Major-element composition of the particulate matter in the near-bottom nepheloid layer of the gulf of Mexico

During cruises 71-A-12 and 73-A-3 of the R/V “Alaminos” eighty-six samples of suspended matter at eleven near-bottom stations in the Gulf of Mexico and northwestern Caribbean Sea were collected, and simultaneously, values for light scattering were measured. Selected samples of the suspended matter were analyzed for particulate aluminum, silicon, iron, calcium, magnesium, organic carbon and inorganic carbon. The results indicate that a permanent but highly variable near-bottom nepheloid layer exists in the Gulf of Mexico but not in the northwestern Caribbean Sea. Average total-suspended loads in the Gulf of Mexico nepheloid layer are two times higher than in the clear water above the nepheloid layer.Since there is a significant increase in the alumino-silicate fraction and a corresponding decrease in the organic fraction of the suspended matter in the nepheloid layer relative to the overlying water, it appears that sediments are the most probable source of the increased concentrations of suspended matter in the nepheloid layer. This hypothesis is supported by X-ray diffraction analyses on the nepheloid material collected at one station which show the same mineral assemblages as the underlying sediments.Time studies over periods of one week and one and one-half years showed large total-suspended-matter variations which indicate that non steady-state processes, primarily vertical eddy diffusion and possibly advection, are controlling the distribution of suspended matter in the nepheloid layer.     

Geological,fluid inclusion and stable isotope studies of Mo mineralization,Galway Granite,Ireland

Mo mineralization within the Galway Granite at Mace Head and Murvey, Connemara, western Ireland, has many features of classic porphyry Mo deposits including a chemically evolved I-type granite host, associated K- and Si-rich alteration, quartz vein(Mace Head) and granite-hosted (Murvey) molybdenite, chalcopyrite, pyrite and magnetite mineralization and a gangue assemblage which includes quartz, muscovite and K-feldspar. Most fluid inclusions in quartz veins homogenize in the range 100–350°C and have a salinity of 1–13 eq. wt.% NaCl. They display Th-salinity covariation consistent with a hypothesis of dilution of magmatic water by influx of meteoric water. CO₂-bearing inclusions in an intensely mineralized vein at Mace Head provide an estimated minimum trapping temperature and pressure for the mineralizing fluid of 355°C and 1.2 kb and are interpreted to represent a H₂O-CO₂ fluid, weakly enriched in Mo, produced in a magma chamber by decompression-activated unmixing from a dense Mo-bearing NaCl-H₂O-CO₂ fluid. ³⁴S values of most sulphides range from c. 0 at Murvey to 3–4 at Mace Head and are consistent with a magmatic origin. Most quartz vein samples have ¹⁸O of 9–10.3 and were precipitated from a hydrothermal fluid with ¹⁸O of 4.6–6.7. Some have ¹⁸O of 6–7 and reflect introduction of meteoric water along vein margins. Quartz-muscovite oxygen isotope geothermometry combined with fluid inclusion data indicate precipitation of mineralized veins in the temperature range 360–450°C and between 1 and 2 kb. Whole rock granite samples display a clear ¹⁸O-D trend towards the composition of Connemara meteoric waters. The mineralization is interpreted as having been produced by highlyfractionated granite magma; meteoric water interaction postdates the main mineralizing event. The differences between the Mace Head and Murvey mineralizations reflect trapping of migrating mineralizing fluid in structural traps at Mace Head and precipitation of mineralization in the granite itself at Murvey.     

Magma mixing and mingling textures in granitoids: examples from the Galway Granite, Connemara, Ireland

Summary ?Many granitoid intrusions display textural evidence for the interaction of mafic and silicic magmas during their genesis. The ∼ 400 Ma Galway Granite exhibits excellent evidence for magma mixing and mingling both at outcrop/map scale (magma mingling and mixing zones), and at thin-section/crystal scale (mixing textures). These textures – quartz ocelli, rapakivi feldspars, acicular and mixed apatite morphologies, inclusion zones in feldspars, anorthite ‘spikes’ in plagioclase, sphene ocelli, K-feldspar megacrysts in mafic microgranular enclaves (MME), and mafic clots – constitute a textural assemblage whose origin can be explained in terms of magma mixing and mingling models. Furthermore, textures from this assemblage have been recorded throughout the Galway batholith indicating that magma mingling and mixing played a key role during its evolution. Received November 18, 2000; revised version accepted November 6, 2001     

Fluid inclusion study of the Ballinglen W-Sn-sulphide mineralization, SE Ireland

Scheelite-mineralized microtonalite sheets occur on the SE margin of the end-Caledonian Leinster Granite in SE Ireland. Scheelite, polymetallic sulphides and minor cassiterite occur in veins in the microtonalites, disseminated throughout the greisened microtonalite sheets and in the adjacent wallrocks. Two major mineralized vein types occur in the microtonalite sheets: (1) Scheelite ± arsenopyrite ± pyrrhotite occur in quartz-fluorite veins, generally without a muscovite selvage; (2) Sphalerite ± chalcopyrite ± pyrite ± galena ± cassiterite ± stannite occur in quartz + fluorite veins with a coarse muscovite selvage and are often intergrown with the muscovite. Quartz-hosted fluid inclusions were examined from representative samples of both vein types using petrographic, microthermometric and laser Raman spectroscopic techniques. Three distinct types of fluid inclusions have been recognized. Primary, vapour rich Type 1 inclusions in quartz from the scheelite-mineralized veins are of H₂O-CO₂-CH₄-N₂ ± H₂S ± NaCl composition and formed between 360–530 °C. Primary and secondary, liquid-rich Type 2 fluid inclusions in the base metal sulphide-mineralized veins are of H₂O-CH₄-N₂ ± H₂S-NaCl composition and formed between 340–480 °C. They also occur as pseudosecondary and secondary inclusions in scheelite-mineralized veins. Late dilute, low temperature H₂O-NaCl + KCl fluid inclusions may be related to late-Caledonian convection of meteoric waters around the cooling Leinster Granite batholith. Received: 4 September 1996 / Accepted: 23 May 1997     

Dissolved trace metals in the surface waters of Puget Sound

Employing clean and quantitative techniques, a marine monitoring programme succeeded in detecting large surface elevations in the concentrations of dissolved Cu, Zn and Pb in the marine surface waters of Puget Sound adjacent to Seattle and Tacoma, Washington. Physical mixing with cleaner waters was the controlling factor in reducing the dissolved concentrations of Cu downstream of these contaminated regions. Comparisons between Puget Sound waters and coastal waters adjacent to Puget Sound suggest that a portion of this Cu, Zn and Pb pollution is being advected out of Puget Sound. The low Ni and Cd concentrations found in this study indicate that these trace metals are not a significant pollution problem in the main basin of Puget Sound.     

Radium isotopes in sub-Arctic waters

Measurements of the²²⁸Ra/²²⁶Ra activity ratio in the waters of the Greenland, Norwegian and Labrador Seas and Baffin Bay reveal strong horizontal gradients in the surface waters. The coastal waters are dominated by²²⁸Ra injection from nearshore sediments. There is an inverse correlation between the²²⁸Ra/²²⁶Ra activity ratio and salinity in the 30–36‰ salinity range. Vertical profiles indicate that the²²⁸Ra/²²⁶Ra activity ratio is also strongly coupled toσ_θ except for some regions where²²⁸Ra is being injected into higher density water as these isopycnals intersect coastal areas. We use these measurements in the area of formation of North Atlantic Deep Water to estimate that this water mass forms with a²²⁸Ra/²²⁶Ra activity ratio of 0.10.     

Features of coastal upwelling regions that determine net air-sea CO<Subscript>2</Subscript> flux

The influence of the coastal ocean on global net annual air-sea CO₂ fluxes remains uncertain. However, it is well known that air-sea pCO₂ disequilibria can be large (ocean pCO₂ ranging from ∼400 μatm above atmospheric saturation to ∼250 μatm below) in eastern boundary currents, and it has been hypothesized that these regions may be an appreciable net carbon sink. In addition it has been shown that the high productivity in these regions (responsible for the exceptionally low surface pCO₂) can cause nutrients and inorganic carbon to become more concentrated in the lower layer of the water column over the shelf relative to adjacent open ocean waters of the same density. This paper explores the potential role of the winter season in determining the net annual CO₂ flux in temperate zone eastern boundary currents, using the results from a box model. The model is parameterized and forced to represent the northernmost part of the upwelling region on the North American Pacific coast. Model results are compared to the few summer data that exist in that region. The model is also used to determine the effect that upwelling and downwelling strength have on the net annual CO₂ flux. Results show that downwelling may play an important role in limiting the amount of CO₂ outgassing that occurs during winter. Finally data from three distinct regions on the Pacific coast are compared to highlight the importance of upwelling and downwelling strength in determining carbon fluxes in eastern boundary currents and to suggest that other features, such as shelf width, are likely to be important.     

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     

Possible evidence for enrichment of trace elements in the hydrous manganese oxide phases of suspended matter from an urbanized embayment

Total and weak-acid-soluble trace elements in suspended matter from the Duwamish River and Elliott Bay were determined from samples collected in February and September 1980. The results indicate that Mn scavenging in the water column is coincident with enrichments of Cr, Ni, Cu, Zn, and Pb in the suspended matter, suggesting a possible enrichment of these trace elements in a hydrous Mn oxide phase. This process occurs primarily in the sub-surface waters of Elliott Bay. Since mass balance calculations show a net export of Mn out of the bay, this mechanism may be an important means of transporting toxic trace metals from polluted estuaries and embayments to cleaner coastal environments.