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Lemmings and voles: present and future

机译:鼠和田鼠:现在和将来

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Lemmings have long been attracting many population ecologists because of large amplitude and cyclicity of their population fluctuations and, in the past, assumed non-adaptive mass-migration at the peaks (but see Henttonen and Kaikusalo 1993, for a recent view). When I was asked by the Editors to write a comment on this Special Feature on "Population Ecology of the Vole Clethrionomys rufocanus, I remembered my young age. That is 40 years ago, when I published the first edition of my book "Comparative Ecology" (Ito 1959) in Japanese. Using correlogram analysis, I demonstrated 4-year cycles of the lemming and the arctic fox, and 9-10 year cycles of the varying hare and lynx populations based on the data from MacLulich (1937), Elton and Nicholson (1942) and Elton (1942). From this, I expressed my opinion that these cycles might be driven and maintained by a classic, Lotka-Volterra type, predator-prey interactions. (The use of correlogram analysis to demonstrate population cycles was first done by Utida (1953), when he supported MacLulich's (1937) view that lynx cycles do not reflect the 11-year sunspot cycles.)
机译:由于种群的波动幅度大且周期性大,并且过去曾假设在高峰期没有自适应种群迁移,因此,旅鼠一直吸引着许多种群生态学家(有关最新观点,请参见Henttonen and Kaikusalo 1993)。当编辑要求我对“田鼠笼草的种群生态学”这一专题报道发表评论时,我想起了我的年纪。那是40年前,当我出版我的第一本书《比较生态学》时(Ito 1959)日文。根据MacLulich(1937),Elton和M.的数据,我用相关图分析证明了旅鼠和北极狐的4年周期,以及不同野兔和山猫种群的9-10年周期。 Nicholson(1942)和Elton(1942)。据此,我认为这些周期可能是由经典的Lotka-Volterra类型的捕食者-猎物相互作用驱动和维持的。最初由Utida(1953)完成,当时他支持MacLulich(1937)的观点,即天猫座周期不反映11年黑子周期。)

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