首页> 美国卫生研究院文献>other >The Effect of Parasite Infection on Stable Isotope Turnover Rates of δ15N δ13C and δ34S in Multiple Tissues of Eurasian Perch Perca fluviatilis
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The Effect of Parasite Infection on Stable Isotope Turnover Rates of δ15N δ13C and δ34S in Multiple Tissues of Eurasian Perch Perca fluviatilis

机译:寄生虫感染对欧亚鲈Perca fluviatilis多个组织中δ15Nδ13C和δ34S稳定同位素转换率的影响

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摘要

Stable isotope analysis of commercially and ecologically important fish can improve understanding of life-history and trophic ecology. However, accurate interpretation of stable isotope values requires knowledge of tissue-specific isotopic turnover that will help to describe differences in the isotopic composition of tissues and diet. We performed a diet-switch experiment using captive-reared parasite-free Eurasian perch (Perca fluviatilis) and wild caught specimens of the same species, infected with the pike tapeworm Triaenophorus nodulosus living in host liver tissue. We hypothesize that metabolic processes related to infection status play a major role in isotopic turnover and examined the influence of parasite infection on isotopic turn-over rate of carbon (δ13C), nitrogen (δ15N) and sulphur (δ34S) in liver, blood and muscle. The δ15N and δ13C turnovers were fastest in liver tissues, followed by blood and muscle. In infected fish, liver and blood δ15N and δ13C turnover rates were similar. However, in infected fish, liver and blood δ13C turnover was faster than that of δ15N. Moreover, in infected subjects, liver δ15N and δ13C turnover rates were three to five times faster than in livers of uninfected subjects (isotopic half-life of ca.3-4 days compared to 16 and 10 days, respectively). Blood δ34S turnover rate were about twice faster in non-infected individuals implying that parasite infection could retard the turnover rate of δ34S and sulphur containing amino acids. Slower turnover rate of essential amino acid could probably decrease individual immune function. These indicate potential hidden costs of chronic and persistent infections that may have accumulated adverse effects and might eventually impair life-history fitness. For the first time, we were able to shift the isotope values of parasites encapsulated in the liver by changing the dietary source of the host. We also report variability in isotopic turnover rates between tissues, elements and between infected and parasite-free individuals. These results contribute to our understanding of data obtained from field and commercial hatcheries; and strongly improve the applicability of the stable isotope method in understanding life-history and trophic ecology of fish populations.
机译:对具有商业意义和生态重要性的鱼类进行稳定的同位素分析可以增进对生命历史和营养生态学的了解。然而,稳定同位素值的准确解释需要了解特定组织的同位素转换,这将有助于描述组织和饮食同位素组成的差异。我们进行了饮食转换实验,使用了圈养的无寄生虫的欧亚鲈鱼(Perca fluviatilis)和野外捕获的相同物种的标本,这些标本感染了生活在宿主肝脏组织中的派克tape虫Triaenophorus nodulosus。我们假设与感染状态有关的代谢过程在同位素转换中起主要作用,并研究了寄生虫感染对碳(δ 13 C),氮(δ 15 N)和硫(δ 34 S)在肝脏,血液和肌肉中的含量。肝脏组织中δ 15 N和δ 13 C的更新最快,其次是血液和肌肉。在受感染的鱼中,肝脏和血液中δ 15 N和δ 13 C的周转率相似。然而,在受感染的鱼类中,肝脏和血液中δ 13 C的周转速度要快于δ 15 N。此外,在受感染的受试者中,肝脏δ 15 N和δ 13 C的更新速度比未受感染的受试者的肝脏快三到五倍(Ca的同位素半衰期为3-4天,而分别为16天和10天)。未感染个体的血液δ 34 S周转速度快约两倍,这表明寄生虫感染可延迟δ 34 S和含硫氨基酸的周转率。必需氨基酸的转换率降低可能会降低个体的免疫功能。这些表明慢性和持续性感染的潜在隐性成本,这些隐性成本可能已累积了不良影响,并最终可能损害生活史适应性。通过改变宿主的饮食来源,我们第一次能够改变包裹在肝脏中的寄生虫的同位素值。我们还报告了组织,元素之间以及受感染和无寄生虫的个体之间同位素转换率的差异。这些结果有助于我们理解从现场和商业孵化场获得的数据;极大地提高了稳定同位素方法在了解鱼类种群的生活史和营养生态学方面的适用性。

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