Paleocene Palynomorph Assemblages from the Nacimiento Formation, San Juan Basin, New Mexico, and Their Biostratigraphic Significance Thomas E

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Paleocene Palynomorph Assemblages from the Nacimiento Formation, San Juan Basin, New Mexico, and Their Biostratigraphic Significance Thomas E Paleocene palynomorph assemblages from the Nacimiento Formation, San Juan Basin, New Mexico, and their biostratigraphic significance Thomas E. Williamson, [email protected], New Mexico Museum of Natural History and Science, 1801 Mountain Road, NW, Albuquerque, New Mexico 87104; Douglas J. Nichols, [email protected], Denver Museum of Nature & Science, 2001 Colorado Boulevard, Denver, Colorado 80205; and Anne Weil, [email protected], Department of Biological Anthropology and Anatomy, Duke University, Box 90383, Durham, North Carolina 27708 (current address: Department of Anatomy and Cell Biology, Oklahoma State University Center for Health Sciences, 1111 W. 17th Street, Tulsa, Oklahoma 74104) Abstract important biochronologic correlation for the Mammal Ages (NALMAs). The continuing Western Interior. goal is to refine NALMAs and tie them to The Nacimiento Formation bears vertebrate other biological and geological time mark- faunas that are types for the Puercan and Introduction ers (Woodburne 2006). A biochronology Torrejonian North American Land Mam- of the early Paleocene of western North mal Ages (NALMAs). A biostratigraphy based on therian mammal distribution in The Paleocene was a time of dramatic America, tied to the geomagnetic polarity the Nacimiento Formation can be tied to restructuring of terrestrial ecosystems and time scale (GPTS), and in some places, con- magnetostratigraphy. This is correlated to a rapid diversification of many groups of ani- strained by radiometric ages obtained from geomagnetic polarity time scale, forming an mals and plants following the Cretaceous– volcanic ashes, is well established (Lofgren important geochronologic and biochronolog- Tertiary (K–T) mass extinction. The San et al. 2004). The type faunas for the two ic framework for regional correlation. Two Juan Basin (Fig. 1), a foreland basin formed NALMAs ushering in the age of mammals, palynomorph assemblages recovered from during the Laramide orogeny, contains a the Puercan and Torrejonian, are from the the Paleocene Nacimiento Formation in Kim- long and relatively continuous deposition- Nacimiento Formation. beto Arroyo, San Juan Basin, New Mexico, al record spanning the K–T boundary and In an effort to refine early Paleocene can be correlated to a Paleocene palynostrati- graphic zonation of western North America, the early Paleocene (Fig. 2). The record of biostratigraphy and biochronology, Wil- providing an independent and significant mammalian succession of the Nacimiento liamson (1996) proposed a therian mam- biochronologic correlation. The first sample Formation is particularly important as it mal biostratigraphy based on lithostrati- (SJB03-17) is from a carbonaceous mudstone is the longest and most complete for the graphic correlation of fossil localities in the ~1 m (~3 ft) below strata of the Puercan (Pu2) early Paleocene of North America. This Nacimiento Formation. This was tied to NALMAs and in a zone of normal magnetic record has been crucial for constructing an existing magnetostratigraphy (Lindsay polarity correlated with polarity subchron a biochronologic framework for the early et al. 1981) that provided tie points to the C29n. It yielded an assemblage including Paleocene based on the succession of mam- GPTS. The resulting biochronology pro- Arecipites sp., Corollina sp., Laevigatosporites malian faunas, the North American Land vided the chief basis for the latest revision sp., Momipites tenuipolus, Nyssapollenites spp., Pityosporites sp., Tricolpites anguloluminosus, Tricolpites spp., and Ulmipollenites krempii. The second sample (SJB03-19) is from a car- bonaceous mudstone approximately 2 m (6.5 ft) above strata that yield a basal Torrejonian (To1) NALMA vertebrate fauna and within a succeeding zone of normal magnetic polar- ity correlated with polarity subchron C28n. It yielded an assemblage including Cicatrico- sisporites sp., Corollina sp. (common), Laevi- gatosporites sp., Momipites triorbicularis (com- mon), Pityosporites spp., Tricolpites angulolu- minosus, Ulmipollenites krempii, and Zlivisporis novomexicanum. SJB03-17 contains Momipites tenuipolus, a taxon that is widespread in the lower Paleo- cene in the Western Interior. Its occurrence in this sample in the lower Nacimiento For- mation is consistent with its known strati- graphic range. SJB03-19 yields Momipites tri- orbicularis, a taxon that indicates a correlation with Paleocene palynostratigraphic Zone P3 (the Momipites actinus–Aquilapollenites spinu- losus Interval Biozone), a zone identified throughout the lower Paleocene of the West- ern Interior. The identification of Zone P3 in the Nacimiento Formation closely associ- ated with a To1 vertebrate assemblage firmly establishes a correlation between a Paleocene palynostratigraphic and vertebrate biostrati- graphic zonation. This is consistent with most recent age correlations proposed for the Nacimiento Formation and provides an FIGURE 1—Geologic map of the San Juan Basin, northwestern New Mexico (after Williamson 1996). February 2008, Volume 30, Number 1 NEW MEXICO GEOLO G Y 3 FIGURE 2—Stratigraphy of the San Juan Basin spanning the Cretaceous–Tertiary boundary and early Paleocene with two differing hypotheses regarding the age correlation of these strata. Radiometric ages from volcanic ashes in the De-na-zin Member are shown as published by Fassett and Steiner (1997) and are not corrected using updated decay constants after Renne et al. (1998) and Knight et al. (2003). The composite stratigraphic section and magnetostratigraphy of Upper Cretaceous and Paleocene deposits are after Lindsay et al. (1981). Fossil zones A–H are from Williamson (1996). The time scale is from Gradstein et al. (2004). 4 NEW MEXICO GEOLO G Y February 2008, Volume 30, Number 1 of the Puercan and Torrejonian NALMAs lithostratigraphy and compiled them into “Taeniolabis zone” (Archibald et al. 1987; (Lofgren et al. 2004). a series of eight successive fossiliferous Lofgren et al. 2004). However, strata yield- Recently, Fassett (2001, 2007) suggested zones, labeled A–H in a composite section ing the Pu3 fauna are not present or are not that age correlation of the Nacimiento For- (Fig. 2). These zones can be considered as fossiliferous in Kimbeto Wash (Williamson mation based on mammals is in error. Fas- ”paleontologically distinct lithozones” as 1996). The fossil localities from the lowest sett and others, in a number of papers (e.g., defined by Walsh (2000). The lowest two fossil zone of the west flank of Kimbeto Fassett et al. 1987; Fassett and Lucas 2000; zones, A and B, yield the type Puercan Wash locale were collectively referred to as Fassett et al. 2000, 2002; Fassett 2001, 2007), NALMA faunas. The succeeding six fossil locality 11 in Williamson (1996, appendix 3; argued that sediments of the Naashoibito zones yield the type Torrejonian NALMA Figs. 3, 4; precise locality information is on Member, Kirtland Formation (sensu Baltz et faunas. file at the NMMNH). This locale includes al. 1966), yielding non-avian dinosaurs are Williamson (1996) erected eight biostrati- the site AMNH locality 5 as well as Stand- Paleocene in age. The Naashoibito Member graphic zones based on interval zones of hardt’s (1980) Black Toe site, a microverte- contains a zone of normal polarity. This fossil mammals as distributed among the brate fossil locality. This fossil zone can be was later attributed to overprinting (But- eight fossiliferous zones. These zones can ler and Lindsay 1985). However, Fassett be tied directly to the Nacimiento Forma- (2001, 2007) argued that this zone of nor- tion lithostratigraphy and magnetostratig- mal polarity reflects remanent magnetiza- raphy, facilitating correlation between tion and is correlated with subchron 29n. If biological and geochronological events. correct, correlation of this zone to subchron Notably, the resulting biochronology dif- 29n would necessitate a revision of the cor- fers conceptually from that of the NALMAs relation of the magnetostratigraphy of the (see Woodburne 1987, 2004). overlying Nacimiento Formation with the In the study area, encompassing the GPTS resulting in a significantly different east and west flanks of Kimbeto Wash, age assessment for the Nacimiento Forma- are several diverse fossil localities within tion and its vertebrate faunas (Fig. 2). Such three distinct fossil zones (Figs. 3, 4). The a conclusion would therefore not only have lowest of these is from close to the base of important implications to extinction across the Nacimiento Formation and is restricted the K–T boundary, but also to the efficacy to a relatively narrow fossiliferous band of early Paleocene mammal biostratigra- bounded above and below by intervals phy, biochronology, and evolutionary stud- barren of vertebrate fossils (Williamson ies (e.g., Alroy 1999). In order to test this 1996). This fossiliferous zone is referred FIGURE 3—Digital elevation model of Kimbe- hypothesis, an independent age assessment to as the “Ectoconus zone” (sensu Sinclair to Wash (portions of the Kimbeto and Blanco Trading Post USGS 7.5-min topographic maps) for key horizons of the Nacimiento Forma- and Granger 1914) or “Hemithlaeus zone” showing location of measured sections on the tion is required. (sensu Van Valen 1978). The fauna recov- west (A–A’) and east (B–B’) flanks of Kimbeto Against this backdrop, two new palyno- ered from this horizon is regarded as the Wash. Locations for samples for palynomorphs morph assemblages from the Nacimiento “type fauna” for the middle Puercan (Pu2) SJB03-17 and SJB03-19
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