Spatial and temporal variability of pCO2 and CO2 efflux in seven Amazonian Rivers

Current estimates of CO₂ outgassing from Amazonian rivers and streams have considerable uncertainty since they are based on limited-time surveys of pCO₂ measurements along the Amazon mainstem and mouths of major tributaries, using conservative estimates of gas exchange velocities. In order to refine basin-scale CO₂ efflux estimates from Amazonian rivers, we present a long time (5-year) dataset of direct measurements of CO₂ fluxes, gas transfer velocities and pCO₂ measurements in seven representative rivers of the lowland Amazon basin fluvial network, six non-tidal (Negro, Solimões, Teles Pires, Cristalino, Araguaia and Javaés) and one tidal river (Caxiuanã), with sizes ranging from 4th to 9th order. Surveys were conducted from January 2006 to December 2010, in a total of 389 campaigns covering all stages of their hydrographs. CO₂ fluxes and gas transfer velocities (k) were measured using floating chambers and pCO₂ was measured simultaneously by headspace extraction followed by gas chromatography analysis. Results show high CO₂ flux rate variability among rivers and hydrograph stages, ranging from ?0.8 to 15.3 μmol CO₂ m^?2 s^?1, with unexpected negative fluxes in clear-water rivers during low waters. Non-tidal rivers showed marked seasonal CO₂ flux patterns, with significantly higher exchange during high waters. Seasonality was modulated by pCO₂, which was positive and strongly correlated with discharge. In these rivers k was well correlated with wind speed, which allowed the use of wind data to model k. We estimate a release of 360 ± 60 Tg C year^?1 from Amazonian rivers and streams within a 1.47 million km² quadrant in the central lowland Amazon. Extrapolating these values to the basin upstream of Óbidos, results in an outgassing of 0.8 Pg C to the atmosphere each year. Our results are a step forward in achieving more accurate gas emission values for Amazonian rivers and their role in the annual carbon budget of the Amazon basin.     

Metabolism,Gas Exchange,and Carbon Spiraling in Rivers

Ecosystem metabolism, that is, gross primary productivity (GPP) and ecosystem respiration (ER), controls organic carbon (OC) cycling in stream and river networks and is expected to vary predictably with network position. However, estimates of metabolism in small streams outnumber those from rivers such that there are limited empirical data comparing metabolism across a range of stream and river sizes. We measured metabolism in 14 rivers (discharge range 14–84 m³ s^?1) in the Western and Midwestern United States (US). We estimated GPP, ER, and gas exchange rates using a Lagrangian, 2-station oxygen model solved in a Bayesian framework. GPP ranged from 0.6–22 g O₂ m^?2 d^?1 and ER tracked GPP, suggesting that autotrophic production supports much of riverine ER in summer. Net ecosystem production, the balance between GPP and ER was 0 or greater in 4 rivers showing autotrophy on that day. River velocity and slope predicted gas exchange estimates from these 14 rivers in agreement with empirical models. Carbon turnover lengths (that is, the distance traveled before OC is mineralized to CO₂) ranged from 38 to 1190 km, with the longest turnover lengths in high-sediment, arid-land rivers. We also compared estimated turnover lengths with the relative length of the river segment between major tributaries or lakes; the mean ratio of carbon turnover length to river length was 1.6, demonstrating that rivers can mineralize much of the OC load along their length at baseflow. Carbon mineralization velocities ranged from 0.05 to 0.81 m d^?1, and were not different than measurements from small streams. Given high GPP relative to ER, combined with generally short OC spiraling lengths, rivers can be highly reactive with regard to OC cycling.     

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.     

Seasonal variability of methane in the rivers and lagoons of Ivory Coast (West Africa)

We report a data-set of dissolved methane (CH₄) in three rivers (Comoé, Bia and Tanoé) and five lagoons (Grand-Lahou, Ebrié, Potou, Aby and Tendo) of Ivory Coast (West Africa), during the four main climatic seasons (high dry season, high rainy season, low dry season and low rainy season). The surface waters of the three rivers were over-saturated in CH₄ with respect to atmospheric equilibrium (2221–38719%), and the seasonal variability of CH₄ seemed to be largely controlled by dilution during the flooding period. The strong correlation of CH₄ concentrations with the partial pressure of CO₂ (pCO₂) and dissolved silicate (DSi) confirm the dominance of a continental sources (from soils) for both CO₂ and CH₄ in these rivers. Diffusive air–water CH₄ fluxes ranged between 25 and 1187 μmol m^?2 day^?1, and annual integrated values were 288 ± 107, 155 ± 38, and 241 ± 91 μmol m^?2 day^?1 in the Comoé, Bia and Tanoé rivers, respectively. In the five lagoons, surface waters were also over-saturated in CH₄ (ranging from 1496 to 51843%). Diffusive air–water CH₄ fluxes ranged between 20 and 2403 μmol m^?2 day^?1, and annual integrated values were 78 ± 34, 338 ± 217, 227 ± 79, 330 ± 153 and 326 ± 181 μmol m^?2 day^?1 in the Grand-Lahou, Ebrié, Potou, Aby and Tendo lagoons, respectively. The largest CH₄ over-saturations were observed in the Tendo and Aby lagoons that are permanently stratified systems (unlike the other three lagoons), leading to anoxic bottom waters favorable for a large CH₄ production. In addition, these two stratified lagoons showed low pCO₂ values due to high primary production, which suggests an efficient transfer of organic matter across the pycnocline. As a result, the stratified Tendo and Aby lagoons were respectively, a low source of CO₂ to the atmosphere and a sink of atmospheric CO₂ while the other three well-mixed lagoons were strong sources of CO₂ to the atmosphere but less over-saturated in CH₄.     

Interannual variability of carbon dioxide drawdown by subantarctic surface water near New Zealand

The ocean-atmosphere flux of carbon dioxide in subantarctic surface water (SASW) east of New Zealand has been determined using data from bi-monthly cruises on a time series transect for 8 years. The 60 km long transect extends from the coast (45.770°S 170.720°E) to a station at 45.833°S 171.500°E. Sea surface temperature, salinity, nutrient concentrations and pCO₂ have been measured at a frequency of about once every 2 months from January 1998 until December 2005. Measured pCO₂ exhibits a seasonal cycle with a maximum in late winter/spring, and a minimum in late summer/autumn, a mean 356 ??atm, and an amplitude of 9 ??atm. The magnitude of ??pCO₂ (the air-sea concentration gradient) has increased over the 8 years, primarily due to the increase in atmospheric CO₂ concentration. The air-sea flux of CO₂ was determined from wind speed data and ??pCO₂. The uptake of atmospheric CO₂ by SASW in the study area changed from + 1 and +82 mmol m^?2 in 1998 and 1999 respectively (ocean as source) to ?870 and ?510 mmol m^?2 in 2004 and 2005 (ocean as sink). These values are substantially less in magnitude than the value obtained from the Takahashi et al. (Deep-Sea Res II, 2009) flux climatology.     

Quantifying the indirect effects of nitrogen deposition on grassland litter chemical traits

The quantitative contribution of tropical estuaries to the atmospheric CO₂ budget has large uncertainties, both spatially and seasonally. We investigated the seasonal and spatial variations of carbon biogeochemistry downstream of Ho Chi Minh City (Southern Vietnam). We sampled four sites distributed from downstream of a highly urbanised watershed through mangroves to the South China Sea coast during the dry and wet seasons. Measured partial pressure of CO₂ (pCO₂) ranged from 660 to 3000 μatm during the dry season, and from 740 to 5000 μatm during the wet season. High organic load, dissolved oxygen saturation down to 17%, and pCO₂ up to 5000 μatm at the freshwater endmember of the estuary reflected the intense human pressure on this ecosystem. We show that releases from mangrove soils affect the water column pCO₂ in this large tropical estuary (~600 m wide and 10–20 m deep). This study is among the few to report direct measurements of both water pCO₂ and CO₂ emissions in a Southeast Asian tropical estuary located in a highly urbanised watershed. It shows that the contribution of such estuaries may have been previously underestimated, with CO₂ emissions ranging from 74 to 876 mmol m^?2 day^?1 at low current velocity (< 0.2 m s^?1). Corresponding gas transfer velocities k₆₀₀, ranging from 1.7 to 11.0 m day^?1, were about 2 to 4 times of k₆₀₀ estimated using published literature equations.     

Disproportionate Contribution of Riparian Inputs to Organic Carbon Pools in Freshwater Systems

A lack of appropriate proxies has traditionally hampered our ability to distinguish riverine organic carbon (OC) sources at the landscape scale. However, the dissection of C₄ grasslands by C₃-enriched riparian vegetation, and the distinct carbon stable isotope signature (δ¹³C) of these two photosynthetic pathways, provides a unique setting to assess the relative contribution of riparian and more distant sources to riverine C pools. Here, we compared δ¹³C signatures of bulk sub-basin vegetation (δ¹³C_VEG) with those of riverine OC pools for a wide range of sites within two contrasting river basins in Madagascar. Although C₃-derived carbon dominated in the eastern Rianala catchment, consistent with the dominant vegetation, we found that in the C₄-dominated Betsiboka basin, riverine OC is disproportionately sourced from the C₃-enriched riparian fringe, irrespective of climatic season, even though δ¹³C_VEG estimates suggest as much as 96% of vegetation cover in some Betsiboka sub-basins may be accounted for by C₄ biomass. For example, δ¹³C values for river bed OC were on average 6.9 ± 2.7‰ depleted in ¹³C compared to paired estimates of δ¹³C_VEG. The disconnection of the wider C₄-dominated basin is considered the primary driver of the under-representation of C₄-derived C within riverine OC pools in the Betsiboka basin, although combustion of grassland biomass by fire is likely a subsidiary constraint on the quantity of terrestrial organic matter available for export to these streams and rivers. Our findings carry implications for the use of sedimentary δ¹³C signatures as proxies for past forest-grassland distribution and climate, as the C₄ component may be considerably underestimated due to its disconnection from riverine OC pools.     

Controls on the origin and cycling of riverine dissolved inorganic carbon in the Brazos River, Texas

Rivers draining watersheds that include carbonate bedrock or organic matter (OM)-rich sedimentary rocks frequently have ¹⁴C-depleted dissolved inorganic carbon (DIC) relative to rivers draining carbonate- and OM-free watersheds, due to dissolution of carbonate and/or decomposition of ancient OM. However, our results from a subtropical river, the Brazos River in Texas, USA, show that in this watershed human activities appear to dominate basin lithology in controlling the origin and metabolism of DIC. The middle Brazos flows through limestone and coal-bearing bedrock, but DIC isotope data suggest no limestone dissolution or respiration of ancient OM, and instead reflect efficient air?Cwater CO₂ exchange, degradation of relatively young OM and photosynthesis in the river as a result of river damming and urban treated wastewater input. The lower Brazos drains only small areas of carbonate and coal-bearing bedrock, but DIC isotope data suggest the strong influence of carbonate dissolution, with a potentially minor contribution from decomposition of old soil organic matter (SOM). Oyster shells and crushed carbonate minerals used in road construction are likely sources of carbonate in the lower Brazos, in addition to natural marl and pedogenic carbonate. Additionally, the generally low pCO₂ and high DIC concentration in the Brazos River lead to a low CO₂ outgassing:DIC export ratio, distinguishing the Brazos River from other rivers.     

Fluvial transport of carbon along the river-to-ocean continuum and its potential impacts on a brackish water food web in the Iwaki River watershed, northern Japan

Riverine transport of dissolved inorganic carbon (DIC) from land to the ocean is an important carbon flux that influences the carbon budget at the watershed scale. However, the dynamics of DIC in an entire river network has remained unknown, especially in mountainous Japanese watersheds. We examined the effects of watershed land use and geology on the transports of inorganic carbon as well as weathered silica (Si) and calcium (Ca) in the Iwaki River system where agricultural and residential areas have developed in the middle and lower parts of the watershed. The concentration and stable carbon isotope ratios (δ¹³C) of DIC showed the longitudinal increase of ¹³C-depleted inorganic carbon along the river. As a result, most streams and rivers were supersaturated in dissolved CO₂ that will eventually be emitted to the atmosphere. The possible origin of ¹³C-depleted carbon is CO₂ derived from the decomposition of organic matter in agricultural and urban landscapes, as well as from in-stream respiration. In addition, agricultural and urban areas, respectively, exported the large amount of dissolved Si and Ca to the rivers, suggesting that CO₂ increased by respiration accelerates the chemical weathering of silicate and carbonate materials in soils, river sediments, and/or urban infrastructure. Furthermore, riverine bicarbonate flux is likely to enter shell carbonates of Corbicula japonica, an aragonitic bivalve, in the downstream brackish lake (Lake Jusan). These results revealed that the flux of DIC from the human-dominated watersheds is a key to understanding the carbon dynamics and food-web structure along the land-to-river-to-ocean continuum.     

Organic carbon transfers in the subtropical Red River system (Viet Nam): insights on CO<Subscript>2</Subscript> sources and sinks

The Red River, draining a 169,000 km² watershed, is the second largest river in Viet Nam and constitutes the main source of water for a large percentage of the population of North Viet Nam. Here we present the results of an investigation into the spatial distribution and temporal dynamics of particulate and dissolved organic carbon (POC and DOC, respectively) in the Red River Basin. POC concentrations ranged from 0.24 to 5.80 mg C L^?1 and DOC concentrations ranged from 0.26 to 5.39 mg C L^?1. The application of the Seneque/Riverstrahler model to monthly POC and DOC measurements showed that, in general, the model simulations of the temporal variations and spatial distribution of organic carbon (OC) concentration followed the observed trends. They also show the impact of high population densities (up to 994 inhab km^?2 in the delta area) on OC inputs in surface runoff from the different land use classes and from urban point sources. A budget of the main fluxes of OC in the whole river network, including diffuse inputs from soil leaching and runoff and point sources from urban centers, as well as algal net primary production and heterotrophic respiration was established using the model results. It shows the predominantly heterotrophic character of the river system and provides an estimate of CO₂ emissions from the river of 330 Gg C year^?1. This value is in reasonable agreement with the few available direct measurements of CO₂ fluxes in the downstream part of the river network.     

CO2 Saturation and Trophic Shift Induced by Microbial Metabolic Processes in a River-Dominated Ocean Margin (Tropical Shallow Lagoon,Chilika, India)

An effort has been made for the first time in Asia's largest brackish water lagoon, Chilika, to investigate the spatio-temporal variability in primary productivity (PP), bacterial productivity (BP), bacterial abundance (BA), bacterial respiration (BR) and bacterial growth efficiency (BGE) in relation to partial pressure of CO₂ (pCO₂) and CO₂ air–water flux and the resultant trophic switchover. Annually, PP ranged between 24 and 376 µg C L^?1 d^?1 with significantly low values throughout the monsoon (MN), caused by light limitation due to inputs of riverine suspended matter. On the contrary, BP and BR ranged from 11.5 to 186.3 µg C L^?1 d^?1 and from 14.1 to 389.4 µg C L^?1 d^?1, respectively, with exceptionally higher values during MN. A wide spatial and temporal variation in the lagoon trophic status was apparent from BP/PP (0.05–6.4) and PP/BR (0.10–18.2) ratios. The seasonal shift in net pelagic production from autotrophy to heterotrophy due to terrestrial organic matter inputs via rivers, enhanced the bacterial metabolism during the MN, as evident from the high pCO₂ (10,134 µatm) and CO₂ air–water flux (714 mm m^?2 d^?1). Large variability in BGE and BP/PP ratios especially during MN led to high bacteria-mediated carbon fluxes which was evident from significantly high bacterial carbon demand (BCD >100% of PP) during this season. This suggested that the net amount of organic carbon (either dissolved or particulate form) synthesized by primary producers in the lagoon was not sufficient to satisfy the bacterial carbon requirements. Lagoon sustained low to moderate autotrophic–heterotrophic coupling with annual mean BCD of 231% relative to the primary production, which depicted that bacterioplankton are the mainstay of the lagoon biogeochemical cycles and principal players that bring changes in trophic status. Study disclosed that the high CO₂ supersaturation and oxygen undersaturation during MN was attributed to the increased heterotrophic respiration (in excess of PP) fuelled by allochthonous organic matter. On a spatial scale, lagoon sectors such as south sector, central sector and outer channel recorded “net autotrophic,” while the northern sector showed “net heterotrophic” throughout the study period.     

The combined effects of temperature and CO2 lead to altered gene expression in Acropora aspera

This study explored the interactive effects of near-term CO₂ increases (40–90 ppm above current ambient) during a simulated bleaching event (34 °C for 5 d) of Acropora aspera by linking physiology to expression patterns of genes involved in carbon metabolism. Symbiodinium photosynthetic efficiency (F _v /F _m ) was significantly depressed by the bleaching event, while elevated pressure of CO₂ (pCO₂) slightly mitigated the effects of increased temperature on F _v /F _m during the final 4 d of the recovery period, however, did not affect the loss of symbionts. Elevated pCO₂ alone had no effect on F _v /F _m or symbiont density. Expression of targeted Symbiodinium genes involved in carbon metabolism and heat stress response was not significantly altered by either increased temperature and/or CO₂. Of the selected host genes, two carbonic anhydrase isoforms (coCA2 and coCA3) exhibited the largest changes, most notably in crossed bleaching and elevated pCO₂ treatments. CA2 was significantly down-regulated on day 14 in all treatments, with the greatest decrease in the crossed treatment (relative expression compared to control = 0.16; p < 0.05); CA3 showed a similar trend, with expression levels 0.20-fold of controls on day 14 (p < 0.05) in the elevated temperature/pCO₂ treatment. The synergistic effects of ocean acidification and bleaching were evident during this study and demonstrate that increased pCO₂ in surface waters will impact corals much sooner than many studies utilising end-of-century pCO₂ concentrations would indicate.     

Influence of drainage basin topography and elevation on carbon dioxide and methane supersaturation of stream water

The partial pressures of CO₂ (pCO₂) andCH₄ (pCH₄) in streams are not only governed byinstream processes, but also by transformations occurring in soil andgroundwater ecosystems. As such, stream water pCO₂ andpCH₄ can provide a tool to assess ecosystem respiration andanaerobic metabolism throughout drainage basins. We conducted three surveyssampling the gas content of streams in eastern Tennessee and western NorthCarolina to assess factors regulating ecosystem metabolism in catchmentswith contrasting geomorphologies, elevations and soil organic matterstorage. In our first survey, the influence of drainage basin geomorphologyon ecosystem respiration was examined by sampling streams drainingcatchments underlain by either shale or dolomite. Geomorphology isinfluenced by geology with shale catchments having shallower soils, broader,unconstrained valley floors compared with dolomite catchments.pCO₂ varied little between catchment types but increased froman average of 3340 ppmv in spring to 9927 ppmv in summer or 9.3 and 28 timesatmospheric equilibrium (pCO_2(equilib)), respectively. Incontrast, pCH₄ was over twice as high in streams drainingshale catchments (306 ppmv; pCH_4(equilib) = 116) compared withmore steeply incised dolomite basins (130 ppmv; pCH_4(equilib)= 51). Using the ratio of pCH₄:pCO₂ as an indexof anaerobic metabolism, shale catchments had nearly twice as muchanaerobiosis (pCH₄:pCO₂ = 0.046) than dolomitedrainages (pCH₄:pCO₂ = 0.024). In our secondsurvey, streams were sampled along an elevational gradient (525 to 1700 m)in the Great Smoky Mountains National Park, USA where soil organic matterstorage increases with elevation. pCO₂ did not vary betweenstreams but increased from 5340 ppmv (pCO_2(equilib) = 15) to8565 ppmv (pCO_2(equilib) = 24) from spring to summer,respectively. During spring pCH₄ was low and constant acrossstreams, but during summer increased with elevation ranging from 17 to 2068ppmv (pCH_4(equilib) = 10 to 1216). The contribution ofanaerobiosis to total respiration was constant during spring(pCH₄:pCO₂ = 0.017) but during summer increasedwith elevation from 0.002 at 524 m to 0.289 at 1286 m. In our last survey,we examined how pCO₂ and pCH₄ changed withcatchment size along two rivers (ca. 60 km stretches in both riverscorresponding to increases in basin size from 1.7–477km² and 2.5–275 km²). pCO₂and pCH₄ showed opposite trends, with pCO₂decreasing ca. 50% along the rivers, whereas pCH₄roughly doubled in concentration downstream. These opposing shifts resultedin a nearly five-fold increase of pCH₄:pCO₂along the rivers from a low of 0.012 in headwaters to a high of 0.266 65-kmdownstream. pCO₂ likely declines moving downstream asgroundwater influences on stream chemistry decreases, whereaspCH₄ may increase as the prevalence of anoxia in riversexpands due to finer-grained sediments and reduced hydrologic exchange withoxygenated surface water.     

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.     

Origin and cycling of riverine inorganic carbon in the Sava River watershed (Slovenia) inferred from major solutes and stable carbon isotopes

The Sava River and its tributaries in Slovenia represent waters strongly influenced by chemical weathering of limestone and dolomite. The carbon isotopic compositions of dissolved inorganic carbon (DIC) and suspended organic carbon (POC) fractions as well as major solute concentrations yielded insights into the origin and fluxes of carbon in the upper Sava River system. The major solute composition was dominated by carbonic acid dissolution of calcite and dolomite. Waters were generally supersaturated with respect to calcite, and dissolved CO₂ was about fivefold supersaturated relative to the atmosphere. The δ¹³C of DIC ranged from −13.5 to −3.3‰. Mass balances for riverine inorganic carbon suggest that carbonate dissolution contributes up to 26%, degradation of organic matter ∼17% and exchange with atmospheric CO₂ up to 5%. The concentration and stable isotope diffusion models indicated that atmospheric exchange of CO₂ predominates in streams draining impermeable shales and clays while in the carbonate-dominated watersheds dissolution of the Mesozoic carbonates predominates.     

Combined effects of CO2 and light on large and small isolates of the unicellular N2-fixing cyanobacterium Crocosphaera watsonii from the western tropical Atlantic Ocean

We examined the combined effects of light and pCO₂ on growth, CO₂-fixation and N₂-fixation rates by strains of the unicellular marine N₂-fixing cyanobacterium Crocosphaera watsonii with small (WH0401) and large (WH0402) cells that were isolated from the western tropical Atlantic Ocean. In low-pCO₂-acclimated cultures (190 ppm) of WH0401, growth, CO₂-fixation and N₂-fixation rates were significantly lower than those in cultures acclimated to higher (present-day ～385 ppm, or future ～750 ppm) pCO₂ treatments. Growth rates were not significantly different, however, in low-pCO₂-acclimated cultures of WH0402 in comparison with higher pCO₂ treatments. Unlike previous reports for C. watsonii (strain WH8501), N₂-fixation rates did not increase further in cultures of WH0401 or WH0402 when acclimated to 750 ppm relative to those maintained at present-day pCO₂. Both light and pCO₂ had a significant negative effect on gross : net N₂-fixation rates in WH0402 and trends were similar in WH0401, implying that retention of fixed N was enhanced under elevated light and pCO₂. These data, along with previously reported results, suggest that C. watsonii may have wide-ranging, strain-specific responses to changing light and pCO₂, emphasizing the need for examining the effects of global change on a range of isolates within this biogeochemically important genus. In general, however, our data suggest that cellular N retention and CO₂-fixation rates of C. watsonii may be positively affected by elevated light and pCO₂ within the next 100 years, potentially increasing trophic transfer efficiency of C and N and thereby facilitating uptake of atmospheric carbon by the marine biota.     

Carbon budget of oligotrophic mire sites in the Southern Taiga of Western Siberia

The results of a long-term (1999–2007) investigation of vegetation productivity and carbon dioxide (CO₂) emission from the surface of an oligotrophic mire in southern taiga in Western Siberia are presented. The studied ecosystems include pine—shrub—sphagnum (PSS) community, a similar community with oppressed (low) tree stand (LPSS), and sedge—sphagnum fen (SSF). Net primary production for PSS, LPSS and SSF are equal to 552, 575, and 561 g m^?2 yr^?1. The mean respiration during the snow-free season determined by chamber method is 165.8, 105.6, 112.4 mgCO₂ m^?2 h^?1 for PSS, LPSS and SSF, respectively. Field measurements of NPP and CO₂ emission in combination with reference data on methane emission, winter CO₂ and CH₄ emissions and carbon export by river run–off were used to develop an overall carbon budget of the mire ecosystems. At present conditions the studied mire ecosystems are net sinks for atmospheric carbon and accumulate peat. Rates of the actual modern carbon accumulation are equal to 21, 112 and 102 g C m^?2 yr^?1 for PSS, LPSS and SSF communities.     

Carbon dioxide as an under-ice lethal control for invasive fishes

Resource managers need effective tools to control invasive fish populations. In this study, we tested under-ice carbon dioxide (CO₂) injection as a novel piscicide method for non-native Silver Carp (Hypophthalmichthys molitrix), Bighead Carp (Hypophthalmichthys nobilis), Grass Carp (Ctenopharyngodon idella), Common Carp (Cyprinus carpio) and native Bigmouth Buffalo (Ictiobus cyprinellus). Fish were held overwinter in nine outdoor ponds (0.04 ha surface area; 340,000 L volume) treated with no CO₂ (control), 43.5–44.0 kg CO₂ (low treatment), and 87.5–88.5 kg CO₂ (high treatment). Ponds were harvested immediately after ice-out to assess survival and condition. Resulting survival in low (mean = 32%) and high (mean = 5%) CO₂-treated ponds was significantly lower than untreated control ponds (mean = 84%). Lethal efficacy varied across species with no Bighead Carp, Silver Carp, or Bigmouth Buffalo surviving the high CO₂ treatment. External infections were observed more frequently after CO₂ treatments (means = 49–67%) relative to untreated ponds (mean = 2%), suggesting a secondary mechanism for poor survival. This study demonstrates that CO₂ can be used as a lethal control for invasive fishes, but effectiveness may vary by species and CO₂ concentration.     

Diurnal patterns of denitrification, oxygen consumption and nitrous oxide production in rivers measured at the whole-reach scale

1. Denitrification, net oxygen consumption and net nitrous oxide flux to the atmosphere were measured in three small rivers (discharge approximately 2–27 m³ s^?1) at the whole reach scale during Spring and Summer, 2002. Two of these rivers (Iroquois River and Sugar Creek in north‐west Indiana – north‐east Illinois, U.S.A.) drained agricultural catchments and the other (Millstone River in central New Jersey, U.S.A.) drained a mixed suburban–agricultural catchment. 2. Denitrification, oxygen consumption and N₂O flux were measured based on net changes in dissolved gas concentrations (N₂, O₂, and N₂O) during riverine transport, correcting for atmospheric exchange. On each date, measurements were made during both light and dark periods. 3. Denitrification rates in these rivers ranged from 0.31 to 15.91 mmol N m^?2 h^?1, and rates within each river reach were consistently higher during the day than during the night. This diurnal pattern could be related to cyclic patterns of nitrification driven by diurnal variations in water column pH and temperature. 4. Oxygen consumption ranged from 2.56 to 241 mmol O₂ m^?2 h^?1. In contrast to denitrification, net oxygen consumption was generally higher during the night than during the day. 5. River water was consistently supersaturated with N₂O, ranging from 102 to 209% saturated. Net flux of N₂O to the atmosphere ranged from 0.4 to 60 μmol N m^?2 h^?1. Net flux of N₂O was generally higher at night than during the day. The high flux of N₂O from these rivers strengthens the argument that rivers are an important contributor to anthropogenic emissions of this greenhouse gas.