The dissolved iodate and iodide distribution in the South Atlantic from the Weddell Sea to Brazil

Iodide and iodate concentrations are reported and discussed for the WOCE A23 transect from the Weddell Sea north to about 25°S. Iodide concentrations are very low in the surface waters of the Weddell Sea (20 nM) and increase steadily northwards to about 100 nM in the surface waters of the south Atlantic gyre. In deep waters iodide concentrations are low but detectable at 0.5–2 nM. There is no detectable total iodine depletion in the surface waters south of the polar front although there is a small depletion evident north of the front. The results are discussed in terms of the hydrography, nutrient concentrations and phytoplankton activity along the transect. In particular, a systematic change in the relationship between iodide and nitrate along the transect is discussed.     

On the possibility of iodide oxidation in the near-surface of the Black Sea and its implications to iodine in the general ocean

Iodide oxidation to iodate in near-surface waters of the open oceans is an elusive process, and an unequivocal demonstration of it would simplify modelling of the marine iodine system. In the open ocean, the upward advection of iodate complicates any mathematical treatment of the problem. In this context, the high concentration (0.1 μM) of iodate in the Black Sea surface waters suggested that this Sea might be a place where oxidation might be demonstrated. Hydrologically, the surface waters of the Black Sea appear to be downstream of the deeper waters and, given the latter's anoxicity, the surface waters seemed likely to gain most of their iodine as iodide by upward advection. To test this further, prior to experimentation, an iodine budget for the near-surface waters, based upon the latest hydrological model of the Sea was prepared; this predicts a minimum oxidation flux of 3.89×10⁻⁴ mol I m⁻² a⁻¹. The chemistry of this oxidation is discussed in the light of existing knowledge of the sulfide system. It is argued that as the redox potential of the IO₃⁻/I⁻ and I₂/I⁻ couples at pHs typical of the Black Sea (7.75) are much higher than that of the sulfate–sulfide couple, iodide is probably oxidized in the near-surface domain. This contrasts with sulfide oxidation in the suboxic zone. The possible role of nitrifying bacteria in the oxidation is discussed.     

Dissolved iodine across the Gulf Stream Front and in the South Atlantic Bight

The distributions of iodide, iodate and total iodine were determined along a transect from the Sargasso Sea and across the Gulf Stream to the continental shelf of the South Atlantic Bight during November 1990. The western boundary of the Gulf Stream at the outer shelf-upper slope was characterized by steeply sloping isotherms and isopleths of iodide and iodate, resulting from a dome of cold water that was rich in iodate and nearly devoid of iodide at the slope. Both the mid and the inner shelf were relatively well mixed vertically. The concentration of iodate in the surface waters decreased shoreward from >0.3 μM in the Sargasso Sea/Gulf Stream/outer shelf, to 0.29 μM in the midshelf, 0.19 μM in the outer-inner shelf and 0.11 /IM in the inner-inner shelf. Concomitantly, the concentration of iodide increased from <161 nM to 175 nM, 257 nM and 300 nM. The concentration changes were more abrupt in the inner-inner shelf within about 30 km from the shore. There was no evidence of significant concentrations of organic iodine. These distributions of iodide and iodate suggest that the South Atlantic Bight may act as a geochemical processor of dissolved iodine. Iodate is added to the shelf during topographically induced upwelling and frontal exchange with the Gulf Stream. In the shelf waters, iodate is reduced to iodide in situ. Iodide is exported from the shelf to the Gulf Stream which may eventually further transport it to the ocean interior. A ☐ model calculation suggests that 28% and 43% of the iodate added to the Bight and the inner shelf, respectively, are converted to another form in these waters, almost all of which is iodide. About a third of the reduction of iodate to iodide in the Bight occurs in the inner shelf. Thus, the inner shelf may be the most geochemically active zone within the Bight. The residence times of iodide relative to its production and that of iodate relative to its removal are 3.1 and 3.6 months in the Bight and 0.9 and 1.8 months in the inner shelf.     

The distribution of particulate organic carbon and nitrogen in some surface waters of the World Ocean

Data is presented for the concentrations of organic carbon and nitrogen, and C:N ratios, in marine particulate matter, and for POC and PN, from surface waters collected in the northeastern Atlantic, South Atlantic, Indian Ocean and China Sea.The organic carbon content of this particulate matter varies between 4.6% and 29.9%, and has an average of 17.8%. The average organic carbon content of particulate matter from the various oceans decreases in the order: Northeastern Atlantic > South Atlantic > Indian Ocean > China Sea.The nitrogen content of the particulate matter varies between 1.0% and 3.9%, with an average of 2.2%, and in general follows the same trend as that of organic carbon.C:N ratios vary between 5.1 and 10.6, and have an average of 7.9.The POC contents of the oceanic waters vary between 6.6 and 211 μg/l, with an average of 52 μg/l. The concentrations in the surface waters decrease in the following order: Northeastern Atlantic τ China Sea > South Atlantic > Indian Ocean.The concentrations, and compositions, of particulate matter from various coastal localities are given for comparison with the oceanic values.     

Dissolved inorganic and organic iodine in the Chesapeake Bay and adjacent Atlantic waters: Speciation changes through an estuarine system

The distributions of iodate, iodide and dissolved organic iodine (DOI) were determined in two deep sub-basins in the Chesapeake Bay, the shallow waters at the mouth of the Bay and the adjacent North Atlantic between the late spring and the early fall along the net flow-path of the water entering and exiting the Chesapeake Bay by using an improved analytical scheme designed for the quantitative recovery of DOI. The concentration of R-DOI found in the surface mixed layer in the upper Bay was about twice of those found at the same location in previous studies. (R-X was the concentration of a dissolved iodine species X that had been normalized to a constant salinity of 35.) Thus, DOI in estuarine waters might have been underestimated significantly in the earlier studies. Following the water along its net flow-path, iodate initially constituted more than 60% of total iodine (TI) in the source water in the Middle Atlantic Bight off the Delmarva Peninsula. As this water entered the Chesapeake Bay through the northern part of its mouth, the concentration of R-iodate decreased while that of R-iodide increased progressively until the former became undetectable in the surface mixed layer while the latter reached a maximum of 0.42 μM in the deep water in the upper Bay. Then, the concentration of R-iodate rebounded while that of R-iodide decreased in the outflowing water that exited through the southern part of the mouth of the Bay and was later entrained by the Gulf Stream. The concentration of R-DOI in the surface waters followed the same pattern as R-iodide and reached a maximum of 0.20 μM in the upper Bay. However, R-DOI was depleted in the deep water in the sub-basins. Its concentration dropped to around the detection limit in the suboxic waters in the upper Bay. R-TI in the Bay far exceeded that in the incoming Middle Atlantic Bight water and reached 0.55 μM in the upper Bay. These distributions of the iodine species suggest that, as water from the Middle Atlantic Bight intruded into the Chesapeake Bay, in the well oxygenated surface mixed layer, iodate was reduced to iodide, and the inorganic iodine species could also be converted to DOI. In the deep water, iodate and DOI were converted to iodide. Superimposed on these inter-conversions among the iodine species, dissolved iodine, possibly in the form of iodide, was also added to the water column from the underlying sediments and the process was especially significant in the suboxic deep water in the upper Bay. Mixing between the surface mixed layer and the deep water could also have increased the concentrations of iodide and total iodine in the former.     

Nutrient distributions in the winter regime of the northern Irish Sea

Quasi-synoptic distributions of salinity and the concentrations of dissolved inorganic nutrients in the winter regime of the northern Irish Sea are presented. Salinity to nutrient regression analyses and the distributions of nutrient ratios show that the characteristics of Atlantic waters are variously modified during their northward passage through the Irish Sea. Inherently different chemical characteristics of the fresh water sources discharging into the Northern Irish Sea generate a conglomeration of water types in the area. Marine waters along the Irish coast are relatively enriched in silicon, while waters adjacent to the eastern coastal boundary are relatively enriched by anthropogenic nitrogen sources. Possible implications of the spatial dichotomy in nutrient status for the seasonal production cycle in the northern Irish Sea are considered.     

The biogeochemical effect of seaweeds upon close-to natural concentrations of dissolved iodate and iodide in seawater – Preliminary study with Laminaria digitata and Fucus serratus

Toward assessing the biogeochemical significance of seaweeds in relation to dissolved iodine in seawater, the effect of whole seaweeds (Laminaria digitata and Fucus serratus) upon iodide and iodate, at essentially natural concentrations, has been studied. The weeds were carefully removed from the sub-littoral zone of the Menai Straits and exposed to iodide and iodate at their natural temperature (6 °C), but under continuous illumination. Laminaria digitata was found to decrease the concentration of iodate with an exponential rate constant of 0.008–0.24 h⁻¹. This is a newly discovered process which, if substantiated, will require an entirely new mechanism. Generally, apparent iodide concentration increased except in a run with seawater augmented with iodide, where it first decreased. The rate constant for loss of iodide was 0.014–0.16 h⁻¹. Meanwhile, F. serratus was found not to decrease iodate concentrations, as did L. digitata. Indeed, after ∼30 h iodate concentrations increased, suggesting that the weed may take in iodide before oxidising and releasing it. If substantiated, this finding may offer a way into one of the most elusive of processes within the iodine cycle – iodide oxidation. With both seaweeds sustained long-term increases of apparent iodide concentration are most easily explained as a secretion by the weeds of organic matter which is capable of reducing the Ce(IV) reagent used in determination of total iodine. Modelling of the catalytic method used is provided to support this contention. The possibility of developing this to measure the strain that seaweeds endure in this kind of biogeochemical flux experiment is discussed. A Chemical Oxygen Demand type of approach is applied using Ce(IV) as oxidant. The results of the iodine experiments are contrasted with the several investigations of ¹³¹I interaction with seaweeds, which have routinely used discs of weed cut from the frond. It is argued that experiments conducted with stable iodine may measure a different variable to that measured in radio-iodine experiments.     

Reduction of iodate in seawater during Arabian Sea shipboard incubations and in laboratory cultures of the marine bacterium Shewanella putrefaciens strain MR-4

Shipboard incubations from the US JGOFS cruise to the Arabian Sea (TN045) March, 1995 showed evidence of iodate reduction in 0.45 μ (Gelman Supor membrane) filtered seawater samples collected from intermediate depths (200–600 m) within the oxygen minimum zone (OMZ). Inorganic chemical reduction of iodate in these samples was ruled out as no free sulfide was measurable and concentrations of ammonia and nitrite were found to be less than 5 μM. To examine whether the reduction of iodate observed at sea could have been the result of bacterial metabolism, reduction of iodate (IO₃⁻) to iodide (I⁻) by Shewanella putrefaciens strain MR-4 was studied in artificial seawater using electrochemical methods. MR-4 is a ubiquitous marine bacterium which may be of considerable importance when considering redox zonation in the water column because it is a facultative anaerobe and may switch amongst a suite of electron acceptors to support metabolism. In all experiments MR-4 reduced all iodate to iodide. The rate of formation of [I⁻]in the culture followed pseudo-first order kinetics. This is the first report of the marine bacterial reduction of iodate where the concentrations of iodide and iodate were measured directly. Our results may help to explain the depth distribution of iodine speciation reported in productive waters like the Arabian Sea and for the first time couple iodine speciation with bacterial productivity in the ocean.     

Sources and distribution of fresh water in the East Greenland Current

Fresh water flowing from the Arctic Ocean via the East Greenland Current influences deep water formation in the Nordic Seas as well as the salinity of the surface and deep waters flowing from there. This fresh water has three sources: Pacific water (relatively fresh cf. Atlantic water), river runoff, and sea ice meltwater. To determine the relative amounts of the three sources of fresh water, in May 2002 we collected water samples across the East Greenland Current in sections from 81.5°N to the Irminger Sea south of Denmark Strait. We used nitrate-phosphate relationships to distinguish Pacific waters from Atlantic waters, salinity to obtain the sum of sea ice melt water and river runoff water, and total alkalinity to distinguish the latter. River runoff contributed the largest part of the total fresh water component, in some regions with some inventories exceeding 12 m. Pacific fresh water (Pacific source water S ∼ 32 cf. Atlantic source water S ∼ 34.9) typically provided about 1/3 of the river runoff contribution. Sea ice meltwater was very nearly non-existent in the surface waters of all sections, likely at least in part as a result of the samples being collected before the onset of the melt season. The fresh water from the Arctic Ocean was strongly confined to near the Greenland coast. We thus conjecture that the main source of fresh water from the Arctic Ocean most strongly impacting deep convection in the Nordic Seas would be sea ice as opposed to fresh water in the liquid phase, i.e., river runoff, Pacific fresh water, and sea ice meltwater.     

Dissolved Iodate and Total Iodine During an Extreme Hypoxic Event in the Southern Benguela System

Dissolved iodate and total iodine were studied in St Helena Bay, South Africa, during a period of acute hypoxia, following upwelling off Cape Columbine. Despite the generally high concentrations of chlorophyll α (10–30 mg m⁻³) total iodine concentration was essentially constant in the main part of the Bay, and similar to that found elsewhere in the oceans. Occasional, lower concentrations of total iodine (0·28 to 0·42 μM) were found with exceptionally high chlorophyll α concentrations (500 mg m⁻³) in shallow waters. In contrast, iodate was found to be reduced to iodide at both the surface and the bottom of the Bay. The implications of these changes are discussed, given that the surface waters reflect sustained eutrophication while the bottom waters are hypoxic as a result of the organic-rich sediment from the waters above.     

Physical and anthropogenic effects on observed long-term nutrient changes in the Irish Sea

The trend in Irish Sea nutrient concentrations over the last four decades has been considered to reflect changes in anthropogenic loading. Comparison of a long-term database for the Menai Strait, North Wales, with an established historic data set for the Cypris station, Isle of Man, indicates that climate also has a significant influence on observations of nutrient concentrations. Data are presented detailing long-term shifts in nitrate, phosphate and silicate measurements since the 1960s at these two fixed sampling sites in the Irish Sea. Broad systematic changes observed in all three nutrients over the decades show a rise from the 1960s through to the 1980s, followed generally by an overall decline in the 1990s. Decadal-scale salinity changes occur in the opposite sense to nutrient changes. Anthropogenic inputs from freshwater cannot fully account for observed nutrient trends, neither is there evidence for shifts in nutrient concentrations in oceanic waters over the past four decades. Climatically forced movement in the geographical position of the freshwater/seawater mixing zone over a decadal time scale could, however, give rise to the observed shifts in nutrient concentration and salinity. This cannot alter nutrient concentration and salinity per se, but causes the measurements taken at fixed sampling sites to fluctuate inversely over this time scale. It is concluded that there is complex interplay between anthropogenic loading and climate affecting the distribution of nutrients in the Irish Sea.     

北太平洋西部和印度洋东部及其邻近海域表层水体中137Cs的分布

对北太平洋西部海域、苏禄海及印尼海、中国南海、印度洋东部海域、孟加拉湾及安达曼海等表层水体中放射性核素137Cs的活度进行了测定。结果表明,上述海域表层水体中137Cs活度显示了较大的变化范围,最低值出现在南极附近的南大洋(1.1Bqm-3),较高的活度值则出现在北太平洋西部海域及中国南海(3Bqm-3)。在所研究水域范围内,137Cs活度的纬度分布特征并没有完全有效地反映出137Cs的全球理论大气沉降趋势及其纬度效应。综合本研究及Miyake等人(1988)的测定结果,我们计算出137Cs自表层海水中的析出速率在苏禄海及印尼海约为0.016/a,在孟加拉湾及安达曼海约为0.033/a,在中国南海约为0.029/a,这一结果明显低于西北太平洋日本沿海表层水体中137Cs的析出速率。这可能是因为在这些海域,横向及纵向的水体混合过程相对都较慢,而且颗粒物对137Cs的吸附析出过程也比较弱所致。     

Water transport from the North-east Irish Sea to western Scottish coastal waters: Further observations from time-trend matching of Sellafield radiocaesium

Radiocaesium isotopes, discharged into the North-east Irish Sea from the Sellafield (formerly Windscale) nuclear fuel reprocessing plant in Cumbria, have been employed as flow monitors to update and extend the record of coastal water movement from the Irish Sea to the Clyde Sea area and, further north, to Loch Etive. The temporal trends in radiocaesium levels have been used to determine the extent of water mixing en route and to define mean advection rates. Flow conditions from the Irish Sea have changed considerably since the mid-1970s, the residence time of northern Irish Sea waters being ～12 months during 1978–1980 inclusive. Average transport times of four and six months are estimated for the Sellafield to Clyde and Sellafield to Etive transects respectively. Sellafield ¹³⁷Cs levels in seawater were diluted by factors of 27 and 50 respectively during current movement to the Clyde and Etive areas. The decrease in salinity-corrected ¹³⁷Cs concentrations between the Clyde and Etive suggests that dilution by Atlantic water occurs, the latter mainly entering the Firth of Lorne from the west. The majority (～94%) of the radiocaesium supply to Loch Etive enters the Firth of Lorne via the portion of the coastal current circulating west of Islay, only ～6% arriving via the Sound of Jura.     

The distribution of iodide and iodate in anchialine cave waters — Evidence for sustained localised oxidation of iodide to iodate in marine water

A study of inorganic iodine speciation in the waters of seven Croatian coastal caves is described. These are anchialine caves as they are connected hydraulically with Adriatic Sea surface water, with the tide inside the cave rising and falling with that outside, but replenishment of the water is restricted by the karst rock. In effect, the water in the cave probably acts more like a piston, and although moving slightly vertically, has a long residence time compared to a fully-flushing cave. Anchialine environments display a number of unusual features, e.g., a well-developed pycnocline, hypoxia and endemic fauna. Iodate and iodide were determined by differential pulse voltammetry and cathodic stripping square wave voltammetry, respectively. Low iodide concentrations (< 10 nM) have been consistently identified in the bottom water of the caves where concentrations of 90–100 nM would ordinarily be expected from intrusion of Eastern Adriatic surface seawater. Where total inorganic iodine concentrations behave conservatively with salinity the loss of the iodide implies oxidation to iodate. As iodide oxidation remains one of the enduring academic problems of the marine iodine system the study of iodine in anchialine caves may help unravel it. Iodate reduction was observed in mid-water, at the halocline, and mechanisms for the reduction involving either respiration or chemolitho-autotrophic bacteria are considered. The respiration mechanism is favoured because of enhanced alkalinity found in the near surface waters of the caves.     

Seasonal variation of water temperature in the Seto Inland Sea

The seasonal variation of water temperature in the Seto Inland Sea, Japan is examined using data analysis and numerical experiments and is shown to be controlled by heat exchange through the sea surface and horizontal heat dispersion from the Pacific Ocean. The average water temperature goes down from the Pacific Ocean to the center of the Seto Inland Sea indicating that 4.0 to 6.0×10¹⁵ cal day^?1 (1.6 to 2.5×10¹⁶ joule day^?1) of heat is transported from the Pacific Ocean to the Seto Inland Sea and is lost through the sea surface. The amplitude of seasonal variation of water temperature is large at the center of the Seto Inland Sea and the maximum water temperature is reached first at Bisan Straits and last at Iyo-Nada.     

The Irish Sea: Is it eutrophic?

The question of whether the Irish Sea is eutrophic is addressed by reviewing the evidence for anthropogenic nutrient enrichment, elevated phytoplankton production and biomass and undesirable disturbance in the context of the EU and OSPAR definitions of eutrophication. Winter concentrations of dissolved available inorganic phosphate (DAIP), nitrogen (DAIN as nitrate and nitrite) and silicate (Si) in coastal waters and concentrations of DAIP and Si in offshore waters of the Irish Sea are elevated relative to winter Celtic Sea shelf break concentrations (0.5 μM DAIP, 7.7 μM DAIN and 2.7 μM Si). Significant, negative nutrient salinity relationships and analysis of the Isle of Man nutrient time-series indicate that the elevated Irish Sea levels of DAIP and DAIN are the result of anthropogenic enrichment with highest concentrations (≈2.0 μM DAIP, 30 μM DAIN and 17 μM Si) measured in near shore eastern Irish Sea waters.     

Marine geochemistry of cadmium

A detailed study of particulate and dissolved cadmium distributions on 83 seawater samples from six profiles in the open North Atlantic Ocean showed a relatively homogenous distribution. The mean concentration of cadmium was 60 ± 27 ng/kg and the median concentration of particulate cadmium was 0.2 ng/kg. Although there are regional differences in dissolved cadmium concentrations among stations, it is suggested that cadmium behaves essentially as an inert element in sea water.Particulate cadmium is enriched by about a factor of four in samples from less than 400 m compared to samples from deeper than 1000 m. The high concentrations in surface waters are suggested to be due to aeolian transport of anthropogenically derived cadmium.Additional analyses of cadmium in the Gulf of Maine show a mean value of 230 ng/kg. The higher values in the Gulf of Maine are ascribed to the influence of continental runoff. Twelve sediment samples from the open North Atlantic show a relatively homogenous distribution, ranging from 0.13 to 0.21 ppm on a dry-weight basis.     

全球热带海洋海表温度场异常对北极海冰的影响

本文利用1951?2021年哈德莱中心提供的海冰和海温最新资料以及美国国家海洋和大气管理局气候预报中心提供的NCEP/NCAR再分析资料,分析探讨了北极海冰70余年的长期变化特征,进而研究了其快速减少与热带海温场异常变化之间的联系,揭示了在全球热带海洋海温场变化与北极海冰之间存在密切联系的事实。结果表明,北极海冰异常变化最显著区域出现在格陵兰海、卡拉海和巴伦支海。热带不同海区对北极海冰的影响存在明显时滞时间和强度差异,热带大西洋的影响相比偏早,印度洋次之,太平洋偏晚。热带大西洋、印度洋和中东太平洋海温异常影响北极海冰的最佳时间分别是后者滞后26个月、30个月和34个月,全球热带海洋影响北极海冰的时滞时间为33个月。印度洋SST对北极海冰的影响程度最强,其次是太平洋,最弱是大西洋。全球热带海洋对北极海冰的影响过程中,热带东太平洋和印度洋起主导作用。当全球热带海洋SST出现正（负）距平时,北极海冰会出现偏少（多）的趋势,而AO、PNA、NAO对北极海冰变化起重要作用,是热带海洋与北极海冰相系数的重要“纽带”。而AO、PNA和NAO不仅受热带海洋SST的影响,同时也受太平洋年代际振荡PDO和大西洋多年代际AMO的影响,这一研究为未来北极海冰快速减少和全球气候变暖机理的深入研究提供理论支撑。     

The biogeochemistry of major elements of the suspended particulate matter of the Cretan Sea

The biogeochemistry of the following elements Al, Fe, Si_bio, POC, PN_tot, Ca_bio, S_org, P and Mn has been studied within waters of the Cretan Sea in March and September 1994, as part of the PELAGOS project. Particulate aluminosilicate concentrations, exemplified by Al, are very low (<1 μgl⁻¹) especially in the upper waters. Higher concentrations occur below 200 m, especially at depths of 200 m and 500–700 m in the central and eastern areas, and are thought to result from sediment injections from the shelf edge and slope. The results for Si_bio, Ca_bio, P and S_org show much higher concentrations within the photic waters. Temporal and spatial high concentrations in these waters closely relate to the existence of cyclonic eddies on the east and west sides of the sea, while low concentrations are associated with an intervening anticyclonic eddy. However in September, discharge of Black Sea Water in the west sufficiently suppresses the thermocline to prevent upwelled water from reaching the surface and hence these substances are prevented from forming.Particulate Fe (expressed as Fe_excess) concentrations show much higher concentrations relative to Al in September, and are thought to result from additional atmospheric inputs. The low particulate Mn concentrations in the upper water compared with deeper waters are considered to be a product of photoinhibition of MnO_x precipitation from Mn(II).An attempt has been made to assess input/output budgets of Al, Ca, Fe and Mn through the Antikithira and Kassos Straits. Much of the outflows leave through the Kassos Strait and, except for Ca, net outflows through the Antikithira Straits are negligible.