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17 results for “Pelodiscus sinensis”
Fig. 15. P in First Records Of New Aquatic Predator Pelodiscus Sinensis (Wiegmann 1835) In Latvia And Preliminary Ecological Risk Assessment Of The Invasion For Autochthonic Emys Orbicularis (Linnaeus 1758)
Fig. 15. P.sinensis laid eggs after breeding in captivity (Latgales Zoo, shelter for exotic turtles).
Fig.13 in First Records Of New Aquatic Predator Pelodiscus Sinensis (Wiegmann 1835) In Latvia And Preliminary Ecological Risk Assessment Of The Invasion For Autochthonic Emys Orbicularis (Linnaeus 1758)
Fig.13. Old adult female of Emys orbicularis from the habitat, where Pelodiscus sinensis #PeSi0003 was found in 2014 (Daugavpils, Latvia) (Photo: 2003).
Fig. 5 in First Records Of New Aquatic Predator Pelodiscus Sinensis (Wiegmann 1835) In Latvia And Preliminary Ecological Risk Assessment Of The Invasion For Autochthonic Emys Orbicularis (Linnaeus 1758)
Fig. 5. Olaines lake, habitat of the first P.sinensis #PeSi0001 recorded in Latvia (Photo: Drezina, 2008).
Fig. 7 in First Records Of New Aquatic Predator Pelodiscus Sinensis (Wiegmann 1835) In Latvia And Preliminary Ecological Risk Assessment Of The Invasion For Autochthonic Emys Orbicularis (Linnaeus 1758)
Fig. 7. Orthophoto of habitat of findings of P.sinensis #PeSi0001 in Olaine, Latvia (Google Earth services).
Fig. 14. Received from owners P in First Records Of New Aquatic Predator Pelodiscus Sinensis (Wiegmann 1835) In Latvia And Preliminary Ecological Risk Assessment Of The Invasion For Autochthonic Emys Orbicularis (Linnaeus 1758)
Fig. 14. Received from owners P.sinensis breeding in captivity (Latgales Zoo, shelter for exotic turtles).
Fig. 9 in First Records Of New Aquatic Predator Pelodiscus Sinensis (Wiegmann 1835) In Latvia And Preliminary Ecological Risk Assessment Of The Invasion For Autochthonic Emys Orbicularis (Linnaeus 1758)
Fig. 9. Orthophoto of habitat of findings of P.sinensis #PeSi0003 in Daugavpils, Latvia (Google Earth services).
Fig.12 in First Records Of New Aquatic Predator Pelodiscus Sinensis (Wiegmann 1835) In Latvia And Preliminary Ecological Risk Assessment Of The Invasion For Autochthonic Emys Orbicularis (Linnaeus 1758)
Fig.12. Peculiarities of P.sinensis findings waterbodies anthropogenic influence and distance potential for species distribution in Latvia.
Fig.11 in First Records Of New Aquatic Predator Pelodiscus Sinensis (Wiegmann 1835) In Latvia And Preliminary Ecological Risk Assessment Of The Invasion For Autochthonic Emys Orbicularis (Linnaeus 1758)
Fig.11. Peculiarities of P.sinensis findings waterbodies water connectivity in Latvia.
Fig.1 in First Records Of New Aquatic Predator Pelodiscus Sinensis (Wiegmann 1835) In Latvia And Preliminary Ecological Risk Assessment Of The Invasion For Autochthonic Emys Orbicularis (Linnaeus 1758)
Fig.1. Placement of the findings of Pelodiscus sinensis in Latvia.
Fig. 4 in First Records Of New Aquatic Predator Pelodiscus Sinensis (Wiegmann 1835) In Latvia And Preliminary Ecological Risk Assessment Of The Invasion For Autochthonic Emys Orbicularis (Linnaeus 1758)
Fig. 4. Ventral side of the first P.sinensis #PeSi0001 found in Latvia.
Fig. 10 in First Records Of New Aquatic Predator Pelodiscus Sinensis (Wiegmann 1835) In Latvia And Preliminary Ecological Risk Assessment Of The Invasion For Autochthonic Emys Orbicularis (Linnaeus 1758)
Fig. 10. Peculiarities of P.sinensis findings waterbodies size in Latvia.
Hibernation habitat selection by the threatened Chinese softshell turtle (Pelodiscus sinensis) in the Yellow River wetlands of Northwest China: Implications for conservation management
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Nocturnal emergence facilitated by thermally-induced hatching in the Chinese Softshell Turtle, Pelodiscus sinensis
<p><span>The coincidence of hatching timing and emergence events with favourable conditions is crucial for survival. Nocturnal emergence has been widely documented across marine and freshwater turtles and has long been suggested as an adaptive behaviour that reduces risk of heat stress and predation. However, our knowledge of emergence timing is mainly based on the observation of emergence events, and whether the timing of hatching is influenced by diel environmental factors remains largely unknown. Herein, we visually monitored the activity of the Chinese softshell turtle (<em>Pelodiscus sinensis</em>)—a shallow-nesting freshwater turtle—from hatching to emergence. Our data demonstrated that (i) the embryos within a single nest exhibited synchronous hatching; in particular, (ii) their synchronous hatching coincided with the period of decreased nest temperature. Further analysis indicated that pipping was specifically more likely to occur during the period of rapidly decreasing nest temperatures. Together, these results provide strong evidence for the existence of synchronous hatching in this freshwater, shallow-nesting turtle species, and that the timing for nest emergence may have already been selected at the hatching stage.</span></p>
Nocturnal emergence facilitated by thermally-induced hatching in the Chinese Softshell Turtle, Pelodiscus sinensis
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Transcriptome data of the interdigital webbing in Chinese Soft-shell Turtle (Pelodiscus sinensis)
GEO Series GSE287055. Pelodiscus sinensis. 8 samples. Type: Expression profiling by high throughput sequencing.
Fig. 2. First P in First Records Of New Aquatic Predator Pelodiscus Sinensis (Wiegmann 1835) In Latvia And Preliminary Ecological Risk Assessment Of The Invasion For Autochthonic Emys Orbicularis (Linnaeus 1758)
Fig. 2. First P.sinensis #PeSi0001 found in Latvia: head, legs and tail of the male are visible.
Wild type and probiotic feeding transcriptome of pelodiscus sinensis
GEO Series GSE183769. Pelodiscus sinensis. 12 samples. Type: Expression profiling by high throughput sequencing.
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