Predominance of phytoplankton-derived dissolved and particulate organic carbon in a highly eutrophic tropical coastal embayment (Guanabara Bay,Rio de Janeiro,Brazil)

We investigate the carbon dynamics in Guanabara Bay, an eutrophic tropical coastal embayment surrounded by the megacity of Rio de Janeiro (southeast coast of Brazil). Nine sampling campaigns were conducted for dissolved, particulate and total organic carbon (DOC, POC and TOC), dissolved inorganic carbon (DIC), partial pressure of CO₂ (pCO₂), chlorophyll a (Chl a), pheo-pigments and ancillary parameters. Highest DOC, POC and Chl a concentrations were found in confined-shallow regions of the bay during the summer period with strong pCO₂ undersaturation, and DOC reached 82 mg L^?1, POC 152 mg L^?1, and Chl a 800 μg L^?1. Spatially and temporally, POC and DOC concentrations varied positively with total pigments, and negatively with DIC. Strong linear correlations between these parameters indicate that the production of TOC translates to an equivalent uptake in DIC, with 85% of the POC and about 50% of the DOC being of phytoplanktonic origin. Despite the shallow depths of the bay, surface waters were enriched in POC and DOC relative to bottom waters in periods of high thermohaline stratification. The seasonal accumulation of phytoplankton-derived TOC in the surface waters reached about 105 g C m^?2 year^?1, representing between 8 and 40% of the net primary production. The calculated turnover time of organic carbon was 117 and 34 days during winter and summer, respectively. Our results indicate that eutrophication of coastal bays in the tropics can generate large stocks of planktonic biomass and detrital organic carbon which are permanently being produced and partially degraded and buried in sediments.     

Carbon flows in eutrophic Lake Rotsee: a <Superscript>13</Superscript>C-labelling experiment

The microbial segment of food webs plays a crucial role in lacustrine food-web functioning and carbon transfer, thereby influencing carbon storage and CO₂ emission and uptake in freshwater environments. Variability in microbial carbon processing (autotrophic and heterotrophic production and respiration based on glucose) with depth was investigated in eutrophic, methane-rich Lake Rotsee, Switzerland. In June 2011, ¹³C-labelling experiments were carried out at six depth intervals in the water column under ambient light as well as dark conditions to evaluate the relative importance of (chemo)autotrophic, mixotrophic and heterotrophic production. Label incorporation rates of phospholipid-derived fatty acid (PLFA) biomarkers allowed us to differentiate between microbial producers and calculate group-specific production. We conclude that at 6 m, net primary production (NPP) rates were highest, dominated by algal photoautotrophic production. At 10 m —the base of the oxycline— a distinct low-light community was able to fix inorganic carbon, while in the hypolimnion, heterotrophic production prevailed. At 2 m depth, high label incorporation into POC could only be traced to nonspecific PLFA, which prevented definite identification, but suggests cyanobacteria as dominating organisms. There was also depth zonation in extracellular carbon release and heterotrophic bacterial growth on recently fixed carbon. Large differences were observed between concentrations and label incorporation of POC and biomarkers, with large pools of inactive biomass settling in the hypolimnion, suggesting late-/post-bloom conditions. Net primary production (115 mmol C m^?2 d^?1) reached highest values in the epilimnion and was higher than glucose-based production (3.3 mmol C m^?2 d^?1, highest rates in the hypolimnion) and respiration (5.9 mmol C m^?2 d^?1, highest rates in the epilimnion). Hence, eutrophic Lake Rotsee was net autotrophic during our experiments, potentially storing large amounts of carbon.     

High heterotrophic CO<Subscript>2</Subscript> emissions from a Malaysian oil palm plantations during dry-season

Tropical peatlands are currently being rapidly cleared and drained for the establishment of oil palm plantations, which threatens their globally significant carbon sequestration capacity. Large-scale land conversion of tropical peatlands is important in the context of greenhouse gas emission factors and sustainable land management. At present, quantification of carbon dioxide losses from tropical peatlands is limited by our understanding of the relative contribution of heterotrophic and autotrophic respiration to net peat surface CO₂ emissions. In this study we separated heterotrophic and autotrophic components of peat CO₂ losses from two oil palm plantations (one established in ‘2000’ and the other in 1978, then replanted in ‘2006’) using chamber-based emissions sampling along a transect from the rooting to non-rooting zones on a peatland in Selangor, Peninsular Malaysia over the course of 3 months (June–August, 2014). Collar CO₂ measurements were compared with soil temperature and moisture at site and also accompanied by depth profiles assessing peat C and bulk density. The soil respiration decreased exponentially with distance from the palm trunks with the sharpest decline found for the plantation with the younger palms with overall fluxes of 1341 and 988 mg CO₂ m^?2 h^?1, respectively, at the 2000 and 2006 plantations, respectively. The mean heterotrophic flux was 909 ± SE 136 and 716 ± SE 201 mg m^?2 h^?1 at the 2000 and 2006 plantations, respectively. Autotrophic emissions adjacent to the palm trunks were 845 ± SE 135 and 1558 ± SE 341 mg m^?2 h^?1 at the 2000 and 2006 plantations, respectively. Heterotrophic CO₂ flux was positively related to peat soil moisture, but not temperature. Total peat C stocks were 60 kg m^?2 (down to 1 m depth) and did not vary among plantations of different ages but SOC concentrations declined significantly with depth at both plantations but the decline was sharper in the second generation 2006 plantation. The CO₂ flux values reported in this study suggest a potential for very high carbon (C) loss from drained tropical peats during the dry season. This is particularly concerning given that more intense dry periods related to climate change are predicted for SE Asia. Taken together, this study highlights the need for careful management of tropical peatlands, and the vulnerability of their carbon storage capability under conditions of drainage.     

A worldwide view of organic carbon export from catchments

Growing interest in the effects of global change on the metabolism, stoichiometry and cycling of carbon in aquatic ecosystems has motivated research on the export of organic carbon (OCE) from catchments. In this article, quantitative and functional features of the annual export rates of total, particulate and dissolved organic carbon (TOC, POC and DOC) were reviewed, and the stoichiometry of export (OC:N, OC:P and N:P) from 550 catchments worldwide was reported. TOC export ranged 2.1–92,474?kg?C?km^?2?year^?1, POC export ranged 0.4–73,979?kg?C?km^?2?year^?1 and DOC export ranged 1.2–56,946?kg?C?km^?2?year^?1. Exports of TOC and DOC were strongly linked, but POC export was unrelated to DOC. The DOC fraction comprised on average 73?±?21% of TOC export. The export rates of organic carbon were poorly related to those of total nitrogen and total phosphorus. Discrete and continuous environmental variables failed to predict TOC export, but DOC export was influenced by discharge and catchment area worldwide. Models of OCE in different catchment types were controlled by different environmental variables; hydrological variables were generally better predictors of OCE than anthropogenic and soil variables. Elemental ratios of carbon export in most catchments were above the Redfield ratio, suggesting that phosphorus may become the limiting nutrient for downstream plant growth. These ratios were marginally related to environmental data. More detailed hydrological data, consideration of in-stream processes and the use of quasi-empirical dynamical models are advocated to improve our knowledge of OCE rates and those of other nutrients.     

Carbon dioxide and methane emissions from interfluvial wetlands in the upper Negro River basin, Brazil

Extensive interfluvial wetlands occur in the upper Negro River basin (Brazil) and contain a mosaic of vegetation dominated by emergent grasses and sedges with patches of shrubs and palms. To characterize the release of carbon dioxide and methane from these habitats, diffusive and ebullitive emissions and transport through plant aerenchyma were measured monthly during 2005 in permanently and seasonally flooded areas. CO₂ emissions averaged 2193 mg C m^?2 day^?1. Methane was consumed in unflooded environments and emitted in flooded environments with average values of ?4.8 and 60 mg C m^?2 day^?1, respectively. Bubbles were emitted primarily during falling water periods when hydrostatic pressure at the sediment?Cwater interface declined. CO₂ and CH₄ emissions increased when dissolved O₂ decreased and vegetation was more abundant. Total area and seasonally varying flooded areas for two wetlands, located north and south of the Negro River, were determined through analysis of synthetic aperture radar and optical remotely sensed data. The combined areas of these two wetlands (3000 km²) emitted 1147 Gg C year^?1 as CO₂ and 31 Gg C year^?1 as CH₄. If these rates are extrapolated to the area occupied by hydromorphic soils in the upper Negro basin, 63 Tg C year^?1 of CO₂ and 1.7 Tg C year^?1 as CH₄ are estimated as the regional evasion to the atmosphere.     

Gaseous and fluvial carbon export from an Amazon forest watershed

The transfer of carbon (C) from Amazon forests to aquatic ecosystems as CO₂ supersaturated in groundwater that outgases to the atmosphere after it reaches small streams has been postulated to be an important component of terrestrial ecosystem C budgets. We measured C losses as soil respiration and methane (CH₄) flux, direct CO₂ and CH₄ fluxes from the stream surface and fluvial export of dissolved inorganic C (DIC), dissolved organic C (DOC), and particulate C over an annual hydrologic cycle from a 1,319-ha forested Amazon perennial first-order headwater watershed at Tanguro Ranch in the southern Amazon state of Mato Grosso. Stream pCO₂ concentrations ranged from 6,491 to 14,976 ??atm and directly-measured stream CO₂ outgassing flux was 5,994 ± 677 g C m^?2 y^?1 of stream surface. Stream pCH₄ concentrations ranged from 291 to 438 ??atm and measured stream CH₄ outgassing flux was 987 ± 221 g C m^?2 y^?1. Despite high flux rates from the stream surface, the small area of stream itself (970 m², or 0.007% of watershed area) led to small directly-measured annual fluxes of CO₂ (0.44 ± 0.05 g C m² y^?1) and CH₄ (0.07 ± 0.02 g C m² y^?1) per unit watershed land area. Measured fluvial export of DIC (0.78 ± 0.04 g C m^?2 y^?1), DOC (0.16 ± 0.03 g C m^?2 y^?1) and coarse plus fine particulate C (0.001 ± 0.001 g C m^?2 y^?1) per unit watershed land area were also small. However, stream discharge accounted for only 12% of the modeled annual watershed water output because deep groundwater flows dominated total runoff from the watershed. When C in this bypassing groundwater was included, total watershed export was 10.83 g C m^?2 y^?1 as CO₂ outgassing, 11.29 g C m^?2 y^?1 as fluvial DIC and 0.64 g C m^?2 y^?1 as fluvial DOC. Outgassing fluxes were somewhat lower than the 40?C50 g C m^?2 y^?1 reported from other Amazon watersheds and may result in part from lower annual rainfall at Tanguro. Total stream-associated gaseous C losses were two orders of magnitude less than soil respiration (696 ± 147 g C m^?2 y^?1), but total losses of C transported by water comprised up to about 20% of the ± 150 g C m^?2 (±1.5 Mg C ha^?1) that is exchanged annually across Amazon tropical forest canopies.     

The Absorption of Light in Lakes: Negative Impact of Dissolved Organic Carbon on Primary Productivity

Colored dissolved organic matter (CDOM) absorbs a substantial fraction of photosynthetically active radiation (PAR) in boreal lakes. However, few studies have systematically estimated how this light absorption influences pelagic primary productivity. In this study, 75 boreal lakes spanning wide and orthogonal gradients in dissolved organic carbon (DOC) and total phosphorus (TP) were sampled during a synoptic survey. We measured absorption spectra of phytoplankton pigments, CDOM, and non-algal particles to quantify the vertical fate of photons in the PAR region. Area-specific rates of gross primary productivity (PP_A) were estimated using a bio-optical approach based on phytoplankton in vivo light absorption and the light-dependent quantum yield of photochemistry in PSII measured by a PAM fluorometer. Subsequently, we calculated the effects of CDOM, DOC, and TP concentration on PP_A. CDOM absorbed the largest fraction of PAR in the majority of lakes (mean 56.3%, range 36.9–76.2%), phytoplankton pigments captured a comparatively minor fraction (mean 6.6%, range 2.2–28.2%). PP_A estimates spanned from 45 to 993 mg C m^?2 day^?1 (median 286 mg C m^?2 day^?1). We found contrasting effects of CDOM (negative) and TP (positive) on PP_A. The use of DOC or CDOM as predictors gave very similar results and the negative effect of these variables on PP_A can probably be attributed to shading. A future scenario of increased DOC, which is highly correlated with CDOM in these lakes, might impose negative effects on areal primary productivity in boreal lakes.     

Small scale variability of vertical water and dissolved organic matter fluxes in sandy Cambisol subsoils as revealed by segmented suction plates

Dissolved organic matter (DOM) is considered as a major carbon source in subsoils. As soil water fluxes are highly variable at small scale, and transport versus sorptive retention of DOM is related to water flux and associated contact time with minerals, knowledge of the small scale spatial variability of the dissolved organic carbon (DOC) concentrations and fluxes into the subsoil is decisive for a solid estimation of organic carbon (OC) translocation into the subsoil. Here, we made advantage of novel segmented suction plates (4 × 4 segments, each 36 cm²) to analyze the small scale spatial and temporal variability of DOC transport at 10, 50 and 150 cm depth of three subsoil observatories (approximately 50 m apart) in a sandy Dystric Cambisol under beech in the Grinderwald, 40 km northwest from Hannover, Germany. Water fluxes, DOC concentrations and fluxes as well as the specific UV absorbance (SUVA) at 280 nm were determined in weekly samples from August 2014 to November 2015 for each individual segment. The DOC fluxes decreased with depth (19.6 g C m^?2 year^?1, 10 cm; 1.2 g C m^?2 year^?1, 150 cm) and were strongly related to the water fluxes. The SUVA at 280 nm also decreased with depth (0.03 L mg C^?1 cm^?1, 10 cm; 0.01 L mg C^?1 cm^?1, 150 cm), indicating a selective retention of aromatic moieties, that was eased with increasing water flux at least in the subsoil. The proportion of temporal fluctuations and small scale variability on the total variance of each parameter where determined by the calculation of intra class correlations. The seasonal heterogeneity and the small scale spatial heterogeneity were identified to be of major importance. The importance of the small scale spatial heterogeneity strongly increased with depth, pointing towards the stability of flow paths and suggesting that at a given substrate hydrological processes rather than physicochemical processes are decisive for the sorptive retention of DOM and the variability of OC accumulation in the subsoil. Our results clearly show the demand of small scale sampling for the identification of processes regarding carbon cycling in the subsoil.     

Riverine nitrogen and carbon exports from the Canadian landmass to estuaries

Dissolved total nitrogen (N_t) and total organic carbon (TOC) exports were measured from 30 catchments and regions draining 76 % of the Canadian landscape in order to estimate reactive N and organic C runoff losses to estuaries and the conditions that control them. N exports from the catchments were lower than measured in most of Europe and the United States due to significantly less agricultural activity and atmospheric deposition, especially in northern Canada. We produce statistical models using a number of geographical, climatic, agricultural, and population factors in order to predict N and C losses from the remaining regions. Using measured and extrapolated data, we estimated that the Canadian landscape exports 884 and 18,210 ktons of N_t and OC per year. Area normalized exports ranged from 29.4 kg km^?2 for the northern Mackenzie River to 299 kg km^?2 for the semi-agricultural Saint John. Area normalized OC exports ranged from 495 kg km^?2 in the high Arctic to 7,295 to the wetland dominated Broadback River in northern Quebec. N exports were best predicted by the latitude of the catchment centroid, mean slope, population density, runoff and % of the catchment as agricultural land. The best model for predicting TOC exports needed only slope and runoff. The N_t/OC ratio in the rivers unsurprisingly was highest in the southern portion of the country where anthropogenic activities were concentrated.     

Gross primary productivity of phytoplankton and planktonic respiration in inland floodplain wetlands of southeast Australia: habitat-dependent patterns and regulating processes

Gross primary productivity (GPP) of phytoplankton and planktonic respiration (PR) (i.e., planktonic metabolism) are critical pathways for carbon transformation in many aquatic ecosystems. In inland floodplain wetlands with variable inundation regimes, quantitative measurements of GPP and PR are rare and their relationships with wetland environmental conditions are largely unknown. We measured PR and the GPP of phytoplankton using light and dark biological oxygen demand bottles in open waters of channel and non-channel floodplain habitats of inland floodplain wetlands of southeast Australia that had been inundated by environmental water. Overall, GPP varied from 3.7 to 405.5 mg C m^?3 h^?1 (mean ± standard error: 89.4 ± 9.2 mg C m^?3 h^?1, n = 81), PR from 1.5 to 251.6 mg C m^?3 h^?1 (43.2 ± 5.6 mg C m^?3 h^?1, n = 81), and GPP/PR from 0.2 to 15.6 (3.0 ± 0.3, n = 81). In terms of wetland environmental conditions, total nitrogen (TN) ranged from 682.0 to 14,700.0 mg m^?3 (mean ± standard error: 2,643.0 ± 241.6 mg m^?3, n = 81), total phosphorus (TP) from 48.0 to 1,405.0 mg m^?3 (316.8 ± 31.4 mg m^?3, n = 81), and dissolved organic carbon (DOC) from 1.9 to 46.3 g m^?3 (22.0 ± 1.6 g m^?3, n = 81). Using ordinary least-squares multiple regression analyses, the rates of GPP and PR, and their ratio (GPP/PR) were modeled as a function of TN, TP, and DOC that had been measured concomitantly. The “best” models predicted GPP and GPP/PR ratio in channel habitats as a function of DOC; and GPP, PR, and GPP/PR in non-channel floodplain habitats as a function of TN and/or TP. The models explained between 46 and 74 % of the variance in channel habitats and between 17 and 87 % of the variance in non-channel floodplain habitats. Net autotrophy (mean GPP/PR 3.0) of planktonic metabolism in our work supports the prevailing view that wetlands are a net sink for carbon dioxide. We propose a nutrient-DOC framework, combined with hydrological and geomorphological delineations, to better predict and understand the planktonic metabolism in inland floodplain wetlands.     

The relative contributions of biological and abiotic processes to carbon dynamics in subarctic sea ice

Knowledge on the relative effects of biological activity and precipitation/dissolution of calcium carbonate (CaCO₃) in influencing the air-ice CO₂ exchange in sea-ice-covered season is currently lacking. Furthermore, the spatial and temporal occurrence of CaCO₃ and other biogeochemical parameters in sea ice are still not well described. Here we investigated autotrophic and heterotrophic activity as well as the precipitation/dissolution of CaCO₃ in subarctic sea ice in South West Greenland. Integrated over the entire ice season (71 days), the sea ice was net autotrophic with a net carbon fixation of 56 mg C m^?2, derived from a sea-ice-related gross primary production of 153 mg C m^?2 and a bacterial carbon demand of 97 mg C m^?2. Primary production contributed only marginally to the TCO₂ depletion of the sea ice (7–25 %), which was mainly controlled by physical export by brine drainage and CaCO₃ precipitation. The net biological production could only explain 4 % of this sea-ice-driven CO₂ uptake. Abiotic processes contributed to an air-sea CO₂ uptake of 1.5 mmol m^?2 sea ice day^?1, and dissolution of CaCO₃ increased the air-sea CO₂ uptake by 36 % compared to a theoretical estimate of melting CaCO₃-free sea ice. There was a considerable spatial and temporal variability of CaCO₃ and the other biogeochemical parameters measured (dissolved organic and inorganic nutrients).     

Potamoplankton and primary productivity in the River Danube

Autochthonous production of potamoplankton has recently attracted greater interest as it was incorporated into expanded river concepts such as the flow pulse concept or the riverine productivity model (RPM). This review assembles data on primary production from the River Danube to evaluate the importance of productivity in large rivers. Results indicate positive net production in the middle reach of the river and in impoundments. These sections are characterised by favourable conditions for algal growth. Reduction in flow, reduced concentrations of suspended solids and improved under-water light result in significant increase in plankton biomass. Maximum chlorophyll concentrations were below 20 mg m^?3 in 2007 but concentrations up to 130 mg m^?3 have been recorded in the past. Since nutrients are not limiting, as in most large rivers, net primary production is largely controlled by availability of photosynthetic active radiation under water, chlorophyll-a, water depth and discharge. Hourly carbon uptake rates of 3–130 mg C m^?3 h^?1 observed in the Danube are well within the range of 0–790 mg C m^?3 h^?1 for large rivers of the world. Autochthonous autotrophic production must be regarded as an important feature of large rivers supporting the RPM concept.     

Vertical change in dissolved organic carbon and oxygen at the water table region of an aquifer recharged with stormwater: biological uptake or mixing?

Decreases in dissolved organic carbon (DOC) and dissolved oxygen (DO) with increasing depth below the groundwater table are often considered as evidence for aerobic respiration; however, they may reflect mixing of infiltrating water and groundwater. We found that groundwater DOC concentration was on average 0.3 mg C l^?1 higher and DO concentration 1.5 mg O₂ l^?1 lower at recharge sites replenished with stormwater than at reference sites fed by direct infiltration of rain water from the land surface. Groundwater DOC increased and DO decreased with increasing vadose zone thickness (VZT) at both recharge and reference sites. There was no significant interaction between the effects of stormwater infiltration and VZT. Vertical changes in DOC and DO below the groundwater table at recharge sites could account for by simple mixing of infiltrating stormwater and groundwater. Moreover, aquifer sediment respiration (SR) was not significantly higher at recharge sites than at reference sites. However, slow filtration column experiments showed that SR increased significantly with an increasing supply of easily biodegradable DOC. We conclude that the observed reduction in DOC below the groundwater table at recharge sites was essentially due to water mixing rather than biological uptake because of the low biodegradability of the DOC and the short transit time of stormwater in the upper layers of groundwater. Our results highlight the need to distinguish between the effect of hydrological and biological processes on DOC and DO patterns below the groundwater before conclusions are made on the efficiency of groundwater in degrading surface-derived DOC.     

Seasonal variation in dissolved carbon concentrations and fluxes in the upper Purus River, southwestern Amazon

One of the less studied components of carbon cycling that could improve our understanding of how and how strongly Amazonian ecosystems act as sinks or sources of carbon is the amount that is carried downstream by rivers. In this paper, we show that a headwater river can carry from 25 to 130 % of the reported sink for Amazonian forests, therefore not being negligible for ecosystem-level carbon budgets. Based on monthly measurements from May 2004 to April 2005 of the upper Purus River, southwestern Amazonia, we found that: water pH, dissolved oxygen, specific electrical conductivity, and dissolved inorganic carbon (DIC) were inversely related to water discharge and precipitation; pCO₂ was directly and strongly related to discharge and precipitation, and to a lesser extent to pH and dissolved oxygen; and dissolved organic carbon (DOC) was not related to any measured variable. Annual flux of dissolved carbon (DIC + DOC) at the sampling site was estimated as 604 ± 55 Gg C a^?1. More than 75 % was in the form of bicarbonate, with the remainder as CO₂ and DOC. This amount is equivalent to 0.15 ± 0.01 Mg C ha^?1 a^?1 in the upstream drainage basin, which is on the same order of magnitude as terrestrial carbon fixation.     

Estimation of carbon biomass and community structure of planktonic bacteria in Lake Biwa using respiratory quinone analysis

The relationship between bacterial respiratory quinone (RQ) concentration and biomass was assessed for Lake Biwa bacterial assemblages to evaluate the utility of bacterial RQ concentration as an indicator of bacterial carbon. The biomass estimated from the RQ concentration correlated well with that from cell volume, indicating that RQ concentration is an appropriate indicator of bacterial biomass. The estimated carbon content per unit of RQ (carbon conversion factor) of bacteria was 0.67 mg C nmol RQ^?1. Bacterial carbon biomass, which was estimated from the RQ concentration using the conversion factor, ranged between 0.008 and 0.054 mg C L^?1 (average 0.025 mg C L^?1) at 5 m depth and between 0.010 and 0.024 mg C L^?1 (average 0.015 mg C L^?1) at 70 m depth. Ubiquinone-8-containing bacteria dominated the epilimnion and hypolimnion. Compared to conventional image analysis, bacterial RQ analysis is a less laborious method of simultaneously determining bacterial biomass and community.     

Evolution of carbon fluxes during initial soil formation along the forefield of Damma glacier, Switzerland

Soil carbon (C) fluxes, soil respiration and dissolved organic carbon (DOC) leaching were explored along the young Damma glacier forefield chronosequence (7–128 years) over a three-year period. To gain insight into the sources of soil CO₂ effluxes, radiocarbon signatures of respired CO₂ were measured and a vegetation-clipping experiment was performed. Our results showed a clear increase in soil CO₂ effluxes with increasing site age from 9 ± 1 to 160 ± 67 g CO₂–C m^?2 year^?1, which was linked to soil C accumulation and development of vegetation cover. Seasonal variations of soil respiration were mainly driven by temperature; between 62 and 70 % of annual CO₂ effluxes were respired during the 4-month long summer season. Sources of soil CO₂ effluxes changed along the glacier forefield. For most recently deglaciated sites, radiocarbon-based age estimates indicated ancient C to be the dominant source of soil-respired CO₂. At intermediate site age (58–78 years), the contribution of new plant-fixed C via rhizosphere respiration amounted up to 90 %, while with further soil formation, heterotrophically respired C probably from accumulated ‘older’ soil organic carbon (SOC) became increasingly important. In comparison with soil respiration, DOC leaching at 10 cm depth was small, but increased similarly from 0.4 ± 0.02 to 7.4 ± 1.6 g DOC m^?2 year^?1 over the chronosequence. A strong rise of the ratio of SOC to secondary iron and aluminium oxides strongly suggests that increasing DOC leaching with site age results from a faster increase of the DOC source, SOC, than of the DOC sink, reactive mineral surfaces. Overall, C losses from soil by soil respiration and DOC leaching increased from 9 ± 1 to 70 ± 17 and further to 168 ± 68 g C m^?2 year^?1 at the <10, 58–78, and 110–128 year old sites. By comparison, total ecosystem C stocks increased from 0.2 to 1.1 and to 3.1 kg C m^?2 from the young to intermediate and old sites. Therefore, the ecosystem evolved from a dominance of C accumulation in the initial phase to a high throughput system. We suggest that the relatively strong increase in soil C stocks compared to C fluxes is a characteristic feature of initial soil formation on freshly exposed rocks.     

<Emphasis Type="Italic">In vitro</Emphasis> effects of GA<Subscript>3</Subscript> on morphogenesis of CIP potato explants and acclimatization of plantlets in field

Improvement of potato has been accomplished using conventional and non-conventional approaches coupled with numerous tissue culture procedures. The aim of the present study was to assess the efficacy of gibberellic acid (GA₃) on the morphogenesis of International Potato Center (CIP) potato explants and acclimatization of plantlets in the field. Nodal segments as an explant source (1–1.5 cm) were isolated from 31 CIP potato plantlets and were inoculated into Murashige and Skoog (MS) medium supplemented with 0.0 (control), 0.1, 0.5, or 1.0 mg L^?1of GA₃. The variation in growth parameters of the cultivars was then observed. The highest shoot induction occurred in MS medium containing 1.0 mg L^?1 GA₃ with an increase in the inter-nodal distance between nodes as compared to other treatments. Higher concentration (1.0 mg L^?1) of GA₃ significantly increased plant height and root length in the treated germplasm however; this concentration was inhibitory to the number of nodes and roots per plant. The number of leaves was significantly increased in plants receiving GA₃ treatment at lower concentration (0.1 mg L^?1). The 31 CIP genotypes were transplanted to the field and checked for yield quality traits. It was concluded from the results that GA₃ had significant effects on morphogenesis and was effective in the acclimatization of CIP potato plantlets in field.     

Spatial and temporal dynamics of diffusive methane emissions in the Okavango Delta,northern Botswana,Africa

Global warming is associated with the continued increase in the atmospheric concentrations of greenhouse gases; carbon dioxide, methane (CH₄) and nitrous oxide. Wetlands constitute the largest single natural source of atmospheric CH₄ in the world contributing between 100 and 231 Tg year^?1 to the total budget of 503–610 Tg year^?1, approximately 60 % of which is emitted from tropical wetlands. We conducted diffusive CH₄ emission measurements using static chambers in river channels, floodplains and lagoons in permanent and seasonal swamps in the Okavango Delta, Botswana. Diffusive CH₄ emission rates varied between 0.24 and 293 mg CH₄ m^?2 h^?1, with a mean (±SE) emission of 23.2 ± 2.2 mg CH₄ m^?2 h^?1 or 558 ± 53 mg CH₄ m^?2 day^?1. These emission rates lie within the range reported for other tropical wetlands. The emission rates were significantly higher (P < 0.007) in permanent than in seasonal swamps. River channels exhibited the highest average fluxes at 31.3 ± 5.4 mg CH₄ m^?2 h^?1 than in floodplains (20.4 ± 2.5 mg CH₄ m^?2 h^?1) and lagoons (16.9 ± 2.6 mg CH₄ m^?2 h^?1). Diffusive CH₄ emissions in the Delta were probably regulated by temperature since emissions were highest (20–300 mg CH₄ m^?2 h^?1) and lowest (0.2–3.0 mg m^?2 h^?1) during the warmer-rainy and cooler winter seasons, respectively. Surface water temperatures between December 2010 and January 2012 varied from 15.3 °C in winter to 33 °C in summer. Assuming mean inundation of 9,000 km², the Delta’s annual diffusive emission was estimated at 1.8 ± 0.2 Tg, accounting for 2.8 ± 0.3 % of the total CH₄ emission from global tropical wetlands.     

Biotrickling filtration of isopropanol under intermittent loading conditions

This paper investigates the removal of isopropanol by gas-phase biotrickling filtration. Two plastic packing materials, one structured and one random, have been evaluated in terms of oxygen mass transfer and isopropanol removal efficiency. Oxygen mass transfer experiments were performed at gas velocities of 104 and 312 m h^?1 and liquid velocities between 3 and 33 m h^?1. Both materials showed similar mass transfer coefficients up to liquid velocities of 15 m h^?1. At greater liquid velocities, the structured packing exhibited greater oxygen mass transfer coefficients. Biotrickling filtration experiments were carried out at inlet loads (IL) from 20 to 65 g C m^?3 h^?1 and empty bed residence times (EBRT) from 14 to 160 s. To simulate typical industrial emissions, intermittent isopropanol loading (16 h/day, 5 day/week) and intermittent spraying frequency (15 min/1.5 h) were applied. Maximum elimination capacity of 51 g C m^?3 h^?1 has been obtained for the random packing (IL of 65 g C m^?3 h^?1, EBRT of 50 s). The decrease in irrigation frequency to 15 min every 3 h caused a decrease in the outlet emissions from 86 to 59 mg C Nm^?3 (inlet of 500 mg C Nm^?3). The expansion of spraying to night and weekend periods promoted the degradation of the isopropanol accumulated in the water tank during the day, reaching effluent concentrations as low as 44 mg C Nm^?3. After a 7-week starvation period, the performance was recovered in less than 10 days, proving the robustness of the process.     

Responses of a new isolated <Emphasis Type="Italic">Cyanobacterium aponinum</Emphasis> strain to temperature,pH, CO<Subscript>2</Subscript> and light quality

A new strain of cyanobacteria was isolated from seawater samples collected near Jimo hot springs, Qingdao, China, and was identified as Cyanobacterium aponinum by 16S rDNA analysis. This study examined the effects of temperature, pH, light quality and high CO₂ concentration on the growth of the cyanobacteria. Results showed that the strain exhibited a higher growth rate (about 168.4 mg L^?1 day^?1) at 35 °C than other temperatures (surviving at up to 50 °C) and a wide growth tolerance to acidic stress (pH 3.0 to 4.0) resulting from either H₂SO₄ or HNO₃. The four light qualities, ranked by greatest to least biomass effect, were as follows: LED white light (LW) > LED red light (LR) > fluorescent white light (FW) > LED blue light (LB), achieving a higher lighting effect at a LW light intensity (60 μmol photons m^?2 s^?1) lower than other light qualities, which implied less energy consumption therewith. This strain demonstrates excellent CO₂ tolerance at least 10% CO₂ with the highest productivity in biomass (about 337.8 mg L^?1 day^?1) measured at 1% CO₂ level. Results indicate that this strain is a promising candidate for use in biofixation of CO₂ from flue gases emitted by thermoelectric plants.