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2010 Overboard in the Mojave - Biological Science - California State ...

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on <strong>in</strong>land lakes, such as <strong>the</strong> Salton Sea, Imperial County.<br />

The rema<strong>in</strong><strong>in</strong>g species frequent coastal mar<strong>in</strong>e waters or<br />

<strong>in</strong>land areas from <strong>the</strong> San Joaqu<strong>in</strong> Valley, central <strong>California</strong><br />

northward (Pyle, 1961; Cogswell and Christman,<br />

1977; Garrett and Dunn, 1981) (Table 2).<br />

Extant species of migratory birds represented <strong>in</strong> <strong>the</strong><br />

assemblage are presently absent from sou<strong>the</strong>rn <strong>California</strong><br />

dur<strong>in</strong>g <strong>the</strong> summer (Pyle, 1961). They migrate northward<br />

<strong>in</strong> <strong>the</strong> spr<strong>in</strong>g follow<strong>in</strong>g <strong>in</strong>land portions of <strong>the</strong> north–<br />

south Pacific Coast fly-way. Dur<strong>in</strong>g Pleistocene pluvial<br />

periods, this fly-way would have <strong>in</strong>cluded <strong>the</strong> lakes of <strong>the</strong><br />

Colorado and <strong>Mojave</strong> Deserts, those east of <strong>the</strong> Sierra<br />

Nevada Mounta<strong>in</strong>s, and <strong>the</strong> western part of Lake Lahontan<br />

(Snyder et al., 1964). Many of <strong>the</strong>se species are also<br />

known from <strong>the</strong> late Pleistocene deposits of Ch<strong>in</strong>a Lake,<br />

Inyo County, <strong>California</strong>, and Fossil Lake, Lake County,<br />

sou<strong>the</strong>astern Oregon ( Jefferson, 1985b).<br />

Two-thirds of <strong>the</strong> extant species (Gavia arctica,<br />

Podiceps nigricollis, Aechmophorus occidentalis, Pelecanus<br />

erythrorhynchos, Phalacrocorax auritus, Mergus merganser,<br />

Haliaeetus leucophalus, Aquila chrysaetos, and Larus spp.),<br />

represented by 80% NISP of <strong>the</strong> fossil avian specimens<br />

(Table 3), presently prefer or feed exclusively on small<br />

fish (Cogswell and Christman, 1977; Garrett and Dunn,<br />

1981). Gila bicolor mojavensis represents an abundant<br />

food source for <strong>the</strong>se predators. Modern representatives<br />

of <strong>the</strong> rema<strong>in</strong><strong>in</strong>g taxa (Cygnus columbianus, Branta<br />

canadensis, Anas crecca, Anas platyrhynchos, Aythya sp.,<br />

Oxyura jamaicensis, Fulica americana, Grus sp., Actitis sp.),<br />

feed on a variety of water plants and freshwater <strong>in</strong>vertebrates<br />

(Cogswell and Christman, 1977; Garrett and<br />

Dunn, 1981). The owl, Bubo virg<strong>in</strong>ianus, is <strong>the</strong> only bird <strong>in</strong><br />

<strong>the</strong> assemblage that feeds primarily on small mammals.<br />

Mammalian herbivores<br />

Among <strong>the</strong> larger herbivores, three taxa of ground sloth,<br />

Megalonyx, Paramylodon, and Nothro<strong>the</strong>riops, are present.<br />

All are poorly represented <strong>in</strong> <strong>the</strong> assemblage (Table<br />

4). Megalonyx is known from <strong>the</strong> West Coast and eastern<br />

two-thirds of <strong>the</strong> United <strong>State</strong>s, and ranged from South<br />

America <strong>in</strong>to Canada and Alaska. Stock (1925) suggested<br />

that this animal was adapted to forest or woodland habitats.<br />

The habitat and dietary preferences of Paramylodon,<br />

which also ranged through North and South America, are<br />

not well known. Given its association with o<strong>the</strong>r presumed<br />

grassland animals, Stock (1925, 1930) ma<strong>in</strong>ta<strong>in</strong>ed<br />

that Paramylodon was a grazer. Based on analysis of <strong>the</strong><br />

feed<strong>in</strong>g mechanism <strong>in</strong> Paramylodon, Naples (1989) argued<br />

that it was a grazer-browser. Consider<strong>in</strong>g <strong>the</strong> varied<br />

environments with<strong>in</strong> an extensive geographic range, both<br />

Megalonyx and Paramylodon were probably mixed feeders.<br />

Nothro<strong>the</strong>riops shastensis ranged throughout <strong>the</strong><br />

george t. jefferson<br />

southwestern United <strong>State</strong>s and nor<strong>the</strong>rn Mexico. It is<br />

well represented <strong>in</strong> cave assemblages from nor<strong>the</strong>astern<br />

<strong>California</strong> through sou<strong>the</strong>rn Nevada, and Arizona<br />

where it browsed on desert shrubs and plants typical of a<br />

juniper-sage brush savannah habitat (Mart<strong>in</strong> et al., 1961;<br />

Hansen, 1978). This selective folivore/browser (Naples,<br />

1987) appears to have <strong>in</strong>habited a broad spectrum of<br />

floral assemblages, but was limited latitud<strong>in</strong>ally and altitud<strong>in</strong>ally<br />

by m<strong>in</strong>imum w<strong>in</strong>ter temperatures (McDonald et<br />

al., 1996).<br />

Lepus sp. is <strong>the</strong> only small mammalian herbivore well<br />

represented <strong>in</strong> <strong>the</strong> assemblage. Jack rabbits typically <strong>in</strong>habit<br />

grassy and brush covered areas. The order Rodentia<br />

is represented by a s<strong>in</strong>gle cricetid humerus.<br />

The relatively abundant but fragmentary rema<strong>in</strong>s of<br />

mammoth can not be identified to species. However, <strong>the</strong>y<br />

probably represent <strong>the</strong> well-known middle and late Pleistocene<br />

form, Mammuthus columbi (= M. imperator). M.<br />

columbi ranged throughout <strong>the</strong> United <strong>State</strong>s and likely<br />

browsed and/or grazed (Davis et al., 1984) <strong>in</strong> small herds<br />

similar to extant elephants. Evans (1961) suggested that<br />

juvenile mammoths were <strong>the</strong> favored prey of <strong>the</strong> scimitartooth<br />

cat, Homo<strong>the</strong>rium serum. The American mastodon,<br />

Mammut americanum, is absent <strong>in</strong> <strong>the</strong> assemblage, and has<br />

not been identified from any Rancholabrean LMA sites<br />

with<strong>in</strong> <strong>the</strong> <strong>Mojave</strong> Desert or Colorado Desert regions<br />

( Jefferson, 1991c).<br />

Fossil horses are well represented <strong>in</strong> <strong>the</strong> assemblage<br />

(Table 4), and at least two forms, Equus conversidens and<br />

Equus sp. (large) have been identified. The occurrence<br />

Table 4. Relative abundance of mammalian taxa,<br />

Manix Formation<br />

Taxon NISP % NISP<br />

Megalonyx sp. _ 1 0.1<br />

Nothro<strong>the</strong>riops sp. cf. N. shastensis _ 2 0.3<br />

Paramylodon sp. _ 1 0.1<br />

Mammuthus sp. _ 37 5.2<br />

Lepus sp. 11 1.6<br />

Cricetidae 1 0.1<br />

Canis sp. cf. C. dirus _ 5 0.7<br />

Canis latrans 5 0.7<br />

Arctodus sp. _ 1 0.1<br />

cf. Ursus sp. 1 0.1<br />

Felis (Puma) sp. 3 0.4<br />

Homo<strong>the</strong>rium sp. cf. H. crenatidens _ 1 0.1<br />

Homo<strong>the</strong>rium sp. cf. H. serum _ 2 0.3<br />

Equus conversidens _ 52* 7.4<br />

Equus sp. (large-size) _ 67* 9.5<br />

Camelops sp. cf. C. hesternus _ 371 54.7<br />

Camelops sp. aff. C. m<strong>in</strong>idokae _ 5 0.7<br />

Hemiauchenia macrocephala _ 117 16.6<br />

Antilocapara sp. 2 0.3<br />

Ovis canadensis 17 2.5<br />

Bison sp. cf. B. antiquus _ 1 0.1<br />

Note: Total number of identified specimens is 703, and total % NISP is<br />

101.5. Data are <strong>in</strong> part from Jefferson (1985a, 1987).<br />

NISP = number of identified specimens<br />

% NISP = number of specimens identified for each taxon divided by <strong>the</strong><br />

total number of identified specimens<br />

* = may represent more than one species _ = ext<strong>in</strong>ct taxon<br />

48 <strong>2010</strong> Desert Symposium

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