三种鱼的磷排泄及其在微型生态系统磷再循环中的作用

PHOSPHORUS EXCRETION OF THREE SPECIES OF FISH AND ITS ROLE IN THE RECYCLING OF PHOSPHORUS IN FRESHWATER MICROCOSMS

  • 摘要: 在考查罗非鱼或鲢、鳙下行影响的微型生态系统实验后期,对三种鱼的特定正磷酸盐(PO4P)排泄率进行了测定,并且估算了系统中实验鱼的PO4P排泄率。结果表明,在个体大小相同的情况下,罗非鱼的特定PO4P排泄率明显地高于链、鳙,似乎同它们的食物含磷量无关而由其体组织含磷量所决定;放养罗非鱼的系统中鱼的PO4P排泄率比放养链、鳙的系统平均高2倍多,其磷排泄对浮游植物的PO4P供给率分别为100%—158%和61%—75%。根据有鱼系统中PO4P的供求关系和实验结束时磷分布的观测结果推断,沉积物的磷释放是系统中磷再生的主要途径,而实验鱼调节系统磷再循环的主要机制是排粪。

     

    Abstract: The freshwater microcosm experiments have demonstrated that the stocking of Nile tilapia (Oreochromis niloticus) or silver carp (Hypophthalmichthys molitrix) and bighead carp (Aristichthys nobilis) not only altered the community structure and metabolism intensity of themicrocosms but also induced themarked changes in the nutrient levels of the microcosms, and the effects of omnivorous Nile tilapia on themicrocosms were far greater than those of planktivorous silver carp and bighead carp. It is generally considered that the major mechanisms by which fish regulate the nutrient recycling in aquatic ecosystems include egestion (voided undigested material), excretion (dissolved metabolicwast material), reducing themean body size of zooplankton via size-selective predationand thereby enhancing nutrient excretion in zooplankton community, the release of nutrients in fish carcasses by microbial decomposition, and accelerating the release of nutrients in sediments by mechanical mixing processes, in which the importance of nutrient excretion by fishes to the regeneration of nutrients in ecosystems has received thegreatest attention. In order to evaluate the role of experimental fish in phosphorus recycling in the microcosms, author estimated orthophosphate (PO4-P) excretion by the experimental fish in the microcosms by measuring the specific PO4-P excretion rates of the three species of fish and fish biomass in the microcosms following the estimation of PO4-P turnover time and PO4-P excretion by zoo plankton in the microcosms in the later period of the experiments. The rates of PO4-P excretion by fishes were directly measured in size-classes of the each species of fish. In the test fish taken from the microcosms or culture aquariawere promptly transferred to clean containers (1) 5 fish per container dependent on fish size) holding tap water prefiltered with active carbon, aerated and stored for 24h at 23) 25e. The tested fish stayed in the containers for 1h, and in the meanwhile feces voided by fishes were immediately drawn out with absorption tubes. The specific PO4-P excretion rate of fish was determined as the increment of PO4-P concentrations in the container in 1h, correcting for the volume of water in the container and the biomass of tested fish, here assuming that a brief stop of feeding by fishes could not bring about the obvious effect on their normal excretion of nutrients. The results of direct measurement of PO4-P excretion by fishes were proved to be reliableby the results of estimation of phosphorus excretion by Nile tilapia using a bioenergetics approach for testing the above assumption. According to the results of direct measurement the specific PO4-P excretion rate of Nile tilapia was much higher than that of silver carp and bighead carp as they were in the same size, which seemed to be independent of phosphorus content in food but dependent on phosphorus content in fish tissues. And the rate of PO4-P excretion by the experimental fish in the microcosms stocked with Nile tilapia, on the average, was more than three times that in themicrocosms with silver carp and bighead carp, and phosphorus excretion by fishes would supply 10.0%) 15. 8% and 6. 1%) 7. 5% of the PO4-P requirements of phytoplankton in the microcosms, respectively. It was inferred from the relation between PO4-P supply and demand for PO4-P in the microcosms with fish and the distribution of phosphorus in the microcosms at the end of the experiments that the release of phosphorus in sediments was the dominant pathway for phosphorus regeneration in the microcosms and egestion by the experimental fish was the major mechanism to regulate the recy cling of phosphorus in the microcosms.

     

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