Engen Steinar, Ringsby Thor Harald, Saether Bernt-Erik, Lande Russell, Jensen Henrik, Lillegård Magnar, Ellegren Hans
Population Biology Center, Department of Mathematical Sciences, Norwegian University of Science and Technology, N-7491 Trondheim, Norway.
Evolution. 2007 Aug;61(8):1873-85. doi: 10.1111/j.1558-5646.2007.00155.x.
We derive formulas that can be applied to estimate the effective population size N(e) for organisms with two sexes reproducing once a year and having constant adult mean vital rates independent of age. Temporal fluctuations in population size are generated by demographic and environmental stochasticity. For populations with even sex ratio at birth, no deterministic population growth and identical mean vital rates for both sexes, the key parameter determining N(e) is simply the mean value of the demographic variance for males and females considered separately. In this case Crow and Kimura's generalization of Wright's formula for N(e) with two sexes, in terms of the effective population sizes for each sex, is applicable even for fluctuating populations with different stochasticity in vital rates for males and females. If the mean vital rates are different for the sexes then a simple linear combination of the demographic variances determines N(e), further extending Wright's formula. For long-lived species an expression is derived for N(e) involving the generation times for both sexes. In the general case with nonzero population growth and uneven sex ratio of newborns, we use the model to investigate numerically the effects of different population parameters on N(e). We also estimate the ratio of effective to actual population size in six populations of house sparrows on islands off the coast of northern Norway. This ratio showed large interisland variation because of demographic differences among the populations. Finally, we calculate how N(e) in a growing house sparrow population will change over time.
我们推导了一些公式,这些公式可用于估计每年繁殖一次且成年平均生命率恒定、与年龄无关的两性生物的有效种群大小N(e)。种群大小的时间波动是由人口统计学和环境随机性产生的。对于出生时性别比例均等、不存在确定性种群增长且两性平均生命率相同的种群,决定N(e)的关键参数仅仅是分别考虑的雄性和雌性人口统计方差的平均值。在这种情况下,克劳和木村对赖特关于两性N(e)公式的推广,就每种性别的有效种群大小而言,即使对于雄性和雌性生命率具有不同随机性的波动种群也是适用的。如果两性的平均生命率不同,那么人口统计方差的简单线性组合决定N(e),这进一步扩展了赖特公式。对于长寿物种,推导了一个涉及两性世代时间的N(e)表达式。在种群增长不为零且新生个体性别比例不均等的一般情况下,我们使用该模型通过数值研究不同种群参数对N(e)的影响。我们还估计了挪威北部海岸外岛屿上六个家麻雀种群的有效种群大小与实际种群大小的比率。由于各种群之间的人口统计学差异,这个比率显示出很大的岛间差异。最后,我们计算了一个不断增长的家麻雀种群中的N(e)将如何随时间变化。