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768


Journal of Paleontology 91(4):767–780


fossil record (Thompson et al., 2015b). Furthermore, the echi- noids described herein demonstrate that some of the morpho- logical innovations associated with the echinoid crown group were in fact present in numerous stem group taxa in the Permian.


Geologic setting


All specimens were collected from the Lamar Member of the Bell Canyon Formation from the Guadalupe Mountains ofWest Texas. From 1939 to 1968, numerous expeditions were made by G. A. Cooper and others to the Permian outcrops of West Texas. The specimens herein described were collected during those excursions. In the Guadalupe Mountains, a number of micro- fossil taxa have yielded good biostratigraphic control. From the concurrent presence of the conodonts Jinogondolella postserrata (Behnken, 1975) and J. shannoni Wardlaw in Wardlaw and Mei, 1998, the Lamar Member of the Bell Canyon Formation has been determined to be Capitanian in age (Lambert et al., 2002; Lambert, 2006). The transition from the J. postserrata Zone to the J. shannoni Zone takes place within the uppermost Lamar Limestone Member (Lambert et al., 2010), thus indicating a lower Capitanian age (ca. 264 ma) (Henderson et al., 2012). The uppermost Lamar Limestone Member also marks the transition from J. shannoni to J. altudaensis (Kozur, 1992). The presence of both of these faunal transitions allows for relatively precise biostratigraphic control and clarifies the age of the Lamar Limestone Member to lower Capitanian (263–264 Ma). The Lamar Member of the Bell Canyon Formation was


deposited in the Delaware Basin and is spatially located to the southeast of the Guadalupe Mountains and the Capitan Forma- tion. The Lamar Member contains carbonate debris flows transported from the reef edge sediments of the Capitan Formation. The unit displays a wedge-shaped morphology, being over 90m thick near the shelf margin, where allochtho- nous sedimentation from the reefal sediments represented by the Capitan Formation was greatest, and thinning basinward to only about 2m(Babcock, 1977). The Capitan Formation and the Bell Canyon Formation are coeval (Lambert et al., 2010), and merge toward the edge of the Delaware Basin. Close to the basin edge, at the type section of the Reef Trail Member (which overlies the Lamar Limestone Member), the Lamar Limestone Member was described as containing medium to dark gray organic-rich mudstones, and skeletal, peloidal wackestones and packstones with interspersed carbonate debris flows containing silicified fossils (Lambert et al., 2010). Babcock (1977) noted the presence of numerous transported silicified reef fossils infilling channels in the zone proximal to the reef. Proximal to the reef edge, the fauna of the Lamar Limestone Member consists of brachiopods, bryozoans, and crinoids (Babcock, 1977). Cooper and Grant (1972) furthermore noted that the brachiopod fauna in the Lamar was similar to that occurring on the ‘reef slope.’ Of special importance to this paper, silicified echinoid spines and plates have been noted as common in these debris flows (Babcock, 1977, p. 365, fig. 5). Basinward, the Lamar Lime- stone Member thins and is composed primarily of finely laminated mud lacking fossils and bioturbation (Babcock, 1977). The specimens discussed in this study were collected from localitiesUSNM725e, 728p, and 738b near the Guadalupe


Mountains (Cooper and Grant, 1972), which are interpreted as having been deposited near a shelf margin.


Materials and methods


Following their collection, specimens were prepared out of bulk limestone blocks at the USNM by using the hydrochloric acid dissolution method of Cooper and Grant (1972). Observations were made using dissecting microscopes, and specimens were measured using calipers. Silicified fossils are common in the Lamar Limestone (Cooper and Grant, 1972; Babcock, 1977), and all Lamar echinoid specimens discussed in this study are silicified. Fine scale details of plate structure and tuberculation are obscured by silicification, and stereomic microstructure is lacking from the surface of specimens. Cooper and Grant (1972) discussed two types of silicification present among the fossils of the Glass Mountains. One of these preservation types results in a thin coat of silica on the surface of the specimens, which, when treated with acid, protects the calcite on the interior of the plate from disintegration. This is the nonpervasive silicification dis- cussed by Butts and Briggs (2011), and indeed, some echinoid specimens within this fauna are preserved with only a thin layer of silica and thus contain calcitic interiors. The second type of silicification mentioned by Cooper and Grant (1972) is complete replacement, where the entire fossil has been recrystallized to silica. This is also common among the specimens described herein.


Repositories and institutional abbreviations.—Institutional abbreviations for specimen repositories are as follows: USNM = United States National Museum, Washington D. C., USA; MGL = Musée d’Histoire Naturelle de Lille, France; NMS G = National Museum of Scotland, Edinburgh, Scotland; RGM = Naturalis Biodiversity Center, Leiden, The Netherlands.


Systematic paleontology


Terminology and classification follows Smith (1984) and Kroh and Smith (2010). Methodology follows Lewis and Donovan (2007).


Class Echinoidea Leske, 1778 Subclass Cidaroidea Smith, 1984


Family Miocidaridae Durham and Melville, 1957 Type genus.—Miocidaris Döderlein, 1887


Other genera.—Eotiaris Lambert, 1899, Couvelardicidaris Vadet, 1991, Procidaris Pomel, 1883 Genus Eotiaris Lambert, 1899


Type species.—Cidaris keyserlingi Geinitz, 1848, from the Wuchiapingian Zechstein of Germany and England.


Diagnosis.—Miocidarid with small test. Interambulacral plates imbricate adapically. Aureoles confluent only at and below ambitus. Spines with spinules.


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