Apatemyids are a unique family of small mammals that are uncommon in Paleogene localities of North America and Europe. Their cranial and postcranial anatomy are known in North America from Paleocene specimens of Labidolemur kayi (Bloch & Boyer, 2001; Silcox et al., 2010) and an Eocene specimen of Apatemys chardini (Von Koenigswald et al., 2005a), while the unusual dental, jaw, and hand adaptations of these and a few skeletons from Europe indicate that apatemyids evolved convergently with living marsupials in the genus Dactylopsila (Petauridae; striped or long-fingered possums) of New Guinea and northeastern Australia, and with the living primate Daubentonia (Daubentoniidae; aye-aye) of Madagascar (McKenna, 1963; West, 1973; Von Koenigswald & Schierning, 1987; Von Koenigswald et al., 2005a; Von Koenigswald et al., 2005b; Rose, 2006). Aspects of apatemyids’ ecology, too, were probably similar to these living mammals as well as possibly that of the extinct Oligocene-Miocene metatherian Yalkaparidon of Australia (Beck, 2009). Like striped possums and the aye-aye, the striped possum-sized apatemyids are presumed (1) to have been arboreal and insectivorous, (2) to have used their pincerlike upper and lower incisors to tear loose bark from trees or rip open rotting wood that might harbor wood-boring insects, and (3) to have used two elongated manual digits to help find and extract the insects from cavities in the wood. The overall time range of the Apatemyidae as presently known spans virtually the entire Paleogene, from the early Paleocene to Eocene in Europe and from the early Paleocene to the late Oligocene (early Arikareean) in North America (McKenna & Bell, 1997; Rose, 2006; Gunnell et al., 2008). Apatemyids are unknown from other continents. The earliest North American genera in this poorly known family are Jepsenella and Unuchinia. Jepsenella is known from the late Torrejonian, Unuchinia from the Torrejonian and Tiffanian (Paleocene), and Labidolemur from the early Tiffanian. West (1973) reviewed the North American Eocene and Oligocene Apatemyidae (not the Paleocene taxa) and reduced several previously named genera (Apatemys, Labidolemur, Stehlinius, Stehlinella, Teilhardella, and Sinclairella) and species to just two genera: Apatemys, with two highly variable species, and Sinclairella, with a single species. So defined, Apatemys has a long temporal range of perhaps 20 million years from the late Paleocene (Tiffanian) until the late middle Eocene (Duchesnean) in North America. All known occurrences of this family in North America are in the western interior or Pacific coastal parts of the continent, in Saskatchewan, Canada, and the states of Montana, Wyoming, South Dakota, Nebraska, Utah, Colorado, New Mexico, and California (West, 1973; Storer, 1996). Some authors (e.g., McKenna & Bell, 1997) followed West’s (1973) synonymy, but Russell et al. (1979) asserted that Labidolemur should be maintained as a separate genus for the species L. kayi. Gingerich & Rose (1982) and Gingerich (1982) also retained Labidolemur for other Paleocene species. Rose (2006) recognized Apatemyidae as the only family within the order Apatotheria, containing six genera, Unuchinia, Jepsenella, Labidolemur, Apatemys, Heterohyus, and Sinclairella. We follow Rose’s (2006) taxonomy herein but also recognize in addition the recently described European genus Carcinella (Von Koenigswald, Ruf & Gingerich, 2009).
The latest known apatemyid is Sinclairella dakotensis Jepsen, 1934, the only recognized member of its genus. Sinclairella occurred in the Duchesnean (late middle Eocene), Chadronian (late Eocene), Orellan (early Oligocene), Whitneyan (early Oligocene) and early Arikareean (early Oligocene) of western North America. Two of the earliest records are identified only as Sinclairella sp. (Storer, 1995; Storer, 1996); later occurrences are published as Sinclairella dakotensis. Ages and localities of occurrence (Fig. 1; ages here are adjusted to reflect those provided by Albright et al., 2008; Janis, Gunnell & Uhen, 2008: appendix 1) are: Duchesnean: Lac Pelletier Lower fauna, Saskatchewan (Storer, 1995); Chadronian: Calf Creek Local Fauna (LF), Saskatchewan (Storer, 1996), Flagstaff Rim area and Bates Hole, Wyoming (Emry, 1973; West, 1973), the type locality at Big Corral Draw, South Dakota (Jepsen, 1934), Medicine Pole Hills Local Fauna, North Dakota (Pearson & Hoganson, 1995), Raben Ranch and Twin Buttes Local Faunas, and harvester ant mounds in Sioux County, Nebraska (Clemens, 1964; Ostrander, 1985; Ostrander, 1987); Orellan: Logan County and Weld County, Colorado (Clemens, 1964), and Shannon County, South Dakota (West, 1973); Whitneyan-early Arikareean: Wh2-Ar1, Harris Ranch badlands, Fall River County, South Dakota (as Sinclairella cf. S. dakotensis; Simpson, 1985); Ar1, Gering Fauna, Nebraska (Gunnell et al., 2008); Ar1, Unit C of Turtle Cove Member, John Day Formation, Oregon (29.75–28.8 Ma; Cavin & Samuels, 2012). Thus, through Sinclairella dakotensis, the North American apatemyid lineage continued into the earliest Arikareean (Ar1).
We report the occurrence of the apatemyid lineage for the first time in the eastern half of North America, and about 5 million years later than the previous latest known occurrences. The occurrence consists of four unassociated, isolated teeth of an apatemyid similar to Sinclairella dakotensis that were found in the Buda locality, Florida, which yielded a mammalian fauna of latest Oligocene age (early late Arikareean, Ar3). The Florida Sinclairella differs in size and qualitative dental characters from S. dakotensis, and clearly represents a distinct new species.
Herein we use the revised chronostratigraphy and biochronology of the Arikareean NALMA of Albright et al. (2008) as recorded in the John Day Formation of Oregon. These authors placed the base of the Arikareean NALMA and subbiochron Ar1 at approximately 30 Ma, with basal temporal boundaries of the other subbiochron intervals as follows: Ar2, 28 Ma; Ar3, 26 Ma; Ar4, 23 Ma; base of Hemingfordian NALMA and He1 subbiochron, 18.5 Ma. Of particular significance to the Buda Local Fauna, Albright et al. (2008) established the boundary between the Ar2 and Ar3 at about 26 Ma (late Oligocene), whereas Tedford et al. (2004) placed this same boundary at about 23 Ma (earliest Miocene). We also use the broader terms, early Arikareean (Ar1 and Ar2), including the earliest Arikareean (Ar1; 30–28 Ma) and late early Arikareean (Ar2; 28–26 Ma), and late Arikareean (Ar3 and Ar4), including the early late Arikareean (Ar3; 26–23 Ma) and latest Arikareean (Ar4; 23-18.5 Ma). Rincon et al. (2015) recently subdivided the Arikareean somewhat differently, still recognizing the Ar1–Ar4 subbiochrons with the same boundaries as in Albright et al. (2008), but using the term early Arikareean only for Ar1 faunas, middle Arikareean for Ar2, Ar3, and earliest Ar4 faunas, and late Arikareean for most Ar4 faunas.
Locality and mammalian biochronology
The Buda Local Fauna (LF) was found in the Buda Quarry, an abandoned limestone mine located about 8 km southwest of High Springs, Alachua County, northern peninsular Florida (29°45′N, 82°38′W). The Buda LF, discovered in February 1965 by SD Webb, N Tessman, JS Waldrop, and E Kayworth, occurred in a clay-filled sinkhole formed in Eocene marine limestone of the Crystal River Formation. The fossiliferous sinkhole deposit, long since destroyed by mining operations, consisted of three shallow vertical chambers from 1 to 3 m in diameter that probably shared a common opening. The remains of large mammals from the Buda Quarry were found mostly in clays in spoil piles, whereas the small mammals were screenwashed from pockets of clayey sand. The fossils occurred primarily as isolated teeth and disarticulated postcranial bones (Frailey, 1979).
About 20 species of mammals are presently recognized in the Buda fauna (Table 1). Frailey (1979) reported 12 taxa of large mammals: five carnivores (the amphicyonid Daphoenodon notionastes and the canid Bassariscops achoros, both described as new species, the canid Cynarctoides sp., a mustelid, and a nimravid); two perissodactyls (the small chalicothere Moropus sp. and an indeterminate equid); and five artiodactyls (the tayassuid Cynorca, a phenacocoeline oreodont, two unidentified camelids, and the hypertragulid Nanotragulus loomisi). The most abundant mammal at Buda is the tiny artiodactyl Nanotragulus loomisi.
Genus and species
Centetodon cf. C. magnus
Undescribed genus and species
Cormocyon cf. C. copei
Moropus cf. M. oregonensis
In a systematic review of the borophagine canids, Wang, Tedford & Taylor (1999) reexamined the canid sample from Buda, and reassigned several specimens to different taxa than in Frailey (1979). Wang, Tedford & Taylor (1999) recognized three small borophagine canids from Buda: Phlaocyon achoros (referred to Bassariscops by Frailey, 1979), Cynarctoides lemur (including some specimens originally referred to Bassariscops achoros by Frailey, 1979), and Cormocyon cf. C. copei. Phlaocyon achoros is known only from Buda, the type locality, but this species is similar to P. multicuspus from the late Arikareean of Wyoming (Wang, Tedford & Taylor, 1999) and P. taylori from the early late Arikareean (Ar3) Brooksville 2 LF in Florida (Hayes, 2000). Cynarctoides lemur is primarily an early Arikareean species, including samples from the John Day Formation in Oregon and the Sharps Formation in South Dakota. Wang, Tedford & Taylor (1999) tentatively referred a single isolated tooth from Buda to Cormocyon copei, a species best known from the early Arikareean of Oregon. In a paper reviewing the earliest North American chalicotheres, Coombs et al. (2001) referred the small Buda chalicothere to Moropus cf. M. oregonensis, a species also known from the early late Arikareean (Ar3) of Oregon and Texas.
Buda also yielded a significant small mammal fauna that remains mostly unstudied. Rich & Patton (1975) reported an isolated lower molar of the erinaceine hedgehog Amphechinus from Buda, which Hayes (2000) reidentified as the erinaceid Parvericius. Other small mammals from Buda include the new apatemyid described herein, the geolabidid insectivore Centetodon cf. C. magnus, a large species of emballonurid bat, and three rodents, the jimomyid Texomys, the large eomyid Arikareeomys, and the heteromyid Proheteromys. The two teeth of Centetodon from Buda represent one of the youngest known records of this genus. Korth (1992) described the new species Centetodon divaricatus from the McCann Canyon LF in Nebraska, which he placed in the early late Arikareean (Ar3). However, Tedford et al. (1996) and Tedford et al. (2004) considered the McCann Canyon LF to be late early Arikareean (Ar2), equivalent in age to faunas from the Monroe Creek Formation. The youngest previous record of Centetodon is based on two early Arikareean specimens of C. magnus from the Monroe Creek Formation in the Wounded Knee area of South Dakota (Lillegraven, McKenna & Krishtalka, 1981). Korth (1992) also described a new genus and species of large eomyid rodent, Arikareeomys skinneri, from McCann Canyon. The only other records of Arikareeomys are represented by an undescribed species from four Florida Arikareean faunas, Buda, Cow House Slough, SB-1A/Live Oak, and White Springs (Morgan, 1993; MacFadden & Morgan, 2003). Texomys occurs in both Buda and the correlative Ar3 Toledo Bend LF in easternmost Texas. These are apparently the only Arikareean records of Texomys, which is otherwise known from the Hemingfordian of Panama and the Barstovian of Texas and Louisiana (Slaughter, 1981; Albright, 1996; MacFadden et al., 2014).
Frailey (1979) considered the Buda LF to be late Arikareean in age. Tedford et al. (1987) placed this fauna in the early part of the late Arikareean (Ar3 of Woodburne & Swisher, 1995). In comparisons with other Arikareean faunas from Florida and Texas, Albright (1998) and Hayes (2000) agreed with Tedford et al. (1987) in placing the Buda LF in the early late Arikareean (Ar3, 24-22 Ma). Tedford et al. (2004) gave the same approximate age range for Buda (24-23 Ma), but placed this fauna in the late early Arikareean (late Ar2). Based on the revised age ranges for the subdivisions (subbiochrons) of the Arikareean NALMA presented by Albright et al. (2008), the Buda LF would be placed in the early late Arikareean (late Ar3; 24-23 Ma; latest Oligocene) (Fig. 2).
Although a number of mammals from the Buda LF are age-diagnostic, depending upon the genus or species, they seem to provide somewhat conflicting evidence pertaining to the site’s age. Some mammals from Buda suggest a late early Arikareean age (Ar2), whereas other taxa are indicative of early late Arikareean faunas (Ar3). Furthermore, most of the previous papers that have discussed the mammalian biochronology of Buda (Frailey, 1979; Tedford et al., 1987; Tedford et al., 2004; Albright, 1998; Hayes, 2000) were written prior to the significant changes in the boundaries for the subbiochrons of the Arikareean NALMA proposed by Albright et al. (2008). Mammals from Buda indicating an Ar3 age are Moropus, Daphoenodon, and Texomys. Moropus and Daphoenodon make their first appearance in the John Day sequence at approximately the same time, in the Ar3 at about 25 Ma (Albright et al., 2008). Texomys does not occur in the John Day Formation, but all other records of this genus are from late Arikareean (Ar3) or younger faunas (Albright, 1996). As noted above, Texomys has a southern distribution, including Florida, Louisiana, Texas, and Panama, and the earliest occurrences of this genus are in Buda and the correlative Ar3 Toledo Bend LF on the Gulf Coastal Plain of Texas (Albright, 1996).
Mammals from Buda indicative of an early Arikareean (Ar1/Ar2) age are the new apatemyid, Centetodon, Cynarctoides lemur, Cormocyon cf. C. copei, Arikareeomys, and Nanotragulus loomisi. Excluding Buda, apatemyids are otherwise unknown after the earliest Arikareean (Ar1) in North America (West, 1973). The youngest records of Centetodon are from the Wounded Knee Fauna of South Dakota (Lillegraven, McKenna & Krishtalka, 1981) and the McCann Canyon LF of Nebraska (Korth, 1992), both of which are correlatives of the Monroe Creek Fauna of late early Arikareean age (Ar2). Wang, Tedford & Taylor (1999) referred specimens of borophagine canids from Buda to Cynarctoides lemur and Cormocyon cf. C. copei, species originally described from the early Arikareean (Ar1/Ar2) Turtle Cove Member of the John Day Formation in Oregon. The fauna from the type locality for Arikareeomys, the McCann Canyon LF in Nebraska, was considered a correlative of the late early Arikareean (Ar2) Monroe Creek Fauna by Tedford et al. (1996) and Tedford et al. (2004). In addition to Buda, the three other faunas from Florida in which Arikareeomys occurs, Cow House Slough, White Springs, and SB-1A/Live Oak, have been considered late early Arikareean in age (Frailey, 1978; Morgan, 1993; Hayes, 2000; MacFadden & Morgan, 2003). However, these three faunas, like Buda, would now be considered early late Arikareean (Ar3) based on the placement of the lower boundary for the Ar3 at 26 Ma (Albright et al., 2008). The tiny ruminant Nanotragulus loomisi from Buda, as well as the Brooksville 2 LF in Florida, is most similar to samples of N. loomisi from early Arikareean faunas in the northern Great Plains (Frailey, 1979; Hayes, 2000).
Albright (1996); Albright (1998) and Albright (1999) considered Buda and the Toledo Bend LF in easternmost Texas to be correlative early late Arikareean (Ar3) faunas based on the co-occurrence of Daphoenodon notionastes, Moropus, and Texomys. However, these two faunas do have different species of Nanotragulus. Buda has the small early Arikareean species N. loomisi, whereas Toledo Bend has a larger species, similar to N. ordinatus and N. matthewi, that is more common in the late Arikareean (Frailey, 1979; Albright, 1999; Hayes, 2000).
The conflicting evidence from certain taxa indicating a late early Arikareean (Ar2) age and other taxa indicating an early late Arikareean (Ar3) age for Buda has led several workers to regard Buda and other Florida Arikareean faunas (e.g., Brooksville 2) as “medial Arikareean,” essentially combining Ar2 and Ar3 (e.g., Albright, 1998; Wang, Tedford & Taylor, 1999; Hayes, 2000). Rincon et al. (2015) used the term “middle Arikareean” for the time interval between about 28 and 22 Ma, encompassing the Ar2, Ar3, and early part of Ar4. The presence of Centetodon cf. C. magnus, the John Day canids Cynarctoides lemur and Cormocyon cf. C. copei, Arikareeomys, and Nanotragulus loomisi provides the most compelling biochronologic evidence for a late early Arikareean (Ar2) age for the Buda LF. None of these species occurs after the early Arikareean in western faunas, and Sinclairella is otherwise unknown in faunas younger than earliest Arikareean (Ar1). However, Dapheonodon and Moropus are unknown from early Arikareean faunas, with their earliest well-dated appearance in the John Day Formation in Oregon in the early late Arikareean (Ar3) at about 25 Ma (Albright et al., 2008). Together with the records from the John Day Formation and the Toledo Bend LF in Texas (Albright, 1998; Albright, 1999; Albright et al., 2008), Buda appears to represent one of the earliest occurrences of both Daphoenodon and Moropus. Pending a more detailed biochronology of Florida Arikareean faunas, we tentatively regard the Buda LF as early late Arikareean in age (Ar3; 25-23 Ma).
Methods and Materials
The electronic version of this article in Portable Document Format (PDF) will represent a published work according to the International Commission on Zoological Nomenclature (ICZN), and hence the new names contained in the electronic version are effectively published under that Code from the electronic edition alone. This published work and the nomenclatural acts it contains have been registered in ZooBank, the online registration system for the ICZN. The ZooBank LSIDs (Life Science Identifiers) can be resolved and the associated information viewed through any standard web browser by appending the LSID to the prefix http://zoobank.org/. The LSID for this publication is: urn:lsid:zoobank.org:pub:76E08309-BD0A-4665-AA39-D36450AAE5FF. The online version of this work is archived and available from the following digital repositories: PeerJ, PubMed Central and CLOCKSS.
Dental terminology follows that used by Van Valen (1966) and Silcox et al. (2010). Specimens were measured and photographed at the Oklahoma Museum of Natural History, University of Oklahoma, using an Olympus SZX9 stereomicroscope with an eyepiece reticle, and a Zeiss digital scanning electron microscope, respectively. Anteroposterior length (APL) was the greatest length measured anteroposteriorly along the labial side of the tooth; transverse width (TW) was the greatest width of the tooth measured transversely from lingualmost extent to the labialmost extent. Additional tooth measurements were made in a manner following Von Koenigswald, Ruf & Gingerich (2009: Table 4): Width 2 was the diagonal width from the lingual base of the protocone to the edge of the tooth labial to the paracone; Width 3 was the diagonal width from the lingual base of he protocone to the edge of the tooth labial to the metacone; Width 4 was the diagonal width from the posterolingual corner of the talon at the hypocone to the anterolabial corner of the tooth at the parastyle.
Holotype. UF 97383, right M2 (Fig. 3).
Hypodigm. Type and UF 97385, right M1; UF 97384, damaged right M2; UF 97382, left M3.
Locality and Horizon. Buda locality, Alachua County, Florida. Fissure fillings in solution cavities formed within the Crystal River Formation, early late Arikareean (Ar3) land mammal age, latest Oligocene (see ‘Locality and Mammalian Biochronology’).
Etymology. simplicis, Latin, “simple;” dens, Latin, “tooth;” in reference to the simplicity of the crowns of the upper molars.
Diagnosis. Upper molars simpler than in Sinclairella dakotensis and all other known apatemyids in that they lack conules except for a weak paraconule on M1, anterior cingula are absent, labial stylar cusps are absent except for a strong parastyle on M1, and stylar shelves (labial cingula) are virtually absent on all three upper molars, the only remnant being a weak shelf labial to the paracone on M3 that is much less prominent than that on any other known apatemyid. Hypocones on M1 and M2 smaller and on M3 larger than in S. dakotensis. Centrocristae (postparacrista and premetacrista) on upper molars straighter than in S. dakotensis. M2 relatively small, having about the same occlusal area as M1 and less than M3, about as long as wide, transversely much narrower than the M2 in S. dakotensis, and with distal edge continuous from hypocone to postmetacrista supporting a large posterior basin. In size, molars are slightly smaller than in S. dakotensis (Table 2). Notes: Anteroposterior length Transverse width Sample size Additional measurements as defined by Von Koenigswald, Ruf & Gingerich (2009) and in the text are provided for Sinclairella simplicidens (Width 2, Width 3, Width 4).
3.36 (N = 1)
3.9–4.1 (N = 3)
2.80 (N = 1)
3.3–3.7 (N = 3)
2.90 (N = 1)
3.10 (N = 1)
4.10 (N = 1)
2.80–2.84 (N = 2)
3.4–3.8 (N = 4)
2.68–3.04 (N = 2)
4.1–4.6 (N = 4)
3.10–3.20 (N = 2)
2.90–3.10 (N = 2)
3.70–3.80 (N = 2)
3.24 (N = 1)
3.2 (N = 1)
3.28 (N = 1)
4.4 (N = 1)
3.60 (N = 1)
3.20 (N = 1)
4.20 (N = 1)
Additional measurements as defined by Von Koenigswald, Ruf & Gingerich (2009) and in the text are provided for Sinclairella simplicidens (Width 2, Width 3, Width 4).
Description. Sinclairella simplicidens is known only by the four isolated teeth listed above (Fig. 3). The four teeth represent a minimum of two individuals based on two right M2s; one of these, UF 97384, also shows more wear than the holotype UF 97383. Size is smaller than in S. dakotensis and larger than in Apatemys uintensis. The molars are brachydont and generally lack sharp crests, although the centrocrista forms a fairly strong ridge between the paracone and metacone of each molar. In occlusal view the centrocrista, preparacrista and postmetacrista form a nearly straight ridge on each upper molar. Paracones and metacones are moderately tall cusps that are oval in occlusal aspect. The molars are simplified by comparison with those of all other known apatemyids.
The M1 is roughly quadrangular in occlusal outline, with a prominent anterior projection formed by the paracone and parastyle. The three main cusps, protocone, paracone, and metacone are roughly equal in size. A smaller hypocone is present on the posterolingual corner of the tooth; it bears weak, short ridges extending anteriorly and posterolabially from its rounded summit. A small, weak paraconule occurs lingual to the paracone. A preprotocrista extends from the protocone anteriorly and labially to the paraconule and parastyle, forming a shelf. A short, notched preparacrista connects the parastyle and paracone. In occlusal view the labial cusps (parastyle-paracone-metacone) are connected by crests (preparacrista-centrocrista-postmetacrista) and aligned nearly straight from anterior to posterior.
Two specimens of M2 are available, the holotype UF 97383 and UF 97384. UF 97384 is somewhat damaged, with minor breakage on its distal edge and preprotocrista, and missing small portions of its enamel on the posterior edge and on the apex of the protocone and labial edge due to breakage or abrasion. The M2 has three main cusps, with the protocone appearing somewhat larger than the paracone and metacone. A small, low hypocone lends a squarish outline to the posterior half of the tooth. The trigon basin between the three main cusps is relatively shallow and featureless. The hypocone is small and less projecting posteriorly than in S. dakotensis. Instead the distal edge of the tooth is nearly straight to barely convex between the hypocone and metacone. A preprotocrista curves forward from the protocone toward the anterior of the paracone, forming a small shelf that closes off the trigon basin anteriorly. There is no parastyle, stylar shelf, or cingula. The preparacrista and centrocrista are aligned nearly straight anterior to posterior in occlusal view; postmetacrista is weak or absent.
The M3 has three main cusps, with the protocone somewhat larger than the subequal paracone and metacone. The hypocone is fairly large, low, rounded, and curved, and is more elongated transversely than in M1 and M2, forming a rounded posterolingual corner on the tooth. As in M1 and M2, the preprotocrista forms a shelf between the protocone and the preparacrista. There is no parastyle. The preparacrista and centrocrista are aligned straight anterior to posterior along the labial half of the tooth; postmetacrista is absent. In occlusal outline, the paracone bulges anteriorly and labially, with a weak labial shelf, but there is no hint of a shelf labial to the metacone. Posterior edge of the M3 is nearly straight, as in M2.
Comparisons. The Buda LF apatemyid consists of four unassociated upper molars representing the loci M1, M2, and M3. The Buda LF specimens can be confidently assigned to the Apatemyidae, whose upper molars are characterized as being relatively low-crowned, transversely rather narrow, bearing three main cusps plus a small hypocone, conules absent or very small, and moderate stylar shelves lacking mesostyles but having strong parastyles (Rose, 2006; Gunnell et al., 2008). The genus Sinclairella is further characterized as being relatively large, with upper molars squarish, lacking ectoflexi, and bearing large hypocones (West, 1973). The genus presently includes only one species, Sinclairella dakotensis. Given the differences in the few known upper molars of S. simplicidens from those of Sinclairella dakotensis it is possible that the apatemyid in the Buda LF represents not only a new species but a new genus. Many named apatemyids are based on more complete material, often lower jaws with teeth, skulls, or even complete or partial skeletons. However, until more and better specimens are found and the diagnosis can be expanded with additional characters of the skeleton, skull, or at least the other teeth besides upper molars, it seems parsimonious at present to consider the Florida apatemyid as a new species.
Silcox et al. (2010) provided the only available phylogenetic analysis of Apatemyidae, and included S. dakotensis in their study. In the characters they developed that can be assessed in the Buda LF molars, two that pertain to the upper molars were found to be synapomorphies of the Apatemyidae: M1 metaconule absent, and M1 paraconule appressed to paracone. In the Buda M1s, metaconules are absent and the paraconule is reduced but situated near the paracone. Several of Silcox et al.’s (2010) characters pertaining to the upper molars appeared as synapomorphies supporting a node containing S. dakotensis and Heterohyus nanus, a European taxon. These synapomorphies are: M1 protocone position central on the tooth, M2 hypocone large, similar in size to the protocone, M3 hypocone large, upper molar stylar shelf narrow (buccal cingulum only) or absent, molar cusps relatively blunt (bunodont). Relative to these character states, the Buda LF specimens resemble S. dakotensis and H. nanus in sharing the M1 protocone position, narrow stylar shelves, and blunt cusps, but differs from them in having the M2 hypocone distinctly smaller than the protocone, and the M3 hypocone small instead of large. Sinclairella dakotensis showed no apomorphies in the upper molars among apatemyids in their study (Silcox et al., 2010); however, another European taxon, Carcinella sigei, showed an upper molar autapomorphy in having the M1 metaconule and paraconule both weak or absent. This condition, too, differs in the Buda LF M1, which has a weak paraconule and no metaconule.
Fossils of apatemyids are generally rare or uncommon in early Paleogene faunas. When they are encountered, the most commonly found elements are lower jaws or fragments; maxillary fragments and upper molars are quite rare in collections (West, 1973; Fig. 4). Thus, the Florida sample is rather unusual in that it consists of isolated upper molars and no lower teeth. When West (1973) reviewed all the North American Eocene and Oligocene apatemyids, he studied the type specimen of S. dakotensis, YPM PU 13585. The type included the only cranium of the species and was one of the few available specimens including upper molars (West, 1973). The holotype YPM PU 13585 was lost in the mail in 1976 and had not been molded before it was loaned (D Brinkman and M Fox, pers. comm., 2001). As a result, our comparisons of S. simplicidens were necessarily based on the diagnoses, illustrations, and measurements of S. dakotensis upper molars provided in Jepsen (1934), Clemens (1964) and West (1973).
The external (labial) shelf in Sinclairella dakotensis (and other earlier apatemyids) forms prominent projections anterolabial to the paracone in M2 and M3 and labial to the metacone in M2 (Fig. 4). Jepsen (1934) noted that the stylar shelf in M1 supported a number of small cuspules, the largest of which occurred in the metastyle and mesostyle positions (although he commented that these cuspules were not true styles). The labial shelf in M2 is wide and elevated as an irregular ridge along its outer border. In M3 the external cingulum is present anterolabial to the paracone but absent or minute labial to the metacone. Clemens (1964) noted no significant differences between Chadronian and Orellan specimens of S. dakotensis from the Great Plains and the type specimen of S. dakotensis, although he did mention minor differences in details of crown morphology of the upper molars. In a maxillary fragment from Colorado (University of Kansas Museum of Natural History 11210), the M1 has a smooth stylar shelf with no evidence of stylar cusps, unlike the holotype, and the M2 in occlusal view has a stylar shelf represented by anterolabial (with a small parastyle) and posterolabial projections separated by a distinct ectoflexus, and a convex rather than concave posterior margin. Another Orellan specimen (University of Colorado Museum, Boulder, no. 20173), an isolated M2 from Colorado, lacks the stylar cusps in the position of a parastyle and mesostyle (Clemens, 1964), but also retains anterolabial and posterolabial projections separated by a deep ectoflexus.
Compared to S. dakotensis, the crowns of the upper molars of S. simplicidens are even less distinctly cuspate and more simplified, with the bases of the cusps merging into smooth-bottomed valleys between cusps. The crests extending from the major cusps are somewhat better developed. Labial shelves are essentially absent and they completely lack cuspules in S. simplicidens compared to S. dakotensis. Although the M1 retains a strong parastyle anterior to the paracone, the only remnant of a labial shelf in S. simplicidens is a smooth rounded shelf anterolabial to the paracone in M3. Unlike S. dakotensis, parastyles are absent on M2 and M3 in S. simplicidens. Sinclairella simplicidens lacks other structures that are present in S. dakotensis, such as a paraconule on M2, a lingual cingulum anterior to the base of the protocone in M1, and a low ridge posterolingual to the base of the metacone in M1. Relative to the other upper molars, the M2 is the smallest molar in the row in S. simplicidens, whereas M2 is the largest upper molar in S. dakotensis (Fig. 4). The hypocone on M2 in S. simplicidens is much smaller than that in S. dakotensis. The hypocone on M3 is present as an elongated ridge in S. simplicidens, whereas it is essentially absent in S. dakotensis.
With the description of S. simplicidens from the latest Oligocene, the overall time range of existence of the Apatemyidae now virtually spans the entire Paleogene (early Paleocene-late Oligocene) in North America and from the early Paleocene to late Eocene in Europe. Apatemyids are generally uncommon in early Paleogene faunas in North America, although, as West (1973) noted, they are not quite as rare as Simpson (1954) and others had previously believed. This paper records the only known Paleogene occurrence of an apatemyid in eastern North America. The Florida apatemyids were discovered some 10° of latitude farther south and 20° of longitude farther east in North America than previously known.
Given their unusual niche as “mammalian woodpeckers” or ecological equivalents of striped possums or aye-ayes, apatemyids probably required stable, mature forests, where deposition, burial, and preservation conditions are usually poor. They may also have required numerous dead snags or at least dead wood in which to forage, or some other specialized niche or habitat feature of restricted availability that could have limited their abundance. Regarding the less distinctly cuspate and more simplified crowns, and the singularly small M2 proportions relative to M1 and M3 in S. simplicidens, these distinctions might point to some unknown difference in the species’ trophic biology from S. dakotensis and other Apatemyidae. Alternatively, it could represent a phylogenetic trend unique to the North American lineage of which S. simplicidens is a part, because there does not seem to be a general trend among North American apatemyids toward simplification of the upper molars.
The Buda fauna preserves certain genera of mammals that are also known in Arikareean faunas of the northern Great Plains and/or the John Day Formation of Oregon (e.g., Sinclairella, Centetodon, Cormocyon, Cynarctoides, Phlaocyon, Daphoenodon, Arikareeomys, Moropus, and Nanotragulus). At the same time, the Buda fauna and other Florida faunas of middle and late Cenozoic age reflect a provinciality in which the relatively subtropical Gulf Coastal Plain supported a different fauna from the Great Plains and other parts of temperate North America (Albright, 1998). The new Florida apatemyid is a significant tie-in both to the Great Plains faunas and the Gulf Coastal Plain endemism noted by several previous authors. Albright (1998, see also references cited therein) summarized old and new evidence from Arikareean faunas from Texas and Florida indicating an Arikareean and early Hemingfordian peak in regional endemism of mammals in the subtropical Gulf Coastal Plain. While the mammalian fauna of this region retained strong continuity with the developing grassland fauna in the northern Great Plains, the coastal plain of the Gulf of Mexico provided a refugium for several genera and species of subtropical-tropical forest-adapted mammals. As a Gulf Coastal endemic member of a genus otherwise known only in late Eocene and early Oligocene northern Great Plains faunas, Sinclairella simplicidens in the Buda LF of Florida lends additional support to Albright’s (1998) interpretation of Gulf Coastal Plain faunal endemism in the Arikareean.
Concomitant with retreat into a subtropical forest refugium, S. simplicidens might also represent the end of the North American apatemyid lineage unless it or other apatemyids occurred farther south into the tropics of Mexico and Central America. Several recently discovered early Miocene (latest Arikareean and early Hemingfordian) vertebrate faunas from Panama contain a moderate diversity of rodents and a bat, but lack apatemyids (MacFadden et al., 2014). The general scarcity of apatemyids in the fossil record and the paucity of Middle American late Oligocene and early Miocene faunas, except those from Panama, will impede confirmation of this possibility until Middle American paleofaunas are much better known.
There are other possible last occurrences of mammalian lineages in the Gulf Coastal Plains faunas, (reviewed by Albright, 1998:180; Albright, 2005). Albright (2005) noted an occurrence of the distinctive primate Ekgmowechashala in the early late Arikareean (Ar3) Toledo Bend LF of Texas as a 4-million-year temporal range extension, and a geographic extension from the northern Great Plain to the Gulf Coastal Plain similar to our record of Sinclairella simplicidens in Florida. However, Samuels, Albright & Fremd (2015) recently questioned the identity of the Toledo Bend specimen as Ekgmowechashala and determined that further study of it will be necessary to determine its true identity. In the Buda LF Centetodon, Texomys, and Arikareeomys probably represent either “holdovers” or Gulf Coast endemics. Centetodon and Sinclairella are almost certainly holdovers that apparently survived in the Gulf Coastal Plain after their earlier local extinction in the Great Plains. Texomys seems to be a Gulf Coastal (and Middle American) endemic because it is currently known only from Panama, Texas, Louisiana, and Florida (Albright, 1996; MacFadden et al., 2014). Arikareeomys is known primarily from Florida (four Arikareean records), with the exception of the type locality—the McCann Canyon LF in Nebraska of Korth (1992).
Gulf Coastal Plain faunas in the Arikareean and early Hemingfordian also reflect an early, temporary expansion of the tropical Middle American fauna into this region (Webb, 1977; MacFadden & Webb, 1982; Albright, 1998). Several bat families with Neotropical affinities in Florida late Oligocene and early Miocene faunas affirm this Neotropical link for at least these volant mammals; the faunas and families include the Buda LF (Emballonuridae) and those from I-75, Brooksville 2, and Thomas Farm (Emballonuridae, Mormoopidae, Speonycteridae, and Natalidae; Morgan & Czaplewski, 2003; Morgan & Czaplewski, 2012; Czaplewski & Morgan, 2012). The bats are not holdovers since none of these families are known in Great Plains Oligocene-early Miocene faunas (nor elsewhere on the continent). However, the Neotropical bats provide further evidence that Florida, and presumably the remainder of the Gulf Coastal Plain, did provide a subtropical/tropical refugium for certain mammals in the Arikareean and on into the early Hemingfordian.