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Ecology Letters · 2019 · Vol. 22 · Issue 11 · Wiley
Tropical soils contain huge carbon stocks, which climate warming is projected to reduce by stimulating organic matter decomposition, creating a positive feedback that will promote further warming. Models predict that the loss of carbon from warming soils will be mediated by microbial physiology, but no empirical data are available on the response of soil carbon and microbial physiology to warming in tropical forests, which dom...
Ecology · 2018 · Vol. 99 · Issue 11 · Wiley
More than 200 years ago, Alexander von Humboldt reported that tropical plant species richness decreased with increasing elevation and decreasing temperature. Surprisingly, coordinated patterns in plant, bacterial, and fungal diversity on tropical mountains have not yet been observed, despite the central role of soil microorganisms in terrestrial biogeochemistry and ecology. We studied an Andean transect traversing 3.5 km in el...
Environmental Microbiology · 2018 · Vol. 20 · Issue 10 · Wiley
Summary Several lines of evidence suggest that the agaricoid, non‐ectomycorrhizal members of the family Hygrophoraceae (waxcaps) are biotrophic with unusual nitrogen nutrition. However, methods for the axenic culture and lab‐based study of these organisms remain to be developed, so our current knowledge is limited to field‐based investigations. Addition of nitrogen, lime or organophosphate pesticide at an experimental field si...
Environmental Microbiology · 2016 · Vol. 18 · Issue 6 · Wiley
Summary Microbial responses to A rctic climate change could radically alter the stability of major stores of soil carbon. However, the sensitivity of plot‐scale experiments simulating climate change effects on A rctic heathland soils to potential confounding effects of spatial and temporal changes in soil microbial communities is unknown. Here, the variation in heathland soil bacterial communities at two survey sites in S wede...
Global Change Biology · 2013 · Vol. 19 · Issue 4 · Wiley
Previous studies have shown a correspondence between the abundance of particular plant species and methane flux. Here, we apply multivariate analyses, and weighted averaging, to assess the suitability of vegetation composition as a predictor of methane flux. We developed a functional classification of the vegetation, in terms of a number of plant traits expected to influence methane production and transport, and compared this...
Global Change Biology · 2012 · Vol. 18 · Issue 11 · Wiley
Dissolved organic carbon ( DOC ) concentrations in surface waters have increased across much of E urope and N orth A merica, with implications for the terrestrial carbon balance, aquatic ecosystem functioning, water treatment costs and human health. Over the past decade, many hypotheses have been put forward to explain this phenomenon, from changing climate and land management to eutrophication and acid deposition. Resolution...
Global Change Biology · 2012 · Vol. 18 · Issue 5 · Wiley
Nearly 5000 chamber measurements of CH 4 flux were collated from 21 sites across the U nited K ingdom, covering a range of soil and vegetation types, to derive a parsimonious model that explains as much of the variability as possible, with the least input requirements. Mean fluxes ranged from −0.3 to 27.4 nmol CH 4 m −2 s −1 , with small emissions or low rates of net uptake in mineral soils (site means of −0.3 to 0.7 nmol m −2...
Environmental Microbiology · 2008 · Vol. 10 · Issue 10 · Wiley
Summary Peatlands represent an enormous carbon reservoir and have a potential impact on the global climate because of the active methanogenesis and methanotrophy in these soils. Uncultivated methanotrophs from seven European peatlands were studied using a combination of molecular methods. Screening for methanotroph diversity using a particulate methane monooxygenase‐based diagnostic gene array revealed that Methylocystis ‐rela...
Global Change Biology · 2007 · Vol. 13 · Issue 12 · Wiley
We present results from modelling studies, which suggest that, at most, only about 10–20% of recently observed soil carbon losses in England and Wales could possibly be attributable to climate warming. Further, we present reasons why the actual losses of SOC from organic soils in England and Wales might be lower than those reported.
Environmental Microbiology · 2005 · Vol. 7 · Issue 6 · Wiley
Summary Rhizosphere microorganisms play an important role in soil carbon flow, through turnover of root exudates, but there is little information on which organisms are actively involved or on the influence of environmental conditions on active communities. In this study, a 13 CO 2 pulse labelling field experiment was performed in an upland grassland soil, followed by RNA‐stable isotope probing (SIP) analysis, to determine the...
Environmental Microbiology · 2005 · Vol. 7 · Issue 4 · Wiley
Summary The influence of liming on rhizosphere microbial biomass C and incorporation of root exudates was studied in the field by in situ pulse labelling of temperate grassland vegetation with 13 CO 2 for a 3‐day period. In plots that had been limed (CaCO 3 amended) annually for 3 years, incorporation into shoots and roots was, respectively, greater and lower than in unlimed plots. Analysis of chloroform‐labile C demonstrated...
Global Change Biology · 2004 · Vol. 10 · Issue 12 · Wiley
The effect of liming on the flow of recently photosynthesized carbon to rhizosphere soil was studied using 13 CO 2 pulse labelling, in an upland grassland ecosystem in Scotland. The use of 13 C enabled detection, in the field, of the effect of a 4‐year liming period of selected soil plots on C allocation from plant biomass to soil, in comparison with unlimed plots. Photosynthetic rates and carbon turnover were higher in plants...