Climatological and hydrographic influences on nearshore food webs off the southeastern United States: bacterioplankton dynamics

Bacterioplankton productivity, numbers, and cell specific activity were studied in nearshore waters of the southeastern U.S. continental shelf during seasons of maximum freshwater discharge. In April 1984, coastal waters were stratified from normal spring discharge and typical northeastward wind stress. In April 1985, shelf waters were vertically homogeneous due to below normal runoff and southwestward wind stress. In 1984, nearshore bacterial productivity ranged from 7.0 to 14.7 × 10⁶ cells l⁻¹ h⁻¹ and midshelf rates were 40–50% less. In 1985, nearshore productivity ranged from 0.9 to 2.4 × 10⁶ cells 1⁻¹ h⁻¹, and productivity was extremely patchy over the entire shelf. The cell-specific activity (thymidine incorporation per cell) suggests that although productivity was high in 1984, only a fraction of the bacterioplankton was actively growing or incorporating thymidine (0.9–2.9 × 10⁻²¹ mol cell⁻¹ h⁻¹). In 1985, a higher percentage of cells appeared to be active and incorporating thymidine (5–13 × 10⁻²¹mol cell⁻¹h⁻¹) even though productivity was low. Hydrographic conditions along the southeastern coastline may have had a significant impact on the overall community structure and carbon flow through the microbial food web. When coastal waters were stratified in 1984, bacterial biomass was a significant percentage (35–320%) of the phytoplankton biomass. During vertically homogeneous conditions of 1985, bacterial production and biomass were a small percentage (2–13%) of the phytoplankton production and biomass across the shelf. The interannual variation in the microbial food web was attributed to the interannual variability of the southeastern U.S. hydrology due to changes in freshwater discharge and wind direction and intensity. The ecological implications of these results extend to the potential impact of seasonal microbial food webs on nearshore allochothonous and autochothonous organics before removal from the southeastern U.S. coastline.     

Chemical and stable isotopic models for boundary creek warm springs, southwestern Yellowstone National Park, Wyoming

Thermal springs of the Boundary Creek hydrothermal system in the southwestern part of Yellowstone Park outside the caldera boundary vary in chemical and isotopic composition, and temperature. The diversity may be accounted for by a combination of processes including boiling of a deep thermal water, mixing of the deep thermal water with cool meteoric water and/or with condensed steam or steam-heated meteoric water, and chemical reactions with surrounding rocks. Dissolved-silica, Na⁺, K⁺ and Ca²⁺ contents of the thermal springs could result from a thermal fluid with a temperature of 200 ± 20°C. Chloride-enthalpy and silica-enthalpy mixing models suggest mixing of 230°C, 220 mg/l Cl⁻ thermal water with cool, low-Cl⁻ components. A 350 to 390°C component with Cl⁻ ≥ 300 mg/l is possibly present in thermal springs inside the caldera but is not required to fit observed spring chemical and isotopic compositions. Irreversible mass transfer models in which a low-temperature water reacts with volcanic glass as it percolates downward and warms, can account for observed pH and dissolved-silica, K⁺, Na⁺, Ca²⁺ and Mg²⁺ concentrations, but produces insufficient Cl⁻ or F⁻ for measured concentrations in the warm springs. The ratio of a_Na/a_H, and Cl⁻ are best accounted for in mixing models. The water-rock interaction model fits compositions of acid-sulfate waters observed at Summit Lake and of low-Cl⁻ waters involved in mixing.The cold waters collected from southwestern Yellowstone Park have δD values ranging from −118 to −145 per mil and δ¹⁸O values of −15.9 to −19.4 per mil. Two samples from nearby Island Park have δD values of −112 and −114 per mil and δ¹⁸O values of −15.1 and −15.3 per mil. All samples of thermal water plot significantly to the right of the meteoric water line. The low Cl⁻ and variable δD values of the thermal waters indicate isotopic compositions are derived by extensive dilution with cold meteoric water and by steam separation on ascent to the surface. Many of the hot springs with higher δD values may contain in addition a significant amount of high-D, low-Cl⁻, acid-sulfate or steam-heated meteoric water. Mixing models, Cl⁻ content and isotopic compositions of thermal springs suggest that 30% or less of a deep thermal component is present. For example, the highest-temperature springs from Three Rivers, Silver Scarf and Upper Boundary Creek thermal areas contain up to 70% cool meteoric water and 30% hot water components, springs at Summit Lake and Middle Boundary Creek spring 57 are acid-sulfate or steam-heated meteoric water; springs 27 and 48 from Middle Boundary Creek and 49 from Mountain Ash contain in excess of 50% acid-sulfate water; and Three Rivers spring 46 and Phillips could result from mixing hot water with 55% cool meteoric water followed by mixing of acid-sulfate water. Extensive dilution by cool meteoric water increases the uncertainties in quantity and nature of the deep meteoric, thermal component.     

Sulfur isotopic effects in the disproportionation reaction of sulfur dioxide in hydrothermal fluids: implications for the δS variations of dissolved bisulfate and elemental sulfur from active crater lakes

Sulfur isotope effects during the SO₂ disproportionation reaction to form elemental sulfur (3SO₂+3H₂O→2HSO₄⁻+S+2H⁺) at 200–330°C and saturated water vapor pressures were experimentally determined. Initially, a large kinetic isotopic fractionation takes place between HSO₄⁻ and S, followed by a slow approach to equilibrium. The equilibrium fractionation factors, estimated from the longest run results, are expressed by 1000 ln α_HSO4⁻–S=6.21×10⁶/T²+3.62. The rates at which the initial kinetic fractionation factors approach the equilibrium ones were evaluated at the experimental conditions.δ³⁴S values of HSO₄⁻ and elemental sulfur were examined for active crater lakes including Noboribetsu and Niseko, (Hokkaido, Japan), Khloridnoe, Bannoe and Maly Semiachik (Kamchatka), Poás (Costa Rica), Ruapehu (New Zealand) and Kawah Ijen and Keli Mutu (Indonesia). Δ_HSO4⁻–S values are 28‰ for Keli Mutu, 26‰ for Kawah Ijen, 24‰ for Ruapehu, 23‰ for Poás, 22‰ for Maly Semiachik, 21‰ for Yugama, 13‰ for Bannoe, 9‰ for Niseko, 4‰ for Khloridonoe, and 0‰ for Noboribetsu, in the decreasing order. The SO₂ disproportionation reaction in the magmatic hydrothermal system below crater lakes where magmatic gases condense is responsible for high Δ_HSO4⁻–S values, whereas contribution of HSO₄⁻ produced through bacterial oxidation of reduced sulfur becomes progressively dominant for lakes with lower Δ_HSO4⁻–S values. Currently, Noboribetsu crater lake contains no HSO₄⁻ of magmatic origin. A 40-year period observation of δ³⁴S_HSO4⁻ and δ³⁴S_S values at Yugama indicated that the isotopic variations reflect changes in the supply rate of SO₂ to the magmatic hydrothermal system. This implies a possibility of volcano monitoring by continuous observation of δ³⁴S_HSO4⁻ values. The δ¹⁸O values of HSO₄⁻ and lake water from the studied lakes covary, indicating oxygen isotopic equilibration between them. The covariance gives strong evidence that lake water circulates through the sublimnic zone at temperatures of 140±30°C.     

Interactions between freshwater input, light, and phytoplankton dynamics on the Louisiana continental shelf

We examined the effects of freshwater flow and light availability on phytoplankton biomass and production along the Louisiana continental shelf in the region characterized by persistent spring–summer stratification and widespread summer hypoxia. Data were collected on 7 cruises from 2005 to 2007, and spatially-averaged estimates of phytoplankton and light variables were calculated for the study area using Voronoi polygon normalization. Shelf-wide phytoplankton production ranged from 0.47 to 1.75 mg C m⁻² d⁻¹ across the 7 cruises. Shelf-wide average light attenuation (k_d) ranged from 0.19–1.01 m⁻¹ and strongly covaried with freshwater discharge from the Mississippi and Atchafalaya Rivers (R²=0.67). Interestingly, we observed that the euphotic zone (as defined by the 1% light depth) extended well below the pycnocline and to the bottom across much of the shelf. Shelf-wide average chlorophyll a (chl a) concentrations ranged from 1.4 to 5.9 mg m⁻³ and, similar to k_d, covaried with river discharge (R²=0.83). Also, chl a concentrations were significantly higher in plume versus non-plume regions of the shelf. When integrated through the water-column, shelf-wide average chl a ranged from 26.3 to 47.6 mg m⁻², but did not covary with river discharge, nor were plume versus non-plume averages statistically different. The high integrated chl a in the non-plume waters resulted from frequent sub-pycnocline chl a maxima. Phytoplankton production rates were highest in the vicinity of the Mississippi River bird's foot delta, but as with integrated chl a were not statistically different in plume versus non-plume waters across the rest of the shelf. Based on the vertical distribution of light and chl a, a substantial fraction of phytoplankton production occurred below the pycnocline, averaging from 25% to 50% among cruises. These results suggest that freshwater and nutrient inputs regulate shelf-wide k_d and, consequently, the vertical distribution of primary production. The substantial below-pycnocline primary production we observed has not been previously quantified for this region, but has important implications about the formation and persistence of hypoxia on the Louisiana continental shelf.     

The high content of polyunsaturated fatty acids in Nannochloropsis limnetica (Eustigmatophyceae) and its implication for food web interactions, freshwater aquaculture and biotechnology

In the eustigmatophycean Nannochloropsis limnetica the content of polyunsaturated fatty acids (PUFA) is extremely high in comparison to different planktonic green algal taxa in freshwater ecosystems. The sums of n-6 and n-3 fatty acids in N. limnetica were ten-fold higher than in the other picoplankton Choricystis minor and Pseudodictyosphaerium jurisii, and higher than in the nanoplanktonic green algae Chlorella vulgaris, Monoraphidium neglectum and Scenedesmus obtusiusculus. The content of fatty acids in N. limnetica was highly variable under different culture conditions. The highest concentrations of PUFA in N. limnetica were found in non-aerated suspension cultures, with a high content of phosphate (40 mg l⁻¹ K₂HPO₄) in the culture medium: linoleic acid 22.19 mg g⁻¹ DW, arachidonic acid 10.52 mg g⁻¹ DW, and eicosapentaenoic acid 55.56 mg g⁻¹ DW. N. limnetica represent a high-quality food resource in freshwater food chains. Furthermore, cultures of this eustigmatophycean alga have a high potential for use in biotechnology and aquaculture.     

Modern and Pleistocene boron isotope composition of the benthic foraminifer Cibicidoides wuellerstorfi

Here we present the first species-specific study of boron isotopes in the epibenthic foraminifer species Cibicidoides wuellerstorfi. Coretop samples from a water depth profile from 1000 to 4500 m on the northern flank of the Walvis Ridge are 4.4‰ lower than the values expected, based on calculations of the δ¹¹B_borate of ambient seawater. Similar values for this foraminifer species are presented from ODP site 668B at the Sierra Leone Rise, in the equatorial Atlantic. The consistency between data of the same species suggests the offsets are primary, rather than diagenetic. Glacial C. wuellerstorfi from ODP 668B and Walvis Ridge have boron isotope compositions only slightly different to interglacial samples, that is no larger than + 0.10 pH units, or + 23 µmol kg^− 1 in [CO₃²⁻] above the reconstructed glacial lysocline, and − 0.07 pH units, or − 14 µmol kg^− 1 in [CO₃²⁻] below. We use these results to suggest that glacial deep water pH in the Atlantic was similar to interglacial pH. The new data resolve the inconsistency between the previously reported high bottom water pH and the lack of significant carbonate preservation of the glacial deep ocean.     

Role of suspended sediments on the distribution of PCB in the Seine Estuary (France)

PCB (polychlorinated biphenyls) contamination and its relationship to SPM (suspended particulate material) have been studied in the Seine Estuary, which is heavily polluted by these persistent and hydrophobic man-made chemicals. Two sampling cruises have been performed during different freshwater discharge conditions. PCB and SPM concentrations, as well as grain-size distributions in the particulate material have been determined. Water samples have been collected at fixed positions during a tidal cycle, and along transects within the estuary.PCB concentrations vary from 2 ng 1⁻¹ in the marine zone to 250 ng 1⁻¹ within the estuary, and reach 1.3 × 10³ ng 1⁻¹ in the turbidity maximum zone. During a tidal cycle, low PCB concentrations are observed at high water, and are in the same range in February as in July. High PCB contamination is observed at low water, but PCB concentrations are about five times higher in February. SPM and PCB variations are well correlated in both periods of observations. Higher PCB contamination during February is explained by higher SPM inputs, mainly due to particles of riverine origin. The transport of PCB within the estuary depends on the quantity and the grainsize composition of suspended material, which varies according to freshwater discharge and tidal amplitude.     

Mathematical modeling of PCB bioaccumulation in Perna viridis

In the present work, we built a mathematical model of polychlorinated biphenyl (PCB) bioaccumulation in Perna viridis, namely, a one-compartment model with a time dependent incorporation rate R (μg g⁻¹ lipid per ppb water per day), with positive substrate cooperativity as the underlying physical mechanism. The temporal change of the PCB concentration Q (μg g⁻¹ lipid) in the soft tissues of the mussel depends on the competition of the input rate RW and the output rate kQ, where W is the concentration of PCB in water (ppb water) and k is the elimination rate (per day). From our experimental data, k=0.181±0.017 d⁻¹. The critical concentration in water W_c for positive substrate cooperativity was found to be 2.4 ppb. Below W_c, R is a constant. For a water concentration of 0.5 ppb Aroclor 1254, R=24.0±2.4 μg g⁻¹ lipid ppb⁻¹ d⁻¹. Above W_c, positive substrate cooperativity comes into effect and R becomes a function of time and dependent on the concentration Q in a form R=γQ/(Q+δ). This is the case for a water concentration of 5 ppb Aroclor 1254, where γ=15.1 μg g⁻¹ lipid ppb⁻¹ d¹ and δ≈200 μg g⁻¹ lipid. From this model, the uptake is exponentially increasing when the PCB concentration in the mussel is small compared to 200 μg g⁻¹ lipid, and hyperbolically increasing when the concentration is large compared to 200 μg g⁻¹ lipid, which are consistent with the experimental data. The model is useful for understanding the true processes taking place during the bioaccumulation and for risk assessment with higher confidence. Future experimental data which challenge the present model are anticipated and in fact desirable for improvement and perfection of the model.     

Authigenic carbonates in sediments from the Gulf of Mexico

The carbon isotopic composition of diagenetic dolomite and calcite in some sediments of the Gulf of Mexico varies between “normal-marine” (δ¹³C ca. 0‰) and −14.6‰ which suggests that biogenic CO₂ contributed to the carbonate formation. The δ¹³O values of dolomite and coexisting calcite are very similar but variable down-core.Dolomite and calcite precipitated early from pore water where SO₄²⁻ was not reduced. However, during (and after?) SO₄²⁻ reduction dolomite and calcite still formed and there are at least two generations of carbonate minerals present.     

Isotope geochemistry of minerals and fluids from Newberry volcano, Oregon

Isotopic compositions were determined for hydrothermal quartz, calcite, and siderite from core samples of the Newberry 2 drill hole, Oregon. The δ¹⁵O values for these minerals decrease with increasing temperatures. The values indicate that these hydrothermal minerals precipitated in isotopic equilibrium with water currently present in the reservoirs. The δ¹⁸O values of quartz and calcite from the andesite and basalt flows (700–932 m) have isotopic values which require that the equilibrated water δ¹⁸O values increase slightly (− 11.3 to −9.2‰) with increasing measured temperatures (150–265°C). The lithic tuffs and brecciated lava flows (300–700 m) contain widespread siderite. Calculated oxygen isotopic compositions of waters in equilibrium with siderite generally increase with increasing temperatures (76–100°C). The δ¹⁸O values of siderite probably result from precipitation in water produced by mixing various amounts of the deep hydrothermal water (− 10.5 ‰) with meteoric water (− 15.5 ‰) recharged within the caldera. The δ¹³C values of calcite and siderite decrease with increasing temperatures and show that these minerals precipitated in isotopic equilibrium with CO₂ of about −8 ‰.The δ¹⁸O values of weakly altered (<5% alteration of plagioclase) whole-rock samples decrease with increasing temperatures above 100°C, indicating that exchange between water and rock is kinetically controlled. The water/rock mass ratios decrease with decreasing temperatures. The δ¹⁸O values of rocks from the bottom of Newberry 2 show about 40% isotopic exchange with the reservoir water.The calculated δ¹⁸O and δD values of bottom hole water determined from the fluid produced during the 20 hour flow test are −10.2 and −109‰, respectively. The δD value of the hydrothermal water indicates recharge from outside the caldera.     

Phytoplankton dynamics within Gulf Stream intrusions on the southeastern United States continental shelf during summer 1981

During July and August 1981 subsurface intrusion of upwelled nutrient-rich Gulf Stream water was the dominant process affecting temporal and spatial changes in phytoplankton biomass and productivity of the southeastern United States continental shelf between 29 and 32°N latitude. Intruded waters in the study area covered as much as 10¹ km including virtually all of the middle and outer shelf and approximately 50% of the inner shelf area.Within 2 weeks following a large intrusion event in late July, middle shelf primary production and Chl a reached 3 to 4 gC m⁻ d⁻¹ and 75 mg m⁻, respectively. At the peak of the bloom 80% of the water column primary production occurred below the surface mixed-layer, and new primary production (i.e., NO₃-supported) exceeded 90% of the total. Chl a-normalized photosynthetic rates were very high as evidenced by high mean assimilation number (15.5 mg C mg Chl a⁻¹ h⁻¹), high mean α (14 mg C mg Chl a⁻¹ Ein⁻¹ m), and no photoinhibition. As a result of the high photosynthetic rates, mean light-utilization index (Ψ) was 2 to 3 times higher than reported for temperature sub-arctic and arctic waters.The results imply a seasonal (June to August) middle shelf production of 150 g C m⁻¹, about 15% higher than previous estimates of annual production on the middle shelf. Intrusions of the scale we observed in 1981 may not occur every summer. However, when such events do occur, they are by far the most important processes controlling summer phytoplankton dynamics of the middle and outer shelf and of the inner shelf in the southern half of the study area.     

Temperature dependence of the oxygen isotopic fractionation between diatom silica and water

We present a new paleotemperature scale, based on the oxygen isotopic ratio of the non-exchangeable fraction of the oxygen from diatom silica. The equation t = 17.2 − 2.4 (δ¹⁸O_silica − δ¹⁸O_water − 40) − 0.2 (δ¹⁸O_silica − δ¹⁸O_water − 40)² was derived using recent sediment samples from different oceanic areas, the temperature and isotopic composition of the local surface water. Comparison of our results with other relationships established for quartz-water or amorphous silica-water at higher temperature suggests no difference in isotopic fractionation between quartz-water and biogenic silica-water couples.     

Distribution, abundance and life history of Mysis relicta (Lovén) in the Feldberg Lake District, Germany

Distribution, abundance and life history characteristics of Mysis relicta were studied in the Feldberg Lake District (Lake Breiter Luzin, Lake Schmaler Luzin, Lake Zansen) located in northeastern Germany. Between July 2001 and November 2002 mysids were collected by vertical net hauls. In order to determine the impact of the current trophic conditions on the distribution of mysids in these lakes, oxygen concentration, total phosphorus, chlorophyll a and water transparency were also measured. All investigated lakes are mesotrophic at present. Lake Breiter Luzin exhibited great seasonal and spatial variations in mysid abundance. Density of adults and juveniles had a mean of 44.9 ± 57.1 and 68.7 ± 99.6 m⁻², respectively. Highest abundance of adults was 110.4 ± 76.5 m⁻² in summer, lowest abundances of 2.0 ± 4.0 m⁻² occurred in spring. For juveniles, highest density of 218.4 ± 174.6 m⁻² was detected in summer and lowest of 0.8 ± 1.8 m⁻² in winter. No mysids were caught in any of the daytime hauls, but they were widely distributed throughout the water column at night. Size frequency distribution of mysids suggested that reproduction occurred year-round, the most consistent influx of juveniles occurred in early summer and a smaller second cohort in autumn. Highest mysid abundance was 189.2 ± 318.6 adults and 127.0 ± 66.3 juveniles m⁻² in Lake Schmaler Luzin, and 59.6 ± 5.6 adults and 79.4 ± 11.2 juveniles m⁻² in Lake Zansen. There were great spatial differences in abundance in both lakes.     

A new analytical solution for water table fluctuations in coastal aquifers with sloping beaches

The Boussinesq equation appears as the zeroth-order term in the shallow water flow expansion of the non-linear equation describing the flow of fluid in an unconfined aquifer. One-dimensional models based on the Boussinesq equation have been used to analyse tide-induced water table fluctuations in coastal aquifers. Previous analytical solutions for a sloping beach are based on the perturbation parameter, _N=αcotβ (in which β is the beach slope, α is the amplitude parameter and is the shallow water parameter) and are limited to tan⁻¹(α)βπ/2. In this paper, a new higher-order solution to the non-linear boundary value problem is derived. The results demonstrate the significant influence of the higher-order components and beach slope on the water table fluctuations. The relative difference between the linear solution and the present solution increases as and α increase, and reaches 7% of the linear solution.     

Fluxes of selected trace metals from the Seine estuary to the eastern English Channel during the period August 1994 to July 1995

Two sampling cruises conducted in the Seine estuary (France) under low-water and flood conditions produced high resolution profiles for dissolved cadmium, lead, copper, zinc and nickel concentrations versus salinity. The distribution of dissolved trace metals differed depending on hydrologic conditions, partly because of the dilution of upstream inputs during flood periods. Daily fluxes of these dissolved trace metals were estimated for the two sampling periods (September 1994 and February 1995) by extrapolating the dilution lines observed in higher salinity waters to salinity=0 and then multiplying the effective freshwater concentrations thus obtained by the corresponding freshwater flow. Several procedures were subsequently applied to deduce each daily flux for the year studied from data for these two periods. A consensus was found among these procedures, allowing the determination of net fluxes of dissolved trace metals with a precision of 20–35%. The net fluxes thus estimated were 4 T yr⁻¹ for Cd, 4 T yr⁻¹ for Pb, 40 T yr⁻¹ for Cu, 130 T yr⁻¹ for Zn and 50 T yr⁻¹ for Ni.     

Organic biomarkers for tracing carbon cycling in the Gulf of Papua (Papua New Guinea)

Sediment traps were deployed in the Gulf of Papua in June–July 1997, to determine fluxes of organic matter and inorganic elements from the photic zone to deeper waters at the base of the continental slope and in the northern Coral Sea. Three stations, ranging from 900 to 1500 m depth, had “shallow” traps at 300 m below the water surface and “deep” traps set 100 m above the bottom. Infiltrex II water samplers collected particulate and dissolved organic matter from the Fly, Purari and Kikori rivers, and near-surface water from the shelf of the Gulf of Papua. Samples were analysed for molecular organic biomarkers to estimate the sources of organic carbon and its cycling processes.Dry weight fluxes from the shallow traps ranged from 115 to 181 mg m⁻² day⁻¹ and particulate organic carbon (POC) fluxes ranged from 1.2 to 1.9 mM OC m⁻² d⁻¹ with molar organic carbon to particulate nitrogen ratios (C/N) ranging from 6.0 to 6.5. Fluxes in deep traps were likely influenced by both early diagenesis and entrapment of resuspended shelf sediments. Dry weight fluxes in deep traps ranged from 106 to 574 mg m⁻² day⁻¹ and POC fluxes ranged from 0.6 to 1.5 mM OC m⁻² d⁻¹, with C/N ratios ranging from 8.5 to 10.8. ¹³C/¹²C ratios were −20.2‰ to −21.7‰ in all trap samples, indicating that most of the settling POC was “marine-derived”. Shallow traps had δ¹⁵N values of 6.3‰ to 7.2‰ while the values in deep traps were 4.9–5.0‰, indicating the N-rich near-surface OC was less degraded than that in the deep traps. The biogenic lipids consisted of hydrocarbon, sterol and fatty acid biomarkers indicative of marine zooplankton, phytoplankton and bacteria. Sterol markers for diatoms and dinoflagellates were abundant in the water samples. Highly branched isoprenoid alkenes, usually attributable to diatoms, were also detected in both water and shallow traps. Traces of C₂₆–C₃₄ n-alcohols indicative of land–plant biomarkers, were found in river water samples and in the shallow sediment traps. A large unresolved complex mixture (UCM) of hydrocarbons, and a uniform distribution of n-alkanes, indicative of petroleum hydrocarbons, were also detected in the traps. Hopane and sterane biomarkers detected in the trap oil were characteristic of a marine carbonate source, and the aromatic hydrocarbon composition distinguished at least two different oil signatures.We concluded that mass and POC fluxes were similar to those reported for other continental shelves and marginal oceans in tropical and subtropical regions. There was a dramatic decrease in POC as particles sank, due to zooplankton repackaging and photochemical and bacterial decomposition. Carbon isotopic and biomarker patterns showed most of the POC in the sediment traps was marine-sourced with only traces of terrestrial input. There was a significant flux of petroleum, which may signal the existence of natural petroleum seeps in this region.     

An anomalous subauroral red arc on 4 August, 1972: comparison of ISIS-2 satellite data with numerical calculations

This study compares the Isis II satellite measurements of the electron density and temperature, the integral airglow intensity and volume emission rate at 630 nm in the SAR arc region, observed at dusk on 4 August, 1972, in the Southern Hemisphere, during the main phase of the geomagnetic storm. The model results were obtained using the time dependent one-dimensional mathematical model of the Earth’s ionosphere and plasmasphere (the IZMIRAN model). The major enhancement to the IZMIRAN model developed in this study to explain the two component 630 nm emission observed is the analytical yield spectrum approach to calculate the fluxes of precipitating electrons and the additional production rates of N⁺₂, O⁺₂, O⁺(⁴S), O⁺(²D), O⁻(²P), and O⁺(²P) ions, and O(¹D) in the SAR arc regions in the Northern and Southern Hemispheres. In order to bring the measured and modelled electron temperatures into agreement, the additional heating electron rate of 1.05 eV cm⁻³ s⁻¹ was added in the energy balance equation of electrons at altitudes above 5000 km during the main phase of the geomagnetic storm. This additional heating electron rate determines the thermally excited 630 nm emission observed. The IZMIRAN model calculates a 630 nm integral intensity above 350 km of 4.1 kR and a total 630 nm integral intensity of 8.1 kR, values which are slightly lower compared to the observed 4.7 kR and 10.6 kR. We conclude that the 630 nm emission observed can be explained considering both the soft energy electron excited component and the thermally excited component. It is found that the inclusion of N₂(v > 0) and O₂(v > 0) in the calculations of the O⁺(⁴S) loss rate improves the agreement between the calculated N_e and the data on 4 August, 1972. The N₂(v > 0) and O₂(v > 0) effects are enough to explain the electron density depression in the SAR arc F-region and above F2 peak altitude. Our calculations show that the increase in the O⁺ + N₂ rate factor due to the vibrationally excited nitrogen produces the 5–19% reductions in the calculated quiet daytime peak density and the 16–24% decrease in NmF2 in the SAR arc region. The increase in the O⁺ + N₂ loss rate due to vibrationally excited O₂ produces the 7–26% decrease in the calculated quiet daytime peak density and the 12–26% decrease in NmF2 in the SAR arc region. We evaluated the role of the electron cooling rates by low-lying electronic excitation of O₂(a¹δ_g) and O₂(b¹σ_g⁺), and rotational excitation of O₂, and found that the effect of these cooling rates on T_e can be considered negligible during the quiet and geomagnetic storm period 3–4 August, 1972. The energy exchange between electron and ion gases, the cooling rate in collisions of O(³P) with thermal electrons with excitation of O(¹D), and the electron cooling rates by vibrational excitation of O₂ and N₂ are the largest cooling rates above 200 km in the SAR arc region on 4 August, 1972. The enhanced IZMIRAN model calculates also number densities of N₂(B³π_g⁺), N₂(C³π_u), and N₂(A³σ_u⁺) at several vibrational levels, O(¹S), and the volume emission rate and integral intensity at 557.7 nm in the region between 120 and 1000 km. We found from the model that the integral integral intensity at 557.7 nm is much less than the integral intensity at 630 nm.     

Ra in the Japan Sea and the residence time of the Japan Sea water

The surface water of the Japan Sea contained²²⁶Ra of70 ± 4dpm m⁻³ which was nearly equal to that of the surface water in the North Pacific. The concentration of²²⁶Ra in the Japan Sea deep water below 500 m was151 ± 8dpm m⁻³, showing a vertically and regionally small variation. This concentration of²²⁶Ra in the deep water is unexpectedly high, because the Japan Sea deep water has a higher Δ¹⁴ C value by about 50‰ than the Atlantic deep water containing the same²²⁶Ra. One of the causes to be considered is larger contribution of²²⁶Ra from biogenic particles dissolving in the Japan Sea deep water, but the Japan Sea is not so fertile in comparison to the Bering Sea. The other more plausible cause is the internal ventilation of the Japan Sea water, which means that the residence time of the Japan Sea Proper water is considerably long although the water is vertically mixed fairly well especially in winter. The ventilation may supply some amounts of radiocarbon and oxygen but does not change the inventory of²²⁶Ra. The residence times of the Japan Sea deep water and of water within the Japan Sea are calculated by solving simultaneous equations for²²⁶Ra and¹⁴C with a three-box model to be 300–400 years and 700–1000 years, respectively.     

Sources of chloride in hydrothermal fluids from the Valles caldera, New Mexico: a Cl study

The Valles caldera in New Mexico hosts a high-temperature geothermal system, which is manifested in a number of hot springs discharging in and around the caldera. In order to determine the fluid pathways and the origin of chloride in this system, we measured ³⁶Cl/Cl ratios in waters from high-temperature drill holes and from surface springs in this region. The waters fall into two general categories: recent meteoric water samples with low Cl⁻ concentrations (< 10 mg/L) and relatively high ³⁶Cl/Cl ratios [(300–1000) × 10⁻¹⁵]; and geothermal brines with high Cl⁻ concentrations (800–9400 mg/L) but low ³⁶Cl/Cl ratios [(11–26) × 10⁻¹⁵]. The ³⁶Cl/Cl ratios for meteoric waters are slightly higher than expected for this region, suggesting a small addition of anthropogenic ³⁶Cl. Because of low ³⁶Cl/Cl ratios and high Cl⁻ concentrations in the brines, chloride in these waters must be derived from subsurface sources. A comparison between the observed ³⁶Cl/Cl ratios in the brines and those calculated for potential source formations in this region indicates that the present host formations, mainly volcanic tuffs, cannot be major sources of chloride, and that formations at greater depth, such as the Paleozoic and Precambrian formations are more likely to be sources of chloride in the brines. The results suggest that brines are meteoric waters which penetrated into the basement where they derive chloride from leaching of basement rocks and/or from saline pore fluids trapped there, along with likely addition of chloride from Paleozoic strata. Although these fluids have since come to reside in the intracaldera volcanic sequence after convective upwelling, they do not derive much Cl⁻ from the volcanic strata; and residence times of fluids in the volcanics are < 100,000 years.     

Seasonal dynamics of zooplankton in Lake Huetzalin, Xochimilco (Mexico City, Mexico)

We quantified the seasonal changes in the zooplankton abundances collected from the Huetzalin Lake (Mexico City, Mexico) for two years (February 2003–January 2004 and then March 2005–February 2006). Selected physicochemical variables (Secchi depth, temperature, pH, conductivity, dissolved oxygen, phosphorus, nitrogen, carbon and chlorophyll a concentration) were also measured at the time of zooplankton collection. The data on zooplankton abundances and the physicochemical variables were subjected to multiple correlation analysis and we also derived Shannon–Wiener species diversity index. Secchi depth ranged from 9 to 65 cm. Generally the lake was alkaline (pH 7–12). The conductivity ranged from 500–1000 mS cm⁻¹, while the mean water temperature was 20.5 °C. Dissolved oxygen levels were generally >3 mg L⁻¹ and were higher in the winter than warmer months. Nitrates (90–95 μg L⁻¹) and phosphates (.2–.5 mg L⁻¹) indicated that the water was eutrophic. Chlorophyll a levels ranged from 143 to 696 μg L⁻¹ during the study period. The zooplankton community was dominated by rotifers (46 species), followed by cladocerans (9 species) and there were only two copepod species. The dominant rotifer species were Brachionus angularis, Brachionus calyciflorus, Brachionus havanaensis, Brachionus quadridentatus, Lecane bulla and Polyarthra vulgaris. Rare rotifer species in Lake Huetzalin were Lecane ohioensis, Dicranophorus forcipatus, Lecane pyriformis, Lindia torulosa, Pleurotrocha petromyzon and Brachionus durgae. Highest densities (occasional peaks of 400 ind L⁻¹) of B. quadridentatus occurred between April and December, while B. havanaensis reached peak densities, during June to October. B. calyciflorus reached densities higher than 1240 ind L⁻¹ during May–September. Cladoceran and copepod densities in Lake Huetzalin were much lower than that of the rotifers. This study confirmed the earlier findings that Xochimilco system of canals is dominated by rotifers and the crustacean zooplankton have much lower abundances possibly due to predation from fish.