Bowen, 1955 dition than do the types. The aperture never become? Subgenus GAUDRYINA Cushman 1937, emend. Bowen, 1955 entirely isolated in the apertural face in the Pierre specimens, although in several it is terminal or nearl;r Gaudryina (Gaudryina) waters! (Cushman) so and maintains contact with the penultimate chambe^ Plate 4, figures 9a-c through only a very small part of the apertural periph­ Plectma watersi Cushman, 1933, Cushman Lab. Foram. Re­ ery. Unfigured specimens from the Nacatoch Sand search Contr., v. 9, pt. 3, p. 57, pi. 7, figs. la-d. (Cushman Collin. 28062) and Selma Group (Cushman collin. 28059) identified as P. watersi also do not have Test elongate, early triserial part prominent, later the aperture isolated in the apertural face. becomes biserial; triserial part tapers, broadly trian­ Because of the close approach of the aperture to isc - gular with well-rounded edges when viewed from initial lation in the apertural face and the very close similarity end, composes at least one-fourth of the length of even in plan, shape, size, and texture of the test to that of the largest specimens, broader than biserial part in side G. watersi (Cushman), the Pierre specimens are placed view; biserial part tapers slightly in side and front in this species. The generic name Plectina is considered views, slightly twisted in some specimens, consists of to be a junior synonym for Gaudryina, following th^ three and sometimes four pairs of chambers; chambers emendation of Bowen (1955, p. 363-364). indistinct in early part of triserial arrangement, later An interesting feature, also noted for the Pierre speci­ fairly distinct and slightly inflated, distinct and mod­ mens of Bathysiplum brosgei Tappan? and G. bcnuera erately inflated in biserial part; sutures become pro­ Mello, is the larger size of arenaceous material compos­ gressively more depressed with addition of chambers, ing the tests of specimens of all three species in samples moderately oblique in biserial portion; wall finely to 14,16, and 18 of section 3. moderately coarsely arenaceous, about 20 percent ce­ Ocourrence. This species has been reported from ment, cement soluble in dilute MCI; aperture in the tri­ beds of Navarro age in the Gulf Coastal Plain by Cush­ serial part a simple high-arched opening ait the basal man (1946, p. 47). It has also been reported from tie margin of the last-formed chamber at the center of the Upper Cretaceous Vidono Shale Member of the Santa upper surface; aperture in the biserial part somewhat Anita Formation of northeastern Venezuela and from recessed into the higher apertural face and becomes beds of Senonian, Maestrichtian, and ages in more recessed as chambers are added, in the largest northeastern Bulgaria. specimens almost completely isolated in the apertural Gaudryina watersi occurs in the upper part of tr^ face, with only a small part of the periphery being Pierre Shale from 80 feet above the upper key bentonite formed by the upper surface of the penultimate cham­ to 144 feet below the lower key bentonite. ber. Dimensions of average-sized specimens: length 0.55 Material. 500 to 1,000 specimens were found. to 0.6 mm; breadth across biserial chambers about 0.25 mm. Locality Sample Locality Sample Remarks. The emendation of the genus Gaudryina ______11 VR 27A______2 VI, 14 RC 3 VF by Bowen (1955, p. 363-364) was made for the pur­ 16 RR 9? S pose of including in this genus a group of fossils which, 18 RR 36______2 S up to that time, had been placed' in separate but similar ______8 VR 4 VF, genera. The genus Plectma Marsson, 1878, was one of ______1 X 5 S 30 RC 37-__---_--_-.-_- 5 S those placed in synonymy. In order to test Bowen's idea 32 S 44______..___-__ 23 S of the 'artificiality of the use of number of chambers in 13. ______40 X 49____ -- - 5 S the initial whorl as a diagnostic character, I etched a 41 X 9 S paratype of P. watersi and found that the initial whorl 20- ______17 VR 15 R consisted of three chambers surrounding a central pro- 27. ______6 S 19? X 7 S 54______---_____- 1 X loculus. Bowen's arguments are supported by this find­ 3 S ing, and I feel that he is correct in placing Plectma in Gaudryina boweni Mello, new name synonymy with Gaudryina. Plate 4, figures lOa, b The early arrangement of chambers in the Pierre specimens is definitely triserial, as determined by etch­ Dorothia stephensoni Cushman, 1936, Cushman Lab. Foram. Re­ ing a number of specimens. In addition, the prominence search, Spec. Pub. 6, p. 28, pi. 4, fig. 15 (not Gaudryira of the triserial part and its rounded angles are very stephensoni Cushman, 1928). similar to these features in the type specimens of P. Test elongate, early part in a low trochoid spire, three watersi. However, the biserial chambers, in the Pierre to four chambers per whorl; later part biserial, slightly specimens show less tendency toward the uniserial con­ twisted, nearly circular viewed from initial end, slightly 48 FORAMINIFERA, STRATIGRAPHY, PIERRE SHALE, FOX HILLS SANDSTONE, S. DAK. to moderately compressed viewed from apertural end; Locality Sample Locality Sample sides moderately taper in front view, nearly parallel in 36____-_-__- ___ 5 X 10 RR 37______.______10 VR 1 S edge view, greatest breadth at apertural end; chambers 41______1 VR 3 X in trochoid part overlapping, indistinct; in later biseriaJ 9 R 5? X part, chambers slightly inflated, distinct; sutures flush Gaudryina bentonensis (Carman) and indistinct in trochoid part, slightly depressed and distinct between later inflated chambers, perpendicular Plate 4, figures Ha, b or nearly so to the axis of elongation; wall finely to Rplroplectammina bentonensis Carman, 1929, Jour. Pileontology. moderately finely arenaceous, rather smoothly finished, v. 3, no. 3, p. 311, pi. 34, figs. 8, 9. reacts with dilute HC1, white or gray; aperture a nar­ Gaudryina bentonensis (Carman). Cushman, 1932, Cushman row elongate slit at the center of the base of the final Lab. Foram. Research Contr., v. 8, pt. 4, p. 96. Cushman, 1937, Cushman Lab. Foram. Research Spec. Pub. chamber surrounded by a slight thickening; base of 7, p. 42, pi. 6, fig. 22. aperture formed by top of preceding chamber. Dimen­ Cushman and Deaderick, 1942, Cushman Lab. Foram. Re­ sions of average-sized specimens: length, about 0.45 search Contr., v. 18, pt. 3, p. 52, pi. 9, figs. 12, 13. mm; breadth of biserial part about 0.25 mm; thickness of biserial part about 0.15 mm. Test elongate, straight, slightly twisted, usually dis­ Remarks. In the Pierre specimens the low trochoid torted, earliest part obscure but probably triserial, fol­ part is generally very short and is always several times lowed by triserial part of variable length and then by shorter than the biserial portion. The amount and a biserial part also of variable length but composing at coarseness of arenaceous material is rather variable, but least half of the longest specimens; chambers in triserial the most coarsely arenaceous specimens were obtained part slightly inflated, spheroidal, with shortest axis from section 3, samples 14, 16 and 18, the same strati- vertical and overlapping, similar in biserial part except graphic interval that yielded the most coarsely arena­ more inflated and less overlapping; chambers increase ceous specimens of Bathysiphon brosgei Tappan? and in size fairly slowly in triserial part, very sic wly or not Gaudryina. u^atersi (Cushman). The surface texture and at all in biserial part so that the sides of the longer appearance of these three species are very similar in specimens are parallel or nearly so; wall ccmposed of this interval. silt grains of medium size relative to test size and em­ The validity of the genus Dorothia is discussed by bedded in a moderate amount of noncalareons cement; Bowen (1955, p. 362-363), who concluded that this sutures obscure in early part of triserial stage, become genus should be considered a junior synonym of the more distinct and depressed in later part of triserial genus Gaudily inn. I find Bowen's arguments to be con­ stage and in biserial stage as chambers become more vincing and have here adopted his recommendation by inflated, perpendicular, or nearly so, to the axis of elon­ placing Dorothia stephemoni Cushman in Gaudryina. gation; aperture obscured by crushing in a]l available The new name G. boweni is proposed because the specific specimens, but in the biserial stage apparently a simple name stephemoni is preoccupied in the genus opening in the midline of the test in the apertural face Gaudryina. of the final chamber at or near the suture line separating this chamber from the preceding one. Dimensions of Occurrence. This species has been reported as average-sized specimens: length, about 0.7 mm; breadth, Dorothia stephemonj Cushman from beds of Austin, Taylor, and Navarro ages in Arkansas, Alabama, and about 0.15 mm. Remarks. In some specimens there is a tendency Texas (Cushman, 1946, p. 45). It has also been reported towards separation of the final few chambers from from the Senonian and Maestrichtian of Bulgaria. those immediately below, as evidenced by increasing In the upper part of the Pierre Shale, the species oc­ incision of the sutures and corresponding decrease in curs from the base of the .section to 64 feet above the chamber overlap. In a few samples containing Gau­ upper key bentonite in the Grand River sequence and dryina ~ben-tonemis, several partial specimen-? of a large from 139 to 25 feet below the lower key bentonite in the Moreau River sections. uniserial form composed of three or four chambers, with wall texture similar to G. bentonensis and with Material. 100 to 200 specimens were observed. a protruding terminal aperture, were observed. These Locality Sample Locality Sample 3______.______12 X 7______1 S may represent a further development of G. bentonensis 14 R 5 R beyond what can be observed in complete specimens. 16 S 6 X However, a uniserial stage has not been found attached 18 RR 9? VR to any biserial specimen. 20 S 15 X 22 R 36______._ 1 S The Pierre specimens are very similar to the holotype 23 X 3 VR and paratypes of ftpiroplectammina bentonensis Car- PALEONTOLOGY man and to the plesiotypes figured in the papers cited ment probably calcareous; aperture terminal, elongate, in the synonymy. They also correspond quite well to narrow, straight to very slightly curved, upper surface nearly all the remaining specimens of G. bentonetwis of the final chamber is at different levels on either sid°, in the U.S. National Museum collections, when allow­ of the aperture, the higher side has an abrupt trunca­ ances are made for the distortion of the specimens. tion forming one side of the aperture, and a distinct Occurrence. The species has been reported from the flap rises from the lower surface to the level of the Upper Cretaceous of Trinidad, British West Indies higher surface to form the other side of the aperture; (Cushman and Renz, 1946, p. 21; 1947, p. 38), from the aperture itself is the elongate narrow slit between rocks of Austin, Taylor, and early Late Cretaceous age the top of this flap and the edge of the higher surface-; in Texas and Arkansas (Cushman, 1946, p. 33), from most specimens have a small lip about the aperture, but the Benton Shale and Niobrara Chalk of Wyoming several have larger lips which give the aperture a pro­ (Carman, 1929, p. 311), from the lower shale member truding aspect; no internal tube is present between of the Niobrara Formation in Wyoming (Shaw, 1953), apertures. Dimensions of average-sized specimens: and from the Carlile and Cocly Formations in South length, about 0.3 mm; breadth, about 0.1 mm. Dakota and Wyoming (Fox, 1954, p. 105,107, 109). Re?JwrJcs. The distinguishing characteristics of this This species is found from 5 feet above the lower key species are the short, broad, roughly triserial trochoid bentonite to the base of the Virgin Creek Member of stage in which the later chambers increase markedly in the Pierre Shale. size as added, the following uniserial stage composed Material. About 170 specimens are found. of inflated globular to spheroidal chambers, the fine­ Locality Sample Locality Sample grained calcareous wall, and the narrow elongate 1-RR 3______--___- 11-R aperture. 3-R 12-R 5-R 18-R The genus Pseudoclavulina has a triserial arrang?/- 7-RR 22-S ment of the early chambers followed by a uniserial se­ 9-RC 23-RR ries of chambers, and in these respects the new species 1-RC 37_.______3-S resembles this genus, but no species of Pseudoclavidina 3-RR 42_-_-___-__--__- 8-R 5-R 9-RC has an aperture similar to that of the new species. A 9-RR 44_-____.-_____-_ 1A-R similar aperture is present in Martinottiella paleocenica Cushman, but this genus has four or more chambers Genus PSEUDOCLAVULINA Cushman, 1936 per whorl in the early trochoid part whereas the new Pseudoclavulina? meidamos Mello, n. sp. species has only three. The new species is tentatively Plate 1, figures 2a-e ; plate 5, figures la-d placed in the genus Pseudoclavulina until further study Test agglutinated, elongate, straight or slightly ir­ of its variability and phylogeny becomes possible. regular; earliest part composed of the proloculus and Examination of crushed specimens under the petro- about eight chambers arranged three to a whorl, graphic microscope revealed that the walls are com­ forms a low relatively broad trochoid spire, be­ posed of very small calcite grains oriented randomly. comes uniserial above the spire with no intervening The apparently poreless nature of the wall and the pres­ biserial stage; chambers in trochoid part, globular, ence of what appear to be silt-sized particles embedded closely appressed, increase rather rapidly in size as in the wall, as determined under X 216 magnification, added, except, much less rapidly for the final three or indicate that the wall is agglutinated. There is no too% four chambers, indistinct when dry, fairly distinct when connected with the aperture, and there is no extension moistened; uniserial part composed of one to five globu­ of any kind from one aperture to the next. lar to spheroidal chambers, usually three or four, each Occurrence. This species occurs from the level of of which is slightly larger than its predecessor, slightly the lower key bentonite to 47 feet below this level. O~ie to moderately overlapping, quite distinct and slightly specimen, placed here with question because of poor inflated; sutures indistinct in trochoid part, distinct preservation, occurs 94 feet above the upper key ben­ and slightly depressed in uniserial part, oblique in the tonite. The holotype and paratypes of PseudoelavuUna? earliest uniserial part of some specimens, later more nieidam-os are from locality 41, sample 1. Holotype, nearly horizontal; wall rather thick, smooth for USNM (U.S. National Museum) 642579; figured para- agglutinated specimens, composed predominantly of type, USNM 642580; unfigured paratypes, USNM small calcite grains with occasional quartz grains, ce­ 642581, 642582. 50 FORAMINIFERA, STRATIGRAPHY, PIERRE SHALE, FOX HILLS SANDSTONE, S. DAK. Material. Fewer than 50 specimens were found. occurrence of var. conca.va in samples with C. trilaterus Locality Sample Locality Sample (Cushman, 1946, p. 38) suggests that it cannot be con­ 7__ __-- _- 11-X 37. 1-S sidered a valid biologic subspecies. Therefore the Pierre 5-S specimens and Cushman's var. concava are here placed 10-S in Clavulinoides trilaterus (Cushman) undifferentiated. 2?-S 41. 1-RC 3-VR 9-S Occurrence. Clavulinoides trilatera, var. concava, 4-VR has been reported from beds of Taylor and Navarro ages Genus CLAVTTLINOIDES Cushman, 1936 in Tennessee, Alabama, Mississippi, Texas, and Ar­ kansas by Cushman (1946, p. 38). It has also been re­ Clavulinoides trilaterus (Cushman) ported from the Upper Cretaceous of Maryland (Cush­ Plate 1, figures 3a, b man, 1948a, p. 246), from beds of Maestrichtian age in trilatera Cushman, 1926, Am. Assoc. Geol­ Egypt, and from the Cretaceous of northeastern Bul­ ogists Bull., no. 6, v. 10, p. 588, pi. 17, fig. 2. garia. Clavulinoides trilatera (Oustonan). Cushman, 1937, Oushman In the upper part of the Pierre Shale this species oc­ Lab. Foram. Research Spec. Pub. 7, p. 121, pi. 16, figs. 12-18. curs from 82 feet below the lower key bentonite to IT Clavulina trilatera Cuishman var. concava Cushman, 1931, Jour. feet above the upper key bentonite. Paleontology, v. 5, no. 4, p. 302, pi. 34, figs. 12a, b. Material. 20 to 30 well-preserved specimens were Clavulinoides trilatera (Cushman) var. concava (Cushman). Cushman, 1937, Cushman Lab. Foram. Research Spec. found. Pub. 7, p. 121, pi. 16, figs. 19-25. Locality Sample Locality Sample 20-VR 27- 1-X Test elongate, early triserial part rather rapidly 22-VR 7?-X tapers, consists of four or five whorls in which chambers 4-VR 39. 1-VR increase rapidly in size as added, sides parallel in later 40?-S uniserial part, triangular throughout, angles distinct, Genus HETEROSTOMELLA Reuss, 1865 keeled; in the uniserial part chambers fairly distinct, Heterostomella americana Cushman overlap considerably, of rather uniform size and shape, increase in size slightly if at all as added; sutures fairly Plate 5, figures 2a-c distinct, slightly depressed, oblique in triserial part and Heterostomella americana Cushman, 1936, Cushman Lab. Foram. form a chevron pattern on each side, in uniserial part Research Spec. Pub. 6, p. 24, pi. 3, fig. 20. slightly convex upward, slightly oblique, become nearly Remarks. A single well-preserved microspheric horizontal in larger specimens; wall distinctly arena­ specimen is assigned to Heterostomella americana.. Its ceous, appears smoothly finished but in detail rather early triserial part is about one-third the lergth of the rough, composed of well-sorted small grains, percent­ test and is followed by a biserial part ornamented with age of cement variable but usually high, either cement four or five longitudinal partially eroded r; dges; the or grains or both are calcareous; aperture in the tri­ aperture is atop a very short neck. The specimen com­ serial stage a simple small, rounded interioareal opening pares well with the holotype and paratypes of this a slight distance above the junction of the final and species. penultimate chambers and near the point of junction of Occurrence. Cushman (1946, p. 41-42) listed the the final three chambers at about the center of the test, species from beds of Taylor and Navarro ages in the in the uniserial part the aperture is a small rounded to Gulf Coastal plain but stated that "So far rs seen, H. irregular opening at the apex of the chamber at about americana is confined to the Taylor marl and its equi­ the center of the test that projects very slightly. Di­ valent of Texas and related areas, with the exception mensions of average-sized specimens: length, about 0.9 of a few specimens from the Navarro that may be iden­ mm; breadth, about 0.45 mm. tical." The species has also been reported from the Remarks. The type specimens of Clamilinoides tri­ Upper Cretaceous of Maryland (Cushman, 1948a, p. latera var. concava (Cushman) differ from the types 247). of C. trilaterus (Cushman) in having more acute angles The single specimen from the upper part of the Pierre and more concave sides, properties shared by the Shale was found 28 feet below the lower key bentonite. Pierre specimens. Varieties no longer have taxonomic Material. One specimen. status, according to the "International Code of Zoo­ Locality Sample logical Nomenclature" (Stoll and others, 1961) and the 41 . 5-X PALEONTOLOGY

Family SHICINIDAE Material. Fewer than 75 specimens were seen, many Genus SILICOSIGMOILINA Cushman and Church, 1929 of which were at least somewhat distorted. Locality Sample Locality Silicosigmoilina f utabaensis Asano 1______._ 5-VR 3 16-R Plate 5, figures 3a, b 3 ._ _- 7-X 18-RR 9-S 22-RR Silicosiffmoilwia futalwensis Asaao, 1950, Pacific Sci., v. 4, no. 11-R 7 9-VR 2, p. 159, pi. 1, figs. 6, 7. 14-RR Silicosigmoilina californica Cusbman and Church. Applin, 1933, Jour. Paleontology, v. 7, no. 2, p. 219. Family Test compressed, oval to nearly circular in equatorial Genus SPIROLOCULHTA d'Orbigny, 1826 outline, periphery subacute; chambers indistinct in Spiroloculina sp. early part, possibly planispirally arranged, later added Remarks. A single specimen referable to this genui in planes not quite 180° apart; sutures flush or slightly was found. The test is very small, narrowly ovate, and depressed, indistinct; wall finely arenaceous, smooth to flat and lacks an early quinqueloculine stage. The final slightly grainy, generally flat white but in some speci­ chamber is broken, and apertural characters could no4' mens slightly vitreous; aperture the open end of the be observed. The specimen seems to be quite similar to final chamber, irregular, somewhat produced and con­ specimens of Spiroloculina cretacea Reuss in the U.S. stricted, apparently without a tooth. Dimensions of National Museum collections and may belong in thi^ average-sized specimens: length, 0.55 to 0.6 mm; species. Dimensions: length, 0.2 mm.; breadth 0.1 mm; breadth, about 0.35 mm; thickness, 0.05 to 0.1 mm. thickness, 0.01 to 0.02 mm. Remarks. Some of the Pierre specimens closely re­ Occurrence. Spiroloculina oretacea Reuss is the only semble some of the paratypes of Silicosigmoilina cali­ species of this genus so far reported from the American fornica Cushman and Church, but in general they are Cretaceous. It ha,s been found in beds of Taylor and much more compressed than S. californica. The Pierre Austin ages (Cushman, 1946, p. 49). specimens seem to be better accommodated in S. futa­ The Pierre specimen was found in locality 37, sample baensis Asano, judging from the type description and 1,47 feet below the lower key bentonite. figures (no comparative specimens were seen). 8. f uta­ baensis and S. californica are certainly closely related Genus QUINQUELOCULINA d'Orbigny, 1826 and may be variants of single species, although this has not been demonstrated yet. ftuinqueloculina sp. Unfigured specimens on Cushman collection slides Plate 5, figures 4a-c 28096 and 2809T labeled "Rzehakina epigona var. lata" Remarks. Included under this designation are speci­ also appear to belong in 8. f utabaensis. These specimens mens from nine samples and four different localities and the specimens from the upper part of the Pierre All specimens but one are preserved as internal mold? cannot be placed in the genus Rzehakina because of the in silica, and this lack of well-preserved specimens has nonplanispiral mode of addition of at least the later made species identification impossible. Dimensions of chambers. average-sized specimens: length, 0.2 to 0.25 mm; A small group of specimens identified as S. calif omica breadth, about 0.2 mm; thickness 0.15 to 0.2 mm. Occurrence. Distribution of this species is sporadic. Cushman and Church by Cushman and listed by Applin It occurs most commonly in the Pierre Shale within (1933, p. 219) from the Pierre Shale in South Dakota 80 feet of the Fox Hills Sandstone but is also found 42 are like the Pierre specimens found in the present in­ feet above the upper key bentonite and 155 feet belov vestigation and are here placed in 8. futabaensis. the lower key bentonite. Occurrence. Silicosigmoilina futabaensis was orig­ Locality Sample Locality Sample inally described from Senonian carbonaceous sand­ 9-VR 5-VR stone and shale at Yokouchi, Honshu, Japan. It has 49_ 13-S 53 11-R since been reported from Hokkaido, Japan (Fukuta, 50_ 5-S 13-VR 52_ 1-S 17-R 1957, p. 10; Yoshida, 1958, p. 259), and from beds of 3-X Coniacian-Santonian age near Redding, Shasta County, Calif. (Trujillo, 1960, p. 303). Genus MASSILINA Schlumberger, 1893 This species is present in the upper part of the Pierre Massilina sp. Shale 174 to 52 feet below the lower key bentonite in Remarks. Six specimens, only one of which is well the Moreau River sections. preserved, are placed here. The well-preserved specimen 52 FORAMINIFERA, STRATIGRAPHY, PIERRE SHALE, FOX HILLS SANDSTONE, S. DAK. has an elliptical outline, elongate cylindrical neck with ing their variety, Parker and Jones mentioned no dif­ a round aperture lacking a tooth, long, narrow, rounded ference in aperture from that of the parent species. L. chambers, an early part not coiled in a single plane, and nautiloidea. (Lamarck). If Parker and Jones' variety a rust-colored slightly calcareous wall which contains does have a cribrate aperture, it cannot be placed in Tro- no silt grains. In shape, plan of coiling, and most other chammina. As Cushman explicitly stated that his speci­ preserved details, the other five specimens exactly re­ mens do have an interiomarginal aperture, he is cor­ semble this specimen; however, they have dull-white or rect in placing them in Trochammina but ir correct in whitish-gray very calcareous tests. The specimens do crediting the species designation to Parker and Jones not seem to belong in any previously described species as their variety (Cushman's species) globigerinif'ormis of MassU'ma and may represent a new species. Dimen­ presumably belongs in the genus Lituola. This question sions of the well-preserved specimen: length, 0.29 mm; cannot be properly resolved until specimens of L. nau­ breadth, 0.17 mm; thickness, 0.01 mm. tiloidea (Lamarck) var. globigerinif ormis Parker and Occurrence. The samples from which the specimens Jones are available for comparison with specimens of came are distributed 25 to about 100 feet below the lower T. globigerinif ormis of Cushman. key bentonite in the Grand River sections. The Pierre specimens are smaller on the average than Material. Six specimens were found. specimens of T. globigerinif ormis Cushman in the U.S. Locality Sample Locality Sample National Museum collections, but there is suf'cient size 36. 3-X 37. 3-X variation to include the Pierre specimens. In other re­ 4-X 5-X spects agreement is good. 5-X 41. 1-X Occurrence. This species has been reported, as Tro- Family TROCHAMMINIDAE chammina globigerinif ormis (Parker and Jones), from Cretaceous deposits of Switzerland, Trinidad, Peru, Genus TROCHAMMINA Parker and Jones, 1859 Venezuela, England, Bulgaria, U.S.S.E., ?.nd tenta­ Trochammina globigerinif ormis Cushman tively from Poland. Plate 1, figures 4a-c The few specimens obtained from the upper part of the Pierre Shale came from 70 feet below the lower key Trochammina gloWgerintformis Cushman (not Parker and bentonite to 64 feet above the upper key bentonite. Jones), 1910, U.S. Natl. Mus. Bull. 71 pt. 1, p. 124, text figs. 193-195. Material. Fewer than 25 specimens were sufficiently well preserved to be identified. Test trochoid, of about four whorls, equatorial pe­ Locality Sample Locality Sample riphery subovate, spiral side strongly convex to conical, 22-X 49. 3-X umbilical side slightly convex with a small shallow um­ 5-X 54. 3-R bilical depression; chambers globular, four in the final 5-X 5-R whorl, inflated, not compressed, distinct; spiral and sep- Trochammina globosa Bolin tal sutures distinct, depressed, septal sutures short, ob­ Plate 5, figures 5a c lique on spiral side, straight and radial on umbilical side; wall very finely arenaceous, noncalcareous, Trochammina globosa Bolin, 1956, Jour. Paleontology, v. 30, no. smoothly finished, with a subordinate amount of ce­ 2, p. 289, pi. 38, figs. 8, 9; text fig. 5, fig. 7a, I. ment ; aperture not well exposed in available specimens, Test in a low trochoid spire, equatorial periphery apparently a low-arched slit between the margin of the lobulate and roughly circular, spiral side moderately final chamber and the previous whorl extending from convex, umbilical side with a prominent central depres­ the periphery onto the umbilical side. Dimensions of sion encircled by the inflated chambers; chambers in the plesiotype, the only well-preserved specimen: maxi­ final whorl vertically compressed, overlapping, mod­ mum diameter, 0.22 mm; minimum diameter, 0.20 mm. erately inflated, indistinct in earlier whorls; sutures Remarks. Cushman (1910, p. 124) placed some Ke- distinct in final whorl, depressed, straight and oblique cent specimens of Trochammina under the specific on spiral side, straight and radial on umbilical side; name globigerinif ormis. He derived this name by plac­ wall rather smoothly finished, white to yellow, com­ ing Lituola nautiloidea (Lamarck) var. globigerini- posed predominantly of clear arenaceous grains the f ormis Parker and Jones in the genus Trocliammina size of which varies quite noticeably, percentage of ce­ and raising the name globigerinif ormis from varietal to ment small; aperture an elongate interiomarginal open­ specific rank. This action seems to me to be in error be­ ing extending from the periphery onto the umbilical cause the aperture of Litiwla is cribrate, whereas Tro­ side but apparently not extending into the umbilicus. chammina has an interiomarginal aperture. In describ­ Dimensions of average-sized specimens: marimuni di- PALEONTOLOGY 53 ameter about 0.3 mm; minimum diameter, about 0.25 Texas, and Arkansas. Since 1945 the species has beer mm; thickness, 0.15 to 0.2 mm. reported from the Arkadelphia Marl of Arkansas Remarks. The above description is based primarily (Cushman, 1949 p. 4) and the Lawson Limestone of on the features exhibited by two well-preserved speci­ Florida (Applin and Jordan, 1945, p. 132 (list)) R. mens. They somewhat resemble Trochatnmina alber- muensteri has also been reported from the Niobrarr, tensis Wickenden but differ in having indistinct earlier Formation of South Dakota (Bolin, 1952, p. 21), from chambers and sutures, and in having the sutures of the the Hilliard Shale of Campanian and Santonian ages last-formed whorl distinctly depressed. The Pierre speci­ in Wyoming (Ganger in Jones, 1953, p. 66-67), and mens agree well with the description and figures of from the Mobrara Formation in Wyoming (Shaw, T. globosa Bolin, but they are somewhat larger and have 1953, table 1). a more easily observable aperture. Other Upper Cretaceous reports of this species are Occurrence. The species was found 172 to 190 feet from Colombia, Spanish Sahara, Venezuela, Germany, above the upper key bentonite in two sections of the Poland, Egypt, California (Graham and Clark, 1961, Grand Kiver stratigraphic sequence. Bolin (1956, p. p. 108 (list)), and Maryland (Cushman, 1948, p. 248) 289) reported it from the Cretaceous of Minnesota. and with question from Puerto Rico. Material. About 10 identifiable specimens were In the upper part of the Pierre Shale this species oc­ found. curs from 1 foot above the upper key bentonite to 14? Locality Sample Locality Sample feet below the lower key bentonite. 50.. 3-VR 52. 3-X Material. Several hundred specimens from a num­ 5-S 5-S ber of samples were found.

Family LAGENIDAE Locality Sample Locality Sample 11-X Genus ROBULUS Montf ort, 1808 15-S 14-RC 13. 5-X Robulus muensteri (Roemer) 16-VR 27. 1-VR 18-VR 4-S Plate 5, figures 6a, b 20-VR 36. 2-S Robulina munsteri Roemer, 1839, Versteinerungen morddeuts- 22-R 3-S chen Oolithengebirges, Nachtrag., p. 48, pi. 22, fig. 29. 4-VR 4-VR Cristellaria munsteri (Roemer). Reuss, 1862, Akad. Wiss. Wien, 5-S 37. 1-X Math.-naturw. KL, Sitzungsber., v. 46, pt. 1, p. 77, pi. 9, 1-S 6-X figs. 3, 4 [1863]. 3-VR 10-X Romulus nmnsteri (Roerner). Cushman, 1932, Jour. Palentol- 5-VR 41. 1-S ogy, v. 6, no. 4, p. 334, pi. 50, figs. 2a, b. 6-X 5-S 9-R 9-R Test planispiral, completely involute, not much com­ 11-S 10-S pressed, with large umbos; periphery sharply angled, 13-S slightly keeled; chambers distinct, of uniform shape Robulus spissocostatus Cushman and increase gradually in size as added, not inflated, Plate 5, figures 8a, b; 9a, b eight or nine in final whorl; sutures distinct, slightly to moderately limbate and raised, tangential, slightly Robulus spisso-oostatus Cushman, 1938, Cushman Lab. Foram. Research Contr., v. 14, pt. 2, p. 32, pi. 5, fig. 2. curved; wall smooth, glassy, without visible perfora­ tions; aperture at the outer peripheral angle, radiate, Test planispiral, completely involute to partially with a more elongate slit extending a short distance evolute, moderately compressed, most specimens not into the apertural face. Dimensions of average-sized umbonate, but umbos developed on some, periphery specimens: maximum diameter, about 0.5 mm; mini­ acute on some specimens, slightly to moderately keelec1 mum diameter, about 0.4 mm; thickness, 0.25 to 0.3 mm. on some specimens, a delicate flangelike keel developed Remarks. The Pierre specimens correspond well on a few specimens; chambers distinct, of unifonr with the description of Robulus muensteri given by shape, increase fairly rapidly in size as added, slightly Cushman (1946, p. 53) and compare favorably with or not at all inflated, six to 10 in final whorl; sutures specimens of this species in the U.S. National Museum usually either flush or raised but occasionally slightly collections. depressed; when raised, sutures are thickest near the Occurrence. Cushman (1946, p. 53) noted the oc­ center where they either join a central boss or coalesce currence of Robulus muensteri in deposits of Austin, into a less well defined mass; wall smooth, glassy, with­ Taylor, and Navarro ages in Tennessee, Mississippi, out visible perforations; aperture radiate, at the apey 54 FORAMINIFERA, STRATIGRAPHY, PIERRE SHALE, FOX HILLS SANDSTONE, S. DAK. of the periphery of the final chamber, without a promi­ Robulus taylorensis (Plummer) nent extension onto the apertural face. Dimensions of Plate 5, figures 7 a, b average-sized specimens: maximum diameter, 0.75 to Astacolus taylorensis Plummer, 1931, Texas Univ. Bull. 3101, 0.8 mm; minimum diameter, about 0.6 mm; thickness, p. 143, pi. 11, fig. 16 ; pi. 15, figs. 8-11. 0.35 to 0.4 mm. Robulus taylorensis (Plummer). Cushman, 1941, Cnshman Lab. Remarks. The specimens here grouped in Robulus Foram. Research Contr., v. 17, pt. 3, p. 57, pi. 15, figs. spissocostatus, if they are in fact members of the same 5 a, b. species, indicate that the species exhibits a wide range Test planispiral, incompletely involute, uncoiling in of variation in several important characters. The degree the final part of largest specimens, only a small part of of limbation and the elevation of sutures, the degree of previous whorls visible in umbilical areas, moderately involution, the presence and nature of the umbo, the compressed, umbilical areas flush with the surface of number of chambers in the final volution, and the na­ the test or slightly depressed; axial peripl °-ry acute, ture of the keel are all variable. This morphologic varia­ with a small keel, equatorial periphery smooth or with tion is impressive, but, as Cifelli (1960) has shown, slight indentations at the sutures ; chambers distinct, of species of Robulus characteristically vary a great deal uniform shape, increase gradually in size as a.dded, very in morphology. Cushman (1946, p. 51) pointed out the slightly if at all inflated, eight to 12 chambers per variability found in Upper Cretaceous species of whorl, usually nine to 11 ; sutures distinct, in some speci­ Robulus. mens slightly limbate but in most not at all limbate, The variations exhibited by the Pierre specimens are nearly radial towards the center but beccme gently all closely matched by similar variations among the curved toward the periphery, flush in most specimens, type specimens of R. spissocostatus, especially the large slightly depressed in some; wall smooth, thick, glassy, group of paratypes of Cushman collection 28380. Cush­ without visible perforations; aperture radial, at the man (1946, p. 52) suggested that there is a great deal of apex of the apertural face, with an elongate, widened similarity between R. spissocostatus and/?, navarroensis slit extending about one-fourth to one-third the distance var. extruatus Cushman but stated (p. 53) that R. spis- down the slightly convex apertural face. Dimensions of socostatus is distinguished from R. navarroensis by the average-sized specimens: maximum diameter, about lack of a thin, flangelike keel and by the presence of 0.6 mm ; minimum diameter, between 0.45 and 0.5 mm ; raised sutures that become thick and rounded at the thickness, between 0.15 and 0.2 mm. inner ends. However, two of the smaller paratypes of Remarks. None of the specimens becomes complete­ R. spissocostat'us do have this thin flangelike keel. More­ ly uncoiled, but in several of the largest specimens, the final few chambers migrate quite far out toward the over, paratypes of R. navarroensis var. ewtruatus have periphery. In most specimens the proloculus is visible in raised and thickened sutures exactly similar to those on the umbilical region, but in larger specimens, cloudy some of the paratypes of R. spissocostatus. In short, shell material covers the proloculus and the erposed part these two forms are very similar and may well belong of earlier whorls as succeeding whorls ir crease the in the same species, although I do not have sufficient thickness of the test. specimens to resolve this question to my own satis­ The specimens closely resemble specimens of Robulus faction. taylorensis in the Cushman Collection but differ from Occwt^ence. Robiilus spissocostatus has been re­ most of these in having a slightly less convex um­ ported from stratigraphic units of Navarro age in bilicus, and slightly less tangential sutures. Texas, Mississippi, Arkansas, and Alabama (Cushman, Occurrence. Cushman (1946, p. 53) reported this 1946, p. 53). Other Cretaceous citations are from Vene­ species from Alabama, Mississippi, Texas, and Ar­ zuela and Japan. kansas from beds of Austin and Taylor ag

Marginulina curvatura Cushman (1826, p. 258). The generic description stated that the Plate 6, figure la, b test is in the form of an arched scabbard, that the aper­ ture is radiate, marginal, and situated at the tip of a Marginulina curvatura Cushman, 1938, Cushman Lab. Foram. prolongation of the final chamber at the anterior angle, Research Contr., v. 14, pt. 2, p. 34, pi. 5, figs. 13, 14. that there is an early coiled part (the degree or amount Remarks. Five fairly well preserved specimens are of coiling is not specified), and that the chambers are placed in this species. They match the type description superposed and slightly oblique. d'Orbigny did not and the holotype of Marginulina. curvatura very well designate a type species for Marginulina. Deshayes except for having a shorter uncoiled part. It seems safe (1832, p. 1107) designated M. raphanus (Linne) = to assume that this difference is due to the failure of the raphanus Linne, 1758) as the type species of Pierre specimens to reach as advanced a stage of growth Marginulina. Cushman (1913, p. 79) designated M. as the holotype. Dimensions of a somewhat larger than glabra d'Orbigny, 1826, as the type species of Marginu­ average-sized specimen: length, 0.45 mm; breadth, 0.22 lina: Marie (1941, p. 105, 257, 258) also decided to con­ mm; thickness, 0.20 mm. sider M. raphanus (Linne) as the type species. The type Occurrence. MarginuUna curvatura has been re­ specimens of N. raphanus and M. glabra have not been ported from the Arkadelphia Marl of Arkansas and the available to me for study, and my conclusions are based Corsicana Marl of Texas (Cushman, 1946, p. 63), from on the type figures and descriptions of these species. The the Upper Cretaceous of Hokkaido, Japan, and ques­ type figures of N. raphanus Linne (Ellis and Mes­ tionably from beds of Cenomanian age near Dresden, sina, 1940-1964) show a straight uniserial, Nodosaria- Germany. like form with no indication of an early coiled part. In the upper part of the Pierre Shale this species This form does not correspond to the type description occurs from 126 to 25 feet below the lower key bentonite. of Marginulina. given by d'Orbigny, and it must be con­ Material. Five specimens were found. cluded that d'Orbigny was ignorant of the true nature Locality Sample Locality Sample of N. raphanus Linne (as this nature is indicated by 14-VR 15-S Linne's figures) when he placed the species in Marginu­ Marginulina sp. lina. Cushman (1945, p. 12) reexamined material from Castel Arquato, Italy, one of the localities from which Remarks. Five similar specimens from four samples d'Orbigny reported M. rapha,nus (Linne), but he found were found which appear to belong in the genus Mar­ no specimens identical with d'Orbigny's figure or model ginulina but which could not be identified to species. of this species. They are composed of three to five small oblique, over­ In view of the apparently incorrect assignment of lapping chambers and are slightly curved in the early N. raphanus Linne to the genus Marginulina, I prefer part. A radiate, moderately produced aperture is at the to consider M. glabra d'Orbigny as the type speoies of apex of the test on the dorsal periphery. The type figure Marginulina, as proposed by Cushman (1913, p. 79). of M. depressa Blake (Tate and Blake, 1876, p. 463, pi. M. glabra corresponds to the type description of Mar­ 19, fig. 9) closely resembles these specimens, but the ginulina in having an early coiled part, a radiate aper­ generalized type description is of little use for making ture situated at the tip of a slight prolongation at the a more detailed comparison. M. depressa has not been apex of the test, and slightly oblique chambers in the reported from the Cretaceous. Dimensions of an aver­ uniserial portion. In addition, this species was named age-sized specimen: length, about 0.25 mm; breadth, by d'Orbigny and placed by him in his genus Mar­ about 0.1 mm. ginulina. Occurrence. The specimens are found 30 to 70 feet The genus Astacolus, erected by Denys de Montfort below the lower key bentonite. in 1808, is poorly described, and the type figure is also Material. Five specimens were found. very poor. However, the type species, Nautilus crepidkila, Locality Sample Locality Sample Fichtel and Moll was well figured by the original au­ 22-S 37. 5-X thors. This species differs from the type species of Mar­ 5-X 41. 3-X ginulina in having the chambers of the uniserial part The genera Astacolus and Marginulina extending well back toward the proloculus on the ven­ Some confusion surrounds the designation of a type tral side and in having the early chambers more loosely species for the genus Marginulina, which makes it im­ coiled. It is primarily on the basis of these two char­ perative that I discuss the removal herein of several acteristics, especially the extension of the uniseriaJ species from Marginulina and their relocation in Asta­ chambers toward the proloculus, that I have separatee? colus. The genus Marginulina was erected by d'Orbigny Astacolus from Marginulina. 56 FORAMINIFERA, STRATIGRAPHY, PIERRE SHALE, FOX HILLS SANDSTONE, S. DAK. The genera Astacolus and Vaginulina In the upper part of the Pierre Shale this species For a number of years the genus Astacolus was occurs from 32 feet below to just above the upper key ignored by most workers in Foraminifera, and species beiitonite. that could have been placed in this genus were placed, Material. Fewer than 10 specimens were found. for the most part, in the genera Margmulina and Locality Sample Locality Sample 27______.______1-X 45..______1-X Vagi-milina. The genus Astacolus is valid and in my 4-S 7-S opinion serves a useful purpose under this generic name can be placed those species that are laterally com­ Astacolus rectus (d'Orbigny) pressed and partially coiled in the early part, become Plate 6, figures 3a, b uniserial and gently curved later, and have rather oblique chambers which extend back toward the proloc- Cristellaria recta- d'Orbigny, 1840, 'Soc. geol. France Mem., v. 4, p. 28, pi. 2, figs. 23-25. ulus. All these characteristics are shown by the type Enantiovagimdina recta (d'Orbigny). Marie, 1941, Mus. His- species of Astacohis, A. crepidulus (Fitchel and Moll) toire Naturelle, Mem., new ser., v. 12, pt. 1, p. 161, pi. 21, (^Nautilus crepidula, Fichtel and Moll). The type figs. 235a-e. species of Vagmitfina, V. legumen (Linne) ( =Nautilu-s Astacolus rectus (d'Orbigny). Hagn, 1953, Paleortographic, v. legumen Linne) is similar to Astacolus in many respects 104, pts. A, p. 39, pi. 5, fig. 16. but differs in being slightly if at all compressed lat­ Test elongate, compressed, early part partially coiled, erally and in having only slightly oblique chambers rapidly uncoiling; ventral periphery smooth, straight which do not extend back appreciably toward the initial to slightly concave, dorsal periphery smooth, convex, end. It seems desirable to utilize these differences in dorsal margin sharply rounded, ventral margin smooth­ placing species in Astacolus and Vaginulina, respec­ ly rounded, uncoiled part, subtriangular in. cross section; tively. chambers distinct, slightly if at all inflated, increase Genus ASTACOLUS Montfort, 1808 rather rapidly in length but more gradually in breadth Astacolus cretaceus (Cushman) and thickness as added; final chambers in large speci­ mens do not reach back to the early coiled pivrt; sutures Plate 6, figures 2a-d distinct, slightly curved, flush to slightly depressed; Marginulina cretacea Cushman, 1937, Cushman Lab. Foram. wall smooth, semitraiisparent, lacks visible perfora­ Research Contr., v. 13, pt. 4, p. 94, pi. 13, figs. 12-15. tions ; aperture radiate, at the outer peripheral angle; Astacolus cretaceus (Cushman). Pozaryska, 1957, Paleont. apertural face slightly convex, with smoothly rounded Polonica. no. 8, p. 98, pi. 11, figs. 11. 12; pi. 13, fig. 7. edges, steeply inclined. Dimensions of an average-sized Remarks. The single complete, well-preserved speci­ specimen with final chamber extending nearly to the men, of the few that are referred to this species, com­ proloculus; length, 0.37 mm; breadth, 0.17 mm; thick­ pares almost perfectly with the holotype of this species ness, 0.12 mm. Dimensions of a specimen in which the and quite well with the paratypes. This species differs final chamber does not extend as far towr.rd the pro­ from Cushmaii's (1946, p. 60, pi. 12, figs. 4, 5) descrip­ loculus: length, 0.47 mm; breadth, 0.14 mm; thickness, tion and figures of Margmulina cf. M. recta, in having 0.11 mm. shorter, ventrally narrower, less oblique chambers, fewer Remarks. The final chamber on several specimens of which reach back to the early part, of the test. The is much smaller than the preceding chambers and only Pierre specimens resemble M. siUqu-a Cushman a great partially covers the apertural face of tlw preceding deal but differ in having a more concave ventral side, chamber. continually increasing size of chambers with growth, This species differs from Astacolus cretaceus (Cush­ and a less pronounced extension of the chambers toward man) in its more smoothly rounded ventral margin and the earlier part of the test. Dimensions of the plesiotype: its subtriangular outline in cross section. d'Orbigny ns length, 0.56 mm; breadth, 0.24 mm; thickness, 0.18 mm. type description of Cristellaria recta and the, type figure Occurrence. Cushman (1946, p. 61) recorded this resemble the Pierre material rather closely, as does the species from 'beds of Taylor and Navarro ages in Texas description and figure given by Hagn fc^ A. rectum and Arkansas. The species has also been recorded from (d'Orbigny). Cushman recognized a form that he con­ the Hilliard Shale in Wyoming (Ganger, in Jones, 1953, sidered similar to A. recta from the Cretaceous rocks p. 68), from the Upper Cretaceous in Maryland (Cush­ of the United States Gulf Coast and designated it Mar- man, 1948a, p. 250), from beds of Campanian age in gimdin-a. cf. M. recta. (d'Orbigny). An examination of California (Graham and Clark, 1961, p. 108 (list)), some of the slides of Margmulina cf. M. recta in the and from the Upper Cretaceous of France, Poland, and U.S. National Museum collections revealed close simi­ Puerto Rico. larity of the Pierre material with the plesiotypes and PALEONTOLOGY 57 identity with those specimens (uiifigured) on Cushman Material. Fewer than 20 specimens were found. collection slide 28733 from the upper part of the Taylor Locality Sample Locality Sample Marl. 7___._. ______5-VR 7 .______9-S Occurrence. This species has been reported from the 6-S 11-X 7-R 13-X upper part of the Taylor Marl and the Pecan Gap Chalk Member of the Taylor Marl in Texas (Cushman, Astacolus navarroanus (Cushman) 1946, p. 60) and from Upper Cretaceous strata near Plate 6, figures 5a, b Salisbury, Md. (Cushman, 1948a, p. 249). It has also Vaginulina navarroana Cushman, 1936, Geol. Soc. America Bull., been reported from the Cretaceous of Czechoslovakia v. 47, no. 3, p. 416, pi. 1, fig. 3. and from the upper Campanian of Germany. Astacolus navarroanm (Cushman). Perlmutter and Todd, 1965, U.S. Geol. Survey Prof. Paper 483-1, p. 11, pi. 1, fig. 9. In the upper part of the Pierre Shale, Astacolus rectus (d'Orbigny) occurs from 115 feet below the lower Test elongate, somewhat compressed, early part key bentonite to 24 feet, above the upper key bentonite. slightly curved, later part straight, periphery rounded, Material. Fewer than 50 specimens were found. ventral side straight to slightly concave, not inter­ Locality Sample Locality Sample rupted, dorsal side straight in later part, convex in early 3______-______16-VR 7______6-X part, initial end with or without a small spine; chambers 18-X 7-S distinct, slightly inflated, oblique, moderately overlap­ 4______-______4-S 25-X ping, higher than broad, appear broader than high 5-R 27______.__ 6-X 5-_-____.---.__-- 4-S 9-X when overlapped, six in the largest specimen, of uni­ 7______1-S 42_..______8-X form shape except for the more bulbous proloculus, in­ crease very gradually in size as added; sutures distinct, Astacolus jarvisellus Mello, new name slightly depressed, oblique, curve slightly downward; Plate 6, figures 4a, b wall ornamented with about 11 longitudinal, nearly Marginulina jarvisi Cushtnan, 1938, Cushman Lab. Forani. Re­ vertical costae, often in the form of thin flanges that are search Contr., v. 14, pt. 2, p. 35, pi. 5, figs. 17. 18. continuous across sutures and chambers alike, best de­ Astacolus jarvisi (Cushman) (not Astacolus jarvisi Brotzen, veloped in early part, become weaker and less numerous 1936). Trujillo, 1960, Jour. Paleontology, v. 34, no. 2, p. in later part, completely absent in upper half of final 317, pi. 46, fig. 2. chamber; aperture radiate, terminal, at the dorsal angle, Remarks. The few specimens found are character­ with a short neck. Dimensions of the only complete ized by a compressed test with early coiled part, straight specimen in addition to the plesiotype: length, 0.72 or slightly concave ventral side, straight or slightly mm; breadth, 0.15 mm; thickness, 0.11 mm. convex dorsal side, an oval outline in cross section, Remarks. Only four specimens from a single sample equally and rather abruptly rounded lateral peripheries, were found, and all are macrospheric forms. They fit and moderately oblique chambers. The Pierre specimens the description of Astacolus navarroanus (Cushman) compare well with plesiotypes of this species. quite well and are closely similar to the holotype except Astacolm jarvi-si Brotzen (Brotzen, 1936, p. 56, pi. 3, that they are less compressed in the early part because figs. 5a, b, 6, 7, text fig. 17) from the Upper Cretaceous of the large size of the proloculus. The Pierre specimens of Sweden is not the same species as Marginulina jarvisi most closely resemble the plesiotype of this species illus­ Cushman. Therefore, in placing M. jarvisi Cushman in trated by Cushman (1946, pi. 29, fig. 22) from the the genus Astacolus, I have changed the species name Bulimina zone of the Corsicana Marl of Texas. to jarvisellus. Dimensions of average-sized specimens: Ocmrrence. This species has been reported from length, 0.35 to 0.4 mm; breadth, 0.1 to 0.15 mm; thick­ beds of Navarro age in Mississippi, Texas, and Arkansas ness 0.05 to 0.1 mm. (Cushman, 1946, p. 81) and from the Arkadelphia Marl Occurrence. Astacolus jarvisellus has been reported, of Navarro age in Arkansas (Cushman, 1949, p. 6). The as Marginulina jarvisi, from the Kemp Clay (Navarro holotype conies from Cretaceous deposits on Georges age) of Texas (Cushman, 1946, p. 63) and from the Bank (Cushman, 1936, p. 416). The species has also Upper Cretaceous of Mexico and Venezuela. It has also been reported from the Cretaceous of New Jersey (Ols- been reported, as Astacolus jarvisi, from beds of Coii- son, 1960, p. 20), New York (Perlmutter and Todd, iacian and Santonian ages in California (Trujillo, 1960, 1965, p. 11), Colombia, and Africa. p. 317). The Pierre specimens come from 12 feet above the lower key bentonite. In the upper part of the Pierre Shale this species Material. Four specimens were found. was found only at locality 7 from 70 to 36 feet below Locality Sample the lower key bentonite. 1______23-VR 58 FORAMINIFERA, STRATIGRAPHY, PIERRE SHALE, FOX HILLS SANDSTONE, S. DAK.

Astacolus dissonus Plummer Locality Sample Locality Sample 157-VR 44______1A-S Plate 6, figure 6 9?-VR 45__.______1-X 10-S Astacolus dissonus Plummer, 1981, Texas Univ. Bull. 3101, p. 145, pi. 11, figs. 17, 18; pi. 15, figs. 2-7. Genus DENTAIINA d'Orbigny, 1826 Test planispiral, completely involute except uncoil­ Dentalina catenula Reuss ing in some larger specimens, quite compressed, not um- bonate, periphery on smaller specimens sharply angled Plate 6, figure 7 and in some slightly keeled, larger specimens with a Dentalina catenula, Reuss, 1860, Akad. Wiss. Wien, Math.- broad, thin, delicate keel; chambers distinct, in the naturw. Kl., Sitzungsber., v. 40, p. 185, pi. 3, fig. 6. shape of elongate curved triangles, increase in length rather rapidly as added, early chambers slightly or not Test elongate, straight, tapers in microspheric indi­ at all inflated, later chambers slightly inflated, seven to viduals, with parallel sides in megalospheric individuals, .nine in the final whorl of larger specimens; sutures dis­ initial end with a distinct spine; chambers, few, pyri- tinct, in smaller specimens generally moderately lim- form, of uniform shape, all but final chamber appears bate and in larger specimens slightly or not at all globular because of slight overlapping; sutures distinct, limbate, nearly radial at the point of junction, gently strongly depressed; wall smooth; aperture terminal, arched away from the aperture as they approach the radiate. Dimensions of an average-sized two-chambered periphery, flush with the surface or slightly depressed specimen: length, 0.55 mm; breadth, 0.24 mm. between slightly inflated chambers; wall smooth, glassy, Remarks. Specimens referable to this species are few, without visible perforations; aperture radiate, at the and no specimen preserves more than five chambers. apex of the final chamber, lacks a prominent slit in the Nevertheless, the smooth surface, pyriforn chamber apertural face; apertural face slightly convex, with shape, deep sutural depressions, and basal snine are di­ rounded edges, not sharply set off from the chamber agnostic criteria which allow a reasonably certain iden­ sides. Dimension of average-sized specimens: maximum tification. diameter, about 0.65 mm; minimum diameter, 0.45 to Occurrence. Dent-alma catenula has been reported from the beds of Taylor and Navarro ages in Alabama, 0.5 mm; thickness, about 0.1 mm. Texas, and Arkansas (Cushman, 1946, p. 68). Other Remarks. Only a few specimens are assigned here United States occurrences are from the Upper Cretace­ with confidence. The other specimens exhibit a wide ous of California (Trujillo, 1960, p. 327; Cushman and range of variation and may in fact belong in another Church, 1929, p. 509) and Maryland (Cushman, 1948a, species. Similar variants, labeled as Plamd-aria dissona, p. 251). It has also been reported from the Cretaceous were found in the U.S. National Museum collections. of Germany, Palestine, Switzerland, tH Spanish The type figures for this species (Plummer, 1931, pi. 11, Sahara, Venezuela, Poland, Egypt, Angola, Japan, figs. 17,18; pi. 15, figs. 2-7) also show a range of varia­ Australia, and Puerto Rico. tion which is similar in most respects to that exhibited In the upper part of the Pierre Shale this species by the Pierre specimens. occurs from just below the lower key bentonite to 103 This species is placed in the genus Astacolus rather feet below this bentonite. than in the genus Planularia, where it has been most Material. Fewer than 20 specimens were found. frequently placed in the past, because it more closely Locality Sample Locality Sample resembles Nautilus crepidula Fichtel and Moll, the type 18-VR 9-VR species of Astacolus, than it does auris De- 20-VR 11-S 22-S 42. 8-S f ranee, the type species of Planufaria.. Occurrence. This species has been reported from Dentalina niobrarensis Loetterle beds of Navarro age in Texas and Arkansas by Gush- Plate 6, figures 8a, b man (1946, p. 57). It has also been reported from the Red B,ank Sand of New Jersey (Olsson, 1960, p. 11) and Dentalina niobrarensis Loetterle, 1937, Nebraska Geol. Survey from Upper Cretaceous deposits in Long Island Sound Bull. 12, 2d ser., p. 24, pi. 2, fig. 3. (Perlmutter and Todd, 1965, pp. 11). Remarks. Assignment of the Pierre specimens to In the upper part of the Pierre Shale this species is this species is made with some hesitation because of the found from 25 feet below to 6 feet above the lower key scarcity of good specimens and because the species does bentonite, not have many distinctive morphologic parameters on Material. Fewer than 20 specimens were found. which to base comparisons. The specimens available PALEONTOLOGY 59 correspond quite well to Loetterle's type figures and specimen in the Pierre samples on which the aperture description, but they also appear to be similar to the is preserved, only a tentative assignment to D. consc- type figures and description of Marginulina subtilis brina is made. Brotzen. No comparative specimens of either species Occurrence. Dentalina consobrina has been reported were seen. Dimensions of average-sized specimens: from beds of Taylor and Navarro ages in Texas and length, 0.25 to 0.3 mm; breadth, about 0.1 mm. Tennessee (Cushman, 1946, p. 69, 70). It has also been Occurrence. Dentalina niobrarensis Loetterle was reported from Europe, Japan, Palestine, South Amer­ originally described from the Niobrara Formation in ica, and from the Campanian of California (Grahar^ Nebraska (Loetterle, 1937, p. 24) and since then has and Clark, 1961, p. 108). only been reported once, from the Niobrara Forma­ This species occurs in samples from 6 feet above th-> tion in South Dakota (Bolin, 1952, p. 28). lower key bentonite to 126 feet below this level. The species occurs from the level of the lower key Material. Fewer than 50 specimens were found. bentonite to 69 feet below this level in the upper part of Locality Sample Locality Sample the Pierre Shale. 3-______--_-__ 14 X 41. 1 R Material. Fewer than 15 specimens were found. 4______._____ 4 VR 9 VR 5 X 10 R Locality Sample Locality Sample 7_____.______5 R 45. 1 X 22-X 37- 6-X 5-VR 10-S Dentalina gracilis d'Orbigny 15-S 41. 3-X 36. 2-X 5-X Plate 6, figures lOa, b Dentalina cf. D. consobrina d'Orbigny Dentalina, gradlis d'Orbigny, 1840, Soc. geol. France Mem., 1st Plate 6, figures 9a, b ser., v. 45 p. 14, pi. 1, fig. 5. Remarks. A slightly bulbous initial chamber, Test elongate, slender, gently arched, initial end straight or very slightly arched test, and chambers that pointed in most specimens, chambers slightly if at all increase considerably in height but little in breadth as inflated, increase gradually in size as added, moderately added are characteristic features of the Pierre speci­ overlapping; sutures flush or slightly depressed, slightly mens. In these respects the specimens are similar to oblique to axis of elongation; wall smooth, finely perfor­ Dentalina consobrina d'Orbigny. Only three of 10 spec­ ate ; in a few well-preserved specimens the upper third imens that have the initial chamber preserved have a of the final chamber is more transparent than the lowe~ sharp basal spine, a character described by d'Orbigny part, and a small triangle of clear shell persists beneath for his species. No specimen with the aperture preserved the aperture of each overlapped chamber; the clear shell was found. Dimensions of an incomplete specimen com­ area is apparently not perforate; aperture radiate, mod­ posed of proloculus and four chambers: length, 1.41 erately produced, at the inner or concave periphery of mm; breadth, 0.08 mm. the test. Dimensions of average-sized specimens: length The Pierre specimens closely correspond to Creta­ about 0.7 mm; breadth, about 0.1 mm. ceous specimens in the U.S. National Museum collec­ Remarks. The specimens with the distinctive pattern tions labeled Dentalina cf. D. consobrina from the Sel- of clear and cloudy shell material are matched perfectly ma Group in McNairy County, Tenii. (Cushman colln. by specimens of Dentalina gradlis from the Kemp Clay 15164), and from 1,410-1,420* feet in the Ohio Oil Co. (Cushman colln. 29236) and from the Matawan Forma­ Hammond well 1 in eastern Maryland (Cushman colln. tion in Ohio Oil Co. Hammond well 1 from 1,410-1,420 62029). These specimens are the best preserved of any feet (Cushman, colln. 62003). These specimens resembh American Cretaceous specimens bearing this designa­ D. lequmen Reuss rather closely but are distinguished by tion in the U.S. National Museum collections. Topo- the less oblique sutures and chambers. types of D. consobrina from Baden, Austria (Cushman Occurrence. Dentalina gracilis has been reported colln, 17167), are also closely similar to the Pierre spe­ cimens and to the specimens from Tennessee and Mary­ from beds of Austin, Taylor, and Navarro ages in tta land mentioned above, but they differ in being somewhat Gulf Coast Cretaceous (Cushman, 1946, p. 65-66), from stouter in proportion to their length. the Hilliard Shale of Campanian and Santonian age^ These similarities indicate that the Pierre specimens in Wyoming, Ganger, in Jones, 1953, p. 70), from th? are morphologically very close to and perhaps are con- Frontier Formation of Campanian and Santonian age? specific with D. consobrina. However, because of the in Utah (Peterson, in Jones, 1953, p. 34), and from tiw difference in proportions between the Pierre specimens Upper Cretaceous of Maryland (Cushman, 1948a, p and the topotypes and because of the absence of any 250). This species has also been reported from the Cre- 60 FORAMINIFERA, STRATIGRAPHY, PIERRE SHALE, FOX HILLS SANDSTONE, S. DAK. taceous of France, Germany, Switzerland, Poland, Eng­ Locality Sample Locality Sample land, Trinidad, Venezuela, Egypt, and Australia. 36_.______3-S 44. 8-VR 4-X 45. 1-S In the upper part of the Pierre Shale the species 41_.____--___-__- 10-VR 7-S ranges from just below to 126 feet below the lower key bentonite. Dentalina pertinens Cushman Material. Fewer than 50 specimens were found, and Plate 6, figures 12a, b well-preserved specimens are very few. Dentalina pertinens Cusbman, 1938, Cushman Lab Foram. Re- Locality Sample Locality Sample searcb Contr., v. 14, pt. 2, p. 40, pi. 6, figs. 15-18. 14-R 6-S 18-R 37. 3-S Test elongate., slightly arched, tapers moderately rap­ 1-S 20-VR 39. idly, rather stout for a species of this genus; chambers 22-S 44. 1A-S of the early part indistinct and not inflated, gradually Dentalina legumen Reuss become more inflated, less overlapping, anc1 more dis­ tinct ; sutures indistinct in early part, become progres­ Plate 6, figure 11 sively depressed and distinct toward apertural end, Dentalina legumen Reuss, 1851, Haidinger's Naturw. Abb., v. 4, slightly limba,te; wall quite thick, ornamented by rather p. 10, pi. 1, fig. 14. heavy costae, which are twisted and continuous across Test elongate, slender, straight to slightly arched, several chambers in the early part and become finer, lacks a basal spine; chambers slightly to moderately more numerous, less continuous, and less twisted on inflated, increase gradually in size as added, slightly to later chambers; aperture radiate, slightly projecting, moderately overlapping; sutures slightly to moderately toward the convex margin of the test. Dimensions of depressed, vary in angle from about 20° to 45° to the the best preserved specimen, the plesiotyoe: length axis of elongation; wall smooth, in some specimens 0.83 mm; breadth, 0.25 mm. transparent, finely perforate; aperture radiate, slightly Remarks. Very few specimens of this species were to moderately produced, at the inner or concave margin found, but their distinctive ornamentation and shape of curved specimens. Dimensions of average-sized speci­ are diagnostic. They agree exactly with th