Sediment–seawater solute flux in a polluted New Zealand estuary

We investigated the sediment–seawater solute flux at five sites in the polluted Avon–Heathcote Estuary, New Zealand, to provide a point of comparison for future studies of the effects of the closure of a major wastewater outfall into the estuary. Sediments collected in winters 2007 and 2008, and summer 2008, ranked consistently in organic matter content. Microelectrode profiling and sediment-core incubations revealed (1) a dominant role of microphytes in regulating solute flux causing significant differences in the dark and light sediment O₂ consumption (R_d, R_l), total sediment O₂ utilisation (TOU_d, TOU_l), and inorganic nutrient flux, (2) consistent ranking of sites in solute flux, and (3) a clear solute-flux signature of the wastewater effluent. Sediment near the wastewater outfall exhibited the highest absolute R and TOU_, the lowest ratio R_l/R_d, the highest dark efflux of dissolved reactive phosphorus and ammonium, and the highest dark and light uptake of nitrate + nitrite.     

Hg bioaccumulation in marine copepods around hydrothermal vents and the adjacent marine environment in northeastern Taiwan

The Hg concentration in seawater and copepod samples collected from the area around hydrothermal vents at Kueishan Island and the adjacent marine environment in northeastern Taiwan were analyzed to study Hg bioaccumulation in copepods living in polluted and clean marine environments. The seawater collected from the hydrothermal vent area had an extremely high concentration of dissolved Hg, 50.6–256 ng l⁻¹. There was slightly higher Hg content in the copepods, 0.08–0.88 μg g⁻¹. The dissolved Hg concentration in the hydrothermal vent seawater was two to three orders of magnitude higher than that in the adjacent environment. The bioconcentration factor of the studied copepods ranged within 10³–10⁶, and showed higher dissolved concentration as the bioconcentration factor was lower. A substantial abundance, but with less copepod diversity was recorded in the seawater around the hydrothermal vent area. Temora turbinata was the species of opportunity under the hydrothermal vent influence.     

Hafnium and neodymium isotopes in seawater and in ferromanganese crusts: The “element perspective”

Hafnium and Nd isotopes are increasingly used as paleoceanographic proxies. Comparing the “mantle–crust array” and the “seawater array” in plots of ε_Hf vs. ε_Nd, it has been observed that for a given ε_Nd value the corresponding ε_Hf value is higher for seawater than it is for terrestrial rocks. While this difference had initially been explained by significant hydrothermal input of mantle Hf into seawater, the currently favoured explanation is incongruent weathering of continental rocks producing radiogenic riverine Hf input.We here address this topic from the perspective of the behaviour of these two elements in seawater and in ferromanganese (Fe–Mn) crusts. We distinguish between a “truly dissolved” and a “dissolved” Hf and Nd pool, the latter being comprised of truly dissolved and colloid-bound (“colloidal”) Hf and Nd. While there exists a hydrothermal pathway for colloid-bound dissolved mantle Hf into the oceans, there is, in marked contrast to Nd, no important riverine pathway for colloidal or truly dissolved continental Hf. Owing to their respective chemical speciation in seawater, there exists truly dissolved Nd in the ocean, while the amount of truly dissolved Hf is insignificant.Neodymium is in exchange equilibrium between local seawater and both, the hydrous Fe and Mn oxides hydrogenetic Fe–Mn crusts are composed of. Due to continuous ad- and desorption there is continuous isotopic re-equilibration and the isotopic composition of Nd in a Fe–Mn crust reflects that of truly dissolved Nd in local ambient seawater. In contrast, Hf is only associated with the hydrous Fe oxides on which it forms surface precipitates that do not exchange with seawater. Due to this lack of isotopic re-equilibration, the isotopic composition of Hf in a Fe–Mn crust is the average of that of all the Hf scavenged during the lifetime of the hydrous Fe oxide particles. Since the Hf-bearing hydrous Fe oxides in a Fe–Mn crust do not form from local ambient seawater at the crust's growth site but are advected as colloids or fine particles, their Hf isotopic composition depends on the origin and migration pathway of these colloids. Hence, while Nd isotopes in Fe–Mn crusts provide reliable information on truly dissolved Nd in local ambient seawater, Hf isotopes rather indicate the origin and pathway of hydrous Fe oxide colloids, and might differ from truly dissolved Hf in local ambient seawater. This may explain the occasional decoupling of Nd and Hf isotopes in Fe–Mn crusts and supports the notion of a significant hydrothermal mantle signal of Hf in seawater.     

Acute toxicity of copper to sea catfish

Sea catfish (Arius felis) were exposed to aqueous solutions of reagent grade cupric chloride in artificial seawater ($\text{30.0±2.0‰}$, 21–23°C) in four static bioassays. The 24, 48, 72 and 96 h LC₅₀ were calculated and found to be 5.43, 4.17, 3.57 and 2.40 mg l.^?1 copper, respectively. Experimental concentrations of copper producing subtle behavioral changes in this species correspond to less than 0.3% of the 72 h LC₅₀. Based on this comparison with literature values, a new, maximum ‘safe’ concentration for copper in marine waters of 0.01 mg l.^?1 is proposed.     

The coagulation of dissolved239, 240Pu in estuaries as determined from a mixing experiment

A mixing experiment, using large volumes (100 l) of filtered (< 1 μm) freshwater and seawater end-members, was performed to simulate and investigate the chemical reactivity of^{239, 240}Pu during estuarine mixing. An organic-rich freshwater with a relatively high concentration (0.8 dpm/100 l) of dissolved^{239, 240}Pu was used as one end-member; Buzzards Bay seawater (dissolved^{239, 240}Pu= 0.04dpm/100l) was the other. The results demonstrate that dissolved^{239, 240}Pu in the freshwater undergoes extensive and rapid coagulation under simulated estuarine conditions. There is a strong correlation between the amount of coagulation of dissolved^{239, 240}Pu, humic acids (HA), and Fe. The extent of coagulation of all three constituents increases with increasing salinity and the net extent of their removal is 53%, 57%, and 100% for Pu, HA, and Fe respectively. As has been documented for Fe in freshwater, dissolved^{239, 240}Pu appears to be stabilized by naturally occurring humic substances to form negatively charged colloids which are then coagulated by seawater cations. The extrapolation of these experimental results to real estuaries will require additional research.     

Interaction of Aquatic Dissolved Organic Matter(DOM) with Amitrole: The Nature of the Bound Residues

In this study the binding behaviour of the herbicide amitrole with humic substances respectively dissolved organic matter (DOM) is presented. The results of the binding and release experiments using radio actively ¹⁴C-labelled amitrole ledto the conclusion that the binding of amitrole is very low. About 70% of amitrole bound to humic substances was not extractable. The releasable amitrole portion of the purified DOM-amitrolecomplexes led to a harmful effect in the cress test. Solid-state cross polarisation (CP) magic angle spinning (MAS) ¹⁵N-NMR spectroscopy is a powerful spectroscopic method to elucidate the structure of bound xenobiotics. In addition extraction experiments were used resulting in a binding scheme of amitrole to DOM, where above all the covalent bonding occurred via acid amide bonds.     

Comparison of marine and river water humic substances in a Patagonian environment (Argentina)

Structural aspects of humic substances (HSs) in marine waters of Engaño Bay (Atlantic Ocean) and water from the Chubut River (Patagonia, Argentina) were compared. The HSs were isolated, purified, and analyzed using a multiple-method approach for structural characterization: elemental analysis, nuclear magnetic resonance (¹³C and ¹H NMR), infrared spectroscopy (FTIR), UV-visible absorption and fluorescence. Similarities between the marine and freshwater components were evaluated on the basis of N and O contents, H/C and C/N atomic ratios, infrared bands from nitrogen-containing and carboxylic groups, percentage of functional groups obtained from NMR spectra, spectral slope coefficient of absorption spectra, absorbance ratios at 250 and 365 nm (E ₂/E ₃), aromaticity, excitation–emission matrices and fluorescence quantum yield. Both the Engaño Bay and Chubut River waters have HSs that are mainly composed of fulvic acids (FAs); although they are very similar, they may be distinguished from one another. Similarities include the predominance of aliphatic carbon content (low aromatic content); however, the water bodies differed in their content of proteins and carboxylic acids. The Engaño Bay FAs have mainly an aquatic origin; although the Chubut River FAs suggest a similar aquagenic origin, there is also evidence of contributions from pedogenic FAs.     

Stable and radiogenic isotopes as tracers for the origin,mixing and subsurface history of fluids in submarine shallow-water hydrothermal systems

The shallow-water hydrothermal system in Tutum Bay on the west side of Ambitle Island, Papua New Guinea provides us with an exceptional opportunity to study isotope systematics in a near shore setting. Compared to seawater, the hydrothermal fluids in Tutum Bay have lower values for δD, δ¹⁸O, δ¹³C, and ⁸⁷Sr and higher values for ³H, δ³⁴S(SO₄) and δ¹⁸O(SO₄). The δ¹⁸O and δD records for vents 1 and 4 indicate that fluid compositions remained stable over an extended period. Interpretation of isotope data clearly demonstrates the predominantly meteoric origin of Tutum Bay hydrothermal fluids, despite their location in a marine environment. δ¹⁸O and δD values are identical to mean average annual precipitation in eastern Papua New Guinea. The hypothesis that these fluids are a simple product of mixing between seawater and onshore hydrothermal fluids from the Waramung (W-1) and Kapkai (W-2) thermal areas has been rejected, because the observed δ³⁷Cl, ³H, δ³⁴S(SO₄) and δ¹⁸O(SO₄) values cannot be explained by a simple mixing model. The application of δ¹⁸O(SO₄) and δ¹³C thermometers in combination with ³H values corroborates the three-step model of Pichler et al. [Pichler, T., Veizer, J., Hall, G.E.M., 1999. The chemical composition of shallow-water hydrothermal fluids in Tutum Bay, Ambitle Island, Papua New Guinea and their effect on ambient seawater. Marine Chemistry 64 (3) 229–252], where (1) phase separation in the deep reservoir beneath Ambitle Island produces a high temperature vapor that rises upward and subsequently reacts with cooler ground water to form a low pH, CO₂-rich water of approximately 150–160 °C, (2) caused by the steep topography, this CO₂-rich fluid moves laterally towards the margin of the hydrothermal system where it mixes with the marginal upflow of the deep reservoir fluid. This produces a dilute chloride water of approximately 165 °C, and (3) possibly the entrainment of minor amounts of ground or seawater during its final ascent.     

Partial pressure and air–sea CO2 flux in the Aegean Sea during February 2006

Data on the distribution of fCO₂ were obtained during a cruise in the Aegean Sea during February 2006. The fCO₂ of surface water (fCO₂^sw) was lower than the atmospheric fCO₂ (fCO₂^atm) throughout the area surveyed and ΔfCO₂ values varied from ?34 to ?61 μatm. The observed under-saturation suggests that surface waters in the Aegean represent a sink for atmospheric CO₂ during the winter of 2006. Higher fCO₂^sw values were recorded in the ‘less warm’ and ‘less saline’ shallow northernmost part of the Aegean Sea implying that the lower seawater temperature and salinity in this area play a crucial role in the spatial distribution of fCO₂^sw.A first estimate of the magnitude of the air–sea CO₂ exchange and the potential role of the Aegean Sea in the transfer of atmospheric CO₂ was also obtained. The air–sea CO₂ fluxes calculated using different gas transfer formulations showed that during February 2006, the Aegean Sea absorbs atmospheric CO₂ at a rate ranging from ?6.2 to ?11.8 mmol m^?2 d^?1 with the shipboard recorded wind speeds and at almost half rate (?3.5 to ?5.5 mmol m^?2 d^?1) with the monthly mean model-derived wind speed. Compared to recent observations from other temperate continental shelves during winter period, the Aegean Sea acts as a moderate to rather strong sink for atmospheric CO₂.Further investigations, including intensive spatial and temporal high-resolution observations, are necessary to elucidate the role of the Aegean Sea in the process of transfer of atmospheric CO₂ into the deep horizons of the Eastern Mediterranean.     

Correlations between13C and ΣCO2 in surface waters and atmospheric CO2

¹³C and ΣCO₂ data from the North and South Atlantic, the Antarctic, and the North and South Pacific are given. The δ¹³C of the ΣCO₂ in the deep water (～3000m) decreases from 1.7‰ in the North Atlantic to ?0.10‰ in the North Pacific. This change is attributed to the addition of about 158 μmoles of CO₂ per kg of seawater. The in-situ oxidation of organic matter accounts for 83% of this increase in ΣCO₂, while the remainder is attributed to dissolution of calcium carbonate.The δ¹³C of the dissolved CO₂ in mid-latitude surface water samples is controlled by a quasi-steady-state equilibrium with atmospheric CO₂ at a mean temperature of 16°C. The δ¹³C and ΣCO₂ values of Antarctic surface water samples suggest that these waters are derived from a mixture of North Atlantic deep water and equilibrated surface water.     

针铁矿对湖泊草、藻来源可溶有机质的非均质吸附

为探究富营养化湖泊中自生源可溶有机质(DOM)在泥水界面的吸附行为,以马来眼子菜(Potamogeton malaianus)和铜绿微囊藻(Microcystis aeruginosa)释放的DOM为代表,考察针铁矿对草、藻源DOM中不同组分的吸附特征.三维荧光平行因子分析表明类富里酸组分C1和类胡敏酸组分C4的含量很低,而类蛋白物质(类酪氨酸组分C2和类色氨酸组分C3)分别占草、藻源DOM荧光组成的70%和93%. 2种DOM均可被针铁矿吸附,吸附过程符合伪一级动力学.通过等温线拟合发现针铁矿吸附藻源DOM的非线性更强,饱和吸附量(23.77 mg/g)高于草源DOM(19.10 mg/g).特别地,类蛋白组分呈现非线性吸附,而类腐殖物质的吸附近似线性,且针铁矿对于DOM各荧光组分的吸附量顺序为:C3C2 C4 C1,此非均质吸附特征与DOM组分的初始含量、分子大小、芳香性及有效吸附位点有关.红外光谱证实氨基、羧基和羟基是吸附过程中的重要官能团.因此,草、藻源DOM显著改变了针铁矿表面的有机物质组成,影响湖泊沉积物的生物地球化学行为.     

Importance of aquatic macrophyte for invertebrate diversity in large subtropical reservoir

The abundance and preferences of individual invertebrate populations (including zooplankton) closely associated with the substrates provided by aquatic plant structures and open-water areas of Lake Nasser were quantified in this study in order to gain understanding of the importance of submerged macrophyte for invertebrate diversity, and their relation to water properties. The following water parameters were measured: temperature, pH, dissolved oxygen (DO), total dissolved salts, electrical conductivity, turbidity, total suspended solids, carbonate, bicarbonate, nitrate, nitrite, phosphate, sulphate, silica, potassium, total hardness, calcium and magnesium.Five macrophyte species were recorded: Myriopyllum spicatum, Najas horrida, Potamogeton schweinfurthii, Potamogeton pectinatus and Vallisneria spiralis. In total 67 invertebrate species were recorded, comprising 39 Rotifera, 12 Cladocera, 4 Copepoda, 4 Insecta, 2 Protozoa, 2 Ostracoda and one species of Turbellaria, Tardigrada, Annelida and Nematoda. Thirty-seven species were exclusively epiphytic, 11 species were collectively planktonic and 19 species were found in both habitats. The greatest abundance of epiphytic invertebrates occurred in association with N. horrida-P. schweinfurthii community.The results indicated that total suspended solids (TSS), TH and NO₂ are the most influential water variables on the distribution of the aquatic macrophyte samples and their invertebrate communities. Also, the study indicates that water variables have a higher impact on the aquatic macrophytes than on the associated invertebrate populations. P, NO₃, K, Na, Mg, Cl and DO were the most influential water variables that dictate the distribution of invertebrate groups recorded in the open-water zone. Water temperature, electric conductivity, pH, NO₂, SO₄⁻⁻, SiO₃⁻, CO₃⁻⁻ and turbidity have a lesser influence of the distribution of the invertebrates recorded in this zone.     

Optimization of nutrient component for diesel oil degradation by Rhodococcus erythropolis

A novel bacterium T7-2 was isolated from the oil-polluted sea-bed mud of Bohai Sea, northern China, which can degrade diesel oil at 15 °C. This bacterium was identified as a strain of Rhodococcus erythropolis according to its 16S rDNA gene. In order to enhance degradation efficiency, a five-level, three-factor central composite design was employed to optimize the nutrition supplied to artificial seawater. The results indicate that a supplement of 2.53 g (NH₄)₂SO₄ L⁻¹, 2.75 g Na₂HPO₄ L⁻¹ and 0.01 g yeast extract L⁻¹ to artificial seawater increases the degradation rate from 12.61% to 75% within 7 d.     

High resolution profiles for arsenic in the Seine Estuary. Seasonal variations and net fluxes to the English Channel

Three sampling cruises were conducted in the Seine Estuary from 1993 to 1995 in varying hydrological and seasonal conditions. The site included all of the lower part of the river under the influence of tidal dynamics and the dilution plume in the Baie de Seine. Chemical speciation of arsenic showed high seasonal variations, especially in September when AsIII represented around 50% of dissolved arsenic. The inclusion of organoarsenic compounds not accessible to direct analysis by hydride generation required preliminary mineralisation of the samples. The ratio of dissolved to particulate arsenic distribution was controlled mainly by the iron content of particles. Biological activity had an influence on chemical speciation and thus on the partition coefficient (K_D 10⁻³=6±1 in September and 12±0.9 in February). The zone of conservative mixing used for Seine River flow calculations was limited to a salinity range of approximately 10–30. Dissolved arsenic concentrations extrapolated to null salinities were lower during the high-water period because of dilution (17.6±1.1 nM), and maximal during the low-water period in summer (35.7±0.9 nM). Mean arsenic export to the English Channel was estimated at 33.2±6 T yr⁻¹ for dissolved arsenic. Observation of an arsenic output greater than the upstream input, as well as a simultaneous increase in dissolved and particulate arsenic concentrations during the mixing of freshwater with seawater, strongly suggested the existence of an important intra-estuarine source of arsenic, either of industrial origin or related to the transport and diagenesis of marine sediments.     

Century-long record of Mo isotopic composition in sediments of a seasonally anoxic estuary (Chesapeake Bay)

A double-spike method was used to obtain Mo isotope data for sediments and waters of the seasonally anoxic Chesapeake Bay, and its primary tributary, the Susquehanna River. The dissolved Mo distribution in the estuary is non-conservative, reflecting minor Mo loss to the sediments, although removal of Mo to the sediments does not have a large influence on the isotopic composition of the water column. The δ⁹⁸Mo of dissolved Mo in most of the estuary is dominated by seawater. Six samples with salinity > 15 have an average δ⁹⁸Mo = + 2.17‰ (± 0.12), which agrees well with a δ⁹⁸Mo value for the CASS-4 seawater standard of + 2.23‰. A single sample of Susquehanna River water has a δ⁹⁸Mo of + 1.02‰, consistent with recent findings of positive δ⁹⁸Mo in rivers worldwide. Susquehanna river sediments, in contrast, have δ⁹⁸Mo ～ ? 0.1‰. The difference between the river water and sediment values implies that isotopic fractionation occurs within the river basin. The δ⁹⁸Mo values for estuarine sediments are offset from values in the overlying water. Most samples deposited before 1925 have δ⁹⁸Mo less than 0‰, similar to the Susquehanna sediments. Subsequently, there is an increase in the variability of δ⁹⁸Mo, with values ranging up to + 0.8‰. The transition to increased variability coincides with the onset of authigenic Mo deposition, which was previously attributed to escalating summertime anoxia. Authigenic Mo concentrations correlate poorly with δ⁹⁸Mo in core samples, suggesting that independent mechanisms influence the two parameters. Authigenic Mo concentrations may be controlled by shifting pore water H₂S levels, while δ⁹⁸Mo may be primarily affected by annual variations in Mn refluxing.     

Rates of dissolution of aluminosilicates in seawater

Dissolution of eight clay minerals, four zeolites, and quartz in seawater has been monitored for81/2 years. For most of the minerals, dissolution can be described as a first-order reaction in which dissolved silica approaches from undersaturation steady concentration values with time. Characteristic reaction rate constants (k₁) are of the order of 10^?7 sec^?1. One of the zeolites, clinoptilolite, shows a different dissolution behavior: SiO₂ concentration in solution reaches a high value within one year, followed by a decline to a lower value, suggestive of precipitation of another silicate phase (possibly sepiolite).A mathematical solution is given for a kinetic equation combining the parabolic-rate and first-order rate processes. It is shown that in a wide range of silicate dissolution reactions taking place over long periods of time, the presence of the parabolic-rate dissolution processes cannot be detected, thereby making its inclusion in the kinetic equations unnecessary. The experimental rates of dissolution are comparable to the SiO₂^? dissolution rates in oceanic sediments near the sediment/water interface. But deeper in the sediment, the calculated dissolution rates are significantly lower than the near-interface and experimental values.     

Neodymium isotopic variations in seawater

New data for the direct measurement of the isotopic composition of neodymium in Atlantic Ocean seawater are compared with previous measurements of Pacific Ocean seawater and ferromanganese sediments from major ocean basins. Data for Atlantic seawater are in excellent agreement with Nd isotopic measurements made on Atlantic ferromanganese sediments and are distinctly different from the observed compositions of Pacific samples. These results clearly demonstrate the existence of distinctive differences in the isotopic composition of Nd in the waters of the major ocean basins and are characteristic of the ocean basin sampled. The average ε_Nd(0) values for the major oceans as determined by data from seawater and ferromanganese sediments are as follows: Atlantic Ocean,ε_Nd(0) ? ?12 ± 2; Indian Ocean,ε_Nd(0) ? ?8 ± 2; Pacific Ocean,ε_Nd(0) ? ?3 ± 2. These values are considerably less than ε_Nd(0) value sources with oceanic mantle affinities indicating that the REE in the oceans are dominated by continental sources. The difference in the absolute abundance of¹⁴³Nd between the Pacific and Atlantic Oceans corresponds to ～10⁶ atoms¹⁴³Nd per gram of seawater. The correspondence between the¹⁴³Nd/¹⁴⁴Nd in seawater and in the associated sediments suggests the possible application of this approach to paleo-oceanography.Distinctive differences in ε_Nd(0) values are observed in the Atlantic Ocean between deep-ocean water associated with North Atlantic Deep Water and near-surface water. This suggests that North Atlantic Deep Water may be relatively well mixed with respect to Nd isotopic composition whereas near-surface water may be quite heterogeneous, reflecting different sources for surface waters relative to deep water. This suggests that it may be possible to distinguish the sources of water masses within an ocean basin on the basis of Nd isotopic composition.The Nd isotopic variations in seawater are used to relate the residence time of Nd and mixing rates between the oceans.     

Dissolved Carbohydrate Concentration,Composition, and Bioavailability to Microbial Heterotrophs in Stream Water

Dissolved total carbohydrates (DTCH), dissolved free monosaccharides (DFMS), dissolved organic carbon (DOC), biodegradable DOC (BDOC), and humic substances (HS) were measured in White Clay Creek (WCC), a stream in southeastern Pennsylvania Piedmont, USA. Samples were collected over different seasons and under baseflow and stormflow conditions. DOC concentrations ranged from 1.0 to 12.8 mg/L C with the highest concentrations associated with stormflows. Carbohydrates ranged from 0.42 to 12.4 μM and accounted for 2.9 to 12.7% of the DOC. Humic substances represented the major DOC fraction, accounting for 55 to 72% of the DOC pool under all flow conditions. The humic fraction had a lower carbohydrate content (4.4%) than the non-humic fraction of DOC (7.2%). Stormflow DOC was enriched in carbohydrates relative to baseflow DOC, but the percentage of humic-C changed little. Carbohydrates were primarily present as dissolved polysaccharides (55%), but a significant fraction was bound to humic substances (40%), while a small proportion was present as monosaccharides (5%). The major monosaccharides in stream water, listed in order of decreasing concentration, included glucose, galactose, rhamnose, xylose, arabinose, mannose, and fucose. On average (30.6 ± 7.4)% (n = 44) of the stream water DOC was biodegradable, and carbohydrates accounted for 9.9 to 17.7% of the BDOC.     

The hydrothermal system of Mendeleev Volcano,Kunashir Island,Kuril Islands: The geochemistry and the transport of magmatic components

This paper reports a detailed geochemical study of thermal occurrences as observed in the edifice and on the flanks of Mendeleev Volcano, Kunashir Island in August and September 2015. We showed that three main types of thermal water are discharged there (neutral chloride sodium, acid chloride sulfate, and acid sulfate types); these waters exhibit a zonality that is typical of volcano-hydrothermal island arc systems. Spontaneous and solfataric gases have relatively low ³He/⁴He ratios, ranging between 5.4Ra and 5.6Ra, and δ¹³C-CO₂ between –4.8‰ and –3.1‰, and contain a light isotope of carbon in methane (δ¹³C ≈ –40‰). Gas and isotope geothermometers yield relatively low temperatures around 200°C. The isotope compositions in all types of water are similar to that of local meteoric water. The distribution of microcomponents varies among different types. The isotope composition of dissolved Sr varies considerably, from 0.7034 as observed in Kunashir rocks on an average to 0.7052 in coastal springs, which may have resulted from admixtures of seawater. The total hydrothermal transport rates of magmatic Cl and SO₄, as observed for Mendeleev Volcano, are 7.8 t/d and 11.6 t/d, respectively. The natural outward transport of heat by the volcano’s hydrothermal system is estimated as 21 MW.