Determining Spatial and Temporal Inputs of Freshwater,Including Submarine Groundwater Discharge,to a Subtropical Estuary Using Geochemical Tracers,Biscayne Bay,South Florida

Geochemical mixing models were used to decipher the dominant source of freshwater (rainfall, canal discharge, or groundwater discharge) to Biscayne Bay, an estuary in south Florida. Discrete samples of precipitation, canal water, groundwater, and bay surface water were collected monthly for 2 years and analyzed for salinity, stable isotopes of oxygen and hydrogen, and Sr²⁺/Ca²⁺ concentrations. These geochemical tracers were used in three separate mixing models and then combined to trace the magnitude and timing of the freshwater inputs to the estuary. Fresh groundwater had an isotopic signature (δ ¹⁸O = −2.66‰, δD −7.60‰) similar to rainfall (δ ¹⁸O = −2.86‰, δD = −4.78‰). Canal water had a heavy isotopic signature (δ ¹⁸O = −0.46‰, δD = −2.48‰) due to evaporation. This made it possible to use stable isotopes of oxygen and hydrogen to separate canal water from precipitation and groundwater as a source of freshwater into the bay. A second model using Sr²⁺/Ca²⁺ ratios was developed to discern fresh groundwater inputs from precipitation inputs. Groundwater had a Sr²⁺/Ca²⁺ ratio of 0.07, while precipitation had a dissimilar ratio of 0.89. When combined, these models showed a freshwater input ratio of canal/precipitation/groundwater of 37%:53%:10% in the wet season and 40%:55%:5% in the dry season with an error of ±25%. For a bay-wide water budget that includes saltwater and freshwater mixing, fresh groundwater accounts for 1–2% of the total fresh and saline water input.     

Variation and uncertainty in evaporation from a subtropical estuary: Florida Bay

Variation and uncertainty in estimated evaporation was determined over time and between two locations in Florida Bay, a subtropical estuary. Meteorological data were collected from September 2001 to August 2002 at Rabbit Key and Butternut Key within the Bay. Evaporation was estimated using both vapor flux and energy budget methods. The results were placed into a long-term context using 33 years of temperature and rainfall data collected in south Florida. Evaporation also was estimated from this long-term data using an empirical formula relating evaporation to clear sky solar radiation and air temperature. Evaporation estimates for the 12-mo period ranged from 144 to 175 cm yr⁻¹, depending on location and method, with an average of 163 cm yr⁻¹ (±9%). Monthly values ranged from 9.2 to 18.5 cm, with the highest value observed in May, corresponding with the maximum in measured net radiation. Uncertainty estimates derived from measurement errors in the data were as much as 10%, and were large enough to obscure differences in evaporation between the two sites. Differences among all estimates for any month indicate the overall uncertainty in monthly evaporation, and ranged from 9% to 26%. Over a 33-yr period (1970–2002), estimated annual evaporation from Florida Bay ranged from 148 to 181 cm yr⁻¹, with an average of 166 cm yr⁻¹. Rainfall was consistently lower in Florida Bay than evaporation, with a long-term average of 106 cm yr⁻¹. Rainfall considered alone was uncorrelated with evaporation at both monthly and annual time scales; when the seasonal variation in clear sky radiation was also taken into account both net radiation and evaporation were significantly suppressed in months with high rainfall.     

Variability of continental riverine freshwater and nutrient inputs into the North Sea for the years 1977–2000 and its consequences for the assessment of eutrophication

We determined the monthly and annual riverine freshwater, nitrogen (N) and phosphorus (P) loading into the North Sea from Belgium, The Netherlands, and Germany for the years 1977–2000. An average of 133 km³ yr⁻¹ of the 309 km³ yr⁻¹ precipitation into the watershed is carried by the rivers into the sea. Total freshwater discharge fluctuates with a strong 6–7 yr periodicity, is strongly correlated with precipitation, and exhibits a slight long-term decrease. The temporal changes of regional patterns of precipitation lead to changing ratios of annual discharge of the western rivers compared to the eastern rivers, varying between 2.2 and 3.5. The long-term oscillations in discharge were more pronounced as discharge increased. The annual means of total and dissolved inorganic N and P loads were estimated to be 722 and 582 kt N yr⁻¹ and 48 and 26 kt P yr⁻¹, respectively. The monthly N loads were much more strongly correlated with discharge, compared to the monthly P loads. Total N and P as well as dissolved inorganic N also demonstrated a 6–7 yr periodicity. The annual N loads decreased by about 17 kt N yr⁻¹ from 1977 to 2000. The total phosphorus and phosphate loads decreased from about 80 and 50 kt P yr⁻¹ in the 1980s to 25 and 12 kt P yr⁻¹, respectively, in the 1990s. The western rivers contributed the major part of the nutrient loads. The long-term oscillations in their nutrient loads were much more pronounced, compared to the eastern rivers. The area-specific loading rates estimated for all rivers are comparable to earlier estimates using shorter data records, smaller sample sizes, and a less complete watershed monitoring program. The monthly and annual average N:P ratios and their variability increased considerably for individual rivers during the study interval. These results confirm that the water quality of European continental rivers is strongly influenced by intense land use. They demonstrate the necessity for using long time series monitoring results to assess change and evaluate the effects of climate change on the North Sea coastal ecosystems, using ecosystem models on decadal time scales.     

Effects of salinity on NH4 + adsorption capacity, nitrification, and denitrification in Danish estuarine sediments

The regulatory effect of salinity on nitrogen dynamics in estuarine sediments was investigated in the Randers Fjord estuary, Denmark, using sediment slurries and intact sediment cores and applying ¹⁵N-isotope techniques. Sediment was sampled at three representative stations varying in salinity, and all experiments were run at 0‰, 10‰, 20‰, and 30‰. The sediment NH₄ ⁺ adsorption capacity decreased markedly at all stations when salinity was increased from 0‰ to 10‰; further increase showed little effect. In situ nitrification and denitrification also decreased with increasing salinities, with the most pronounced reduction of approximately 50% being observed when the salinity was raised from 0‰ to 10‰. The salinity-induced reduction in NH₄ ⁺ adsorption capacity and stimulation of NH₄ ⁺ efflux has previously been argued to cause a reduction in nitrification activity since the nitrifying bacteria become limited by NH₄ ⁺ availability at higher salinities. However, using a potential nitrification assay where NH₄ ⁺ was added in excess, it was demonstrated that potential nitrification activity also decreased with increasing salinity, indicating that the inhibitory salinity effect may also be a physiological effect on the microorganisms. This hypothesis was supported by the finding that denitrification based on NO₃ ⁻ from the overlying water (D_w), which is independent of the nitrification process, and hence NH₄ ⁺ availability, also decreased with increasing salinity. We conclude that changes in salinity have a significant effect on nitrogen dynamics in estuarine sediments, which must be considered when nitrogen transformations are measured and evaluated.     

Plankton and dissolved inorganic carbon isotopic composition in a river-dominated estuary: Apalachicola Bay, Florida

To characterize the isotopic composition of organisms at the base of the food web and the controls on their variability, the concentration and δ¹³C isotopic composition of dissolved inorganic carbon (DIC) and plankton δ¹³C, δ¹⁵N, and δ³⁴S were measured. The measurements were made during periods of high and low river flow in Apalachicola Bay, Florida, United States, over 3 yr. DIC concentration and δ¹³C values were related to salinity, indicating that conservative mixing of riverine and marine waters was responsible for the overall distributions. The usefulness of DIC δ^13C data for characterizing the trophic processes within the estuary was dependent upon the residence time of water within the season. Plankton δ¹³C values varied from −22‰ to −30‰ and were directly related to estuarine DIC δ¹³C, offset by a factor of roughly −20‰. This offset factor varied with salinity. Values of δ³⁴S in estuarine plankton (station means ranged from 11.4‰ to 13.1‰) were depleted relative to marine plankton (17.7±0.4‰) possibly due to the admixture of³⁴S-depleted sedimentary sulfide with estuarine samples. Values of δ³⁴S in plankton were not related to δ¹³C values of plankton and were only weakly correlated to the salinity of the water from which the plankton were collected, indicating that marine sulfate was the primary source of planktonic sulfur. Values of δ¹⁵N in plankton varied from 5.5‰ to 10.7‰ and appeared related to dominance of the sample by phytoplankton or zooplankton. Estuarine plankton was¹⁵N enriched relative to offshore plankton and estuarine sediment.     

Stable isotope characteristics and origin of ore-forming fluids in copper-gold-polymetallic deposits within strike-slip pull-apart basin of Weishan-Yongping continental collision orogenic belt, Yunnan Province, China

More than 140 middle-small sized deposits or minerals are present in the Weishan-Yongping ore concentration area which is located in the southern part of a typical Lanping strike-slip and pull-apart basin. It has plenty of mineral resources derived from the collision between the Indian and Asian plates. The ore-forming fluid system in the Weishan-Yongping ore concentration area can be divided into two subsystems, namely, the Zijinshan subsystem and Gonglang arc subsystem. The ore-forming fluids of Cu, Co deposits in the Gonglang arc fluid subsystem have δD values between −83.8‰ and −69‰, δ¹⁸O values between 4.17‰ and 10.45‰, and δ¹³C values between −13.6‰ and 3.7‰, suggesting that the ore-forming fluids of Cu, Co deposits were derived mainly from magmatic water and partly from formation water. The ore-forming fluids of Au, Pb, Zn, Fe deposits in the Zijinshan subsystem have δD values between −117.4‰ and −76‰, δ¹⁸O values between 5.32‰ and 9.56‰, and Δ¹³C values between −10.07‰ and −1.5‰. The ore-forming fluids of Sb deposits have δD values between −95‰ and −78‰, δ¹⁸O values between 4.5‰ and 32.3‰, and Δ¹³C values between −26.4‰ and −1.9‰. Hence, the ore-forming fluids of the Zijinshan subsystem must have been derived mainly from formation water and partly from magmatic water. Affected by the collision between the Indian and Asian plates, ore-forming fluids in Weishan-Yongping basin migrated considerably from southwest to northeast. At first, the Gonglang arc subsystem with high temperature and high salinity was formed. With the development of the ore-forming fluids, the Zijinshan subsystem with lower temperature and lower salinity was subsequently formed. Translated from Mineral Deposits, 2006, 25(1): 60–70 [译自: 矿床地质]     

A comparative study on isotopic composition of precipitation in wet tropic and semi-arid stations across southern India

Isotopic composition of monthly composite precipitation samples from Kozhikode (n = 31), a wet tropic station and Hyderabad (n = 25), a semi-arid station across southern India were studied for a period of four years from 2005 to 2008. During the study period, the Kozhikode station recorded an average rainfall of 3500 mm while the Hyderabad station showed an average rainfall of 790 mm. The average stable isotope values in precipitation at the Kozhikode station were δ ¹⁸O = −3.52‰, d-excess = 13.72‰; δ ¹⁸O = −2.94‰, d-excess = 10.57‰; and δ ¹⁸O = −7.53‰, d-excess = 13.79‰, respectively during the pre-monsoon (March–May), monsoon (June–September) and post-monsoon (October–February) seasons. For the Hyderabad station, the average stable isotope values were δ ¹⁸O = −5.88‰, d-excess = 2.34‰; δ ¹⁸O = −4.39‰, d-excess = 9.21‰; and δ ¹⁸O = −8.69‰, d-excess = 14.29‰, respectively for the three seasons. The precipitation at the two stations showed distinctive isotopic signatures. The stable isotopic composition of precipitation at the Hyderabad station showed significant variations from the global trend while the Kozhikode station almost followed the global value. These differences are mainly attributed to the latitudinal differences of the two stations coupled with the differences in climatic conditions.     

A fluid inclusion and stable isotope study of 200 Ma of fluid evolution in the Galway Granite, Connemara, Ireland

Fluid inclusions in granite quartz and three generations of veins indicate that three fluids have affected the Caledonian Galway Granite. These fluids were examined by petrography, microthermometry, chlorite thermometry, fluid chemistry and stable isotope studies. The earliest fluid was a H₂O-CO₂-NaCl fluid of moderate salinity (4–10 wt% NaCl eq.) that deposited late-magmatic molybdenite mineralised quartz veins (V₁) and formed the earliest secondary inclusions in granite quartz. This fluid is more abundant in the west of the batholith, corresponding to a decrease in emplacement depth. Within veins, and to the east, this fluid was trapped homogeneously, but in granite quartz in the west it unmixed at 305–390 °C and 0.7–1.8 kbar. Homogeneous quartz δ¹⁸O across the batholith (9.5 ± 0.4‰n = 12) suggests V₁ precipitation at high temperatures (perhaps 600 °C) and pressures (1–3 kbar) from magmatic fluids. Microthermometric data for V₁ indicate lower temperatures, suggesting inclusion volumes re-equilibrated during cooling. The second fluid was a H₂O-NaCl-KCl, low-moderate salinity (0–10 wt% NaCl eq.), moderate temperature (270–340 °C), high δD (−18 ± 2‰), low δ¹⁸O (0.5–2.0‰) fluid of meteoric origin. This fluid penetrated the batholith via quartz veins (V₂) which infill faults active during post-consolidation uplift of the batholith. It forms the most common inclusion type in granite quartz throughout the batholith and is responsible for widespread retrograde alteration involving chloritization of biotite and hornblende, sericitization and saussuritization of plagioclase, and reddening of K-feldspar. The salinity was generated by fluid-rock interactions within the granite. Within granite quartz this fluid was trapped at 0.5–2.3 kbar, having become overpressured. This fluid probably infiltrated the Granite in a meteoric-convection system during cooling after intrusion, but a later age cannot be ruled out. The final fluid to enter the Granite and its host rocks was a H₂O-NaCl-CaCl₂-KCl fluid with variable salinity (8–28 wt% NaCl eq.), temperature (125–205 °C), δD (−17 to −45‰), δ¹⁸O (−3 to + 1.2‰), δ¹³C_CO2 (−19 to 0‰) and δ³⁴S_sulphate (13–23‰) that deposited veins containing quartz, fluorite, calcite, barite, galena, chalcopyrite sphalerite and pyrite (V₃). Correlations of salinity, temperature, δD and δ¹⁸O are interpreted as the result of mixing of two fluid end-members, one a high-δD (−17 to −8‰), moderate-δ¹⁸O (1.2–2.5‰), high-δ¹³C_CO2 (> −4‰), low-δ³⁴S_sulphate (13‰), high-temperature (205–230 °C), moderate-salinity (8–12 wt% NaCl eq.) fluid, the other a low-δD (−61 to −45‰), low-δ¹⁸O (−5.4 to −3‰), low-δ¹³C (<−10‰), high-δ³⁴S_sulphate (20–23‰) low-temperature (80–125 °C), high-salinity (21–28 wt% NaCl eq.) fluid. Geochronological evidence suggests V₃ veins are late Triassic; the high-δD end-member is interpreted as a contemporaneous surface fluid, probably mixed meteoric water and evaporated seawater and/or dissolved evaporites, whereas the low-δD end-member is interpreted as a basinal brine derived from the adjacent Carboniferous sequence. This study demonstrates that the Galway Granite was a locus for repeated fluid events for a variety of reasons; from expulsion of magmatic fluids during the final stages of crystallisation, through a meteoric convection system, probably driven by waning magmatic heat, to much later mineralisation, concentrated in its vicinity due to thermal, tectonic and compositional properties of granite batholiths which encourage mineralisation long after magmatic heat has abated. Received: 3 April 1996 / Accepted: 5 May 1997     

Setting load limits for nutrients and suspended solids based upon seagrass depth-limit targets

Total nitrogen (TN), total phosphorus (TP), and total suspended solids (TSS) loadings [log (kg ha⁻¹ yr⁻¹)] were regressed against seagrass depth limits (percent of depth-limit targets) to back-predict the load limits or allocations (kg ha⁻¹ yr⁻¹ or kg yr⁻¹) necessary to meet targeted seagrass depth limits in the Indian River and Banana River (IRBR) lagoons, Florida. Because the load allocations can be applied as total maximum daily loads (TMDL) for the IRBR (U.S. Environmental Protection Agency mandate), the method and results are developed and presented toward that end. The regression analyses indicate that the range of surface-discharge load limits (nonpoint + point source), per watershed area, required to achieve the desired depth limits for seagrass in the IRBR are approximately 2.4–3.2 kg ha⁻¹ yr⁻¹ TN, 0.41–0.64 kg ha⁻¹ yr⁻¹ TP, and 48–64 kg ha⁻¹ yr⁻¹ TSS. This simple regression method may have application to other shallow estuarine lagoons or bays where seagrass growth is limited by light and water transparency, water transparency is strongly affected by watershed pollutant loadings, water residence times are sufficiently long to allow seagrass coverage to respond to and covary with total load inputs, and multiyear monitoring has yielded sufficient variability in both pollutant loadings and seagrass coverages to develop a statistically meaningful relationship.     

Carbon and oxygen isotopic composition of car- bonate cements of different phases in terrigenous siliciclastic reservoirs and significance for their origin： A case study from sandstones of the Triassic Yanchang Formation, southwestern Ordos Basin, China

Early carbonate cements in the Yanchang Formation sandstones are composed mainly of calcite with relatively heavier carbon isotope （their δ^18O values range from -0.3‰- -0.1‰） and lighter oxygen isotope （their δ^18O values range from -22.1‰- -19.5‰）. Generally, they are closely related to the direct precipitation of oversaturated calcium carbonate from alkaline lake water. This kind of cementation plays an important role in enhancing the anti-compaction ability of sandstones, preserving intragranular volume and providing the mass basis for later disso- lution caused by acidic fluid flow to produce secondary porosity. Ferriferous calcites are characterized by relatively light carbon isotope with δ^13C values ranging from -8.02‰ to -3.23‰, and lighter oxygen isotope with δ^18O values ranging from -22.9‰ to -19.7‰, which is obviously related to the decarboxylation of organic matter during the late period of early diagenesis to the early period of late diagenesis. As the mid-late diagenetic products, ferriferous cal- cites in the study area are considered as the characteristic authigenic minerals for indicating large-scaled hydrocarbon influx and migration within the clastic reservoir. The late ankerite is relatively heavy in carbon isotope with δ^13C values ranging from -1.92‰ to -0.84‰, and shows a wide range of variations in oxygen isotopic composition, with δ^18O values ranging from -20.5‰ to -12.6‰. They are believed to have nothing to do with decarboxylation, but the previously formed marine carbonate rock fragments may serve as the chief carbon source for their precipitation, and the alkaline diagenetic environment at the mid-late stage would promote this process.     

Growth and production of the mummichog (<Emphasis Type="Italic">Fundulus heteroclitus</Emphasis>) in a restored salt marsh

The mummichog,Fundulus heteroclitus, is one of the most important macrofaunal components of salt marsh surfaces and an important link to subtidal areas of the adjacent estuary along the east coast of the U.S. We estimated growth, population size, and production of the mummichog in a restored marsh in order to improve our understanding of the role of this resident fish and to evaluate the success of the restoration. The restored marsh, covering 234 ha, was a former salt hay farm located in the mesohaline portion of Delaware Bay that was restored to tidal influence in August 1996. We separated the mummichog population into two components based on life history stage and summer habitat use patterns. One component, consisting of adults and large young-of-the-year (YOY), exhibited tidal movements to and from the marsh surface and the subtidal creeks. These were examined with an intensive mark and recapture program using coded wire tags. Another component, consisting of small YOY, remained on the marsh surface throughout the tidal cycle. Throw traps were used to sample these small YOY. The mean annual population density of adults and large YOY for the entire marsh was approximately 1.2 fish m⁻² and mean monthly density peaked at 2.9 fish m⁻². The mean annual density of small YOY on the marsh surface was 15.1 fish m⁻² and mean monthly density peaked at 41.4 fish m⁻². Size and season influenced the growth rate of individual fish and instantaneous growth rates ranged from 0.03 to 2.26 mo⁻¹. Total annual mummichog production was estimated to be 8.37 g dw m⁻² yr⁻¹, with adults and large YOY contributing 28.4% (2.38 g dw m⁻² yr⁻¹) and small YOY on the marsh surface contributing 71.6% (5.99 g dw m⁻² yr⁻¹). The seasonal use and population densities were comparable to previous studies in natural marshes while growth and production of mummichog in this restored marsh appeared to be higher. Coupled with the results of other studies on the feeding, movement, and habitat use of this species in this restored marsh, the species has responded well to the restoration.     

Hydrochemical characteristics of groundwater in the Zhangye Basin, Northwestern China

The Zhangye Basin, located in arid northwest China, is an important agricultural and industrial center. In recent years rapid development has created an increased demand for water, which is increasingly being fulfilled by groundwater abstraction. Detailed knowledge of the geochemical evolution of groundwater and water quality can enhance understanding of the hydrochemical system, promoting sustainable development and effective management of groundwater resources. To this end, a hydrochemical investigation was conducted in the Zhangye Basin. Types of shallow groundwater in the Zhangye Basin were found to be HCO₃ ⁻, HCO₃ ⁻–SO₄ ²⁻, SO₄ ²⁻–HCO₃ ⁻, SO₄ ²⁻–Cl⁻, Cl⁻–SO₄ ²⁻ and Cl⁻ . The deep aquifer groundwater type was found to be HCO₃⁻–SO₄²⁻ throughout the entire area. Ionic ratio and saturation index calculations suggest that silicate rock weathering and evaporation deposition are the main processes that determine the ionic composition in the study area. The suitability of the groundwater for irrigation was assessed based on the US Salinity Laboratory salinity classification and the Wilcox diagram. In the study area, the compositions of the stable isotopes δ¹⁸O and δD in groundwater samples were found to range from −4.00 to −9.28‰ and from −34.0 to −65.0‰, respectively. These values indicate that precipitation is the main recharge source for the groundwater system; some local values indicate high levels of evaporation. Tritium analysis was used to estimate the ages of the different groundwaters; the tritium values of the groundwater samples varied from 3.13 to 36.62 TU. The age of the groundwater at depths of less than 30 m is about 5–10 years. The age of the groundwater at depths of 30–50 m is about 10–23 years. The age of the groundwater at depths of 50–100 m is about 12–29 years. For groundwater samples at depths of greater than 100 m, the renewal time is about 40 years.     

Air-sea exchange of CO2 in the Gulf of Kutch,northern Arabian Sea based on bomb-carbon in corals and tree rings

Radiocarbon analyses were carried out in the annual bands of a 40 year old coral collected from the Gulf of Kutch (22.6°N, 70°E) in the northern Arabian Sea and in the annual rings of a teak tree from Thane (19°14′N, 73°24′E) near Bombay. These measurements were made in order to obtain the rates of air-sea exchange of CO₂ and the advective mixing of water in the Gulf of Kutch. The Δ¹⁴C peak in the Thane tree occurs in the year 1964, with a value of ∼630‰, significantly lower than that of the mean atmospheric Δ¹⁴C of the northern hemisphere (∼ 1000‰). The radiocarbon time series of the coral was modelled considering the supply of carbon and radiocarbon to the gulf through air-sea exchange and advective water transport from the open Arabian Sea. A reasonable fit for the coral data was obtained with an air-sea CO₂ exchange rate of 11–12 mol m⁻² yr⁻¹, and an advective velocity of 28 m yr⁻¹ between the Arabian Sea and the Gulf of Kutch; this was based on a model generated time series for radiocarbon in the Arabian Sea. The deduced velocity (∼ 28 m yr⁻¹) of the advective transport of water between the gulf and the Arabian Sea is much lower than the surface tidal current velocity in this region, but can be understood in terms of net fluxes of carbon and radiocarbon to the gulf to match the observed coral Δ¹⁴C time series.     

Distribution of Hydrogen and Oxygen Isotopes in Salt Lakes of the Qinghai—Xizang Plateau,China

The Qinghai-Xizang Plateau is an area where a large number of salt lakes are distributed. We have collected several hundred samples of natural waters over the Plateau since 1976 and carried out researches on their hydrogen and oxygen isotopes. The results indicate that the^δD and δ¹⁸O values of the salt lake waters over the Plateau range from −64.1 to +12.4‰ and from −11.19 to +8.62‰, respectively. From the different types of surfaces, ground and lake waters of various salinities it is inferred that the compositions of H and O isotopes in the initial water of Qinghai Lake are^δD=−55.0‰ and {ie336-1}; and those in the original water from the lakes in northern Xizang, are^δD=−116.0‰ and {ie336-2}. Brines in the salt lakes are derived from rain water through prolonged circulation. Oilfield water also makes some contribution to the salt lakes in the Qaidam Basin. Similar slopes of evaporation lines of water isotopes are noticed for the Qinghai Lake area and northern Xizang. This is attributed to the evolution of the isotopes in these water bodies in an environment of middle latitude and high elevation.     

Water quality analysis of a freshwater diversion at Caernarvon, Louisiana

Since 1991, Mississippi River water has been diverted at Caernarvon, Louisiana, into Breton Sound estuary. Breton Sound estuary encompasses 1100 km² of fresh and brackish, rapidly subsiding wetlands. Nitrite + nitrate, total Kjeldahl nitrogen, ammonium, total phosphorus, total suspended sediments, and salinity concentrations were monitored at seven locations in Breton Sound from 1988 to 1994. Statistical analysis of the data indicated decreased total Kjeldahl nitrogen with associated decrease in total nitrogen, and decreased salinity concentrations in the estuary due to the diversion. Spring and summer water quality transects indicated rapid reduction of nitrite + nitrate and total suspended sediment concentration as diverted Mississippi River water entered the estuary, suggesting near complete assimilation of these constituents by the ecosystem. Loading rates of nitrite + nitrate (5.6–13.4 g m⁻² yr⁻¹), total nitrogen (8.9–23.4 g m⁻² yr⁻¹), and total phosphorus (0.9–2.0 g m⁻² yr⁻¹) were calculated along with removal efficiencies for these constituents (nitrite + nitrate 88–97%; total nitrogen 32–57%; total phosphorus 0–46%). The low impact of the diversion on water quality in the Breton Sound estuary, along with assimilation of TSS over a very short distance, suggests that more water may be introduced into the estuary without detrimental affects. This would be necessary if freshwater diversions are to be used to distribute nitrients and sediments into the lower reaches of the estuary, in an effort to compensate for relative sea-level rise, and reverse the current trend of rapid loss of wetlands in coastal Louisiana.     

Fluctuations in a magmatic sulphur isotope signature from the Pinnacles Mine,New South Wales,Australia

Sulphur isotopic compositions of 29 sulphide samples from the Broken Hill-type Pinnacles Deposit, NSW, are found to cluster at 0%. (mean −0.8‰). The restricted range of the (δ³⁴S) values between −3.5 and + 3.7‰ with a mean of −0.8‰, is interpreted as reflecting partial oxidation of a dominantly magmatic sulphur source. δ³⁴S data for galena samples fall into two groups: (1) isotopically heavier galenas (range −0.7 to 0.0‰; mean −0.4‰) which come mainly from the footwall Zn lode and (2) isotopically lighter galenas (range −3.5 to −0.8‰; mean −2.2‰) which are from the main Pb lode. Sphalerite, pyrrhotite and chalcopyrite have slightly heavier isotopic compositions (range −1.6 to +3.7‰ mean +0.3‰) but exhibit the same stratigraphic differentiation. These data are interpreted as representing fluctuating conditions at the site of ore deposition, in which upwelling hydrothermal fluids were subject to increasing fO₂ and decreasing temperature with time.     

The Sarylakh and Sentachan gold-antimony deposits,Sakha-Yakutia: A case of combined mesothermal gold-quartz and epithermal stibnite ores

New mineralogical, thermobarometric, isotopic, and geochemical data provide evidence for long and complex formation history of the Sarylakh and Sentachan Au-Sb deposits conditioned by regional geodynamics and various types of ore mineralization, differing in age and source of ore matter combined in the same ore-localizing structural units. The deposits are situated in the Taryn metallogenic zone of the East Yakutian metallogenic belt in the central Verkhoyansk-Kolyma Fold Region. They are controlled by the regional Adycha-Taryn Fault Zone that separates the Kular-Nera Terrane and the western part of the Verkhoyansk Fold-Thrust Belt. The fault extends along the strike of the northwest-trending linear folds and is deep-rooted and repeatedly reactivated. The orebodies are mineralized crush zones accompanied by sulfidated (up to 100 m wide) quartz-sericite metasomatic rocks and replacing dickite-pyrophyllite alteration near stibnite veinlets. Two stages of low-sulfide gold-quartz and stibnite mineralization are distinguished. The formation conditions of the early milk white quartz in orebodies with stibnite mineralization at the Sarylakh and Sentachan deposits are similar: temperature interval 340–280°C, salt concentration in fluids 6.8–1.6 wt % NaCl equiv, fluid pressure 3430–1050 bar, and sodic bicarbonate fluid composition. The ranges of fluid salinity overlapped at both deposits. In the late regenerated quartz that attends stibnite mineralization, fluid inclusions contain an aqueous solution with salinity of 3.2 wt % NaCl equiv and are homogenized into liquid at 304–189°C. Syngenetic gas inclusions contain nitrogen 0.19 g/cm³ in density. The pressure of 300 bar is estimated at 189°C. The composition of the captured fluid is characterized as K-Ca bicarbonatesulfate. The sulfur isotopic composition has been analyzed in pyrite and arsenopyrite from ore and metasomatic zones, as well as in coarse-, medium-, and fine-grained stibnite varieties subjected to dynamometamorphism. The following δ³⁴S values, ‰ have been established at the Sarylakh deposit: −2.0 to −0.9 in arsenopyrite, −5.5 to −1.1 in pyrite, and −5.5 to −3.6 in stibnite. At the Sentachan deposit: −0.8 to +1.0 in arsenopyrite, +0.5 to +2.6 in pyrite, and −3.9 to +0.6 in stibnite. Sulfides from the Sentachan deposit is somewhat enriched in ³⁴S. The ¹⁸O of milk white quartz at the Sarylakh deposit varies from +14.8 to 17.0‰ and from +16.4 to + 19.3‰ at the Sentachan. The δ¹⁸O of regenerated quartz is +16.5‰ at the Sarylakh and +17.6 to +19.8‰ at the Sentachan. The δ¹⁸O of carbonates varies from +15.0 to 16.3% at the Sarylakh and from +16.7 to +18.2‰ at the Sentachan. The δ¹³C of carbonates ranges from −9.5 to −12.1‰ and −7.8 to −8.5‰, respectively. The calculated $ \delta ^{18} O_{H_2 O} $ \delta ^{18} O_{H_2 O} of the early fluid in equilibrium with quartz and dolomite at 300δC are +7.9 to +10.1‰ for the Sarylakh deposit and +9.5 to +12.4‰ for the Sentachan deposit (+4.9 and 6.0‰ at 200°C for the late fluid, respectively). Most estimates fall into the interval characteristic of magmatic water (°¹⁸O = +5.5 to +9.5‰).     

Fluid origin and structural enhancement during mineralization of the Jinshan orogenic gold deposit, South China

The Jinshan orogenic gold deposit is a world-class deposit hosted by a ductile shear zone caused by a transpressional terrane collision during Neoproterozoic time. Ore bodies at the deposit include laminated quartz veins and disseminated pyrite-bearing mylonite. Most quartz veins in the shear zone, with and without gold mineralization, were boudinaged during progressive shear deformation with three generations of boudinage structures produced at different stages of progressive deformation. Observations of ore-controlling structures at various scales indicate syn-deformational mineralization. Fluid inclusions from pyrite intergrown with auriferous quartz have ³He/⁴He ratios of 0.15–0.24 Ra and ⁴⁰Ar/³⁶Ar ratios 575–3,060. δ¹⁸O_fluid values calculated from quartz are 5.5–8.4‰, and δD values of fluid inclusions contained in quartz range between −61‰ and −75‰. The δ¹³C values of ankerite range from −5.0‰ to −4.2‰, and ankerite δ¹⁸O values from 4.4‰ to 8.0‰. The noble gas and stable isotope data suggest a predominant crustal source of ore fluids with less than 5% mantle component. Data also show that in situ fluids were generated locally by pervasive pressure solution, and that widespread dissolution seams acted as pathways of fluid flow, migration, and precipitation. The in situ fluids and fluids derived from deeper levels of the crust were focused by deformation and deformation structures at various scales through solution-dissolution creep, crack-seal slip, and cyclic fault-valve mechanisms during progressively localized deformation and gold mineralization.     

Hydrogeochemical controls and usability of groundwater in the semi-arid Mayo Tsanaga River Basin: far north province,Cameroon

Deuterium, δ ¹⁸O, major ions and dissolved silica in groundwater from semi-arid Mayo-Tsanaga river basin in the Far North Province, Cameroon were used to trace hydrogeochemical processes that control their concentrations and to explore for usability of the water. Electrical conductivity ranges from 57–2,581 μs/cm with alternating low and high values along the hydraulic gradient. Waters from piedmont alluvium show low concentrations in major cations, which peak in Mg within basalt, Na within plain alluvium, and Ca within basalt and the sandy Limani-Yagoua ridge. The initial dominant groundwater composition is CaHCO₃, which did not evolve within the basalt and piedmont alluvium, but evolved to NaHCO₃ in the granite and plain alluvium. The main processes controlling the major ions composition include the following: (1) dissolution of silicates and fluorite; (2) precipitation of fluorite and carbonate; (3) cation exchange of Ca in water for Na in clay; (4) and anthropogenic activities. The δD and δ ¹⁸O ratios vary from −35 to 0.7 and −5.3 to 1.1‰, respectively. The lowest and highest isotope ratios are observed in groundwater within the downstream sandy Limani-Yagoua ridge and the upstream graintes respectively. Variation in isotope ratios depends on altitude effect of −0.48‰ per 100 m between 600 and 850 m asl, and on evaporation, which had insignificant effect on the water salinity. Seventy percent of the groundwater shows poor drinking quality and 90% is suitable for irrigation. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

An organic carbon budget for the Mississippi River turbidity plume and plume contributions to air-sea CO2 fluxes and bottom water hypoxia

We investigated seasonal variability in organic carbon (OC) budgets using a physical-biological model for the Mississippi River turbidity plume. Plume volume was calculated from mixed layer depth and area in each of four salinity subregions based on an extensive set of cruise data and satellite-derived suspended sediment distributions. These physical measurements were coupled with an existing food web model to determine seasonally dependent budgets for labile (reactive on time scales of days to weeks) OC in each salinity subregion. Autochthonous gross primary production (GPP) equaled 1.3×10¹² g C yr⁻¹ and dominated labile OC inputs (88% of the budget) because riverine OC was assumed mostly refractory (nonreactive). For perspective, riverine OC inputs amounted to 3.9×10¹² g C yr⁻¹, such that physical inputs were 3 times greater than biological inputs to the plume. Annually, microbial respiration (R) accounted for 65% of labile OC losses and net metabolism (GPP—R) for the entire plume was, autotrophic, equaling 5.1×10¹¹ g C yr⁻¹. Smaller losses of labile OC occurred via sedimentation (20%), advection (10%), and export to higher trophic levels (5%). In our present model, annual losses of labile OC are 10% higher than inputs, indicating future improvements are required. Application of our model to estimate air-sea carbon dioxide (CO₂) fluxes indicated the plume was a net sink of 2.0×10⁹ mol CO₂ yr⁻¹, of which 90% of the total drawdown was from biotic factors. In all seasons, low salinity waters were a source of CO₂ (pCO₂=560–890 μatm), and intermediate to high salinity waters were a sink of CO₂ (pCO₂=200–370 μatm). Our model was also used to calculate O₂ demand for the development, of regional hypoxia, and our spring and early summer budgets indicated that sedimentation of autochthonous OC from the immediate plume contributed 23% of the O₂ demand necessary for establishment of hypoxia in the region.