scholarly journals High Rates of Ecosytem Metabolism in Five Western Rivers

Author(s):  
Robert Hall ◽  
Jennifer Tank ◽  
Michelle Baker ◽  
Emma Rosi-Marshall ◽  
Michael Grace ◽  
...  

Primary production and respiration are core functions of river ecosystems that in part determine the carbon balance. Gross primary production (GPP) is the total rate of carbon fixation by autotrophs such as algae and higher plants and is equivalent to photosynthesis. Ecosystem respiration (ER) measures rate at which organic carbon is mineralized to CO2 by all organisms in an ecosystem. Together these fluxes can indicate the base of the food web to support animal production (Marcarelli et al. 2011), can predict the cycling of other elements (Hall and Tank 2003), and can link ecosystems to global carbon cycling (Cole et al. 2007).

2021 ◽  
Vol 9 (1) ◽  
pp. 9
Author(s):  
Víctor Cicuéndez ◽  
Javier Litago ◽  
Víctor Sánchez-Girón ◽  
Laura Recuero ◽  
César Sáenz ◽  
...  

Gross primary production (GPP) represents the carbon (C) uptake of ecosystems through photosynthesis and it is the largest flux of the global carbon balance. Our overall objective in this research is to identify and model GPP dynamics and its relationship with meteorological variables and energy fluxes based on time series analysis of eddy covariance (EC) data in two different agroecosystems, a Mediterranean rice crop in Spain and a rainfed cropland in Germany. Crops exerted an important influence on the energy and water fluxes dynamics existing a clear feedback between GPP, meteorological variables and energy fluxes in both type of crops.


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.


2008 ◽  
Vol 5 (5) ◽  
pp. 4035-4069 ◽  
Author(s):  
U. Weber ◽  
M. Jung ◽  
M. Reichstein ◽  
C. Beer ◽  
M. Braakhekke ◽  
...  

Abstract. We are comparing spatially explicit process-model based estimates of the terrestrial carbon balance and its components over Africa and confront them with remote sensing based proxies of vegetation productivity and atmospheric inversions of land-atmosphere net carbon exchange. Particular emphasis is on characterizing the patterns of interannual variability of carbon fluxes and analyzing the factors and processes responsible for it. For this purpose simulations with the terrestrial biosphere models ORCHIDEE, LPJ-DGVM, LPJ-Guess and JULES have been performed using a standardized modeling protocol and a uniform set of corrected climate forcing data. While the models differ concerning the absolute magnitude of carbon fluxes, we find several robust patterns of interannual variability among the models. Models exhibit largest interannual variability in southern and eastern Africa, regions which are primarily covered by herbaceous vegetation. Interannual variability of the net carbon balance appears to be more strongly influenced by gross primary production than by ecosystem respiration. A principal component analysis indicates that moisture is the main driving factor of interannual gross primary production variability for those regions. On the contrary in a large part of the inner tropics radiation appears to be limiting in two models. These patterns are corroborated by remotely sensed vegetation properties from the SeaWiFS satellite sensor. Inverse atmospheric modeling estimates of surface carbon fluxes are less conclusive at this point, implying the need for a denser network of observation stations over Africa.


2009 ◽  
Vol 6 (2) ◽  
pp. 285-295 ◽  
Author(s):  
U. Weber ◽  
M. Jung ◽  
M. Reichstein ◽  
C. Beer ◽  
M. C. Braakhekke ◽  
...  

Abstract. We are comparing spatially explicit process-model based estimates of the terrestrial carbon balance and its components over Africa and confront them with remote sensing based proxies of vegetation productivity and atmospheric inversions of land-atmosphere net carbon exchange. Particular emphasis is on characterizing the patterns of interannual variability of carbon fluxes and analyzing the factors and processes responsible for it. For this purpose simulations with the terrestrial biosphere models ORCHIDEE, LPJ-DGVM, LPJ-Guess and JULES have been performed using a standardized modeling protocol and a uniform set of corrected climate forcing data. While the models differ concerning the absolute magnitude of carbon fluxes, we find several robust patterns of interannual variability among the models. Models exhibit largest interannual variability in southern and eastern Africa, regions which are primarily covered by herbaceous vegetation. Interannual variability of the net carbon balance appears to be more strongly influenced by gross primary production than by ecosystem respiration. A principal component analysis indicates that moisture is the main driving factor of interannual gross primary production variability for those regions. On the contrary in a large part of the inner tropics radiation appears to be limiting in two models. These patterns are partly corroborated by remotely sensed vegetation properties from the SeaWiFS satellite sensor. Inverse atmospheric modeling estimates of surface carbon fluxes are less conclusive at this point, implying the need for a denser network of observation stations over Africa.


2021 ◽  
Author(s):  
Julie Rotschi ◽  
Isabelle Domaizon ◽  
Irene Gregory-Eaves ◽  
Andrea Lami ◽  
Cécilia Barouillet ◽  
...  

<p>Although lakes only represent a small fraction of the surface of the earth, a growing number of studies have shown that they play a critical role in the global carbon cycle (<sup>[i],[ii],[iii]</sup>), mediating carbon transfer from land to the atmosphere, and burying organic carbon in their sediments. The magnitude and temporal variability of carbon burial is, however, poorly constrained, and the degree to which lake productivity has influenced lake carbon cycling has not been systematically assessed (<sup>[iv]</sup>). Here, trends in total organic carbon (TOC) sequestration and primary production are reconstructed from sediment records for the last 300 years in four perialpine deep lakes. We rely on High Performance Liquid Chromatography (HPLC) and geochemical proxies to investigate changes in algal communities. Then, we evaluate the temporal contribution of algal assemblages to the variability of lake primary production, as well as the potential effects on carbon sequestration magnitude. Other contributors to carbon sequestration derived from the IPER RETRO project (2009-2013) are also investigated, such as past oxygen conditions, lake thermal structure or allochthonous supplies of carbon. Our results suggest that despite reoligotrophication of all lakes (e.g., decrease in dissolved phosphorus concentration in water column and relative restoration of diatoms communities (<sup>[v]</sup>)) over the last 3 decades, TOC in lakes sediments is still increasing in the sediment. The study of algal pigments suggests that changes in algal assemblages and oxygen conditions could be responsible of this persistent increase in carbon burial. Future development (e.g., DNA analysis) should provide more detail on algal communities to validate these results.</p><div><br><div> <p>[i] J. J. Cole et al., ‘Plumbing the Global Carbon Cycle: Integrating Inland Waters into the Terrestrial Carbon Budget’, Ecosystems 10, no. 1 (May 2007): 172–85, https://doi.org/10.1007/s10021-006-9013-8.</p> </div> <div> <p>[ii] Tom J. Battin et al., ‘Biophysical Controls on Organic Carbon Fluxes in Fluvial Networks’, Nature Geoscience 1, no. 2 (February 2008): 95–100, https://doi.org/10.1038/ngeo101.</p> </div> <div> <p>[iii] Lars J. Tranvik et al., ‘Lakes and Reservoirs as Regulators of Carbon Cycling and Climate’, Limnology and Oceanography 54, no. 6part2 (November 2009): 2298–2314, https://doi.org/10.4319/lo.2009.54.6_part_2.2298.</p> </div> <div> <p>[iv] N. J. Anderson et al., ‘Anthropogenic Alteration of Nutrient Supply Increases the Global Freshwater Carbon Sink’, Science Advances 6, no. 16 (April 2020): eaaw2145, https://doi.org/10.1126/sciadv.aaw2145.</p> </div> <div> <p>[v] Vincent Berthon et al., ‘Trophic History of French Sub-Alpine Lakes over the Last 150 Years: Phosphorus Reconstruction and Assessment of Taphonomic Biases’, Journal of Limnology 72, no. 3 (September 2013): 34, https://doi.org/10.4081/jlimnol.2013.e34.</p> </div> </div>


2009 ◽  
Vol 6 (4) ◽  
pp. 6601-6634 ◽  
Author(s):  
B. Bjarnadottir ◽  
B. D. Sigurdsson ◽  
A. Lindroth

Abstract. This study reports 3-year measurements (2004–2006) of net ecosystem exchange (NEE) over a 12–14 year old Siberian larch forest in Iceland established on previously grazed heath land pasture that had been site-prepared prior to planting. The study evaluated interannual and seasonal variation of NEE and its component fluxes, gross primary production (GPP) and ecosystem respiration (Re), with the aim to clarify how climatic factors controlled the site's carbon balance. The young plantation acted as a relatively strong sink for CO2 during all of the three years, with a net sequestration of −375, −566 and −245 g CO2 m−2 for years 2004, 2005 and 2006, respectively. The annual carbon balance was strongly influenced by climatic factors leading to a high inter-annual variability in NEE. This variation was more related to variation in carbon efflux (Re) than carbon uptake (GPP). The abiotic factors that showed the strongest correlation to Re were air temperature during the growing season and soil water potential. The GPP mostly followed the seasonal pattern in irradiance, except in 2005, when the plantation experienced severe spring frost damage that set the GPP back to zero. It was not expected that the rather slow-growing Siberian larch plantation would be such a strong sink for atmospheric CO2 only twelve years after site preparation and afforestation.


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.


2021 ◽  
Author(s):  
Junbin Zhao ◽  
Holger Lange ◽  
Helge Meissner

<p>Forests have climate change mitigation potential since they sequester carbon. However, their carbon sink strength might depend on management. As a result of the balance between CO<sub>2</sub> uptake and emission, forest net ecosystem exchange (NEE) reaches optimal values (maximum sink strength) at young stand ages, followed by a gradual NEE decline over many years. Traditionally, this peak of NEE is believed to be concurrent with the peak of primary production (e.g., gross primary production, GPP); however, in theory, this concurrence may potentially vary depending on tree species, site conditions and the patterns of ecosystem respiration (R<sub>eco</sub>). In this study, we used eddy-covariance (EC)-based CO<sub>2</sub> flux measurements from 8 forest sites that are dominated by Norway spruce (Picea abies L.) and built machine learning models to find the optimal age of ecosystem productivity and that of CO<sub>2</sub> sequestration. We found that the net CO<sub>2</sub> uptake of Norway spruce forests peaked at ages of 30-40 yrs. Surprisingly, this NEE peak did not overlap with the peak of GPP, which appeared later at ages of 60-90 yrs. The mismatch between NEE and GPP was a result of the R<sub>eco</sub> increase that lagged behind the GPP increase associated with the tree growth at early age. Moreover, we also found that newly planted Norway spruce stands had a high probability (up to 90%) of being a C source in the first year, while, at an age as young as 5 yrs, they were likely to be a sink already. Further, using common climate change scenarios, our model results suggest that net CO<sub>2</sub> uptake of Norway spruce forests will increase under the future climate with young stands in the high latitude areas being more beneficial. Overall, the results suggest that forest management practices should consider NEE and forest productivity separately and harvests should be performed only after the optimal ages of both the CO<sub>2</sub> sequestration and productivity to gain full ecological and economic benefits.</p>


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