FACTORS CONTROLLING HYPORHEIC RESPIRATION IN A DESERT STREAM

被引:65
作者
JONES, JB [1 ]
机构
[1] ARIZONA STATE UNIV,DEPT ZOOL,TEMPE,AZ 85287
关键词
D O I
10.1111/j.1365-2427.1995.tb00426.x
中图分类号
Q14 [生态学(生物生态学)];
学科分类号
071012 ; 0713 ;
摘要
1. Experimental manipulations were performed to determine the biological, chemical and physical attributes that govern sediment respiration in the hyporheic zone of Sycamore Creek, a Sonoran Desert stream. 2. Hyporheic respiration per unit volume of sediment was inversely related to diameter of sediment particles, indicating that respiration is affected by availability of substrate for microbial colonization (i.e. sediment surfaces). Respiration rate per unit surface area on sediments was positively correlated with particle diameter, indicating greater metabolic activity of microbes on larger sediments. 3. Hyporheic respiration was more than twice as high in water collected from the surface flow than from subsurface flow. Further, hyporheic respiration was highest immediately following exposure of sediments to surface water and declined over time, presumably due to exhaustion of labile organic matter. 4. Microbial activity was stimulated by addition of algal leachate; however, amendments of leaf leachate had little effect. Respiration was also elevated with dextrose and leucine amendments, but not with inorganic nitrogen additions, indicating hyporheic respiration is carbon limited. 5. Water from the stream surface is probably enriched in labile organic matter derived from algae and stimulates respiration at points of hydrologic downwelling where surface water enters hyporheic sediments. The physical structure of sediments further affects metabolism by affecting the area available for microbial attachment.
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页码:91 / 99
页数:9
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共 41 条
[1]  
Barlocher F., Murdoch J.H., Hyporheic biofilms ‐a potential food source for interstitial animals, Hydrobiologia, 184, pp. 61-67, (1989)
[2]  
Bengtsson G., Patterns of amino acid utilization by aquatic hyphomycetes, Oecologia, 55, pp. 355-363, (1982)
[3]  
Benner R., Lay J., K'ness E., Hodson R.E., Carbon conversion efficiency for bacterial growth on lignocellulose: implications for detritus‐based food webs, Limnology and Oceanography, 33, pp. 1514-1526, (1988)
[4]  
Bott T.L., Kaplan L.A., Bacterial biomass, metabolic state, and activity in stream sediments: relation to environmental variables and multiple assay comparisons, Appl Environ Microbiol, 50, pp. 508-522, (1985)
[5]  
Bott T.L., Kaplan L.A., Kuserk FT., Benthic bacterial biomass supported by stream‐water dissolved organic matter, Microbial Ecology, 10, pp. 335-344, (1984)
[6]  
Cummins K.W., Klug M.J., Wetzel R.G., Petersen R.C., Suberkropp K.F., Manny B.A., Wuycheck J.C., Howard F.O., Organic enrichment with leaf leachate in experimental lotic ecosystems, BioScience, 22, pp. 719-722, (1972)
[7]  
Dahm C.N., Uptake of dissolved organic carbon in mountain streams, Verhandlungen der Internatianalen Vereinigung für Theoretische ünd Angewandte Limnologie, 22, pp. 1842-1846, (1984)
[8]  
Fiebig M., Marxsen J., Immobilization and mineralization of dissolved free amino acids by streambed biofilms, Freshwater Biology, 28, pp. 129-140, (1992)
[9]  
Findlay S., Smith P.J., Meyer J.L., Effect of detritus addition on metabolism of river sediment, Hydrobiologia, 137, pp. 257-263, (1986)
[10]  
Fisher S.G., Gray L.J., Grimm N.B., Busch D.E., Temporal succession in a desert stream ecosystem following flash flooding, Ecological Monographs, 52, pp. 92-110, (1982)