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Durations (days: meanSD) of copepodid stages (CI- CVI) of Hemicyclops gomsoensis maintained at 15°C and 25°C. The values for CVI indicate days to death after final molt.

Durations (days: meanSD) of copepodid stages (CI- CVI) of Hemicyclops gomsoensis maintained at 15°C and 25°C. The values for CVI indicate days to death after final molt.

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A 17-month field survey and laboratory experiments were conducted to investigate the life cycle, seasonal population fluctuations, and salinity tolerance in the poecilostomatoid copepod Hemicyclops gomsoensis associated with the burrows of the mud shrimp Upogebia major and the ocypodid crab Macrophthalmus japonicus in the mud-flats of the Tama-Rive...

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Context 1
... of the copepod deaths occurred when the copepods crept up the wall of the rearing vessel and got out of the water, which is similar to the observation by Gurney (1944) during his experiment with the Saphirella-like copepodids. There were considerable variations in the durations both among and within stages, and between sexes and temperatures ( Table 1). The total aver- Copepod survival was significantly affected by salinity (one-way ANOVA, F 6, 133 579.9, p0.001). ...
Context 2
... present estimates of the stage durations (Table 1) should be viewed with caution because of the high mortalities during the experiments and the large variation among and within stages that may partly be attributable to the experimental conditions applied in this study that were considerably different from those in situ. Under this limitation, if we assume an average duration from the CIs to adult females of 24.0 d at 25°C and a duration from NI to CI of 9 d at 20°C (Itoh, unpublished data), a maximum average generation time from April to November may be roughly estimated at 1 month, which implies the presence of at least 7 generations per year. ...

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... Adults of some species of the Family Ergasilidae that are parasitic on fish have been reported to occur frequently in plankton communities (Ohtsuka et al. 2004a,b). Hemicyclops are loosely associated with benthic animals, such as polychaetes, ghost shrimps, and crabs (Itoh & Nishida 2007, 2013, and their adults are occasionally found in plankton (Mulyadi 2005, Ohtsuka et al. 2010. In Chinese brackish waters, adults of H. xiamenensis Ohtsuka, Ko & Xu, 2010 occur exclusively in plankton at night, but copepodids do not (Ohtsuka et al. 2010). ...
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... In the Tama-River estuary five species of Hemicyclops have been recorded from the burrows of invertebrates, among which H. gomsoensis Ho & Kim is the most abundant, followed by H. spinulosus Itoh & Nishida and H. ctenidis Ho & Kim which are much rarer (Itoh 2001, Itoh & Nishida 2007. These copepods are planktonic during naupliar stages, and shift from the water column to the mudflat substratum during the first copepodid (CI) stage to inhabit invertebrate burrows (Itoh 2001, Itoh & Nishida 2007. ...
... In the Tama-River estuary five species of Hemicyclops have been recorded from the burrows of invertebrates, among which H. gomsoensis Ho & Kim is the most abundant, followed by H. spinulosus Itoh & Nishida and H. ctenidis Ho & Kim which are much rarer (Itoh 2001, Itoh & Nishida 2007. These copepods are planktonic during naupliar stages, and shift from the water column to the mudflat substratum during the first copepodid (CI) stage to inhabit invertebrate burrows (Itoh 2001, Itoh & Nishida 2007. The major benthic habitats of H. gomsoensis are the burrows of the mud shrimp Upogebia major (de Haan) and those of the ocypodid crab Macrophthalmus japonicus (de Haan). ...
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We examined the potential advantage of the association of Hemicyclops species with decapod burrows in their avoidance from fish predators through gut-content analysis of fishes collected from the estuary of the Tama River, Japan, and an experiment applying model burrows. The small gobiid species Pseudogobius masago, collected from an area dominated by burrows of the ocypodid crab Macrophthalmus japonicus, showed a high frequency of Hemicyclops gomsoensis in their guts relative to the other co-occurring fish species. In the experiment, no significant difference was observed in the numbers of H. gomsoensis eaten by the goby between the treatments with and without the model burrows. Another goby, Acanthogobius flavimanus, from an area dominated by burrows of the mud shrimp Upogebia major, showed very low frequencies of H. gomsoensis in their guts, as compared with those in P. masago. They had also ingested H. spinulosus and H. ctenidis, in spite of the overwhelmingly high abundance of H. gomsoensis in the burrows. The number of H. gomsoensis eaten by A. flavimanus was significantly lower in the treatments with the model burrows than in the absence of burrows. Since A. flavimanus was the most dominant demersal fish in the study area, H. gomsoensis seemed to avoid predation from this potentially strong predator by inhabiting the decapod burrows. H. ctenidis and H. spinulosus seemed to avoid predation by trespassers by inhabiting the smaller burrows of polychaetes, but this strategy may be less efficient against large predators that feed on polychaetes.
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