Isotope (δD, δ<Superscript>18</Superscript>О) systematics in waters of the Russian Arctic seas

Oxygen and hydrogen isotope analysis was performed to study the processes of distribution of water masses and modification of their salinity in the Russian Arctic seas. A wealth of new isotopic data was obtained for freshwater (river runoff, Novaya Zemlya glaciers) and seawater samples collected along a set of extended 2D profiles in the Barents, Kara, and Laptev Seas. The study presents the first δD values measured for the Northeast Atlantic Deep Water NEADW dominated the water column of the Barents Sea (S = 34.90 ± 0.05, δD = +1.55 ± 0.4‰, δ¹⁸O = +0.26 ± 0.1‰, n = 44). This water mass is present in the Kara Sea and western Laptev Sea. The relationship between δD, δ18О, and salinity data was used to calculate the fractions of waters of different origin, including the fractions of continental runoff in waters of the Barents, Kara, and Laptev Seas. It was shown that the relationships between the isotopic parameters (δD, δ¹⁸О) and salinity in waters of the Kara and Laptev Seas is controlled by the intensity of continental runoff and sea ice processes. Sea ice formation is the main factor controlling the formation of the water column on the Laptev Sea shelf, whereas the surface waters of the middle Kara Sea are dominated by the contribution of river runoff. A very strong stratification in the Kara Sea is caused by the presence of a relatively fresh surface layer mostly contributed by estuarine water inputs from the Ob and Yenisei Rivers. The contribution of river waters reaches 40–60% in the surface layer in the central part of the sea and decreases to a few percent down 100 m water depth. Stratification in the western part of the Laptev Sea is controlled by the contribution of freshwater input from the Lena River and modification of salinity by sea ice formation.     

A bi-polar signal recorded in the western tropical Pacific: Northern and Southern Hemisphere climate records from the Pacific warm pool during the last Ice Age

Western tropical Pacific sea surface temperatures and Pacific Deep Water temperatures during Marine Isotope Stage 3 have been reconstructed from the δ¹⁸O and Mg/Ca of planktonic and benthic foraminifera from Marion Dufresne core MD98-2181. This 36 m marine core was collected at 6.3°N from a water depth of 2114 m. With sediment accumulation rates of up to 80 cm/ky, it provides a decadally resolved history of ocean variability during the Last Glacial period. Surface temperatures and salinities at this site varied in close association with millennial-scale atmospheric temperature swings at high northern latitudes as reflected in the GISP2 ice core. At times of colder atmospheric temperatures over Greenland, the western Pacific was more saline and summer season SSTs were ～2 °C colder. These millennial-scale changes within the tropics are attributed to a southward displacement of the summer season ITCZ in response to steeper meridional temperature gradients within the Pacific. The benthic δ¹⁸O record from MD98-2181 documents upper Pacific Deep Water temperature and salinity variability. Benthic δ¹⁸O variations of 0.3–0.5‰ during MIS 3 indicate deep waters within the Pacific were varying by ～1–1.5 °C, with the possibility that some of the variability was due to changing salinity and minor glacial–eustatic changes. The observed deep-water variability correlates to changes in Antarctic surface temperatures and thus reflects changes in Southern Ocean temperatures at the site of Pacific Deep Water formation. The combined planktonic and benthic records from MD98-2181 thus provide a northern and southern hemispheric climate record of anti-phased variability during MIS 3 as has been inferred previously from ice core records. Furthermore, the deep sea temperature excursions appear to have led millennial variations in atmospheric CO₂ as recorded in the EDML ice core by ～1 kyr.     

Marine conditions in central Sweden during the early Preboreal as inferred from a stable oxygen isotope gradient

The marine benthic fauna and the δ¹⁸O_c of foraminifers and ostracods from six sites situated on a west–east transect through central Sweden have been analysed in order to estimate the palaeosalinity and palaeocirculation in this shallow‐marine environment. The measurements have been undertaken on material from the early Preboreal, when the Baltic Basin was in contact with the North Sea through straits in central Sweden. The δ¹⁸O_c values have a more negative value towards the east, indicating decreasing salinity. This was the result of limited possibilities for marine water to penetrate into the Baltic Basin and the mixing with freshwater from the melting Fennoscandian ice‐sheet. Four water masses existed in the area: a surface layer of freshwater, marine water from the North Sea, brackish–marine intermediate water on the Swedish west coast and brackish Yoldia Sea water in the Baltic Basin. The chronology is based on radiocarbon dates of marine fossils and, at one site, on the occurrence of the Vedde Ash (10 400–10 300 ¹⁴C yr BP). This is the first record from marine settings in Sweden. Copyright © 2001 John Wiley & Sons, Ltd.     

Holocene hydrographical changes of the eastern Laptev Sea (Siberian Arctic) recorded in δO profiles of bivalve shells

Oxygen isotope profiles along the growth axis of fossil bivalve shells of Macoma calcarea were established to reconstruct hydrographical changes in the eastern Laptev Sea since 8400 cal yr B.P.. The variability of the oxygen isotopes (δ¹⁸O) in the individual records is mainly attributed to variations in the salinity of bottom waters in the Laptev Sea with a modern ratio of 0.50‰/salinity. The high-resolution δ¹⁸O profiles exhibit distinct and annual cycles from which the seasonal and annual salinity variations at the investigated site can be reconstructed. Based on the modern analogue approach oxygen isotope profiles of radiocarbon-dated bivalve shells from a sediment core located northeast of the Lena Delta provide seasonal and subdecadal insights into past hydrological conditions and their relation to the Holocene transgressional history of the Laptev Sea shelf. Under the assumption that the modern relationship between δ¹⁸O_w and salinity has been constant throughout the time, the δ¹⁸O of an 8400-cal-yr-old bivalves would suggest that bottom-water salinity was reduced and the temperature was slightly warmer, both suggesting a stronger mixture of riverine water to the bottom water. Reconstruction of the inundation history of the Laptev Sea shelf indicates local sea level ∼27 m below present at this time and a closer proximity of the site to the coastline and the Lena River mouth. Due to continuing sea level rise and a southward retreat of the river mouth, bottom-water salinity increased at 7200 cal yr B.P. along with an increase in seasonal variability. Conditions comparable to the modern hydrography were achieved by 3800 cal yr B.P.     

Spatial Distribution of Nitrous Oxide (N<Subscript>2</Subscript>O) in the Reloncaví Estuary–Sound and Adjacent Sea (41°–43° S), Chilean Patagonia

Fjords and estuaries exchange large amounts of solutes, gases, and particulates between fluvial and marine systems. These exchanges and their relative distributions of compounds/particles are partially controlled by stratification and water circulation. The spatial and vertical distributions of N₂O, an important greenhouse gas, along with other oceanographic variables, are analyzed from the Reloncaví estuary (RE) (~41° 30′ S) to the gulf of Corcovado in the interior sea of Chiloé (43° 45′ S) during the austral winter. Freshwater runoff into the estuary regulated salinity and stratification of the water column, clearly demarking the surface (<5 m depth) and subsurface layer (>5 m depth) and also separating estuarine and marine influenced areas. N₂O levels varied between 8.3 and 21 nM (corresponding to 80 and 170 % saturation, respectively), being significantly lower (11.8 ± 1.70) at the surface than in subsurface waters in the Reloncaví estuary (14.5 ± 1.73). Low salinity and NO₃ ^?, NO₂ ^?, and PO₄ ^3? levels, as well as high Si(OH)₄ values were associated with low surface N₂O levels. Remarkably, an accumulation of N₂O was observed in the subsurface waters of the Reloncaví sound, associated with a relatively high consumption of O₂. The sound is exposed to increasing anthropogenic impacts from aquaculture and urban discharge, occurring simultaneously with an internal recirculation, which leads to potential signals of early eutrophication. In contrast, within the interior sea of Chiloé (ISC), most of water column was quasi homohaline and occupied by modified subantarctic water (MSAAW), which was relatively rich in N₂O (12.6 ± 2.36 nM) and NO₃ ^? (18.3 ± 1.63 μM). The relationship between salinity, nutrients, and N₂O revealed that water from the open ocean, entering into ISC (the Gulf of Corcovado) through the Guafo mouth, was the main source of N₂O (up to 21 nM), as it gradually mixed with estuarine water. In addition, significant relationships between N₂O excess vs. AOU and N₂O excess vs. NO₃ ^? suggest that part of N₂O is also produced by nitrification. Our results show that the estuarine and marine waters can act as light source or sink of N₂O to the atmosphere (air–sea N₂O fluxes ranged from ?1.57 to 5.75 μmol m^?2 day^?1), respectively; influxes seem to be associated to brackish water depleted in N₂O that also caused a strong stratification, creating a barrier to gas exchange.     

Dolomitization by penesaline sea water in Early Jurassic peritidal platform carbonates, Gibraltar, western Mediterranean

Peritidal carbonates of the Lower Jurassic (Liassic) Gibraltar Limestone Formation, which form the main mass of the Rock of Gibraltar, are replaced by fine and medium crystalline dolomites. Replacement occurs as massive bedded or laminated dolomites in the lower 100 m of an ≈460‐m‐thick platform succession. The fine crystalline dolomite has δ¹⁸Ο values either similar to, or slightly higher than, those expected from Early Jurassic marine dolomite, and δ¹³C values together with ⁸⁷Sr/⁸⁶Sr ratios that overlap with sea‐water values for that time, indicating that the dolomitizing fluid was Early Jurassic sea water. Absence of massive evaporitic minerals and/or evaporite solution‐collapse breccias in these carbonate rocks indicates that the salinity of sea water during dolomitization was below that of gypsum precipitation. The occurrence of peritidal facies, a restricted microbiota and rare gypsum pseudomorphs are also consistent with penesaline conditions (salinity 72–199‰). The medium crystalline dolomite has some δ¹⁸Ο and δ¹³C values and ⁸⁷Sr/⁸⁶Sr ratios similar to those of Early Jurassic marine dolomites, which indicates that ambient sea water was again a likely dolomitizing fluid. However, the spread of δ¹⁸Ο, δ¹³C and ⁸⁷Sr/⁸⁶Sr values indicates that dolomitization occurred at slightly increased temperatures as a result of shallow (≈500 m) burial or that dolomitization was multistage. These data support the hypothesis that penesaline sea water can produce massive dolomitization in thick peritidal carbonates in the absence of evaporite precipitation. Taking earlier models into consideration, it appears that replacement dolomites can be produced by sea water or modified sea water with a wide range of salinities (normal, penesaline to hypersaline), provided that there is a driving mechanism for fluid migration. The Gibraltar dolomites confirm other reports of significant Early Jurassic dolomitization in the western Tethys carbonate platforms.     

Hydrologic Dynamics of a Subtropical Estuary Using Geochemical Tracers,Celestún,Yucatan, Mexico

Oxygen isotopes and strontium concentrations were used as geochemical tracers to discern the sources of water to Celestún Lagoon, a small subtropical estuary on the western side of the Yucatán Peninsula of Mexico. Celestún Lagoon is underlain by karstified limestone with numerous locations where groundwater is observed discharging directly to the lagoon. In this study, samples of groundwater, lagoon surface water, and seawater (SW) were collected in April 2008 and June 2009 and analyzed for salinity, stable isotopes of oxygen, and strontium (Sr²⁺) concentrations. These geochemical tracers were used in two tertiary mixing models to calculate the relative ratio inputs of fresh groundwater, brackish groundwater, and SW to the lagoon. Two sources of groundwater were found to contribute to the surface water in the lagoon; one fresh and the other brackish with an average salinity of 19 psu. The fresh groundwater had an oxygen isotopic signature (δ¹⁸O) and strontium concentration (Sr²⁺) of δ¹⁸O?=?-3.30‰ and Sr²⁺?=?0.03 mmol/l, respectively. The brackish groundwater observed in the northern end of the lagoon add a dissimilar oxygen isotopic signature and Sr²⁺ concentration of δ¹⁸O?=?3.01‰ and Sr²⁺?=?0.12 mmol/l, respectively. Local SW had an isotopic oxygen signature and Sr²⁺ concentration between the two fresher sources (δ¹⁸O?=?1.40‰, Sr²⁺?=?0.09 mmol/l). The lagoonwide results of the two tracer mixing models (δ¹⁸O and Sr²⁺) agreed well (within 5 %) and indicated a ratio of brackish groundwater–fresh groundwater– SW of 31 %–26 %–43 % (±5 %) for the Sr²⁺ model and 35 %–25 %–40 % (± 5 %) for the δ¹⁸O model. Brackish groundwater is dominant in the northern portion of the lagoon, while SW dominates the southern portion. Fresh groundwater discharge is a significant contributor of water along the entire eastern boundary of the lagoon where mangrove forests are the dominant vegetation.     

Salinity reflux and dolomitization of southern Australian slope sediments: the importance of low carbonate saturation levels

Anomalously saline waters in Ocean Drilling Program Holes 1127, 1129, 1130, 1131 and 1132, which penetrate southern Australian slope sediments, and isotopic analyses of large benthic foraminifera from southern Australian continental shelf sediments, indicate that Pleistocene–Holocene meso‐haline salinity reflux is occurring along the southern Australian margin. Ongoing dolomite formation is observed in slope sediments associated with marine waters commonly exceeding 50‰ salinity. A well‐flushed zone at the top of all holes contains pore waters with normal marine trace element contents, alkalinities and pH values. Dolomite precipitation occurs directly below the well‐flushed zone in two phases. Phase 1 is a nucleation stage associated with waters of relatively low pH (ca 7) caused by oxidation of H₂S diffusing upward from below. This dolomite precipitates in sediments < 80 m below the sea floor and has δ¹³C values consistent with having formed from normal sea water (? 1‰ to + 1‰ Vienna Pee Dee Belemnite). The Sr content of Phase 1 dolomite indicates that precipitation can occur prior to substantial metastable carbonate dissolution (< 300 ppm in Holes 1129 and 1127). Dolomite nucleation is interpreted to occur because the system is undersaturated with respect to the less stable minerals aragonite and Mg‐calcite, which form more readily in normal ocean water. Phase 2 is a growth stage associated with the dissolution of metastable carbonate in the acidified sea water. Analysis of large dolomite rhombs demonstrates that at depths > 80 m below the sea floor, Phase 2 dolomite grows on dolomite cores precipitated during Phase 1. Phase 2 dolomite has δ¹³C values similar to those of the surrounding bulk carbonate and high Sr values relative to Phase 1 dolomite, consistent with having formed in waters affected by aragonite and calcite dissolution. The nucleation stage in this model (Phase 1) challenges the more commonly accepted paradigm that inhibition of dolomitization by sea water is overcome by effectively increasing the saturation state of dolomite in sea water.     

Fingerprinting groundwater salinity sources in the Gulf Coast Aquifer System,USA

Understanding groundwater salinity sources in the Gulf Coast Aquifer System (GCAS) is a critical issue due to depletion of fresh groundwater and concerns for potential seawater intrusion. The study objective was to assess sources of groundwater salinity in the GCAS using ～1,400 chemical analyses and ～90 isotopic analyses along nine well transects in the Texas Gulf Coast, USA. Salinity increases from northeast (median total dissolved solids (TDS) 340 mg/L) to southwest (median TDS 1,160 mg/L), which inversely correlates with the precipitation distribution pattern (1,370– 600 mm/yr, respectively). Molar Cl/Br ratios (median 540–600), depleted δ²H and δ¹⁸O (?24.7‰, ?4.5‰) relative to seawater (Cl/Br ～655 and δ²H, δ¹⁸O 0‰, 0‰, respectively), and elevated ³⁶Cl/Cl ratios (～100), suggest precipitation enriched with marine aerosols as the dominant salinity source. Mass balance estimates suggest that marine aerosols could adequately explain salt loading over the large expanse of the GCAS. Evapotranspiration enrichment to the southwest is supported by elevated chloride concentrations in soil profiles and higher δ¹⁸O. Secondary salinity sources include dissolution of salt domes or upwelling brines from geopressured zones along growth faults, mainly near the coast in the northeast. The regional extent and large quantities of brackish water have the potential to support moderate-sized desalination plants in this location. These results have important implications for groundwater management, suggesting a current lack of regional seawater intrusion and a suitable source of relatively low TDS water for desalination.     

Sea surface temperature record off central Japan since the Last Glacial Maximum using planktonic foraminiferal Mg/Ca thermometry

We conducted paired measurements of the Mg/Ca ratio and δ¹⁸O of planktonic foraminifera, Globigerina bulloides, from a sediment core (MD01‐2420) off central Japan in the northwest Pacific, to reconstruct current movements since the Last Glacial Maximum (LGM). These methods make it possible to determine the magnitude and timing of the sea surface temperature (SST) changes and to reconstruct the variations of the past seawater δ¹⁸O (δ¹⁸Ow) off central Japan. The amplitude of Mg/Ca‐based SST changes between the Holocene and the LGM was about 10°C. The strong resemblance of the SSTs estimated from both methods, Mg/Ca‐based and δ¹⁸O‐based, suggests that the SST changes were caused primarily by latitudinal displacement of the Kuroshio–Oyashio currents and no distinct change in the carbonate dissolution of the core. The southward migration of the water mass was 5–6° in latitude at the LGM. The values for regional δ¹⁸Ow changes, which were obtained by subtracting the ice volume contribution from the calculated δ¹⁸Ow, describe the millennial‐scale water mass migration over the last 30 kyr. Copyright © 2005 John Wiley & Sons, Ltd.     

The Use of Stable Sulfur, Oxygen and Hydrogen Isotope Ratios as Geochemical Tracers of Sulfates in the Podwiśniówka Acid Drainage Area (South-Central Poland)

The paper presents the results of determinations of stable S and O isotopes of dissolved sulfates and O and H stable isotopes of waters from three ponds, that is, Marczakowe Do?y acid pond, Marczakowe Do?y fish pond and Podwi?niówka acid pit pond, located in the Holy Cross Mountains (south-central Poland). The δ³⁴S_V-CDT and δ¹⁸O_V-SMOW of SO₄ ^2? in waters of three ponds (n = 14) varied from ?16.2 to ?9.5 ‰ (mean of ?13.6 ‰) and from ?8.1 to ?3.2 ‰ (mean of ?4.8 ‰), respectively. The mean δ³⁴S–SO₄ ^2? values were closer to those of pyrite (mean of ?25.4 ‰) and efflorescent sulfate salts (mean of ?25.6 ‰), recorded previously in the Podwi?niówka quarry, than to sulfates derived from other anthropogenic or soil and bedrock sources. The SO₄ ^2? ions formed by bacterially induced pyrite oxidation combined with bacterial (dissimilatory) dissolved sulfate reduction, and presumably with subordinate mineralization of carbon-bonded sulfur compounds, especially in both Marczakowe Do?y ponds. In addition, the comparison of δ¹⁸O–SO₄ ^2? and δ¹⁸O–H₂O values indicated that 75–100 % of sulfate oxygen was derived from water. Due to the largest size, the Podwi?niówka acid pit pond revealed distinct seasonal variations in both δ¹⁸O–H₂O (?9.2 to ?1.6) and δD–H₂O (?29.7 to ?71.3) values. The strong correlation coefficient (r ² = 0.99) was noted between δ¹⁸O–H₂O and δD–H₂O values, which points to atmospheric precipitation as the only source of water. The sediments of both acid ponds display different mineral inventory: the Marczakowe Do?y acid pond sediment consists of schwertmannite and goethite, whereas Podwi?niówka acid pit pond sediment is composed of quartz, illite, chlorite and kaolinite with some admixture of jarosite reflecting a more acidic environment. Geochemical modeling of two acid ponds indicated that the saturation indices of schwertmannite and nanosized ε-Fe₂O₃ (Fe³⁺ oxide polymorph) were closest to thermodynamic equilibrium state with water, varying from ?1.44 to 3.05 and from ?3.42 to 6.04, respectively. This evidence matches well with the obtained mineralogical results.     

Norwegian sea‐surface palaeoenvironments of marine oxygen‐isotope stage 3: the paradoxical response of dinoflagellate cysts

High‐resolution marine palynological data have been obtained from two very long sediment cores (MD952009 and MD952010) retrieved from the southern Norwegian Sea. The dinoflagellate cyst assemblages show pronounced fluctuations in composition, which correlate strongly with magnetic susceptibility records and also mimic the δ¹⁸O signal of the GISP2 Greenland ice‐core. If focusing on the period from 48 to 30 cal. kyr BP, this correlation suggests a paradoxical response of the sea‐surface environments to the atmospheric conditions over Greenland: when the Greenland δ¹⁸O signal reflects warm interstadial conditions, the Norwegian Sea depicts cold sea‐surface temperatures with quasi‐perennial sea‐ice cover (based on dinoflagellate cysts). In contrast, when the Greenland δ¹⁸O records cold stadial periods, the Norwegian Sea‐surface temperatures are warm (based on dinoflagellate cysts), probably linked to inflow of the North Atlantic Drift. These results, similar in both cores, are contrary to those of previous studies and shed light on a possible decoupling of Norwegian sea surface‐water conditions and atmospheric conditions over Greenland. This decoupling could be linked to an atmosphere–ocean system behaving similar to that which the Northern Hemisphere is experiencing at present, i.e. strongly variable owing to the North Atlantic Oscillation. Copyright © 2002 John Wiley & Sons, Ltd.     

Salinization of porewater in a multiple aquitard-aquifer system in Jiangsu coastal plain,China

Chemical and isotopic compositions were analyzed in porewater squeezed from a clayey aquitard in Jiangsu coastal plain, eastern China, to interpret the salinity origin, chemical evolution and water-mass mixing process. A strong geochemical fingerprint was obtained with an aligned Cl/Br ratio of 154 in the salinized aquitard porewater over a wide Cl^? concentration range (396–9,720 mg/L), indicating that porewater salinity is likely derived from a mixing with old brine with a proportion of less than 20%. Very small contributions of brine exerted limited effects on water stable isotopes. The relationships between porewater δ¹⁸O and δD indicate that shallow and intermediate porewaters could be original seawater and were subsequently diluted with modern meteoric water, whereas deep porewaters with depleted stable isotopic values were probably recharged during a cooler period and modified by evaporation and seawater infiltration. The cation–Cl relationship and mineralogy of associated strata indicate that porewater has been chemically modified by silicate weathering and ion-exchange reactions. ⁸⁷Sr/⁸⁶Sr ratios of 0.7094–0.7112 further confirm the input source of silicate minerals. Numerical simulations were used to evaluate the long-term salinity evolution of the deep porewater. The alternations of boundary conditions (i.e., the third aquifer mixed with brine at approximately 70 ka BP, followed by recharge of glacial meltwater at 20–25 ka BP, and then mixing with Holocene seawater at 7–10 ka BP) are responsible for the shift in porewater salinity. These timeframes correspond with the results of previous studies on ancient marine transgression-regression in Jiangsu coastal plain.     

Oxygen isotope composition of water and snow-ice cover of isolated lakes at various stages of separation from the White Sea

This study aimed to analyze the oxygen isotope composition of water, ice, and snow in water bodies isolated from the White Sea and to identify the structural peculiarities of these pools during the winter period. The studies were performed during early spring in Kandalaksha Bay of the White Sea, in Velikaya Salma Strait and in Rugoserskaya Inlet. The studied water bodies differ in their degree of isolation from the sea. In particular, Ermolinskaya Inlet has normal water exchange with the sea; the Lake on Zelenyi Cape represents the first stage of isolation; i. e., it has permanent water exchange with the sea by the tide. Kislo-Sladkoe Lake receives sea water from time to time. Trekhtsvetnoe Lake is totally isolated from the sea and is a typical meromictic lake. Finally, Nizhnee Ershovskoe Lake exhibits some features of a saline water body. The oxygen isotope profile of the water column in Trekhtsvetnoe Lake allows defining three layers; this lake may be called typically meromictic. The oxygen isotope profile of the water column in Kislo-Sladkoe Lake is even from the surface to the bottom. The variability of δ¹⁸O is minor in Lake on Zelenyi Cape. A surface layer (0–1 m) exists in Nizhnee Ershovskoe Lake, and the oxygen isotope variability is well pronounced. Deeper, where the freshwater dominates, the values of ?18Îvary insignificantly disregarding the water depth and temperature. This fresh water lake is not affected by the seawater and is not stratified according to the isotope profile. It is found that applying the values of ?18Î and profiles of temperature and salinity may appear as an effective method in defining the water sources feeding the water bodies isolated from the sea environment.     

Spatio-Temporal Patterns of Submerged Macrophytes in Three Hydrologically Altered Mediterranean Coastal Lagoons

Rice cultivation in the Ebro Delta (Catalonia, Spain) has inverted the natural hydrological cycles of coastal lagoons and decreased water salinities for over 150 years. Adjustments in the water management practices—in terms of source and amount of freshwater inputs—have resulted in changes in the diversity, distribution and productivity of submerged angiosperms. Between the 1970s and late 1980s, a massive decline of the aquatic vegetation occurred in the Encanyissada–Clot and Tancada lagoons, but little information on the status is available after the recovery of macrophytes in the 1990s. Here, we evaluate the influence of salinity regimes resulting from current water management practices on the composition, distribution, seasonal abundance and flowering rates of submersed macrophytes, as well as on the occurrence of epiphyte and drift macroalgae blooms in three coastal lagoons. Our results show that Ruppia cirrhosa is the dominant species in the Encanyissada lagoon (185.97?±?29.74 g?DW?m^?2?year^?1; 12–27?‰ salinity) and the only plant species found in the Tancada lagoon (53.26?±?10.94 g?DW?m²?year^?1; 16–28?‰ salinity). Flowering of R. cirrhosa (up to 1,011?±?121 flowers?m^?2) was only observed within the Encanyissada and suggests that mesohaline summer conditions may favor these events. In contrast, low salinities in Clot lagoon (～3–12?‰) favor the development of Potamogeton pectinatus (130.53?±?13.79 g?DW?m²?year^?1) with intersperse R. cirrhosa (8.58?±?1.71 g?DW?m^?2) and mixed stands of P. pectinatus and Najas marina (up to ～57 g?DW?m^?2?year^?1) in some reduced areas. The peak biomasses observed during the study are 88 to 95 % lower than maximum values reported in the literature at similar salinities, and there is also little or no recovery in some areas compared to last reports more than 20 years ago. The main management actions to restore the natural diversity and productivity of submersed angiosperms, such as the recovering of the seagrass Zostera noltii, should be the increase of salinity during the period of rice cultivation, by reducing freshwater inputs and increasing flushing connections with the bays.     

Physical and chemical growth conditions of Ordovician organogenic deep-water dolomite concretions: implications for the δ18O of Early Palaeozoic sea water

The estimated depth of formation of authigenic dolomite concretions in the Middle Ordovician Cloridorme Formation, Quebec, ranges from < 1 m to 150–200 m below sea floor (mbsf) (mostly between < 1 and 25 mbsf), based on centre‐to‐margin variations in minus‐cement porosity (80–90% to 45–75%). Formation depths are > 350 mbsf (25–17% porosity) in the Lower Ordovician Levis Formation. Outward‐decreasing δ¹³C_VPDB values (10·2–0·8‰) suggest precipitation in the methane generation zone with an increasing contribution of light carbonate derived by advection from thermocatalytic reactions at depth. Anomalously low δ¹⁸O_VPDB values (centre‐to‐margin variations of ?0·4 to ?7·5‰) give reasonable temperatures for the concretion centres only if the δ¹⁸O of Ordovician sea water was negative (?6‰) and the bottom water was warm (> 15 °C). The 3–5‰ lower values for the concretion margins compared with the centres can be explained if, in addition, volcanic‐ash alteration, organic‐matter decomposition and/or advection of ¹⁸O‐depleted water lowered the δ¹⁸O of the pore water further by 2·0–4·0‰ during the first 25–200 m of burial. Reasonable growth temperatures for the margins of 17–20 °C are compatible with a lowering of the isotopic ratios by 1 to < 1·3‰ as a temperature effect. The systematic concentric isotope zonation of the concretions suggests that the well‐ordered near‐stoichiometric dolomite is a primary feature and not the result of recrystallization. Diagenetic dolomite beds of the Cloridorme Formation appear to have formed by coalescence of concretions, as shown by randomly sampled traverses that indicate formation at different subsurface depths. Growth of the Cloridorme dolomites was probably limited by calcium availability, at least 50% of which was derived from connate water, and the remainder by diffusion from sea water. Dolomite precipitation was favoured over calcite by very high sedimentation rates, the abundance of marine organic matter in the host sediment and a correspondingly thin sulphate reduction zone. Deep‐seated concretion growth in the Levis Formation required either internal sources for the participating ions (carbonate dissolution event) or porewater advection along faults.     

Stable isotopic information for hydrological investigation in Hailuogou watershed on the eastern slope of Mount Gongga, China

Hydrological systems have been seriously affected by changes of glaciations and snow covers in Mount Gongga, Sichuan, China, but the relevance of ice-snow melt for alpine river basin hydrology is so far not well known. To better understand hydrological features of the Hailuogou River, changes of δ¹⁸O and δ²H were investigated by analyzing 117 water samples collected from May 2008 to November 2009. Our results show that the stream water contains a relatively intermediate magnitude of isotopic variations, with δ¹⁸O ranging from ?18.09 to ?13.08 ‰ and δ²H from ?126.5 to ?88.8 ‰. The average values are both higher than those of ice-snow meltwater, but lower than those of meteoric water. These data also show a gradually increasing trend from upstream to downstream, and these changes might document the fingerprint of ice-snow melt in the headwater region and indicate the increasing recharge of heavy isotope-enriched waters with flow distance. The similarity in slopes of δ²H and δ¹⁸O relationship for meteoric waters and stream waters suggests that the isotopic signature of precipitation is well preserved in stream flow, and during the rainfall and stream flow the evaporation is only minor. Based on δ¹⁸O model, the results suggested that the fraction of ice-snow meltwater input over the total stream flow ranged from 84.50 to 86.52 % in the headwater region, but the fraction of ice-snow meltwater input from upper basin downward was significantly decreased. The study demonstrates that ice-snow meltwater is a substantially important water source in alpine regions on the edge of Tibetan Plateau.     

The use of proxy chemical records in Coral skeletons to ascertain past environmental conditions in Florida Bay

This paper will discuss the use of chemical proxies in coral skeletons to reconstruct the history of salinity (from the δ¹⁸O of the skeleton) and nutrients in the water (from the δ¹³C) in Florida Bay between 1824 and 1994. Monthly salinity and water temperature data collected since 1989 were used to establish a correlation between salinity, temperature, and the δ¹⁸O of the skeleton of the coralSolenastrea bournoni from Lignumvitae Basin in Florida Bay. This relationship explains over 50% of the variance in the δ¹⁸O of the skeleton. Assuming that interannual variations in the temperature of the water are small, we have applied this relationship to the δ¹⁸O measured in the coral skeleton collected from Lignumvitae Basin which has a record between 1824 and 1993. These data provide a revised estimate of salinity variation in Lignumvitae Basin for the period when historical records for salinity were not available, and show that the highest salinity events occurred in the past 30 yr. Using the relationships between the salinity in Lignumvitate Basin and other basins, obtained using a modern dataset, we are able to estimate ranges in salinity for other portions of Florida Bay. Skeletons of specimens of the coral speciesSiderastrea radians collected from other areas of Florida Bay show similar patterns in the δ¹⁸O over the past 10 yr, indicating that corals in most portions of Florida Bay are recording salinity variations in their skeletons and therefore support the idea that salinity variations in different portions of Florida Bay can be related. Fluorescence analysis of the coral from Lignumvitae Basin shows a large change in the magnitude of the 10-yr signal coincident with the construction of the railway, confirming that this event had a significant impact upon Florida Bay. The δ¹³C of the coral skeletons reveals a long-term history of the oxidation of organic material, fixation of carbon by photosynthesis (algal blooms), and the intrusion of marine water into the bay. Since the construction of the railway from Miami to Key West there has been a long-term decrease in the δ¹³C of the coral skeleton from Lignumvitae Basin, suggesting the increased oxidation of organic material in this area. This decrease in δ¹³C appears to have reached a minimum value around 1984 and has increased since this time in the western portions of Florida Bay. The increase may be related to the algal blooms prevalent in the area or alternatively could result from intrusion of more marine water. In the eastern areas, a small increase in the δ¹⁸C between 1984 and 1988 was followed by further decline suggesting more oxidation of organic material. We have also attempted to use the concentration of barium in the coral skeleton as a proxy indicator of the nutrient status in Florida Bay.     

Ordovician low- to intermediate-Mg calcite marine cements from Sweden: marine alteration and implications for oxygen isotopes in Ordovician seawater

Petrography demonstrates the presence of three types of fibrous calcite cement in buildup deposits of the Kullsberg Limestone (middle Caradoc), central Sweden. Translucent fibrous calcite has intrinsic blue luminescence (CL) indicative of pure calcite. This cement has 2–5 mol% MgCO₃, low Mn and Fe (≤ 100 p.p.m.), and is considered to be slightly altered to unaltered, primary low- to intermediate-Mg calcite. Grey turbid fibrous calcite has variable but generally low MgCO₃ content (most analyses <2 mol%) and variable CL response, with Mn and Fe concentrations up to 1200 and 500 p.p.m., respectively. The heterogeneous characteristics of this variety of fibrous calcite are caused by diagenetic alteration of a translucent fibrous calcite precursor. Light-brown turbid fibrous calcite has low MgCO₃ (near 1 mol%) and variable Mn (up to 800 p.p.m.) and Fe (up to 500 p.p.m.) concentrations, with an abundance of bright luminescent patches, which formed during alteration caused by reducing diagenetic fluids. The δ¹³C and δ¹⁸O values of all fibrous calcite form a tight field (δ¹³C=1·7 to 3·1‰ PDB, δ¹⁸O= ? 2·6 to ? 4·1‰ PDB) compared with fibrous calcite isotope values from other units. Fibrous calcite δ¹⁸O values are larger than adjacent meteoric or burial cements, which have δ¹⁸O δ ? 8‰ PDB. Consequently, most diagenetic alteration of Kullsberg fibrous calcite is interpreted to have occurred in the marine diagenetic realm. First-generation equant and bladed calcite cements, which pre-date fibrous calcite, are interpreted as unaltered, low-Mg calcite marine cements based on δ¹³C and δ¹⁸O data (δ¹³C = 2·3 to 2·7‰ PDB, δ¹⁸O= ? 2·8 to ? 3·5‰ PDB). Unlike fibrous cement, which reflects global sea water chemistry, first-generation equant and bladed calcite are indicators of localized modification of seawater chemistry in restricted settings. Kullsberg abiotic marine cements have larger δ¹⁸O values than most Caradoc marine precipitates from equatorial Laurentia. Positive Kullsberg δ¹⁸O values are attributed to lower seawater temperatures and/or slightly elevated salinity on the Baltic platform relative to seawater from which other marine precipitates formed.     

Holocene migration of oceanic front systems over the Conrad Rise in the Indian Sector of the Southern Ocean

There has been limited previous research about Holocene climate variability in the Indian Sector of the Southern Ocean. Here we examine centennial‐scale changes in diatom assemblages and stable isotopic ratios since 10 000 cal a BP in a high‐accumulation‐rate sediment core from the Conrad Rise. Although abundances of dominant diatom taxa (Fragilariopsis kerguelensis and Thalassiothrix antarctica) are comparatively constant, relative abundances of secondary taxa fluctuate. Before c. 9900 cal a BP, winter sea‐ice and cold water covered the Conrad Rise. Following deglaciation the sea‐ice retreated from the Conrad Rise, lagging that of the Atlantic and eastern Indian Sectors by about 1500 a. The Polar Front moved southward during the early Holocene optimum and north Antarctic Zone waters covered the Conrad Rise for about 650 a. After 9300 cal a BP, solar insolation strongly influenced sea surface temperature and primary productivity in the Southern Ocean. In the high‐latitude Indian Sector, productivity increased 1500 a after the onset of late Holocene neoglaciation. Periodic δ¹⁸O and cold‐water diatom taxa spikes (at intervals of 200 and 300–500 a, respectively) occurred after 9300 cal a BP, probably associated with solar activity. Fluctuations in short‐term sea surface temperature and cold‐water taxa are synchronous with changes in δD observed in an east Antarctic ice core. Copyright © 2011 John Wiley & Sons, Ltd.