1981
DOI: 10.1080/10236248109386988
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Salinity preference behaviour inCarcinus

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1986
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Cited by 30 publications
(19 citation statements)
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“…The general assumption is that salinities with osmolalities near the osmolality of the blood (isosmotic) minimize the physiological cost of osmoregulation, allowing more energy for other processes, such as growth and reproduction (Lankford & Targett, 1994; Cardona, 2000; Hurst & Conover, 2002). Two different types of salinity preference apparatus have been used: salinity gradient tanks that present a continuum of different salinities (Davenport, 1972; Keiser & Aldrich, 1976; Moser, 1988; Chung, 2001) and salinity choice chambers with pre‐established salinities which appear to work well for crustaceans (Thomas et al , 1981; McGaw & Naylor, 1992 a , b ; McGaw, 2001). The main limitation of both of these experimental set‐ups is that they often require a very shallow depth to prevent vertical stratification, thus precluding the testing of relatively large, mobile organisms, such as L. griseus .…”
Section: Introductionmentioning
confidence: 99%
“…The general assumption is that salinities with osmolalities near the osmolality of the blood (isosmotic) minimize the physiological cost of osmoregulation, allowing more energy for other processes, such as growth and reproduction (Lankford & Targett, 1994; Cardona, 2000; Hurst & Conover, 2002). Two different types of salinity preference apparatus have been used: salinity gradient tanks that present a continuum of different salinities (Davenport, 1972; Keiser & Aldrich, 1976; Moser, 1988; Chung, 2001) and salinity choice chambers with pre‐established salinities which appear to work well for crustaceans (Thomas et al , 1981; McGaw & Naylor, 1992 a , b ; McGaw, 2001). The main limitation of both of these experimental set‐ups is that they often require a very shallow depth to prevent vertical stratification, thus precluding the testing of relatively large, mobile organisms, such as L. griseus .…”
Section: Introductionmentioning
confidence: 99%
“…There are marked halokinetic responses to reduce salinity, whether applied suddenly (Taylor and Naylor, 1977;Thomas et al, 1981) or sinusoidally (Bolt and Naylor, 1985), and such responses appear to be purely exogenous. In contrast, The phase relation of the activity peaks to the salinity cycle of a, crabs exposed to a salinity cycle with low salinity timed to coincide with expected high tide, (data from Figure 4).…”
Section: Discussionmentioning
confidence: 93%
“…There is evidence to support the hypothesis that rhythmic activity in Carcinus is modulated by the release of a peptidic neurodepressing hormone (NDH) from the eyestalk neurosecretory complex , but previous attempts to test that hypothesis have studied the effects of tissue ablation only on the persistence or absence of endogenous rhythmicity. Now, in view of the complexity of the responses of Carcinus to salinity cycles (Taylor and Naylor, 1977, Thomas et al, 1981, Bolt and Naylor, 1985, it is of particular interest to make a comparative study of the effects of eyestalk ablation on the exogenous and endogenous aspects of the crab's locomotor rhythm.…”
Section: Introductionmentioning
confidence: 99%
“…Green crabs in an estuary appear to become habituated to episodes of falling salinity, crabs retained in the estuary clearly exhibiting tidal and daily rhythmic locomotor patterns as though they were on the open shore, with no apparent mechanism to induce escape. This initial high halokinesis (Taylor & Naylor, 1977), presumed to enable the crabs to avoid adverse salinities (Thomas et al, 1981;Ameyaw-Akumfi & Naylor, 1987), would also account for differences in choice behaviour between the red and green crabs (McGaw & Naylor, in press). Exposure to constant low salinity in winter has been shown in Carcinus to induce a locomotor rhythm of circatidal periodicity (Bolt & Naylor, 1985;.…”
Section: Discussionmentioning
confidence: 99%