Time-series sediment trap record of alkenones from the western Sea of Okhotsk     

Osamu Seki  Takeshi Nakatsuka  Kimitaka Kawamura  Sei-Ichi Saitoh  Masaaki Wakatsuchi 《Marine Chemistry》2007,104(3-4):253-265

C₃₇–C₃₉ alkenones were measured in time-series sediment trap samples collected from August 1998 to June 2000 at two depths in the seasonal sea ice region of the western Sea of Okhotsk, off Sakhalin, in order to investigate alkenone production and water-column processes in the region. Measurable export fluxes of alkenones are ranged from < 0.1 to 5.8 μg/m²/day and clearly showed that the alkenone production was restricted to autumn. In 1998, maximum export flux of alkenones occurred in September when surface water column was well stratified with low nutrients in the surface mixing layer. In the next year, the maximum flux is observed in October. Comparison between alkenone temperature and satellite based sea surface temperature (SST) shows that the estimated alkenone temperatures in August 1998 were found to be  10 °C lower than the temporal satellite SST, suggesting that alkenones are produced in surface to subsurface thermocline layers during the period. Annual mean flux of alkenones is lower in the lower traps than that of the upper traps, suggesting rapid degradation of alkenones in water column, but the U^K₃₇′ value is not significantly altered. This study indicates that U^K₃₇′ values preserved in the surface sediments off Sakhalin reflect the seasonal temperature signal of near surface water, rather than annual mean surface temperature.  相似文献   

Anomalously low alkenone temperatures caused by lateral particle and sediment transport in the Malvinas Current region, western Argentine Basin     

Albert Benthien  Peter J. Müller 《Deep Sea Research Part I: Oceanographic Research Papers》2000,47(12):373

We analysed the alkenone unsaturation ratio (U^K′₃₇) in 87 surface sediment samples from the western South Atlantic (5°N–50°S) in order to evaluate its applicability as a paleotemperature tool for this part of the ocean. The measured U^K′₃₇ ratios were converted into temperature using the global core-top calibration of Müller et al. (1998) and compared with annual mean atlas sea-surface temperatures (SSTs) of overlying surface waters. The results reveal a close correspondence (<1.5°C) between atlas and alkenone temperatures for the Western Tropical Atlantic and the Brazil Current region north of 32°S, but deviating low alkenone temperatures by −2° to −6°C are found in the regions of the Brazil–Malvinas Confluence (35–39°S) and the Malvinas Current (41–48°S). From the oceanographic evidence these low U^K′₃₇ values cannot be explained by preferential alkenone production below the mixed layer or during the cold season. Higher nutrient availability and algal growth rates are also unlikely causes. Instead, our results imply that lateral displacement of suspended particles and sediments, caused by strong surface and bottom currents, benthic storms, and downslope processes is responsible for the deviating U^K′₃₇ temperatures. In this way, particles and sediments carrying a cold water U^K′₃₇ signal of coastal or southern origin are transported northward and offshore into areas with warmer surface waters. In the northern Argentine Basin the depth between displaced and unaffected sediments appears to coincide with the boundary between the northward flowing Lower Circumpolar Deep Water (LCDW) and the southward flowing North Atlantic Deep Water (NADW) at about 4000 m.  相似文献   

Seasonal and depth variations in molecular and isotopic alkenone composition of sinking particles from the western North Pacific     

《Deep Sea Research Part I: Oceanographic Research Papers》2007,54(9):1571-1592

Seasonal and depth variations in alkenone flux and molecular and isotopic composition of sinking particles were examined using a 21-month time-series sediment trap experiment at a mooring station WCT-2 (39°N, 147°E) in the mid-latitude NW Pacific to assess the influences of seasonality, production depth, and degradation in the water column on the alkenone unsaturation index U^K′₃₇. Analysis of the underlying sediments was also conducted to evaluate the effects of alkenone degradation at the water–sediment interface on U^K′₃₇. Alkenone sinking flux and U^K′₃₇-based temperature showed strong seasonal variability. Alkenone fluxes were higher from spring to fall than they were from fall to spring. During periods of high alkenone flux, the U^K′₃₇-based temperatures were lower than the contemporary sea-surface temperatures (SSTs), suggesting alkenone production in a well-developed thermocline (shallower than 30 m). During low alkenone flux periods, the U^K′₃₇-based temperatures were nearly constant and were higher than the contemporary SSTs. The nearly constant carbon isotopic ratios of C_37:2 and C_38:2 alkenones suggest that alkenones produced in early fall were suspended in the surface water until sinking. The alkenone sinking flux decreased exponentially with increasing depth. The decreasing trend was enhanced during the periods of high alkenone flux, suggesting that fresh and labile particles sank from spring to fall, while old and stable particles sank from fall to spring. The U^K′₃₇-based temperature usually increased with increasing depth. The preservation efficiency of alkenones was ∼2.7–5.2% at the water–sediment interface. Despite the significant degradation of the alkenones, there was little difference in U^K′₃₇ levels between sinking particles and the surface sediment.  相似文献   

Alkenone distribution in surface sediments of the southern Yellow Sea and implications for the {\text{U}}^{{{\text{K}}\prime}}_{{37}} thermometer     

Shuqin Tao  Lei Xing  Xiaofan Luo  Hao Wei  Yanguang Liu  Meixun Zhao 《Geo-Marine Letters》2012,32(1):61-71

The \textU^\textK￠₃₇ {\text{U}}^{{{\text{K}}\prime}}_{{37}} index has been widely applied for sea surface temperature (SST) reconstruction in open ocean environments, but has inherently limited applications at smaller, regional scales including some marginal seas where both historical and reconstructed SST records are urgently needed for understanding regional climate evolution. We determined the spatial distribution of alkenone contents in surface sediments from the southern Yellow Sea to assess the regional \textU₃₇^\textK￠ {\text{U}}_{{{37}}}^{{{\text{K'}}}} —SST relationship for paleo-SST reconstructions. C_37:2 and C_37:3 alkenones were detected at all 36 sites covering most of the southern Yellow Sea. Alkenone content ranges from 17 to 1,063 ng/g, with high values (ca. 400 to 1,000 ng/g) at deep water sites and a decreasing trend shoreward. For six samples at shallower depths near the coast and further offshore, the values were too low for statistical evaluation. This spatial pattern of alkenone contents is consistent with existing knowledge on the spatial distribution and productivity of alkenone-producing coccolithophorid species in the region. There is a significant positive relationship ( \textU₃₇^\textK￠ = 0.059\textSST - 0.350 {\text{U}}_{{{37}}}^{{{\text{K'}}}} = 0.059{\text{SST}} - 0.350 , R = 0.912, n = 30) between the \textU₃₇^\textK￠ {\text{U}}_{{{37}}}^{{{\text{K'}}}} values and satellite-derived annual mean SSTs (0 m) for the last 27 years, providing support for the application of a region-specific \textU₃₇^\textK￠ {\text{U}}_{{{37}}}^{{{\text{K'}}}} index as paleothermometer in the southern Yellow Sea. However, the slope of the southern Yellow Sea calibration (0.059) is considerably larger than that of the well-known global core-top calibration (0.033). This implies that global SST trends may not adequately encompass regional SST patterns and/or that environmental factors other than temperature may gain importance in explaining coccolithophore dynamics in marginal seas.  相似文献   

Biomarker records from core GH02-1030 off Tokachi in the northwestern Pacific over the last 23,000 years: Environmental changes during the last deglaciation     

Masaki Inagaki  Masanobu Yamamoto  Yaeko Igarashi  Ken Ikehara 《Journal of Oceanography》2009,65(6):847-858

We investigated marine and terrestrial environmental changes at the northern Japan margin in the northwestern Pacific during the last 23,000 years by analyzing biomarkers (alkenones, long-chain n-alkanes, long-chain n-fatty acids, and lignin-derived materials) in Core GH02-1030. The U ₃₇^K′-derived temperature in the last glacial maximum (LGM) centered at 21 ka was ∼10°C, which was 2°C lower than the core-top temperature (∼12°C). This small temperature drop does not agree with pollen evidence of a large air temperature drop (more than 4°C) in the Tokachi area. This disagreement might be attributed to a bias of U ₃₇^K′-derived temperature within 2.5°C by a seasonal shift in alkenone production. The U ₃₇^K′-derived temperature was significantly low during the last deglaciation. Because this cooling was significant in the Kuroshio-Oyashio transition zone, the temperature drops are attributable to the southward displacement of the Kuroshio-Oyashio boundary. Abundant lignin-derived materials, long-chain n-alkanes and long-chain n-fatty acids indicate a higher contribution of terrigenous organic matter from 17 to 12 ka. This phenomenon might have resulted from an enhanced coastal erosion of terrestrial soils due to marine transgression and/or an efficient inflow of higher plant debris to river waters from 17 to 12 ka.  相似文献   

长链烯酮及U₃₇k值在北极海洋古温度的应用研究   总被引：1，自引：1，他引：1  

卢冰  陈荣华  王自磐  陈建芳  刘镇盛 《海洋学报》2001,23(5):49-57

在北极楚科奇海和白令海表层沉积物中检出长链烯酮化合物,研究结果表明楚科奇海和白令海沉积物中长链烯酮以C_37:3甲基酮占优势,C₃₇～C₃₉不饱和烯酮丰度变化顺序为C₃₇>C₃₈>C₃₉.根据∑C₃₇/∑C₃₈比值,所检出的长链烯酮母质生物主要是颗石藻(Emiliania huxleyi).应用U₃₇k和U₃₇k'标准校正关系式估算了表层海水古温度,其中U₃₇k'估算值为4.147～5.706℃(平均为5.092℃).  相似文献   

Seasonal record for alkenones in sedimentary particles from the Gulf of Maine     

《Deep Sea Research Part I: Oceanographic Research Papers》2001,48(2):515-528

C_37–39 alkenones and C₃₆ alkenoates, biomarkers of haptophyte origin, were measured in a 10-month sediment trap times series from the Wilkinson Basin in the Gulf of Maine (GOM). Highest biomarker flux to the seabed was observed in summertime, the period when surface waters are stratified and a persistent, subsurface chlorophyll maximum (SCM) exists within the upper thermocline and at the base of the euphotic zone throughout the GOM. Comparison of biomarker content and composition of sediment trap particles and underlying surface sediments indicates significant loss (>50%) of signal due to the impact of early diagenesis. Despite such loss, however, C₃₇ alkenone unsaturation patterns (U₃₇^K′) are not altered. Estimates of algal growth temperature made from analysis of U₃₇^K′ in these sedimentary materials correspond with water temperature measured at the SCM, identifying this biological oceanographic feature as a key site of alkenone export production to the GOM sediment record. Given the common occurrence of SCM in surface waters of the world ocean, particularly the expansive oligotrophic regions of the subtropical to temperate ocean, export of alkenones produced within such features is a potentially widespread biological oceanographic phenomenon which shapes the sediment record for these biomarkers.  相似文献   

Spectrophotometric pH measurement in estuaries using thymol blue and m-cresol purple     

Luke M. Mosley  Shamus L.G. Husheer  Keith A. Hunter   《Marine Chemistry》2004,91(1-4):175-186

The conditional acid dissociation constants (pK_a′) of two sulfonephthalein dyes, thymol blue (TB) and m-cresol purple (mCP), were assessed throughout the estuarine salinity range (0<S<40) using a tris/tris–HCl buffer and spectrophotometric measurement. The salinity dependence of the pK_a′ of both dyes was fitted to the equations (25 °C, total proton pH scale, mol kg soln⁻¹):The estimated accuracy of pH measurements using these calculated pK_a′ values is considered to be comparable to that possible with careful use of a glass electrode (±0.01 pH unit) but spectrophotometric measurements in an estuary have the significant advantage that it is not necessary to calibrate an electrode at different salinities. pH was measured in an estuary over a tidal cycle with a precision of ±0.0005 pH unit at high (S>30) salinity, and ±0.002 pH unit at low (S<5) salinity. The pH increased rapidly in the lower salinity ranges (0<S<15) but less rapidly at higher salinities.  相似文献   

Solubility of calcite in the ocean     

S. E. Ingle 《Marine Chemistry》1975,3(4):301-319

The apparent solubility product K′_sp of calcite in seawater was measured as a function of temperature, salinity, and pressure using potentiometric saturometry techniques. The temperature effect was hardly discernible experimentally. The value of K′_sp at 25°C was 4.59·10⁻⁷ mole²/(kg seawater)² at 35‰S, 5.34·10⁻⁷ at 43‰S, and 3.24·10⁻⁷ at 27‰S. The apparent partial molal volume was found to be −34.4 cm³ at 25°C and −42.3 cm³ at 2°C from a linear fit of log(K′_sp ^P/K′_sp ¹). These results were used in conjunction with field data to calculate the degree of saturation in the oceans and showed undersaturation at shallower depths than previously reported.  相似文献   

The solubility of CaCO₃ in seawater at 2°C based upon in-situ sampled pore water composition     

Frederick L. Sayles 《Marine Chemistry》1980,9(4):223-235

Analyses of the concentration product (Ca²⁺) × (CO₃²⁻) in the pore waters of marine sediments have been used to estimate the apparent solubility products of sedimentary calcite (K′_SPc) and aragonite (K′_SPa) in seawater. Regression of the data gives the relation In K′^P_SPc = 1.94 × 10⁻³ δP − 14.59 The 2°C, 1 atm value of K′_SPc is, then, 4.61 × 10⁻⁷ mol² l⁻². The pressure coefficient yields a at 2°C of −43.8 cm³ atm⁻¹. A single station where aragonite is present in the sediments gives a value of K′_SPa = 9.2 × 10⁻⁷ (4°C, 81 atm). The calcite data are very similar to those determined experimentally by Ingle et al. (1973) for K′_SPc at 2°C and 1 atm. The calculated is also indistinguishable from the experimental results of Ingle (1975) if is assumed to be independent of pressure.  相似文献   

The C₃₇ alkenone record of seawater temperature during seasonal thermocline stratification     

I. Bentaleb  J. O. Grimalt  F. Vidussi  J. -C. Marty  V. Martin  M. Denis  C. Hatt  M. Fontugne 《Marine Chemistry》1999,64(4):255

  相似文献   

Glucuronidation in the polar bear (Ursus maritimus)     

James C. Sacco  Margaret O. James   《Marine environmental research》2004,58(2-5):475

Polar bears bioaccumulate lipophilic pollutants, including polychlorinated biphenyls (PCBs), into their bodies from their exclusive diet of marine organisms. Hydroxylated PCB metabolites (OH-PCBs) have been found in plasma, presumably due to CYP-dependent biotransformation of PCBs in liver. Little is known about the phase 2 metabolism of hydroxylated xenobiotics in polar bears. The objective of this study was to examine UDP-glucuronosyltransferase (UGT) activity with OH-PCBs and a hydroxylated polycyclic aromatic hydrocarbon, 3-hydroxy-benzo(a)pyrene (3-OH-BaP), in polar bear liver. Samples of frozen polar bear liver were used to prepare microsomes. UGT activity with 3-OH-BaP in Brij-treated microsomes, measured by a fluorescence assay, was readily measurable with protein concentrations in assay tubes of up to 10 μg/ml, but dropped off very sharply at higher protein concentrations. The apparent K_m for 3-OH-BaP was 1.71 ± 0.04 μM, and V_max 1.26 ± 0.16 nmol/min/mg protein (mean ± SD, n=3). UGT activities with a model tetrachloro-OH-PCB (4^′-OH-CB72) and a model hexachloro-OH-PCB (4^′-OH-CB159) were assayed with [¹⁴-C]-UDPGA and separation of the [¹⁴-C]-glucuronide by ion-pair extraction and thin-layer chromatography. [¹⁴-C]-glucuronide conjugates were readily formed by polar bear liver microsomes in the absence of added substrate, apparently from contaminants present in liver. This phenomenon was not observed using hepatic microsomes from laboratory-held catfish. Glucuronidation efficiency was much higher with 4^′-OH-CB72 (K_m 7.3 μM; V_max 1.55 nmol/min/mg) than 4^′-OH-CB159 (K_m 16.1 μM; V_max 0.46 nmol/min/mg). The identities of the aglycones present in polar bear liver are not known, but could include OH-PCBs or hydroxylated metabolites of other persistent organic pollutants. This study demonstrates that UGT with high activity for 3-OH-BaP and other substrates is present in polar bear liver.  相似文献   

The fate of marine lipids: Biotic vs. abiotic degradation of particulate sterols and alkenones in the Northwestern Mediterranean Sea     

J.-F. Rontani  N. Zabeti  S.G. Wakeham 《Marine Chemistry》2009,113(1-2):9-18

Sterol and alkenone compositions in suspended particle and surface sediment samples collected in the Northwestern Mediterranean Sea during the MEDFLUX program were used to evaluate the relative importance of biotic and abiotic degradation processes on marine organic matter. Alkenone concentrations decreased much more rapidly (~ 500 fold) between 5 and 800 m than Δ⁵-sterols (~ 100-fold) or POC (~ 100-fold). The diverse functional groups attached to the stable tetracyclic carbon skeleton of Δ⁵-sterols appeared to be useful for estimating the relative effects of biotic vs. abiotic (photooxidation and autoxidation) degradation. Products of abiotic degradation predominated over products of biotic degradation in suspended particles in the NW Mediterranean. For alkenones, the U₃₇^K′ index increased from 0.43 to 0.55 with increasing water depth, and a good correlation between variations of U₃₇^K′ and concentrations of specific Δ⁵-sterol autoxidation products points to selective autoxidation of alkenones in suspended particles. Stereomutated alkenones (with cis double bonds) were detected in the surface sediment, allowing us to estimate that stereomutation resulted in a + 0.05 increase in U₃₇^K′. Therefore, abiotic degradation may be another factor effect on alkenone-derived paleothermometry.  相似文献   

N₂O Production, Nitrification and Denitrification in an Estuarine Sediment   总被引：1，自引：0，他引：1  

T. Usui  I. Koike  N. Ogura 《Estuarine, Coastal and Shelf Science》2001,52(6):769

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.  相似文献   

The reliability of the thermodynamic constants for the dissociation of carbonic acid in seawater     

Kitack Lee  Frank J. Millero  Douglas M. Campbell 《Marine Chemistry》1996,55(3-4)

Laboratory measurements of all four CO₂ parameters [f_CO2 ( = fugacity of CO₂), pH, TCO₂ ( = total dissolved inorganic carbon), and TA ( = total alkalinity)] were made on the same sample of Gulf Stream seawater (S = 35) as a function of temperature (5–35 °C) and the ratio of TA/TCO₂ (X) (1.0–1.2). Overall the measurements were consistent to ±8 μ atm in f_CO2, ± 0.004 in pH, ± 3 μ mol kg⁻¹ in TCO₂, and ± 3 μ mol kg⁻¹ in TA with the thermodynamic constants of Goyet and Poisson (1989), Roy et al. (1993), and Millero (1995). Deviations between the measured pH, TCO₂, TA and those calculated from various input combinations increase with increasing X when the same constants are used. This trend in the deviations indicates that the uncertainties in pK₂ become important with increasing X (surface waters), but are negligible for samples with the lower X (deep waters). This trend is < 5 μ mol kg⁻¹ when the pK₂ values of Lee and Millero (1995) are used.The overall probable error of the calculated f_CO2 due to uncertainties in the accuracy of the parameters (pH, TCO₂, TA, pK₀, pk₁, and pK₂) is ± 1.2%, which is similar to the differences between the measured values and those calculated using the thermodynamic constants of Millero (1995).The calculated values of pK₁, (from f_CO2-TCO₂-TA) agree to within ± 0.004 compared to the results of Dickson and Millero (1987), Goyet and Poisson (1989), Roy et al. (1993), and Millero (1995) over the same experimental conditions. The calculated values of pK₂ (from pH-TCO₂-TA) are in good agreement (± 0.004) with the results of Lee and Millero (1995) and also in reasonable agreement (± 0.008) with the results of Goyet and Poisson (1989), Roy et al. (1993), and Millero (1995). The salinity dependence of our derived values of pK₁ and pK₂, (S = 35) can be estimated using the equations determined by Millero (1995).  相似文献   

Apparent copper complexation capacity and conditional stability constants in north atlantic waters     

Cees J.M Kramer 《Marine Chemistry》1986,18(2-4)

Surface water samples were collected in the north Atlantic Ocean in July–August 1983. Their apparent complexation capacity for copper (CC_Cu) was determined on board, using differential pulse anodic stripping voltammetry under clean room conditions. Measurements were carried out by direct titrations as well as after equilibration of copper spikes. CC_Cu and conditional stability constants (K′) were calculated, by means of three different methods, which are compared.On the basis of salinity, temperature, silicate and phosphate concentrations the following surface waters could be distinguished: North Atlantic Drift (I), East Greenland Current (II), Labrador Current (III) and Gulf Stream waters (IV, V). CC_Cu and K′ were found to differ between these waters. The range of values for CC_Cu and their mean values given in parentheses, as calculated from van den Berg plots for waters I–IV are: I, 53–65 (59); II, 47–66 (55); III, 37–53 (45); IV, 20–42 (33) nM Cu. The range and mean values for log K′ are: I, 8.23–8.33 (8.28); II, 7.89–8.11 (7.98); III, 8.40–8.41 (8.41); IV, 7.90–8.21 (8.06).Information on complexation kinetics extracted from the titration curve revealed that k_f^′ is area-specific. The complexation rate constant in the northern part (Area I) is about two times larger than that in the southern area IV, (3.6 ± 0.3) and (2.2 ± 0.2) × 10⁴s⁻¹M⁻¹ Cu, respectively.Preliminary results for deep water samples suggest smaller but still existent CC_Cu and higher K′ than those found for surface waters.  相似文献   

High-resolution measurement of Southern Ocean CO₂ and O₂/Ar by membrane inlet mass spectrometry     

C. Guguen  P.D. Tortell 《Marine Chemistry》2008,108(3-4):184-194

This paper evaluates the simultaneous measurement of dissolved gases (CO₂ and O₂/Ar ratios) by membrane inlet mass spectrometry (MIMS) along the 180° meridian in the Southern Ocean. The calibration of pCO₂ measurements by MIMS is reported for the first time using two independent methods of temperature correction. Multiple calibrations and method comparison exercises conducted in the Southern Ocean between New Zealand and the Ross Sea showed that the MIMS method provides pCO₂ measurements that are consistent with those obtained by standard techniques (i.e. headspace equilibrator equipped with a Li–Cor NDIR analyser). The overall MIMS accuracy compared to Li–Cor measurements was 0.8 μatm. The O₂/Ar ratio measurements were calibrated with air-equilibrated seawater standards stored at constant temperature (0 ± 1 °C). The reproducibility of the O₂/Ar standards was better than 0.07% during the 9 days of transect between New Zealand and the Ross Sea.The high frequency, real-time measurements of dissolved gases with MIMS revealed significant small-scale heterogeneity in the distribution of pCO₂ and biologically-induced O₂ supersaturation (ΔO₂/Ar). North of 65°S several prominent thermal fronts influenced CO₂ concentrations, with biological factors also contributing to local variability. In contrast, the spatial variation of pCO₂ in the Ross Sea gyre was almost entirely attributed to the biological utilization of CO_2, with only small temperature effects. This high productivity region showed a strong inverse relationship between pCO₂ and biologically-induced O₂ disequilibria (r² = 0.93). The daily sea air CO₂ flux ranged from − 0.2 mmol/m² in the Northern Sub-Antarctic Front to − 6.4 mmol/m² on the Ross Sea shelves where the maximum CO₂ influx reached values up to − 13.9 mmol/m². This suggests that the Southern Ocean water (south of 58°S) acts as a seasonal sink for atmospheric CO₂ at the time of our field study.  相似文献   

Water masses and currents of deep circulation southwest of the Shatsky Rise in the western North Pacific     

Masaki Kawabe  Shinzou Fujio  Daigo Yanagimoto  Kiyoshi Tanaka   《Deep Sea Research Part I: Oceanographic Research Papers》2009,56(10):1675-1687

We conducted full-depth hydrographic observations in the southwestern region of the Northwest Pacific Basin in September 2004 and November 2005. Deep-circulation currents crossed the observation line between the East Mariana Ridge and the Shatsky Rise, carrying Lower Circumpolar Deep Water westward in the lower deep layer (θ<1.2 °C) and Upper Circumpolar Deep Water (UCDW) and North Pacific Deep Water (NPDW) eastward in the upper deep layer (1.3–2.2 °C). In the lower deep layer at depths greater than approximately 3500 m, the eastern branch current of the deep circulation was located south of the Shatsky Rise at 30°24′–30°59′N with volume transport of 3.9 Sv (1 Sv=10⁶ m³ s⁻¹) in 2004 and at 30°06′–31°15′N with 1.6 Sv in 2005. The western branch current of the deep circulation was located north of the Ogasawara Plateau at 26°27′–27°03′N with almost 2.1 Sv in 2004 and at 26°27′–26°45′N with 2.7 Sv in 2005. Integrating past and present results, volume transport southwest of the Shatsky Rise is concluded to be a little less than 4 Sv for the eastern branch current and a little more than 2 Sv for the western branch current. In the upper deep layer at depths of approximately 2000–3500 m, UCDW and NPDW, characterized by high and low dissolved oxygen, respectively, were carried eastward at the observation line by the return flow of the deep circulation composing meridional overturning circulation. UCDW was confined between the East Mariana Ridge and the Ogasawara Plateau (22°03′–25°33′N) in 2004, whereas it extended to 26°45′N north of the Ogasawara Plateau in 2005. NPDW existed over the foot and slope of the Shatsky Rise from 29°48′N in 2004 and 30°06′N in 2005 to at least 32°30′N at the top of the Shatsky Rise. Volume transport of UCDW was estimated to be 4.6 Sv in 2004, whereas that of NPDW was 1.4 Sv in 2004 and 2.6 Sv in 2005, although the values for NPDW may be slightly underestimated, because they do not include the component north of the top of the Shatsky Rise. Volume transport of UCDW and NPDW southwest of the Shatsky Rise is concluded to be approximately 5 and 3 Sv, respectively. The pathways of UCDW and NPDW are new findings and suggest a correction for the past view of the deep circulation in the Pacific Ocean.  相似文献   

fCO₂ variability at the CARIACO tropical coastal upwelling time series station     

Y.M. Astor  M.I. Scranton  F. Muller-Karger  R. Bohrer  J. García   《Marine Chemistry》2005,97(3-4):245-261

Monthly seawater pH and alkalinity measurements were collected between January 1996 and December 2000 at 10°30′N, 64°40′W as part of the CARIACO (CArbon Retention In A Colored Ocean) oceanographic time series. One key objective of CARIACO is to study temporal variability in Total CO₂ (TCO₂) concentrations and CO₂ fugacity (fCO₂) at this tropical coastal wind-driven upwelling site. Between 1996 and 2000, the difference between atmospheric and surface ocean CO₂ concentrations ranged from about − 64.3 to + 62.3 μatm. Physical and biochemical factors, specifically upwelling, temperature, primary production, and TCO₂ concentrations interacted to control temporal variations in fCO₂. Air–sea CO₂ fluxes were typically depressed (0 to + 10 mmol C m^{− 2} day^{− 1}) in the first few months of the year during upwelling. Fluxes were higher during June–November (+ 10 to 20 mmol C m^{− 2} day^{− 1}). Fluxes were generally independent of the slight changes in salinity normally seen at the station, but low positive flux values were seen in the second half of 1999 during a period of anomalously heavy rains and land-derived runoff. During the 5 years of monthly data examined, only two episodes of negative air–sea CO₂ flux were observed. These occurred during short but intense upwelling events in March 1997 (−10 mmol C m^{− 2} day^{− 1}) and March 1998 (− 50 mmol C m^{− 2} day^{− 1}). Therefore, the Cariaco Basin generally acted as a source of CO₂ to the atmosphere in spite of primary productivity in excess of between 300 and 600 g C m^{− 2} year^{− 1}.  相似文献   

Chemical speciation of copper and zinc in surface waters of the western Black Sea     

Franois L. L. Muller  Sergei B. Gulin  shild Kalvy 《Marine Chemistry》2001,76(4):62

The chemical speciation of Cu and Zn was investigated by voltammetric titration methods in the surface waters (10 m) of the western Black Sea during an Istanbul–Sevastopol cruise conducted in November 1998. Supporting parameters (temperature (T), salinity (S), pH, alkalinity (Alk), suspended particulate matter (SPM) and dissolved and particulate ²³⁴Th) were obtained in order to distinguish hydrographic features against involvement of the metals in biogeochemical processes. In the Turkish continental slope region, the cruise track intersected a narrow vein of colder water originating on the western shelf. The core of this cold water vein was characterised by a relatively low salinity, higher specific alkalinity and higher metal (especially Cu) and metal-binding ligand concentrations.A very large portion of Cu (93–99.8%) and Zn (82–97%) was organically complexed. The degree of complexation was highest in shelf waters and lowest in the central gyre. Titration data for Cu were modelled by two classes of organic binding ligands characterised by (C_L1=3–12 nM, log K₁′=13.1–13.9) and (C_L2=20–70 nM, log K₂′=9.4–11.2). These ligands occurred mainly in the ‘dissolved’ phase, as defined by 0.4-μm filtration. The stronger Cu-binding ligand seemed to be produced in situ in response to Cu concentration, whereas the weaker Cu-binding ligand appeared to be derived from terrestrial sources and/or reducing shelf sediments. Titration results for Zn were generally represented by one class of ligands (C_L1=8–23 nM, log K₁′=9.4–10.2), which were almost uniformly distributed between the ‘dissolved’ (78±8%) and the particulate phase (22±8%). The concentration of these strong Zn-binding ligands showed a very good correlation with SPM (r²=0.64), which improved when the dissolved ligands alone were considered (r²=0.78). It is hypothesised that these ligands were produced in situ by the bacterial breakdown of particulate organic matter.  相似文献