Studies of hydrocarbons in the waters and snow-ice cover of the southeast sector of the antarctic

Data are presented on the content of hydrocarbons (HC) relative to the concentrations of particulate matter, lipids, C_org, and chlorophyll a in the surface waters and snow-ice cover of the East Antarctic coastal areas. It was shown that the growth of the concentrations of aliphatic HC (AHC) to 30 μg/l in the surface waters takes place in the frontal zones and under the young ice formation. The AHC content in the snow increases with the growth of the aerosol content in the atmosphere. In the lower part of the ice at the boundary with the seawater, despite the low temperatures, the autochthonous processes may provide high AHC concentrations (up to 289 μg/l). Within the snow-ice cover on fast ice, synchronous content variations of all the compounds considered take place.     

Organic tracers from biomass burning in atmospheric particulate matter over the ocean

Particulate matter from the atmosphere over the Atlantic Ocean along the South American and African Continents has been analyzed for organic tracers from natural and biomass burning emissions. The major biomarker compounds characterized are natural products from continental vegetation consisting primarily of epicuticular wax components. For example, n-alkanes ranged from C₂₅ to C₃₅, with an odd carbon number predominance and carbon maxima (C_max) at 29 or 31. Concentrations of n-alkanes varied from 0.3 to 680 ng/m³. Nevertheless, n-alkanols are the dominant terrestrial tracers in almost all samples (concentrations from 0.1 to 780 ng/m³) and ranged from C₂₂ to C₃₄ with an even carbon number predominance. Despite the major presence of the natural tracers, organic components from biomass burning emissions are also present in the particulate matter. The major tracers from this source are thermal degradation products from the biopolymer cellulose, namely the dianhydromonosaccharide derivatives levoglucosan, galactosan, and mannosan. In general, the concentrations of levoglucosan, the major derivative from this source in all samples, varied from 0.0008 to 0.15 ng/m³ in atmospheric samples collected over the ocean and from 0.04 to 4860 ng/m³ in terrestrial particulate matter, used as reference in this study. Dehydroabietic acid, another marker compound emitted from burning of Gymnosperm fuel, is also detectable in most oceanic samples at concentrations ranging from 0.0001 to 0.4 ng/m³, whereas in terrestrial aerosol particulate matter, this component is present at much higher concentrations (0.23–440 ng/m³). The presence of these tracers in atmospheric particulate matter over the ocean confirms the long-range transport of smoke from biomass burning off the continents.     

南大洋大气有机胺分布及来源特征研究

依托中国第36次南极科学考察,利用船载走航气溶胶及气体组分在线分析仪对南大洋大气中气态和颗粒态有机胺进行了在线观测。获得了南大洋开阔海域及普里兹湾大气中高分辨气态和颗粒态有机胺的组成及分布,并对其来源特征进行了分析。结果表明：南大洋大气有机胺以气态三甲胺（TMA）和二甲胺（DMA）为主要存在形态,其均值分别为(104.0±285.2)、(3.5±6.0) ng/m3。普里兹湾大气中有机胺的平均浓度显著高于南大洋开阔海域,气态TMA和DMA均值分别达到(289.0±396.6)、(5.6±16.1) ng/m3。南大洋大气中气态TMA、DMA和氨气（NH3）在不同区域内均具有良好的线性关系,表明三者具有同源性。从来源分析,南大洋大气有机胺主要受到海洋生物活动的影响,但在海冰边缘区及南极近岸海域,企鹅等动物的生物活动会导致大气中有机胺的浓度显著升高。     

Long-term (1998–2007) trends on the spatial distribution of heterotrophic ciliates in the East China Sea in summer: effect of the Three Gorges Dam construction

The spatial distribution of heterotrophic ciliates, environmental factors and potential food items (bacteria, Synechococcus spp. and nanoflagellates) were measured in the East China Sea to examine which variables contributed importantly to the long-term distribution of ciliates between 1998 and 2007. In July 1998 and June 2003, heterotrophic ciliates were found to be abundant (1,000–2,000 × 10³ cells m⁻³) in regions where surface salinity <32 but extremely low (<500 × 10³ cells m⁻³) in shelf waters of surface salinity >32. After August 2003, shortly after the completion of the Three Gorges Dam, we found no significant areal differences in the abundance of heterotrophic ciliates (HC). However, we found a significantly negative correlation between temperature and HC abundance of surface water after the completion of the dam, suggesting that temperature had a greater influence on HC abundance, once the original saline state had changed. For the long-term trends on the vertical distribution of HC, their abundance was significantly higher in the upper 50 m of the water column than at either 75 or 100 m. Abundance of Synechococcus spp. at these levels varied significantly in regions of surface salinity <32, suggesting that ciliates and picophytoplankton contribute greatly to mediating the transfer of organic matter to higher trophic levels in this marine ecosystem.     

Seasonal variations in nutrients and chlorophyll-a concentrations in the Northern east China sea

Nutrients, chlorophyll-a, particulate organic carbon (POC), and environmental conditions were extensively investigated in the northern East China Sea (ECS) near Cheju Island during three seasonal cruises from 2003 to 2005. In spring and autumn, relatively high concentrations of nitrate (2.6~12.4 μmol kg^-1) and phosphate (0.17~0.61 μmol kg^-1) were observed in the surface waters in the western part of the study area because of the large supply of nutrients from deep waters by vertical mixing. The surface concentrations of nitrate and phosphate in summer were much lower than those in spring and autumn, which is ascribed to a reduced nutrient supply from the deep waters in summer because of surface layer stratification. While previous studies indicate that upwellings of the Kuroshio Current and the Changjiang (Yangtze River) are main sources of nutrients in the ECS, these two inputs seem not to have contributed significantly to the build-up of nutrients in the northern ECS during the time of this study. The lower nitrate:phosphate (N:P) ratio in the surface waters and the positive correlation between the surface N:P ratio and nitrate concentration indicate that nitrate acts as a main nutrient limiting phytoplankton growth in the northern ECS, contrary to previous reports of phosphate-limited phytoplankton growth in the ECS. This difference arises because most surface water nutrients are supplied by vertical mixing from deep waters with low N:P ratios and are not directly influenced by the Changjiang, which has a high N:P ratio. Surface chlorophyll-a levels showed large seasonal variation, with high concentrations (0.38~4.14 mg m^-3) in spring and autumn and low concentrations (0.22~1.05 mg m^-3) in summer. The surface distribution of chlorophyll-a coincided fairly well with that of nitrate in the northern ECS, implying that nitrate is an important nutrient controlling phytoplankton biomass. The POC:chlorophyll-a ratio was 4~6 times higher in summer than in spring and autumn, presumably because of the high summer phytoplankton death rate caused by nutrient depletion in the surface waters.     

Particulate matter and components of the organic substance in the surface waters of the Southern and Atlantic Oceans

The integrated studies of the particulate matter and organic compounds in the surface waters and the snow-ice cover by means of geochemical (the concentrations of the particulate matter, the Corg, the hydrocarbons, the lipids, and the chlorophyll a) and optical techniques were performed in the Southern Ocean and in the east of the Atlantic Ocean along the vessel’s route: Africa-Antarctica-Africa-St. Petersburg. The correlations between the treated compounds were found. It was shown that the supply of pollutants affects not only the concentrations but also the proportions of the considered compounds. New data were obtained on the processes of the accumulation of particulate matter and organic compounds under the ice formation.     

The concentration and composition of hydrocarbons in water,particulate matter,and bottom sediments of the Kara Sea

Data are presented on the content of aliphatic and polycyclic aromatic hydrocarbons (AHC and PAH, respectively) in the interstitial waters and bottom sediments of the Kara Sea compared to the distribution of the particulate matter and organic carbon. It was found that the AHC concentrations within the water mass (16 μg/l on average) are mainly formed by natural processes. The AHC distribution represents the variability of the hydrological and sedimentation processes in different regions of the sea. The widest ranges of the concentrations were registered in the Ob Bay-Kara Sea section: in the water (10–310 μg/l for the AHC and 0.4–7.2 ng/l for the PAH) and in the surface layer of the bottom sediments (8–42 μg/l for the AHC and 9–94 ng/g for the PAH). The differentiation of the hydrocarbons (HC) in the different media follows the marginal filter’s regularities; therefore, no oil and pyrogenic compounds are supplied to the open parts of the sea. In the sediment mass, the HC content is determined by the variations in the oxidative conditions in the sediment and its material’s composition.     

Particulate organic matter in the coastal and estuarine waters of Goa and its relationship with phytoplankton production

In the coastal and estuarine waters of Goa, particulate organic carbon (POC) varied from 0.52 to 2.51 mg l^?1 and from 0.28 to 5.24 mg l^?1 and particulate phosphorus (PP) varied from 0.71 to 5.18 μg l^?1 and from 0.78 to 20.34 μg l^?1, respectively. The mean values of chlorophyll and primary productivity were 1.94 mg m^?3 and 938.1 mg C m^?2 day^?1 in the coastal waters and 4.3 mg m^?3 and 636.5 mg C m^?1 day^?1 in the estuarine waters, respectively.$\text{POC}\text{chl}$ ratios were low in June and October even when POC values were quite high. The POC in surface waters was linearly correlated with the chlorophyll content. Also PP increased when chlorophyll and primary productivity remained high. The results suggest that the phytoplankton was sharply increasing and contributed to POC and PP content. The percentage of detritus calculated from the intercept values of chlorophyll on POC varied from 46 to 76% depending on season. Results indicate that the major portion of POC and PP during postmonsoon (October–January) is derived from phytoplankton production while the allochthonous matter predominate during monsoon (June–September).     

Origin of hydrocarbons in the particulate matter and bottom sediments of the northern shelf of the Caspian Sea

Data are presented on the content and composition of hydrocarbons (HC) (aliphatic, AHC and polyaromatic, PAH) in the filtered particulate matter and in the surface layer of the bottom sediments on the northern shelf of the Caspian Sea and related to the data on their content in the Volga River estuary. Because of the transformation and precipitation of anthropogenic and natural compounds, the HC composition in the particulate matter and bottom sediments undergoes transformations caused by the mixing of fresh and saline waters (in the bottom sediments, within the concentration ranges 70.4–4557.9 μ g/g for AHC and 3.8–4800 ng/g for PAH). It was found that the greatest concentrating of HC proceeds in the region of the avalanche sedimentation, and their content is independent of the grain-size type of the sediments. The anthropogenic HC (oil and pyrogenous) do not get over the marginal filter of the Volga River and do not pass to the open part of the sea.     

Chemical and GC-MS characterization of marine dissolved lipids

The chloroform-extractable ‘lipid’ fraction of dissolved organic matter in seawater was analyzed by gravimetry, liquid chromatography, gas chromatography (GC), and gas chromatography—mass spectrometry (GC—MS). Gravimetric concentrations of dissolved lipids in the Gulf of Mexico were in the range of 60–160 μg 1^?1 in near-surface waters and 61–116 μg 1^?1 in near bottom waters and accounted for ～4% of the dissolved organic carbon. Over a 12-h sampling period and a 5-d sampling period extensive variability in dissolved lipid quantity and quality were observed. The major percentage of extractable weight was collected in the polar liquid chromatographic fraction (55–95%). Gas chromatographic concentrations of the aliphatic fractions were in the range of 0.014-0.187 μg 1^?1. Concentrations derived from gas chromatography were consistently lower than gravimetrically-derived concentrations. A number of compounds were tentatively identified by a combination of GC, GC—MS, and authentic standards. The major components of the analyzable dissolved lipids were n-alkanes (C₁₆C₃₂), pristane, phytane, methyl, ethyl and propyl esters of fatty acids. Minor components included olefins and cycloalkanes, aromatics, short-chained acids, and possibly a lactone and an alcohol. All concentrations and compounds were indicative of a fairly pristine environment. The n-alkane distribution appears to be the result of marine and terrestrial inputs superimposed on a chronic low-level background of oil pollution. It is suggested that the fatty acid esters and other fragment molecules are the résult of the degradation of humic substances. A number of potential indicators of source were isolated.     

Chlorinated hydrocarbons in the seawater and surface sediments of Blanca Bay,Argentina

In order to characterize our study area and to provide reference values to be used in the future to measure the changes produced by an increase in contamination, the concentrations of chlorinated hydrocarbons have been investigated in fifty-one samples of seawater, taken at four different depths: air-sea interface, surface, one metre and bottom waters, and in twenty-three samples of surface sediments from Blanca Bay, Argentina. Of eleven organochlorine compounds we were looking for (α BHC, lindane, heptachlor, δ BHC. aldrin, heptachlor epoxide, dieldrin, o-p′DDD, p-p′DDD, o-p′DDT and p-p′DDT), seven could be detected in seawater and three in surface sediments with the following mean concentrations: α-BHC=48·2 ng l^?1; lindane=54·2 ng l^?1; heptachlor=45·0 ng l^?1; δ BHC=12·5 ng l^?1; aldrin=61·8 ng l^?1 and ΣDDT=67·0 ng l^?1; and δ BHC=3·2 ng g^?1; lindane=4·2 ng g^?1 and heptachlor=1·0 ng g^?1 for seawater, regarding the surface waters, and sediment samples, respectively.Concentration factors among the different water layers were also studied to see if there was any correlation between chlorinated hydrocarbon contents and the water depths from which the samples were taken. As a mean value, the air-sea interface water contains 18 times more of these compounds than that of the water near the bottom. A comparison of the values corresponding to seawater and surface sediments from our study area with those levels measured in samples from other geographic locations is also presented.With the purpose to detect a relationship between chlorinated hydrocarbon concentrations and the contents of particulate matter (PM) on the one hand, and particulate organic material (POM) on the other hand, four groups of samples containing different amounts of PM and POM, respectively were formed. From a comparison of the results obtained, lindane, heptachlor and δ BHC showed a tendency to lower concentrations in those samples containing little PM whereas α BHC and aldrin remained without important changes. No significant correlation was found between organochlorine levels and contents of POM.     

Primary production and chlorophyll distributions in the subtropical and tropical waters of the Atlantic Ocean in the autumn of 2002

In October and November 2002, high and relatively high values of the chlorophyll a concentration at the sea surface (C _chl) were observed in the English Channel (0.47 mg/m³), in the waters of the North Atlantic Current (0.25 mg/m³), in the tropical and subtropical anticyclonic gyres (0.07–0.42 mg/m³), and also in the southwestern region of the southern subtropical anticyclonic gyre (usually 0.11–0.23 mg/m³). The central regions of the southern subtropical anticyclonic gyre (SATG) and the North Atlantic tropical gyre (NATR) were characterized by lower values of C _chl (0.02–0.08 mg/m³ for the SATG and 0.07–0.14 mg/m³ for the NATR). At most of the SATG stations, the values of the surface primary production (C _phs) varied from 2.5 to 5.5 mg C/m³ per day and were mainly defined by the fluctuations of C _chl (r = +0.78) rather than by those of the assimilation number (r = +0.54). The low assimilation activity of phytoplankton in these waters (1.3–4.6 mg chl a per hour) pointed to a lack of nutrients. An analysis of the variability of their concentration and the composition of photosynthetic pigments showed that, in the waters north of 30° N, the growth of phytoplankton was mostly restricted by the deficiency of nitrogen, while, in more southern areas, at the majority of stations (about 60%), the phosphorus concentrations were the minimum. At the low concentrations of nitrates and nitrites, ammonium represented itself as a buffer that prevented planktonic algae from extreme degrees of nitric starvation. In the tropical waters and in the waters of the SATG, the primary production throughout the water column varied from 240 to 380 mg C/m² 30° per day. This level of productivity at stations with low values of C _chl (<0.08 mg/m³) was provided by a well-developed deep chlorophyll maximum and a high transparency of the water. The light curves of photosynthesis based on in situ measurements point to the high efficiency of utilizing the penetrating solar radiation by phytoplankton on cloudy days.     

Nutrient (N,P and Si) and carbon partitioning in the stratified NW Mediterranean

The distribution of nutrients and carbon in the different pools present in the three functional layers (the upper, biogenic layer, the thermocline layer, and the deeper, biolythic layer) of the stratified NW Mediterranean Sea was examined. The stoichiometry between dissolved inorganic nutrients, which had low concentrations in the surface waters, indicated a deficiency in nitrogen, relative to phosphorus, and an excess nitrogen relative to phosphorus within the thermocline, as well as a general silicate deficiency relative to both N and P, even extending to the biolythic layer. The dissolved organic matter was highly depleted in N and, particularly, in P relative to C, with average DOC/DON ratios >60 and DOC/DOP ratios >1500 in all three layers. The particulate pool was also depleted in N and P relative to C, particularly in the biolythic layer. The concentration of biogenic silica was low relative to C, N and P, indicating that diatoms were unlikely to contribute a significant fraction of the seston biomass. Most (>80%) of the organic carbon was present as dissolved organic carbon. Total organic N and P comprised 50–80% of the N and P pool in the biogenic layer, and decreased with depth to represent 10–25% of these nutrient pools in the biolythic layer. The high total N:P ratios in all three depth layers (N/P ratio >20) indicated an overall phosphorus deficiency in the system. The high P depletion of the dissolved organic matter must derive from a very rapid recycling of the P-rich molecules within DOM, and the increasing C/N ratio of DOM with depth indicates that N is also recycled faster than C in the DOM. Because of the uniform depth distribution of the total dissolved nitrogen concentration, the increase in the percent inorganic N and the decline in the percent dissolved organic N with depth indicates that there must be biological transformations between these pools, with a dominance of DON production in surface waters and remineralisation in the underlying layers, from which dissolved inorganic nitrogen is supplied back to the biogenic layer. Downward fluxes of DON and DOC were estimated at 200–250 μmol N m⁻² d⁻¹ and 1.4–2.1 mmol C m⁻² d⁻¹, respectively, while there should be little or no export of P as dissolved organic matter. The downward DON flux exceeded the diffusive DIN supply of about 145 μmol N m⁻² d⁻¹ to the biogenic layer, suggesting that allochthonous N inputs must be important in the region.     

Structure and Productivity of the Phytocenosis in the Southwestern Kara Sea in Early Spring

Results of plankton biota studies in the southwestern Kara are presented. The spatial distribution of hydrochemical and hydrophysical parameters related to structural and functional characteristics of phytoplankton in the surface water is considered. The chlorophyll a concentration varied in the surface layer of the Kara Sea from 0.08 to 3.22 mg m^–3 (mean value 0.62 mg m^–3). Primary production varied from 0 to 1.92 mg C m^–3 day^–1 (the mean value of 0.42 mg C m^–3 day^–1) in the ice-covered water areas and was greater by a factor of four, ranging from 1.01 to 3.46 mg C m^–3 day^–1 (the mean value of 1.79 mg C m^–3 day^–1) in ice-free areas. In this case, the total algal biomass varied from 0.8 to 110.7 mg C m^–3 (mean value 10.6 mg C m^–3). It is shown that in the study period, waters from the western Kara Sea were more productive than the estuarine water areas of the Ob and Yenisei rivers. The activity of phototrophic phytoplankton in river waters was almost completely absent. It is established that the contents of nutrients and iron were higher than the threshold for limitation of phytoplankton development. The experiments showed that the production activity of phototrophic algae is restrained by light deficit beneath the ice.     

Was a carbon balance measured in the equatorial Pacific during JGOFS?

The likelihood that the carbon fluxes measured as part of the US-JGOFS field program in the equatorial Pacific ocean (EgPac) during 1992 yielded a balanced carbon budget for the surface ocean was determined. The major carbon fluxes incorporated into a surface carbon budget were: new production, particulate organic carbon (POC) and dissolved organic carbon (DOC) export, CaC0₃ export, C0₂ gas evasion, dissolved inorganic carbon (DIC) supply, and the time rate of charge. The ratio of the measured concentration gradients of DOC and DIC provided a constraint on the ratio of POC/DOC export. Uncertainties of ±30–50% for individual carbon flux measurements reduce the likelihood that a carbon balance can be measured during a JGOFS process-type study. As a benchmark, carbon fluxes were prescribed to yield a hypothetical surface carbon budget that was, on average, balanced. Given the typical errors in the individual carbon fluxes, however, there was only about a 30% chance that this hypothetical budget could be measured to be balanced to ±50%. Using this benchmark, it was determined that there was a 95 % chance that the carbon flux measurements yielded a surface DIC budget balanced (to ±50%) during El Nino conditions in boreal spring 1992, when the total organic carbon export rate was - 5 mmol C m-2 day- 1 and the POC export was 3 mmol C m⁻² day⁻¹. In boreal fall 1992, during cold period conditions, there was a 70% chance that the surface carbon DIC budget was balanced when the total organic carbon export rate was 20 mmol C m⁻² day⁻¹ and export was -13 mmol C m-2 day-'. The DOC to DIC concentration gradient ratio of - -0.15, measured in depth profiles down to 100m and in surface waters, was used as an important constraint that most (> 70%) of the organic carbon exported from the euphotic zone was POC rather than DOC. If a balanced surface DIC budget was used to test the compatibility of individual carbon fluxes measured during EgPac, then a three- to four-fold increase in total and particulate organic carbon export between spring and fall is indicated. This increase was not reflected in the POC loss rates measured by drifting sediment trap collections or estimated by²³⁴Th deficiencies coupled with the C/Th measured on suspended particles.     

The atmospheric cycling and air–sea exchange of mercury species in the South and equatorial Atlantic Ocean

Measurements of gas-, particle- and precipitation-phases of atmospheric mercury (Hg) were made in the South and equatorial Atlantic Ocean as part of the 1996 IOC Trace Metal Baseline Study (Montevideo, Uruguay to Barbados). Total gaseous mercury (TGM) ranged from 1.17 to 1.99 ng m⁻³, with a weighted mean of 1.61±0.09 ng m⁻³. These values compare well with Pacific Ocean data and earlier results from the Atlantic. The open-ocean samples recorded a distinctive inter-hemispheric gradient, which is consistent with a long-lived trace gas emitted to a greater extent from the Northern than from the Southern Hemisphere. Correlations with surface ²²²Rn measurements indicate an influence of regional terrestrial sources on open-ocean TGM concentrations. Total Hg in precipitation ranged from 10 to 99 pM (volume-weighted average: 17.8±2.9 pM). On average, about 72% of the total Hg was “reactive” (i.e., reducible by SnCl₂). The data showed an apparent rapid nonlinear decrease in concentration with event size (“washout curve”). The wet depositional flux was estimated at 18–36 nmol m⁻² yr⁻¹ (4–7 μg m⁻² yr⁻¹), which is slightly lower than that found in mid-continental locations of North America (6–12 μg m⁻² yr⁻¹). ²¹⁰Pb analyses indicate a strong impact of particles on rain Hg concentrations. Particle-phase Hg (range 5–25 fmol m⁻³; mean 12±1 fmol m⁻³; 66% “reactive”) was comparable to values over the equatorial Pacific. The dry depositional flux is ca. 0.4 nmol m⁻² yr⁻¹, or 0.4–1.0% of the wet flux. Particle-phase Hg concentrations did not change significantly when African dust was present during sampling. However, the Hg/Al ratios were consistent with crustal values during the dust periods. The residence time of TGM was calculated to be 1.3–3.4 yr in this region, based on standing stock estimates. Incubation of rainwater added to surface seawater gave reduction rates [i.e., production of elemental Hg (Hg°); 1.6–4.3% d of total Hg added] comparable to additions of inorganic ionic standards, indicating that Hg⁺² from precipitation is reduced in a similar manner in surface waters. Thus, precipitation-phase Hg is generally available for evasion to the atmosphere following deposition to the surface ocean, effectively enhancing the mobility and residence time of Hg at the Earth's surface.     

Primary production and deep-water oxygen content of two British Columbian fjords

Vertical profiles of ¹⁴C-uptake were acquired monthly from the mouths and landward stations of periodically anoxic Saanich Inlet and oxygenated Jervis Inlet, British Columbia, Canada from August 1985 to October 1989. Saanich Inlet (490 g C m⁻² year⁻¹) was 1.7 times more productive than Jervis Inlet (290 g C m⁻² year⁻¹) and primary production toward the mouths of both inlets was 1.4 times higher than at the landward stations. The elevated rates of primary production in Saanich Inlet may have been due to exchange with the nutrient-rich surface waters of the passages leading to the Pacific Ocean and the up-inlet gradients in both fjords also may have reflected relative nutrient supply. Sediment-trap results show enhanced fluxes of biogenic silica to the deep waters of Saanich Inlet; associated organic matter is likely to have caused a large oxygen demand. Combined with the high primary production and export flux, low rates of vertical mixing and particle-entrapment within the fjord, factors associated with weak estuarine circulation as well as weak winds and tides in Saanich Inlet, may also stimulate anoxia.Although in Jervis Inlet there is more stagnant water behind the sill and deep-water renewals appear to be less frequent than in Saanich Inlet, the deep sill allows degradation of a significant fraction of the sinking organic matter before the stagnant waters are reached, reducing the chances of oxygen depletion in the bottom waters.     

The distributions of particulate atmospheric trace metals and mineral aerosols over the Indian Ocean

Data are presented for the concentrations of Al, Fe, Mn, Ni, Co, Cr, V, Cu, Zn, Pb and Cd in aerosols collected over two contrasting regions of the Indian Ocean. These are: (1) the northern Arabian Sea (AS), from which samples were collected in the northeast monsoon, during which the region receives an input of crustal material from the surrounding arid land masses; and (2) the Tropical Southern Indian Ocean (TSIO), a remote region from which samples were collected from air masses for which there were no large-scale up-wind continental aerosol sources. The TSIO samples can be divided into two populations: Population I aerosols, collected from air masses which have probably impinged on Madagascar, and Population II aerosols, which have been confined to open-ocean regions to the south of the area.The data indicate that there are strong latitudinal variations in the chemical signatures of aerosols over the Indian Ocean. The input of crustal material to the Arabian Sea gives rise to an average Al concentration of about 1000 ng m⁻³ of air in the northeast monsoon regime. As a result, the concentrations of all trace metals are relatively high, and the values of crustal enrichment factors are less than 10 for most metals, in the AS aerosols. In contrast, TSIO Population II ‘open-ocean southern air’ sampled during the southwest monsoon season, has an average Al concentration of only about 10 ng m⁻³ of air. Trace metal concentrations in the TSIO ‘open-ocean southern air’ during the southwest monsoon season are representative of ‘clean’ remote marine air and are generally similar to those reported over the central North Pacific.Mineral dust concentrations over the Indian Ocean decrease in a north to south direction, from about 15–20 μg m⁻³ of air in the extreme north to about 0.01–0.25 μg m⁻³ of air in the far south. The deposition of mineral dust over the northern Arabian Sea can account for approximately 75% of the non-carbonate material incorporated into the underlying sediments.In the Arabian Sea the dissolved atmospheric inputs of all the trace metals, with the exception of Cu and Co, exceed those from fluvial run-off by factors which range from 9.6 for Pb to 1.6 for Cr.     

Recovery of benthic macroinvertebrate and epilithic communities following a large flood,in an unstable,braided, New Zealand river

Benthic macroinvertebrates and small stones were collected from a riffle in the Ashley River, North Canterbury, New Zealand, on 12 occasions within a 132‐day period following a particularly large flood in 1986. Despite the occurrence of smaller floods during this period, benthic macroinvertebrate communities and stone surface organic layers recovered rapidly. Mean concentration of stone surface organic carbon increased from 0.23 g/m² to 1.01 g/m² stone surface in the first 23 days after the flood and chlorophyll a concentration increased from 0.13 mg/m² (day 3) to 9.2 mg/m² by day 132. Minor floods during the recovery period had little effect on organic layer biomass. Mean faunal density increased from 230/m² to 7920/m² during this time and taxon richness from 7 to 21 per 5 benthic samples. Immediately after the flood and throughout the study period the fauna was dominated by larvae of Deleatidium (Ephemeroptera: Leptophlebiidae), Hydora (Coleoptera: Elmidae), and Chironomidae. Re‐establishment of Deleatidium populations in previously denuded brands was effected by oviposition, egg‐hatching, and larval immigration. Minor braids are likely to represent important epicentres from which recolonisation proceeds.     

Waters of the western springs catchment,Auckland

Abstract

Aquifers occur in basalt deposits infilling valleys in the Western Springs catchment of Auckland City, and they discharge into small streams incised along the edges of major lava flows. Total run‐off from the area is >0.261 m³·s^?1. Analyses by standard methods of twelve subsurface and surface waters show that flowing groundwaters have a low level of pollution (dissolved oxygen x = 7.6 mg·l^?1, abuminoid nitrogen x = 0.038 mg·l^?1, and total solids x = 188 mg·l^?1). Surface waters and stagnant groundwater have high, but varying levels of biological activity. Although much of the dissolved solid content of all the waters (e.g., Ca²⁺, Mg²⁺, Na⁺, K⁺, SiO₂) is consistent with the chemistry of the rocks of the catchment, particularly the glassy volcanic tuffs, for surface waters various sources of pollution also make significant contributions (e.g., leaking sewers, sewage overflows, combustion of fossil fuels, fertilisers, zoo animals). Apart from its iron level, the moderate volume (～.0.13 m³·s^?1) of flowing groundwater is of suitable quality for domestic, industrial and irrigation needs.