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无机磷对中营养型湖泊中细菌浮游生物产量的刺激作用。

Inorganic phosphorus stimulation of bacterioplankton production in a meso-eutrophic lake.

机构信息

Louis Calder Center, Fordham University, P.O. Drawer K, Armonk, New York 10504, and Institute of Ecosystem Studies, The New York Botanical Garden, Mary Flagler Cary Arboretum, Millbrook, New York 12545.

出版信息

Appl Environ Microbiol. 1991 Jul;57(7):2074-8. doi: 10.1128/aem.57.7.2074-2078.1991.

Abstract

Experiments were conducted to determine whether production of heterotrophic bacterioplankton in a small meso-eutrophic lake was influenced by the dissolved inorganic phosphorus (DIP) supply. DIP may indirectly limit bacterial production by limiting phytoplankton, which in turn may limit the carbon available to bacteria. Direct DIP limitation of bacteria occurs where the availability of DIP for bacteria is insufficient to maintain growth. This work examined direct DIP limitation of bacteria by removing phytoplankton and incubating flasks with or without added P in the dark. Bacterial production was measured via the rate of incorporation of [H]thymidine ([H]TdR) into DNA. Bacterial abundance was followed with epifluorescent direct counts. Rates of [H]TdR incorporation were significantly greater in flasks with added DIP, and changes in cell abundances generally paralleled increases in [H]TdR incorporation. Even very small additions of P (0.05 muM) were sufficient to stimulate production. DIP addition to whole lakewater also stimulated [H]TdR incorporation relative to that in zero-addition controls, but there was not a concurrent increase in bacterial cell numbers. The stimulation of [H]TdR incorporation after DIP addition to whole lakewater was significantly less than the stimulation due to DIP addition to 1-mum-pore-size-filtered lakewater. In this study, addition of DIP caused as much as an eightfold stimulation of [H]TdR incorporation.

摘要

进行了实验以确定溶解无机磷(DIP)供应是否会影响小型中营养湖中异养浮游细菌的产生。DIP 可能通过限制浮游植物间接限制细菌的产生,而浮游植物反过来又可能限制细菌可用的碳。当 DIP 的可用性不足以维持细菌生长时,就会发生直接的 DIP 对细菌的限制。本研究通过去除浮游植物并用或不用添加的 P 在黑暗中孵育培养瓶来检查细菌对 DIP 的直接限制。通过将 [H]胸苷([H]TdR)掺入 DNA 的速率来测量细菌的生产力。用荧光直接计数法跟踪细菌的丰度。添加 DIP 的培养瓶中的 [H]TdR 掺入率明显更高,细胞丰度的变化通常与 [H]TdR 掺入率的增加平行。即使添加非常少量的 P(0.05 μM)也足以刺激生产。与零添加对照相比,向整个湖水添加 DIP 也刺激了 [H]TdR 的掺入,但细菌细胞数量没有同时增加。与向 1 微米孔径过滤的湖水添加 DIP 相比,向整个湖水中添加 DIP 后 [H]TdR 掺入的刺激作用明显较小。在这项研究中,添加 DIP 可使 [H]TdR 掺入的刺激作用增加多达八倍。

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