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Enzymatic activities and microbial communities in an Antarctic dry valley soil: Responses to C and N supplementation
Authors:D.W. Hopkins   A.D. Sparrow   L.L. Shillam   L.C. English   P.G. Dennis   P. Novis   B. Elberling   E.G. Gregorich  L.G. Greenfield
Affiliation:1. Scottish Crop Research Institute, Invergowrie, Dundee, DD2 5DA, Scotland, UK;2. School of Biological and Environmental Sciences, University of Stirling, Stirling, FK9 4LA, Scotland, UK;3. Department of Natural Resources and Environmental Sciences, University of Nevada, 1000 Valley Road, Reno, NV 89512, USA;4. Manaaki Whenua - Landcare Research, PO Box 69, Lincoln, 8152, New Zealand;5. Institute of Geography and Geology, University of Copenhagen, Øster Voldgade 10, DK-1350, Copenhagen K., Denmark;6. The University Centre in Svalbard, Longyearbyen, Norway;7. Agriculture and Agri-Food Canada, Central Experimental Farm, Ottawa, K1A 0C6, Canada;8. School of Biological Sciences, University of Canterbury, Private Bag 4800, Christchurch, 8020, New Zealand
Abstract:
The soils of the Antarctic dry valleys are exposed to extremely dry and cold conditions. Nevertheless, they contain small communities of micro-organisms that contribute to the biogeochemical transformations of the bioelements, albeit at slow rates. We have determined the dehydrogenase, β-glucosidase, acid and alkaline phosphatase and arylsulphatase activities and the rates of respiration (CO2 production) in laboratory assays of soils collected from a field experiment in an Antarctic dry valley. The objective of the field experiment was to test the responses of the soil microbial community to additions of C and N in simple (glucose and NH4Cl) and complex forms (glycine and lacustrine detritus from the adjacent lake comprising principally cyanobacterial necromass). The soil samples were taken 3 years after the experimental treatments had been applied. In unamended soil, all enzyme activities and respiration were detected indicating that the enzymatic capacity to mineralize organic C, P and S compounds existed in the soil, despite the very low organic matter content. Relative to the control (unamended soil), respiration was significantly increased by all the experimental additions of C and N except the smallest NH4Cl addition (1 mg N g−1 soil) and the smallest detritus addition (1.5 mg C g−1 soil and 0.13 mg N g−1 soil). The activities of all enzymes except dehydrogenase were increased by C and combined large C (10 mg C g−1 soil) and N additions, but either unchanged or diminished by addition of either N only or N (up to 10 mg N g−1 soil) with only small C (1 mg C g−1 soil) additions in the form of glucose and NH4Cl. This suggests that in the presence of a large amount of N, the C supply for enzyme biosynthesis was limited. When normalized with respect to soil respiration, only arylsulphatase per unit of respiration showed a significant increase with C and N additions as glucose and NH4Cl, consistent with S limitation when C and N limitations have been alleviated. Based on the positive responses of enzyme activity, detritus appeared to provide either conditions or resources which led to a larger biological response than a similar amount of C and more N added in the form of defined compounds (glucose, NH4Cl or glycine). Assessment of the soil microbial community by ester-linked fatty acid (ELFA) analysis provided no evidence of changes in the community structure as a result of the C and N supplementation treatments. Thus the respiration and enzyme activity responses to supplementation occurred in an apparently structurally stable or unresponsive microbial community.
Keywords:Acid phosphatase   Alkaline phosphatase   Antarctica   Arylsulphatase   Dehydrogenase   Ester-linked fatty acids   Soil respiration   β  -Glucosidase
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