Elevated Dissolved Inorganic Carbon Research Articles

Coupling between chromophoric dissolved organic matter and dissolved inorganic carbon in Indian estuaries

This study investigates the coupling between Chromophoric Dissolved Organic Matter (CDOM) and Dissolved Inorganic Carbon (DIC) in eighteen Indian estuaries across salinity gradient of the east and west coasts during the monsoon season, characterized by significant river discharge. The hypothesis that humic acids (HA) and fulvic acids (FA), prominent in estuarine CDOM, closely correspond to the ‘organic alkalinity’ (Aorg) component of total alkalinity is examined. In most estuaries, specifically those along the northeast coast (NE) and southwest coast (SW), a significant linear relationship exists between DIC, CDOM abundance, and pH level. Notably, minor estuaries along the southeast coast (SE) and northwest coast (NW) exhibit elevated DIC levels beyond what this relationship predicts. These estuaries also reveal heightened ammonium levels, increased δ15N values, and decreased δ13C values, indicative of anthropogenic influence. CDOM properties, such as spectral slope (S300–500) and spectral slope ratio (SR, S275–295:S350–400), align with these findings, with SE and NW estuaries displaying higher values. On average, CDOM contributes 110.5 μM (6.8 %) to DIC in NE, 390.7 μM (11 %) in SE, 24.4 μM (4.8 %) in SW, and 122.2 μM (4 %) in NW estuaries. The relationship between total alkalinity minus DIC (TA-DIC) and pH25 suggests that CDOM, mediated by HA/FA, buffers the inorganic carbon system in estuaries. This buffering capacity weakens at elevated DIC levels, and this condition is marked by anomalous SR values compared to the baseline salinity-SR linear regression. This Study suggests that estuarine CDOM could largely represent “organic alkalinity” and could help monitor acidification in estuaries.

Fingerprint of Climate Change on Southern Ocean Carbon Storage

AbstractThe Southern Ocean plays a critical role in the uptake, transport, and storage of carbon by the global oceans. It is the ocean's largest sink of CO2, yet it is also among the regions with the lowest storage of anthropogenic carbon. This behavior results from a unique combination of high winds driving the upwelling of deep waters and the subduction and northward transport of surface carbon. Here we isolate the direct effect of increasing anthropogenic CO2 in the atmosphere from the indirect effect of climate variability and climate change on the reorganization of carbon in the Southern Ocean interior using a combination of modeling and observations. We show that the effect of climate variability and climate change on the storage of carbon in the Southern Ocean is nearly as large as the effect of anthropogenic CO2 during the period 1998–2018 compared with the climatology around the year 1995. We identify a distinct climate fingerprint in dissolved inorganic carbon (DIC), with elevated DIC concentration in the ocean at 300–600 m that reinforces the anthropogenic CO2 signal, and reduced DIC concentration in the ocean around 2,000 m that offsets the anthropogenic CO2 signal. The fingerprint is strongest at lower latitudes (30°–55°S). This fingerprint could serve to monitor the highly uncertain evolution of carbon within this critical ocean basin, and better identify its drivers.

Disentangling the Effects of Ocean Carbonation and Acidification on Elemental Contents and Macromolecules of the Coccolithophore Emiliania huxleyi.

Elemental contents change with shifts in macromolecular composition of marine phytoplankton. Recent studies focus on the responses of elemental contents of coccolithophores, a major calcifying phytoplankton group, to changing carbonate chemistry, caused by the dissolution of anthropogenically derived CO2 into the surface ocean. However, the effects of changing carbonate chemistry on biomacromolecules, such as protein and carbohydrate of coccolithophores, are less documented. Here, we disentangled the effects of elevated dissolved inorganic carbon (DIC) concentration (900 to 4,930μmolkg−1) and reduced pH value (8.04 to 7.70) on physiological rates, elemental contents, and macromolecules of the coccolithophore Emiliania huxleyi. Compared to present DIC concentration and pH value, combinations of high DIC concentration and low pH value (ocean acidification) significantly increased pigments content, particulate organic carbon (POC), and carbohydrate content and had less impact on growth rate, maximal relative electron transport rate (rETRmax), particulate organic nitrogen (PON), and protein content. In high pH treatments, elevated DIC concentration significantly increased growth rate, pigments content, rETRmax, POC, particulate inorganic carbon (PIC), protein, and carbohydrate contents. In low pH treatments, the extents of the increase in growth rate, pigments and carbohydrate content were reduced. Compared to high pH value, under low DIC concentration, low pH value significantly increased POC and PON contents and showed less impact on protein and carbohydrate contents; however, under high DIC concentration, low pH value significantly reduced POC, PON, protein, and carbohydrate contents. These results showed that reduced pH counteracted the positive effects of elevated DIC concentration on growth rate, rETRmax, POC, PON, carbohydrate, and protein contents. Elevated DIC concentration and reduced pH acted synergistically to increase the contribution of carbohydrate–carbon to POC, and antagonistically to affect the contribution of protein–nitrogen to PON, which further shifted the carbon/nitrogen ratio of E. huxleyi.

Seasonal Variability of the CO2 System in a Large Coastal Plain Estuary

AbstractThe Chesapeake Bay, a large coastal plain estuary, has been studied extensively in terms of its water quality, and yet, comparatively less is known about its carbonate system. Here we present discrete observations of dissolved inorganic carbon (DIC) and total alkalinity from four seasonal cruises in 2016–2017. These new observations are used to characterize the regional CO2 system and to construct a DIC budget of the mainstem. In all seasons, elevated DIC concentrations were observed at the mouth of the bay associated with inflowing Atlantic Ocean waters, while minimum concentrations of DIC were associated with fresher waters at the head of the bay. Significant spatial variability of the partial pressure of CO2 was observed throughout the mainstem, with net uptake of atmospheric CO2 during each season in the upper mainstem and weak seasonal outgassing of CO2 near the outflow to the Atlantic Ocean. During the time frame of this study, the Chesapeake Bay mainstem was (1) net autotrophic in the mixed layer (net community production of 0.31‐mol C m−2·year−1) and net heterotrophic throughout the water column (net community production of −0.48‐mol C m−2·year−1), (2) a sink of 0.38‐mol C m−2·year−1 for atmospheric CO2, and (3) significantly seasonally and spatially variable with respect to biologically driven changes in DIC.

Seasonal Carbonate Chemistry Dynamics on Southeast Florida Coral Reefs: Localized Acidification Hotspots From Navigational Inlets

Seawater carbonate chemistry varies across temporal and spatial scales. Shallow-water environments can exhibit especially dynamic fluctuations as biological and physical processes operate on a smaller water volume, relative to open ocean environments. Water was collected on a bi-monthly basis from seven sites off of southeast Florida (Miami-Dade and Broward counties), including four reef, and three closely-associated inlets. Significant seasonal fluctuations in carbonate chemistry were observed on reef sites, with elevated pCO2 in the warmer wet season. Inlets demonstrated a more dynamic range, with periodic pulses of acidified water contributing to, on average, more advanced acidification conditions than those found at nearby reefs. Within inlet environments, there was a significant negative correlation between seawater salinity and both total alkalinity (TA) and dissolved inorganic carbon (DIC), which was in contrast to the patterns observed on reefs. Elevated TA and DIC in low salinity waters likely reflect carbonate dissolution as a result of organic matter decomposition. Together, these data highlight the important role that inlets play on shallow-water carbonate chemistry dynamics within southeast Florida waters and underscore the degree to which engineered freshwater systems can contribute to coastal acidification on localized scales.

Seasonal carbonate chemistry variability in marine surface waters of the US Pacific Northwest

Abstract. Fingerprinting ocean acidification (OA) in US West Coast waters is extremely challenging due to the large magnitude of natural carbonate chemistry variations common to these regions. Additionally, quantifying a change requires information about the initial conditions, which is not readily available in most coastal systems. In an effort to address this issue, we have collated high-quality publicly available data to characterize the modern seasonal carbonate chemistry variability in marine surface waters of the US Pacific Northwest. Underway ship data from version 4 of the Surface Ocean CO2 Atlas, discrete observations from various sampling platforms, and sustained measurements from regional moorings were incorporated to provide ∼ 100 000 inorganic carbon observations from which modern seasonal cycles were estimated. Underway ship and discrete observations were merged and gridded to a 0.1° × 0.1° scale. Eight unique regions were identified and seasonal cycles from grid cells within each region were averaged. Data from nine surface moorings were also compiled and used to develop robust estimates of mean seasonal cycles for comparison with the eight regions. This manuscript describes our methodology and the resulting mean seasonal cycles for multiple OA metrics in an effort to provide a large-scale environmental context for ongoing research, adaptation, and management efforts throughout the US Pacific Northwest. Major findings include the identification of unique chemical characteristics across the study domain. There is a clear increase in the ratio of dissolved inorganic carbon (DIC) to total alkalinity (TA) and in the seasonal cycle amplitude of carbonate system parameters when moving from the open ocean North Pacific into the Salish Sea. Due to the logarithmic nature of the pH scale (pH = −log10[H+], where [H+] is the hydrogen ion concentration), lower annual mean pH values (associated with elevated DIC : TA ratios) coupled with larger magnitude seasonal pH cycles results in seasonal [H+] ranges that are ∼ 27 times larger in Hood Canal than in the neighboring North Pacific open ocean. Organisms living in the Salish Sea are thus exposed to much larger seasonal acidity changes than those living in nearby open ocean waters. Additionally, our findings suggest that lower buffering capacities in the Salish Sea make these waters less efficient at absorbing anthropogenic carbon than open ocean waters at the same latitude.All data used in this analysis are publically available at the following websites: Surface Ocean CO2 Atlas version 4 coastal data, https://doi.pangaea.de/10.1594/PANGAEA.866856 (Bakker et al., 2016a);National Oceanic and Atmospheric Administration (NOAA) West Coast Ocean Acidification cruise data, https://doi.org/10.3334/CDIAC/otg.CLIVAR_NACP_West_Coast_Cruise_2007 (Feely and Sabine, 2013); https://doi.org/10.7289/V5JQ0XZ1 (Feely et al., 2015b); https://data.nodc.noaa.gov/cgi-bin/iso?id=gov.noaa.nodc:0157445 (Feely et al., 2016a); https://doi.org/10.7289/V5C53HXP (Feely et al., 2015a);University of Washington (UW) and Washington Ocean Acidification Center cruise data, https://doi.org/10.5281/zenodo.1184657 (Fassbender et al., 2018);Washington State Department of Ecology seaplane data, https://doi.org/10.5281/zenodo.1184657 (Fassbender et al., 2018);NOAA Moored Autonomous pCO2 (MAPCO2) buoy data, https://doi.org/10.3334/CDIAC/OTG.TSM_LAPUSH_125W_48N (Sutton et al., 2012); https://doi.org/10.3334/CDIAC/OTG.TSM_WA_125W_47N (Sutton et al., 2013); https://doi.org/10.3334/CDIAC/OTG.TSM_DABOB_122W_478N (Sutton et al., 2014a); https://doi.org/10.3334/CDIAC/OTG.TSM_TWANOH_123W_47N (Sutton et al., 2016a);UW Oceanic Remote Chemical/Optical Analyzer buoy data, https://doi.org/10.5281/zenodo.1184657 (Fassbender et al., 2018);NOAA Pacific Coast Ocean Observing System cruise data, https://doi.org/10.5281/zenodo.1184657 (Fassbender et al., 2018).

Potential ecotoxicological effects of elevated bicarbonate ion concentrations on marine organisms

Recently, a novel method for carbon capture and storage has been proposed, which converts gaseous CO2 into aqueous bicarbonate ions (HCO3−), allowing it to be deposited into the ocean. This alkalinization method could be used to dispose large amounts of CO2 without acidifying seawater pH, but there is no information on the potential adverse effects of consequently elevated HCO3− concentrations on marine organisms. In this study, we evaluated the ecotoxicological effects of elevated concentrations of dissolved inorganic carbon (DIC) (max 193 mM) on 10 marine organisms. We found species-specific ecotoxicological effects of elevated DIC on marine organisms, with EC50-DIC (causing 50% inhibition) of 11–85 mM. The tentative criteria for protecting 80% of individuals of marine organisms are suggested to be pH 7.8 and 11 mM DIC, based on acidification data previously documented and alkalinization data newly obtained from this study. Overall, the results of this study are useful for providing baseline information on ecotoxicological effects of elevated DIC on marine organisms. More complementary studies are needed on the alkalinization method to determine DIC effects on seawater chemistry and marine organisms.

Seasonal variability of the inorganic carbon system in a large coastal plain estuary

Abstract. Carbonate geochemistry research in large estuarine systems is limited. More work is needed to understand how changes in land-use activity influence watershed export of organic and inorganic carbon, acids, and nutrients to the coastal ocean. To investigate the seasonal variation of the inorganic carbon system in the Delaware Estuary, one of the largest estuaries along the US east coast, dissolved inorganic carbon (DIC), total alkalinity (TA), and pH were measured along the estuary from June 2013 to April 2015. In addition, DIC, TA, and pH were periodically measured from March to October 2015 in the nontidal freshwater Delaware, Schuylkill, and Christina rivers over a range of discharge conditions. There were strong negative relationships between river TA and discharge, suggesting that changes in HCO3− concentrations reflect dilution of weathering products in the drainage basin. The ratio of DIC to TA, an understudied but important property, was high (1.11) during high discharge and low (0.94) during low discharge, reflecting additional DIC input in the form of carbon dioxide (CO2), most likely from terrestrial organic matter decomposition, rather than bicarbonate (HCO3−) inputs due to drainage basin weathering processes. This is also a result of CO2 loss to the atmosphere due to rapid water transit during the wet season. Our data further show that elevated DIC in the Schuylkill River is substantially different than that in the Delaware River. Thus, tributary contributions must be considered when attributing estuarine DIC sources to the internal carbon cycle versus external processes such as drainage basin mineralogy, weathering intensity, and discharge patterns. Long-term records in the Delaware and Schuylkill rivers indicate shifts toward higher alkalinity in estuarine waters over time, as has been found in other estuaries worldwide. Annual DIC input flux to the estuary and export flux to the coastal ocean are estimated to be 15.7 ± 8.2 × 109 mol C yr−1 and 16.5 ± 10.6 × 109 mol C yr−1, respectively, while net DIC production within the estuary including inputs from intertidal marshes is estimated to be 5.1 × 109 mol C yr−1. The small difference between riverine input and export flux suggests that, in the case of the Delaware Estuary and perhaps other large coastal systems with long freshwater residence times, the majority of the DIC produced in the estuary by biological processes is exchanged with the atmosphere rather than exported to the sea.

Effect of Inorganic and Organic Carbon Enrichments (DIC and DOC) on the Photosynthesis and Calcification Rates of Two Calcifying Green Algae from a Caribbean Reef Lagoon.

Coral reefs worldwide are affected by increasing dissolved inorganic carbon (DIC) and organic carbon (DOC) concentrations due to ocean acidification (OA) and coastal eutrophication. These two stressors can occur simultaneously, particularly in near-shore reef environments with increasing anthropogenic pressure. However, experimental studies on how elevated DIC and DOC interact are scarce and fundamental to understanding potential synergistic effects and foreseeing future changes in coral reef function. Using an open mesocosm experiment, the present study investigated the impact of elevated DIC (pHNBS: 8.2 and 7.8; pCO2: 377 and 1076 μatm) and DOC (added as 833 μmol L-1 of glucose) on calcification and photosynthesis rates of two common calcifying green algae, Halimeda incrassata and Udotea flabellum, in a shallow reef environment. Our results revealed that under elevated DIC, algal photosynthesis decreased similarly for both species, but calcification was more affected in H. incrassata, which also showed carbonate dissolution rates. Elevated DOC reduced photosynthesis and calcification rates in H. incrassata, while in U. flabellum photosynthesis was unaffected and thalus calcification was severely impaired. The combined treatment showed an antagonistic effect of elevated DIC and DOC on the photosynthesis and calcification rates of H. incrassata, and an additive effect in U. flabellum. We conclude that the dominant sand dweller H. incrassata is more negatively affected by both DIC and DOC enrichments, but that their impact could be mitigated when they occur simultaneously. In contrast, U. flabellum can be less affected in coastal eutrophic waters by elevated DIC, but its contribution to reef carbonate sediment production could be further reduced. Accordingly, while the capacity of environmental eutrophication to exacerbate the impact of OA on algal-derived carbonate sand production seems to be species-specific, significant reductions can be expected under future OA scenarios, with important consequences for beach erosion and coastal sediment dynamics.

Effects of High Dissolved Inorganic and Organic Carbon Availability on the Physiology of the Hard Coral Acropora millepora from the Great Barrier Reef.

Coral reefs are facing major global and local threats due to climate change-induced increases in dissolved inorganic carbon (DIC) and because of land-derived increases in organic and inorganic nutrients. Recent research revealed that high availability of labile dissolved organic carbon (DOC) negatively affects scleractinian corals. Studies on the interplay of these factors, however, are lacking, but urgently needed to understand coral reef functioning under present and near future conditions. This experimental study investigated the individual and combined effects of ambient and high DIC (pCO2 403 μatm/ pHTotal 8.2 and 996 μatm/pHTotal 7.8) and DOC (added as Glucose 0 and 294 μmol L-1, background DOC concentration of 83 μmol L-1) availability on the physiology (net and gross photosynthesis, respiration, dark and light calcification, and growth) of the scleractinian coral Acropora millepora (Ehrenberg, 1834) from the Great Barrier Reef over a 16 day interval. High DIC availability did not affect photosynthesis, respiration and light calcification, but significantly reduced dark calcification and growth by 50 and 23%, respectively. High DOC availability reduced net and gross photosynthesis by 51% and 39%, respectively, but did not affect respiration. DOC addition did not influence calcification, but significantly increased growth by 42%. Combination of high DIC and high DOC availability did not affect photosynthesis, light calcification, respiration or growth, but significantly decreased dark calcification when compared to both controls and DIC treatments. On the ecosystem level, high DIC concentrations may lead to reduced accretion and growth of reefs dominated by Acropora that under elevated DOC concentrations will likely exhibit reduced primary production rates, ultimately leading to loss of hard substrate and reef erosion. It is therefore important to consider the potential impacts of elevated DOC and DIC simultaneously to assess real world scenarios, as multiple rather than single factors influence key physiological processes in coral reefs.

The physiological response of two green calcifying algae from the Great Barrier Reef towards high dissolved inorganic and organic carbon (DIC and DOC) availability.

Increasing dissolved inorganic carbon (DIC) concentrations associated with ocean acidification can affect marine calcifiers, but local factors, such as high dissolved organic carbon (DOC) concentrations through sewage and algal blooms, may interact with this global factor. For calcifying green algae of the genus Halimeda, a key tropical carbonate producer that often occurs in coral reefs, no studies on these interactions have been reported. These data are however urgently needed to understand future carbonate production. Thus, we investigated the independent and combined effects of DIC (pCO2 402 μatm/ pHtot 8.0 and 996 μatm/ pHtot 7.7) and DOC (added as glucose in 0 and 294 μmol L-1) on growth, calcification and photosynthesis of H. macroloba and H. opuntia from the Great Barrier Reef in an incubation experiment over 16 days. High DIC concentrations significantly reduced dark calcification of H. opuntia by 130 % and led to net dissolution, but did not affect H. macroloba. High DOC concentrations significantly reduced daily oxygen production of H. opuntia and H. macroloba by 78 % and 43 %, respectively, and significantly reduced dark calcification of H. opuntia by 70%. Combined high DIC and DOC did not show any interactive effects for both algae, but revealed additive effects for H. opuntia where the combination of both factors reduced dark calcification by 162 % compared to controls. Such species-specific differences in treatment responses indicate H. opuntia is more susceptible to a combination of high DIC and DOC than H. macroloba. From an ecological perspective, results further suggest a reduction of primary production for Halimeda-dominated benthic reef communities under high DOC concentrations and additional decreases of carbonate accretion under elevated DIC concentrations, where H. opuntia dominates the benthic community. This may reduce biogenic carbonate sedimentation rates and hence the buffering capacity against further ocean acidification.

Spatial variation in shallow sediment methane sources and cycling on the Alaskan Beaufort Sea Shelf/Slope

The MITAS (Methane in the Arctic Shelf/Slope) expedition was conducted during September, 2009 onboard the U.S. Coast Guard Cutter (USCGC) Polar Sea (WAGB-11), on the Alaskan Shelf/Slope of the Beaufort Sea. Expedition goals were to investigate spatial variations in methane source(s), vertical methane flux in shallow sediments (<10 mbsf), and methane contributions to shallow sediment carbon cycling. Three nearshore to offshore transects were conducted across the slope at locations approximately 200 km apart in water column depths from 20 to 2100 m. Shallow sediments were collected by piston cores and vibracores and samples were analyzed for sediment headspace methane (CH4), porewater sulfate (SO42−), chloride (Cl−), and dissolved inorganic carbon (DIC) concentrations, and CH4 and DIC stable carbon isotope ratios (δ13C). Downward SO42− diffusion rates estimated from sediment porewater SO42− profiles were between −15.4 and −154.8 mmol m−2 a−1 and imply a large spatial variation in vertical CH4 flux between transects in the study region. Lowest inferred CH4 fluxes were estimated along the easternmost transect. Higher inferred CH4 flux rates were observed in the western transects. Sediment headspace δ13CCH4 values ranged from −138 to −48‰, suggesting strong differences in shallow sediment CH4 cycling within and among sample locations. Measured porewater DIC concentrations ranged from 2.53 mM to 79.39 mM with δ13CDIC values ranging from −36.4‰ to 5.1‰. Higher down-core DIC concentrations were observed to occur with lower δ13C where an increase in δ13CCH4 was measured, indicating locations with active anaerobic oxidation of methane. Shallow core CH4 production was inferred at the two western most transects (i.e. Thetis Island and Halkett) through observations of low δ13CCH4 coupled with elevated DIC concentrations. At the easternmost Hammerhead transect and offshore locations, δ13CCH4 and DIC concentrations were not coupled suggesting less rapid methane cycling. Results from the MITAS expedition represent one of the most comprehensive studies of methane source(s) and vertical methane flux in shallow sediments of the U.S. Alaskan Beaufort Shelf to date and show geospatially variable sediment methane flux that is highly influenced by the local geophysical environment.

Mobilization of metals and phosphorus from intact forest soil cores by dissolved inorganic carbon

Increased dissolved inorganic carbon (DIC) enhances the mobilization of metals and nutrients in soil solutions. Our objective was to investigate the mobilization of Al, Ca, Fe, and P in forest soils due to fluctuating DIC concentrations. Intact soil cores were taken from the O and B horizons at the Bear Brook Watershed in Maine (BBWM) to conduct soil column transport experiments. Solutions with DIC concentrations (∼20-600 ppm) were introduced into the columns. DIC was reversibly sorbed and its migration was retarded by a factor of 1.2 to 2.1 compared to the conservative sodium bromide tracer, corresponding to a log K (D) = -0.82 to -0.07. Elevated DIC significantly enhanced the mobilization of all Al, Fe, Ca, and P. Particulate (>0.4 μm) Al and Fe were mobilized during chemical and flow transitions, such as increasing DIC and dissolved organic carbon (DOC), and resumption of flow after draining the columns. Calcium and P were primarily in dissolved forms. Mechanisms such as ion exchange (Al, Fe, Ca), ligand- and proton-promoted dissolution (Al and Fe), and ligand exchange (P) were the likely chemical mechanisms for the mobilization of these species. One column was packed with dried and sieved B-horizon soil. The effluent from this column had DOC, Al, and Fe concentrations considerably higher than those in the intact columns, suggesting that these species were mobilized from soil's microporous structure that was otherwise not exposed to the advective flow. Calcium and P concentrations, however, were similar to those in the intact columns, suggesting that these elements were less occluded in soil particles.

Ecosystem responses to increased precipitation and permafrost decay in subarctic Sweden inferred from peat and lake sediments

AbstractRecent accelerated decay of discontinuous permafrost at the Stordalen Mire in northern Sweden has been attributed to increased temperature and snow depth, and has caused expansion of wet minerotrophic areas leading to significant changes in carbon cycling in the mire. In order to track these changes through time and evaluate potential forcing mechanisms, this paper analyses a peat succession and a lake sediment sequence from within the mire, providing a record for the last 100 years, and compares these with monitored climate and active layer thickness data. The peat core was analysed for testate amoebae to reconstruct changes in peatland surface moisture conditions and water table fluctuations. The lake sediment core was analysed by near infrared spectroscopy to infer changes in the total organic carbon (TOC) concentration of the lake‐water, and changes in δ13C and C, N and δ15N to track changes in the dissolved inorganic carbon (DIC) pool and the influence of diagenetic effects on sediment organic matter, respectively. Results showed that major shifts towards increased peat surface moisture and TOC concentration of the lake‐water occurred around 1980, one to two decades earlier than a temperature driven increase in active layer thickness. Comparison with monitored temperature and precipitation from a nearby climate station indicates that this change in peat surface moisture is related to June–September (JJAS) precipitation and that the increase in lake‐water TOC concentration reflects an increase in total annual precipitation. A significant depletion in 13C of sediment organic matter in the early 1980s probably reflects the effect of a single or a few consecutive years with anomalously high summer precipitation, resulting in elevated DIC content of the lake water, predominantly originating from increased export and subsequent respiration of organic carbon from the mire. Based on these results, it was not possible to link proxy data obtained on peat and lake‐sediment records directly to permafrost decay. Instead our data indicate that increased precipitation and anomalously high rainfall during summers had a significant impact on the mire and the adjacent lake ecosystem. We therefore propose that effects of increased precipitation should be considered when evaluating potential forcing mechanisms of recent changes in carbon cycling in the subarctic.

Temporal variations in organic carbon species and fluxes from the Chena River, Alaska

Water samples were collected biweekly from the Chena River, Alaska, during 2005‐2006 for analysis of dissolved organic carbon (DOC), dissolved inorganic carbon (DIC), total dissolved carbohydrate (TCHO), including monosaccharide (MCHO) and polysaccharide (PCHO), particulate organic carbon (POC) and its isotopic compositions, and Si(OH)4. Carbon species exhibit strong temporal variations with elevated DOC, POC, and TCHO but depleted DIC and Si(OH)4 during the spring freshet and decreased DOC, POC, and TCHO but elevated DIC and Si(OH)4 concentrations under winter ice. Organic matter is mostly derived from surface soil leaching, whereas DIC and Si(OH)4 are associated with groundwater and mineral layer leaching. On average, DIC was the predominant carbon species, accounting for 77% ± 13% of the total carbon pool, whereas DOC and POC comprised 19% ± 10% and 4% ± 4%, respectively. However, DOC became the dominant carbon species during the spring freshet. TCHO comprised 15% ± 4% of DOC with higher CHO:DOC ratios during spring runoff and summer. Within the TCHO pool, MCHO was the predominant CHO component (89% ± 10%), leaving 11% ± 10% as PCHO. The particulate organic matter source during the summer drought season was mostly autochthonous, with low POC: chlorophyll a and C:N but high POC: suspended particulate matter ratios and depleted δ13C values. The annual yields of DOC, DIC, and POC from the basin are 133 ± 8, 361 ± 7, and 27 ± 4 x 103 mol C km‐2, corresponding to an export flux of 6.9 ± 0.4, 18.8 ± 0.4, and 1.4 ± 0.2 x 108 mol C yr‐1, respectively. Anticipated changes in hydrological and biogeochemical cycles in high‐latitude watersheds undergoing climate warming will likely be reflected in the chemical and phase speciation of carbon and other elements.

Rapid decline of the CO2 buffering capacity in the North Sea and implications for the North Atlantic Ocean

New observations from the North Sea, a NW European shelf sea, show that between 2001 and 2005 the CO2 partial pressure (pCO2) in surface waters rose by 22 μatm, thus faster than atmospheric pCO2, which in the same period rose approximately 11 μatm. The surprisingly rapid decline in air‐sea partial pressure difference (ΔpCO2) is primarily a response to an elevated water column inventory of dissolved inorganic carbon (DIC), which, in turn, reflects mostly anthropogenic CO2 input rather than natural interannual variability. The resulting decline in the buffering capacity of the inorganic carbonate system (increasing Revelle factor) sets up a theoretically predicted feedback loop whereby the invasion of anthropogenic CO2 reduces the ocean's ability to uptake additional CO2. Model simulations for the North Atlantic Ocean and thermodynamic principles reveal that this feedback should be stronger, at present, in colder midlatitude and subpolar waters because of the lower present‐day buffer capacity and elevated DIC levels driven either by northward advected surface water and/or excess local air‐sea CO2 uptake. This buffer capacity feedback mechanism helps to explain at least part of the observed trend of decreasing air‐sea ΔpCO2 over time as reported in several other recent North Atlantic studies.

Time-series study of the biogeochemistry of the North East subarctic Pacific: reconciliation of the Corg/N remineralization and uptake ratios with the Redfield ratios

Abstract Ten years of a time-series study at Station P or OSP (50°N, 145°W) in the NE subarctic Pacific are presented in this paper. Measurements of nutrients, primary production, dissolved inorganic carbon (DIC), total alkalinity (TA), dissolved organic carbon and nitrogen (DOC and DON), and sinking organic and inorganic particulate fluxes (derived from free-drifting sediment traps positioned every 100 m in the upper 1000 m) were made. One-dimensional C and N budgets were calculated in the mixed layer and in 4 layers below 50 m down to 1000 m. The remineralization and uptake stoichiometric ratios were determined, with an emphasis on the C org /N ratios. Three independent approaches were used: (1) nutrient vertical gradients in the 100–1000 m, (2) nutrient seasonal drawdown in the 0–50 m upper layer, and (3) nutrient regeneration from sinking particles. Analysis of the nutrient vertical gradients showed that the P/N/C org /−O 2 remineralization molar ratios were 1/16.6/107.9/−170.7 and that the average C org /N was about 6.5 in the upper 400 m. In contrast, the seasonal DIC:NO 3 − drawdown molar ratio varied widely from 6.9 to 12.1 and averaged 9.3. However, when corrections were made for CO 2 gas exchange, dissolved organic matter (DOM) production and CaCO 3 production, the true average C org /N uptake ratio was estimated to be 6.1. This study suggested that the elevated DIC:NO 3 − depletion ratios were mostly due to calcification, and that the net effect of gas exchange and DOM production was small at station P. Furthermore, whereas the POC/PON flux (particulate organic C and N fluxes) ratio ranged from 8 to 12 (mole ratio) and increased with depth, there was a linear relationship between the POC and PON fluxes, with a slope of 7.2±0.2. This indicated that the C org /N remineralization ratio from sinking particles was relatively low and that there was a methodological problem with free-drifting sediment traps.

Seasonal cycles of nutrients and dissolved inorganic carbon at high and mid latitudes in the North Pacific Ocean during the Skaugran cruises: determination of new production and nutrient uptake ratios

Abstract The results of a 2-yr monitoring program in the North Pacific (March 1995–April 1997) using the commercial cargo carrier M/V Skaugran are presented in this paper. Seasonal changes in macronutrients (nitrate, phosphate and silicate), dissolved inorganic carbon (DIC) and total alkalinity (TA) were recorded in the surface waters of 12 major provinces of the North Pacific Ocean (35–55°N). North of the subarctic boundary (40°N), nitrate rarely decreased to below detection limit except in the more near-shore provinces, with nitrate concentrations remaining as high as 8–9 μmol kg −1 in the summer in the northern provinces of the Bering Sea, the central and western subarctic Pacific. There were also strong latitudinal nutrient gradients. In most provinces of the subarctic Pacific, there was little interannual change in the nutrient cycles, except in the western subarctic Pacific where nitrate concentration fell to 2.6 μmol kg −1 in the summer of 1996. We suggest that this large nitrate depletion was due to enhanced diatom production triggered by the supply of iron from the Asian continent. The relationship between salinity-normalized TA and DIC revealed that calcification was low or negligible in the surface waters of the Bering Sea and the western subarctic Pacific. In contrast, the percent of CaCO 3 production to organic carbon production was found to be at times as high as 70–75% in the eastern subarctic Pacific and the southern region off east Japan. This study also revealed east–west contrasts in the seasonal nutrient-depletion ratios. In the east, the elevated DIC:NO 3 ratios and low Si(OH) 4 :NO 3 ratios were due to high CaCO 3 production and low diatom production in surface waters. On the contrary, in the western subarctic Pacific and the Bering Sea, the low Redfieldian DIC:NO 3 ratios and the high Si(OH) 4 :NO 3 ratios were due to low calcification and high diatom production. The annual new production was estimated from the seasonal drawdown of nitrate at the surface. It ranged from 10.1 g C m −2 yr −1 in the subtropical gyre to 76–83 g C m −2 yr −1 in the western subarctic Pacific. Overall, horizontal advection was the major source of uncertainty in the estimation of new production. Finally, the net removal of carbon from the surface by the biological pump was then estimated to be 0.58 Gt C yr −1 north of 35°N in the Pacific Ocean. The subarctic North Pacific and the Bering Sea accounted for 93% of the carbon removal.

The influence of dissolved inorganic carbon in the rhizosphere on carbon and nitrogen metabolism in salinity‐treated tomato plants

The influence of variation in the concentration of dissolved inorganic carbon (DIC) in the form of CO2 and HCO3− in the root media on the C and N metabolism of Lycopersicon esculentum cv. F144 was investigated under both saline and non‐saline conditions. Tomato seedlings were grown in hydroponic culture (pH 6.5) with or without NaCl, and the root solution was aerated with either ambient CO2 (360 μmol mol−1) or CO2‐enriched air (5000 μmol mol−1). Nitrate uptake and root tissue NO3− concentrations were increased slightly by elevated rhizosphere DIC concentrations in both control and salinity‐treated plants. This was associated with 46% higher nitrate reductase activity in the roots of control plants supplied with elevated DIC than in those supplied with ambient DIC. The activity of phosphoenolpyruvate carboxylase (PEPc) in vitro in control and salinity‐treated plants was unaffected by the supply of elevated rhizosphere DIC concentrations. However, PEPc activity in vitro was considerably higher than the rates of PEPc activity in vivo reported previously, indicating that PEPc activity was not in itself a limitation on the provision of anaplerotic C. Therefore elevated DIC concentration in the rhizosphere stimulated the uptake of NO3− and provided alternative C skeletons for the assimilation of the NH4+ resulting from NO3− reduction into amino acids within the roots. Salinity stimulated root glutamine synthetase (GS) activity up to double that in control plants. Furthermore, elevated DIC caused an increase in leaf and root GS activity of control plants while inhibiting GS activity in the roots of salinity‐treated plants. Glutamine∶2‐ oxoglutarate aminotransferase (GOGAT) activity of salinity‐treated plants was doubled by elevated rhizosphere DIC concentrations. These changes in GS and GOGAT activity must reflect changes in amino acid synthesis. Under saline conditions the xylem transport of NO3− is partly blocked and a larger root assimilation develops, requiring not only the transamination of 2‐oxoglutarate to glutamate but also that of oxaloacetate to aspartate and the transamidation of aspartate to asparagine.

Carbon isotopes in aquatic plants, Long Valley Caldera, California as records of past hydrothermal and magmatic activity

Hot and cold springs contribute “dead” (14C free) dissolved inorganic carbon (DIC) to the Owens River and Hot Creek. Headwaters aquatic plants have modern 14C, but live plants downstream of the intracaldera springs are depleted in 14C, (as low as 19% modern, with apparent ages up to 13.3 kyrs). In an abandoned meander of the upper Owens River, preserved streambed plants are buried by 600 year old Inyo Craters pumice. Apparent 14C ages of these plants exceed true ages by ∼ 1100 years indicating that they also incorporated dead DIC as they grew. The preserved plants are downstream of Big Springs, whose elevated dead DIC may represent magmatic ‘CO2. The buried plants incorporated ∼10% dead carbon, although modern plants here have ∼50% dead carbon, suggesting that more magmatic CO2 is now entering the upper Owens River than at the time of the Inyo Craters eruptions 600 years ago.