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Sturgeon biodiversity and conservation

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408<br />

sturgeon life history. <strong>Sturgeon</strong> are uniquely adapt- variety of prey <strong>and</strong> switch as prey availability<br />

ed to the large mainstem river systems upon which changes. These fish can also withst<strong>and</strong> long periods<br />

all species rely during all or part of their life cycle of starvation during periods of low food availability<br />

(Rochard et al. 1990). Rivers include diverse hab- or spawning migrations (Dadswell 1979, Mason &<br />

itats which are distributed in large scale patterns Clugston 1993). <strong>Sturgeon</strong> generally feed on invercorresponding<br />

to the surrounding topography. Typ- tebrates in the benthic food chain (Held 1969, Dadical<br />

transitions include headwaters through tribu- swell 1979, Carlson et al. 1985, S<strong>and</strong>il<strong>and</strong>s 1987,<br />

taries. mainstem, <strong>and</strong> estuary into an ocean, sea, or McCabe et al. 1993) where most production occurs<br />

large lake. In large basins, rivers may traverse many in large river systems (Sheehan & Rasmussen 1993).<br />

different regions <strong>and</strong> climatic zones. Rivers are also Fish may also be an important diet component of<br />

extremely dynamic habitats featuring large season- some sturgeon species (Semakula & Larkin 1968).<br />

al <strong>and</strong> annual variations in physical conditions <strong>and</strong> Large sturgeon can consume large prey. Pursuit <strong>and</strong><br />

resource availability (Sheehan & Rasmussen 1993). capture of active prey belie an image of sturgeon as<br />

Seasonal cycles in weather <strong>and</strong> runoff drive changes sluggish bottom scavengers.<br />

in velocity. morphometry, temperature, substrate, Populations of sturgeon are buffered from an<strong>and</strong><br />

turbidity. Conditions vary from year to year in nual variation in environmental conditions by deunpredictable<br />

patterns based on regional weather layed maturation, longevity, <strong>and</strong> high individual fepatterns.<br />

Periodic floods <strong>and</strong> droughts may radical- cundity. Delayed maturation (Roussow 1957,<br />

ly alter the riverine environment. Distribution <strong>and</strong> Sunde 1961, Dadswell 1979, Conte et al. 2 , Chapman<br />

abundance ofmany species of fishes <strong>and</strong> other orga- 1989, Guenette et al. 1992, Keenlyne & Jenkins<br />

nisms vary widely in response to spatial <strong>and</strong> tempo- 1993) speeds growth to large sizes as energy is deral<br />

patterns. For instance, anadromous fishes are voted to somatic rather than gonadal development.<br />

seasonally abundant as they move between spawn- Large size helps reduce predation. lowering natural<br />

ing <strong>and</strong> feeding areas in portions of many temperate mortality rate <strong>and</strong> increasing longevity. A long liferivers<br />

<strong>and</strong> estuaries.<br />

span (Pycha1956.Wilson 1987, Rien &Beamesder-<br />

<strong>Sturgeon</strong> have evolved life history characteristics fer 1994) allows fish numerous opportunities to<br />

which allow them to thrive in these large, diverse. spawn <strong>and</strong> reduces the need to spawn in years when<br />

<strong>and</strong> dynamic river systems. Individuals often range conditions are not suitable. Many species have been<br />

widely to take advantage of scattered <strong>and</strong> season- observed to resorb eggs under these conditions<br />

ally abundant resources. Regular migrations for (Artyukhinetal. 1979, Chapman 1989). Highfecunspawning<br />

<strong>and</strong> short-term movements for feeding dity associated with large size improves spawning<br />

have been observed for many species (Chadwick success in years when suitable conditions are en-<br />

1959, Miller 1972a, Haynes et al. 1978, Haynes & countered.<br />

Gray 1981, Smith 1985, Wooley & Crateau 1985, Many sturgeon species depend on free-flowing<br />

S<strong>and</strong>il<strong>and</strong>s 1987, Kempinger 1988, Odenkirk 1989, rivers <strong>and</strong> seasonal floods to provide suitable<br />

Hall et al. 1991, Mosindy & Rusak 1 , O’Herron et al. spawning conditions. Adhesive eggs are typically<br />

1993). Many species are euryhaline <strong>and</strong> move freely broadcast over rocky substrates in turbulent. highbetween<br />

freshwater, estuaries, <strong>and</strong> saltwater (Ro- velocity areas during high spring runoff (Magnin<br />

chard et al. 1990) to further broaden their resource 1966, Buckley & Kynard 1985, Smith 1985, Kempbase.<br />

Long-distance movements are facilitated by inger 1988, Hall et al. 1991, Mosindy & Rusak1, Latheir<br />

large size, shape, <strong>and</strong> swimming ability which Haye et al. 1992, Parsley et al. 1993). Recruitment<br />

allow them to move through heavy current.<br />

<strong>Sturgeon</strong> are opportunistic predators that eat a<br />

1 Mosindy, T. & J. Rusak. 1991. An assesment of lake sturgeon<br />

populations in Lake of the Woods <strong>and</strong> the Rainy River 1987–90<br />

Ontario Ministry of Natural Resources 66 pp.<br />

, 2<br />

Conte, F.S., S.I. Doroshov & P.B. Lutes. 1988. Hatchery manual<br />

for the white sturgeon Acipenser transmontanus Richardson<br />

with application to other North American Acipenseridae. University<br />

of California Cooperative Extension Publication 3322.<br />

104pp.

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