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1

PEISKER, M., and S. A. HENDERSON. "Carbon: terrestrial C4 plants." Plant, Cell and Environment 15, no. 9 (December 1992): 987–1004. http://dx.doi.org/10.1111/j.1365-3040.1992.tb01651.x.

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2

Keenan, T. F., and C. A. Williams. "The Terrestrial Carbon Sink." Annual Review of Environment and Resources 43, no. 1 (October 17, 2018): 219–43. http://dx.doi.org/10.1146/annurev-environ-102017-030204.

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Life on Earth comes in many forms, but all life-forms share a common element in carbon. It is the basic building block of biology, and by trapping radiation it also plays an important role in maintaining the Earth's atmosphere at a temperature hospitable to life. Like all matter, carbon can neither be created nor destroyed, but instead is continuously exchanged between ecosystems and the environment through a complex combination of physics and biology. In recent decades, these exchanges have led to an increased accumulation of carbon on the land surface: the terrestrial carbon sink. Over the past 10 years (2007–2016) the sink has removed an estimated 3.61 Pg C year−1from the atmosphere, which amounts to 33.7% of total anthropogenic emissions from industrial activity and land-use change. This sink constitutes a valuable ecosystem service, which has significantly slowed the rate of climate change. Here, we review current understanding of the underlying biological processes that govern the terrestrial carbon sink and their dependence on climate, atmospheric composition, and human interventions.
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3

Baldocchi, Dennis, Youngryel Ryu, and Trevor Keenan. "Terrestrial Carbon Cycle Variability." F1000Research 5 (September 26, 2016): 2371. http://dx.doi.org/10.12688/f1000research.8962.1.

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A growing literature is reporting on how the terrestrial carbon cycle is experiencing year-to-year variability because of climate anomalies and trends caused by global change. As CO2 concentration records in the atmosphere exceed 50 years and as satellite records reach over 30 years in length, we are becoming better able to address carbon cycle variability and trends. Here we review how variable the carbon cycle is, how large the trends in its gross and net fluxes are, and how well the signal can be separated from noise. We explore mechanisms that explain year-to-year variability and trends by deconstructing the global carbon budget. The CO2 concentration record is detecting a significant increase in the seasonal amplitude between 1958 and now. Inferential methods provide a variety of explanations for this result, but a conclusive attribution remains elusive. Scientists have reported that this trend is a consequence of the greening of the biosphere, stronger northern latitude photosynthesis, more photosynthesis by semi-arid ecosystems, agriculture and the green revolution, tropical temperature anomalies, or increased winter respiration. At the global scale, variability in the terrestrial carbon cycle can be due to changes in constituent fluxes, gross primary productivity, plant respiration and heterotrophic (microbial) respiration, and losses due to fire, land use change, soil erosion, or harvesting. It remains controversial whether or not there is a significant trend in global primary productivity (due to rising CO2, temperature, nitrogen deposition, changing land use, and preponderance of wet and dry regions). The degree to which year-to-year variability in temperature and precipitation anomalies affect global primary productivity also remains uncertain. For perspective, interannual variability in global gross primary productivity is relatively small (on the order of 2 Pg-C y-1) with respect to a large and uncertain background (123 +/- 4 Pg-C y-1), and detected trends in global primary productivity are even smaller (33 Tg-C y-2). Yet residual carbon balance methods infer that the terrestrial biosphere is experiencing a significant and growing carbon sink. Possible explanations for this large and growing net land sink include roles of land use change and greening of the land, regional enhancement of photosynthesis, and down regulation of plant and soil respiration with warming temperatures. Longer time series of variables needed to provide top-down and bottom-up assessments of the carbon cycle are needed to resolve these pressing and unresolved issues regarding how, why, and at what rates gross and net carbon fluxes are changing.
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4

Grossman, Jesse Muir. "Carbon in Terrestrial Systems." Journal of Sustainable Forestry 25, no. 1-2 (September 14, 2007): 17–41. http://dx.doi.org/10.1300/j091v25n01_02.

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5

Lalonde, K., A. V. Vähätalo, and Y. Gélinas. "Revisiting the disappearance of terrestrial dissolved organic matter in the ocean: a <i>δ</i><sup>13</sup>C study." Biogeosciences 11, no. 13 (July 15, 2014): 3707–19. http://dx.doi.org/10.5194/bg-11-3707-2014.

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Abstract. Organic carbon (OC) depleted in 13C is a widely used tracer for terrestrial organic matter (OM) in aquatic systems. Photochemical reactions can, however, change δ13C of dissolved organic carbon (DOC) when chromophoric, aromatic-rich terrestrial OC is selectively mineralized. We assessed the robustness of the δ13C signature of DOC (δ13CDOC) as a tracer for terrestrial OM by estimating its change during the photobleaching of chromophoric DOM (CDOM) from 10 large rivers. These rivers cumulatively account for approximately one-third of the world's freshwater discharge to the global ocean. Photobleaching of CDOM by simulated solar radiation was associated with the photochemical mineralization of 16 to 43% of the DOC and, by preferentially removing compounds depleted in 13C, caused a 1 to 2.9‰ enrichment in δ13C in the residual DOC. Such solar-radiation-induced photochemical isotopic shift could bias the calculations of terrestrial OM discharge in coastal oceans towards the marine end-member. Shifts in terrestrial δ13CDOC should be taken into account when constraining the terrestrial end-member in global calculation of terrestrially derived DOM in the world ocean.
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Lalonde, K., A. V. Vähätalo, and Y. Gélinas. "Revisiting the disappearance of terrestrial dissolved organic matter in the ocean: a <i>δ</i><sup>13</sup>C study." Biogeosciences Discussions 10, no. 11 (November 1, 2013): 17117–44. http://dx.doi.org/10.5194/bgd-10-17117-2013.

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Abstract. Organic carbon (OC) depleted in 13C is a widely used tracer for terrestrial OM in aquatic systems. Photochemical reactions can however change δ13C of dissolved organic carbon (DOC) when chromophoric, aromatic-rich terrestrial OC is selectively mineralized. We assessed the robustness of the δ13C signature of DOC (δ13CDOC) as a tracer for terrestrial OM by estimating its change during the photobleaching of chromophoric DOM (CDOM) from ten large rivers. These rivers cumulatively account for approximately 1/3 of the world's freshwater discharge to the global ocean. Photobleaching of CDOM by simulated solar radiation was associated with the photochemical mineralization of 16 to 43% of the DOC and, by preferentially removing compounds depleted in 13C, caused a 1 to 2.9‰ enrichment in δ13C in the residual DOC. Such solar radiation-induced photochemical isotopic shift biases the calculations of terrestrial OM discharge in coastal oceans towards the marine end-member. Shifts in terrestrial δ13CDOC should be taken into account when constraining the terrestrial end-member in global calculation of terrestrially derived DOM in the world ocean.
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7

Haverd, V., M. R. Raupach, P. R. Briggs, S. J. Davis, R. M. Law, C. P. Meyer, G. P. Peters, C. Pickett-Heaps, and B. Sherman. "The Australian terrestrial carbon budget." Biogeosciences 10, no. 2 (February 7, 2013): 851–69. http://dx.doi.org/10.5194/bg-10-851-2013.

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Abstract. This paper reports a study of the full carbon (C-CO2) budget of the Australian continent, focussing on 1990–2011 in the context of estimates over two centuries. The work is a contribution to the RECCAP (REgional Carbon Cycle Assessment and Processes) project, as one of numerous regional studies. In constructing the budget, we estimate the following component carbon fluxes: net primary production (NPP); net ecosystem production (NEP); fire; land use change (LUC); riverine export; dust export; harvest (wood, crop and livestock) and fossil fuel emissions (both territorial and non-territorial). Major biospheric fluxes were derived using BIOS2 (Haverd et al., 2012), a fine-spatial-resolution (0.05°) offline modelling environment in which predictions of CABLE (Wang et al., 2011), a sophisticated land surface model with carbon cycle, are constrained by multiple observation types. The mean NEP reveals that climate variability and rising CO2 contributed 12 &amp;pm; 24 (1σ error on mean) and 68 &amp;pm; 15 TgC yr−1, respectively. However these gains were partially offset by fire and LUC (along with other minor fluxes), which caused net losses of 26 &amp;pm; 4 TgC yr−1 and 18 &amp;pm; 7 TgC yr−1, respectively. The resultant net biome production (NBP) is 36 &amp;pm; 29 TgC yr−1, in which the largest contributions to uncertainty are NEP, fire and LUC. This NBP offset fossil fuel emissions (95 &amp;pm; 6 TgC yr−1) by 38 &amp;pm; 30%. The interannual variability (IAV) in the Australian carbon budget exceeds Australia's total carbon emissions by fossil fuel combustion and is dominated by IAV in NEP. Territorial fossil fuel emissions are significantly smaller than the rapidly growing fossil fuel exports: in 2009–2010, Australia exported 2.5 times more carbon in fossil fuels than it emitted by burning fossil fuels.
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8

Haverd, V., M. R. Raupach, P. R. Briggs, J. G. Canadell, S. J. Davis, R. M. Law, C. P. Meyer, G. P. Peters, C. Pickett-Heaps, and B. Sherman. "The Australian terrestrial carbon budget." Biogeosciences Discussions 9, no. 9 (September 12, 2012): 12259–308. http://dx.doi.org/10.5194/bgd-9-12259-2012.

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Abstract. This paper reports a study of the full carbon (C-CO2) budget of the Australian continent, focussing on 1990–2011 in the context of estimates over two centuries. The work is a contribution to the RECCAP (REgional Carbon Cycle Assessment and Processes) project, as one of numerous regional studies being synthesised in RECCAP. In constructing the budget, we estimate the following component carbon fluxes: Net Primary Production (NPP); Net Ecosystem Production (NEP); fire; Land Use Change (LUC); riverine export; dust export; harvest (wood, crop and livestock) and fossil fuel emissions (both territorial and non-territorial). The mean NEP reveals that climate variability and rising CO2 contributed 12 ± 29 (1σ error on mean) and 68 ± 35 Tg C yr−1 respectively. However these gains were partially offset by fire and LUC (along with other minor fluxes), which caused net losses of 31 ± 5 Tg C yr−1 and 18 ± 7 Tg C yr−1 respectively. The resultant Net Biome Production (NBP) of 31 ± 35 Tg C yr−1 offset fossil fuel emissions (95 ± 6 Tg C yr−1) by 32 ± 36%. The interannual variability (IAV) in the Australian carbon budget exceeds Australia's total carbon emissions by fossil fuel combustion and is dominated by IAV in NEP. Territorial fossil fuel emissions are significantly smaller than the rapidly growing fossil fuel exports: in 2009–2010, Australia exported 2.5 times more carbon in fossil fuels than it emitted by burning fossil fuels.
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9

Long, Steve, G. W. Koch, and H. A. Mooney. "Carbon Dioxide and Terrestrial Ecosystems." Journal of Applied Ecology 34, no. 2 (April 1997): 543. http://dx.doi.org/10.2307/2404900.

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10

Tranvik, L. J., and M. Jansson. "Terrestrial export of organic carbon." Nature 415, no. 6874 (February 2002): 861–62. http://dx.doi.org/10.1038/415861b.

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11

Evans, C. D., C. Freeman, D. T. Monteith, B. Reynolds, and N. Fenner. "Terrestrial export of organic carbon." Nature 415, no. 6874 (February 2002): 862. http://dx.doi.org/10.1038/415862a.

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12

Morison, James I. L. "Carbon dioxide and terrestrial ecosystems." Trends in Ecology & Evolution 11, no. 12 (December 1996): 526–27. http://dx.doi.org/10.1016/0169-5347(96)88914-2.

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13

Smith, T. M., W. P. Cramer, R. K. Dixon, R. Leemans, R. P. Neilson, and A. M. Solomon. "The global terrestrial carbon cycle." Water, Air, & Soil Pollution 70, no. 1-4 (October 1993): 19–37. http://dx.doi.org/10.1007/bf01104986.

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14

Evans, Martin, Timothy Quine, and Nikolaus Kuhn. "Geomorphology and terrestrial carbon cycling." Earth Surface Processes and Landforms 38, no. 1 (October 24, 2012): 103–5. http://dx.doi.org/10.1002/esp.3337.

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15

He, Qiaoning, Weimin Ju, and Xinchuan Li. "Response of Global Terrestrial Carbon Fluxes to Drought from 1981 to 2016." Atmosphere 14, no. 2 (January 23, 2023): 229. http://dx.doi.org/10.3390/atmos14020229.

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Precipitation plays a dominant role in regulating terrestrial carbon fluxes. In concert with global warming, aridity has been increasing during recent decades in most parts of the world. How global terrestrial carbon fluxes respond to this change, however, is still unclear. Using a remote-sensing-driven, process-based model, the Boreal Ecosystem Productivity Simulator (BEPS), this study investigated the responses of global terrestrial carbon fluxes to meteorological drought, which were characterized by the standardized precipitation evapotranspiration index (SPEI). The results showed that the response of terrestrial carbon fluxes to drought exhibited distinguishable spatial heterogeneity. In most regions, terrestrial carbon fluxes responded strongly to drought. With an increase in annual water balance (annual precipitation minus annual potential evapotranspiration), the response of carbon fluxes to drought became weaker. The lagged time of terrestrial carbon fluxes responding to drought decreased with the increasing strength of carbon fluxes in response to drought. The sensitivity of terrestrial carbon fluxes to drought also showed noticeable spatial heterogeneity. With an increase in annual water balance, the sensitivity first increased and then decreased. Terrestrial carbon fluxes exhibited the highest sensitivity to drought in semi-arid areas.
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16

Houghton, R. A. "Terrestrial sources and sinks of carbon inferred from terrestrial data." Tellus B: Chemical and Physical Meteorology 48, no. 4 (January 1996): 420–32. http://dx.doi.org/10.3402/tellusb.v48i4.15923.

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17

HOUGHTON, R. A. "Terrestrial sources and sinks of carbon inferred from terrestrial data." Tellus B 48, no. 4 (September 1996): 420–32. http://dx.doi.org/10.1034/j.1600-0889.1996.t01-3-00002.x.

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18

Houghton, Richard A. "Terrestrial fluxes of carbon in GCP carbon budgets." Global Change Biology 26, no. 5 (March 24, 2020): 3006–14. http://dx.doi.org/10.1111/gcb.15050.

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19

Jing, Zhen, and Jing Yi Li. "Comment on Credible Terrestrial Carbon Market Mechanism and Future Development." Advanced Materials Research 734-737 (August 2013): 1824–28. http://dx.doi.org/10.4028/www.scientific.net/amr.734-737.1824.

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Credible terrestrial carbon market mechanism is a new mechanism which terrestrial carbon Organization proposed in July 2008, namely using the credible way carbon market, bring terrestrial carbon of developing countries into the international action to combat climate change. The paper starts from the background of credible terrestrial carbon market mechanism, introduces the content and implementation of the mechanism and discusses the related legal issues, lastly explores its future development prospect.
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20

Lin, Tong, Dafang Wu, Muzhuang Yang, Peifang Ma, Yanyan Liu, Feng Liu, and Ziying Gan. "Evolution and Simulation of Terrestrial Ecosystem Carbon Storage and Sustainability Assessment in Karst Areas: A Case Study of Guizhou Province." International Journal of Environmental Research and Public Health 19, no. 23 (December 4, 2022): 16219. http://dx.doi.org/10.3390/ijerph192316219.

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Against the background of “carbon neutrality” and sustainable development goals, it is of great significance to assess the carbon storage changes and sustainability of terrestrial ecosystems in order to maintain the coordinated sustainable development of regional ecological economies and the balance of terrestrial ecosystems. In this study, the terrestrial ecosystem carbon storage in Guizhou from 2010 to 2020 was assessed with the InVEST model. Using the PLUS model, the distribution of terrestrial ecosystem carbon storage by 2030 and 2050 was predicted. The current sustainable development level of the terrestrial ecosystem of Guizhou was evaluated after establishing an index system based on SDGs. The results showed the following: (1) From 2010 to 2020, the terrestrial ecosystem carbon storage decreased by 1106.68 × 104 Mg. The area and carbon storage of the forest and farmland ecosystems decreased while the area and carbon storage of the grassland and settlement ecosystems increased. (2) Compared with 2020, the terrestrial ecosystem carbon storage will be reduced by 4091.43 × 104 Mg by 2030. Compared with 2030, the terrestrial ecosystem carbon storage will continue to decrease by 3833.25 × 104 Mg by 2050. (3) In 2020, the average score of the sustainable development of the terrestrial ecosystem was 0.4300. Zunyi City had the highest sustainable development score of 0.6255, and Anshun had the lowest sustainable development score of 0.3236. Overall, the sustainable development of the terrestrial ecosystem of Guizhou was found to be high in the north, low in the south, high in the east, and low in the west. The sustainable regional development of the terrestrial ecosystem of Guizhou was found to be unbalanced, and the carbon storage of the terrestrial ecosystem will keep decreasing in the future. In order to improve the sustainable development capacity of the terrestrial ecosystem, the government needs to take certain measures, such as returning farmland to forests and grasslands, curbing soil erosion, and actively supervising.
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21

Sokolov, Andrei P., David W. Kicklighter, Jerry M. Melillo, Benjamin S. Felzer, C. Adam Schlosser, and Timothy W. Cronin. "Consequences of Considering Carbon–Nitrogen Interactions on the Feedbacks between Climate and the Terrestrial Carbon Cycle." Journal of Climate 21, no. 15 (August 1, 2008): 3776–96. http://dx.doi.org/10.1175/2008jcli2038.1.

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Abstract The impact of carbon–nitrogen dynamics in terrestrial ecosystems on the interaction between the carbon cycle and climate is studied using an earth system model of intermediate complexity, the MIT Integrated Global Systems Model (IGSM). Numerical simulations were carried out with two versions of the IGSM’s Terrestrial Ecosystems Model, one with and one without carbon–nitrogen dynamics. Simulations show that consideration of carbon–nitrogen interactions not only limits the effect of CO2 fertilization but also changes the sign of the feedback between the climate and terrestrial carbon cycle. In the absence of carbon–nitrogen interactions, surface warming significantly reduces carbon sequestration in both vegetation and soil by increasing respiration and decomposition (a positive feedback). If plant carbon uptake, however, is assumed to be nitrogen limited, an increase in decomposition leads to an increase in nitrogen availability stimulating plant growth. The resulting increase in carbon uptake by vegetation exceeds carbon loss from the soil, leading to enhanced carbon sequestration (a negative feedback). Under very strong surface warming, however, terrestrial ecosystems become a carbon source whether or not carbon–nitrogen interactions are considered. Overall, for small or moderate increases in surface temperatures, consideration of carbon–nitrogen interactions result in a larger increase in atmospheric CO2 concentration in the simulations with prescribed carbon emissions. This suggests that models that ignore terrestrial carbon–nitrogen dynamics will underestimate reductions in carbon emissions required to achieve atmospheric CO2 stabilization at a given level. At the same time, compensation between climate-related changes in the terrestrial and oceanic carbon uptakes significantly reduces uncertainty in projected CO2 concentration.
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22

Keaveney, Evelyn M., Paula J. Reimer, and Robert H. Foy. "Young, Old, and Weathered Carbon—Part 2: Using Radiocarbon and Stable Isotopes to Identify Terrestrial Carbon Support of the Food Web in an Alkaline, Humic Lake." Radiocarbon 57, no. 3 (2015): 425–38. http://dx.doi.org/10.2458/azu_rc.57.18355.

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Carbon (C) and nitrogen (N) stable isotope analysis (SIA) has been used to identify the terrestrial subsidy of freshwater food webs. However, SIA fails to differentiate between the contributions of old and recently fixed terrestrial C and consequently cannot fully determine the source, age, and biochemical quality of terrestrial carbon. Natural abundance radiocarbon (Δ14C) was used to examine the age and origin of carbon in Lower Lough Erne, Northern Ireland. 14C and stable isotope values were obtained from invertebrate, algae, and fish samples, and the results indicate that terrestrial organic C is evident at all trophic levels. High winter δ15N values in calanoid zooplankton (δ15N = 24‰) relative to phytoplankton and particulate organic matter (δ15N = 6‰ and 12‰, respectively) may reflect several microbial trophic levels between terrestrial C and calanoid invertebrates. Winter and summer calanoid Δ14C values show a seasonal switch between autochthonous and terrestrial carbon sources. Fish Δ14C values indicate terrestrial support at the highest trophic levels in littoral and pelagic food webs. 14C therefore is useful in attributing the source of carbon in freshwater in addition to tracing the pathway of terrestrial carbon through the food web.
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23

Zaehle, S. "Terrestrial nitrogen–carbon cycle interactions at the global scale." Philosophical Transactions of the Royal Society B: Biological Sciences 368, no. 1621 (July 5, 2013): 20130125. http://dx.doi.org/10.1098/rstb.2013.0125.

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Interactions between the terrestrial nitrogen (N) and carbon (C) cycles shape the response of ecosystems to global change. However, the global distribution of nitrogen availability and its importance in global biogeochemistry and biogeochemical interactions with the climate system remain uncertain. Based on projections of a terrestrial biosphere model scaling ecological understanding of nitrogen–carbon cycle interactions to global scales, anthropogenic nitrogen additions since 1860 are estimated to have enriched the terrestrial biosphere by 1.3 Pg N, supporting the sequestration of 11.2 Pg C. Over the same time period, CO 2 fertilization has increased terrestrial carbon storage by 134.0 Pg C, increasing the terrestrial nitrogen stock by 1.2 Pg N. In 2001–2010, terrestrial ecosystems sequestered an estimated total of 27 Tg N yr −1 (1.9 Pg C yr −1 ), of which 10 Tg N yr −1 (0.2 Pg C yr −1 ) are due to anthropogenic nitrogen deposition. Nitrogen availability already limits terrestrial carbon sequestration in the boreal and temperate zone, and will constrain future carbon sequestration in response to CO 2 fertilization (regionally by up to 70% compared with an estimate without considering nitrogen–carbon interactions). This reduced terrestrial carbon uptake will probably dominate the role of the terrestrial nitrogen cycle in the climate system, as it accelerates the accumulation of anthropogenic CO 2 in the atmosphere. However, increases of N 2 O emissions owing to anthropogenic nitrogen and climate change (at a rate of approx. 0.5 Tg N yr −1 per 1°C degree climate warming) will add an important long-term climate forcing.
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Wei, Ning, Jianyang Xia, Jian Zhou, Lifen Jiang, Erqian Cui, Jiaye Ping, and Yiqi Luo. "Evolution of Uncertainty in Terrestrial Carbon Storage in Earth System Models from CMIP5 to CMIP6." Journal of Climate 35, no. 17 (September 1, 2022): 5483–99. http://dx.doi.org/10.1175/jcli-d-21-0763.1.

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Abstract The spatial and temporal variations in terrestrial carbon storage play a pivotal role in regulating future climate change. However, Earth system models (ESMs), which have coupled the terrestrial biosphere and atmosphere, show great uncertainty in simulating the global land carbon storage. Here, based on multiple global datasets and a traceability analysis, we diagnosed the uncertainty source of terrestrial carbon storage in 22 ESMs that participated in phases 5 and 6 of the Coupled Model Intercomparison Project (CMIP5 and CMIP6). The modeled global terrestrial carbon storage has converged among ESMs from CMIP5 (1936.9 ± 739.3 PgC) to CMIP6 (1774.4 ± 439.0 PgC) but is persistently lower than the observation-based estimates (2285 ± 669 PgC). By further decomposing terrestrial carbon storage into net primary production (NPP) and ecosystem carbon residence time (τE), we found that the decreased intermodel spread in land carbon storage primarily resulted from more accurate simulations on NPP among ESMs from CMIP5 to CMIP6. The persistent underestimation of land carbon storage was caused by the biased τE. In CMIP5 and CMIP6, the modeled τE was far shorter than the observation-based estimates. The potential reasons for the biased τE could be the lack of or incomplete representation of nutrient limitation, vertical soil biogeochemistry, and the permafrost carbon cycle. Moreover, the modeled τE became the key driver for the intermodel spread in global land carbon storage in CMIP6. Overall, our study indicates that CMIP6 models have greatly improved the terrestrial carbon cycle, with a decreased model spread in global terrestrial carbon storage and less uncertain productivity. However, more efforts are needed to understand and reduce the persistent data–model disagreement on carbon storage and residence time in the terrestrial biosphere.
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Butman, David, Sarah Stackpoole, Edward Stets, Cory P. McDonald, David W. Clow, and Robert G. Striegl. "Aquatic carbon cycling in the conterminous United States and implications for terrestrial carbon accounting." Proceedings of the National Academy of Sciences 113, no. 1 (December 22, 2015): 58–63. http://dx.doi.org/10.1073/pnas.1512651112.

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Inland water ecosystems dynamically process, transport, and sequester carbon. However, the transport of carbon through aquatic environments has not been quantitatively integrated in the context of terrestrial ecosystems. Here, we present the first integrated assessment, to our knowledge, of freshwater carbon fluxes for the conterminous United States, where 106 (range: 71–149) teragrams of carbon per year (TgC⋅y−1) is exported downstream or emitted to the atmosphere and sedimentation stores 21 (range: 9–65) TgC⋅y−1in lakes and reservoirs. We show that there is significant regional variation in aquatic carbon flux, but verify that emission across stream and river surfaces represents the dominant flux at 69 (range: 36–110) TgC⋅y−1or 65% of the total aquatic carbon flux for the conterminous United States. Comparing our results with the output of a suite of terrestrial biosphere models (TBMs), we suggest that within the current modeling framework, calculations of net ecosystem production (NEP) defined as terrestrial only may be overestimated by as much as 27%. However, the internal production and mineralization of carbon in freshwaters remain to be quantified and would reduce the effect of including aquatic carbon fluxes within calculations of terrestrial NEP. Reconciliation of carbon mass–flux interactions between terrestrial and aquatic carbon sources and sinks will require significant additional research and modeling capacity.
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26

Cole, Jonathan J., Jonathan J. Cole, Nina F. Caraco, and Nina F. Caraco. "Carbon in catchments: connecting terrestrial carbon losses with aquatic metabolism." Marine and Freshwater Research 52, no. 1 (2001): 101. http://dx.doi.org/10.1071/mf00084.

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For a majority of aquatic ecosystems, respiration (R) exceeds autochthonous gross primary production (GPP). These systems have negative net ecosystem production ([NEP]=[GPP]–R) and ratios of [GPP]/R of <1. This net heterotrophy can be sustained only if aquatic respiration is subsidized by organic inputs from the catchment. Such subsidies imply that organic materials that escaped decomposition in the terrestrial environment must become susceptible to decomposition in the linked aquatic environment. Using a moderate-sized catchment in North America, the Hudson River (catchment area 33500 km2), evidence is presented for the magnitude of net heterotrophy. All approaches (CO2 gas flux; O2 gas flux; budget and gradient of dissolved organic C; and the summed components of primary production and respiration within the ecosystem) indicate that system respiration exceeds gross primary production by ~200 g C m-2 year-1. Highly 14C-depleted C of ancient terrestrial origin (1000–5000 years old) may be an important source of labile organic matter to this riverine system and support this excess respiration. The mechanisms by which organic matter is preserved for centuries to millennia in terrestrial soils and decomposed in a matter of weeks in a river connect modern riverine metabolism to historical terrestrial conditions.
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27

Kao, S. J., R. G. Hilton, K. Selvaraj, M. Dai, F. Zehetner, J. C. Huang, S. C. Hsu, et al. "Preservation of terrestrial organic carbon in marine sediments off shore Taiwan: mountain building and atmospheric carbon dioxide sequestration." Earth Surface Dynamics Discussions 1, no. 1 (July 17, 2013): 177–206. http://dx.doi.org/10.5194/esurfd-1-177-2013.

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Abstract. Geological sequestration of atmospheric carbon dioxide (CO2) can be achieved by the erosion of organic carbon (OC) from the terrestrial biosphere and its burial in long-lived marine sediments. Rivers on mountain islands of Oceania in the western Pacific have very high rates of OC export to the ocean, yet its preservation offshore remains poorly constrained. Here we use the OC content (Corg, %), radiocarbon (Δ14Corg) and stable isotope (δ13Corg) composition of sediments offshore Taiwan to assess the fate of terrestrial OC. We account for rock-derived fossil OC to assess the preservation of OC eroded from the terrestrial biosphere (non-fossil OC) during flood discharges (hyperpycnal river plumes) and when river inputs are dispersed more widely (hypopycnal). The Corg, Δ14Corg and δ13Corg of marine sediment traps and cores indicate that during flood discharges, terrestrial OC is transferred efficiently to the deep ocean and accumulates offshore with little evidence for terrestrial OC loss. In marine sediments fed by dispersive river inputs, the Corg, Δ14Corg and δ13Corg are consistent with mixing of marine OC and terrestrial OC and suggest that efficient preservation of terrestrial OC (> 70%) is also associated with hypopycnal delivery. Re-burial of fossil OC is pervasive. Our findings from Taiwan suggest that erosion and marine burial of terrestrial non-fossil OC may sequester > 8 TgC yr−1 across Oceania, a significant geological CO2 sink which requires better constraint. We postulate that mountain islands of Oceania provide strong link between tectonic uplift and the carbon cycle, one moderated by the climatic variability that controls terrestrial OC delivery to the ocean.
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28

Kao, S. J., R. G. Hilton, K. Selvaraj, M. Dai, F. Zehetner, J. C. Huang, S. C. Hsu, et al. "Preservation of terrestrial organic carbon in marine sediments offshore Taiwan: mountain building and atmospheric carbon dioxide sequestration." Earth Surface Dynamics 2, no. 1 (March 4, 2014): 127–39. http://dx.doi.org/10.5194/esurf-2-127-2014.

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Abstract. Geological sequestration of atmospheric carbon dioxide (CO2) can be achieved by the erosion of organic carbon (OC) from the terrestrial biosphere and its burial in long-lived marine sediments. Rivers on mountain islands of Oceania in the western Pacific have very high rates of OC export to the ocean, yet its preservation offshore remains poorly constrained. Here we use the OC content (Corg, %), radiocarbon (Δ 14Corg) and stable isotope (δ13Corg) composition of sediments offshore Taiwan to assess the fate of terrestrial OC, using surface, sub-surface and Holocene sediments. We account for rock-derived OC to assess the preservation of OC eroded from the terrestrial biosphere and the associated CO2 sink during flood discharges (hyperpycnal river plumes) and when river inputs are dispersed more widely (hypopycnal). The Corg, Δ14Corg and δ 13Corg of marine sediment traps and cores indicate that during flood discharges, terrestrial OC can be transferred efficiently down submarine canyons to the deep ocean and accumulates offshore with little evidence for terrestrial OC loss. In marine sediments fed by dispersive river inputs, the Corg, Δ14Corg and δ 13Corg are consistent with mixing of terrestrial OC with marine OC and suggest that efficient preservation of terrestrial OC (>70%) is also associated with hypopycnal delivery. Sub-surface and Holocene sediments indicate that this preservation is long-lived on millennial timescales. Re-burial of rock-derived OC is pervasive. Our findings from Taiwan suggest that erosion and offshore burial of OC from the terrestrial biosphere may sequester >8 TgC yr−1 across Oceania, a significant geological CO2 sink which requires better constraint. We postulate that mountain islands of Oceania provide a strong link between tectonic uplift and the carbon cycle, one moderated by the climatic variability which controls terrestrial OC delivery to the ocean.
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29

Wisniewski, J., RK Dixon, JD Kinsman, RN Sampson, and AE Lugo. "Carbon dioxide sequestration in terrestrial ecosystems." Climate Research 3 (1993): 1–5. http://dx.doi.org/10.3354/cr003001.

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30

SCHIMEL, DAVID S. "Terrestrial ecosystems and the carbon cycle." Global Change Biology 1, no. 1 (February 1995): 77–91. http://dx.doi.org/10.1111/j.1365-2486.1995.tb00008.x.

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31

Crowley, Thomas J. "Ice Age terrestrial carbon changes revisited." Global Biogeochemical Cycles 9, no. 3 (September 1995): 377–89. http://dx.doi.org/10.1029/95gb01107.

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32

Bird, Michael I., Jon Lloyd, and Graham D. Farquhar. "Terrestrial carbon storage at the LGM." Nature 371, no. 6498 (October 1994): 566. http://dx.doi.org/10.1038/371566a0.

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33

Seneviratne, Gamini. "Global warming and terrestrial carbon sequestration." Journal of Biosciences 28, no. 6 (December 2003): 653–55. http://dx.doi.org/10.1007/bf02708423.

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34

Luo, Yiqi, Trevor F. Keenan, and Matthew Smith. "Predictability of the terrestrial carbon cycle." Global Change Biology 21, no. 5 (December 3, 2014): 1737–51. http://dx.doi.org/10.1111/gcb.12766.

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35

Kinsman, John D., and Mark C. Trexler. "Terrestrial carbon management and electric utilities." Water, Air, & Soil Pollution 70, no. 1-4 (October 1993): 545–60. http://dx.doi.org/10.1007/bf01105021.

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36

Bloom, A. Anthony, Jean-François Exbrayat, Ivar R. van der Velde, Liang Feng, and Mathew Williams. "The decadal state of the terrestrial carbon cycle: Global retrievals of terrestrial carbon allocation, pools, and residence times." Proceedings of the National Academy of Sciences 113, no. 5 (January 19, 2016): 1285–90. http://dx.doi.org/10.1073/pnas.1515160113.

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The terrestrial carbon cycle is currently the least constrained component of the global carbon budget. Large uncertainties stem from a poor understanding of plant carbon allocation, stocks, residence times, and carbon use efficiency. Imposing observational constraints on the terrestrial carbon cycle and its processes is, therefore, necessary to better understand its current state and predict its future state. We combine a diagnostic ecosystem carbon model with satellite observations of leaf area and biomass (where and when available) and soil carbon data to retrieve the first global estimates, to our knowledge, of carbon cycle state and process variables at a 1° × 1° resolution; retrieved variables are independent from the plant functional type and steady-state paradigms. Our results reveal global emergent relationships in the spatial distribution of key carbon cycle states and processes. Live biomass and dead organic carbon residence times exhibit contrasting spatial features (r = 0.3). Allocation to structural carbon is highest in the wet tropics (85–88%) in contrast to higher latitudes (73–82%), where allocation shifts toward photosynthetic carbon. Carbon use efficiency is lowest (0.42–0.44) in the wet tropics. We find an emergent global correlation between retrievals of leaf mass per leaf area and leaf lifespan (r = 0.64–0.80) that matches independent trait studies. We show that conventional land cover types cannot adequately describe the spatial variability of key carbon states and processes (multiple correlation median = 0.41). This mismatch has strong implications for the prediction of terrestrial carbon dynamics, which are currently based on globally applied parameters linked to land cover or plant functional types.
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37

Keaveney, Evelyn M., Paula J. Reimer, and Robert H. Foy. "Young, Old, and Weathered Carbon-Part 1: Using Radiocarbon and Stable Isotopes to Identify Carbon Sources in an Alkaline, Humic Lake." Radiocarbon 57, no. 3 (2015): 407–23. http://dx.doi.org/10.2458/azu_rc.57.18354.

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This article presents a case study of Lower Lough Erne, a humic, alkaline lake in northwest Ireland, and uses the radiocarbon method to determine the source and age of carbon to establish whether terrestrial carbon is utilized by heterotrophic organisms or buried in sediment. Stepped combustion was used to estimate the degree of the burial of terrestrial carbon in surface sediment. Δ14C, δ13C, and δ15N values were measured for phytoplankton, dissolved inorganic carbon (DIC), dissolved organic carbon (DOC), and particulate organic carbon (POC). Δ14C values were used to indicate the presence of different sources of carbon, including bedrock-derived inorganic carbon, “modern,” “recent,” “subsurface,” and “subfossil” terrestrial carbon in the lake. The use of 14C in conjunction with novel methods (e.g. stepped combustion) allows the determination of the pathway of terrestrial carbon in the system, which has implications for regional and global carbon cycling.
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38

Olson, Jerry, and Garland R. Upchurch. "Patterns of terrestrial plant carbon: late Mesozoic and Cenozoic." Paleontological Society Special Publications 6 (1992): 225. http://dx.doi.org/10.1017/s2475262200007851.

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Variation in terrestrial productivity and biomass impacts evolution through linkages between productivity and biodiversity and through the types of resources available for consumption by herbivores. Geographic variation in terrestrial plant carbon is known on a global scale for extant biomes and is strongly correlated with precipitation, temperature, and the area of wetlands. Although estimates of extant terrestrial plant carbon density are still somewhat uncertain, the highest densities clearly occur in tropical and temperate rainforests, and the lowest occur in deserts, semideserts, and arctic/alpine tundra. Patterns of variation in ancient terrestrial plant carbon can be estimated through the correlation between biome/climate and carbon density, provided individual biomes show little change through time in primary productivity or density of plant carbon.Density of terrestrial plant carbon has been estimated on a global scale for the latest Cretaceous, late Paleocene/Eocene, middle-late Eocene, early Miocene, and Holocene/Recent using the biomal reconstructions of Wolfe (1984), Upchurch (this symposium), and others. Latest Cretaceous (Maastrichtian) estimates indicate a relatively low value of 700-800 gigatons, which may underestimate carbon due to the presence of extensive latest Cretaceous coastal wetlands. However, much of this figure is readliy explainable by extensive deserts in Asia and little evidence for areally extensive tropical rainforest.Major increase in terrestrial plant carbon occurred during the Paleocene/earliest Eocene in conjunction with a major areal increase in rainforest. During the early Miocene terrestrial global carbon was approximately 1200-1300 gigatons. This figure decreased by about half between the early Miocene and Holocene/Recent. The decrease in terrestrial carbon density resulted from a decrease in area of tropical and subtropical forests and increase in area of deserts, grasslands, and mediterranean woodlands/chapparal.
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39

Kramer, J. R., P. Brassard, G. Patry, and I. Takacs. "Sensivity of terrestrial carbon cycle on atmospheric carbon dioxide." Chemical Geology 84, no. 1-4 (July 1990): 166–68. http://dx.doi.org/10.1016/0009-2541(90)90201-h.

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40

Goodwin, Philip. "Quantifying the Terrestrial Carbon Feedback to Anthropogenic Carbon Emission." Earth's Future 7, no. 12 (December 2019): 1417–33. http://dx.doi.org/10.1029/2019ef001258.

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41

Wang, Lian Kuan, Pei Yong Lian, and Yun Jiang Fu. "Impact of Land-Use Change on Grassland Carbon Stocks: An Overview of the Literature." Applied Mechanics and Materials 448-453 (October 2013): 948–51. http://dx.doi.org/10.4028/www.scientific.net/amm.448-453.948.

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Terrestrial vegetation and soils in the terrestrial biosphere play an active role in shaping the environmental systems of the Earth. An improved understanding of changes in carbon storage of terrestrial ecosystems is very important for assessing the impacts of increasing atmospheric CO2concentration and climate change on the terrestrial biosphere. Accurately predicting terrestrial carbon (C) storage requires understanding the stock and storage potential of C, because it helps us understand how ecosystems would respond to natural and anthropogenic disturbances under different management strategies. Grasslands are important for global carbon balance both for their large area and significant sink or source capacities, depending on the factors of climatic and land-use. Land-use change is often associated with changes in land cover and carbon (C) stocks. Land-use and land cover strongly influence carbon (C) storage and distribution within the grassland ecosystems.
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42

Hoogakker, B. A. A., R. S. Smith, J. S. Singarayer, R. Marchant, I. C. Prentice, J. R. M. Allen, R. S. Anderson, et al. "Terrestrial biosphere changes over the last 120 kyr and their impact on ocean δ <sup>13</sup>C." Climate of the Past Discussions 11, no. 2 (March 31, 2015): 1031–91. http://dx.doi.org/10.5194/cpd-11-1031-2015.

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Abstract. A new global synthesis and biomization of long (>40 kyr) pollen-data records is presented, and used with simulations from the HadCM3 and FAMOUS climate models to analyse the dynamics of the global terrestrial biosphere and carbon storage over the last glacial–interglacial cycle. Global modelled (BIOME4) biome distributions over time generally agree well with those inferred from pollen data. The two climate models show good agreement in global net primary productivity (NPP). NPP is strongly influenced by atmospheric carbon dioxide (CO2) concentrations through CO2 fertilization. The combined effects of modelled changes in vegetation and (via a simple model) soil carbon result in a global terrestrial carbon storage at the Last Glacial Maximum that is 210–470 Pg C less than in pre-industrial time. Without the contribution from exposed glacial continental shelves the reduction would be larger, 330–960 Pg C. Other intervals of low terrestrial carbon storage include stadial intervals at 108 and 85 ka BP, and between 60 and 65 ka BP during Marine Isotope Stage 4. Terrestrial carbon storage, determined by the balance of global NPP and decomposition, influences the stable carbon isotope composition (δ13C) of seawater because terrestrial organic carbon is depleted in 13C. Using a simple carbon-isotope mass balance equation we find agreement in trends between modelled ocean δ13C based on modelled land carbon storage, and palaeo-archives of ocean δ13C, confirming that terrestrial carbon storage variations may be important drivers of ocean δ13C changes.
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43

Matthews, H. Damon, Andrew J. Weaver, and Katrin J. Meissner. "Terrestrial Carbon Cycle Dynamics under Recent and Future Climate Change." Journal of Climate 18, no. 10 (May 15, 2005): 1609–28. http://dx.doi.org/10.1175/jcli3359.1.

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Abstract The behavior of the terrestrial carbon cycle under historical and future climate change is examined using the University of Victoria Earth System Climate Model, now coupled to a dynamic terrestrial vegetation and global carbon cycle model. When forced by historical emissions of CO2 from fossil fuels and land-use change, the coupled climate–carbon cycle model accurately reproduces historical atmospheric CO2 trends, as well as terrestrial and oceanic uptake for the past two decades. Under six twenty-first-century CO2 emissions scenarios, both terrestrial and oceanic carbon sinks continue to increase, though terrestrial uptake slows in the latter half of the century. Climate–carbon cycle feedbacks are isolated by comparing a coupled model run with a run where climate and the carbon cycle are uncoupled. The modeled positive feedback between the carbon cycle and climate is found to be relatively small, resulting in an increase in simulated CO2 of 60 ppmv at the year 2100. Including non-CO2 greenhouse gas forcing and increasing the model’s climate sensitivity increase the effect of this feedback to 140 ppmv. The UVic model does not, however, simulate a switch from a terrestrial carbon sink to a source during the twenty-first century, as earlier studies have suggested. This can be explained by a lack of substantial reductions in simulated vegetation productivity due to climate changes.
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44

Schimel, David, Britton B. Stephens, and Joshua B. Fisher. "Effect of increasing CO2 on the terrestrial carbon cycle." Proceedings of the National Academy of Sciences 112, no. 2 (December 29, 2014): 436–41. http://dx.doi.org/10.1073/pnas.1407302112.

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Feedbacks from the terrestrial carbon cycle significantly affect future climate change. The CO2 concentration dependence of global terrestrial carbon storage is one of the largest and most uncertain feedbacks. Theory predicts the CO2 effect should have a tropical maximum, but a large terrestrial sink has been contradicted by analyses of atmospheric CO2 that do not show large tropical uptake. Our results, however, show significant tropical uptake and, combining tropical and extratropical fluxes, suggest that up to 60% of the present-day terrestrial sink is caused by increasing atmospheric CO2. This conclusion is consistent with a validated subset of atmospheric analyses, but uncertainty remains. Improved model diagnostics and new space-based observations can reduce the uncertainty of tropical and temperate zone carbon flux estimates. This analysis supports a significant feedback to future atmospheric CO2 concentrations from carbon uptake in terrestrial ecosystems caused by rising atmospheric CO2 concentrations. This feedback will have substantial tropical contributions, but the magnitude of future carbon uptake by tropical forests also depends on how they respond to climate change and requires their protection from deforestation.
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45

Pilli, R., and G. Grassi. "The carbon balance of terrestrial ecosystems of China." Forest@ - Rivista di Selvicoltura ed Ecologia Forestale 6, no. 1 (May 19, 2009): 137–39. http://dx.doi.org/10.3832/efor0584-006.

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46

Schulze, E. D. "Biological control of the terrestrial carbon sink." Biogeosciences 3, no. 2 (March 29, 2006): 147–66. http://dx.doi.org/10.5194/bg-3-147-2006.

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Abstract. This lecture reviews the past (since 1964 when the International Biological Program began) and the future of our understanding of terrestrial carbon fluxes with focus on photosynthesis, respiration, primary-, ecosystem-, and biome-productivity. Photosynthetic capacity is related to the nitrogen concentration of leaves, but the capacity is only rarely reached under field conditions. Average rates of photosynthesis and stomatal conductance are closely correlated and operate near 50% of their maximal rate, with light being the limiting factor in humid regions and air humidity and soil water the limiting factor in arid climates. Leaf area is the main factor to extrapolate from leaves to canopies, with maximum surface conductance being dependent on leaf level stomatal conductance. Additionally, gas exchange depends also on rooting depth which determines the water and nutrient availability and on mycorrhizae which regulate the nutrient status. An important anthropogenic disturbance is the nitrogen uptake from air pollutants, which is not balanced by cation uptake from roots and this may lead to damage and breakdown of the plant cover. Photosynthesis is the main carbon input into ecosystems, but it alone does not represent the ecosystem carbon balance, which is determined by respiration of various kinds. Plant respiration and photosynthesis determine growth (net primary production) and microbial respiration balances the net ecosystem flux. In a spruce forest, 30% of the assimilatory carbon gain is used for respiration of needles, 20% is used for respiration in stems. Soil respiration is about 50% the carbon gain, half of which is root respiration, half is microbial respiration. In addition, disturbances lead to carbon losses, where fire, harvest and grazing bypass the chain of respiration. In total, the carbon balance at the biome level is only about 1% of the photosynthetic carbon input, or may indeed become negative. The recent observed increase in plant growth has different reasons depending on the region of the world: anthropogenic nitrogen deposition is the controlling factor in Europe, increasing global temperatures is the main factor in Siberia, and maybe rising CO2 the factor controlling the carbon fluxes in Amazonia. However, this has not lead to increases in net biome productivity, due to associated losses. Also important is the interaction between biodiversity and biogeochemical processes. It is shown that net primary productivity increases with plant species diversity (50% species loss equals 20% loss in productivity). However, in this extrapolation the action of soil biota is poorly understood although soils contribute the largest number of species and of taxonomic groups to an ecosystem. The global terrestrial carbon budget strongly depends on areas with pristine old growth forests which are carbon sinks. The management options are very limited, mostly short term, and usually associated with high uncertainty. Unmanaged grasslands appear to be a carbon sink of similar magnitude as forest, but generally these ecosystems lost their C with grazing and agricultural use. Extrapolation to the future of Earth climate shows that the biota will not be able to balance fossil fuel emissions, and that it will be essential to develop a carbon free energy system in order to maintain the living conditions on earth.
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47

Eglinton, Timothy I., Valier V. Galy, Jordon D. Hemingway, Xiaojuan Feng, Hongyan Bao, Thomas M. Blattmann, Angela F. Dickens, et al. "Climate control on terrestrial biospheric carbon turnover." Proceedings of the National Academy of Sciences 118, no. 8 (February 16, 2021): e2011585118. http://dx.doi.org/10.1073/pnas.2011585118.

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Terrestrial vegetation and soils hold three times more carbon than the atmosphere. Much debate concerns how anthropogenic activity will perturb these surface reservoirs, potentially exacerbating ongoing changes to the climate system. Uncertainties specifically persist in extrapolating point-source observations to ecosystem-scale budgets and fluxes, which require consideration of vertical and lateral processes on multiple temporal and spatial scales. To explore controls on organic carbon (OC) turnover at the river basin scale, we present radiocarbon (14C) ages on two groups of molecular tracers of plant-derived carbon—leaf-wax lipids and lignin phenols—from a globally distributed suite of rivers. We find significant negative relationships between the 14C age of these biomarkers and mean annual temperature and precipitation. Moreover, riverine biospheric-carbon ages scale proportionally with basin-wide soil carbon turnover times and soil 14C ages, implicating OC cycling within soils as a primary control on exported biomarker ages and revealing a broad distribution of soil OC reactivities. The ubiquitous occurrence of a long-lived soil OC pool suggests soil OC is globally vulnerable to perturbations by future temperature and precipitation increase. Scaling of riverine biospheric-carbon ages with soil OC turnover shows the former can constrain the sensitivity of carbon dynamics to environmental controls on broad spatial scales. Extracting this information from fluvially dominated sedimentary sequences may inform past variations in soil OC turnover in response to anthropogenic and/or climate perturbations. In turn, monitoring riverine OC composition may help detect future climate-change–induced perturbations of soil OC turnover and stocks.
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48

Kolchugina, Tatyana P., and Ted S. Vinson. "Equilibrium analysis of carbon pools and fluxes of forest biomes in the former Soviet Union." Canadian Journal of Forest Research 23, no. 1 (January 1, 1993): 81–88. http://dx.doi.org/10.1139/x93-013.

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Natural processes in ocean and terrestrial ecosystems together with human activities have caused a measurable increase in the atmospheric concentration of CO2. It is predicted that an increase in the concentration of CO2 will cause the Earth's temperatures to rise and will accelerate rates of plant respiration and the decay of organic matter, disrupting the equilibrium of the terrestrial carbon cycle. Forests are an important component of the biosphere, and sequestration of carbon in boreal forests may represent one of the few realistic alternatives to ameliorate changes in atmospheric chemistry. The former Soviet Union has the greatest expanse of boreal forests in the world; however, the role of Soviet forests in the terrestrial carbon cycle is not fully understood because the carbon budget of the Soviet forest sector has not been established. In recognition of the need to determine the role of Soviet forests in the global carbon cycle, the carbon budget of forest biomes in the former Soviet Union was assessed based on an equilibrium analysis of carbon cycle pools and fluxes. Net primary productivity was used to identify the rate of carbon turnover in the forest biomes. Net primary productivity was estimated at 4360 Mt of carbon, the vegetation carbon pool was estimated at 110 255 Mt, the litter carbon pool was estimated at 17 525 Mt, and the soil carbon pool was estimated at 319 100 Mt. Net primary productivity of Soviet forest biomes exceeded industrial CO2 emissions in the former Soviet Union by a factor of four and represented approximately 7% of the global terrestrial carbon turnover. Carbon stores in the phytomass and soils of forest biomes of the former Soviet Union represented 16% of the carbon concentrated in the biomass and soils of the world's terrestrial ecosystems. All carbon pools of Soviet forest biomes represented approximately one-seventh of the world's terrestrial carbon pool.
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49

Ran, Lishan, Mingyang Tian, Nufang Fang, Suiji Wang, Xixi Lu, Xiankun Yang, and Frankie Cho. "Riverine carbon export in the arid to semiarid Wuding River catchment on the Chinese Loess Plateau." Biogeosciences 15, no. 12 (June 27, 2018): 3857–71. http://dx.doi.org/10.5194/bg-15-3857-2018.

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Abstract. Riverine export of terrestrially derived carbon represents a key component of the global carbon cycle. In this study we quantify the fate of riverine carbon within the Wuding River catchment on the Chinese Loess Plateau. Export of dissolved organic and inorganic carbon (DOC and DIC) exhibited pronounced spatial and temporal variability. While DOC concentration first presented a downward trend along the river course and then increased in the main-stem river, it showed no significant seasonal differences and was not sensitive to flow dynamics. This likely reflects the predominance of groundwater input over the entire year and its highly stable DOC. DIC concentration in the loess subcatchment is significantly higher than that in the sandy subcatchment, due largely to dissolution of carbonates that are abundant in loess. In addition, bulk particulate organic carbon content (POC%) showed strong seasonal variability with low values in the wet season owing to input of deeper soils by gully erosion. The downstream carbon flux was (7.0 ± 1.9) × 1010 g C yr−1 and dominated by DIC and POC. Total CO2 emissions from water surface were (3.7 ± 0.6) × 1010 g C yr−1. Radiocarbon analysis revealed that the degassed CO2 was 810–1890 years old, indicating the release of old carbon previously stored in soil horizons. Riverine carbon export in the Wuding River catchment has been greatly modified by check dams. Our estimate shows that carbon burial through sediment storage was (7.8 ± 4.1) × 1010 g C yr−1, representing 42 % of the total riverine carbon export from terrestrial ecosystems on an annual basis ((18.5 ± 4.5) × 1010 g C yr−1). Moreover, the riverine carbon export accounted for 16 % of the catchment's net ecosystem production (NEP). It appears that a significant fraction of terrestrial NEP in this arid to semiarid catchment is laterally transported from the terrestrial biosphere to the drainage network.
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50

Köhler, P., H. Fischer, J. Schmitt, and G. Munhoven. "On the application and interpretation of Keeling plots in paleo climate research – deciphering δ<sup>13</sup>C of atmospheric CO<sub>2</sub> measured in ice cores." Biogeosciences 3, no. 4 (November 15, 2006): 539–56. http://dx.doi.org/10.5194/bg-3-539-2006.

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Abstract. The Keeling plot analysis is an interpretation method widely used in terrestrial carbon cycle research to quantify exchange processes of carbon between terrestrial reservoirs and the atmosphere. Here, we analyse measured data sets and artificial time series of the partial pressure of atmospheric carbon dioxide (pCO2) and of δ13C of CO2 over industrial and glacial/interglacial time scales and investigate to what extent the Keeling plot methodology can be applied to longer time scales. The artificial time series are simulation results of the global carbon cycle box model BICYCLE. The signals recorded in ice cores caused by abrupt terrestrial carbon uptake or release loose information due to air mixing in the firn before bubble enclosure and limited sampling frequency. Carbon uptake by the ocean cannot longer be neglected for less abrupt changes as occurring during glacial cycles. We introduce an equation for the calculation of long-term changes in the isotopic signature of atmospheric CO2 caused by an injection of terrestrial carbon to the atmosphere, in which the ocean is introduced as third reservoir. This is a paleo extension of the two reservoir mass balance equations of the Keeling plot approach. It gives an explanation for the bias between the isotopic signature of the terrestrial release and the signature deduced with the Keeling plot approach for long-term processes, in which the oceanic reservoir cannot be neglected. These deduced isotopic signatures are similar (−8.6‰) for steady state analyses of long-term changes in the terrestrial and marine biosphere which both perturb the atmospheric carbon reservoir. They are more positive than the δ13C signals of the sources, e.g. the terrestrial carbon pools themselves (−25‰). A distinction of specific processes acting on the global carbon cycle from the Keeling plot approach is not straightforward. In general, processes related to biogenic fixation or release of carbon have lower y-intercepts in the Keeling plot than changes in physical processes, however in many case they are indistinguishable (e.g. ocean circulation from biogenic carbon fixation).
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