Charophytivory, Playas y Papalotes, a Local Paradigm of Global Relevance

1999 ◽  
Vol 47 (3) ◽  
pp. 399 ◽  
Author(s):  
Vernon W. Proctor

The Llano Estacado region of western Texas and adjacent New Mexico has one of the most species-rich charophyte floras known for North America, but upon closer inspection this flora is seen to consist of two, strictly non-overlapping segments, one of 12 taxa, the other of nine. The larger group of species is confined to a vast series of shallow, ephemerally inundated depressions known as playas. These normally fill with run-off rainwater in late May or early June, remain flooded through early to mid-September before eventually drying to the curling polygon stage near the end of September. Approximately 8 months later the cycle is repeated. The remaining nine charophytes are confined to permanently inundated sites, the most common of which are livestock-watering windmill complexes, known as papalotes. Rarely, if ever, are members of the playa-12 encountered in papalotes or members of the papalote-9 in playas. The underlying bases for this ‘two flora’ dichotomy stem from the contrasting amphipod populations engendered by the two habitat types. Most freshwater amphipods (scuds), including the common North American herbivore Hyalella azteca (Saussure), cannot withstand complete desiccation which, accordingly, prevents its colonisation of playas. By contrast, scuds often reach exceptionally high densities in the associated concrete or metal tanques of papalotes, since such specialised habitats are usually free of vertebrate predators, e.g. birds, fish, turtles, salamanders. Scud- resistant charophytes are larger and slower to develop gametangia, features inimical to success in short- lived playas. By contrast, precocious charophyte opportunists–typical of playa floras–cannot withstand the grazing pressures of papalote (or papalote-like) environments. While charophytivory is assumed to be of worldwide occurrence and significance, it has been clearly demonstrated only in the unique juxtaposition of ‘playas y papalotes’.

1992 ◽  
Vol 6 ◽  
pp. 305-305
Author(s):  
Mahito Watabe

The late Miocene Chinese hipparions are morphologically diversified showing similarity to both western Old World's and North American forms. Two Chinese taxa that are phylogenetically related to western Old World's forms are Hipparion fossatum (= H. forstende) from Baode (Shanxi) and H. hippidiodus from Qingyang (Gansu) and Baode. The former is related to H. mediterraneum and the latter to H. urmiense - platygenys from the Turolian localities in the western Old World. H. fossatum and H. hippidiodus are associated with the “dorcadoides” (open-land) and “mixed” faunas in northern China. Hipparion fossatum that is characterized by POF located close to the orbit co-occurs with large and morphologically specialized form, H. dermatorhinum in Baode (Loc.30). H. hippidiodus with reduced POF is discovered with smaller H. coelophyes in Loc. 43, 44 (Baode) and Loc. 115 (Gansu).The hipparions associated with the “gaudryi” (forest) fauna are characterized by well defined and small POF located far from the orbit. Those forms are: H. platyodus from Loc. 70; H. ptychodus from Loc. 73; H. tylodus from Hsi-Liang in Yushe - Wuxiang basins; and H. sefvei from Loc. 12 at Xin-an in Henan province. H. coelophyes from Baode (Loc.43 & 44) and Qingyang (Loc. 115) also show similar facial morphology to the these forms, although it has small size and shallow POF. Those forms are similar in facial and dental morphology to Hipparion sensu stricto and some species of Cormohipparion in North America.The assemblages of Chinese hipparions are composed of two groups whose members are phylogenetically similar to the forms from both western part of Eurasia and North America. The “gaudryi” fauna is considered younger than the other two on the basis of faunal analyses. The similarity in hipparionine taxonomy between northern China and North America in the latest Miocene is an evidences for possible faunal interchange(s) occurred during that period, as suggested by taxonomic analyses on carnivores and proboscideans in eastern half of Eurasia and North America.


1955 ◽  
Vol 87 (6) ◽  
pp. 249-252
Author(s):  
Eugene Munroe

Hübner ([1824-25] p. 357) defined the genus Epipagis, citing three species. Hampson (1918: 277) chose fenestralis Hübner as type, and sank Sameodes Snellen to Epipagis. The arrangement of the British Museum Pyralidae shows that Hampson thought fenestralis Hübner was the same as phyllisalis Walker; but so far as I know this synonymy was never published. Actually, Hübner's figure of fenestralis represents a female of the genus usually known as Stenophyes Lederer, wrongly synonymized by Hampson (1899) with Crocidophora Lederer. The size and coloration suggest that the species Hübner figured is the common North American one universally called buronalis Guenée.


1967 ◽  
Vol 45 (5) ◽  
pp. 663-666 ◽  
Author(s):  
R. Hartland-Rowe

The name Chirocephalopsis bundyi (Forbes 1876) has been applied to two species. One of these is Eubranchipus bundyi (Forbes), of which Eubranchipus gelidus (Hay and Hay, 1889) is a synonym. The other, referred to by Brtek (1966) as E. gelidus (Hay and Hay), is described as E. intricatus n.sp. Both species are widely distributed in North America and occur in temporary pools of low salinity.


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.


1986 ◽  
Vol 60 (2) ◽  
pp. 302-326 ◽  
Author(s):  
J. Bowman Bailey

Although past authors have regarded the Carydiidae as a European family, six species of Carydium are reported here from the Devonian of eastern North America. Two of these belong to a single morphocline common in the Hamilton shales; another (Carydium clarkei) is new. Due to lack of well preserved hinges most of these species were earlier placed in Nucula because serrations or striations on dental elements were mistaken for a taxodont dentition.New data require modification of carydiid phylogenies of earlier authors. 1) Two independent pre-Devonian derivations from Lyrodesma are inferred. 2) Noradonta shergoldi, a carydiid-like lyrodesmatid from the Ordovician of Australia, is recognized as an important phyletic link between the Carydiidae and the Lyrodesmatidae. 3) The previous view of three distinct lineages within Carydium is not supported. Anamorphic data suggest as few as two main lineages and show two of the hinge types to be homeomorphic grades appearing separately or within one or the other of the main lineages.Though too young to be directly involved in the early diversification of the Bivalvia, the actinodont, subheterodont, and pseudotaxodont hinge morphologies of Carydium supply models for the origin of heterodont and taxodont hinges. Anamorphic and other evidence suggests that both are iterative types, and fundamental differences between them may be few. Hence, their preeminence as diagnostic criteria among higher taxa is diminished.


2010 ◽  
Vol 75 (2) ◽  
pp. 259-286 ◽  
Author(s):  
Jim A. Railey

Parry and Kelly (1987) argued for a causal link between expedient technologies and sedentism, and their explanation has widely influenced lithic analysts. There are some problems with their explanation, however, including disconnects in the reported timing of the shifts to expedient technologies, agricultural intensification, and sedentism. On the other hand, across much of North America the transition to an expedient technology appears to correlate more closely to the arrival of the bow and arrow. This is supported by data from a large excavation project in southern New Mexico, which shows that indicators of the shift to an expedient technology cannot be attributed to reduced mobility or any observable changes in subsistence practices, but do appear to correlate temporally with the appearance of arrow points.


1866 ◽  
Vol 3 (26) ◽  
pp. 356-362 ◽  
Author(s):  
Gustave Lindström

Professor Steenstrup, some years ago, questioned the fact as to whether the Zoantharia tabulata and rugosa, included by him under the common name of “Cyathophylla,” might be considered as true polyps. MM. Edwards and Haime in framing those great subdivisions of their “Coralliaria,” remarked their striking dissimilarity from the other Actinozoa. Professor Agassiz, in his grand monograph on the Acalephæ of North America, considers these differences so important that henceforth all connection between the above-named groups and the Zoantharia aporosa and perforata will be impossible. But besides these peculiar characteristics of the Rugosa, such, for instance, as the compact imperforate structure of the calyx and septa (the septa originating from four primary ones), the absence of costæ, the strange septal fossæ in the bottom of the calyx, the processes resembling rootlets, the transverse floors or tabulæ in the interior, which often have a cellular or vesicular structure; there is another peculiarity as yet not much known.


1990 ◽  
Vol 68 (11) ◽  
pp. 2306-2309 ◽  
Author(s):  
Richard S. Stemberger

The rotifer Keratella armadura n.sp. is described from a shallow alkaline bog lake from Michigan's lower peninsula. The facet pattern of the dorsal plate is similar to that of the common North American phenotype of Keratella cochlearis and K. taurocephala. The rigid, thickened lorica, long recurving posterior spine, and constriction of the body near the base of the anterior spines is distinctive from known congenors. The species was abundant (> 300 individuals/L) within a well-defined habitat, and appears to have a narrow geographic range. Keratella armadura occurred in spring and summer months and was absent from fall and winter collections. This restricted distribution, if common among rotifers, suggests that many undescribed species still exist in Michigan and in North America.


2001 ◽  
Vol 79 (2) ◽  
pp. 154-169 ◽  
Author(s):  
Félix Forest ◽  
Josée Nadia Drouin ◽  
René Charest ◽  
Luc Brouillet ◽  
Anne Bruneau

The hippocastanaceous Sapindaceae (family Hippocastanaceae) consists of two genera: Aesculus and Billia. The genus Aesculus (buckeyes) is distributed throughout the northern hemisphere. Twelve of the thirteen species of Aesculus are found in eastern Asia and North America, and one is native to Europe. The two species of the genus Billia are found in South and Central America. Aesculus is traditionally divided into five sections. This analysis, based on morphological characters, suggests that the monotypic section Parryanae (Aesculus parryi Gray) is sister to the remainder of the genus, and the other species are divided into two clades. One clade comprises all species from southeastern North America with the monotypic section Macrothyrsus (Aesculus parviflora Walt.) as sister to section Pavia. The other clade consists of all species found in Eurasia included in sections Aesculus and Calothyrsus, with the only North American member of this clade (Aesculus californica (Spach) Nutall) as sister to the rest of the group. According to this analysis, section Calothyrsus is rendered paraphyletic by the inclusion of section Aesculus. In contrast to previous studies that suggest an Asian origin for the genus, our study suggests an American origin for Aesculus from an ancestor similar to Billia with a single migration to Eurasia via the Bering land bridge.Key words: Aesculus, Billia, character evolution, Hippocastanaceae, morphology, phylogeny, Sapindaceae.


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