Reducing conditions, reactive metals, and their interactions can explain spatial patterns of surface soil carbon in a humid tropical forest

Verfasser / Beitragende:
[Steven Hall, Whendee Silver]
Ort, Verlag, Jahr:
2015
Enthalten in:
Biogeochemistry, 125/2(2015-09-01), 149-165
Format:
Artikel (online)
ID: 605517738
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024 7 0 |a 10.1007/s10533-015-0120-5  |2 doi 
035 |a (NATIONALLICENCE)springer-10.1007/s10533-015-0120-5 
245 0 0 |a Reducing conditions, reactive metals, and their interactions can explain spatial patterns of surface soil carbon in a humid tropical forest  |h [Elektronische Daten]  |c [Steven Hall, Whendee Silver] 
520 3 |a Humid tropical forests support large stocks of surface soil carbon (C) that exhibit high spatial variability over scales of meters to landscapes (km). Reactive minerals and organo-metal complexes are known to contribute to C accumulation in these ecosystems, although potential interactions with environmental factors such as oxygen (O2) availability have received much less attention. Reducing conditions can potentially contribute to C accumulation, yet anaerobic metabolic processes such as iron (Fe) reduction can also drive substantial C losses. We tested whether these factors could explain variation in soil C (0-10 and 10-20cm depths) over multiple spatial scales in the Luquillo Experimental Forest, Puerto Rico, using reduced iron (Fe(II)) concentrations as an index of reducing conditions across sites differing in vegetation, topographic position, and/or climate. Fine root biomass and Fe(II) were the best overall correlates of site (n=6) mean C concentrations and stocks from 0 to 20cm depth (r=0.99 and 0.98, respectively). Litterfall decreased as reducing conditions, total and dead fine root biomass, and soil C increased among sites, suggesting that decomposition rates rather than C inputs regulated soil C content at the landscape scale. Strong relationships between Fe(II) and dead fine root biomass suggest that reducing conditions suppressed particulate organic matter decomposition. The optimal mixed-effects regression model for individual soil samples (n=149) showed that aluminum (Al) and Fe in citrate/ascorbate and oxalate extractions, Fe(II), fine root biomass, and interactions between Fe(II) and Al explained most of the variation in C concentrations (pseudo R2=0.82). The optimal model of C stocks was similar but did not include fine root biomass (pseudo R2=0.62). In these models, soil C concentrations and stocks increased with citrate/ascorbate-extractable Al and oxalate-extractable Fe. However, soil C decreased with citrate/ascorbate-extractable Fe, an index of Fe susceptible to anaerobic microbial reduction. At the site scale (n=6), ratios of citrate/ascorbate to oxalate-extractable Fe consistently decreased across a landscape O2 gradient as C increased. We suggest that the impact of reducing conditions on organic matter decomposition and the presence of organo-metal complexes and C sorption by short-range order Fe and Al contribute to C accumulation, whereas the availability of an Fe pool to sustain anaerobic respiration in soil microsites partially attenuates soil C accumulation in these ecosystems. 
540 |a Springer International Publishing Switzerland, 2015 
690 7 |a Iron reduction  |2 nationallicence 
690 7 |a Poorly-crystalline minerals  |2 nationallicence 
690 7 |a Redox  |2 nationallicence 
690 7 |a Root biomass  |2 nationallicence 
690 7 |a Soil carbon  |2 nationallicence 
690 7 |a Soil oxygen  |2 nationallicence 
700 1 |a Hall  |D Steven  |u Department of Environmental Science, Policy, and Management, University of California-Berkeley, 130 Mulford Hall, UC Berkeley, 94720, Berkeley, CA, USA  |4 aut 
700 1 |a Silver  |D Whendee  |u Department of Environmental Science, Policy, and Management, University of California-Berkeley, 130 Mulford Hall, UC Berkeley, 94720, Berkeley, CA, USA  |4 aut 
773 0 |t Biogeochemistry  |d Springer International Publishing  |g 125/2(2015-09-01), 149-165  |x 0168-2563  |q 125:2<149  |1 2015  |2 125  |o 10533 
856 4 0 |u https://doi.org/10.1007/s10533-015-0120-5  |q text/html  |z Onlinezugriff via DOI 
898 |a BK010053  |b XK010053  |c XK010000 
900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
908 |D 1  |a research-article  |2 jats 
949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-springer 
950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1007/s10533-015-0120-5  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Hall  |D Steven  |u Department of Environmental Science, Policy, and Management, University of California-Berkeley, 130 Mulford Hall, UC Berkeley, 94720, Berkeley, CA, USA  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Silver  |D Whendee  |u Department of Environmental Science, Policy, and Management, University of California-Berkeley, 130 Mulford Hall, UC Berkeley, 94720, Berkeley, CA, USA  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Biogeochemistry  |d Springer International Publishing  |g 125/2(2015-09-01), 149-165  |x 0168-2563  |q 125:2<149  |1 2015  |2 125  |o 10533