Ivanova M B
Zoological Institute, Russian Academy of Science, Universitetskaya nab. 1, St.-Petersburg, 199034 Russia.
Zh Obshch Biol. 2001 Nov-Dec;62(6):512-24.
Changes of structure and functioning of pelagic zooplankton under lake eutrophication were studied in a group of small (without outlet) lakes in southern Karelia and Leningrad region. The lakes were morphologically similar and located within the same climatic zone. Differences in their trophic status were connected with anthropogenic eutrophication. Correlation between species number and feeding resources of a lake is determined as: Y = (8.01 +/- 3.85) + (0.29 +/- 0.07)X1 + (6.75 +/- 1.52)X2, r2 = 0.95, (1) Y--number of zooplankton species, X1--average chlorophyll concentration for the season, mg/1; X2--average value of biochemical oxygen demand (expressed in mgC/1). Average biomass of zooplankton for season also depends on food: logY = (-0.054 +/- 0.224) + (0.242 +/- 0.094)logX1 + (0.170 +/- 0.179)logX2, n = 13, r2 = 0.87, (2) Y--average zooplankton biomass for the season, kcal/m3, X1 and X2 the same as (1). Increase in species number and zooplankton bimass determined primarily by Rotatoria occur in parallel to chlorophyll concentration and activity of bacteria. In acid lakes rotifers are not important in energy balance. In mezotrophic lakes two main energy paths are formed--through rotifers and through Crustacea. The role of rotifers is extremely important in eutrophic lakes where about 80% of energy paths through them. The ratio community production to energy consumption for the growing season is also depended on the community structure (species number, equitability, connectence): Y = (2.257 +/- 0.026) - (0.368 +/- 0.031)X1 + (5.160 +/- 0.442)X2, r2 = 0.99, (3) Y--average seasonal production of zooplankton, kcal/m2; X1--maximal meaning of Shannon index (bites), calculated on biomass value; X2--connectence of the community, calculated according Briand (1983). Eutrophication changes the stability of lakes relative to external influences, while low productive lakes are very sensitive to the increase in nutrient load, high productive lakes are more influenced by changes in fish predation.
在卡累利阿南部和列宁格勒地区的一组小型(无出水口)湖泊中,研究了湖泊富营养化状态下浮游动物结构和功能的变化。这些湖泊在形态上相似,且位于同一气候带内。它们营养状态的差异与人为富营养化有关。湖泊物种数量与食物资源之间的相关性确定为:Y = (8.01 ± 3.85) + (0.29 ± 0.07)X1 + (6.75 ± 1.52)X2,r2 = 0.95,(1)Y——浮游动物物种数量,X1——该季节叶绿素平均浓度,mg/1;X2——生化需氧量的平均值(以mgC/1表示)。浮游动物的季节平均生物量也取决于食物:logY = (-0.054 ± 0.224) + (0.242 ± 0.094)logX1 + (0.170 ± 0.179)logX2,n = 13,r2 = 0.87,(2)Y——浮游动物季节平均生物量,kcal/m3,X1和X2与(1)相同。物种数量和主要由轮虫导致的浮游动物生物量增加与叶绿素浓度及细菌活性平行发生。在酸性湖泊中,轮虫在能量平衡中并不重要。在中营养湖泊中形成了两条主要能量路径——通过轮虫和通过甲壳类动物。轮虫在富营养湖泊中的作用极其重要,约80%的能量路径通过它们。生长季节群落产量与能量消耗的比率也取决于群落结构(物种数量、公平性、连通性):Y = (2.257 ± 0.026) - (0.368 ± 0.031)X1 + (5.160 ± 0.442)X2,r2 = 0.99,(3)Y——浮游动物季节平均产量,kcal/m2;X1——基于生物量值计算的香农指数(比特)的最大值;X2——根据布赖恩(1983年)计算的群落连通性。富营养化改变了湖泊相对于外部影响的稳定性,而低生产力湖泊对营养负荷增加非常敏感,高生产力湖泊则更多地受到鱼类捕食变化的影响。