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CRABS (BRACHYURA) OF THE GULF OF MEXICO

CRABS (BRACHYURA) OF THE GULF OF MEXICO

CRABS (BRACHYURA) OF THE GULF OF MEXICO

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Crabs of the Gulf of Mexico 79<br />

tolerated for short periods. Mahood et al., (1970) showed that temperature and<br />

salinity tolerances were interdependent. Blue crabs are also able to tolerate low<br />

oxygen conditions and they are occasionally found in very polluted and anoxic<br />

waters. Along the Texas coast, blue crabs in shallow ponds on sand flats are<br />

exposed to temperatures in excess of 40°C. during midday. These crabs have<br />

been observed to leave the water for Salicornia patches around the pools, where<br />

they rely on aerial respiration for 2 to 4 hours in the cooler (30 to 35°C.),<br />

humidity-saturated environment (personal observations). Blue crabs can travel<br />

some distance overland at night and during wet periods, again relying on aerial<br />

respiration.<br />

Remarks: The vast literature, much of it non-technical or of a commercial<br />

nature, precludes anything approaching a complete bibliography on this species.<br />

The original type for this species was obtained from the eastern coast of the<br />

United States, a variant of the form that is more typical throughout its range.<br />

The "typical" form, most often encountered from Florida southward, was considered<br />

a subspecies by Rathbun (1930) and many others, C. sapidus acutidens,<br />

so-named because of the surface features and pronounced spines, teeth, and<br />

prominent ridges. Because the type-based form from farther north was the basis<br />

for comparison, confusion existed for some years over the designation of a type<br />

to replace the original, which had been lost. Williams (1974a) discusses these<br />

variations and the nomenclatural historj^ of this crab, agreeing with Chace and<br />

Hobbs (1969) that a variety of extreme forms exist and that they could be considered<br />

separate species if they were considered in isolation from each other.<br />

However, these forms are intergraded and form a continuum, without morphological,<br />

bathymetrical, or geographical discontinuity, thus all the forms of Callinectes<br />

sapidus are considered, at present, to represent a single species in the<br />

process of local speciation which is still morphologically incomplete.<br />

Recent literature compilations on this species were provided by Cronin et al.<br />

(1957) and by Tagatz and Hall (1971). Gulf regional Hsts include Florida<br />

(Wass, 1955; Tabb and Manning, 1961; Dragovich and Kelly, 1964; Rouse,<br />

1970; Menzel, 1971; Lyons et al, 1971), Mississippi (Richmond, 1962; Franks<br />

et al., 1972; Christmas and Langley, 1973), Louisiana (Behre, 1950; Darnell,<br />

1959; Hoese and Valentine, 1972), Texas (Gunter, 1950; Lledgpeth, 1950; Hoese,<br />

1960; Copeland, 1965; Leary, 1967; More, 1969; Copeland and Bechtel, 1974),<br />

Mexico (Contreras, 1930; Hildebrand, 1957), and north coast of Cuba (Chace,<br />

1940).<br />

Hay (1905) and Churchill (1919) provided comprehensive life history studies.<br />

Other information on ecology includes: habitat relationships in Texas (Hedgpeth,<br />

1953; Simmons, 1957; Breuer, 1962; Fotheringham and Brunenmeister, 1975;<br />

Trent, Pullen and Proctor, 1976), megalops ecology in Maryland (Cargo, 1960),<br />

habitat notes in Mississippi (Franks et al., 1972; Christmas and Langley, 1973),<br />

effects of environmental variables on juveniles (Holland, Aldrich and Strawn,<br />

1971), larval ecology in Virginia (Sandifer, 1973), seasonal population changes<br />

in Chesapeake Bight (Musick and McEachran, 1972), field observations of freshwater<br />

populations (Gunter, 1938), temperature and thermal tolerance (Tagatz,<br />

1969a), and habitats in Jamaica (Norse, 1972).

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