Réponses Physiologiques De Sept Espèces De Poissons Lacustres À Un Stress De Capture (Filet Maillant Et Épuisette).

Bau, F.; Ferroni-Claverie, N.; Parent, Jean-Paul

doi:10.1051/kmae/2001042

Cited by 4 publications

(4 citation statements)

References 51 publications

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“…Differences between the two families were also evident with regard to indicators of stress‐induced energy mobilization. Plasma glucose levels in unstressed salmonids and cyprinids were similar ( c. 2·5–5·5 mmol l −1 ) and in the latter, as was the case for the salmonids, broadly consistent with earlier reports (Pottinger et al , 1999, 2000; Bau et al , 2001; Ruane et al , 2001, 2002 a , b ; Bracewell et al , 2004). The dynamics of the response profile for glucose, however, were different.…”

Section: Discussionsupporting

confidence: 90%

“…Probably as a result of this, R. rutilus cortisol data presented here are in the lower part of the full range of reported values. For L. cephalus , comparable data are again limited, but the values reported here are similar to earlier data for confined fish (Pottinger et al , 2000) and fish following capture from the wild (Bau et al , 2001). There was also a greater tendency among the salmonids for a decline in plasma cortisol levels during the course of confinement, whereas the reverse was true for the cyprinid species.…”

Section: Discussionsupporting

confidence: 87%

“… (a) Mean values for plasma cortisol levels in six cyprinid and eight salmonid species subjected to a range of stressors. The data plotted were obtained from: Aaltonen et al (2000); Barton (2000); Basu et al (2001); Bau et al (2001); Benfey & Biron (2000); Blahová et al (2007); Cairns et al (2008); Clements et al (2002); Congleton et al (2000); Dabrowska et al (1991); Davis & Schreck (1997); Dror et al (2006); Einarsdóttir & Nilssen (1996); Elofsson et al (2000); Fevolden et al (1999); Gagnona et al (2006); Høgåsen & Prunet (1997); Iversen et al (1998); Jeney et al (1996); Jhingan et al (2003); Jørgensen et al (2001, 2002); Kagawa & Mugiya (2000); Kakuta (1998); Kubokawa et al (1999); Lister et al (2008); McDonald & Robinson (1993); McDonald et al (1993); Mesa (1994); Mesa et al (2000); Momoda et al (2007); Øverli et al (1999); Pankhurst & Dedual (1994); Pankhurst et al (2008); Pickering et al (1982, 1986); Pottinger & Carrick (2000); Pottinger & Moran (1993); Pottinger (1998); Pottinger et al (1992, 1999, 2000); Quabius et al (2000); Quigley et al (2006); Reddy et al (1995); Ruane et al (1999, 2001, 2002 a , b ); Sadler et al (2000); Sandodden et al (2001); Sharpe (2007); Sharpe et al (1998); Sink et al (2007); Skjervold et al (2001); Sloman et al (2001); Smith et al (2004); Stone et al (2008); Stratholt et al (1997); Sumpter et al (1985); Tanck et al (2000); Thomas et al (1999); Van Dijk et al (1993); Vianen et al (2001); Waring et al (1992); Weber et al (2002); Winberg & Lepage (1998); Yin et al (1995). (b) A box plot of the data presented in (a) where the boundary of the box closest to zero indicates the 25th percentile, the unbroken line within the box marks the median, the broken line denotes the mean and the...…”

Section: Resultsmentioning

confidence: 99%

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A multivariate comparison of the stress response in three salmonid and three cyprinid species: evidence for inter‐family differences

Pottinger

2010

Journal of Fish Biology

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The response of six species of freshwater fishes, from the families Cyprinidae (common carp Cyprinus carpio, roach Rutilus rutilus and chub Leuciscus cephalus) and Salmonidae (rainbow trout Oncorhynchus mykiss, brown trout Salmo trutta and Arctic charr Salvelinus alpinus), to a standardized stressor was evaluated. A 6 h period of confinement resulted in changes to plasma cortisol, glucose, amino acid and lactate levels compared with unconfined controls. There were significant differences in the response profiles both within and between families. The cyprinid species exhibited higher and more sustained stress-induced increases in plasma cortisol and glucose than the salmonid species. In cyprinids, plasma lactate and plasma amino acid concentration showed less disturbance following stress than in salmonids. The results of the study, together with an evaluation of previously published data for eight salmonid species and six cyprinid species, support the hypothesis that differences in core elements of the stress response exist between species of fishes, and that this variation may have a systematic basis.

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Section: Discussionsupporting

confidence: 90%

Section: Discussionsupporting

confidence: 87%

Section: Resultsmentioning

confidence: 99%

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A multivariate comparison of the stress response in three salmonid and three cyprinid species: evidence for inter‐family differences

Pottinger

2010

Journal of Fish Biology

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“…The tolerance of Schizothorax davidi to low temperature and UVR was slightly stronger than that of Spinibarbus sinensis, but its salinity tolerance was the weakest among the six species. As a carnivorous fish, Percocypris pingi has a higher oxygen consumption rate under emergency conditions (Bau and Parent, 2001), and histological sections showed that the density of mucous cells and club cells in its epidermis was higher, while the epithelial cells that play a major role in resisting UVR were thinner (Gu et al, 2022a;Gu et al, 2022b). Therefore, its tolerance to low oxygen and UVR was slightly lower than that of Schizothorax davidi with similar altitude distribution.…”

Section: Factors Limiting the Spread Of Lowaltitude Fishes To The Pla...mentioning

confidence: 98%

Factors limiting the spread of middle- and low-altitude fishes to the Qinghai-Tibet plateau

Yuanfu

et al. 2023

Front. Mar. Sci.

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The distribution pattern of species is determined by the environment and their adaptability to the environment. Qinghai-Tibet Plateau has become a natural laboratory for studying adaptive evolution due to its extreme environmental characteristics such as low temperature, low oxygen, high salinity and high ultraviolet radiation (UVR). Fish are sensitive to the environmental stress, so they are ideal materials for studying high-altitude adaptation of animals. Previous studies have mainly focused on the adaptability of plateau species, but the reasons why plain species cannot spread to the plateau have been ignored. In this study, stress experiments and histological experiments were used to compare the tolerance of six Barbini fishes (family: Cyprinidae) distributed at different altitudes and regions to low temperature, low oxygen, salinity and UVR. Results showed that the tolerance of fishes to high-altitude environmental stress factors was closely related to the environmental stress of their main habitats. The high-altitude fish Gymnocypris eckloni had strong tolerance to all stress factors, while the other five fishes from middle and low altitudes could not adapt to single or multiple stress factors, with significant interspecific differences. Among these factors, middle- and low-altitude fishes showed common low tolerance to UVR, suggesting that high UVR, the factor lacking at low altitude areas, plays an important role. Moreover, during the uplift of the Qinghai-Tibet Plateau, Schizothorax fish disappeared from the middle of the plateau. We speculate that this was caused by its intolerance to the increasingly extreme plateau environment, especially salinity.

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Haematological and biochemical profile of harvest-size carp during harvest and post-harvest storage

Svobodová

Vykusová²,

Modrá

et al. 2006

Aquaculture Res

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Stress load on harvest‐size common carp (Cyprinus carpio L.) just before harvest, during harvest and during the post‐harvest storage were assessed using haematological and biochemical indices. The study was carried out at the 60 ha Dřemliny pond for 28, 7 and 1 day before harvest, during 3‐day harvest and after a 28‐day post‐harvest period. Indices monitored included the relative spleen weight (SSI), erythrocyte count (Er), haemoglobin levels (Hb), haematocrit (PCV), MCV, MCH, MCHC, leucocrit (Bc), differential leucocyte count (leucogram), blood plasma cortisol, glucose, total proteins (TP), cholesterol and chloride. During harvest, a significant decrease of SSI (P<0.05; P<0.01), increase of PCV (P<0.01), decrease of Bc (P<0.01, P<0.05), lymphopenia (P<0.05) and neutrophilia (P<0.01) were observed. A significant increase in the levels of blood plasma cortisol was found 1 day before harvest (P<0.05) due to draining off the pond before harvest itself, hyperglycaemia was observed 1 day before harvest (P<0.05) and during harvest (P<0.01); a decrease, on the other hand, was found in cholesterol and chloride levels (P<0.01). The relationships between oxygen content in water and SSI and MCHC were positive (P>0.05) and between oxygen and glucose were negative (P>0.01). A 28‐day post‐harvest storage returned the indices investigated back to physiological interval of values. Persistently lower levels of Bc, lymphopenia, neutrophilia and lower TP concentrations are indicative of deepening immunosuppression during the post‐harvest storage period. Changes of haematological and biochemical indices during harvest in relation to hypoxia, fish handling and higher stocking rates are also discussed.

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Réponses Physiologiques De Sept Espèces De Poissons Lacustres À Un Stress De Capture (Filet Maillant Et Épuisette).

Cited by 4 publications

References 51 publications

A multivariate comparison of the stress response in three salmonid and three cyprinid species: evidence for inter‐family differences

A multivariate comparison of the stress response in three salmonid and three cyprinid species: evidence for inter‐family differences

Factors limiting the spread of middle- and low-altitude fishes to the Qinghai-Tibet plateau

Haematological and biochemical profile of harvest-size carp during harvest and post-harvest storage

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