Photochemical production of hydrogen peroxide in Antarctic Waters

Photochemical production rates of hydrogen peroxide (H₂O₂) were determined in Antarctic waters during two research cruises. The first cruise was from mid-October to mid-November, 1993, in the confluence of the Weddell and Scotia Seas, and the second cruise was in December, 1994, along the coast of the Antarctic Peninsula. During these cruises, midday sea-surface production rates ranged from 2.1 to 9.6 nM h⁻¹, with an average rate of 4.5 nM h⁻¹. Production rates were consistently smaller than rates determined at lower latitudes (>9 nM h⁻¹), primarily due to the colder temperatures and lower ultraviolet irradiances in polar waters. In situ production rates were determined with a free-floating drifter that was deployed for 12–14 h. Production rates, averaged over the deployment time, were highest at or near the surface (ca. 2.4–3.5 nM h⁻¹) and decreased rapidly with depth to 0.1–0.7 nM h⁻¹ at 10–20 m. The decrease in production rates with depth generally paralleled the decrease in ultraviolet irradiance in the water column. Production rates of hydrogen peroxide in Antarctic seawater were largely controlled by the ultraviolet irradiance in the water column, although there was some evidence for production in the blue region of the solar spectrum. A laboratory study was conducted to determine the wavelength dependence of the apparent quantum yield for the photochemical formation of hydrogen peroxide in Antarctic waters. Apparent quantum yields determined at 0°C decreased from 0.74×10⁻³ mol einstein⁻¹ at 290 nm to 1.0×10⁻⁵ mol einstein⁻¹ 410 nm. At 20°C, apparent quantum yields for the photochemical production of hydrogen peroxide were within a factor of two of apparent quantum yields determined in temperate waters at 20–25°C. Sunlight-normalized H₂O₂ production rates were determined as a function of wavelength using noontime irradiance data from Palmer Station, Antarctica. A decrease in stratospheric ozone from 336 to 151 Dobson units resulted in a predicted 19–42% increase in the photoproduction of H₂O₂ at the sea surface in Antarctic waters. The magnitude of this increase depends on the concentration and absorbance characteristics of dissolved organic matter in the photic zone, as well as on other factors such as cloudiness and decreasing solar zenith angle that tend to lower photochemical rates offsetting increases due to stratospheric ozone depletion.     

The influence of UV irradiation on the photoreduction of iron in the Southern Ocean

An iron enrichment experiment, EisenEx, was performed in the Atlantic sector of the Southern Ocean during the Antarctic spring of 2000. Deck incubations of open ocean water were performed to investigate the influence of ultraviolet B (UVB: 280–315 nm) and ultraviolet A (UVA: 315–400 nm) on the speciation of iron in seawater, using an addition of the radioisotopes ⁵⁹Fe(III) (1.25 nM) or ⁵⁵Fe(III) (0.5 nM). Seawater was sampled inside and outside the iron-enriched region. The radioisotopic Fe(II) concentration was monitored during daylight under three different light conditions: the full solar spectrum (total), total minus UVB, and total minus UVB+UVA. A distinct diel cycle was observed with a clear distinction between the three different light regimes. A clear linear relationship was found for the concentration of radioisotopic Fe(II) versus irradiance. UVB produced most of the Fe(II) followed by UVA and visible light (VIS: 400–700 nm), respectively. UVB produced 4.89 and 0.69 pM m² W⁻¹ radioisotopic Fe(II) followed by UVA with 0.33 and 0.10 pM m² W⁻¹ radioisotopic Fe(II) and VIS with 0.04 and 0.03 pM m² W⁻¹ radioisotopic Fe(II).     

Influence of giant kelp beds (Macrocystis pyrifera) on diel cycles of pCO2 and DIC in the Sub-Antarctic coastal area

The partial pressure of CO₂ (pCO₂) and dissolved inorganic carbon (DIC) were monitored in shallow coastal waters located inside and outside giant kelp beds (Macrocystis pyrifera) located in the Kerguelen Archipelago (Southern Ocean). Photosynthesis and respiration by microplankton and kelp lead to marked pCO₂ and DIC diel cycles. Daily variations of pCO₂ and DIC are significant in the spring and summer, but absent in the winter, reflecting the seasonal cycle of biological activity in the kelp beds. If the kelp beds seem to favour the onset of phytoplankton blooms, most of the primary production inside the kelp beds is due to the kelp itself. The primary production of Macrocystis kelp beds in the Sub-Antarctic high-nutrient, low-chlorophyll (HNLC) waters off the Kerguelen Archipelago is elevated and closely linked to light availability. This production is significant from October to March and reaches its climax in December at the solar radiation maximum.     

Amorphous Er2O3 films for antireflection coatings

This paper reports that stoichiometric, amorphous, and uniform Er₂O₃ films are deposited on Si(001) substrates by a radio frequency magnetron sputtering technique. Ellipsometry measurements show that the refractive index of the Er₂O₃ films is very close to that of a single layer antireflection coating for a solar cell with an air surrounding medium during its working wavelength. For the 90-nm-thick film, the reflectance has a minimum lower than 3% at the wavelength of 600 nm and the weighted average reflectances (400--1000 nm) is 11.6%. The obtained characteristics indicate that Er₂O₃ films could be a promising candidate for antireflection coatings in solar cells.     

New estimates of Southern Ocean biological production rates from O2/Ar ratios and the triple isotope composition of O2

We report O₂/Ar ratios (a constraint on net community production) and the triple isotopic composition of dissolved O₂ (a constraint on gross primary production) in samples collected from the surface mixed layer on 23 Southern Ocean transits. Samples were collected at 1–2° meridional resolution during the austral summer. Methodological limitations notwithstanding, the results constrain the net/gross production ratio, net O₂ production, and gross O₂ production at unprecedented resolution throughout the Southern Ocean mixed layer. Gross O₂ production rates inferred from the oxygen triple isotopes are greater than production rates calculated from a model based on remotely sensed chlorophyll. This result agrees with previous ¹⁸O and ¹⁴C incubations along 170°W. O₂/Ar ratios exceeding saturation are consistently observed within the Subantarctic and Polar Frontal Zones south of New Zealand and Australia, showing that a net autotrophic community predominates during austral summer. Lower O₂/Ar values are observed within the Drake Passage and Antarctic Zone, suggesting unresolved influences of low net community production, net heterotrophy, and upwelling of O₂-undersaturated waters. In autotrophic waters of the austral summer mixed layer, ratios of net community production/gross O₂ production scatter about 0.13, corresponding to f ratios of ∼0.25. Net community/gross O₂ production ratios show no meridional gradient across the Antarctic Circumpolar Current, suggesting that an approximately constant fraction of gross primary productivity is regenerated or exported. Our calculated net O₂ production rates are in satisfactory agreement with comparable published estimates. Net and gross O₂ production rates are highest in the Subantarctic and decline to the south, paralleling the well-known trend of chlorophyll a concentrations. In an analysis of variance of net O₂ production and gross O₂ production with other environmental variables, the strongest correlations are between net O₂ production and sea surface temperature (SST) (direct correlation), climatological [NO₃⁻] (inverse correlation), and estimates of primary productivity derived from a remote sensing (direct correlation). These trends are as expected if aerosol iron input is the most important influence on production. They are unexpected if upwelling-derived SiO₂ and iron are the leading influence or if lower SSTs promote greater export in this region.     

Effect of different wavelengths of light on the antioxidant and immunity status of juvenile rock bream, <Emphasis Type="Italic">Oplegnathus fasciatus</Emphasis>, exposed to thermal stress

We investigated the effect of light wavelengths on antioxidant and immunity parameters in juvenile rock bream, Oplegnathus fasciatus, exposed to thermal stress (25 and 30°C). We exposed the fish to light emitting diodes (LEDs) emitting green (520 nm) and red light (630 nm) of 0.25 and 0.5 W/m² intensity, and measured the activity, and mRNA and protein expression levels of the antioxidant enzymes, superoxide dismutase, catalase, and glutathione peroxidase. We also determined the levels of plasma hydrogen peroxide (H₂O₂), melatonin, and lysozyme. Furthermore, the mRNA and protein levels of caspase-3 were measured and terminal transferase dUTP nick end labeling (TUNEL) assays were performed. We observed that mRNA expression and activities of antioxidant enzymes and plasma H₂O₂ levels were significantly higher after exposure to high temperatures. However, increases in these parameters were significantly lower after exposure to green LED light. The plasma melatonin and lysozyme levels were significantly lower in the different groups after exposure to high temperatures; however, in groups exposed to green LED light, their levels were significantly higher than those in the control group. The expression pattern of caspase-3 mRNA was similar to that of H₂O₂. The TUNEL assay showed that apoptosis was markedly higher at higher water temperatures than that at 20°C. These results indicate that high water temperatures induce oxidative stress and decrease the immunity in juvenile rock bream but green LED light inhibits the rise in oxidative stress and combats the decrease in immunity and should, thus, be useful in the culture of rock bream.     

The distributions of uranium, radium and thorium isotopes in two anoxic fjords: Framvaren Fjord (Norway) and Saanich Inlet (British Columbia)

Depth profiles of the naturally-occurring radionuclides ²³⁸U, ²³⁴U, ²²⁶Ra, ²²⁸Ra and ²²⁸Th were obtained in two diverse anoxic marine environments; the permanently anoxic Framvaren Fjord in southern Norway and the intermittently anoxic Saanich Inlet in British Columbia. Concentrations of total H₂S were over three orders of magnitude greater in the anoxic bottom waters of Framvaren Fjord compared to those in Saanich Inlet.In Framvaren Fjord, the O₂/H₂S interface was located at 17 m. While dissolved ²³⁸U behaved conservatively throughout the oxic and anoxic water columns, concentrations based on the ²³⁸U/salinity ratio in oxic oceanic waters were almost 30% lower. Dissolved ²²⁶Ra displayed a sharp maximum just below the O₂/H₂S interface, coinciding with dissolved Mn (II) and Fe (II) maxima in this zone. It is suggested that reductive dissolution of Fe-Mn oxyhydroxides remobilizes ²²⁶Ra in this region.In Saanich Inlet, the O₂/H₂S interface was located at 175 m. Dissolved ²³⁸U displayed a strongly nonconservative distribution. The depth profiles of dissolved ²²⁶Ra and ²²⁸Th correlated well with the distribution of dissolved Mn (II) in the suboxic waters above the O₂/H₂S interface, suggesting that reduction of particulate Mn regulates the behavior of ²²⁶Ra and ²²⁸Th in this region.Removal residence times for dissolved ²²⁸Th in the surface oxic waters of both systems are longer than those generally reported for particle-reactive radionuclides in coastal marine environments. In the anoxic waters of Framvaren Fjord and Saanich Inlet, however, the dissolved ²²⁸Th removal residence times are quite similar to values reported for dissolved ²¹⁰Pb in the anoxic waters of the Cariaco Trench and the Orca Basin. This implies that the geochemistries of Th and Pb may be similar in anoxic marine waters.     

Pb and Po, manganese and iron cycling across the O2/H2S interface of a permanently anoxic fjord: Framvaren, Norway

Vertical profiles of dissolved and particulate ²¹⁰Po and ²¹⁰Pb were measured across the redox transition zone at Station F1 in Framvaren Fjord, Norway. In this fjord, a sharp decrease in pH above the O₂/H₂S interface facilitates the aerobic dissolution of MnO₂. In contrast, Fe(II) concentrations begin to increase only at the O₂/H₂S interface depth. Activity profiles reveal that dissolved ²¹⁰Po and ²¹⁰Pb are sequestered efficiently by particulates in surface waters. As polonium-210 and lead-210 activities descend down into the aerobic manganese reduction (AMR) zone, they are remobilized during the reductive dissolution of the carrier phase oxyhydroxides. Both ²¹⁰Po and ²¹⁰Pb are highly enriched at the O₂/H₂S interface where an active community of microbes, such as anoxygenic phototrophs (e.g., Chromatium, Chlorobium sp.), thrives. The coincident peaks in ²¹⁰Po, ²¹⁰Pb and microbial biomass suggest a strong biological influence on the behavior of these radionuclides. There is a strong covariance between the vertical distribution of Mn and Pb, indicating that their redox cycling is closely coupled and is likely microbially mediated.     

Estimation of the upwelling rate of deep waters in the Black Sea from the H2S vertical distribution

The expression for the bottom convection intensity is derived from the equality of the advective vertical flux of H₂S within 1000–2000 m to the diffusion turbulent flow close to the H₂S zone upper boundary. The upwelling rate, which is expressed via the H₂S concentration in deep waters and the gradient of the H₂S concentration near the upper boundary, is 10^–4 cm/s. It is shown that the H₂S diffusion flux in deep waters is an order less than the advective one. The conclusion that below 1000 m the age of H₂S does not exceed 30 years and H₂S reaches the upper boundary in approximately 150 years is derived.Translated by Mikhail M. Trufanov.     

Si2O2 molecule: structure of ground state and the excited properties under different external electric fields

Geometry and vibrational frequencies of the ground state of Si₂O₂ molecule are studied using density function theory (DFT) at the level of cc-pvtz and 6-311++G^**. It is found that the optimizing value by B3lyp/cc-pvtz is closer to the experimental data. The excited properties under different external electric fields are also investigated by the time-dependent-DFT method. Transitions from the ground state of Si₂O₂ molecule to the first singlet state under different external electric fields can take place more easily. The corresponding absorption spectral line is about 360 nm in wavelength and the excitation energy is about 3.4 eV.     

Nitrogen and oxygen isotopic composition of N2O from suboxic waters of the eastern tropical North Pacific and the Arabian Sea—measurement by continuous-flow isotope-ratio monitoring

Nitrous oxide (N₂O) is a trace gas that is increasing in the atmosphere. It contributes to the greenhouse effect and influences the global ozone distribution. Recent reports suggest that regions such as the Arabian Sea may be significant sources of atmospheric N₂O.In the ocean, N₂O is formed as a by-product of nitrification and as an intermediary of denitrification. In the latter process, N₂O can be further reduced to N₂. These processes, which operate on different source pools and have different magnitudes of isotopic fractionation, make separate contributions to the ¹⁵N and¹⁸O isotopic composition of N₂O. In the case of nitrification in oxic waters, the isotopic composition of N₂O appears to depend mainly on the ¹⁵N/¹⁴N ratio of NH⁺₄ and the ¹⁸O/¹⁶O ratio of O₂ and H₂O. In suboxic waters, denitrification causes progressive ¹⁵N and ¹⁸O enrichment of N₂O as a function of degree of depletion of nitrate and dissolved oxygen. Thus the isotopic signature of N₂O should be a useful tool for studying the sources and sinks for N₂O in the ocean and its impact on the atmosphere.We have made observations of N₂O concentrations and of the dual stable isotopic composition of N₂O in the eastern tropical North Pacific (ETNP) and the Arabian Sea. The stable isotopic composition of N₂O was determined by a new method that required only 80–100 nmol of N₂O per sample analysis. Our observations include determinations across the oxic/suboxic boundaries that occur in the water columns of the ETNP and Arabian Sea. In these suboxic waters, the values of δ¹⁵N and δ¹⁸O increased linearly with one another and with decreasing N₂O concentrations, presumably reflecting the effects of denitrification. Our results suggest that the ocean could be an important source of isotopically enriched N₂O to the atmosphere.     

Organic complexation of iron in the Southern Ocean

The chemical speciation of iron was determined in the Southern Ocean along a transect from 48 to 70°S at 20°E. Dissolved iron concentrations were low at 0.1–0.6 nM, with average concentrations of 0.25±0.13 nM. Organic iron complexing ligands were found to occur in excess of the dissolved iron concentration at 0.72±0.23 nM (equivalent to an excess of 0.5 nM), with a complex stability of log K_FeL′=22.1±0.5 (on the basis of Fe³⁺ and L′). Ligand concentrations were higher in the upper water column (top 200 m) suggesting in situ production by microorganisms, and less at the surface consistent with photochemical breakdown. Our data are consistent with the presence of stable organic iron-complexing ligands in deep global ocean waters at a background level of ∼0.7 nM. It has been suggested that this might help stabilise iron at levels of ∼0.7 nM in deep ocean waters. However, much lower iron concentrations in the waters of the Southern Ocean suggest that these ligands do not prevent the removal of iron (by scavenging or biological uptake) to well below the concentration of these ligands. Scavenging reactions are probably inhibited by such ligand competition, so it is likely that biological uptake is the chief cause for the further removal of iron to these low levels in waters that suffer from very low iron inputs.     

Use of voltammetric solid-state (micro)electrodes for studying biogeochemical processes: Laboratory measurements to real time measurements with an in situ electrochemical analyzer (ISEA)

Solid-state voltammetric (micro)electrodes have been used in a variety of environments to study biogeochemical processes. Here we show the wealth of information that has been obtained in the study of sediments, microbial mats, cultures and the water column including hydrothermal vents. Voltammetric analyzers have been developed to function with operator guidance and in unattended mode for temporal studies with an in situ electrochemical analyzer (ISEA). The electrodes can detect the presence (or absence) of a host of redox species and trace metals simultaneously. The multi-species capacity of the voltammetric electrode can be used to examine complex heterogeneous environments such as the root zone of salt marsh sediments. The data obtained with these systems clearly show that O₂ and Mn²⁺ profiles in marine sedimentary porewaters and in microbial biofilms on metal surfaces rarely overlap indicating that O₂ is not a direct oxidant for Mn²⁺. This lack of overlap was suggested originally by Joris Gieskes' group. In waters emanating from hydrothermal vents, Fe²⁺, H₂S and soluble molecular FeS clusters (FeS_aq) are detected indicating that the reactants for the pyrite formation reaction are H₂S and soluble molecular FeS clusters. Using the ISEA with electrodes at fixed positions, data collected continuously over three days near a Riftia pachyptila tubeworm field generally show that O₂ and H₂S anti-correlate and that H₂S and temperature generally correlate. Unlike sedimentary environments, the data clearly show that Riftia live in areas where both O₂ and H₂S co-exist so that its endosymbiont bacteria can perform chemosynthesis. However, physical mixing of diffuse flow vent waters with oceanic bottom waters above or to the side of the tubeworm field can dampen these correlations or even reverse them. Voltammetry is a powerful technique because it provides chemical speciation data (e.g.; oxidation state and different elemental compounds/ions) as well as quantitative data. Because (micro)organisms occupy environmental niches due to the system's chemistry, it is necessary to know chemical speciation. Voltammetric methods allow us to study how chemistry drives biology and how biology can affect chemistry for its own benefit.     

Trends of trace metal (Mn, Fe, Co, Ni, Cu, Zn, Cd and Pb) distributions at the oxic-anoxic interface and in sulfidic water of the Drammensfjord

Anoxic sulfidic waters provide important media for studying the effect of reducing conditions on the cycling of trace metals. In 1987–1988, dissolved and particulate trace metal (Mn, Fe, Co, Ni, Cu, Zn, Cd and Pb) concentrations were determined in the water column of the anoxic Drammensfjord basins, southeastern Norway. The iminodiacetic acid type chelating resin (Chelex 100) was used for the preconcentration of trace metals. The trace metal concentrations were determined using atomic absorption spectrophotometry (AAS), differential pulse polarography (DPP), and differential pulse-anodic stripping voltammetry (DP-ASV).It was observed that the trace metals Mn and Fe were actively involved in the processes of redox cycling (oxidationreduction and precipitation-dissolution) at the O₂/H₂S interface. The dissolved concentrations of Mn, Fe and Co showed maxima just below the O₂/H₂S interface. The seasonal enhancement in the maxima of both dissolved and particulate Mn and Fe at the redox cline is mainly governed by the downward movement of water which carries oxygen. An association of Co with the Mn cycle was observed, while the total dissolved Ni was decreased by only 10–35% in the anoxic waters. The dissolved concentrations of Cu, Zn, Pb and, to a lesser extent, Cd decreased in the anoxic zone.     

Thickness of the mixed bottom layer in the Northern Atlantic

The thickness of the mixed bottom boundary layer (BBL) has been analyzed based on the CTD data at transoceanic sections in abyssal waters of the Northern Atlantic. The measurements were carried out at two transoceanic sections approximately along 48° N (ASV-99) and 5° N (AI-2000) in 1999 and 2000. These data, and the WOCE data obtained at four zonal sections (AR7E and AR12 along 57° N, AR01 along 24.5° S, and A06 along 7.5° N), were used for the calculation of the statistical characteristics of the BBL??s thickness H _B . The probability distribution function F(H _B ) was close to lognormal. The mean value ??H _B ?? at different latitudes was in the range from 30 to 60 m. The averaged BBL thickness = 46.1 m. The BBL??s thickness was about 1% of the ocean??s depth D; the ratio H _B /D was the minimum (0.8%) near the equator and increased up to 1.6% in the polar latitudes.     

Effects of solar radiation on dimethylsulfide cycling in the western Atlantic Ocean

The influence of solar radiation on springtime rates of photochemical and biological consumption of dimethylsulfide (DMS) in surface waters from the western Atlantic Ocean was examined by exposing 0.2 μm filtered and unfiltered surface seawater to natural sunlight at five depths in the upper 30 m. Parallel deck incubations of 0.2 μm filtered seawater under various long-pass optical filters were also carried out to aid in assessing the wavelength dependence of DMS photolysis. DMS photolysis rate constants for mid-day exposure (∼10:30–17:30 local time) to surface irradiance ranged from 0.026 to 0.086 h⁻¹ and were highest in coastal and shelf waters. Photolysis rate constants decreased with increasing irradiation depth, in accordance with the attenuation of ultraviolet radiation (UVR, 280–400 nm). Total DMS consumption rates (photochemical+biological) in unfiltered surface samples also decreased with increasing incubation depth and were larger than photolysis rates at nearly all depths and all stations. The decrease in photolysis rate constants with exposure depth was mirrored by biological DMS consumption rate constants that were severely inhibited at surface irradiances, and approached or exceeded dark rate constants at deeper exposure depths. Photolysis rates were 2–19 times greater than estimated biological consumption rates in the surface light exposed samples, while biological consumption rates were significantly larger than photolysis rates at incubation depths below the 1% light level for UV–B radiation (280–320 nm). Total DMS loss rates increased up to nine-fold with UVR exposure, but changes in DMS concentrations were not strongly correlated to light dose, presumably due to parallel, light-mediated DMS production processes. The primary loss process for DMS depended mainly on the depth interval considered and the attenuation of UVR; in general, photochemical removal dominated shallow layers characterized by high UV–B intensities, whereas biological removal dominated in deeper layers where UV–B was absent, but UV–A (320–400 nm) and visible (400–700 nm) light fluxes were still relatively high. These results demonstrate that UVR exposure significantly influences the spatial and temporal pattern of DMS production and loss processes, and ultimately the DMS flux to the atmosphere.     

The distribution of oxygen and hydrogen sulfide in Black Sea waters during winter-spring period

Regularities of oxygen and hydrogen sulfide are examined, using the method of spatial isopycnic analysis. The contribution that ventilation of winter-time surface waters over the domes of cyclonic gyres makes to the transfer of O₂ towards the upper boundary of the constant pycnocline and to the oxicline layer is demonstrated. The paper provides spatial scales of this phenomenon and indicates the areas where the upper boundary of the anoxic layer in the Black Sea, relative to the conventional density, is located much higher compared with the rest of the sea. The suboxic zone is shown to be a specific feature of the O₂/H₂S distribution in the Black Sea waters, typical, at least, of the northern part of the basin. Analysis of the suboxic spatial variability in the vertical has been conducted. Translated by Vladimir A. Puchkin.     

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.     

The influence of organics on the adsorption of copper (II) on γ-Al2O3 in seawater,model studies with EDTA

The natural “complexing capacity” of aquatic systems was determined using titration with cupric ions. It was compared with “complexing capacity” determined in the presence of both EDTA, used as a model for organic substances, and of EDTA and γ-Al₂O₃. The γ-Al₂O₃ was used as a model for solid particles of hydrous oxide in natural waters. The adsorption isotherm of copper in seawater on γ-Al₂O₃ particles was determined with and without EDTA.For EDTA alone and for the Cu—EDTA complex, it was found that they are not adsorbed on γ-Al₂O₃ in the natural seawater. However, by adsorption on solid particles, the labile ionic Cu-complex can be removed from the seawater.     

Estimation of net ecosystem metabolism of seagrass meadows in the coastal waters of the East Sea and Black Sea using the noninvasive eddy covariance technique

We measured the community-scale metabolism of seagrass meadows in Bulgaria (Byala [BY]) and Korea (Hoopo Bay [HP]) to understand their ecosystem function in coastal waters. A noninvasive in situ eddy covariance technique was applied to estimate net O₂ flux in the seagrass meadows. From the high-quality and high-resolution time series O₂ data acquired over > 24 h, the O₂ flux driven by turbulence was extracted at 15-min intervals. The spectrum analysis of vertical flow velocity and O₂ concentration clearly showed well-developed turbulence characteristics in the inertial subrange region. The hourly averaged net O₂ fluxes per day ranged from -474 to 326 mmol O₂ m^-2 d^-1 (-19 ± 41 mmol O₂ m^-2 d^-1) at BY and from -74 to 482 mmol O₂ m^-2 d^-1 (31 ± 17 mmol O₂ m^-2 d^-1) at HP. The net O₂ production rapidly responded to photosynthetically available radiation (PAR) and showed a good relationship between production and irradiance (P-I curve). The hysteresis pattern of P-I relationships during daytime also suggested increasing heterotrophic respiration in the afternoon. With the flow velocity between 3.30 and 6.70 cm s^-1, the community metabolism during daytime and nighttime was significantly increased by 20 times and 5 times, respectively. The local hydrodynamic characteristics may be vital to determining the efficiency of community photosynthesis. The net ecosystem metabolism at BY was estimated to be -17 mmol O₂ m^-2 d^-1, which was assessed as heterotrophy. However, that at HP was 36 mmol O₂ m^-2 d^-1, which suggested an autotrophic state.