N2 fixation variability in the oligotrophic Sulu Sea, western equatorial Pacific region over the past 83 kyr

N₂ fixation is an important biological process that adds new nitrogen to oceans and plays a key role in modulating the oceanic nitrate inventory. However, it is not known how, when, and where N₂ fixation rates have varied in response to past climate changes. This study presents a new record of nitrogen isotopic composition (δ¹⁵N) over the last 83 kyr from a sediment core (KH02-4 SUP8) taken in the Sulu Sea in the western equatorial Pacific region; data allow the N₂ fixation variability in the sea to be reconstructed. Sediments, sinking, and suspended particulate organic matter (POM) all have lighter isotopic values compared to the δ¹⁵N values of substrate nitrate (av. 5.8‰) in North Pacific Intermediate Water. These lighter δ¹⁵N values are regarded as reflecting N₂ fixation in the Sulu Sea surface water. A δ¹⁵N mass balance model shows that N₂ fixation rates were significantly enhanced during 54–34 kyr in MIS-3 and MIS-2. It has been speculated that higher interglacial denitrification rates in the Arabian Sea and the eastern tropical Pacific would have markedly decreased the global oceanic N inventory and contributed to the increase in N₂ fixation in oligotrophic regions, but such a model was not revealed by our study. It is possible that changes in N₂ fixation rates in the Sulu Sea were regional response, and accumulation of phosphate in the surface waters due to enhanced monsoon-driven mixing is thought to have stimulated enhancements of N₂ fixation during MIS-3 and MIS-2.     

The oxygen isotope composition of water masses within the North Sea

Based on measurements of the ¹⁸O isotope composition of 247 samples collected over a 3-year period we have assessed the oxygen isotope composition of water masses in the North Sea. This is the first δ¹⁸O data set that covers the entire North Sea basin. The waters lie on a mixing line: δ¹⁸O (‰_VSMOW) = −9.300 + 0.274(S) with North Atlantic sub-polar mode water (SPMW) and surface waters, and Baltic Sea water representing the saline and freshwater end members respectively. Patterns exhibited in surface and bottom water δ¹⁸O distributions are representative of the general circulation of the North Sea. Oxygen-18 enriched waters from the North Atlantic enter the North Sea between Scotland and Norway and to a lesser extent through the English Channel. In contrast, oxygen-18 depleted waters mainly inflow from the Baltic Sea, the rivers Rhine and Elbe, and to a lesser degree, the Norwegian Fjords and other river sources. Locally the δ¹⁸O–salinity relationship will be controlled by the isotopic composition of the freshwater inputs. However, the range of local freshwater compositions around the North Sea basin is too narrow to characterise the relative contributions of individual sources to the overall seawater composition. This dataset provides important information for a number of related disciplines including biogeochemical research and oceanographic studies.     

N2O Production, Nitrification and Denitrification in an Estuarine Sediment

The mechanisms regulating N₂O production in an estuarine sediment (Tama Estuary, Japan) were studied by comparing the change in N₂O production with those in nitrification and denitrification using an experimental continuous-flow sediment–water system with¹⁵N tracer (¹⁵N-NO−3 addition). From Feburary to May, both nitrification and denitrification in the sediment increased (246 to 716 μmol N m⁻² h⁻¹and 214 to 1260 μmol N m⁻² h⁻¹, respectively), while benthic N₂O evolution decreased slightly (1560 to 1250 nmol N m⁻² h⁻¹). Apparent diffusion coefficients of inorganic nitrogen compounds and O₂at the sediment–water interface, calculated from the respective concentration gradients and benthic fluxes, were close to the molecular diffusion coefficients (0·68–2·0 times) in February. However, they increased to 8·8–52 times in May except for that of NO−2, suggesting that the enhanced NO−3 and O₂supply from the overlying water by benthic irrigation likely stimulated nitrification and denitrification. Since the progress of anoxic condition by the rise of temperature from February to May (9 to 16 °C) presumably accelerated N₂O production through nitrification, the observed decrease in sedimentary N₂O production seems to be attributed to the decrease in N₂O production/occurrence of its consumption by denitrification. In addition to the activities of both nitrification and denitrification, the change in N₂O metabolism during denitrification by the balance between total demand of the electron acceptor and supply of NO−3+NO−2 can be an important factor regulating N₂O production in nearshore sediments.     

Isotopic analyses of nitrate and nitrite from reference mixtures and application to Eastern Tropical North Pacific waters

Isotopic analyses of nitrate by the denitrifier method, and indeed by many other analytical methods, do not discriminate between nitrate and nitrite. For samples containing both chemical species, accurate isotopic analysis of nitrate requires either removal of nitrite or independent isotopic analysis of nitrite and subtraction of its contribution to the mixed isotopic signal. This study evaluates the application of a variety of available analytical approaches to the isotopic analysis of mixed nitrate and nitrite solutions, with the goal of producing accurate coupled isotopic analyses of both nitrate and nitrite. These methods are tested on mixtures of standard solutions of nitrate and nitrite, and then applied to the coupled δ¹⁵N and δ¹⁸O analyses of nitrate and nitrite in waters of the Eastern Tropical North Pacific (ETNP). Results from standard mixtures show that even for extreme values of nitrate and nitrite δ¹⁵N and δ¹⁸O, both nitrite removal by ascorbate and nitrite isotopic analysis and subtraction from the mixed isotopic signal yield nitrate δ¹⁵N and δ¹⁸O values that are close to the expected values. Application of these analyses to samples from the ETNP yielded δ¹⁵N_NO3 and δ¹⁸O_NO3 values as high as 21‰ vs. AIR and 19‰ vs. VSMOW, respectively. Conversely, very low δ¹⁵N values were observed in nitrite, with values ranging from − 7.2 to − 18.5‰ vs. AIR. Removal of nitrite from ETNP samples thus revealed differences of up to 5‰ between NO₃^- and NO₂^- + NO₃^- for both δ¹⁵N and δ¹⁸O. Moreover, the δ¹⁵N offset between co-occurring nitrate and nitrite is greater than expected from the action of denitrification alone and may provide a unique constraint on the processes involved in the cycling of nitrite in and around oxygen deficient zones. Finally, subtraction of the nitrite δ¹⁵N and δ¹⁸O from ETNP samples allows the extension of the Δ(15,18) tracer into suboxic regions containing nitrite. The magnitude and distribution of Δ(15,18) in these samples suggests an important role for nitrite reoxidation in nitrate isotope variations.     

O<Subscript>2</Subscript> consumption rate and its isotopic fractionation factor in the deep water of the Philippine Sea

Concentration and stable isotopic compositions (δ ¹⁸O) of dissolved O₂ were measured in seawater samples collected from the Philippine Sea in June 2006. The in-situ O₂ consumption rate and the isotopic fractionation factor (α _r ) during dissolved O₂ consumption were obtained from field observations by applying a vertical one-dimensional advection diffusion model to the deep water mass of about 1000–4000 m. The average O₂ consumption rate and α _r were, respectively, 0.11 ± 0.07 μmol kg⁻¹yr⁻¹ and 0.990 ± 0.001. These estimated values agree well with values from earlier estimations of Pacific deep water. The in-situ O₂ consumption rates are two or more times higher north of 20°N, although the value of α _r was not significantly different between the north and south. Its levels varied rapidly in the water mass of less about 2000 m depth. These results suggest that organic matter from the continent imparts a meaningful contribution to the upper water in the northern part of the area; it might produce the strong O₂ minimum that is evident in the water mass from about 1000–2000 m in the northern part of the Philippine Sea.     

生物固氮速率测定中15N2同位素示踪剂的引入

生物固氮作用是一个重要的海洋新氮来源，在海洋生物地球化学循环中扮演着不可替代的角色。基于稳定同位素（15N₂）示踪吸收法，是目前直接测定海洋生物固氮速率最有效的手段。其中，高效、洁净地将15N₂引入海水培养体系，并准确定量培养体系底物的同位素示踪水平，是同位素示踪吸收法准确获取固氮速率的关键。本研究针对15N₂同位素示踪剂引入这一关键环节进行了探讨，确认改进气泡法是将15N₂引入海水培养体系的首选操作。在对培养体系造成的较小扰动的情况下，可将培养体系氮气底物的15N原子丰度提升至10%以上，相对于另一种导入同位素示踪剂的手段——预溶解海水法，改进气泡法将培养瓶中氮气底物的15N原子丰度提升了近200%。此外，改进气泡法还具有最小化痕量金属沾污、操作简便等优点。将改进气泡法结合与稳定同位素比值质谱测定结合，是准确测定水体生物固氮速率的推荐方法。     

The Air-Sea Exchange of CO2 in the East Sea (Japan Sea)

During CREAMS expeditions, fCO₂ for surface waters was measured continuously along the cruise tracks. The fCO₂ in surface waters in summer varied in the range 320–440 μatm, showing moderate supersaturation with respect to atmospheric CO₂. In winter, however, fCO₂ showed under-saturation of CO₂ in most of the area, while varying in a much wider range from 180 to 520 μatm. Some very high fCO₂ values observed in the northern East Sea (Japan Sea) appeared to be associated with the intensive convection system developed in the area. A gas-exchange model was developed for describing the annual variation of fCO₂ and for estimating the annual flux of CO₂ at the air-sea interface. The model incorporated annual variations in SST, the thickness of the mixed layer, gas exchange associated with wind velocity, biological activity and atmospheric concentration of CO₂. The model shows that the East Sea releases CO₂ into the atmosphere from June to September, and absorbs CO₂ during the rest of the year, from October through May. The net annual CO₂ flux at the air-sea interface was estimated to be 0.032 (±0.012) Gt-C per year from the atmosphere into the East Sea. Water column chemistry shows penetration of CO₂ into the whole water column, supporting a short turnover time for deep waters in the East Sea. This revised version was published online in August 2006 with corrections to the Cover Date.     

~(15)N示踪法测定海洋反硝化速率中~(29)N_2浓度的准确定量

利用15 N示踪法实测南海水体反硝化速率的研究发现,培养水样在长时间密闭放置过程中也会受到外界空气的污染,且其29N2/28N2比值恒定为0.007 35。根据空气背景中29N2/28N2比值恒定的特征,提出基于质量平衡关系校正空气N2污染的方法,通过将样品实测29N2浓度扣除由外界空气贡献的29N2浓度,可获得由生物反硝化作用所产生的29N2准确浓度,进而可计算出准确的反硝化速率。经空气29N2背景校正后,29N2浓度的偏差明显小于未经校正的结果,且29N2浓度与培养时间之间的线性相关性显著加强,凸显出空气29N2背景校正是获取准确反硝化速率的关键。鉴于15 N示踪法已被广泛应用于海洋水体与沉积物反硝化速率的测定中,所提出的空气29N2背景校正方法具有重要的意义。     

Seasonal Study of Methane and Nitrous Oxide in the Coastal Waters of the Southern Baltic Sea

Atmospheric and dissolved methane (CH₄) and nitrous oxide (N₂O) were measured in the unique coastal ecosystem of theBoddenwaters, including the western Oder estuary, (southern Baltic Sea) during five campaigns between 1994 and 1997. The CH₄saturations, ranging from 105–15 500%, showed great spatial and temporal variability with maximum values in September and minimum values in December. The N₂O saturations were in the range of 91–312% with a maximum in March. Enhanced concentrations of both gases were observed only in the western Oder estuary near the mouth of the Peene River. Thus, we conclude that the distributions of CH₄and N₂O in the investigatedBoddenwaters are, directly or indirectly, linked to the Peene River runoff and not to the Oder River. Our estimate of the annual CH₄emissions from theBoddenwaters to the atmosphere indicates a significant contribution (c. 17%) to the overall CH₄emissions from the Baltic Sea. In contrast, theBoddenwaters represent only a small source for atmospheric N₂O.CH₄production rates estimated from sediment slurry experiments revealed a significant spatial variability and indicated that methanogenic activity was related to acetate consumption in the surface sediment layer. Sedimentary CH₄production might depend on different amounts of accumulation of organic material.     

Uptake of atmospheric carbon dioxide in Arctic shelf seas: evaluation of the relative importance of processes that influence pCO2 in water transported over the Bering–Chukchi Sea shelf

The uptake of atmospheric carbon dioxide in the water transported over the Bering–Chukchi shelves has been assessed from the change in carbon-related chemical constituents. The calculated uptake of atmospheric CO₂ from the time that the water enters the Bering Sea shelf until it reaches the northern Chukchi Sea shelf slope (1 year) was estimated to be 86±22 g C m⁻² in the upper 100 m. Combining the average uptake per m³ with a volume flow of 0.83×10⁶ m³ s⁻¹ through the Bering Strait yields a flux of 22×10¹² g C year⁻¹. We have also estimated the relative contribution from cooling, biology, freshening, CaCO₃ dissolution, and denitrification for the modification of the seawater pCO₂ over the shelf. The latter three had negligible impact on pCO₂ compared to biology and cooling. Biology was found to be almost twice as important as cooling for lowering the pCO₂ in the water on the Bering–Chukchi shelves. Those results were compared with earlier surveys made in the Barents Sea, where the uptake of atmospheric CO₂ was about half that estimated in the Bering–Chukchi Seas. Cooling and biology were of nearly equal significance in the Barents Sea in driving the flux of CO₂ into the ocean. The differences between the two regions are discussed. The loss of inorganic carbon due to primary production was estimated from the change in phosphate concentration in the water column. A larger loss of nitrate relative to phosphate compared to the classical ΔN/ΔP ratio of 16 was found. This excess loss was about 30% of the initial nitrate concentration and could possibly be explained by denitrification in the sediment of the Bering and Chukchi Seas.     

Vertical profiles of nitrous oxide and dissolved oxygen in marine sediments

The whole core squeezing method was used to simultaneously obtain profiles of nitrous oxide (N₂O), nitrogenous nutrients, and dissolved oxygen in sediments of Koaziro Bay, Japan (coastal water), the East China Sea (marginal sea), and the central Pacific Ocean (open ocean). In the spring of Koaziro Bay, subsurface peaks of interstitial N₂O (0.5–3.5 cm depth) were observed, at which concentrations were higher than in the overlying water. This was also true for nitrate (NO₃⁻) and nitrite (NO₂⁻) profiles, suggesting that the transport of oxic overlying water to the depth through faunal burrows induced in situ N₂O production depending on nitrification. In the summer of Koaziro Bay, sediment concentrations of N₂O, NO₃⁻ and NO₂⁻ were lower than in the overlying water. In most East China Sea sediments, both N₂O and NO₃⁻ decreased sharply in the top 0.5–2 cm oxic layer (oxygen: 15–130 μM), which may have indicated N₂O and NO₃⁻ consumption by denitrification at anoxic microsites. N₂O peaks at subsurface depth (0.5–6.5 cm) implied in situ production of N₂O and/or its supply from the overlying water through faunal burrows. However, the occurrence of the latter process was not confirmed by the profiles of other constituents. In the central Pacific Ocean, the accumulation of N₂O and NO₃⁻ in the sediments likely resulted from nitrification. Nitrous oxide fluxes from the sediments, calculated using its gradient at the sediment–water interface and the molecular diffusion coefficient, were −45 to 6.9 nmolN m⁻² h⁻¹ in Koaziro Bay in the spring, −29 to −21 nmolN m⁻² h⁻¹ in the summer, −46 to 37 nmolN m⁻² h⁻¹ in the East China Sea, 0.17 to 0.23 nmolN m⁻² h⁻¹ in the equatorial Pacific, and <±0.2 nmolN m⁻² h⁻¹ in the subtropical North Pacific, respectively.     

Spatiotemporal variations of the δ18O–salinity relation in the northern Indian Ocean

A new data set of oxygen isotopic composition (δ¹⁸O) and salinity (S) of surface and sub-surface waters of the northern Indian Ocean, collected during the period 1987–2009, is presented. While the results are consistent with positive P?E (excess of precipitation over evaporation) over the Bay of Bengal and negative P?E over the eastern Arabian Sea, a significant spatiotemporal variability in the slope (also intercept) of the δ¹⁸O–S relation is observed in the Bay; the temporal variability is difficult to discern in the Arabian Sea. The slope and intercept are positively and negatively correlated, respectively, with the annual rainfall over India, a rough measure of river runoff. Both the slope and intercept appear to be sensitive to rainfall; the slope (intercept) is higher (lower) during years of stronger monsoon. The observed variability in the δ¹⁸O–S relation implies that caution needs to be exercised in paleosalinity estimations, especially from the Bay of Bengal, based on δ¹⁸O of marine organisms.     

An improvement in the small-volume technique for determining thorium-234 in seawater

The recently developed 2–5 L small-volume MnO₂ coprecipitation method for determining ²³⁴Th in seawater has provided a new way to substantially increase, both temporally and spatially, the sampling resolution of ²³⁴Th and ²³⁴Th-based particulate organic carbon export estimates in the upper ocean. In this study, we further optimize the technique by reducing reagent quantities and the use of an additional water bath heating step. This optimization allows the filtration of the MnO₂ precipitate onto a 25-mm diameter, 1.0 μm pore size QMA filter to be completed within < 30 min for unfiltered waters from the South China Sea. In addition, we have modified the MnO₂ purification procedure to allow for alpha spectrometric measurements of ²³⁴Th recoveries. Results from recovery experiments suggest that reagent amounts can be reduced to 0.0375 mg KMnO₄ and 0.1 mg MnCl₂·4H₂O per liter of sample, while still maintaining high ²³⁴Th recovery. This study further confirms that the addition of a yield monitor is necessary for the application of the small-volume method.     

Denitrification and the nitrogen gas excess in the eastern tropical South Pacific oxygen deficient zone

Recent studies of the nitrogen gas excess produced during water column denitrification have indicated that water column denitrification rates calculated using nitrate deficit-type methods could be a substantial underestimate. Since there are no other significant processes that produce (or consume) N₂ in the oxygen deficient zone (ODZ), its excess above background can be used to estimate the amount of denitrification, avoiding assumptions made in nitrate deficit calculations of the composition of the respired organic matter and also uncertainties in the nitrogen removal pathways. Dissolved N₂, Ar, and nutrient concentrations were measured at 2 stations in the ODZ of the eastern tropical South Pacific (ETSP) in order to compare the nitrogen gas excess with the dissolved inorganic nitrogen (DIN) deficit due to denitrification. In contrast with previous findings in the Arabian Sea ODZ, the shapes of the N₂ excess and DIN deficit profiles were similar in the ETSP ODZ, with maxima at the top of the ODZ. Maximum DIN deficits at each station were 19 and 18 μM N compared to the maximum N₂ excesses of 15 and 20 μM N, respectively. Given the same considerations of the volume and residence time for the oxygen deficient zone waters, denitrification rates for the ETSP estimated from the N₂ excess would be comparable or no greater than 30% larger than the one determined using the DIN deficit. This implies that the source of the DIN removed from the ODZ is either deep sea nitrate or organic matter with an N:P ratio close to Redfield.     

Stable isotope composition of modern bryozoan skeletal carbonate from the Otago Shelf,New Zealand

The oxygen (δ¹⁸O) and carbon (δ¹³C) isotope ratios of 10 species of living Bryozoa collected from the Otago Shelf, New Zealand were analysed to assess the extent to which isotopic equilibrium (relative to inorganic equilibrium isotope fractionation) is attained during the precipitation of skeletal calcium carbonate. The data reveal that whereas eight species of Bryozoa synthesise skeletal carbonate in apparent oxygen isotope equilibrium with respect to environmental conditions, two species (Celleporina grandis and Hippomonavella flexuosa) yield δ¹⁸O_calcite values which indicate significant disequilibrium oxygen isotope fractionation during calcification. Sufficient data are available from one species (C. grandis) to demonstrate that disequilibrium is probably related to kinetic factors associated with diffusion‐controlled transport of HCO₃‐ to the site of calcite precipitation. Carbon isotope signatures indicate significant departures from inorganic isotope equilibrium in all but one bryozoan species (Hippomenella vellicata). Although greater uncertainties are associated with estimates of the isotopic composition of total dissolved inorganic carbon (δ¹³C_SDIC), the data suggest that two factors—kinetic fractionation and incorporation of respiratory CO₂—are important in controlling carbon isotope disequilibrium. Where bryozoan species exhibit evidence for disequilibrium in both oxygen and carbon isotope systems (C. grandis, H. flexuosa), it is likely that kinetic factors are primarily responsible for observed departures from carbon isotope equilibrium. In contrast, the probable explanation for those species which display evidence for carbon isotope disequilibrium only, is that skeletal carbonate is precipitated from a DIC pool modified by the incorporation of respiratory CO₂. Differences between the carbon isotope composition of skeletal elements from the same species and co‐existing species living in the same community suggests that significant variations may occur in the extent to which marine DIC and respiratory CO₂ are utilised during calcification. Additional studies of carbon pathways associated with calcification are required to assess the relative effects of kinetic, metabolic, and environmental factors on the carbon isotopic composition of bryozoan skeletal carbonate.     

Spatial variability in the partial pressures of CO2 in the northern Bering and Chukchi seas

In the summers of 1999 and 2003, the 1st and 2nd Chinese National Arctic Research Expeditions measured the partial pressure of CO₂ in the air and surface waters (pCO₂) of the Bering Sea and the western Arctic Ocean. The lowest pCO₂ values were found in continental shelf waters, increased values over the Bering Sea shelf slope, and the highest values in the waters of the Bering Abyssal Plain (BAP) and the Canadian Basin. These differences arise from a combination of various source waters, biological uptake, and seasonal warming. The Chukchi Sea was found to be a carbon dioxide sink, a result of the increased open water due to rapid sea-ice melting, high primary production over the shelf and in marginal ice zones (MIZ), and transport of low pCO₂ waters from the Bering Sea. As a consequence of differences in inflow water masses, relatively low pCO₂ concentrations occurred in the Anadyr waters that dominate the western Bering Strait, and relatively high values in the waters of the Alaskan Coastal Current (ACC) in the eastern strait. The generally lower pCO₂ values found in mid-August compared to at the end of July in the Bering Strait region (66–69°N) are attributed to the presence of phytoplankton blooms. In August, higher pCO₂ than in July between 68.5 and 69°N along 169°W was associated with higher sea-surface temperatures (SST), possibly as an influence of the ACC. In August in the MIZ, pCO₂ was observed to increase along with the temperature, indicating that SST plays an important role when the pack ice melts and recedes.     

Nitrogen transformations as inferred from the activities of key enzymes in the Arabian Sea oxygen minimum zone

Vertical distributions of the potential activities of some key enzymes mediating nitrification and denitrification were investigated within the oxygen (O₂) minimum zone of the Arabian Sea at a number of locations between latitudes 17°N and 21°N and longitudes 63°E and 68°E so as to get an insight into the predominant biochemical mode(s) of production and consumption of nitrous oxide (N₂O). Results revealed that the dissimilatory nitrate (NO⁻₃) reduction activity was generally very low or absent within the σ_θ range 26.6–26.8, which corresponds to the Persian Gulf Watermass (PGW). Depth profiles of nitrate reductase (NaR), nitrite reductase (NiR) and ammonia monooxygenase (AMO) activities were compared with those of O₂, NO⁻₃, nitrite (NO⁻₂) and N₂O, and it is concluded that nitrifier denitrification rather than heterotrophic denitrification is active within the core of PGW. The presence of multiple peaks of AMO activity coinciding with distinct maxima in the O₂ profile and with a trend opposite to that of NaR activity indicates that the two processes, viz., classical and nitrifier denitrification, occur in discrete layers, probably determined by the variations in the ambient O₂ concentrations at various depths surrounding the PGW core. Further, it appears that at the depths where nitrifier denitrification is active in the absence of heterotrophic denitrification, N₂O builds up as its consumption may be inhibited by O₂. Possible reasons for the occurrence of appreciable nitrate deficit within the core of PGW, where dissimilatory NO⁻₃ reduction is lacking, are discussed.     

Stable carbon isotope distribution of particulate organic matter in the ocean: a model study

The stable carbon isotopic composition of particulate organic matter in the ocean, δ¹³C_POC, shows characteristic spatial variations with high values in low latitudes and low values in high latitudes. The lowest δ¹³C_POC values (−32‰ to −35‰) have been reported in the Southern Ocean, whereas in arctic and subarctic regions δ¹³C_POC values do not drop below −27‰. This interhemispheric asymmetry is still unexplained. Global gradients in δ¹³C_POC are much greater than in δ¹³C_DIC, suggesting that variations in isotopic fractionation during organic matter production are primarily responsible for the observed range in δ¹³C_POC. Understanding the factors that control isotope variability is a prerequisite when applying δ¹³C_POC to the study of marine carbon biogeochemistry. The present model study attempts to reproduce the δ¹³C_POC distribution pattern in the ocean. The three-dimensional (3D) Hamburg Model of the Oceanic Carbon Cycle version 3.1 (HAMOCC3.1) was combined with two different parametrizations of the biological fractionation of stable carbon isotopes. In the first parametrization, it is assumed that the isotopic fractionation between CO₂ in seawater and the organic material produced by algae, _P, is a function of the ambient CO₂ concentration. The two parameters of this function are derived from observations and are not based on an assumption of any specific mechanism. Thus, this parametrization is purely empirical. The second parametrization is based on fractionation models for microalgae. It is supported by several laboratory experiments. Here the fractionation, _P, depends on the CO₂ concentration in seawater and on the (instantaneous) growth rates, μ_i, of the phytoplankton. In the Atlantic Ocean, where most field data are available, both parametrizations reproduce the latitudinal variability of the mean δ¹³C_POC distribution. The interhemispheric asymmetry of δ¹³C_POC can mostly be attributed to the interhemispheric asymmetry of CO₂ concentration in the water. However, the strong seasonal variations of δ¹³C_POC as reported by several authors, can only be explained by a growth rate-dependent fractionation, which reflects variations in the cellular carbon demand.     

Hydrographical characteristics and oxygen isotopic signatures of water in a coastal environment (Mangalore) along the southeastern Arabian Sea

Coastal marine environments are important links between the continents and the open ocean. The coast off Mangalore forms part of the upwelling zone along the southeastern Arabian Sea. The temperature, salinity, density, dissolved oxygen and stable oxygen isotope ratio (δ¹⁸O) of surface waters as well as those of bottom waters off coastal Mangalore were studied every month from October 2010 to May 2011. The coastal waters were stratified in October and November due to precipitation and runoff. The region was characterised by upwelled bottom waters in October, whereas the region exhibited a temperature inversion in November. The surface and bottom waters presented almost uniform properties from December until April. The coastal waters were observed to be most dense in January and May. Comparatively cold and poorly oxygenated bottom waters during the May sampling indicated the onset of upwelling along the region. δ¹⁸O of the coastal waters successfully documented the observed variations in the hydrographical characteristics of the Mangalore coast during the monthly sampling period. We also noted that the monthly variability in the properties of the coastal waters of Mangalore was related to the hydrographical characteristics of the adjacent open ocean inferred from satellite-derived surface winds, sea surface height anomaly data and sea surface temperatures.     

Seasonal and spatial variations in settling manganese fluxes in the Northern Arabian Sea

Particulate manganese (Mn) fluxes measured with six time series sediment traps showed that the annual settling fluxes were 3–6 times higher in the west compared to those in the east and central Arabian Sea. Annual detrital Mn (Mn_dt) flux was nearly the same in the eastern and western Arabian Sea, but excess Mn (Mn_ex) fluxes were much higher (>4 times) in the western Arabian Sea. Atmospheric inputs cannot account for these high-Mn fluxes. Central and eastern Arabian Sea traps are overlain by a thick and intense denitrification layer, which may cause reductive dissolution of Mn oxides from settling particles and consequently low Mn_ex fluxes. As the exchange of intermediate waters between the Arabian Sea and the rest of the Indian Ocean is confined largely to the western Arabian Sea, relatively more oxic and dynamic conditions prevail in this region. Increased oxidizing conditions coupled with higher inputs of dissolved Mn through intermediate and surface advective processes might have led to in situ oxidation of Mn, thus resulting in higher vertical fluxes of Mn_ex. Mn_ex fluxes in traps at ∼1000 m depth exhibited seasonal variability with a minimum during the winter monsoon (January–February) and maximum during the pre- and early- south-west monsoon (March–June). This variation is correlated with water mass movements and bacterial abundance observed during the Joint Global Ocean Flux Study (JGOFS). The possible involvement of bacteria and the microbial loop is suggested for the concentration and vertical transport of excess Mn.