Ontogenetic behavior and migration of Volga River Russian sturgeon, Acipenser gueldenstaedtii, with a note on adaptive significance of body color
Identifieur interne : 000304 ( PascalFrancis/Checkpoint ); précédent : 000303; suivant : 000305Ontogenetic behavior and migration of Volga River Russian sturgeon, Acipenser gueldenstaedtii, with a note on adaptive significance of body color
Auteurs : Boyd Kynard [États-Unis] ; PING ZHUANG [États-Unis, République populaire de Chine] ; LONGZHEN ZHANG [République populaire de Chine] ; TAO ZHANG [République populaire de Chine] ; ZHENG ZHANG [République populaire de Chine]Source :
- Environmental biology of fishes [ 0378-1909 ] ; 2002.
Descripteurs français
- Pascal (Inist)
- Wicri :
- geographic : Russie.
English descriptors
- KwdEn :
Abstract
We conducted laboratory experiments with Volga River Russian sturgeon, Acipenser gueldenstaedtii, to develop a conceptual model of early behavior. We daily observed fish from day-0 (embryos, first life interval after hatching) to day-29 feeding larvae for preference of bright habitat and cover, swimming distance above the bottom, up- and downstream movement, and diel activity. Hatchling embryos initiated a downstream migration, which suggests that predation risk of embryos at spawning sites is high. Migration peaked on days 0-5 and ceased on day 7 (8-day migration). Migrants preferred bright, open habitat and early migrants swam-up far above the bottom (maximum daily median, 140 cm) in a vertical swim tube. Post-migrant embryos did not prefer bright illumination but continued to prefer white substrate, increased use of cover habitat, and swam on the bottom. Larvae initiated feeding on day 10 after 170.6 cumulative temperature degree-days. Larvae did not migrate, weakly preferred bright illumination, preferred white substrate and open habitat, and swam near the bottom (daily median 5-78 cm). The lack of a strong preference by larvae for bright illumination suggests foraging relies more on olfaction than vision for locating prey. A short migration by embryos would disperse wild sturgeon from a spawning area, but larvae did not migrate, so a second later migration by juveniles disperses young sturgeon to the sea (2-step migration). Embryo and larva body color was light tan and tail color was black. The migration, behavior, and light body color of Russian sturgeon embryos was similar to species of Acipenser and Scaphirhynchus in North America and to Acipenser in Asia that migrate after hatching as embryos. The similarity in migration style and body color among species with diverse phylogenies likely reflects convergence for common adaptations across biogeographic regions.
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<term>Color</term>
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<term>Embryo</term>
<term>Habitat selection</term>
<term>Larva</term>
<term>Russia</term>
<term>Stream</term>
<term>Substrate selection</term>
<term>Swimming</term>
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<keywords scheme="Pascal" xml:lang="fr"><term>Comportement</term>
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<front><div type="abstract" xml:lang="en">We conducted laboratory experiments with Volga River Russian sturgeon, Acipenser gueldenstaedtii, to develop a conceptual model of early behavior. We daily observed fish from day-0 (embryos, first life interval after hatching) to day-29 feeding larvae for preference of bright habitat and cover, swimming distance above the bottom, up- and downstream movement, and diel activity. Hatchling embryos initiated a downstream migration, which suggests that predation risk of embryos at spawning sites is high. Migration peaked on days 0-5 and ceased on day 7 (8-day migration). Migrants preferred bright, open habitat and early migrants swam-up far above the bottom (maximum daily median, 140 cm) in a vertical swim tube. Post-migrant embryos did not prefer bright illumination but continued to prefer white substrate, increased use of cover habitat, and swam on the bottom. Larvae initiated feeding on day 10 after 170.6 cumulative temperature degree-days. Larvae did not migrate, weakly preferred bright illumination, preferred white substrate and open habitat, and swam near the bottom (daily median 5-78 cm). The lack of a strong preference by larvae for bright illumination suggests foraging relies more on olfaction than vision for locating prey. A short migration by embryos would disperse wild sturgeon from a spawning area, but larvae did not migrate, so a second later migration by juveniles disperses young sturgeon to the sea (2-step migration). Embryo and larva body color was light tan and tail color was black. The migration, behavior, and light body color of Russian sturgeon embryos was similar to species of Acipenser and Scaphirhynchus in North America and to Acipenser in Asia that migrate after hatching as embryos. The similarity in migration style and body color among species with diverse phylogenies likely reflects convergence for common adaptations across biogeographic regions.</div>
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<fC01 i1="01" l="ENG"><s0>We conducted laboratory experiments with Volga River Russian sturgeon, Acipenser gueldenstaedtii, to develop a conceptual model of early behavior. We daily observed fish from day-0 (embryos, first life interval after hatching) to day-29 feeding larvae for preference of bright habitat and cover, swimming distance above the bottom, up- and downstream movement, and diel activity. Hatchling embryos initiated a downstream migration, which suggests that predation risk of embryos at spawning sites is high. Migration peaked on days 0-5 and ceased on day 7 (8-day migration). Migrants preferred bright, open habitat and early migrants swam-up far above the bottom (maximum daily median, 140 cm) in a vertical swim tube. Post-migrant embryos did not prefer bright illumination but continued to prefer white substrate, increased use of cover habitat, and swam on the bottom. Larvae initiated feeding on day 10 after 170.6 cumulative temperature degree-days. Larvae did not migrate, weakly preferred bright illumination, preferred white substrate and open habitat, and swam near the bottom (daily median 5-78 cm). The lack of a strong preference by larvae for bright illumination suggests foraging relies more on olfaction than vision for locating prey. A short migration by embryos would disperse wild sturgeon from a spawning area, but larvae did not migrate, so a second later migration by juveniles disperses young sturgeon to the sea (2-step migration). Embryo and larva body color was light tan and tail color was black. The migration, behavior, and light body color of Russian sturgeon embryos was similar to species of Acipenser and Scaphirhynchus in North America and to Acipenser in Asia that migrate after hatching as embryos. The similarity in migration style and body color among species with diverse phylogenies likely reflects convergence for common adaptations across biogeographic regions.</s0>
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<s5>11</s5>
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<s5>11</s5>
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<s5>12</s5>
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<s5>14</s5>
</fC03>
<fC03 i1="14" i2="X" l="ENG"><s0>Stream</s0>
<s5>14</s5>
</fC03>
<fC03 i1="14" i2="X" l="SPA"><s0>Curso agua</s0>
<s5>14</s5>
</fC03>
<fC03 i1="15" i2="X" l="FRE"><s0>Russie</s0>
<s2>NG</s2>
<s5>49</s5>
</fC03>
<fC03 i1="15" i2="X" l="ENG"><s0>Russia</s0>
<s2>NG</s2>
<s5>49</s5>
</fC03>
<fC03 i1="15" i2="X" l="SPA"><s0>Rusia</s0>
<s2>NG</s2>
<s5>49</s5>
</fC03>
<fC03 i1="16" i2="X" l="FRE"><s0>Acipenser gueldenstaedti</s0>
<s2>NS</s2>
<s4>INC</s4>
<s5>64</s5>
</fC03>
<fC03 i1="17" i2="X" l="FRE"><s0>Rivière Volga</s0>
<s2>NG</s2>
<s4>CD</s4>
<s5>96</s5>
</fC03>
<fC03 i1="17" i2="X" l="ENG"><s0>Volga River</s0>
<s2>NG</s2>
<s4>CD</s4>
<s5>96</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE"><s0>Milieu eau douce</s0>
<s5>17</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG"><s0>Freshwater environment</s0>
<s5>17</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA"><s0>Medio agua dulce</s0>
<s5>17</s5>
</fC07>
<fC07 i1="02" i2="X" l="FRE"><s0>Rythme biologique</s0>
<s5>18</s5>
</fC07>
<fC07 i1="02" i2="X" l="ENG"><s0>Biological rhythm</s0>
<s5>18</s5>
</fC07>
<fC07 i1="02" i2="X" l="SPA"><s0>Ritmo biológico</s0>
<s5>18</s5>
</fC07>
<fC07 i1="03" i2="X" l="FRE"><s0>Locomotion</s0>
<s5>19</s5>
</fC07>
<fC07 i1="03" i2="X" l="ENG"><s0>Locomotion</s0>
<s5>19</s5>
</fC07>
<fC07 i1="03" i2="X" l="SPA"><s0>Locomoción</s0>
<s5>19</s5>
</fC07>
<fC07 i1="04" i2="X" l="FRE"><s0>Eurasie</s0>
<s2>NG</s2>
</fC07>
<fC07 i1="04" i2="X" l="ENG"><s0>Eurasia</s0>
<s2>NG</s2>
</fC07>
<fC07 i1="04" i2="X" l="SPA"><s0>Eurasia</s0>
<s2>NG</s2>
</fC07>
<fC07 i1="05" i2="X" l="FRE"><s0>Pisces</s0>
<s2>NS</s2>
<s5>60</s5>
</fC07>
<fC07 i1="05" i2="X" l="ENG"><s0>Pisces</s0>
<s2>NS</s2>
<s5>60</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA"><s0>Pisces</s0>
<s2>NS</s2>
<s5>60</s5>
</fC07>
<fC07 i1="06" i2="X" l="FRE"><s0>Vertebrata</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="06" i2="X" l="ENG"><s0>Vertebrata</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="06" i2="X" l="SPA"><s0>Vertebrata</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="07" i2="X" l="FRE"><s0>Acipenseridae</s0>
<s2>NS</s2>
<s4>INC</s4>
<s5>70</s5>
</fC07>
<fN21><s1>034</s1>
</fN21>
<fN82><s1>PSI</s1>
</fN82>
</pA>
</standard>
</inist>
<affiliations><list><country><li>République populaire de Chine</li>
<li>États-Unis</li>
</country>
<region><li>Massachusetts</li>
</region>
</list>
<tree><country name="États-Unis"><region name="Massachusetts"><name sortKey="Kynard, Boyd" sort="Kynard, Boyd" uniqKey="Kynard B" first="Boyd" last="Kynard">Boyd Kynard</name>
</region>
<name sortKey="Ping Zhuang" sort="Ping Zhuang" uniqKey="Ping Zhuang" last="Ping Zhuang">PING ZHUANG</name>
</country>
<country name="République populaire de Chine"><noRegion><name sortKey="Ping Zhuang" sort="Ping Zhuang" uniqKey="Ping Zhuang" last="Ping Zhuang">PING ZHUANG</name>
</noRegion>
<name sortKey="Longzhen Zhang" sort="Longzhen Zhang" uniqKey="Longzhen Zhang" last="Longzhen Zhang">LONGZHEN ZHANG</name>
<name sortKey="Tao Zhang" sort="Tao Zhang" uniqKey="Tao Zhang" last="Tao Zhang">TAO ZHANG</name>
<name sortKey="Zheng Zhang" sort="Zheng Zhang" uniqKey="Zheng Zhang" last="Zheng Zhang">ZHENG ZHANG</name>
</country>
</tree>
</affiliations>
</record>
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