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Middle Eocene Ostracoda from Baja California Sur, Mexico

ANA LUISA CARRENO THOMAS M. CRONIN lnstituto de Geologia, Paleontology G. Stratigraphy Branch, Universidad Nacional Aiitdnoma de Mexico, U.S. Geological Survey, Delegacidn Coyoacan, Reston, Virginia, 04510 D.F., Mexico. U.S.A.

ABSTRACT One genus and six new species of ostracodes are described from the Bateque Formation on the Pacific of Baja California Sur, Mexico. Planktonic foraminifers indicate a mid Eocene age and the whole assemblage is characteristic of a shallow warm-water environment. Paijenborchella rnezquitalensis sp. nov. is the second record of the genus Puijenborchella from the Eocene of North America. Except for this species and the new genus Bujacythere, the ostracode association has strong affinities with those described from the lower Tertiary Coast region. 1. Micropalaeontol. 12 (2): 141-153, December 1993.

INTRODUCTION During the last few decades, geological research in the Baja California has been focused on the study of deep sea Miocene and Pliocene sequences that were deposited during or immediately after the formation of the . The objective of those efforts has been to understand the origin and evolution of the gulf in relation to neotectonics. A great part of the Peninsula of Baja California, particularly its western slope, is covered by lower Cenozoic outcrops that have been assigned to different formational units: the Tepetate Formation (Upper Cretaceous to mid Eocene), the Malarrimo Formation (Paleocene), the Ballenas Formation (Paleocene), the Santo Doming0 Formation (Paleocene and only recognised in boreholes), the Sepultura Formation (lower Eocene), and the Bateque Formation (lower and mid Eocene).The sediments referred to as the Bateque (Mina-Uhink,l957) and/ or the Tepetate (Heim, 1922) Formations include marine fossiliferous beds containing abundant microfossils. The main objective of this paper is to document the Ostracoda from the Bateque Formation. The paleozoogeographic and biostratigraphic significance of this fauna is included.

MATERIAL AND METHODS Two localities of the Bateque Formation yielded the ostracodes discussed in this paper. The first locality (IGM- 2,515) is located 32 km southwest of San Ignacio, Baja California Sur, Mexico (Fig. l),and is the type locality of the Bateque Formation (Mina-Uhink, 1957). Sampling was made in a section at the northern side of Arroyo San Fig. 1. Location map showing the sampled localities of the Ramon, near Rancho Batequi del Monreal (Rancho Bateque Formation: IGM-2,515 and the USGS-84TC-51.

141 Carreiio & Cronin

Bateque), approximately 2.5 km northeast of latitude upper Hantkenina nuttalli - Globigerinateka subconglobata 27'00" and longitude 113"OO'W (San Jose de Gracia subconglobata zones of Toumarkine & Luterbacher (1985). Quadrangle, Baja California Sur, Mexico, 1: 50,000 chart number G12A64, INEGI, 1983). The measured section is 52 SYSTEMATIC PALAEONTOLOGY m thick and consists mainly of medium to very fine Only new taxa are systematically treated here. The reduced micaceous, feldspathic sandstone with interbedded number of specimens, poor preservation and /or the fossiliferous lenses and siltstones. The base of the formation presence of closed carapaces, did not allow the assignment is not exposed; the unit is unconformably overlain by the of Haze 1 in a, Po kor n ye1 1a, B u n tonia, " Trig i n g 1y m us ", Miocene volcanics of the San Isidro Formation. The Loxoconcha, Paracytheridea and Paracypris to new species; ostracode collection comes from 16 to 40 m above the base thus, these new forms are illustrated and left in open of the outcrop, where fossiliferous lenses bearing nomenclature. Smooth and/or very fragile carapaces or discocyclinids occur. valves are not illustrated. All measurements were done The second locality (USGS-84TC51) is a north-facing 35 m with an eyepiece micrometer and are given in millimeters. high bluff at the southern side of Arroyo Mezquital (Fig. I), Each valve or carapace was considered as an individual. just south of the dirt road leading to San Juanico (13.5 km to Primary and secondary types have been deposited in the north 26'14" - 112"23'W, San Isidro Quadrangle, Baja Instituto de Geologia, micropaleontological collection at the California Sur Mexico, 1: 250, 000 chart number NG12-4, Universidad Nacional Autonoma de Mexico (IGM- -Mi). CGSNEGI, 1982). The ostracode samples were collected at Abbreviations used in this section and in plate captions are: the base of a 30 m thick section, that consists of very RV=right valve; LV=left valve; C=carapace; L=length; H= weathered reddish-gray mudstone and very fine-grained height. sandstone beds. From the two localities, 30 samples were Subclass Ostracoda Latreille, 1806 examined for ostracodes. Detailed geological map and Order Podocopida Muller, 1894 information including both localities was published by Suborder Platycopa Sars, 1866 McLean and coworkers (1985,1987). Family Cytherellidae Sars, 1866 Genus Cytherella Jones, 1849 BIOSTRATIGRAPHIC FRAMEWORK Cytherella spp. Mina-Uhink (1957) studied several localities from this area Remarks. Cytlzerella occurs rather commonly in the Bateque and considered that the Bateque Formation was deposited Formation. Two groups can be recognised based on shape: during the early and mid Eocene, based on the presence of one with an ovate outline, and the other subquadrate. We Turritella pachecoensis Stanton, Morozovella aragoneiisis do not fully understand the Cytherella in our material; thus, (Nuttall) and Acarinina crassata (Cushman). Carrillo de it does not seem advisable to give specific designations to Isolbi (1976) assigned a later early Eocene and mid Eocene the material studied herein. age to the outcrops exposed in the PEMEX San Ignacio- Hypotypes. RV ovate form IGM-302-Mi; LV ovate form Cadeje Project, based on the planktonic foraminifers and IGM-303-Mi; carapace ovate form IGM-304-Mi; RV calcareous nannoplankton. subquadrate form IGM-305-Mi; LV subquadrate form IGM- From the Arroyo San Raymundo section, located near our 306-Mi; carapace subquadrate form IGM-307-Mi. Arroyo Mezquital locality, McLean & Barron (1988) Material. Ovate form, 33 specimens; subquadrate form, 22 recovered a diatom assemblage assigned to the Triceratium specimens. iriconspicuuni var. triloba Partial Range Zone, equivalent to a Distribution. Present at locality IGM 2,515 later mid Eocene age. Recently, Squires & Demetrion (1989, 1990a,1990b), based Suborder Podocopa Sars, 1866 on the presence of Morozovella aragoizensis (Nuttall) and M. Family Bairdiidae Sars, 1866 caucasica (Glaessner), gave a later early Eocene age to a Genus Bairdoppilata Coryell, Sample & Jennings, 1935 locality closely situated to the IGM-2,515-UNAM locality Bairdoppilata spp. and, based on the calcareous nannofossils content, a mid Remarks. The material is poorly preserved, and mostly Eocene age (Discoaster bifax - CP14a Zone of Okada & consists of carapaces. Two groups, based on shape can be Bukry, 1980) to locality USGS-84TC51. recognised; one group is of large, subpyriform and inflated The ostracodes recovered at locality IGM-2,515-UNAM forms, similar to Bairdoppilatn taxodoiitn Howe & Law (1935). are associated with very abundant Pseudopliragmiiia Forms in the other group are also large sized, but elongated, (Proporocyclina) flintensis (Cushman) and Awzphistegiria sharply pointed posteriorly and broadly pointed anteriorly. lopeztrigoi (Palmer), suggesting a mid Eocene age (Butterlin, They resemble Bairdoppilatn zwiioiii Howe (1951). 1981). Hypotypes. RV inflated form IGM-308-Mi; LV inflated form The presence at locality USGS-84TC51 of Morozovella IGM-309-Mi; carapace inflated form IGM-310-Mi; RV aragoiiensis and Tririicorotaloides topileiisis (Cushman), elongate form IGM-311-Mi; LV elongate form IGM-312-Mi; carapace elongate form IGM-313-Mi. asso c i a te d with T u r b o r o t a 1 ia ce Y r o a z u 1en s is p o m e r o 1 i Material. 115 specimens of the elongate form and 87 (Toumarkine & Bolli), "Globigcrinoides" higginsi Bolli and Globigerinatheka subconglobata subconglobata (Shutskaya), specimens of the inflated form. indicates an age earlier than mid Eocene, equivalent to the Distribution. Locality IGM 2,515

142 Mexican Eocene Ostracoda

Family Cytheridae Baird, 1850 Distribution. Locality USGS-84TC51 Subfamily Cytherinae Baird, 1850 Tribe Paijenborchellirri Deroo, 1960 Paijenborchella trigona Marianos & Valentine, 1958 Genus Paijenborchella Kingma, 1948 (PI 1 figs 4-6) PaijenborcheZla mezquitalerrsis Carreiio & Cronin, sp. nov 1958 Paijtvrl7orchrlla friprra Marianos & Valentine: p. 367, PI. (PI 1 figs 1-3) 2, figs. 3a-b, 4, 5a-b Derivation of name. After Arroyo Mezquital, Baja Diagnosis. Carapace small, ornamentated with a deep California Sur, Mexico. median sulcus, longitudinal ridges, pits and a short caudal Diagnosis. Carapace small, thick, ventrally inflated with a process. deep median sulcus and longitudinal ridges; wide anterior Hypotypes. LV female IGM-320-Mi; RV male IGM-321-Mi; fringe bearing at the RV six larger pits parallel to the C male IGM-322-Mi; RV male IGM-323-Mi; C male IGM- anterior margin; at the LV an anterior flange with an 324-Mi. irregularly dentate fringe; dorsal margin obscured by four Material. 103 specimens. strong like-spine projections. Remarks. See P. rrrt~quifnlcirsisCarreiio & Cronin, sp. nov. Holotype. LV female IGM-314-Mi Distribution. This species was described from the Eocene Material. 140 specimens Capay Formation at Marysville Buttes, Sacramento Valley, Locality and horizon. Locality USGS-84TC51 on the California. In Baja California Sur, it was found only at southern side of Arroyo Mezquital, near San Juanico locality IGM-2,515 (26'14" - 112"23'W), Baja California Sur, Mexico. Bateque Formation, mid Eocene age. Unconsolidated foraminifera- Family Trachyleberididae Sylvester-Bradley, 1948 rich, fine-grained sandstone. Subfamily Trachyleberidinae Sylvester-Bradley, 1948 Description. Carapace small, thick, highest at the anterior Tribe Trachyleberidini Sylvester-Bradley, 1948 cardinal angle; widest posterior to the center. Dorsal margin Genus Acanthocythereis Howe, 1963 of the LV is almost straight and slightly inclined, dipping Acanthocythereis washburni (Stephenson, 1944) posteriorly with four strong spine-like projections, the (PI 1 figs 7-8) dorsal margin of the RV straight; ventral margin strongly 194.1 Cytlicwis zuaslibirriii Stephenson: p. 452, pl. 76, fig. 8. convex; anterior margin broadly rounded, bearing at the RV Diagnosis. Carapace medium sized, thick, robust, six large parallel pits and at the LV, the anterior flange subrectangular in lateral view. Dorsal and ventral margins being an irregular dentate fringe. Posterior margin nearly straight and gently converging towards subangular subtriangular, with caudal process. Surface ornamentated posterior end; anterior margin broadly rounded. Anterior by a deep median sulcus, longitudinal ridges, pits, and and posterior margins bear denticulations that are most irregular reticulate pattern; sulcus extends ventrally from prominent ventrally. Dorsal margin slightly obscured by a anterior cardinal angle, terminating against a prominent row of large, rounded, nearly pointed nodes. Surface ventral longitudinal ridge; between this ridge and ventral coarsely reticulated, deep and polygonal pits surrounded margin, a short, weak ridge; a shorter prominent ridge by ridges of nearly equal height bearing blunt rounded bridges the sulcus near center line; surface anteriorly nodes at their intersections. Anterior with five to six large smooth, most part of the valve coarsely and evenly pitted; blunt rounded nodes. Eye tubercle very prominent, nearly mid-posterior surface rough, following an irregular surrounded by blunt nodes. Hinge of RV with a blunt, reticulated pattern. Cardinal tubercle prominent. anterior tooth connected by a narrow, smooth, straight Inner lamella wide, line of concrescence and inner margin dorsal furrow to a large subpyramidal posterior tooth, LV coincide throughout; hinge of the LV with an anterior large complementary. Radial pore canals, numerous and straight. socket and postjacent crenulate tooth connected by narrow Muscle scars obscured. crenulate median element to subrounded posterior socket. Hypotypes. LV IGM-325-Mi; C IGM-326-Mi; RV IGM-327- Radial pore canals straight and numerous; muscle scars Mi. obscured. Sexual dimorphism strong, males larger than Material. 33 specimens. females. Remarks. In spite of the fact that the Bateque Formation Dimensions. (mm) L H specimens have lost most of their surface spines, due to Holotype LV female IGM-314-Mi 0.411 0.240 preservation effect, they appear to be identical to A. Paratype RV female IGM-315-Mi 0.405 0.236 waskhmriri (Stephenson, 1944), described from the mid Paratype LV female IGM-316-Mi 0.415 0.242 Eocene Reklaw Formation, Bastrop Country, Texas. Allotype LV male IGM-317-Mi 0.320 0.160 Allotype C male IGM-318-Mi 0.340 0.220 Distribution. Locality IGM 2, 515, and Bastrop County, Paratype RV female 1GM-319-Mi 0.405 0.221 Texas. Remarks. Paij~rrborclrcllnviezquifalmsis sp. nov. has four Genus Bajacythere Carreiio & Cronin, gen. nov. spine-like strong projections in LV instead of a dorsal ridge Type species. Bujucythere bajaensis Carreiio & Cronin, sp. nov. as present in Paijedxvdirlln trigma Marianos & Valentine Derivation of name. After Baja California Sur, Mexico. (1958); also, the median ridge is only developed posteriorly Diagnosis. A trachyleberidinid genus characterized by to the sulcus; an additional short, weak ridge is ventrally medium size; thinly calcified; subrectangular, laterally prcsent and the caudal process is strongly upturned compressed carapace; asymmetrical valves, the LV higher

143 Carretio & Cronin

anterodorsally with a thick subrounded projection cardinal angle; greatest width at the posterior end of the extending over the RV; denticulate anterior and posterior submedian ridge; LV with a thick subrounded hinge ear- margins; smooth and polished with few and widely like projection anterior to the eye node. Narrowly distributed, apparently open normal pore canals; two cuneiform in dorsal view, compressed in the anterior and submedian parallel ridges; narrow ventral ridge extending posterior with truncated extremities. Dorsal and ventral from anteroventral margin to posteroventral end; moderate margins almost straight in lateral view; anterior margin broad anterior rim; eye tubercle present; moderately broad broadly rounded with 20-25 denticles; posteroventrally inner lamella, narrowing ventrally; moderate number of denticulate, postdorsal and postventral margins forming a long, wavy marginal pore canals; holamphidont hinge; four blunt angle. Surface smooth and polished; two longitudinal elongated adductor scars in a vertical row; V-shaped frontal and parallel ridges extending about half the length of the scar. carapace, rising from anteromedial area and terminating Remarks. This genus is distinguished from other posteromedially; marginal rim low; ventral ridge oblique, trachyleberidinid tricostate genera by its broad inner extending from the mid-anteroventral margin to the margin. It resembles Occdtocythereis but differs by its larger posterior end of the median ridges; normal pore canals size, the presence of a prominent submedian ridge and open and moderate in number. Inner lamella moderately simple, long and sinuous marginal pore canals. broad, narrowing ventromedially; line of concrescence and Phacorhabdotus is similar, but its carapace is much shorter, inner margin coincide throughout; marginal pore canals its anterior frill is thin, it has no marginal ridge, its muscle simple, long, wavy with distal thickening; selvage swelling is pronounced, and its pore canals are paired. prominent, peripheral. Hinge in the RV with a strong tooth In its general outline and the characteristic strong hinge, having a higher large and rounded distal part, a lower Bajacythere resembles Recent Australian Cythereis (Cythereisi reniform proximal part and a large postjacent socket cristatella Brady (1866), later reported by Brady (1880) as anteroventrally opened to the inside; median groove Cythere cristatella from Recent sediments off Booby , straight and smooth; posterior tooth large rounded. LV southern New Guinea. complementary. Sexes distinct, males longer and lower than females. Bajacythere bajaensis Carreiio & Cronin, sp. nov. Dimensions (mm) L H (P1 1 figs 9-13) Holotype LV female IGM-328-Mi 0.730 0.111 Derivation of name. After Baja California Sur, Mexico. Paratype RV female 1GM-329-Mi 0.670 0.340 Diagnosis. A tricostate species characterized by a smooth Paratype RV female IGM-330-Mi 0.690 0.370 Allotype LV male IGM-331-Mi 0.770 0.380 and polished surface with small deep pits, moderately Allotype C male IGM-332-Mi 0.670 0.370 broad inner margin; denticulate anterior and posterior Allotype RV male TGM-333-Mi 0 745 0.380 margins, valves asymmetrical. Remarks. This species was compared with material Holotype. LV female IGM-328-Mi deposited at the Reston, Virginia, United States Geological Material. 40 specimens. Survey collection assigned by Cronin (unpublished report) Locality and horizon. Locality USGS-84TC51 southern side to the upper Miocene "Cnliricoruio" cristntelln (Brady, 1866), of Arroyo Mezquital, near San Juanico (26'14" - 112"23'W), from Enewetak , Marshall , Equatorial Pacific Baja California Sur, Mexico. Bateque Formation, mid Eocene boreholes. This Micronesian species is very similar to age. Unconsolidated foraminifera-rich, fine-grained Bajacythere hajnei1si.s Carreiio & Cronin, sp. nov., particularly sandstone. with respect to the strong hinge both have, but it differs in Description. Carapace with greatest height at the anterior having a smooth surface and a moderately broad inner

Explanation of Plate 1 Figs. 1-3. Puijenborckrllu mczquitalensis sp. nov. Carrefio & Cronin. Locality USGS-84TC51. All specimens are approximately X 130: fig. 1, Holotype IGM-314-Mi, female LV, external view; fig. 2, Paratype IGM-315-Mi, female RV, external view; fig. 3, Paratype IGM-316- Mi, female LV, internal view. Figs. 4-6. Paijrriborchrlla trigoria Marianos & Valentine, 1958. Locality IGM-2, 515. All specimens are approximately X 130; fig. 4, Hypotype IGM-320-Mi, female LV, external view; fig. 5, Hypotype IGM-321-Mi, male RV, external view; fig. 6, Hypotype IGM-322- Mi, male C, dorsal view. Figs. 7-8, Acanthocythereis wushburni (Stephenson 1944). Locality IGM-2, 515, All specimens are approximately X 60; fig. 7, Hypotype IGM-325-Mi, LV, external view; fig. 8, Hypotype IGM-326-Mi, C, dorsal view. Figs. 9-13, Bajacythere bujarnsis gen. nov., sp. nov., Carrefio & Cronin. Locality USGS-84TC51. All specimens are approximately X 60: fig. 9, Holotype IGM-328-Mi, female LV, external view; fig. 10, Paratype IGM-329-Mi, female RV, external view; fig. 11, Paratype IGM-330-Mi, female RV, internal view; fig. 12, Allotype IGM-331-Mi, male LV, external view; fig. 13, Paratype IGM-332-Mi, female C, dorsal view. Figs.14-16 Hazrlina sp. Locality IGM-2, 515. All specimens are approximately X 100: fig. 14, Hypotype IGM-334-Mi, C, dorsal view; fig 15, Hypotype IGM-335-Mi, C, external view of the RV; fig. 16, Hypotype IGM-336-Mi, C, external view of the LV. Figure 17-19, Occultocythereis gioargaezi Carretio & Cronin, sp. nov. Locality USGS-84TC51. All specimens are approximately X100; fig. 17, Holotype IGM-337-Mi, C, dorsal view; fig. 18, Paratype IGM-338-Mi, RV, external view; fig. 19, Paratype IGM-339-Mi, LV, external view.

144 Mexican Eoceiic Ostracoda

145 Carreiio & Cronin

margin instead of a finely pitted surface and broad inner Baja California Sur, Mexico. Bateque Formation, mid Eocene margin. age . U n c o n s o 1id a t e d for ami n i f e r a - rich, fine- g r a i ned Distribution. Locality USCS-84TC51. sandstone. Description. Carapace small, thinly calcified; Genus Hazelina MoosJ966 subrectangular, laterally very compressed; highest at the Hazelina sp. anterior cardinal angle, widest at the posterior end of the (P1 1 figs 14-16) dorsal ridge; valves slightly asymmetrical, LV moderately Description. Small sized carapace, subrectangular in lateral overlapping RV anterodorsally. Dorsal and ventral margins view, highest at the anterior cardinal angle, widest at 1/3 of nearly str

146 Mexican Eou.~iicOstracoda

147 Carreiio & Cronin

(1'1 2 figs 1-4) Holotype LV IGM-340-Mi 0.610 0.360 Derivation of name. Derived after the formational name Paratype RV IGM-341-Mi 0.650 0.340 Bateque. Paratype RV IGM-342-Mi 0.640 0.340 Diagnosis. Characterized by an elongated, subrectangular Paratype C IGM-343-Mi 0.650 0.340 carapace, with dorsal and ventral ridges and a very low, Remarks. This species was placed in the genus Hermanites submedian ridge, surface of the valves foveolate, anterior because of the general outline, ornamentation and hinge; margin denticulate, and the posterior end bearing marginal nevertheless, the dorsal ridge is not well-developed. Also, spines. an unusual low submedian ridge is present, possibly due to Holotype. LV IGM-340-Mi. the replacement of foveolate with reticulated pattern of Material. 30 specimens. ornamentation. Hermanites batequensis sp. nov. resembles H. Locality and horizon. Locality USGS-84TC51 southern side paijenborchiana (Keij, 1957) from the mid Eocene (Lutetian) of Arroyo Mezquital, near San Juanico (26"14'N-l12"23'W), of Grignon, France. It is different from H. batequensis sp. Baja California Sur, Mexico. Bateque Formation, mid Eocene nov. because it lacks the submedian ridge and a well- age. Unconsolidated foraminifera-rich, fine-grained developed reticulated pattern. sandstone. Distribution. Locality USGS-84TC51 Description. Medium sized carapace; with flattened extremities in dorsal view, in lateral view elongated, Genus Jugosocythereis Puri, 1957 subrectangular, greatest height at the anterior cardinal Jugosocythereis bermejoensis Carreiio & Cronin, sp. nov. angle, greatest width posteriorly due to the projection of the (PI 2 figs 5-8) posterior end of the submedian ridge. Dorsal margin almost Derivation of name. Referring to the original Spanish name straight, ventral margin of LV concave, RV almost straight. of the Gulf of California: "Mar Bermejo". Anterior margin broadly and obliquely rounded, fringed Diagnosis. Carapace subquadrate in lateral view; straight with numerous small denticles, posterior margin truncated dorsal and sinuous margin; anterior margin rounded, with in the LV, at the RV its dorsal portion is concave, in both denticles and a heavy rim; posterior end short, subrounded valves the ventral portion bears five marginal spines and with five strong spines. Surface covered with weak two in the dorsal portion. Subcentral swelling low, surface reticulation, ventral and dorsal ridges, and two subparallel of valves foveolate with strong coarse pits projecting over longitudinal median ridges. the dorsal margin, with a very low dorsal ridge, a rounded Holotype. LV IGM-344-Mi. knob at the posterior cardinal angle. A low, rounded Material. 67 specimens. submedian ridge starting at the anterior margin runs back Locality and horizon. Locality (USGS-84TC51) southern to the central swelling where it becomes more evident, side of Arroyo Mezquital, near San Juanico (26'14"- turning upwards and ending at the rounded knob of the 112"23'W), Baja California Sur, Mexico. Bateque Formation, posterior cardinal angle. Another ridge runs parallel to the mid Eocene age. Unconsolidated foraminiferal-rich, fine- grained sandstone. ventral margin in the RV, whereas in the LV it runs Description. Carapace subquadrate in lateral view with an obliquely to the ventral margin. almost straight dorsal margin and slightly sinuous ventral Inner lamella moderately wide, line of concrescence and margin; greatest height at the anterior cardinal angle; inner margin coincide, radial pore canals straight and greatest width at the posterior end of the projecting ribs. numerous. Central muscle scars consist of a posterior Anterior margin almost evenly rounded, wider dorsally vertical row of four elongated scars, with two closely than ventrally, with about 20 denticles along a heavy situated frontal scars. Hinge of RV consists of a high conical marginal ridge. This ridge merges with the anteroventral anterior tooth, a postjacent socket connected by a straight margin, ending dorsally in a moderate eye tubercle; groove to a lobed posterior tooth, hinge of LV posterior end short, laterally compressed, angled complementary. Marginal pore canals numerous, simple subventrally, concave above, subrounded and with five and straight, dorsally widely spaced, anteriorly paired, and strong spines. In dorsal view, sides are parallel and inflated; ventrally numerous and closely spaced. LV overlapping right at the anterodorsal angle. Surface Dimensions (mm) L H covered with weak reticulation, the ventral ridge rising at the anterior ridge and runs almost parallel to the ventral Explanation of Plate 3

Figs. 1-3, Pokornyella sp. Locality IGM-2, 515. All specimens are approximately X 70: fig. 1, Hypotype IGM-353-Mi, C, external view of the RV; fig. 2, Hypotype IGM-354-Mi, C, external view of the LV; fig. 3, Hypotype IGM-355-Mi, C, dorsal view. Figs. 4-6, Buntonia sp. Locality IGM-2,515, All specimens approximately X 100: fig. 4, Hypotype IGM-356-Mi, C, dorsal view; fig. 5, Hypotype IGM-357-Mi, C, external view of LV; fig. 6, Hypotype IGM-358-Mi, C, external view of RV. Fig. 7-8, "Triginglyrnus" sp. Locality IGM-2, 515. All specimens approximately X 60: fig. 7, Hypotype IGM-359-Mi, male C, external view of LV; fig. 8, Hypotype IGM-360-Mi, female LV, external view. Figs. 9-11, Loxoconcha sp. Locality USGS-84-TC-51. All specimens are approximately X 135; fig. 9, Hypotype IGM-361-Mi, C, dorsal view; fig. 10, Hypotype IGM-362-Mi, LV, external view; fig. 11, Hypotype IGM-363-Mi, RV, external view. Fig. 12, Paracytherid~nsp. Locality IGM- 2,515. Hypotype IGM-364-Mi, LV, external view, X 80.

148 Mexican Eocene Ostracoda

149 Carrefio & Cronin

margin ending at 115 of the length from the posterior end; numerous, large and irregular fossae formed by thin murae, dorsal ridge oblique, extending from just below the eye forming a reticulated pattern. Six large fossae occupy the tubercle and obscuring the posterior part of the dorsal anterior margin. Below the eye tubercle and behind the margin, to a strong lateral wing-like projection in front of most anterodorsal fossae, there is a sulcus which is the posterior cardinal angle, where it turns downward and bordered by the emerging oblique dorsal ridge. This ridge runs parallel to the posterodorsal margin. extends back, obscuring the posterior part of the dorsal Two subparallel longitudinal median ridges run 1/ 5 from margin and ending in a strong lateral projection in front of the anterior margin, where they are high, to 115 before the the posterior cardinal angle. At this point, it turns posterior end. At the central point of the swelling, both downward running parallel to the posterodorsal margin ridges are interrupted and continue back as low ridges. almost to join the terminus of the ventral ridge. The ventral In internal view, valves are deep, hinge consists of a large ridge is subparallel to the ventral margin. The characteristic rounded socket with a postjacent small subconical tooth, the median ridge of the genus is weakly developed in some median element is a smooth straight bar that ends in a very specimens (females?), where it forms a short reticulated row deep, large rounded socket. The adductor muscle scars of tubercles in RV. In other specimens (males?), one upper consist of a vertical row of four scars and two frontal scars submedian ridge, emerging from the flattened anterior obscured by a shallow depression at the muscle platform. margin, runs slightly upward and disappears in front of the Sexual dimorphism, females higher than males. posterior cardinal angle. A second low submedian ridge, Dimensions (mm) L H more evident in the RV and in juveniles, runs subparallel to Holotype LV IGM-344-Mi 0.844 0.533 the upper one, disappearing at about 1/6 of the length from Paratype RV IGM-345-Mi 0.800 0.450 the posterior end. In the LV, this ridge is weaker and ends Paratype C IGM-346-Mi 0.780 0.430 near the muscle platform, where a concentric reticulated Paratype LV IGM-347-Mi 0.730 0.440 Remarks. The general outline of this species resembles the pattern occurs. Internally, the valve is deep. In the RV, the hinge has a female carapace of Keij's (1957) Bradleya kaassckieteri from strong conical anterior tooth and a small subovate the upper Eocene of Belgium. It differs from the latter in the postjacent socket with a medial smooth groove ending in a presence of two submedian ridges and in the pattern of the large ovate posterior socket. Adductor muscle scars pattern smaller ones. partially obscured, consists of an oblique row of four scars; Distribution. Locality USGS-84TC51. there are numerous straight radial pore canals. Dimensions (mm) L H Jugosocythereis monrealensis Carreiio & Cronin, sp. nov. Holotype LV female IGM-348-Mi 0.760 0.470 (P12 figs 9-12) Paratype RV female IGM-349-Mi 1.000 0.522 Derivation of name. After Rancho Batequi del Monreal. Allotype RV male IGM-350-Mi 0.922 0.544 Diagnosis. Carapace inflated, covered with numerous, Paratype C female IGM-351-Mi 1.000 0.522 large and irregular reticulated pattern; the median ridges Paratype C female IGM-352-Mi 0.900 0.520 characteristic of the genus very weakly developed. Remarks. This species is similar to several other species Holotype. LV female IGM-348-Mi described from the Gulf and Florida. In dorsal Material. 27 specimens. view, it is similar to Jzigosocytlzereis zddnrrgeizsis (Howe & Locality and horizon. Locality IGM-2,515, 32 km southwest Law, 1936) from the mid Oligocene, Vicksburg Group. of San Ignacio, Baja California Sur, Mexico, northern side of Byram, Hinds County, Mississippi and J. bialntn (Howe, Arroyo San Ramon, near Rancho Batequi del Monreal. 1951) from the mid Eocene, Avon Park limestone at Levy Approximately 2.5 km northeast of the intersection of 27'00' County, Florida. Nevertheless, this species is latitude N - 113"OO' longitude W. Mid Eocene age. Medium distinguishable by its conspicuous, flattened anterior to very fine-grained, micaceous sandstone. margin and somewhat obliquely rounded margin, which Description. The carapace is heavily calcified, bears a large rim like-fringe projection, carrying six large subrectangular in lateral view; dorsal view irregularly fossae. In addition, the characteristic median ridges of the sagittated with the anterior and posterior ends depressed. genus are weakly developed in the species from the Bateque Laterally, dorsal margin nearly straight; ventral margin Formation. slightly convex; greatest convexity just anterior to the Distribution. Locality IGM 2,251 middle; greatest height at the anterior cardinal angle; greatest width at the mid-center because of the projection of Tribe Pokornyellini Puri, 1974 the subcentral swelling. Anterior margin flattened and Genus PokomyelIa Oertli, 1956 somewhat obliquely rounded, bearing a large rim like- Pokornyella sp. fringe projection, more evident from the mid-anterior to the (P13 figs 1-3) cardinal angle, with approximately 23 small denticles, more Diagnosis. Carapace medium size, heavy, thickest along conspicuous at the anteroventral margin. Posterior dorsal median portion and near middle, subrectangular in lateral margin truncated and slightly concave, resulting in a blunt view, lenticular in dorsal view. Dorsal margin straight in angle with the posteroventral margin, which has four blunt, LV, slightly curved in RV, ventral margin slightly sinuous, large spines. The entire valve surface is covered by anterior margin broadly and obliquely rounded, posterior

150 Mexican Eocene Ostracoda

Remarks. The hinge structure observed in this species end blunt bearing two small ribs above where the suggests inclusion in the genus Triginglymus. posterodorsal slope is concave. A lower small rib extends Ornamentation is similar to that exhibited in T. longicostata from the posterior end, nearly parallel to ventral margin; (Blake, 1950) described from the mid Eocene of the Gosport near the anterior end, it forms a distinct ventral ridge. from Clarke County, Alabama; nevertheless, the Surface ornamented with deep oval to quadrate coarse species from the Bateque Formation is bigger, more coarsely reticulation. Eye tubercle small. Internal characters were not reticulated and with a denticulated anterior mid-ventral observed because of the absence of isolated valves. margin. We left this species in open nomenclature due to Hypotypes. C IGM-353-Mi; C IGM-354-Mi; C IGM-355-Mi. the lack of valves. Material. 47 specimens. Hypotypes. C IGM-359-Mi; LV IGM-360-Mi. Remarks. Disarticulated valves were not found and Material. 7 specimens. detailed observation of the internal characters ~7asnot possible. The abundance of well preserved carapaces Distribution. Locality IGM 2, 251. permits comparison with other mid Eocene Pokovrryella, particularly with similar species described from the Avon Family Loxoconchidae Sars, 1861 Park limestone, Levy County, Florida as P. cribaria (Howe, Genus Loxoconcha Sars, 1866 1951) and P. bellzrla (Howe, 1951). The Bateque Formation Loxoconcha sp. species is bigger, more strongly ornamented, much slender (P13 figs 9-11) in dorsal view and less quadrate in lateral view than the Diagnosis. Carapace small, inflated and ovate in dorsal other species. In our opinion, this species represent a new view, dorsal margin straight, ventral margin concave. taxa, but we prefer to leave it in open nomenclature because Anterior margin obliquely rounded, posterior margin in RV at the moment we can not fully describe it. truncated dorsally, broadly rounded from mid-dorsally to Distribution. Locality IGM 2, 515 ventrally; LV is dorsally concave and slightly acute; ventrally LV is obliquely rounded. Surface entirely covered Subfamily Buntoniinae Apostelescu, 1961 with a quadrate to rectangular reticulated pattern. Genus Buntonia Howe, 1935 Hypotypes. C IGM-361 -Mi; LV IGM-362-Mi; RV IGM-363- Buntonia sp. Mi. (P1 3 fig 4-6) Material. 9 specimens. Remarks. Due to the scarce material and its poor Remarks. This species is very close to Loxoconclza preservation, it was impossible to identify this form to a marionensis Puri, 1957 from the upper Eocene of the Crystal specific level. Nevertheless, this species appears to be River Formation of Florida in its general outline, except for related to Burrtoilia shubutaensis Howe in Howe & Chambers the presence in the Bateque material of a low dorsal keel. L. (1935), except for the fact that Runfonia shiibzitaeiisis-is larger. cocoaensis Krutak, 1961 is also similar but, in that species, Hypotypes. C IGM-356-Mi; C IGM-357-Mi; C IGM-358-Mi. the dorsal ridge is blade-like, instead of rounded as in Material. 19 specimens. Loxoconclia sp. from Baja California. Distribution. Locality IGM 2, 515 Distribution. Locality USGS-84TC51.

Subfamily Campylocytherinae Puri, 1960 Family Paracytherideidae Puri, 1957 Tribe Leguminocythereidini Howe, 1961 Genus Paracytheridea Muller, 1894 Genus Triginglymus Blake, 1950 Paracytheridea sp. "Triginglyrnus" sp. (P13 fig 12) (PI 3 figs 7,8) Diagnosis. Carapace subrectangular in lateral view, Diagnosis. Carapace elongated in lateral view, lanceolated strongly alated. Dorsal and ventral margins straight, in dorsal view with compressed posterior end; dorsal and anterior margin broadly rounded, posterior end draw out ventral margins almost straight. Anterior end broadly and into a distinct caudal process. Each valve bears a strong ala evenly rounded carrying several denticles in the mid- which projects from the midventral zone, terminating at ventral portion; posterior margin subangular with the about 1 /3 the shell length from the posterior. Surface dorsal portion slightly concave, ventral portion with six ornamented with a pattern of low, anastomosing ridges; small rounded spines. Valves covered anteriorly with two anteriorly a group of four ridges radiates out from a point low parallel rims, which continue along ventral and dorsal near the antero-ventral zone. Internal features typical for margins; surface coarsely reticulated with several the genus. prominent sinuate longitudinal ridges. Eye tubercle well Hypotypes. LV IGM-364-Mi; RV IGM-365-Mi. developed. Inner characters were not observed because Material. 4 specimens. material consists of carapaces; nevertheless, it was possible Remarks. Compared to other Eocene Paracytheridea species, to observe the LV hinge in a broken specimen, which the material from the Bateque Formation is similar to P. consists of a large, rounded anterior socket and a postjacent basfropensis Stephenson, 1947, but the former has a more blunt tooth followed by a triangular anti-slip tooth elevated ventral alar projection, and a subacute posterior projection connected to an ovate socket by a median smooth end. It is very closely related to P. belhavenensis Howe & bar. Males are more elongated than females. Chambers, 1935, but detailed comparison to the type

151 Carreiio & Cronin

specimen of this species shows that the distribution of the upper-slope paleodepths affected by strong upwelling valves surface ridges is different and the subcircular (McLean & Barron, 1988). depression located in the anteriomedian zone is not evident At locality IGM 2,215, the presence of Pseudophragmina in the Bateque Formation species. (Proporocyclina) flintensis and Amphistegina lopeztrigoi Distribution. Locality IGM 2, 251. indicates a shallow, warm-water environment, deposited at a depth of no more than 100 m (Vaughan, 1945); whereas Family Paracyprididae Sars, 1923 Thaerocytherinii, that constitutes more than 90%, reinforces Genus Paracypris Sars, 1866 the interpretation that deposition occured in an outer-neritic Paracypris sp. environment. Dominance of carapaces vs. valves could Diagnosis. Medium-sized carapace, smooth, elongated, indicate rapid burial in a deeper part of the basin. subpyriform in lateral view, dorsal margin arched forming At USGS 84TC51 locality the exposed lithology consists an angular peak at mid-portion, more conspicuous in LV, mostly of very fine sandstone with interbedding ventral margin straight to slightly concave particularly at fossiliferous lenses, locally rich in well preserved the center, posterior end is narrow, subacute. LV overlaps stromatolites, coralline algae, foraminifers, calcareous RV throughoc:, more strongly dorsally and ventrally. sponges, gastropods, and bivalves (Squires & Demetrion, Hypotypes. C IGM-366-Mi; C IGM-367-Mi. 1989, 1990a,b). No deep-water ostracods were found and Material. 21 specimens. the assemblage is dominated by thick-shelled Remarks. The material consisted only of carapaces. This Trachyleberdidae (Bajacythere, Occultocythereis, species resembles Paracypris licina (Huff, 1970), but differs in Jugosocythereis), suggesting an outer-neritic environment. that it is smaller, and the dorsal margin has a small The associated benthic foraminifers are characteristically concavity at the anterior cardinal angle. P.franquesi Howe & outer-neritic morphotypes. Chambers (1935) is much larger, and the dorsal margin has The ostracod assemblage is a mixture of faunas from an angular peak at the anterior cardinal angle instead of at different paleobiogeographic provinces. In general, the the mid-portion. whole ostracod assemblage has strong taxonomic affinities Distribution. Locality IGM 2, 251. with the Eocene of the Gulf Coast and the Mediterranean. This suggests a marked influence of the Tethyan corridor as Family Pontocyprididae Muller, 1894 a means for tropical species latitudinal dispersal during the Genus Argilloecia Sars, 1866 Eocene. Argilloecia sp. The species Paijeiiborcliella trigom has previously been Diagnosis. Carapace elongated, highest just anterior to the reported from the Californian Province and, together with middle. Anterior margin irregularly rounded, almost the six new species (including Paijrtiborchelh mqilitnleiisis) angulated just above the middle. Dorsal margin straight or and the new genus Bajacythere, constitutes an isolated very gently convex in the middle, curving gently record of the Eocene ostracod fauna in the area. downward at each extremity. Ventral margin very slightly Paijeiiborcheila is a typical Mesozoic and Paleogene genus convex along its whole length. Posterior margin obliquely from Europe and its presence in America's Eocene rounded, blunt. Muscle scars typical of the genus. sediments strongly reinforces its Tethyan origin. Hypotypes. C IGM-368-Mi; C IGM-369-Mi; C IGM-370-Mi. Paijelzhorchella is also present in California during the Late Material. 12 specimens. Cretaceous (Holden, 1964). Remarks. This species resembles Argilloecia in all respects The new genus Bajacythere raises an interesting except that it has reversed hinge overlap. The material of paleogeographic problem. This species is similar to species the Bateque Formation only consists of carapaces so the found in the Equatorial Pacific Ocean at Enewetak Atoll in muscle scars could only be observed through the upper Miocene to Holocene sediments (Cronin, semitransparent carapace. The marginal area was not unpublished data) and also seems to be closely related to observed in detail. Maastrichtian species reported from Europe (i. e. Cythereis Distribution. Locality USGS-84TC51 aiiorchidea Veen, 1935). The Tethyan influence on the paleogeographic distribution of this genus is presently not DISCUSSION certain. The foraminifers associated with the ostracod fauna of the In summary, the Eocene Baja ostracod assemblage Bateque Formation are characteristic of the Haiitkeiiiira provides important new data to our understanding of iiuttallz Interval Zone and Globigerinatheka subcoiiglobatn circum tropical Tethyan ostracod paleobiogeography. suhconglohata Concurrent Range Zone, suggesting a mid Eocene age of 50.3 - 54.1 Ma (Toumarkine & Luterbacher, ACKNOWLEDGMENTS 1985). A. L. Carreiio gratefully acknowledges Dr. J. Pojeta, for the Sorensen (1982) and McLean and coworkers (1987) provided facilities during my stay at the United States reported Bateque sandstones, yielding abundant Geological Survey, Reston, Virginia, supported by Consejo fragmented shallow-water fossils, in a predominantly deep- Nacional de Ciencia y Tecnologia. Direccion General de water assemblage interpreted as significant downslope Asuntos del Personal Acadhmico, UNAM and Universidad transport. The diatomaceous deposits suggest outer-shelf to Autonoma de Baja California Sur, gave logistic support.

152 Mexican Eocene Ostracoda

Brussels, (136):1-210. Technical assistance of M. Alcayde-Orraca, from the staff of Krutak, P.R. 1961. Jackson Eocene Ostracoda from the Cocoa the Instituto de Geologia, was also very valuable. I am Sand of Alabama. Journal of Paleontology, Tulsa, Okla., indebted to Margarita Cronin for all her kindnesses. We 35( 4):769-788. thank Dr. J. E. Hazel (Louisiana State University), Dr. K. L. Marianos, A.W. & Valentine, J.W. 1958. Eocene ostracode fauna Finger (Chevron Oil Field Research Company) and R. from Marysville Buttes, California. Micropaleontology, New Blodgett (United State Geological Survey) for their patience York, N.Y., 4(4): 363-372. in improving early drafts. Thanks also to Alvin M. Phillips, McLean, H. & Barron, J.A. 1988. A late middle Eocene Curator of the Henry V. Howe Collection (Museum of diatomite in northwestern Baja California Sur, Mexico: Geosciences Louisiana State University) for his help. The implications for tectonic translation. In Filewicz, M.V., & authors are also indebted with two anonymous reviewers. Squires, R.L., (Eds.), Paleogene Stratigraphy, west coast of Manuscript received April 1992 North America. Pacific Section, Society of Economic Manuscript accepted August 1993 Paleontologist and Mineralogists, West Coast Paleogene Symposium, Santa Barbara, Calif., 58:l-8. REFERENCES McLean, H., Hausback, B.P. & Knapp, J.H. 1985. Blake, D.B. 1950. Gosport Eocene Ostracoda from Little Stave Reconnaissance geological map of part of the San Isidro Creek, Alabama. journal of Paleontology, Menasha, Wis., quadrangle, Baja California Sur, Mexico. U.S. Geological 24(2):172-284. Survey, Miscellaneous Field Studies Map, MF-1779, scale Brady, G.S. 1866. On new or imperfectly known species of 1:250,000, Reston, Va., one sheet. Ostracoda. Transactions of the Zoological Society of London, McLean, H., Hausback, B.P. & Knapp, J.H. 1987. The geology of London, 5:359-398. west-central Baja California Sur, Mexico. U.S.Geological Brady, G.S. 1880. Report on the Ostracoda dredged by H.M.S. Survey Bulletin, Reston, Va., 1579:l-19 Challenger during the years 1873-1876. Reports of the Voyage Mina-Uhink, F. 1957. Bosquejo geoldgico del territorio de la of H. M. S. Challenger, Zoology, London, l(pt. 3):l-184. Baja California. Boletin de la Asociacidn Mexicana de Gedlogos Butterlin, J. 1981. Claves para la determinacidn de rnacroforarnin~eros Petroleum, Mexico, D.F., 9(3-4):139-269. de Mixico y del Caribe, del Cretucico Superior a1 Mioceno medio. Okada, H. & Bukry, D. 1980. Supplementary modification and Instituto Mexican0 del Petrdeo, Subdireccih de Tecnologia y introduction of code numbers to the low-latitude coccolith Exploracih, Mexico, D.F.:l-219. biostratigraphic zonation (Bukry, 1973; 1975). Marine Carrillo de Isolbi, G. 1976. Geologia regional semidetallada del Micropaleon tology, Amsterdam, 5(3):321-325. prospecto Sun Ignacio-Cadeji, Baja California Sur. Unpub. B. Sc. Puri, H.S. 1957. Stratigraphy and zonation of the Ocala Group, thesis, Universidad Nacional Aut6noma de Mexico, Facultad Part 3. Ostracoda. Florida Geological Survey, Bulletin, de Ingenieria:l-210. Tallahassee, Fla., (38):l-248. Gooch, D.D. 1938. Some Ostracoda of the genus Cythereis from Sorensen, P.A. 1982. Sedimentology and sedimentary petrology of a the Cook Mountain Eocene of Louisiana. Journal of Paleocene basin near Laguna Sun Ignacio, Estado de Baja Paleontology, Menasha, Wis., 13(6):580-588. California Sur Mexico. Unpub. M. Sc. thesis, University of CGSNECI, 1983. San Jose de Gracia, Baja California Sur. California Santa Barbara, 114 p. Mexico, D.F., Secretaria de Programacidn y Presupuesto, Squires, R.L. & Demetrion, R. 1989. An early Eocene pharetronid Coordinacidn General de 10s Servicios Nacionaks de Estadistica, sponge from the Bateque Formation, Baja California Sur, Geografia e lnformatica, Direccidn General de Geografin, Mexico. journal of Paleontology, Lawrence, Ka., 63(4):440-442. topographic chart number G12A64, scale 1:50,000. Squires, R.L. & Demetrion, R. 1990. New early Eocene marine Heim, A. 1922. Notes on the Tertiary of southern lower gastropods from Baja California Sur, Mexico. Journal of California. Geological Magazine, London, 59(702):529-547. Paleontology, Lawrence, Ka., 64 (1):99-103. Holden, J.C. 1964. Upper Cretaceous ostracods from California. Squires, R.L. & Demetrion, R. 1990. New Eocene marine Palaeontology, London, 7(3):393-429. bivalves from Baja California Sur, Mexico. Journal of Howe, H.V. 1952. New Tertiary ostracode fauna from Levy Paleontology, Lawrence, Ka., 64(3):382-391. County, Florida. Florida Geological Suroey, Bulletin, Florida, Fla., Stephenson, M.B. 1944. Ostracoda from the Reklaw Eocene of (34):l-32. Bastrop County, Texas. Journal of Paleontology, Tulsa, Okla. Howe, H.V. & Chambers, J. 1935. Louisiana Jackson Eocene 18(5):448-454. Ostracoda. Department of Conservation Louisiana Geological Stephenson, M.B. 1947. Weches Eocene Ostracoda: corrections. Survey, Bulletin, New Orleans, La., (5):l-65. Journal of Paleontology, Menasha, Wiss., 21 (6):579. Howe, H.V. & Law, J. 1936. Louisiana Vicksburg Oligocene Toumarkine, M. & Luterbacher, H. 1985. Paleocene and Eocene Ostracoda. Department of Conservation Louisiana Geologicnl planktic foraminifera. In Bolli, H.M., Saunders, J.B., & Perch- Survey, Bulktin, New Orleans, La. (7):l-96. Nielsen, K., (Eds.), Plankton Stratigraphy, 87-154, Cambridge INEGI, 1982. San Isidro, Baja California Sur. Mexico, D.F., University Press. Secretaria de Programacidn y Presupuesto, lnstituto Nacional de Vaughan, T.W. 1945. American Paleocene and Eocene larger Estadistica, Geografia e Znformutica, topographic chart number Foraminifera. Geological Society of America Memoir, Baltimore, NG12-4, scale 1:50,000. Md., 9(1):1-175. Huff, W.J. 1970. The Jackson Eocene Ostracoda of Mississippi. Veen, J.E. 1936. Die Cytheridae der Maastrichter Tuffkreide Mississippi Geological, Economic and Topographical Survey, und des Kunrader Korallenkalkes von sud-Limburg. IV Die Bulletin, Jackson, Miss.:l-289. Gat t u n ge n C y t h e re is, A r cl?i cy t he re is u nd C y t h c r ide is. Keij, A.J. 1957. Eocene and Oligocene Ostracoda from Belgium. Natuurhistorisch Maandb/. Maastricht, 25(11-12):131-168. Institut Royal des Sciences Naturelles de Belgique, Mimoires,

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