Tanyrhinichthys mcallisteri, a long-rostrumed Pennsylvanian ray-finned fish (Actinopterygii) and the simultaneous appearance of novel ecomorphologies in Late Palaeozoic fishes

Author(s):  
Jack Stack ◽  
John-Paul Hodnett ◽  
Spencer G Lucas ◽  
Lauren Sallan

Abstract The Carboniferous radiation of fishes was marked by the convergent appearance of then-novel but now common ecomorphologies resulting from changes in the relative proportions of traits, including elongation of the front of the skull (rostrum). The earliest ray-finned fishes (Actinopterygii) with elongate rostra are poorly known, obscuring the earliest appearances of a now widespread feature in actinopterygians. We redescribe Tanyrhinichthys mcallisteri, a long-rostrumed actinopterygian from the Upper Pennsylvanian (Missourian) of the Kinney Brick Quarry, New Mexico. Tanyrhinichthys has a lengthened rostrum bearing a sensory canal, ventrally inserted paired fins, posteriorly placed median fins unequal in size and shape, and a heterocercal caudal fin. Tanyrhinichthys shares these features with sturgeons, but lacks chondrostean synapomorphies, indicating convergence on a bottom-feeding lifestyle. Elongate rostra evolved independently in two lineages of bottom-dwelling, freshwater actinopterygians in the Late Pennsylvanian of Euramerica, as well as in at least one North American chondrichthyan (Bandringa rayi). The near-simultaneous appearance of novel ecomorphologies among multiple, distantly related lineages of actinopterygians and chondrichthyans was common during the Carboniferous radiation of fishes. This may reflect global shifts in marine and freshwater ecosystems and environments during the Carboniferous favouring such ecomorphologies, or it may have been contingent on the plasticity of early actinopterygians and chondrichthyans.

Ecohydrology ◽  
2008 ◽  
Vol 1 (3) ◽  
pp. 225-238 ◽  
Author(s):  
Enrique R. Vivoni ◽  
Alex J. Rinehart ◽  
Luis A. Méndez-Barroso ◽  
Carlos A. Aragón ◽  
Gautam Bisht ◽  
...  

1965 ◽  
Vol 97 (6) ◽  
pp. 561-580 ◽  
Author(s):  
Richard B. Selander

Abstract>Three species are recognized in the North American genus Megetra LeConte. The most distinctive of these anatomically and ecologically is M. cancellata (Brandt and Erichson), which ranges discontinuously from Arizona and New Mexico to the state of Hidalgo in México and occurs in limited sympatry with both of its congeners. Megetra vittata (LeConte) ranges from northern Arizona to western Texas. It appears to be strictly allopatric with, and similar ecologically to, M. punctata, new species, which ranges from southern Arizona and New Mexico to Durango, México. Specific diagnoses are made on the basis of characters of adult and, for M. cancellata and M. punctata, larval anatomy. Intraspecific variation in several adult characters is analyzed. Notes on the seasonal distribution, habitat, and behavior of the adult beetles are included.


Author(s):  
Stephen Aron

Columbus discovered an Old World in 1492. Steep population declines reduced Indian numbers by more than 90 percent in the following four centuries. European maps of the seventeenth and eighteenth centuries claimed to have carved up most of North America, but ‘Empires and enclaves’ shows that control over North American lands remained hotly contested during this time. Well into the eighteenth century, the vast majority of North American Indians had not become the subordinates of European colonizers and in most places there were no European settlements yet. The first contacts between European and Indians are described along with seventeenth-century English settlements in New England, the Spanish conquest in New Mexico, and the alternative approaches of the French.


1997 ◽  
Vol 67 (1) ◽  
pp. 9-70 ◽  
Author(s):  
H.-P. Schultze ◽  
J. Chorn

The lungfish Sagenodus is a widespread Permo-Carboniferous genus found in Europe and North America. Important localities in the U.S.A. include Middle Pennsylvanian coals near Linton, Ohio, Upper Pennsylvanian deposits near Robinson and Hamilton, Kansas, and Peoria, Illinois; Lower Permian sediments near Cameron, Ohio; and Lower Permian “Red Beds” of Texas and Oklahoma. At least three species of Sagenodus were present in North America S. copeanus, S. periprion, S. serratus). S. ohiensis is represented solely by one skull. Knowledge of the osteology of Sagenodus is enhanced by the study of well-preserved but disassociated elements from Robinson, Kansas (S. copeanus) and Little Bitter Creek, Texas (S. serratus). The orbital series is now known to be comprised of six elements and the sensory canal system is more complex than previously realized. The only known articulated skeleton of this genus, from Hamilton Quarry, Kansas, permits a restoration of the entire animal including the median fins. The dorsal and anal fins are not separate; there is instead, a continuous fin around the caudal end of the body, as found in other post-Devonian lungfishes. Sagenodus is structurally intermediate between more primitive Devonian dipnoans and post-Paleozoic lungfishes. Evident trends can be seen in the reduction of bone (both number of bones and degree of ossification), the loss of cosmine, the nature of the scales, the structure and histology of tooth plates, and the configuration of the median fins. Sagenodus is a member of a euryhaline faunal assemblage that can be found from shallow marine to freshwater deposits.


1989 ◽  
Vol 63 (6) ◽  
pp. 919-930 ◽  
Author(s):  
Walter W. Dalquest ◽  
M. John Kocurko ◽  
John V. Grimes

A newly discovered locality of aestivation burrow casts containing the lungfish, Gnathorhiza serrata, is reported from the early Permian Arroyo Formation of Wilbarger County, north-central Texas. Remains preserved in the burrow casts provide sections of mummified Gnathorhiza and new information about the postcranial skeleton of this fish. Scales of Gnathorhiza resemble those of the modern lungfishes such as Lepidosiren in their microanatomy. No traces of paddle-like pectoral or pelvic fins were found and paired fins of Gnathorhiza may have resembled those of Lepidosiren. The axial skeleton and median fins of Gnathorhiza seem to resemble those of Lepidosiren except that the tail area and caudal fin of Gnathorhiza were stout and strong rather than slender and tapering. Gnathorhiza, which aestivated tail-down in its burrow, may have required a stout tail for support.


1988 ◽  
Vol 62 (2) ◽  
pp. 309-311 ◽  
Author(s):  
Gregory D. Edgecombe

The pseudorthoceratid subfamily Macroloxoceratinae Flower, 1957, comprises a rare group of nautiloid cephalopods homeomorphic with the Actinoceratida in the development of a siphonal canal system. With the exception of Macroloxoceras Flower, 1957, from the Upper Devonian of Colorado and New Mexico, this subfamily has previously been reported only from the Mississippian of Europe. A specimen described herein from the late Viséan–?early Namurian Kennetcook Limestone of the Windsor Group of Nova Scotia, assigned to Campyloceras cf. C. unguis (Phillips, 1836), extends the range of the Macroloxoceratinae into the North American Mississippian. This discovery further provides new data on the complex siphonal morphology of this poorly known group of nautiloids, and supplements the recent documentation of the pseudorthoceratids in the Windsor Group cephalopod fauna (Edgecombe, 1987).


1993 ◽  
Vol 125 (S168) ◽  
pp. 1-193 ◽  
Author(s):  
Valerie M. Behan-Pelletier

AbstractThe oribatid family Eremaeidae is represented in North America by two genera, Eremaeus and Eueremaeus, both widely distributed throughout the Palaearctic and Nearctic regions. In North America species in both genera are found in moist to arid habitats from New Mexico to the High Arctic. Reproduction is sexual, and both immatures and adults feed mainly on fungi.Revised diagnoses are presented for the Eremaeidae and genera Eremaeus and Eueremaeus. Eighteen species of Eremaeus, of which 14 are newly proposed, and 24 species of Eueremaeus, of which 15 are newly proposed, are recognized. Identification keys are provided for the world genera of Eremaeidae, and for adults of Eremaeus and Eueremaeus of North America. All but one North American species of these genera are described, and their geographical distributions mapped.North American Eremaeus species include E. appalachicus sp. no v., E. boreomontanus sp. nov., E. brevitarsus (Ewing), E. californiensis sp. nov., E. gracilis sp. nov., E. grandis Hammer, E. kananaskis sp. nov., E. kevani sp. nov., E. megistos sp. nov., E. monticolus sp. nov., E. nortoni sp. nov., E. occidentalis sp. nov., E. oresbios sp. nov., E. plumosus Woolley, E. porosus sp. nov., E. salish sp. nov., E. translamellatus Hammer, and E. walteri sp. nov. The immatures of four of these, E. kananaskis, E. occidentalis, E. oresbios, and E. translamellatus, are described.North American Eueremaeus include Eu. acostulatus sp. nov., Eu. aridulus sp. nov., Eu. columbianus (Berlese), Eu. foveolatus (Hammer), Eu. marshalli sp. nov., Eu. masinasin sp. nov., Eu. michaeli sp. nov., Eu. nahani sp. nov., Eu. nemoralis sp. nov., Eu. proximus (Berlese) comb, nov., Eu. woolleyi (Higgins) comb, nov., Eu. yukonensis sp. nov., and three informal species groups with the following included species in North America: (1) Eu. trionus group—Eu. trionus (Higgins) comb, nov., (2) Eu. stiktos group—Eu. carinatus sp. nov., Eu. higginsi sp. nov., Eu. stiktos (Higgins) comb, nov., Eu. tetrosus (Higgins) comb, nov., (3) Eu. chiatous group—Eu. alvordensis sp. nov., Eu. aysineep sp. nov., Eu. chiatous (Higgins) comb, nov., Eu. danos sp. nov., Eu. lindquisti sp. nov., Eu. magniporosus (Wallwork) comb, nov., and Eu. osoyoosensis sp. nov. The immatures of nine of these, Eu. masinasin, Eu. nahani, Eu. carinatus, Eu. higginsi, Eu. columbianus, Eu. proximus, Eu. woolleyi, Eu. stiktos, and Eu. tetrosus, are described. Kartoeremaeus reevesi Higgins and Eremaeus politus Banks are considered junior subjective synonyms of Eueremaeus columbianus (Berlese).A cladistic analysis of the genera comprising Eremaeidae: Eremaeus, Tricheremaeus, Eueremaeus (and included species groups), Proteremaeus, Carinabella, and Asperemaeus, indicates that Eremaeus is the sister taxon of Carinabella, and that Eueremaeus is the sister taxon of Proteremaeus. Tricheremaeus is the sister taxon of Eremaeus + Carinabella, and Asperemaeus is the sister taxon of Eueremaeus + Proteremaeus. The relationship of the Eremaeidae to the Megeremaeidae and Zetorchestidae is presented. Finally, I discuss the ecology and distribution of North American species of Eremaeidae.


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