Glyphosate Alters Aboveground Net Primary Production, Soil Organic Carbon, and Nutrients in Pampean Grasslands (Argentina)

2018 ◽  
Vol 71 (1) ◽  
pp. 119-125 ◽  
Author(s):  
Adriana M. Rodriguez ◽  
Elizabeth J. Jacobo ◽  
Rodolfo A. Golluscio
2020 ◽  
Vol 117 (33) ◽  
pp. 20038-20043 ◽  
Author(s):  
Laureano A. Gherardi ◽  
Osvaldo E. Sala

Carbon allocated underground through belowground net primary production represents the main input to soil organic carbon. This is of significant importance, because soil organic carbon is the third-largest carbon stock after oceanic and geological pools. However, drivers and controls of belowground productivity and the fraction of total carbon fixation allocated belowground remain uncertain. Here we estimate global belowground net primary productivity as the difference between satellite-based total net primary productivity and field observations of aboveground net primary production and assess climatic controls among biomes. On average, belowground carbon productivity is estimated as 24.7 Pg y−1, accounting for 46% of total terrestrial carbon fixation. Across biomes, belowground productivity increases with mean annual precipitation, although the rate of increase diminishes with increasing precipitation. The fraction of total net productivity allocated belowground exceeds 50% in a large fraction of terrestrial ecosystems and decreases from arid to humid ecosystems. This work adds to our understanding of the belowground carbon productivity response to climate change and provides a comprehensive global quantification of root/belowground productivity that will aid the budgeting and modeling of the global carbon cycle.


2020 ◽  
Author(s):  
Jake D. Graham

Northern peatlands are a major terrestrial carbon (C) store, with an annual sink of 0.1 Pg C yr-1 and a total storage estimate of 547 Pg C. Northern peatlands are also major contributors of atmospheric methane, a potent greenhouse gas. The microtopography of peatlands helps modulate peatland carbon fluxes; however, there is a lack of quantitative characterizations of microtopography in the literature. The lack of formalized schemes to characterize microtopography makes comparisons between studies difficult. Further, many land surface models do not accurately simulate peatland C emissions, in part because they do not adequately represent peatland microtopography and hydrology. The C balance of peatlands is determined by differences in C influxes and effluxes, with the largest being net primary production and heterotrophic respiration, respectively. Tree net primary production at a treed bog in northern Minnesota represented about 13% of C inputs to the peatland, and marks tree aboveground net primary production (ANPP) as an important pathway for C to enter peatlands. Tree species Picea mariana (Black spruce) and Larix Laricina (Tamarack) are typically found in wooded peatlands in North America, and are widely distributed in the North American boreal zone. Therefore, understanding how these species will respond to environmental change is needed to make predictions of peatland C budgets in the future. As the climate warms, peatlands are expected to increase C release to the atmosphere, resulting in a positive feedback loop. Further, climate warming is expected to occur faster in northern latitudes compared to the rest of the globe. The Spruce and Peatland Responses Under Changing Environments (SPRUCE; https://mnspruce.ornl.gov/) manipulates temperature and CO2 concentrations to evaluate the in-situ response of a peatland to environmental change and is located in Minnesota, USA. In this dissertation, I documented surface roughness metrics for peatland microtopography in SPRUCE plots and developed three explicit methods for classifying frequently used microtopographic classes (microforms) for different scientific applications. Subsequently I used one of these characterizations to perform a sensitivity analysis and improve the parameterization of microtopography in a land surface model that was calibrated at the SPRUCE site. The modeled outputs of C from the analyses ranged from 0.8-34.8% when microtopographical parameters were allowed to vary within observed ranges. Further, C related outputs when using our data-driven parameterization differed from outputs when using the default parameterization by -7.9 - 12.2%. Finally, I utilized TLS point clouds to assess the effect elevated temperature and CO2 concentrations had on P. mariana and L. laricina after the first four years of SPRUCE treatments. I observed that P. mariana growth (aboveground net primary production) had a negative response to temperature initially, but the relationship became less pronounced through time. Conversely, L. laricina had no growth response to temperature initially, but developed a positive relationship through time. The divergent growth responses of P. mariana and L. laricina resulted in no detectable change in aboveground net primary production at the community level. Results from this dissertation help improve how peatland microtopography is represented, and improves understanding of how peatland tree growth will respond to environmental change in the future.


2017 ◽  
Vol 14 (2) ◽  
pp. 301-310 ◽  
Author(s):  
Carlos M. Duarte

Abstract. Vegetated coastal habitats, including seagrass and macroalgal beds, mangrove forests and salt marshes, form highly productive ecosystems, but their contribution to the global carbon budget remains overlooked, and these forests remain hidden in representations of the global carbon budget. Despite being confined to a narrow belt around the shoreline of the world's oceans, where they cover less than 7 million km2, vegetated coastal habitats support about 1 to 10 % of the global marine net primary production and generate a large organic carbon surplus of about 40 % of their net primary production (NPP), which is either buried in sediments within these habitats or exported away. Large, 10-fold uncertainties in the area covered by vegetated coastal habitats, along with variability about carbon flux estimates, result in a 10-fold bracket around the estimates of their contribution to organic carbon sequestration in sediments and the deep sea from 73 to 866 Tg C yr−1, representing between 3 % and 1∕3 of oceanic CO2 uptake. Up to 1∕2 of this carbon sequestration occurs in sink reservoirs (sediments or the deep sea) beyond these habitats. The organic carbon exported that does not reach depositional sites subsidizes the metabolism of heterotrophic organisms. In addition to a significant contribution to organic carbon production and sequestration, vegetated coastal habitats contribute as much to carbonate accumulation as coral reefs do. While globally relevant, the magnitude of global carbon fluxes supported by salt-marsh, mangrove, seagrass and macroalgal habitats is declining due to rapid habitat loss, contributing to loss of CO2 sequestration, storage capacity and carbon subsidies. Incorporating the carbon fluxes' vegetated coastal habitats' support into depictions of the carbon budget of the global ocean and its perturbations will improve current representations of the carbon budget of the global ocean.


2020 ◽  
Vol 11 (1) ◽  
Author(s):  
S. Hernández-León ◽  
R. Koppelmann ◽  
E. Fraile-Nuez ◽  
A. Bode ◽  
C. Mompeán ◽  
...  

AbstractThe biological pump transports organic carbon produced by photosynthesis to the meso- and bathypelagic zones, the latter removing carbon from exchanging with the atmosphere over centennial time scales. Organisms living in both zones are supported by a passive flux of particles, and carbon transported to the deep-sea through vertical zooplankton migrations. Here we report globally-coherent positive relationships between zooplankton biomass in the epi-, meso-, and bathypelagic layers and average net primary production (NPP). We do so based on a global assessment of available deep-sea zooplankton biomass data and large-scale estimates of average NPP. The relationships obtained imply that increased NPP leads to enhanced transference of organic carbon to the deep ocean. Estimated remineralization from respiration rates by deep-sea zooplankton requires a minimum supply of 0.44 Pg C y−1 transported into the bathypelagic ocean, comparable to the passive carbon sequestration. We suggest that the global coupling between NPP and bathypelagic zooplankton biomass must be also supported by an active transport mechanism associated to vertical zooplankton migration.


Trees ◽  
2000 ◽  
Vol 14 (7) ◽  
pp. 415-421 ◽  
Author(s):  
J. Oleksyn ◽  
P.B. Reich ◽  
L. Rachwal ◽  
M.G. Tjoelker ◽  
P. Karolewski

2011 ◽  
Vol 8 (8) ◽  
pp. 2099-2106 ◽  
Author(s):  
Y. Wang ◽  
J. Y. Fang ◽  
T. Kato ◽  
Z. D. Guo ◽  
B. Zhu ◽  
...  

Abstract. Recent studies based on remote sensing and carbon process models have revealed that terrestrial net primary production (NPP) in the middle and high latitudes of the Northern Hemisphere has increased significantly; this is crucial for explaining the increased terrestrial carbon sink in the past several decades. Regional NPP estimation based on significant field data, however, has been rare. In this study, we estimated the long-term changes in aboveground NPP (ANPP) for Japan's forests from 1980 to 2005 using forest inventory data, direct field measurements, and an allometric method. The overall ANPP for all forest types averaged 10.5 Mg ha−1 yr−1, with a range of 9.6 to 11.5 Mg ha−1 yr−1, and ANPP for the whole country totaled 249.1 Tg yr−1 (range: 230.0 to 271.4 Tg yr−1) during the study period. Over the 25 years, the net effect of increased ANPP in needle-leaf forests and decreased ANPP in broadleaf forests has led to an increase of 1.9 Mg ha−1 yr−1 (i.e., 0.79 % yr−1). This increase may be mainly due to the establishment of plantations and the rapid early growth of these planted forests.


2020 ◽  
Vol 8 (10) ◽  
pp. 767 ◽  
Author(s):  
Daniel M. Alongi

Mangroves and salt marshes are among the most productive ecosystems in the global coastal ocean. Mangroves store more carbon (739 Mg CORG ha−1) than salt marshes (334 Mg CORG ha−1), but the latter sequester proportionally more (24%) net primary production (NPP) than mangroves (12%). Mangroves exhibit greater rates of gross primary production (GPP), aboveground net primary production (AGNPP) and plant respiration (RC), with higher PGPP/RC ratios, but salt marshes exhibit greater rates of below-ground NPP (BGNPP). Mangroves have greater rates of subsurface DIC production and, unlike salt marshes, exhibit active microbial decomposition to a soil depth of 1 m. Salt marshes release more CH4 from soil and creek waters and export more dissolved CH4, but mangroves release more CO2 from tidal waters and export greater amounts of particulate organic carbon (POC), dissolved organic carbon (DOC) and dissolved inorganic carbon (DIC), to adjacent waters. Both ecosystems contribute only a small proportion of GPP, RE (ecosystem respiration) and NEP (net ecosystem production) to the global coastal ocean due to their small global area, but contribute 72% of air–sea CO2 exchange of the world’s wetlands and estuaries and contribute 34% of DIC export and 17% of DOC + POC export to the world’s coastal ocean. Thus, both wetland ecosystems contribute disproportionately to carbon flow of the global coastal ocean.


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