Geochemical significance of tricyclic and tetracyclic terpanes in source rock extracts from the Offshore Niger Delta Basin,Nigeria

Tricyclic and tetracyclic terpanes are important constituents of crude oil and source rock extracts.However,they have not been reported in the Offshore Niger Delta Basin,Nigeria.Thus,the present study investigated the geochemical significance of tricyclic and tetracyclic terpanes in source rock extracts from the Offshore Niger Delta Bain,Nigeria with gas chromatography-mass spectrometry(GC-MS).The total relative abundances of tricyclic terpanes,C_(19)TT-C_(21)TT,and C23 TT in the rock samples ranged from 82.50 to 96.37%,50.08 to 74.17%,and 25.83 to 49.92%,respectively.These values showed the source rocks were formed from a mixed origin(terrestrial and marine).Among the tricyclic and tetracyclic terpanes identified in the rock extracts,the conventional(C_(20)TT,C_(23)TT,C_(24)TT,C_(24)TeT) and recent(Y1,X1,Z1)were more prominent than all others,indicating mixed input of terrigenous and marine organic matter.The C_(24)TT/C_(23)TT,C_(24)TeT/(C_(24)TeT+C_(26)TT),C_(19)TT/C_(23)TT,C_(20)TT/C_(23)TT,C_(25)TT/C_(24)TeT,C_(25)TT/C_(26)TT,C_(19)TT/C_(20)TT,C_(24)TeT/C_(26)TT,Z1/(Z1+C_(24)TT),and Y1/(Y1+C~(24)TT)in the rock samples range from 0.33 to 1.30,0.76 to 0.90,0.18 to 0.73,0.34 to 1.05,0.33 to 1.74,0.30 to 1.39,0.31 to0.89,1.66 to 4.33,0.36 to 0.83,and 0.34 to 0.79,respectively.These values further showed that the rock samples were formed from mixed input of terrigenous and marine organic matter and deposited under oxic to suboxic conditions in lacustrine-fluvial/deltaic environments.Also,the C_(24)TeT/C_(20-26)TT,C_(24)TeT/C_(30)HOP,and C_(23)TT/C_(30)HOP ranged from 0.16 to 0.45,0.02 to 0.42,and 0.01 to 0.48,respectively.This range of values suggests that source rocks were within immature to early mature stage.Thus,this study showed that tricyclic and tetracyclic terpanes were effective in determining the origin,depositional environments,and thermal maturity of source rocks in the Niger Delta Basin,Nigeria.     

In situ cosmogenic ~(10)Be,~(26)Al,and ~(21)Ne dating in sediments from the Guizhou Plateau,southwest China

Landscape evolution is modulated by the regional tectonic uplift,climate change,and river dynamics.However,how to distinguish these mechanisms through the research of surface exhumation and fluvial incision remains controversial.In this study,cosmogenic~(10)Be,~(26)Al,and~(21)Ne concentrations in quartz from cave deposits,modern river sediments,and bedrocks were measured to constrain the applicability of cosmogenic~(21)Ne and discuss Quaternary landscape evolution history in the Guizhou Plateau,southeast China.Using the~(26)Al-~(10)Be and~(21)Ne-~(10)Be pairs to distinguish the cosmogenic~(21)Ne concentration from the excess~(21)Ne,we found that the nucleogenic~(21)Ne produced by the U and Th decay in quartz is significant in the samples although there is the possibility of inherited cosmogenic~(21)Ne.Combining with previous studies,we suggest that the precise approach for applying the cosmogenic~(21)Ne could be reached by (1) estimating the contribution from nucleogenic~(21)Ne,(2) avoiding samples with complex burial histories to exclude inherited cosmogenic~(21)Ne,and (3) combining the~(10)Be-~(26)Al-~(21)Ne nuclides method for the Quaternary samples.In addition,both pre-burial basin denudation rates and burial ages derived from the~(26)Al-~(10)Be pair were used to determine the different timescale surface denudation rate and fluvial incision rate in relation to previous work.The consistency of the different timescales pre-burial basin denudation rate,~(36)Cl surface denudation rate,and modern basin denudation rate indicates that the landscape-scale surface denudation has been likely stabilized since the Quaternary in the Guizhou Plateau area.The slightly higher river incision rates than the local surface denudation rate show that the river dynamics may not have reached a steady-state due to the regional tectonic uplift in the Guizhou Plateau.     

Toxicities of ten metals to Crassostrea gigas and Mytilus edulis embryos and Cancer magister larvae

Pacific oyster (Crassostrea gigas Thunberg) embryos, bay mussel (Mytilus edulis Linnaeus) embryos, and Dungeness crab (Cancer magister Dana) zoea I stage larvae were exposed to arsenic, cadmium, chromium, copper, lead, mercury, nickel, selenium, silver, and zinc salts. The two bivalve species were exposed through the completion of embryogenesis (48 h), and the effects of the metals upon abnormal development were monitored. The crab larval stages were exposed to the metal solutions for 96 h. Concentrations (μg l_.^?1 as metal) which caused 50% abnormal development in the two species of bivalve larvae and which were fatal to 50% of the crab larvae ranged from 5.3 (oyster) to 49 (crab) for copper; 5.8 (mussel) to 8.2 (crab) for mercury; 14 (mussel) to 55 (crab) for silver; 119 (oyster) to 456 (crab) for zinc; 232 (crab) to 3000 (mussel) for arsenic; 247 (crab) to 1200 (mussel) for cadmium; 349 (oyster) to 4360 (crab) for nickel; 476 (mussel) to 758 (oyster) for lead; 3440 (crab) to 4538 (oyster) for hexavalent chromium; and selenium greater than 10 000 for the three species. The acute toxicity testing of C. gigas embryo together with two California native species confirmed its usefulness for predicting toxicity to the latter species.     

210Po and 210Pb variations in fish species from the Aegean Sea and the contribution of 210Po to the radiation dose

In recent years, there has been increasing interest in the significance of natural radionuclides, particularly (210)Po, in the marine environment. (210)Po, a naturally occurring alpha emitter, accumulates in marine organisms and reflects differences in their diets. In the literature, there is no data for (210)Po and (210)Pb activity concentrations for fish species on the Turkish coast of Aegean Sea. Therefore, in this study, multiple fish species were collected from six stations seasonally on the Turkish coast of Aegean Sea and were analyzed for their (210)Po and (210)Pb content. The (210)Po and (210)Pb concentrations in the fish samples were found to vary from undetectable levels to 499 ± 44 Bq kg(-1) dry weight (dw) and from 1.0 ± 0.3 Bq kg(-1) to 35 ± 4.0 Bq kg(-1) (dw), respectively. There were no significant differences in the activity concentrations of (210)Po and (210)Pb in fish samples between seasons (ANOVA, P>0.05). The highest dose contribution of (210)Po to humans was calculated to be 10,530 μSv year(-1).     

Carbon and nitrogen cycling in the Zhubi coral reef lagoon of the South China Sea as revealed by 210Po and 210Pb

The radionuclides (210)Po and (210)Pb were examined to trace the cycling of particulate organic carbon (POC) and particulate organic nitrogen (PON) in the Zhubi coral reef lagoon. The net export flux of POC to the open sea is 14 mg Cm(-2) d(-1). However, the net exchange of PON has not yet been observed. On average, the vertical export fluxes in the lagoon of POC and PON, as derived from (210)Po/(210)Pb disequilibria, are 43 mg Cm(-2) d(-1) and 13.8 mg Nm(-2) d(-1), respectively. The deficit of (210)Po relative to (210)Pb in particulate matter provides evidence for the degradation of particulate organic matter. According to the mass balance budgets, 310 mg Cm(-2) d(-1) and 121 mg Nm(-2) d(-1) were recycled into dissolved fractions. Based on a first-order kinetics model, the degradation rate constants of POC and PON are 0.28 and 0.30 m(-1), respectively. Thus, (210)Po and (210)Pb can quantify the cycling of carbon and nitrogen in this coral lagoon.     

Determination of arsenic(III) for the investigation of the microbial oxidation of arsenic(III) to arsenic(V)

Recent evaluations of acute and chronical toxicity of arsenic resulted in a reduction of the standard value for total arsenic from 40 μg/L to 10 μg/L in drinking water which will be valid in Germany after a transition period as from January 1996. Arsenic is well known as substance of deep groundwaters, mainly of geogenic origin and normally found as As(III) or As(V). As(V) is well removable by flocculation and filtration after adding iron salts. As(III), however, has to be oxidized first to As(V). Therefore, it is important for treatment techniques to be able to distinguish between As(III) and As(V). A modified determination of As(III) using flow injection analysis was installed and optimized in order to investigate whether As(III) may be oxidized to As(V) by bacteria in natural waters. The results showed that at 4°C, no As(III)-oxidation was observed within 14 days. At room temperature, however, in the bacteria-containing samples, an As(III)-oxidation was found starting after 3 to 7 days. After 14 days, no As(III) was left over. In contrast, in the sterile samples, no As(III)-oxidation could be observed within 14 days. These results demonstrated that microbial processes influence the oxidation of As(III) to As(V) in natural waters.     

Mycorrhizal Colonization Affects the Survival of Vetiveria zizanioides (L.) Nash Grown in Water Containing As(III)

The presence of arsenic (As) in water is of great public concern. Arsenic exists in three common valence states viz., As(0) metalloid arsenic, As(III) (arsenite) and As(V) (arsenate). Arsenite [As(III)] is the most toxic form among arsenicals which, predominates in anaerobic conditions, generally in flooded soils and in the water with high BOD. Experiments were conducted to investigate the effect of As(III) on the mycorrhization in vetiver (Vetiveria zizanioides (L.) Nash) grass in hydroponics. Studies showed significant alteration in the mycorrhizal colonization in the roots of vetiver exposed to higher concentrations of As(III) starting from 1.0, 2.0, 3.0, 4.0 to 5.0 mg/L prepared in 5% Hoagland nutrient solution without addition of phosphate ions. Considerable reduction in the mycorrhizal intensity (M) was observed in all the treatment sets as compared to the control suggesting a negative impact of the As(III) on the mycorrhizal association. Simultaneously, the study also showed that, As(III) is toxic to the vetiver plants having mycorrhizal association however plants with non‐mycorrhizal (cleansed) roots were found to be able to survive for a longer period exposed to As(III).     

Peroxymonosulfate Improves the Activity and Stability of Manganese Oxide for Oxidation of Arsenite to Arsenate

Manganese oxide has been widely investigated for oxidation of arsenite (As(III)) to arsenate (As(V)) due to its high redox potential; however, it becomes extremely unstable after reuse. Here, As(III) oxidation activity and stability of manganese oxide in the presence of peroxymonosulfate (PMS) is investigated. Batch experimental results reveal that manganese oxide/PMS exhibits high catalytic activity for As(III) oxidation compared to manganese oxide or PMS alone. Addition of PMS to manganese oxide not only reveals long‐term stability for As(III) oxidation, but also shows high As(III) oxidation activity in the presence of coexisting ions such as As(V) and phosphate. Quenching tests reveal that As(III) oxidation in the manganese oxide/PMS system is attributed to activation of PMS by manganese oxide at different oxidation states (Mn(III) and Mn(IV)), and the generation of sulfate radicals that are responsible for As(III) oxidation.     

First experiments on the maternal transfer of metals in the cuttlefish Sepia officinalis

The aim of this study was to provide a first insight on the incorporation of eight metals in the eggs of the cuttlefish Sepia officinalis via maternal transfer, using radiotracer techniques ((110m)Ag, (241)Am, (109)Cd, (60)Co, (134)Cs, (54)Mn, (75)Se and (65)Zn). The cuttlefish was fed daily with radiolabelled crabs for two weeks; it then started to spawn every three days. Among the eight tracers, only (110m)Ag, (75)Se and (65)Zn were significantly transferred to the eggs. The radiotracer distribution among the egg compartments showed that (75)Se and (65)Zn were accumulated mainly in the vitellus whereas (110m)Ag was found in similar proportion in the vitellus and the eggshell. During the embryonic development, (75)Se and (65)Zn contained in the vitellus were progressively transferred to the embryo, likely to supply its metabolic needs in these essential elements. Although it has no known biological functions, Ag contained in both vitellus and eggshell was also transferred to the embryo. Overall, our results showed that transfer of Ag, Se, and Zn does actually occur from a female cuttlefish to its eggs, at least during the last two weeks before spawning.     

Effect of prolonged hypoxia on food consumption, respiration, growth and reproduction in marine scavenging gastropod Nassarius festivus

The effects of prolonged exposure to reduced oxygen levels (3.0 and 1.5 mg O(2)l(-1)) on marine scavenging gastropods Nassarius festivus were studied for 8 weeks. The percentages of individuals engaged in feeding and amount of food consumed were reduced as oxygen level decreased; absorption efficiency, however, did not vary significantly with oxygen level. Oxygen consumption rates and specific oxygen consumption rates were lower at reduced oxygen levels. Reproduction occurred at all oxygen levels with less egg capsules being produced at lower oxygen levels. Egg size and number of eggs per capsule, however, were not significantly affected by oxygen level. The increase in shell length was 12%, 6% and 5% at 6.0 mgO(2)l(-1) (normoxia), 3.0 mgO(2)l(-1) and 1.5 mgO(2)l(-1), respectively. At the end of the experiment, the amount of energy allocated to growth and reproduction decreased at reduced oxygen levels with values obtained at 3.0 mgO(2)l(-1) and 1.5 mgO(2)l(-1) being 48% and 70% lower than those at 6.0 mgO(2)l(-1). At all oxygen levels, most of the accumulated energy was allocated to shell growth and reproduction, and the amount allocated to somatic growth was relatively insignificant. The reduction in energy allocated to reproduction was greater than that to shell growth as the oxygen level was reduced, indicating a strategic energy allocation of marine scavengers under stressful conditions to enhance survival.     

Acute toxicity of temporally varying seawater CO2 conditions on juveniles of Japanese sillago (Sillago japonica)

CO(2) ocean storage by which liquefied CO(2) is injected into the deep-sea to mitigate the climate change would increase the CO(2) concentrations of the surrounding seawater. The biological impacts of such dynamic CO(2) environments are, however, unknown. We examined the acute toxicity of temporally changing seawater CO(2) concentrations on juveniles of Sillago japonica. Step-wise increases in ambient CO(2) to fCO(2) (fractional CO(2) concentration of the gas mixture bubbled into seawater) levels of 7% and 9% resulted in mortalities of 0.15 and 0.40-0.67 after 18 h, respectively. In contrast, one-step increases to these CO(2) levels killed all fish within 15 min. Further, a sudden drop of fCO(2) from 9-10% CO(2) to normocapnia (0.038%) killed all the surviving fish within a few minutes. These results demonstrate that impacts of ocean CO(2) storage need to be examined under conditions mimicking the dynamic changes in CO(2) levels expected to occur by the CO(2) injection procedure.     

Humic Substances as a Mediator for Microbially Catalyzed Metal Reduction

The potential for humic substances to serve as a terminal electron acceptor in microbial respiration and to function as an electron shuttle between Fe(III)-reducing microorganisms and insoluble Fe(III) oxides was investigated. The Fe(III)-reducing microorganism Geobacter metallireducens conserved energy to support growth from electron transport to humics as evidenced by continued oxidation of acetate to carbon dioxide after as many as nine transfers in a medium with acetate as the electron donor and soil humic acids as the electron acceptor. Growth of G. metallireducens with poorly crystalline Fe(III) oxide as the electron acceptor was greatly stimulated by the addition of as little as 100 μM of the humics analog, anthraquinone-2,6-disulfonate. Other quinones investigated, including lawsone, menadione, and anthraquinone-2-sulfonate, also stimulated Fe(III) oxide reduction. A wide phylogenetic diversity of microorganisms capable of Fe(III) reduction were also able to transfer electrons to humics. Microorganisms which can not reduce Fe(III) could not reduce humics. Humics stimulated the reduction of structural Fe(III) in clay and the crystalline Fe(III) forms, goethite and hematite. These results demonstrate that electron shuttling between Fe(III)-reducing microorganisms and Fe(III) via humics not only accelerates the microbial reduction of poorly crystalline Fe(III) oxide, but also can facilitate the reduction of Fe(III) forms that are not typically reduced by microorganisms in the absence of humics. Addition of humic substances to enhance electron shuttling between Fe(III)-reducing microorganisms and Fe(III) oxides may be a useful strategy to stimulate the remediation of soils and sediments contaminated with organic or metal pollutants.     

Depth-related influences on biodegradation rates of phenanthrene in polluted marine sediments of Puget Sound, WA

A whole-core injection method was used to determine depth-related rates of microbial mineralization of (14)C-phenanthrene added to both contaminated and clean marine sediments of Puget Sound, WA. For 26-day incubations under micro-aerobic conditions, conversions of (14)C-phenanthrene to (14)CO(2) in heavily PAH-contaminated sediments from two sites in Eagle Harbor were much higher (up to 30%) than those in clean sediments from nearby Blakely Harbor (<3%). The averaged (14)C-phenanthrene degradation rates in the surface sediment horizons (0-3 cm) were more rapid (2-3 times) than in the deeper sediment horizons examined (>6 cm), especially in the most PAH polluted EH9 site. Differences in mineralization were associated with properties of the sediments as a function of sediment depth, including grain-size distribution, PAH concentration, total organic matter and total bacterial abundance. When strictly anaerobic incubations (in N(2)/H(2)/CO(2) atmosphere) were used, the phenanthrene biodegradation rates at all sediment depths were two times slower than under micro-aerobic conditions, with methanogenesis observed after 24 days. The main rate-limiting factor for phenanthrene degradation under anaerobic conditions appeared to be the availability of suitable electron acceptors. Addition of calcium sulfate enhanced the first order rate coefficient (k(1) increased from 0.003 to 0.006 day(-1)), whereas addition of soluble nitrate, even at very low concentration (<0.5 mM), inhibited mineralization. Long-term storage of heavily polluted Eagle Harbor sediment as intact cores under micro-aerobic conditions also appeared to enhance anaerobic biodegradation rates (k(1) up to 0.11 day(-1)).     

Effect of iron type on kinetics and carbon isotopic enrichment of chlorinated ethylenes during abiotic reduction on Fe(0)

Four samples of two commercially available iron brands used as substrate for iron permeable reactive barriers (PRBs) were tested for suitability for remediation of perchloroethylene (PCE), trichloroethylene (TCE), cis-dichloroethylene (cDCE) and vinyl chloride (VC). Kinetic studies indicate that rates of reaction are enhanced for cDCE and VC on Connelly iron (2.8 x 10(-4) to 6.9 x 10(-4) L/m2/hr and 2.0 x 10(-4) to 9.0 x 10(-4) L/m2/hr, for cDCE and VC, respectively) vs. Peerless iron (3.1 x 10(-5) to 4.6 x 10(-5) L/m2/hr and 2.4 x 10(-5) to 4.1 x 10(-5) L/m2/hr, for cDCE and VC, respectively). Carbon isotopic analyses of the residual chlorinated ethylene (CE) during degradation indicate significant fractionation occurs during reductive dechlorination, with, for example, up to 70% enrichment in carbon isotopic values observed when VC is more than 99% degraded. Comparison of fractionation factors (epsilon) indicates significant differences in carbon isotopic fractionation for different iron types and for different CEs. For the lower CEs (cDCE and VC) in particular, both slower reaction rates and larger fractionation are observed for degradation on Peerless vs. Connelly iron. This is the first study to establish a correlation between the rate of abiotic degradation on Fe(0) and the extent of isotopic fractionation, and the first to confirm consistent differences in these two parameters as a function of iron type. The possibility that these differences in kinetics and carbon isotopic fractionation for cDCE and VC are related to differences in branching ratios between competing hydrogenolysis and beta-elimination reactions during reductive dechlorination on the iron surfaces is discussed.     

“Dead Zone” dynamics in Lake Erie: the importance of weather and sampling intensity for calculated hypolimnetic oxygen depletion rates

Calculated hypolimnetic oxygen depletion (HOD) rates depend not only on environmental factors but also logistical ones. In particular, lack of understanding of the effects of weather in addition to how sampling effort determines calculated HOD rates complicates ecological understanding and environmental management of lake ecosystems. To better determine the roles of weather and sampling effort, we combined (1) weekly measurements of temperature and dissolved oxygen (DO) concentrations from seven stations in the Sandusky subbasin of Lake Erie’s central basin during 2005, (2) contemporaneous measures of storm activity and tributary discharge, and (3) a two-dimensional coupled hydrodynamic, chemical, and biological model of Lake Erie to investigate (1) how increased storm activity and tributary discharge affected short- (daily) and long-term (seasonal) dynamics of hypolimnetic hypoxia, and (2) how spatial (number of sites sampled) and temporal (sampling frequency) sampling effort affected calculated HOD rates. Our model closely replicated field-observed DO dynamics. When comparing baseline modeled dynamics to those in a second simulation with twice the number of days with high winds, however, we found that with more storm activity (1) periods of entrainment became more frequent, (2) the hypolimnion was warmer, (3) thermal stratification occurred 1 month later, whereas autumnal turnover occurred at least 1 week earlier shortening the duration of stratification by 1–2 months, and (4) HOD rates increased 12%. Further, spatial and temporal sampling intensity also affected calculated HOD rates. Consequently, adequately quantifying actual HOD rates requires sufficient sampling effort and the particular role of weather should be assessed with rigorous field and simulation studies, especially if HOD rates are used to indicate management success.     

PAHs contamination and bacterial communities in mangrove surface sediments of the Jiulong River Estuary, China

Sixteen sediment samples collected from eight transects in a mangrove swamp of the Jiulong River Estuary, Fujian, China were investigated for their content of polycyclic aromatic hydrocarbons (PAHs) and the biodegradation potential of the indigenous microorganisms. The bacterial community structures in the mangrove sediments and in enrichment cultures were also investigated. The results showed that the total PAHs concentration of mangrove sediments ranged from 280 to 1074 ng g(-1) dry weight, that the PAHs composition pattern in the mangrove sediments was dominated by high molecular weight PAH components (4-6 rings), and that Benzo[ghi]perylene and Indeno[1,2,3-cd]pyrene were the most dominant at different stations. Abundant PAH-degrading bacteria were found in all the stations, the values of phenanthrene-degrading bacteria ranged from 5.85 x 10(4) to 7.80 x 10(5) CFU g(-1) dry weight, fluoranthene-degrading bacteria ranged from 5.25 x 10(4) to 5.79 x 10(5) CFU g(-1) dry weight, pyrene-degrading bacteria ranged from 3.10 x 10(4) to 6.97 x 10(5) CFU g(-1) dry weight and the benzo(a)pyrene-degrading bacteria ranged from 5.25 x 10(4) to 7.26 x 10(5) CFU g(-1) dry weight. DGGE analysis of PCR-amplified 16S rDNA gene fragments confirmed that there was a remarkable shift in the composition of the bacterial community due to the addition of the different model PAH compound phenanthrene (three ring PAH), fluoranthene(four ring PAH), pyrene(four ring PAH) and benzo(a)pyrene(five ring PAH) during enrichment batch culture. Eleven strains were obtained with different morphology and different degradation ability. The presence of common bands for microbial species in the cultures and in the native mangrove sediment DNA indicated that these strains could be potential in situ PAH-degraders.     

利用~(210)Pb、~(137)Cs和~(241)Am计年法测算云南抚仙湖现代沉积速率

通过对云南抚仙湖沉积物柱芯样品的~(210)Pb、~(137)Cs和~(241)Am测试表明,柱芯剖面上有明显的1963年和1986年~(137)Cs蓄积峰,验证了1975年次级蓄积峰存在的可能性,这些峰形完好的蓄积峰对抚仙湖的现代沉积环境有明显的时标意义。利用~(137)Cs计年法得到抚仙湖沉积物自1963年、1975年及1986年以来到2007年的平均沉积速率分别为0.063g/(cm~2·a)、0.052g/(cm~2·a)和0.039g/(cm~2·a),说明了过去近五十年抚仙湖沉积速率整体上经历了一个由快到慢的过程。借助于~(241)Am的1963年蓄积峰可以提高~(137)Cs计年的准确性。根据~(210)Pb CRS计年模式,计算出每个样品深度所对应的年代,与~(137)Cs计年法比较存在一定的偏差,分析了两种计年方法存在差异性的原因。通过质量深度和年代分析,抚仙湖的沉积速率变化幅度比较大,表明抚仙湖近129年来的沉积环境不稳定,可能与相应历史时期的人类活动有密切的关系。     

Benthic primary production during emersion: In situ measurements and potential primary production in the Seine Estuary (English Channel, France)

A two year survey of benthic primary production during periods of emersion was performed on two stations of an intertidal mudflat (a muddy-sand station and a muddy station) in the Seine Estuary (English Channel, France). The goals of this study were to investigate the seasonal variations of metabolism, to estimate daily potential primary production variation at the annual scale and to estimate the annual potential primary production of the mudflat. Primary production and respiration were estimated by in situ measurements of carbon dioxide fluxes. Chlorophyll a concentration exhibited a great variability on both locations. Gross community production ranged from ca. 0 to 77 mg C m(-2) h(-1) at the muddy-sand location and from ca. 0 to 122 mg C m(-2) h(-1) at the muddy location. Community respiration showed a seasonal trend following temperature variations (up to 28.51 mg C m(-2) h(-1) in the muddy-sand and up to 23.40 mg C m(-2) h(-1) in the mud). Daily potential primary production was calculated, according to seasonal variations of photosynthetic parameters calculated using three photosynthesis versus irradiance curves obtained for the muddy location. The annual gross community primary production was 135 g C m(-2) yr(-1), leading to a low autotrophic annual budget, considering an annual community respiration of 110 g C m(-2) yr(-1).     

Boron isotopes as an artificial tracer

A field study was conducted using a combination of intrinsic and artificial tracers to estimate travel times and dilution during transport of infiltrate from a reclaimed water infiltration basin to nearby monitoring wells. A major study objective was to validate boric acid enriched in (10)B as an artificial tracer. Basin 10E at the Rio Hondo Spreading Grounds in Whittier, California, was the site of the test. The basin normally receives a mixture of treated municipal waste water, purchased State Project water, and local runoff from the San Gabriel River. Approximately 3.5 kg of (10)B-enriched boric acid was dispersed among 2.05 x 10(5) m(3) of basin water to initiate the experiment. The resultant median delta(11)B in the infiltration basin was -71 per thousand. Prior to tracer addition, the basin water had an intrinsic delta(11)B of +2 per thousand. Local monitoring wells that were used to assess travel times had delta(11)B values of +5 per thousand and +8 per thousand at the time of tracer addition. Analytic results supported an assumption that boron is conserved during ground water transport and that boron enriched in (10)B is a useful artificial tracer. Several intrinsic tracers were used to reinforce the boric acid tracer findings. These included stable isotopes of oxygen (delta(18)O) and hydrogen (deltaD), sulfate concentration, and the boron to chloride ratio. Xenon isotopes, (136)Xe and (124)Xe, also supported boron isotope results. Xenon isotopes were added to the recharge basin as dissolved gases by investigators from the Lawrence Livermore National Laboratory.