Temporal variability of freshwater and pore water recirculation components of submarine groundwater discharges at Baffin Bay,Texas

Submarine groundwater discharges (SGDs) are an important source of freshwater as well as nutrients and other chemicals to bays and estuaries. SGDs are particularly important for coastal bodies in arid and semi-arid regions that are not fed by perennial streams. The Baffin Bay, TX is a shallow coastal water body that is weakly connected to the Gulf of Mexico and has no major rivers or streams draining into it. A year-long submarine groundwater discharge measurement study was carried out at the Loyola Beach of the Baffin Bay during the months of July 2005–June 2006. A total of 23 synoptic SGD sampling events were carried out with most events collecting SGD data continuously over a period of 24 h at a 1-min temporal resolution using an ultrasonic seepage meter. The median SGD was noted to be 3.83 cm/d with an inter-quartile range (IQR) of 11.36 cm/d. Four sampling events had anomalously high SGD values (~27–48 cm/d) which are hypothesized to be due to the geologic heterogeneity of the sea bed and meteorological effects. Eight of the 23 sampling events had a negative average SGD flux indicating landward flow. The short-term diurnal variability of SGD was comparable or sometimes higher than the longer-term and between-events variability. No long-term trend could be inferred. In the short-term, SGD measurements showed considerable persistence and the effective sample size analysis indicated each sampling event (consisting of over 1,000 samples) yielded only a handful of statistically independent measurements of SGD. The measured SGD values exhibited both negative (hydraulically controlled) and positive (wave set-up controlled) correlations with the bay water levels. Marine controls appeared to be the most significant SGD drivers and are in turn controlled by prevailing aeolian forcings. The salinity of the SGDs were estimated from measured sonic velocities and used in conjunction with the end-member mixing models to estimate fresh (meteoric) and re-circulated pore-water fractions. The freshwater fraction of the SGD was estimated to vary between nearly 4 and 89 % with a median value of 9.96 % and an IQR of 7.16 %. Three events were noted to have abnormally high freshwater fractions (~28, 50 and 84 %) which are likely artifacts caused by bay water freshening from rainfall and plausible thermal expansion. The meteoric and pore-water partitioning was sensitive to the assumed end-member concentrations. This study provides preliminary estimates for SGDs along the South Texas coast line and is useful for calibrating groundwater flow models and understanding the relative importance of terrestrial and marine controls on SGD. However, the heterogeneous nature of the sedimentary geology of the Texas Gulf Coast implies the SGD fluxes are likely to exhibit considerable spatial variation that has not been characterized yet. Therefore, the study provides useful insights for such future data collection and monitoring activities. The measured SGD values at Baffin Bay, TX are comparable to those reported at other parts of the Gulf of Mexico.     

Levels of cadmium, manganese and lead in water and algae; Spirogyra aequinoctialis

This study assessed the ability of filamentous green algae; Spirogyra aequinoctialis to accumulate manganese, cadmium and lead from water. Water pH was also determined. Samples of S. aequinoctialis and their respective water environments were taken from designated sampling points in the city of Blantyre and Malawi during the rainy and dry season in order to capture seasonal variations. The concentration of metals in S. aequinoctialis were higher than in the corresponding water environment in both seasons, but lower in the rainy season than the dry season. In the rainy season the concentrations were (in S. aequinoctialis and (water)): Mn 0.432–5.641 mg/L (ND-0.530 mg/L), CdND- 0.016 mg/L (0.07–0.111 mg/L) andPbND- 0.965 mg/L (0.011–0.098 mg/L). In the dry season the concentrations were: Mn 0.281-16.132 mg/L (0.035–0.626 mg/L), Cd 0.22–0.912 mg/L (0.014–0.111 mg/L) and Pb ND- 0.972 mg/L (ND- 0.23 mg/L). This study has shown that S. aequinoctialis has the capability of accumulating manganese, cadmium and lead. Therefore it can be used as a biological indicator for long term heavy metal water pollution monitoring.     

Spatial and temporal variability of trace element concentrations in an urban subtropical watershed,Honolulu, Hawaii

Trace metal concentrations in soils and in stream and estuarine sediments from a subtropical urban watershed in Hawaii are presented. The results are placed in the context of historical studies of environmental quality (water, soils, and sediment) in Hawaii to elucidate sources of trace elements and the processes responsible for their distribution. This work builds on earlier studies on sediments of Ala Wai Canal of urban Honolulu by examining spatial and temporal variations in the trace elements throughout the watershed. Natural processes and anthropogenic activity in urban Honolulu contribute to spatial and temporal variations of trace element concentrations throughout the watershed. Enrichment of trace elements in watershed soils result, in some cases, from contributions attributed to the weathering of volcanic rocks, as well as to a more variable anthropogenic input that reflects changes in land use in Honolulu. Varying concentrations of As, Cd, Cu, Pb and Zn in sediments reflect about 60 a of anthropogenic activity in Honolulu. Land use has a strong impact on the spatial distribution and abundance of selected trace elements in soils and stream sediments. As noted in continental US settings, the phasing out of Pb-alkyl fuel additives has decreased Pb inputs to recently deposited estuarine sediments. Yet, a substantial historical anthropogenic Pb inventory remains in soils of the watershed and erosion of surface soils continues to contribute to its enrichment in estuarine sediments. Concentrations of other elements (e.g., Cu, Zn, Cd), however, have not decreased with time, suggesting continued active inputs. Concentrations of Ba, Co, Cr, Ni, V and U, although elevated in some cases, typically reflect greater proportions attributed to natural sources rather than anthropogenic input.     

Mineralogy, geochemistry, and origin of hydrothermal manganese veins at Wadi Maliek, Southern Eastern Desert, Egypt

The present work deals with the geology, mineralogy, geochemistry, and origin of the metagabbroic-hosted manganese deposits at Wadi Maliek in the southern Eastern Desert of Egypt. The manganese veins are found in the shear zones and channel ways of the fault planes within the metagabbroic rocks pointing to those hydrothermal solutions carrying manganese and iron load penetrating along these fractures. These faults are striking N 80° E?CS 80° W with dipping 65°. These veins vary in thickness from 15?cm up to 125?cm wide; each vein may show difference in thickness from bottom to top. Microscopic examinations, X-ray diffraction, infrared spectral, differential thermal (DTA), thermogravimetric (TGA), and ESEM-EDAX analyses revealed that the manganese minerals consist mainly of pyrolusite, psilomelane, and ramsdellite. Goethite and hematite are the common iron minerals. Petrographically, the manganese deposits can be classified into three ore types based on the predominance of manganese and iron minerals: manganese, manganese?Ciron, and iron ore types. The geochemistry of Maliek deposits indicated that the total averages of some major oxides in manganese, manganese?Ciron, and iron ore types are respectively as follows: SiO₂ (15.64%, 11.52%, and 20.58%), MnO (39.9%, 17.81%, and 0.77%), FeO* (7.13%, 33.31%, and 37.08%), CaO (5.89%, 5.82%, and 5.32%), and Na₂O (1.04%, 1.61%, and 1.53%). With regard to trace elements, the Maliek manganese deposits are rich in Zn, Ba, Pb, Sr, and V. Based on the geological, mineralogical, and geochemical results, the studied manganese deposits are considered to be precipitated from hydrothermal solution.     

The Escanaba Trough, Gorda Ridge hydrothermal system: Temporal stability and subseafloor complexity

The composition and temperature of vent fluids sampled from the active hydrothermal system in Escanaba Trough, Gorda Ridge in 2000 and 2002 remain unchanged from the only time this field was previously sampled, in 1988. ODP Leg 169 drilled nine bore holes at this site in 1996, some within meters of the vents, yet this disturbance has not impacted the measured compositions or temperatures of the fluids exiting at the seafloor. The fluids have maximum measured temperatures of 218°C and contain ∼20% more chloride than local ambient seawater. Our interpretation is that the fluid compositions are generated by supercritical phase separation of seawater, with much of the water-rock reaction occurring within the ∼400m thick sedimentary section that overlies the basalt at this site. The ODP drilling results provide information on the mineralogy and composition of materials below the seafloor, as well as direct constraints not typically available on the physical conditions occurring below the seafloor hydrothermal system. Calculations utilizing geochemical modeling software suggest the fluids are close to saturation with a suite of minerals found subsurface, suggesting equilibrium between the fluids and substrate. These results provide an explanation for why the fluids have remained chemically stable for 14 yrs. The pore water data from drilling suggest that the hydrology and chemistry of the hydrothermal system are much more complex within the sediment cover than would be expected from the surface manifestations of the hydrothermal system. While the pore waters have chloride contents both greater and less than the local seawater, only fluids with higher chloride contents vent at the seafloor. Our calculations suggest that at the current conditions the “brines” (fluids with chlorinity greater than seawater) are actually less dense than the “vapors” (fluids with chlorinity less than seawater). These density relationships may provide an explanation for why the “brines” are now venting preferentially to the “vapors,” a situation opposite to what is usually observed or inferred.     

Rare earth, major and trace elements in Jurassic manganese shales of the Northern Calcareous Alps: hydrothermal versus hydrogenous origin of stratiform manganese deposits

Summary ?The rare earth, major and trace element geochemistry of Jurassic deep marine manganese shales allow insight into their environment of deposition. We present data of 24 samples from the Northern Calcareous Alps (Eastern Alps), collected from Late Jurassic strata of the Tennengebirge and from Early Jurassic strata of the Karwendel Mts. Whereas major and trace element geochemistry is controlled by the detrital input, rare earth element data and the relationship between total organic carbon and (pyritic) sulfur can be used to constrain the origin of the manganese accumulation. The data of this study are compatible with a hydrogenous precipitation of manganese by strongly varying redox-conditions at the sediment–water interface of a slope basin. Received December 21, 2001; revised version accepted February 18, 2002     

Temporal relationship between granite cooling and hydrothermal uranium mineralization at Dalongshan in China: a combined radiometric and oxygen isotopic study

A combined study using multi-radiometric dating and oxygen isotopic geothermometry was carried out for Mesozoic quartz syenite, alkali-feldspar granite and associated hydrothermal uranium mineralization at Dalongshan in the Middle-Lower Yangtze valley of east-central China. Radiometric dating of the quartz syenite yields a whole-rock Rb–Sr isochron age of 135.6±4.3 Ma, a zircon U–Pb isochron age of 132.9±2.2 Ma, and K–Ar ages of 126±2, 118±3 and 94±4 Ma for hornblende, biotite and orthoclase, respectively. The alkali-feldspar granite yields a whole-rock Rb–Sr isochron age of 117.3±3.3 Ma, a zircon U–Pb isochron age of 114.7±2.1 Ma, and K–Ar ages of 112±2, 109±3 and 88±4 Ma for hornblende, biotite and orthoclase, respectively. Oxygen isotope thermometry for both granites gives temperatures of 685 to 720, 555 to 580, 435 to 460 and 320 to 330 °C, for hornblende, magnetite, biotite and orthoclase respectively, when paired with quartz. The systematic differences among the ages by the different techniques on the different minerals are used to reconstruct the cooling history of the granite. The results yield rapid cooling rates of 27.4 to 58.6 °C/Ma from 800 to 300 °C in the early stage, but slow cooling rates of 6.3 to 7.2 °C/Ma from 300 to 150 °C in the late stage. The regular sequence of oxygen isotope temperatures for the different quartz–mineral pairs demonstrates that diffusion is a dominant factor controlling the closure of both radiometric and O isotopic systems during granite cooling. Pitchblende U–Pb isochron dating yields an uranium mineralization age of 106.4±2.9 Ma, which is younger than the age of the granite emplacement and thus considerably postdates the time of magma crystallization, but is close to the closure time of the K–Ar system in the biotite. This points to a close relationship between granite cooling and ore-forming process. It appears that hydrothermal mineralization took place in the stage of slow cooling of the granite, whereas the rapid cooling of the granite was concurrent with the migration of hydrothermal fluids along fault structures. Therefore, the activity of the ore-forming hydrothermal system is temporally dictated by the cooling rates of the granite and may lag about 25 to 30 Ma behind the crystallization timing of associated granite.     

Shallow and deep aquifer hydrochemistry and chemical variability of water quality at Shariatpur district, Bangladesh

Water quality and hydrochemistry of Shariatpur district were evaluated in terms of hydrochemical composition and some important physico-chemical parameters. The groundwater of the study area is good for drinking, domestic as well as for irrigation purposes. Among the major ions, shallow tube well waters give higher concentration of Ca²⁺ which ranges from 24 to 260 mg/L. The deep tubewell waters show higher concentration of Na⁺ which varies from 74 to 582 mg/L during dry season. Among the trace elements most of the shallow aquifer samples show higher concentration of Fe²⁺, Mn²⁺ and As. Concentration of Fe²⁺ varies from 0.655 to 18.8 mg/L, and Mn²⁺ from trace to 0.868 mg/L during dry period. Hydrochemical analyses reveal significant seasonal variation in water quality of shallow aquifer. Both the shallow aquifer and the surface water of the study area are predominantly of Ca–Mg–HCO₃ type, while the deep aquifer water is mainly of Na–K–Cl–SO₄ type with slight inclination to Ca–Mg–HCO₃ type. The study area is suitable for groundwater development if comprehensive and holistic approaches towards water resource management are taken into consideration.     

Timing and duration of hydrothermal activity at the Los Bronces porphyry cluster: an update

New geochronological data from the Los Bronces cluster of the Río Blanco-Los Bronces mega-porphyry Cu-Mo district establish a wide range of magmatism, hydrothermal alteration, and mineralization ages, both in terms of areal extent and time. The northern El Plomo and southernmost Los Piches exploration areas contain the oldest barren porphyritic intrusions with U-Pb ages of 10.8?±?0.1 Ma and 13.4?±?0.1 Ma, respectively. A hypabyssal barren intrusion adjacent northwesterly to the main pit area yields a slightly younger age of 10.2?±?0.3 Ma (San Manuel sector, U-Pb), whereas in the Los Bronces (LB) open-pit area, the present day mineral extraction zone, porphyries range from 8.49 to 6.02 Ma (U-Pb). Hydrothermal biotite and sericite ages are up to 0.5 Ma younger but consistent with the cooling of the corresponding intrusion events of each area. Two quartz-molybdenite B-type veins from the LB open pit have Re-Os molybdenite ages of 5.65?±?0.03 Ma and 5.35?±?0.03 Ma consistent with published data for the contiguous Río Blanco cluster. The San Manuel exploration area within the Los Bronces cluster, located about 1.5–2 km southeast of the open-pit extraction zone, shows both the oldest hydrothermal biotite (7.70?±?0.07 Ma; ⁴⁰Ar/³⁹Ar) and breccia cement molybdenite ages (8.36?±?0.06 Ma; Re-Os) registered in the entire Río Blanco-Los Bronces district. These are also older than those reported from the El Teniente porphyry Cu(-Mo) deposit, suggesting that mineralization in the late Miocene to early Pliocene porphyry belt of Central Chile commenced 2 Ma before the previously accepted age of 6.3 Ma.     

New geochemical and mineralogical constraints on the genesis of the Vani hydrothermal manganese deposit at NW Milos island,Greece: Comparison with the Aspro Gialoudi deposit and implications for the formation of the Milos manganese mineralization

The Mn-Ba-Pb deposit at Aspro Gialoudi in NW Milos is shown to be a fossil inhalative-exhalative hydrothermal deposit that represents the deepest part of the Vani succession at the western extremity of the main Vani manganese deposit. The geology of the Vani-Aspro Gialoudi area is characterized by Upper Pliocene-Lower Pleistocene dacitic and rhyodacitic lava domes, which are overlain by the Vani volcaniclastic unit considered to be part of the 2.66–1.44 Ma magmatic event at Milos Island. The presence of in-situ and intrusive hyaloclastite breccias surrounding the coherent lava domes at Aspro Gialoudi and Vani areas indicates submarine emplacement for the domes. The dacitic-rhyodacitic domes are variously altered (mainly propylitic and/or argillic alteration, silicified and in some cases locally exhibiting adularia alteration). Both Aspro Gialoudi and main Vani deposit are located proximal to fault systems: the main Vani manganese deposit is adjacent to the NW-trending Kondaros-Katsimouti-Vani Dome fault, whereas the Aspro Gialoudi deposit is adjacent to the relatively minor NE-trending fault on the west coast of Milos. At Aspro Gialoudi, mineralization took place in a subseafloor and/or seafloor environment and is characterized by a stratabound Mn-barite-rich deposit mainly within a package of propylitized intrusive hyaloclastites and within the overlying sandstones. Banded epithermal veins trending NE-SW and composed of chalcedonic silica/quartz + barite + Mn-oxide ± sulfides crosscut the dacitic lavas, the hyaloclastites and the overlying volcaniclastic sequence at Aspro Gialoudi and are considered to represent the feeder zones of the manganese-barite mineralization. Within the veins, early sulfide (galena-sphalerite) barite and quartz deposition is followed by manganese oxides and aragonite, thus resembling the epithermal-style Pb-Zn-Ag-Mn mineralization across the NW-trending Katsimoutis-Kondaros-Vani fault. Mineralization in Aspro Gialoudi and Vani deposits seems to be controlled by alternating cycles of deposition of sulfides and hydrothermal manganese oxides within the faults. Manganese deposition in both deposits formed in a similar manner, namely by transport of hydrothermal fluids through the adjacent fault systems into a reservoir of volcanoclastic sandstone and hyaloclastites to produce a deposit initially consisting of principally of pyrolusite and occasionally ramsdellite, which were subsequently replaced by cryptomelane, hollandite, coronadite and hydrohaeterolite. Precipitation of hydrothermal manganese oxides took place very quick and under microbial Mn(II) oxidation. Compositional data show that metallic elements most enriched in the Aspro Gialoudi and Vani manganese deposits relative to the average continental crust, lie in the sequences Pb > Cd > Mn > As > Sb > Zn > W > Tl > Ba > Cu > Mo > Co > Bi and As > Sb > Pb > Mn > Tl > Cd > Zn > W > Cu > Ba > Mo > Co, respectively. Mineralogical and geochemical (e.g. REE) data from both Aspro Gialoudi and main Vani deposit are taken to indicate mainly a seawater source for the hydrothermal fluids. These two deposits are genetically and spatially related to base- and precious metal intermediate-sulfidation epithermal mineralization. They formed successively by similar processes and are considered to be integral parts of the same hydrothermal system.     

On the distribution of iron and manganese at the sediment/water interface: thermodynamic versus kinetic control

Iron and manganese solubility at the sediment/water interface has been studied at a water depth of 20 m in Kiel Bight, Western Baltic. By means of an in situ bell jar system enclosing 3.14 m² sediment surface and 2094 l water a complete redox turn-over in the bottom water was simulated in an experiment lasting 99 days. The concentration of dissolved Fe in the bell jar water never exceeded 0.041 μmol · dm^?3during the first 50 days of the experiment and then rose abruptly as the Eh fell from +600 to ?200 mV. The concentration of dissolved Fe under oxic and anoxic conditions seems to be limited by equilibria with solid Fe-phases (hydroxides and amorphous sulphide, respectively). In contrast to Fe, manganese was released continuously from the bottom during the first 50 days of the experiment leading to exponentially increasing manganese concentrations in the bell jar water. During this time dissolved O₂ had become ready depleted and pH had dropped from 8.3 to 7.5. Contrary to iron, manganese being solubilized in reduced sediment layers can penetrate oxic strata in metastable form due to slow oxidation kinetics; when the redoxcline moves upwards Mn²⁺ is enriched in bottom waters. The maximum concentration of dissolved Mn under anoxic conditions is controlled by a solid phase with solubility properties similar to MnCO₃ (rhodochrosite). Bottom water enrichment in dissolved Mn²⁺ could be traced to originate from excess solid manganese within the top 3 cm of the sediment.     

Petrology and geochemistry of basalts from the American-Antarctic Ridge,Southern Ocean: implications for the westward influence of the Bouvet mantle plume

Ridge segments and fracture zones from the American-Antarctic Ridge have been systematically dredge sampled from 4° W to 18° W. Petrographic studies of the dredged basalts show that the dominant basalt variety is olivine-plagioclase basalt, although olivine-plagioclase-clinopyroxene basalt is relatively common at some localities. Selected samples have been analysed for major and trace elements, rare earth elements and Sr and Nd isotopes. These data show that the majority of samples are slightly evolved (Mg#=69-35) N-type MORB, although a small group of samples from a number of localities have enriched geochemical characteristics (T- and P-type MORB).These different types of MORB are readily distinguished in terms of their incompatible trace element and isotopic characteristics: N-type MORB have high Zr/Nb (17–78), Y/Nb (4.6–23) and ¹⁴³Nd/¹⁴⁴Nd (0.51303–0.51308) ratios, low Zr/Y (2.2–4.2) and ⁸⁷Sr/⁸⁶Sr (0.70263–0.70295) ratios and have (La/Sm)_N<1.0; T-type MORB have lower than chondritic Zr/Nb ratios (8.8–15.5), relatively low Y/Nb (1.9–4.3) and ¹⁴³Nd/¹⁴⁴Nd (0.51296–0.51288) ratios and relatively high Zr/Y (3.1–4.7), ⁸⁷Sr/⁸⁶Sr (0.70307–0.70334) and (La/Sm)_N (1.1–1.5) ratios; the single sample of P-type MORB has low Zr/Nb (6.3), Y/Nb (0.9) and ¹⁴³Nd/¹⁴⁴Nd (0.51287) ratios and high Zr/Y (7.1), ⁸⁷Sr/⁸⁶Sr (0.70351) and (La/Sm)_N (2.4) ratios. The geochemical characteristics of this sample are essentially identical to those of the Bouvet Island lavas.Geochemically enriched MORB are less abundant on the American-Antarctic Ridge than on the Southwest Indian Ridge but their geochemical characteristics are identical. The compositions of T- and P-type MORB are consistent with a regional mixing model involving normal depleted mantle and Bouvet plume type magma. On a local scale the composition of T-type MORB is consistent with derivation from depleted mantle which contains 4% veins of P-type melt.We propose a model for the evolution of the American-Antarctic Ridge lavas in which N-type MORB is derived from mantle with negligible to low vein/mantle ratios, T-type MORB is derived from domains with moderate and variable vein/mantle ratios and P-type MORB from regions with very high vein/mantle ratios where vein material comprises the major portion of the melt. The sparse occurrence of enriched lavas and by implication enriched mantle beneath the American-Antarctic Ridge, some distance (500–1,200 km) from the Bouvet plume location, is interpreted to be the result of lateral dispersion of enriched mantle domains by asthenospheric flow away from the Bouvet mantle plume towards the American-Antarctic Ridge.     

Origin of the Neoproterozoic Baijianshan Banded Iron Formation at the Southeastern Margin of the Tarim Block in NW China: Implication for an Extremely Reducing Ocean

The Neoproterozoic banded iron formations(BIFs)were closely associated with the“Snowball Earth”during the breakup of the Rodinia,thus they played an important role in our understanding of the atmospheric and oceanic oxygen levels during this period.In this contribution,the Neoproterozoic(ca.737 Ma)Baijianshan BIF at Southeast Tarim,northwestern China was identified.Magnetite is the dominated iron-species,which occurs as the lamina interbedded with chert.The BIF contains low concentrations of trace elements,and is depleted in light rare earth elements(LREEs)based on comparison with the Post-Archean Australian Shale(PAAS).In addition,the BIF exhibits slightly positive La-Eu anomalies,negligible Ce anomalies,insignificant Y anomalies,chondritic Y/Ho ratios(23-32),and slightly chondritic initial ε_Nd(t=737 Ma)values(?0.45 to 1.46,averaging 0.37).All these features indicate that the precipitation of Baijianshan BIF was closely related to the submarine low-T hydrothermal fluids with little detrital contribution.Moreover,the Baijianshan BIF is characterized by the significant enrichment of heavy Fe isotopes,with δ⁵⁷Fe_IRMM-014 values ranging from 1.78‰ to 3.05‰,revealing the partial oxidation of Fe²⁺ into Fe³⁺ during the precipitation of this BIF.Our data suggest that the formation of Baijianshan BIF was closely associated with a significantly reducing ocean,which most likely was isolated from the oxidized atmosphere by a local ice sheet.This Neoproterozoic Baijianshan ocean has the initial oxygen levels as low as,or even lower than that of Archean and Paleoproterozoic oceans.     

Nature and origin of the Vani manganese deposit, Milos, Greece: an overview

The Vani manganese deposit is located in the rugged NW sector of Milos Island. It occurs within the Vani volcano-sedimentary basin, which is underlain by dacitic domes and flows of Upper Pliocene age (3.5–2.0 Ma). The end of the emplacement of the dacites was marked by the collapse of the magma chamber, which resulted in a huge pyroclastic episode and the deposition of a thick layer of pyroclastic material within a shallow submarine basin. This pyroclastic material subsequently compacted to form the volcaniclastic sandstone, which became the host for the manganese ore beds which were about 4 m thick in the two sections studied. Hydrothermal fluids penetrated these sandstone horizons via fractures and fissures to produce the manganese deposit. The permeable nature of the sandstone facilitated the retention of the hydrothermal fluids within these layers. This permitted the fluids to cool slowly and deposit the manganese oxides almost quantitatively. Formation of the hydrothermal manganese deposit took place fairly rapidly over a period of several tens of thousands of years at most. Strong tectonic activity resulted in rapid uplift of the area which elevated the deposit above sea level.Two generations of manganese oxides have been identified within this deposit; the first generation consists of pyrolusite and ramsdellite; the second generation of oxides of the isostructural series cryptomelane–hollandite–coronadite plus hydrohetaerolite characterized by high contents of K, Ba, Pb and Zn, respectively. This sequence is the result of a two-stage process of formation of the manganese-oxide minerals in which a second high-salinity hydrothermal fluid enriched in Ba, Pb and Zn as a result of the dissolution of sulphide minerals remineralized the original manganese-oxide assemblage. It is this two-stage process of formation, which was mainly responsible for the unique characteristics of this deposit. Although formed in a submarine setting, the deposit shows marked differences in mineralogy and composition from known submarine hydrothermal manganese deposits and is most analogous to the epithermal vein deposits of the southwestern United States.     

Physicochemical formation parameters of hydrothermal mineral deposits: Evidence from fluid inclusions. II. Gold,silver, lead,and zink deposits

Information from a database, which was compiled and continuously updated by the authors of this paper and now includes information from 19500 publication on fluid and melt inclusions in minerals, is used to summarize results on the physicochemical formation parameters of hydrothermal Au, Ag, Pb, and Zn deposits. The database provides information on fluid inclusions in minerals from 970 Pb-Zn, 220 Au-Ag-Pb-Zn, and 825 Au-Ag deposits in various settings worldwide. Histograms for the homogenization temperatures of fluid inclusion are presented for the most typical minerals of the deposits. In sphalerite, most homogenization temperatures (1327 measurements) of fluid inclusions lie within the range of 50–200°C with a maximum at 100–200°C for this mineral from Pb-Zn deposits and within the range of 100–350°C (802 measurements) with a maximum at 200–300°C for this mineral from Au deposits. Data are presented on fluid pressures at Au (1495 measurements) and Pb-Zn (180 measurements) deposits. The pressure during the preore, ore-forming, and postore stages at these deposits ranged from 4–10 to 6000 bar. The reason for the high pressures during preore stages at the deposits is the relations of the fluids to acid magmatic and metamorphic processes. More than 70% of the fluid pressures values measured at Pb-Zn deposits lie within the range of 1–1500 bar. Au-Ag deposits are characterized by higher fluid pressures of 500–2000 bar (61% of the measurements). The overall ranges of the salinity and temperature of the mineral-forming fluid at Au-Ag (6778 measurements) and Pb-Zn (3395 measurements) deposits are 0.1–80 wt % equiv. NaCl and 20–800°C. Most measurements (～64%) for Au-Ag deposits yield fluid salinity <10 wt % equiv. NaCl and temperatures of 200–400°C (63%). Fluids at Pb-Zn deposits are typically more saline (10–25 wt % equiv. NaCl, 51% measurements) and lower temperature (100–300°C, 74% measurements). Several measurements of the fluid density fall within the range of 0.8–1.2 g/cm³. The average composition of volatile components of the fluids was evaluated by various techniques. The average composition of volatile components of fluid inclusions in minerals is calculated for hydrothermal W, Au, Ag, Sn, and Pb-Zn deposits, metamorphic rocks, and all geological objects. The Au, Ag, Pb, and Zn concentrations in magmatic melts and mineral-forming fluids is evaluated based on analyses of individual inclusions.     

Seasonal variability of oxygen and hydrogen stable isotopes in precipitation and cave drip water at Guilin,southwest China

The interpretation of climatic information from stalagmites has traditionally been a complex research problem, with oxygen isotopes playing a particularly important role in global climate change studies. This study investigates the relationship between oxygen isotope composition of the atmospheric in precipitation and cave drip water at Panlong cave in southwest China on seasonal timescales of variability. Time series seasonal variability was derived from Panlong cave in Guilin by collecting daily precipitation samples for stable isotope analysis during 2012. Results indicate that δ¹⁸O of precipitation contains a clear seasonal variation whereby higher values are mainly distributed during winter and lower values during summer. Seasonal variations in water sources affect the precipitation δ¹⁸O values. Drip water δ¹⁸O also displayed a seasonal cycle which is attenuated relative to δ¹⁸O of precipitation. Drip water time series display seasonal cycle ranges from 1.5 to 3.5 ‰ relative to Vienna Standard Mean Ocean Water, which mainly follow the precipitation δ¹⁸O seasonal cycle. Seasonal variation in drip water δ¹⁸O supports interpretations of the stalagmite δ¹⁸O record as a paleoclimate proxy sensitive to the local environment. This monitoring experiment revealed that drip water must be transported through the epikarst in approximately 1.5 months during cold periods, and <0.5 months during warm periods. Different residence time percolation is mainly affected by the atmospheric precipitation amount, depending on whether soil moisture reaches saturation.     

Temporal and spatial variability of cross-fault groundwater-level differences: the impact of fault-induced permeability reduction,precipitation and evapotranspiration

Hydrogeology Journal - Faults in the Roer Valley Rift System (Netherlands, Belgium, and Germany) act as barriers to lateral groundwater flow in unconsolidated sedimentary aquifers. This causes a...     

Late Holocene (0–2.4 ka BP) surface water temperature and salinity variability, Feni Drift, NE Atlantic Ocean

Planktonic foraminiferal Mg/Ca ratios and oxygen isotopic compositions of a spliced sediment record from Feni Drift, NE Atlantic Ocean (box core M200309 and piston core ENAM9606) trace late Holocene sea surface temperature (SST) and salinity changes over the past 2400 years. At this location, the variability of SST and oxygen isotopic composition of seawater (δ¹⁸O_w) reflects variable northward advection of warm and saline surface waters, which appears linked to climate variability over the adjacent European continent. Our records reveal a general long-term cooling trend. Superimposed on this overall trend, partly higher temperatures and salinities from 180 to 560 AD and 750 to 1160 AD may be ascribed to the Roman and Medieval Warm Periods, respectively. Subsequently, our record displays highly variable surface water conditions; the main Little Ice Age SST minimum is restricted to the 15th and 16th centuries AD. Pervasive multidecadal- to centennial-scale variability throughout the sedimentary proxy records can be partly attributed to solar forcing and/or variable heat extraction from the surface ocean caused by shifts in the prevailing state of the North Atlantic Oscillation (NAO). High salinities in the 17th and 18th centuries are considered to reflect tropical anomalies linked to a southward shift of the Intertropical Convergence Zone, propagating across the North Atlantic Ocean.     

Perspectives on basaltic magma crystallization and differentiation: Lava-lake blocks erupted at Mauna Loa volcano summit, Hawaii

Explosive eruptions at Mauna Loa summit ejected coarse-grained blocks (free of lava coatings) from Moku'aweoweo caldera. Most are gabbronorites and gabbros that have 0–26 vol.% olivine and 1–29 vol.% oikocrystic orthopyroxene. Some blocks are ferrogabbros and diorites with micrographic matrices, and diorite veins (≤ 2 cm) cross-cut some gabbronorites and gabbros. One block is an open-textured dunite.

The MgO of the gabbronorites and gabbros ranges  7–21 wt.%. Those with MgO > 10 wt.% have some incompatible-element abundances (Zr, Y, REE; positive Eu anomalies) lower than those in Mauna Loa lavas of comparable MgO; gabbros (MgO < 10 wt.%) generally overlap lava compositions. Olivines range Fo_83–58, clinopyroxenes have Mg#s  83–62, and orthopyroxene Mg#s are 84–63 — all evolved beyond the mineral-Mg#s of Mauna Loa lavas. Plagioclase is An_75–50. Ferrogabbro and diorite blocks have  3–5 wt.% MgO (TiO₂ 3.2–5.4%; K₂O 0.8–1.3%; La 16–27 ppm), and a diorite vein is the most evolved (SiO₂ 59%, K₂O 1.5%, La 38 ppm). They have clinopyroxene Mg#s 67–46, and plagioclase An_57–40. The open-textured dunite has olivine  Fo_83.5. Seven isotope ratios are ⁸⁷Sr/⁸⁶Sr 0.70394–0.70374 and ¹⁴³Nd/¹⁴⁴Nd 0.51293–0.51286, and identify the suite as belonging to the Mauna Loa system.

Gabbronorites and gabbros originated in solidification zones of Moku'aweoweo lava lakes where they acquired orthocumulate textures and incompatible-element depletions. These features suggest deeper and slower cooling lakes than the lava lake paradigm, Kilauea Iki, which is basalt and picrite. Clinopyroxene geobarometry suggests crystallization at < 1 kbar P. Highly evolved mineral Mg#s, < 75, are largely explained by cumulus phases exposed to evolving intercumulus liquids causing compositional ‘shifts.’ Ferrogabbro and diorite represent segregation veins from differentiated intercumulus liquids filter pressed into rigid zones of cooling lakes. Clinopyroxene geobarometry suggests < 300 bar P. Open-textured dunite represents olivine-melt mush, precursor to vertical olivine-rich bodies (as in Kilauea Iki). Its Fo_83.5 identifies the most primitive lake magma as  8.3 wt.% MgO. Mass balancing and MELTS show that such a magma could have yielded both ferrogabbro and diorite by ≥ 50% fractional crystallization, but under different fO₂: < FMQ (250 bar) led to diorite, and FMQ (250 bar) yielded ferrogabbro. These segregation veins, documented as similar to those of Kilauea, testify to appreciable volumes of ‘rhyolitic’ liquid forming in oceanic environments. Namely, SiO₂-rich veins are intrinsic to all shields that reached caldera stage to accommodate various-sized cooling, differentiating lava lakes.