The use of fossil fuels and fertilizers has increased the amount of biologically reactive nitrogen in the atmosphere over the past century. As a consequence, forests in industrialized regions have experienced greater rates of nitrogen deposition in recent decades. This unintended fertilization has stimulated forest growth, but has also affected soil microbial activity, and thus the recycling of soil carbon and nutrients. A meta-analysis suggests that nitrogen deposition impedes organic matter decomposition, and thus stimulates carbon sequestration, in temperate forest soils where nitrogen is not limiting microbial growth. The concomitant reduction in soil carbon emissions is substantial, and equivalent in magnitude to the amount of carbon taken up by trees owing to nitrogen fertilization. As atmospheric nitrogen levels continue to rise, increased nitrogen deposition could spread to older, more weathered soils, as found in the tropics; however, soil carbon cycling in tropical forests cannot yet be assessed

During each of the late Pleistocene glacial-interglacial transitions, atmospheric carbon dioxide concentrations rose by almost 100 ppm. The sources of this carbon are unclear, and efforts to identify them are hampered by uncertainties in the magnitude of carbon reservoirs and fluxes under glacial conditions. Here we use oxygen isotope measurements from air trapped in ice cores and ocean carbon-cycle modelling to estimate terrestrial and oceanic gross primary productivity during the Last Glacial Maximum. We find that the rate of gross terrestrial primary production during the Last Glacial Maximum was about 40 +/- 10 Pg C yr(-1), half that of the pre-industrial Holocene. Despite the low levels of photosynthesis, we estimate that the late glacial terrestrial biosphere contained only 330 Pg less carbon than pre-industrial levels. We infer that the area covered by carbon-rich but unproductive biomes such as tundra and cold steppes was significantly larger during the Last Glacial Maximum, consistent with palaeoecological data. Our data also indicate the presence of an inert carbon pool of 2,300 Pg C, about 700 Pg larger than the inert carbon locked in permafrost today. We suggest that the disappearance of this carbon pool at the end of the Last Glacial Maximum may have contributed to the deglacial rise in atmospheric carbon dioxide concentrations

Abstract. Since the mid-20th century, nitrogen (N) deposition has shown an increasing trend in the Tibetan Plateau (TP), where alpine ecosystems are sensitive to elevated N deposition. However, the quantitative characterization of N deposition in the TP remains unclear, due in most part to the lack of in situ measurement. Using the Tibetan Observation and Research Platform network, we conducted short-term in situ measurements of major ions (NO3−, Cl−, SO42−, NH4+, Na+, K+, Ca2+, and Mg2+) wet deposition at five remote sites in the TP during 2011–2013. At Southeast Tibet Station, Nam Co Station, Qomolangma Station, Ngari Station, and Muztagh Ata Station, the NH4+–N wet deposition was 0.63, 0.68, 0.92, 0.36, and 1.25 kg N ha−1 yr−1, respectively; the NO3−–N wet deposition was 0.28, 0.24, 0.03, 0.08, and 0.30 kg N ha−1 yr−1, respectively; and the inorganic N wet deposition was 0.91, 0.92, 0.94, 0.44, and 1.55 kg N ha−1 yr−1, respectively. The inorganic N wet deposition mainly occurred in the form of NH4+–N during summer at all sites. Results of enrichment factor analysis and principal component analysis demonstrated that both NH4+–N and NO3−–N wet deposition in the TP were mainly influenced by anthropogenic activities. Backward trajectory analysis showed that the inorganic N deposition at Muztagh Ata Station was mainly transported from central Asia and the Middle East through westerlies. At Southeast Tibet Station, Nam Co Station, Qomolangma Station, and Ngari Station, the inorganic N deposition was mainly contributed by anthropogenic sources in south Asia, and was mainly transported by the Indian monsoon. Combining site-scale in situ measurements of inorganic N wet deposition in this and previous studies, the average wet deposition of atmospheric NH4+–N, NO3−–N, and inorganic N in the TP was estimated to be 1.06, 0.51, and 1.58 kg N ha−1 yr−1, respectively. The average NH4+–N : NO3−–N ratio in precipitation in the TP was approximately 2 : 1. Results from the present study suggest that earlier estimations based on chemical transport model simulations and/or limited field measurements likely overestimated substantially the regional inorganic N wet deposition in the TP. To clarify the total N deposition in the TP more clearly, it is essential to conduct long-term monitoring of both wet and dry deposition of atmospheric N in various climate zones in the TP in the future.

Abstract. Future climate change will have impact on global and regional terrestrial carbon balances. The fate of African tropical forests over the 21st century has been investigated through global coupled climate carbon cycle model simulations. Under the SRES-A2 socio-economic CO 2 emission scenario of the IPCC, and using the Institut Pierre Simon Laplace coupled ocean-terrestrial carbon cycle and climate model, IPSL-CM4-LOOP, we found that the warming over African ecosystems induces a reduction of net ecosystem productivity, making a 38% contribution to the global climate-carbon cycle positive feedback. Most of this contribution comes from African grasslands, followed by African savannahs, African tropical forest contributing little to the global climate-carbon feedback. However, the vulnerability of the African rainforest ecosystem is quite large. In contrast, the Amazon forest, despite its lower vulnerability, has a much larger overall contribution due to its 6 times larger extent.

Stand-replacing fires are the dominant fire type in North American boreal forest and leave a historical legacy of a mosaic landscape of different aged forest cohorts. To accurately quantify the role of fire in historical and current regional forest carbon balance using models, one needs to explicitly simulate the new forest cohort that is established after fire. The present study adapted the global process-based vegetation model ORCHIDEE to simulate boreal forest fire CO₂ emissions and follow-up recovery after a stand-replacing fire, with representation of postfire new cohort establishment, forest stand structure and the following self-thinning process. Simulation results are evaluated against three clusters of postfire forest chronosequence observations in Canada and Alaska. Evaluation variables for simulated postfire carbon dynamics include: fire carbon emissions, CO₂ fluxes (gross primary production, total ecosystem respiration and net ecosystem exchange), leaf area index (LAI), and biometric measurements (aboveground biomass carbon, forest floor carbon, woody debris carbon, stand individual density, stand basal area, and mean diameter at breast height). The model simulation results, when forced by local climate and the atmospheric CO₂ history on each chronosequence site, generally match the observed CO₂ fluxes and carbon stock data well, with model-measurement mean square root of deviation comparable with measurement accuracy (for CO₂ flux ~100 g C m⁻² yr⁻¹, for biomass carbon ~1000 g C m⁻² and for soil carbon ~2000 g C m⁻²). We find that current postfire forest carbon sink on evaluation sites observed by chronosequence methods is mainly driven by historical atmospheric CO₂ increase when forests recover from fire disturbance. Historical climate generally exerts a negative effect, probably due to increasing water stress caused by significant temperature increase without sufficient increase in precipitation. Our simulation results demonstrate that a global vegetation model such as ORCHIDEE is able to capture the essential ecosystem processes in fire-disturbed boreal forests and produces satisfactory results in terms of both carbon fluxes and carbon stocks evolution after fire, making it suitable for regional simulations in boreal regions where fire regimes play a key role on ecosystem carbon balance