scholarly journals The evolution of photosynthesis…again?

2008 ◽  
Vol 363 (1504) ◽  
pp. 2787-2801 ◽  
Author(s):  
Lynn J Rothschild
Keyword(s):  
Organic Carbon ◽  
Life Form ◽  
Inorganic Carbon ◽  
Carbon Fixation ◽  
Light Harvesting ◽  
Oxygenic Photosynthesis ◽  
Early Earth ◽  
Carboxylating Enzymes ◽  
Evolution Of Photosynthesis ◽  
Carbon Based

‘Replaying the tape’ is an intriguing ‘would it happen again?’ exercise. With respect to broad evolutionary innovations, such as photosynthesis, the answers are central to our search for life elsewhere. Photosynthesis permits a large planetary biomass on Earth. Specifically, oxygenic photosynthesis has allowed an oxygenated atmosphere and the evolution of large metabolically demanding creatures, including ourselves. There are at least six prerequisites for the evolution of biological carbon fixation: a carbon-based life form; the presence of inorganic carbon; the availability of reductants; the presence of light; a light-harvesting mechanism to convert the light energy into chemical energy; and carboxylating enzymes. All were present on the early Earth. To provide the evolutionary pressure, organic carbon must be a scarce resource in contrast to inorganic carbon. The probability of evolving a carboxylase is approached by creating an inventory of carbon-fixation enzymes and comparing them, leading to the conclusion that carbon fixation in general is basic to life and has arisen multiple times. Certainly, the evolutionary pressure to evolve new pathways for carbon fixation would have been present early in evolution. From knowledge about planetary systems and extraterrestrial chemistry, if organic carbon-based life occurs elsewhere, photosynthesis—although perhaps not oxygenic photosynthesis—would also have evolved.

Differential visible spectral influence on carbon metabolism in heterotrophic marine flavobacteria

2020 ◽  
Vol 96 (3) ◽  
Author(s):  
Asif Hameed ◽  
Wei-An Lai ◽  
Mariyam Shahina ◽  
Paul Stothard ◽  
Li-Sen Young ◽  
...  
Keyword(s):  
Carbon Sequestration ◽  
Organic Carbon ◽  
Visible Light ◽  
Blue Light ◽  
Carbon Metabolism ◽  
Inorganic Carbon ◽  
Carbon Fixation ◽  
Heterotrophic Bacteria ◽  
Hydrolytic Enzymes ◽  
Full Spectrum

ABSTRACT The visible spectrum of solar radiation is known to stimulate photoheterotrophic bacterial carbon metabolism. However, its impact on ‘strictly’ heterotrophic bacteria remains less explored. Here, we show that heterotrophic flavobacteria exhibit enhanced uptake and mineralization of dissolved organic carbon with increasing wavelengths of visible light, without employing any ‘known’ light-harvesting mechanisms. RNA sequencing identified blue light as a major constraint in the extracellular enzymatic hydrolysis of polymeric carbohydrates and acquisition of sugars, despite acting as a stimulus for inorganic carbon sequestration. In contrast, green–red and continuous full-spectrum lights activated diverse hydrolytic enzymes and sugar transporters, but obstructed inorganic carbon fixation. This ‘metabolic switching’ was apparent through limited nutrient uptake, suppressed light-sensitivity, oxidative stress response and promotion of inorganic carbon sequestration pathways under blue light. The visible light impact on metabolism may be of significant ecological relevance as it appears to promote cell-mediated mineralization of organic carbon in ‘green-colored’ chlorophyll-rich copiotrophic coastal seawater and inorganic carbon sequestration in ‘blue-colored’ oligotrophic open ocean. Thus, a novel regulatory role played by light on heterotrophic metabolism and a hidden potential of flavobacteria to sense and respond differentially to monochromatic lights influencing marine carbon cycling were unraveled.

scholarly journals Deforestation in Amazonia impacts riverine carbon dynamics

2016 ◽  
Vol 7 (4) ◽  
pp. 953-968 ◽  
Author(s):  
Fanny Langerwisch ◽  
Ariane Walz ◽  
Anja Rammig ◽  
Britta Tietjen ◽  
Kirsten Thonicke ◽  
...  
Keyword(s):  
Land Use ◽  
Organic Carbon ◽  
Land Use Change ◽  
Atlantic Ocean ◽  
Amazon Basin ◽  
Inorganic Carbon ◽  
Carbon Dynamics ◽  
Model System ◽  
Atmospheric Co2 ◽  
Terrestrial Productivity

Abstract. Fluxes of organic and inorganic carbon within the Amazon basin are considerably controlled by annual flooding, which triggers the export of terrigenous organic material to the river and ultimately to the Atlantic Ocean. The amount of carbon imported to the river and the further conversion, transport and export of it depend on temperature, atmospheric CO2, terrestrial productivity and carbon storage, as well as discharge. Both terrestrial productivity and discharge are influenced by climate and land use change. The coupled LPJmL and RivCM model system (Langerwisch et al., 2016) has been applied to assess the combined impacts of climate and land use change on the Amazon riverine carbon dynamics. Vegetation dynamics (in LPJmL) as well as export and conversion of terrigenous carbon to and within the river (RivCM) are included. The model system has been applied for the years 1901 to 2099 under two deforestation scenarios and with climate forcing of three SRES emission scenarios, each for five climate models. We find that high deforestation (business-as-usual scenario) will strongly decrease (locally by up to 90 %) riverine particulate and dissolved organic carbon amount until the end of the current century. At the same time, increase in discharge leaves net carbon transport during the first decades of the century roughly unchanged only if a sufficient area is still forested. After 2050 the amount of transported carbon will decrease drastically. In contrast to that, increased temperature and atmospheric CO2 concentration determine the amount of riverine inorganic carbon stored in the Amazon basin. Higher atmospheric CO2 concentrations increase riverine inorganic carbon amount by up to 20 % (SRES A2). The changes in riverine carbon fluxes have direct effects on carbon export, either to the atmosphere via outgassing or to the Atlantic Ocean via discharge. The outgassed carbon will increase slightly in the Amazon basin, but can be regionally reduced by up to 60 % due to deforestation. The discharge of organic carbon to the ocean will be reduced by about 40 % under the most severe deforestation and climate change scenario. These changes would have local and regional consequences on the carbon balance and habitat characteristics in the Amazon basin itself as well as in the adjacent Atlantic Ocean.

scholarly journals Particulate organic carbon (POC) in relation to other pore water carbon fractions in drained and rewetted fens in Southern Germany

2008 ◽  
Vol 5 (6) ◽  
pp. 1615-1623 ◽  
Author(s):  
S. Fiedler ◽  
B. S. Höll ◽  
A. Freibauer ◽  
K. Stahr ◽  
M. Drösler ◽  
...  
Keyword(s):  
Organic Carbon ◽  
Particulate Organic Carbon ◽  
Pore Water ◽  
Inorganic Carbon ◽  
Dissolved Inorganic Carbon ◽  
Relative Importance ◽  
Pore Waters ◽  
Calcareous Fens ◽  
Essential Components ◽  
The Individual

Abstract. Numerous studies have dealt with carbon (C) contents in Histosols, but there are no studies quantifying the relative importance of the individual C components in pore waters. For this study, measurements were taken of all the carbon components (particulate organic carbon, POC; dissolved organic carbon, DOC; dissolved inorganic carbon, DIC; dissolved methane, CH4) in the soil pore water of calcareous fens under three different water management regimes (re-wetted, deeply and moderately drained). Pore water was collected weekly or biweekly (April 2004 to April 2006) at depths between 10 and 150 cm. The main results obtained were: (1) DIC (94–280 mg C l−1) was the main C-component. (2) POC and DOC concentrations in the pore water (14–125 mg C l−1 vs. 41–95 mg C l−1) were pari passu. (3) Dissolved CH4 was the smallest C component (0.005–0.9 mg C l−1). Interestingly, about 30% of the POM particles were colonized by microbes indicating that they are active in the internal C turnover. Certainly, both POC and DOC fractions are essential components of the C budget of peatlands. Furthermore, dissolved CO2 in all forms of DIC appears to be an important part of peatland C-balance.

scholarly journals Soil organic carbon dynamics following afforestation in the Loess Plateau of China

2013 ◽  
Vol 10 (7) ◽  
pp. 11181-11211 ◽  
Author(s):  
N. Lu ◽  
J. Liski ◽  
R. Y. Chang ◽  
A. Akujärvi ◽  
X. Wu ◽  
...  
Keyword(s):  
Organic Carbon ◽  
Soil Organic Carbon ◽  
Loess Plateau ◽  
Carbon Fixation ◽  
Temporal Dynamics ◽  
Climatic Factors ◽  
Early Stage ◽  
Arable Land ◽  
The Loess Plateau ◽  
Successional Stage

Abstract. Soil organic carbon (SOC) is the largest terrestrial carbon pool and sensitive to land use and cover change; its dynamics is critical for carbon cycling in terrestrial ecosystems and the atmosphere. In this study, we combined a modeling approach and field measurements to examine the temporal dynamics of SOC following afforestation of former arable land at six sites under different climatic conditions in the Loess Plateau during 1980–2010. The results showed that the measured mean SOC increased to levels higher than before afforestation when taking the last measurements (i.e., at age 25 to 30 yr), although it decreased in the first few years at the wetter sites. The accumulation rates of SOC were 1.58 to 6.22% yr–1 in the upper 20 cm and 1.62 to 5.15% yr–1 in the upper 40 cm of soil. The simulations reproduced the basic characteristics of measured SOC dynamics, suggesting that litter input and climatic factors (temperature and precipitation) were the major causes for SOC dynamics and the differences among the sites. They explained 88–96, 48–86 and 57–74% of the variations in annual SOC changes at the soil depths of 0–20, 0–40, and 0–100 cm, respectively. Notably, the simulated SOC decreased during the first few years at all the sites, although the magnitudes of decreases were small at the drier sites. This suggested that the modeling may be advantageous in capturing SOC changes at finer time scale. The discrepancy between the simulation and measurement was a result of uncertainties in model structure, data input, and sampling design. Our findings indicated that afforestation promoted soil carbon sequestration at the study sites, which is favorable for further restoration of the vegetation and environment. Afforestation activities should decrease soil disturbances to reduce carbon release in the early stage. The long-term strategy for carbon fixation capability of the plantations should also consider the climate and site conditions, species adaptability, and successional stage of recovery.

scholarly journals High Rates of Ecosytem Metabolism in Five Western Rivers

2011 ◽  
Vol 33 ◽  
pp. 115-118
Author(s):  
Robert Hall ◽  
Jennifer Tank ◽  
Michelle Baker ◽  
Emma Rosi-Marshall ◽  
Michael Grace ◽  
...  
Keyword(s):  
Organic Carbon ◽  
Primary Production ◽  
Carbon Cycling ◽  
Carbon Balance ◽  
Carbon Fixation ◽  
Higher Plants ◽  
Ecosystem Respiration ◽  
Gross Primary Production ◽  
Total Rate ◽  
Global Carbon

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).

A Syringe Gas-Stripping Procedure for Gas-Chromatographic Determination of Dissolved Inorganic and Organic Carbon in Fresh Water and Carbonates in Sediments

1973 ◽  
Vol 30 (10) ◽  
pp. 1441-1445 ◽  
Author(s):  
Michael P. Stainton
Keyword(s):  
Organic Carbon ◽  
Gas Phase ◽  
Atmospheric Pressure ◽  
Inorganic Carbon ◽  
Dissolved Inorganic Carbon ◽  
Chromatographic Determination ◽  
Canadian Shield ◽  
Gas Stripping ◽  
Inorganic And Organic

A simple, rapid method for determining dissolved inorganic carbon in water is described. A 20-cm3 sample of water is drawn into a 50-cm3 polypropylene syringe and acidified by injection of 1 cm3 of dilute sulphuric acid. Twenty-nine cubic centimeters of helium at atmospheric pressure is injected into the syringe followed by 10 sec of manual agitation to partition CO2 between gas and liquid phase. The gas phase containing 60% of CO2 from the sample is then analyzed by gas chromatography. This method has been used to determine dissolved inorganic and organic carbon in Canadian Shield waters and to determine total carbonates in sediments.

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