USGS Science⌕ Search

USGS · 70047659

Response of global soil consumption of atmospheric methane to changes in atmospheric climate and nitrogen deposition

Abstract

Soil consumption of atmospheric methane plays an important secondary role in regulating the atmospheric CH 4 budget, next to the dominant loss mechanism involving reaction with the hydroxyl radical (OH). Here we used a process-based biogeochemistry model to quantify soil consumption during the 20th and 21st centuries. We estimated that global soils consumed 32–36 Tg CH 4 yr −1 during the 1990s. Natural ecosystems accounted for 84% of the total consumption, and agricultural ecosystems only consumed 5 Tg CH 4 yr −1 in our estimations. During the twentieth century, the consumption rates increased at 0.03–0.20 Tg CH 4 yr −2 with seasonal amplitudes increasing from 1.44 to 3.13 Tg CH 4 month −1 . Deserts, shrublands, and xeric woodlands were the largest sinks. Atmospheric CH 4 concentrations and soil moisture exerted significant effects on the soil consumption while nitrogen deposition had a moderate effect. During the 21st century, the consumption is predicted to increase at 0.05-1.0 Tg CH 4 yr −2 , and total consumption will reach 45–140 Tg CH 4 yr −1 at the end of the 2090s, varying under different future climate scenarios. Dry areas will persist as sinks, boreal ecosystems will become stronger sinks, mainly due to increasing soil temperatures. Nitrogen deposition will modestly reduce the future sink strength at the global scale. When we incorporated the estimated global soil consumption into our chemical transport model simulations, we found that nitrogen deposition suppressed the total methane sink by 26 Tg during the period 1998–2004, resulting in 6.6 ppb higher atmospheric CH 4 mixing ratios compared to without considering nitrogen deposition effects. On average, a cumulative increase of every 1 Tg soil CH 4 consumption decreased atmospheric CH 4 mixing ratios by 0.26 ppb during the period 1998–2004.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Qianlai Zhuang, Min Chen, Kai Xu, Jinyun Tang, Eri Saikawa, Yanyu Lu, Jerry M. Melillo, Ronald G. Prinn, A. David McGuire. 2013-08-09. Response of global soil consumption of atmospheric methane to changes in atmospheric climate and nitrogen deposition. https://doi.org/10.1002/gbc.20057

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related USGS reports

Blind spots in our understanding of the tropical nitrogen cycle

Understanding environmental controls on tropical nitrogen (N) cycling is critical for projecting flux rates and modeling ecosystem responses to rising CO 2 . Here, we ask whether geographic bias in field sampling may shape our understanding of N cycling by failing to capture the breadth of environmental heterogeneity within the tropics. We mapped empirical sampling locations of two major ecosystem N inputs and outputs—biological nitrogen fixation and denitrification—paired with a wide range of variables thought to influence N cycling. Both single and multi-variate analyses revealed that sampling density is greater in productive, wet, fertile, warmer tropical ecosystems with low seasonality—areas expected to have higher process rates—but biased away from spatially extensive biomes which may have high process rate variability and thus higher uncertainty. Even within tropical broadleaf forests, sampling is biased toward sites with unusually high soil fertility (N and phosphorus), potentially skewing biome-wide averages. Although some geographically undersampled regions share environmental characteristics with well-studied sites, others are unique, compromising inference from existing data. Finally, we find that while sampled field locations capture the range of N cycle process means/variances predicted by an ensemble of terrestrial biosphere models, this may be the result of circularity in model parameters and driving data rather than true coverage, including overrepresentation of forest plant functional types that may be parameterized from a small subset of sites. Data coverage expansion into areas with novel environmental conditions and higher uncertainty could be used to assess and improve model parameterization, as well as test general hypotheses.

Global Biogeochemical Cycles↗

Global carbon investment in terrestrial biological nitrogen fixation

Biological nitrogen (N) fixation (BNF) provides the N needed to produce proteins and other biological building blocks, helping feed humanity and mitigate climate change. Due to its high energetic cost compared to other forms of N acquisition, biotic investment in BNF indicates N limitation. Globally gridded BNF flux data provide an opportunity to determine the energetic investment in BNF across ecosystems, which would help reconcile conflicting indicators of N limitation. Here, we use a new BNF synthesis to quantify the relative importance of BNF in different N-fixing niches, in different biomes, and across the globe by calculating the fraction of net primary productivity (NPP) invested in BNF and the fraction of plant N acquisition provided by BNF. Larger fractions of non-agricultural NPP were invested in BNF in less-productive, higher-latitude biomes. This pattern was driven by biocrusts and mosses. Similarly, non-agricultural symbiotic N-fixing plants invested relatively more of their own NPP in BNF in less-productive, higher-latitude biomes. This symbiotic plant pattern was driven by shrubs and herbs, overriding the opposite pattern in trees. Symbiotic plants also acquired a higher fraction of their N from BNF at higher latitudes and in less productive biomes. Investments in symbiotic BNF were 10× higher in agricultural (2.9% of NPP) versus natural (0.29%) biomes, providing 26% versus 3.1% of ecosystem-scale plant N acquisition. These results support the paradigm of strong N limitation at higher latitudes, help understand the rarity of N-fixing trees at higher latitudes, underscore the dominance of human activity, and inform terrestrial biosphere models.

Global Biogeochemical Cycles↗

Erosional and hydrological controls on the age and thermochemical stability of particulate organic carbon in an Arctic river

Understanding the mechanisms that drive the mobilization and fate of organic carbon (OC) in Arctic landscapes is important for modeling the feedbacks among permafrost thaw, carbon cycling, and climate change. While significant progress has been made toward measuring in situ OC decomposition in permafrost soils and bulk particulate organic carbon (POC) export from Arctic rivers, few studies have distinguished the source and lability of POC across Arctic landscapes, limiting our ability to predict whether mobilized POC will be oxidized to CO 2 and CH 4 or buried in downstream depositional environments. This study uses ramped pyrolysis/oxidation radiocarbon (RPO- 14 C) analyses to investigate spatial and temporal variations in the thermochemical stability and radiocarbon content of fluvial POC during downstream transport from mountains to the coast in the Canning River (North Slope, Alaska). Fluvial POC in the headwaters is predominantly comprised of high activation energy, thermally recalcitrant petrogenic OC (OC petro ) derived from shale bedrock. Moving into the foothills and low-relief coastal plains, river bank erosion primarily drives mobilization of labile, low activation energy, soil-derived OC (OC soil ). Fluvial POC in mountainous upstream reaches consisted of ∼70% OC petro and just ∼30% OC soil , while POC in the downstream coastal plain reaches comprised ∼85% OC soil and ∼15% OC petro . The high relative lability of POC exported to the coast indicates high susceptibility to oxidation and microbial decomposition, which could enhance CO 2 release as the Arctic hydrologic cycle intensifies. However, the persistence of refractory OC petro in the suspended load indicates the potential for long-term burial of rock organic carbon in marine sediments.

Alaska↗