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1.
Unlike many reactive continental shelf mud deposits in temperate regions, bacteria and microfauna rather than macrofauna typically dominate benthic biomass and activities over large areas of the Gulf of Papua (GoP) deltaic complex, Papua New Guinea. During mid NW monsoon periods (Jan–Feb), macrofaunal densities at Gulf stations were relatively low (), large macroinfauna were absent (upper 25 cm), and small (), surface deposit-feeding polychaetes and tubiculous amphipods were dominant, reflecting a frequently destabilized seabed and high sedimentation/erosion rates. Although frequent physical disturbance generally inhibits development of macrobenthic communities, some regions of the Gulf deposits are periodically colonized and extensively bioturbated during quiescent periods, as shown by preserved biogenic sedimentary structures. Bacterial inventories integrated over the top 20 cm were extremely variable within each sub region of the clinoform complex. A possible bimodal pattern with bathymetric depth and distance offshore may occur: lowest-inventories within the sandy, proximal Fly River delta, an open Gulf inner topset zone (10–20 m) having sites of relatively high inventories, an open Gulf mid-topset region with intermediate values and less extreme variation, and the outer topset—upper foreset zone (40–50 m) where highest values are attained (). Various measures of microbial activity, including measures proportional to the cellular rRNA content and the proportion of dividing cells, indicate extremely productive populations over the upper 1-m of the seabed throughout the Gulf of Papua region. Bacterial biomass (0–20 cm) including data of Alongi et al. (1991, 1992, 1995) varied from a low of in intertidal mud banks to a high of in the topset—foreset zone. Macrofaunal biomass did not exceed in any sampled region, ranging from 0.009±0 to with no obvious correlation with bathymetric depth (1–63 m). Meiofaunal biomass was generally an order of magnitude lower than macrofaunal biomass. Relatively elevated bacterial biomass and high turnover rates are consistent with high measured rates of benthic remineralization, presumably reflecting the rapid response time of bacteria to physical reworking, the associated entrainment of organic substrate, and flushing of metabolites. Solute exchange is also enhanced below the directly mixed surface region, possibly producing ‘far field’ stimulation of microbes in underlying deposits. Physical reworking and reoxidation of sediments between 10 and 50 m water depth maintain suboxic, nonsulfidic conditions in the upper 0.5–1 m despite active microbial communities and high benthic remineralization rates.  相似文献   

2.
《Continental Shelf Research》2006,26(17-18):2241-2259
The Amazon River spawns a vast mobile mudbelt extending ∼1600 km from the equator to the Orinoco delta. Deposits along the Amazon–Guianas coastline are characterized by some of the highest Corg remineralization rates reported for estuarine, deltaic, or shelf deposits, however, paradoxically, except where stabilized by mangroves or intertidal algal mats, they are usually suboxic and nonsulfidic. A combination of tides, wind-driven waves, and coastal currents forms massive fluid muds and mobile surface sediment layers ∼0.5–2 m thick which are dynamically refluxed and frequently reoxidized. Overall, the seabed functions as a periodically mixed batch reactor, efficiently remineralizing organic matter in a gigantic sedimentary incinerator of global importance. Amazon River material entering the head of this dynamic dispersal system carries an initial terrestrial sedimentary Corg loading of ∼ 0.7 mg C m−2 particle surface area. Total Corg loading is lowered to ∼ 0.2 mg C m−2 in the proximal delta topset, ∼60–70% of which remains of terrestrial origin. Loading decreases further to 0.12–0.14 mg C m−2 (∼60% terrestrial) in mudbanks ∼600 km downdrift along French Guiana, values comparable to those found in the oligotrophic deepsea. DOC/ΣCO2 ratios in pore waters of French Guiana mudbanks indicate that >90% of metabolized organic substrates are completely oxidized. Within the Amazon delta topset at the head of the dispersal system, both terrestrial and marine organic matter contribute substantially to early diagenetic remineralization, although reactive marine substrate dominates (∼60–70%). The conditional rate constant for terrestrial Corg in the delta topset is ∼0.2 a−1. As sedimentary Corg is depleted during transit, marine sources become virtually the exclusive substrate for remineralization except very near the mangrove shoreline. The δ13C and Δ14C values of pore water ΣCO2 in mudbanks demonstrate that the primary source of remineralized organic matter within ∼1 km of shore is a small quantity of bomb signature marine plankton (+80‰). Thus, fresh marine organic material is constantly entrained into mobile deposits and increasingly drives early diagenetic reactions along the transit path. Relatively refractory terrestrial Corg is lost more slowly but steadily during sedimentary refluxing and suboxic diagenesis. Amazon Fan deposits formed during low sea level stand largely bypassed this suboxic sedimentary incinerator and stored material with up to ∼3X the modern high stand inner shelf Corg load (Keil et al., 1997b. Proceedings of the Ocean Drilling Program, Scientific Results. Vol. 155. pp. 531–537). Sedimentary dynamics, including frequency and magnitude of remobilization, and the nature of dispersal systems are clearly key controls on diagenetic processes, biogeochemical cycling, and global C storage along the continental margins.  相似文献   

3.
Clinoform mechanics in the Gulf of Papua, New Guinea   总被引：1，自引：0，他引：1  
The largest islands of the Indo-Pacific Archipelago are estimated to account for 20–25% of the global sediment discharge to the ocean, and much (>50%) of this sediment is supplied to wide (>150 km) continental shelves. These conditions are conducive to creation of large-scale morphologic features known as clinoforms—sigmoidal-shaped deposits on the continental shelf. The Gulf of Papua (GOP) receives 3.84 ×108 tons of sediment annually from three principal sediment suppliers, the Fly, Kikori and Purari Rivers, and its prograding clinoform is the focus of this study. During three research cruises, 80 cores and 37 CTD/optical backscatter casts were collected, and an instrumented tripod was deployed twice. Sedimentological and radiochemical results indicate that the GOP clinoform has characteristics similar to those seaward of other major rivers (e.g., Amazon, Ganges–Brahmaputra), specifically sand/mud interbedding on the topset, rapidly accumulating muds on the foreset, and siliciclastic mud mixed with carbonate sand on the bottomset.Using core data and field observations, the mechanics of clinoform progradation are examined. Discrete, large sedimentation events are identified as processes building the clinoform feature. X-radiographs from foreset cores reveal thick beds (>5 cm) between bioturbated sections. Detailed 210Pb and grain-size data indicate that low activities and increased clay contents are associated with these beds. They are hypothesized to be formed by fluid–mud deposition in response to periods of large wave-tide bed shear stresses, more likely during the SE-tradewind season, and their regular occurrence produces high rates of mean accumulation (4 cm/y). Bed preservation is determined by the rates of sediment accumulation and bioturbation.To assess the influence of physical oceanographic factors on clinoform shape, bottom shear stresses from tides and surface waves were calculated using available wave and tripod data. This effort reveals that the depth range (25–40 m) of the clinoform rollover point (seaward edge of the topset region) is roughly consistent with the sediment-transport regime. Furthermore, calculations corroborate the core data that suggest possible seasonal sediment storage in the inner topset region (<15-m water depth, during the NW-monsoon winds) with subsequent transfer to foreset beds (more probable during SE-tradewind conditions).A 100-yr sediment budget created with accumulation rate data suggests approximately 20% of the total sediment supplied to the GOP accumulates on the clinoform (creating the clinoform morphology). Less than 5% is believed to escape to the adjacent slope, and much of the remaining 75% is likely trapped on the inner-topset region (<20 m water depth) and within the mangrove forests and flood/delta plains of the northern GOP.  相似文献   

4.
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5.
This paper builds on a recently published one-dimensional moving-boundary model of the coevolution of topset, foreset and bottomset in a reservoir that captures the dynamics of the internal muddy pond typical to reservoirs. This model was modified to account for different outlet locations at the reservoir＇s downstream end. This model considers a river carrying two sustained phases of sediments： coarse （sand） and fine （mud）. The coarse phase deposits in the topset and delta foreset, while the fine phase forms a dilute suspension of wash load in the river. As the river enters the reservoir, the muddy water plunges on the foreset to form a Froude-supercritical （purely depositional） turbidity current. This turbidity current emplaces the bottomset. The modified numerical model was tested against five laboratory experiments previously reported by the author. The model successfully locates the muddy-water/clear-water interface. In addition, modeled and measured bed deposits are in good agreement. Results clearly indicate that the location of the internal hydraulic jump plays a key role in the final bed deposit.  相似文献   

6.
δ87Sr values and Ca/Sr ratios were employed to quantify solute inputs from atmospheric and lithogenic sources to a catchment in NW Germany. The aquifer consists primarily of unconsolidated Pleistocene eolian and fluviatile deposits predominated by >90% quartz sand. Accessory minerals include feldspar, glauconite, and mica, as well as disperse calcium carbonate in deeper levels. Decalcification of near-surface sediment induces groundwater pH values up to 4.4 that lead to enhanced silicate weathering. Consequently, low mineralized Ca–Na–Cl- and Ca–Cl-groundwater types are common in shallow depths, while in deeper located calcareous sediment Ca–HCO3-type groundwater prevails. δ87Sr values and Ca/Sr ratios of the dissolved pool range from 7.3 to −2.6 and 88 to 493, respectively. Positive δ87Sr values and low Ca/Sr ratios indicate enhanced feldspar dissolution in shallow depths of less than 20 m below soil surface (BSS), while equilibrium with calcite governs negative δ87Sr values and elevated Ca/Sr ratios in deep groundwater (>30 m BSS). Both positive and negative δ87Sr values are evolved in intermediate depths (20–30 m BSS). For groundwater that is undersaturated with respect to calcite, atmospheric supplies range from 4% to 20%, while feldspar-weathering accounts for 8–26% and calcium carbonate for 62–90% of dissolved Sr2+. In contrast, more than 95% of Sr2+ is derived by calcium carbonate and less than 5% by feldspar dissolution in Ca–HCO3-type groundwater. The surprisingly high content of carbonate-derived Sr2+ in groundwater of the decalcified portion of the aquifer may account for considerable contributions from Ca-containing fertilizers. Complementary tritium analyses show that equilibrium with calcite is restricted to old groundwater sources.  相似文献   

7.
Submersible observations and sampling were carried out in the rift valley of the Mid-Atlantic Ridge (MAR) near 34°40′N–35°N. The 4-km-wide rift valley consists of a Neo Volcanic Zone (NVZ) (<1 km wide) bounded at the west by a Median Ridge (MR) (5 km wide and 20 km long) and at the east by the first scarps of the eastern wall. The MR and the eastern wall are characterized by volcanic cones about 200–300 m height culminating at depths of 1500–1900 m which are made up of volcaniclastic deposits (pyroclasts and hyaloclasts) suggestive of explosive volcanism. Based on their surface morphology, degree of vesicularity, and composition, the erupted deposits are classified into four groups: (1) poorly vesicular (<15% vesicles) N- and T-MORBs (K/Ti <0.25, Na2O+K2O<2.9%) consisting of sheet flows and pillows formed during fissure eruptions in the NVZ at 2000–2300 m depths; (2) vesicular (15–30% vesicles) E-MORBs (K/Ti=0.25−0.45,Na2O+K2O>2.8−3.2%) and alkali basalts (K/Ti=0.45−0.70,Na2O+K2O>3.3−4) made up mainly of pillows; (3) highly vesicular (>35% vesicles) pillow lava and pyroclastic (scoria-like) alkali basalts (K/Ti>0.45−0.80,Na2O+K2O>3−4%); and (4) hyaloclastites consisting of glassy shards of alkali basalt composition. The total water and carbon contents of the deposits increase with the incompatible element concentrations. The estimated initial H2O content for the N- and T-MORBs is less than 3500 ppm, whereas for the E-MORBs and alkali basalts the H2O content is near 4000 and 7000 ppm, respectively. While the H2O is mainly in the melt, the carbon is in the form of CO2 filling vesicles. The vesicles are formed from magma with an initial carbon content of 1000–3000 for the N- and T-MORBs, 3000–6500 ppm for the E-MORBs and higher than 1 wt% for the alkali basalts.The various lava types were derived from a heterogeneous mantle source composed of enriched and depleted components during sequential eruptions of N-, T- and E-MORBs and alkali basalts (K/Ti>0.7). The amount of CO2 and H2O in equilibrium with the dissolved species present in the vesicles indicates that CO2 (XCO2=1−0.84) was the main exsolved compound responsible for bubble nucleation. The increase in the degree of vesicularity and pressure of the volatile phases is mainly due to the early exsolution of CO2 from an alkali melt. The exsolution of significant amounts of dissolved water occurred only for the alkali basalt a few hundred meters beneath the seafloor and contributed to late bubble expansion. This subsequent addition of magmatic water to the vesicles increased the gas pressure and triggered explosions. An alternative hypothesis for the explosive volcanism is based on field observations. During crater collapsed, seawater could have been trapped in fractured volcanic conduits and later sealed by hydrothermal fluid circulation and precipitation. In such an environment, this seawater will be heated and vaporized during renewed magmatic upwelling. Both scenarios give rise to fragmented debris (hyaloclasts and pyroclasts) and the explosive events create turbulent flows followed by differential gravity settling of the particles (shards versus lapilli) through the seawater.  相似文献   

8.
Sulfur isotope effects during the SO2 disproportionation reaction to form elemental sulfur (3SO2+3H2O→2HSO4−+S+2H+) at 200–330°C and saturated water vapor pressures were experimentally determined. Initially, a large kinetic isotopic fractionation takes place between HSO4− and S, followed by a slow approach to equilibrium. The equilibrium fractionation factors, estimated from the longest run results, are expressed by 1000 ln αHSO4−–S=6.21×106/T2+3.62. The rates at which the initial kinetic fractionation factors approach the equilibrium ones were evaluated at the experimental conditions.δ34S values of HSO4− and elemental sulfur were examined for active crater lakes including Noboribetsu and Niseko, (Hokkaido, Japan), Khloridnoe, Bannoe and Maly Semiachik (Kamchatka), Poás (Costa Rica), Ruapehu (New Zealand) and Kawah Ijen and Keli Mutu (Indonesia). ΔHSO4−–S values are 28‰ for Keli Mutu, 26‰ for Kawah Ijen, 24‰ for Ruapehu, 23‰ for Poás, 22‰ for Maly Semiachik, 21‰ for Yugama, 13‰ for Bannoe, 9‰ for Niseko, 4‰ for Khloridonoe, and 0‰ for Noboribetsu, in the decreasing order. The SO2 disproportionation reaction in the magmatic hydrothermal system below crater lakes where magmatic gases condense is responsible for high ΔHSO4−–S values, whereas contribution of HSO4− produced through bacterial oxidation of reduced sulfur becomes progressively dominant for lakes with lower ΔHSO4−–S values. Currently, Noboribetsu crater lake contains no HSO4− of magmatic origin. A 40-year period observation of δ34SHSO4− and δ34SS values at Yugama indicated that the isotopic variations reflect changes in the supply rate of SO2 to the magmatic hydrothermal system. This implies a possibility of volcano monitoring by continuous observation of δ34SHSO4− values. The δ18O values of HSO4− and lake water from the studied lakes covary, indicating oxygen isotopic equilibration between them. The covariance gives strong evidence that lake water circulates through the sublimnic zone at temperatures of 140±30°C.  相似文献   

9.
The influence of a further developed inlake restoration method on the P-immobilisation and microbial activities, especially under anoxic conditions was investigated. The impact of nitrate and iron dosing with a newly developed nitrate storage compound (Depox®Fe) was tested in enclosures in the eutrophic dimictic Lake Dagowsee, Germany. Additions of 50 g m−2 of NO3−–N and 66 g m−2 of Fe3+ ensured availability of nitrate at the sediment surface during a 2-months period.As a result the phosphate release from the anoxic sediments was completely suppressed even 1 year after the application. The hypolimnetic deoxygenation was unaffected by the Depox®Fe addition. However, sulfur reduction and methanogenesis were inhibited and the phosphatase activity increased.  相似文献   

10.
Airborne and ground-based (correlation spectrometer, cascade impactor, and photoelectric counter together with intake filter probes) measurements are described for the volcanic emissions from Popocatépetl volcano (Mexico) from December 23, 1994 to January 28, 1995. Measurements of SO2 restarted 48 h after the eruption onset of December 21, 1994. Maximum sulfur dioxide (4560 t d−1) plus 3.8×104 t d−1 of particulate matter were ejected on December 24, 1994. The maximum rate of ejection occurred coincidentally with the maximum amplitude of harmonic tremor and the maximum number of seismic type B events. Sulfur dioxide emission rates ranged from 1790 to 2070 t d−1 (December 23–24, 1994). Afterwards, sulfur dioxide emission rates clearly indicated a consistent decline. However, frequent gas and ash emission puffs exhibited SO2 fluxes reaching values as high as 3060 t d−1. The emission SO2 baseline for the period of study (February 1994–January 1995) was about 1000 t d−1. Ejection velocity of particulate matter was approximately 270 m s−1 reaching a height of about 2.5 km over the summit. The immediate aerosol dispersion area was estimated at 6.0×104 km2 maximum. The microscopic structure of particles (aerosol and tephra) showed a fragile material, probably coming from weathered crustal layers. X-ray fluorescence and neutron-activation analysis from the impactor samples found the following elements: Si, Al, Ca, S, P, Cl, K, Ni, Fe, Ti, Sc, Cu, Zn, Mn, Sr, Cr, Co, Y, Br, Se, Ga, Rb, Hg and Pb. Morphological analysis shows that ash samples might be from pulverized basaltic rock indicating that the Popocatépetl eruption of December 21, 1994 was at low temperature. The microscopic structure of puff material showed substance aggregates consisted of fragile rock, water and adsorbed SO2. These aggregates were observed within water droplets of approximately 1 mm and even larger. Sulfur transformations in the droplets occurred intensively. Volcanic ash contained 5–6% of sulfur during the first expulsion hours. Elemental relative concentrations with respect to Al show that both Si and S have relative concentrations >1, i.e., 13.73 and 2.17, respectively in agreement with the photoelectric counter and COSPEC measurements.  相似文献   

11.
Gas concentrations and isotopic compositions of water have been measured in hydrothermal waters from 13°N on the East Pacific Rise. In the most Mg-depleted samples ( 5 × 10−3 moles/kg) the gas concentrations are: 3–4.5 × 10−5 cm3 STP/kg helium, 0.62–1.24 cm3 STP/kg CH4, 10.80–16.71 × 10−3 moles/kg CO2. The samples contain large quantities (95–126 cm3/kg) of H2 and some carbon monoxide (0.26–0.36 cm3/kg) which result from reaction with the titanium sampling bottles. δ13C in methane and CO2 (−16.6 to −19.5 and −4.1 to −5.5 respectively) indicate temperatures between 475 and 550°C, whereas δ13CCO is compatible with formation by reduction of CO2 on Ti at 350°C close to the sampling temperature.3He/4He are very homogeneous at (7.5 ± 0.1)RA(3He/4He = 1.0 × 10−5) and very similar to already published data as well as CH4/3He ratios between 1.4 and 2.1 × 106.18O and D in water show enrichments from 0.39 to 0.69‰ and from 0.62 to 1.49‰ respectively. These values correspond to W/R ratios of 0.4–7. The distinct18O enrichments indicate that the isotopic composition of the oceans is not completely buffered by the hydrothermal circulations. The3He-enthalpy relationship is discussed in terms of both hydrothermal heat flux and3He mantle flux.  相似文献   

12.
Isotopic compositions were determined for hydrothermal quartz, calcite, and siderite from core samples of the Newberry 2 drill hole, Oregon. The δ15O values for these minerals decrease with increasing temperatures. The values indicate that these hydrothermal minerals precipitated in isotopic equilibrium with water currently present in the reservoirs. The δ18O values of quartz and calcite from the andesite and basalt flows (700–932 m) have isotopic values which require that the equilibrated water δ18O values increase slightly (− 11.3 to −9.2‰) with increasing measured temperatures (150–265°C). The lithic tuffs and brecciated lava flows (300–700 m) contain widespread siderite. Calculated oxygen isotopic compositions of waters in equilibrium with siderite generally increase with increasing temperatures (76–100°C). The δ18O values of siderite probably result from precipitation in water produced by mixing various amounts of the deep hydrothermal water (− 10.5 ‰) with meteoric water (− 15.5 ‰) recharged within the caldera. The δ13C values of calcite and siderite decrease with increasing temperatures and show that these minerals precipitated in isotopic equilibrium with CO2 of about −8 ‰.The δ18O values of weakly altered (<5% alteration of plagioclase) whole-rock samples decrease with increasing temperatures above 100°C, indicating that exchange between water and rock is kinetically controlled. The water/rock mass ratios decrease with decreasing temperatures. The δ18O values of rocks from the bottom of Newberry 2 show about 40% isotopic exchange with the reservoir water.The calculated δ18O and δD values of bottom hole water determined from the fluid produced during the 20 hour flow test are −10.2 and −109‰, respectively. The δD value of the hydrothermal water indicates recharge from outside the caldera.  相似文献   

13.
Kawah Putih is a summit crater of Patuha volcano, West Java, Indonesia, which contains a shallow, 300 m-wide lake with strongly mineralized acid–sulfate–chloride water. The lake water has a temperature of 26–34°C, pH=<0.5–1.3, Stot=2500–4600 ppm and Cl=5300–12 600 ppm, and floating sulfur globules with sulfide inclusions are common. Sulfur oxyanion concentrations are unusually high, with S4O62−+S5O62−+S6O62−=2400 – 4200 ppm. Subaerial fumaroles (<93°C) on the lake shore have low molar SO2/H2S ratios (<2), which is a favorable condition to produce the observed distribution of sulfur oxyanion species. Sulfur isotope data of dissolved sulfate and native sulfur show a significant 34S fractionation (ΔSO4–Se of 20‰), probably the result of SO2 disproportionation in or below the lake. The lake waters show strong enrichments in 18O and D relative to local meteoric waters, a result of the combined effects of mixing between isotopically heavy fluids of deep origin and meteoric water, and evaporation-induced fractionation at the lake surface. The stable-isotope systematics combined with energy-balance considerations support very rapid fluid cycling through the lake system. Lake levels and element concentrations show strong seasonal fluctuations, indicative of a short water residence time in the lake as well.Thermodynamic modeling of the lake fluids indicates that the lake water is saturated with silica phases, barite, pyrite and various Pb, Sb, Cu, As, Bi-bearing sulfides when sulfur saturation is assumed. Precipitating phases predicted by the model calculations are consistent with the bulk chemistry of the sulfur-rich bottom sediments and their identified mineral phases. Much of the lake water chemistry can be explained by congruent rock dissolution in combination with preferential enrichments from entering fumarolic gases or brines and element removal by precipitating mineral phases, as indicated by a comparison of the fluids, volcanic rocks and lake bed sediment.Flank springs on the mountain at different elevations vary in composition, and are consistent with local rock dissolution as a dominant factor and pH-dependent element mobility. Discharges of warm sulfate- and chloride-rich water at the highest elevation and a near-neutral spring at lower level may contain a small contribution of crater-lake water. The acid fluid-induced processes at Patuha have led to the accumulation of elements that are commonly associated with volcano-hosted epithermal ore deposits. The dispersal of heavy metals and other potentially toxic elements from the volcano via the local drainage system is a matter of serious environmental concern.  相似文献   

14.
Uzon caldera, located in the eastern volcanic belt of the Kamchatka peninsula, is a complicated structure of Middle Pleistocene age. The composition of the co-existing solid and fluid phases, temperature and pH were determined with the aim of establishing the distribution of sulphur species, As, Sb and the main ore-forming metals. In the solid samples, the following sulphur-bearing minerals were identified: pyrite, realgar, orpiment, alacranite (As8S9), uzonite (As4S5), amorphous As-sulphide, stibnite, cinnabar and native sulphur. The following sulphur-bearing species H2S, H2S2+S52−(aq)(aqueous polysulphanes), S0(aq), SO32−(aq), S2O32−, SO42− and total concentration of sulphur were determined in solutions. Eh, pH and H2S concentration were measured potentiometrically in situ. Zero-valent sulphur (S0(aq)+H2S2+S52−(aq)) predominates in Uzon solutions. The pair H2S–Scolloidal is Eh-determining in Uzon solutions up to 75–85°C. A quantitative thermodynamic model of the mineral deposition process at Uzon was constructed using the collected data. It was obtained that the composition of the hydrothermal solution and the precipitation of Sb–As–Hg species can be described using two only main factors: the initial composition of fluid and the temperature variation.  相似文献   

15.
Sediment traps were deployed in the Gulf of Papua in June–July 1997, to determine fluxes of organic matter and inorganic elements from the photic zone to deeper waters at the base of the continental slope and in the northern Coral Sea. Three stations, ranging from 900 to 1500 m depth, had “shallow” traps at 300 m below the water surface and “deep” traps set 100 m above the bottom. Infiltrex II water samplers collected particulate and dissolved organic matter from the Fly, Purari and Kikori rivers, and near-surface water from the shelf of the Gulf of Papua. Samples were analysed for molecular organic biomarkers to estimate the sources of organic carbon and its cycling processes.Dry weight fluxes from the shallow traps ranged from 115 to 181 mg m−2 day−1 and particulate organic carbon (POC) fluxes ranged from 1.2 to 1.9 mM OC m−2 d−1 with molar organic carbon to particulate nitrogen ratios (C/N) ranging from 6.0 to 6.5. Fluxes in deep traps were likely influenced by both early diagenesis and entrapment of resuspended shelf sediments. Dry weight fluxes in deep traps ranged from 106 to 574 mg m−2 day−1 and POC fluxes ranged from 0.6 to 1.5 mM OC m−2 d−1, with C/N ratios ranging from 8.5 to 10.8. 13C/12C ratios were −20.2‰ to −21.7‰ in all trap samples, indicating that most of the settling POC was “marine-derived”. Shallow traps had δ15N values of 6.3‰ to 7.2‰ while the values in deep traps were 4.9–5.0‰, indicating the N-rich near-surface OC was less degraded than that in the deep traps. The biogenic lipids consisted of hydrocarbon, sterol and fatty acid biomarkers indicative of marine zooplankton, phytoplankton and bacteria. Sterol markers for diatoms and dinoflagellates were abundant in the water samples. Highly branched isoprenoid alkenes, usually attributable to diatoms, were also detected in both water and shallow traps. Traces of C26–C34 n-alcohols indicative of land–plant biomarkers, were found in river water samples and in the shallow sediment traps. A large unresolved complex mixture (UCM) of hydrocarbons, and a uniform distribution of n-alkanes, indicative of petroleum hydrocarbons, were also detected in the traps. Hopane and sterane biomarkers detected in the trap oil were characteristic of a marine carbonate source, and the aromatic hydrocarbon composition distinguished at least two different oil signatures.We concluded that mass and POC fluxes were similar to those reported for other continental shelves and marginal oceans in tropical and subtropical regions. There was a dramatic decrease in POC as particles sank, due to zooplankton repackaging and photochemical and bacterial decomposition. Carbon isotopic and biomarker patterns showed most of the POC in the sediment traps was marine-sourced with only traces of terrestrial input. There was a significant flux of petroleum, which may signal the existence of natural petroleum seeps in this region.  相似文献   

16.
Stable isotopic data are presented for 112 samples of francolite from 18 separate phosphate deposits. Values ofδ13C andδ34S in most offshore deposits suggest formation within oxic or suboxic environments either by carbonate replacement or direct precipitation of francolite from water of normal marine compositions. The exceptions are concretionary francolite from Namibia, which has an isotopic composition in keeping with its formation within organic-rich sediments, and that from offshore Morocco, which has an isotopic signature of the anoxic/suboxic interface. Onshore deposits from Jordan, Mexico, South Africa and, possibly, the Permian Phosphoria Formation in the western U.S.A., are substantially depleted in18O: they appear to be too altered for deductions to be made about their environments of formation. In other onshore deposits which are unaltered, or minimally altered, the isotopic composition suggests that some formed within sulphate-reducing sediments (Sedhura, Morocco) whilst francolite from the Georgina Basin of Australia formed at the oxic/anoxic boundary, where oxidation of biogenic H2S decreases theδ34S of pore water. In general, pelletal samples show non-oxic isotopic signatures, whilst non-pelletal samples show oxic isotopic signatures, but samples from Namibia, Peru (Ica Plateau) and the Californian and Moroccan margins are exceptions to this rule. Morphology may therefore be a misleading indicator of francolite genesis as no definitive relation exists between phosphorite type and isotopic signature.  相似文献   

17.
The consequences of a coastal upwelling event on physical and chemical patterns were studied in the central Gulf of Finland. Weekly mapping of hydrographical and -chemical fields were carried out across the Gulf between Tallinn and Helsinki in July–August 2006. In each survey, vertical profiles of temperature and salinity were recorded at 27 stations and water samples for chemical analyses (PO43−, NO2−+NO3−) were collected at 14 stations along the transect. An ordinary distribution of hydrophysical and -chemical variables with the seasonal thermocline at the depths of 10–20 m was observed in the beginning of the measurements in July. Nutrient concentrations in the upper mixed layer were below the detection limit and nutriclines were located just below or in the lower part of the thermocline. In the first half of August, a very intense upwelling event occurred near the southern coast of the Gulf when waters with low temperature and high salinity from the intermediate layer surfaced. High nutrient concentrations were measured in the upwelled water – 0.4 μmol l−1 of phosphates and 0.6 μmol l−1 of nitrates+nitrites. We estimated the amount of nutrients transported into the surface layer as 238–290 tons of phosphorus (P)-PO43− and 175–255 tons of N-NOx for a 12 m thick, 20 km wide and 100 km long coastal stretch. Taking into account a characteristic along-shore extension of the upwelling of 200 km, the phosphate-phosphorus amount is approximately equal to the average total monthly riverine load of phosphorus to the Gulf of Finland. It is shown that TS-characteristics of water masses and vertical distribution of nutrients along the study transect experienced drastic changes caused by the upwelling event in the entire studied water column. TS-analysis of profiles obtained before and during the upwelling event suggests that while welled up, the cold intermediate layer water was mixed with the water from the upper mixed layer with a share of 85% and 15%. We suggest that the coastal upwelling events contribute remarkably to the vertical mixing of waters in the Gulf of Finland. Intrusions of nutrient-rich waters along the inclined isopycnal surfaces in the vicinity of upwelling front were revealed. The upwelling event widened the separation of phosphocline and nitracline which in turn prevented surfacing of nitrate+nitrite-nitrogen during the next upwelling event observed a week after the upwelling relaxation. A suggestion is made that such widening of nutricline separation caused by similar upwelling events in early summer could create favourable conditions for late summer cyanobacterial blooms.  相似文献   

18.
The flow of carbon and nitrogen in sediments of the far northern and northern sections of the Great Barrier Reef continental shelf was examined. Most of the organic carbon (81–94%) and total nitrogen (74–92%) depositing to the seabed was mineralized, with burial of carbon (6–19%) and nitrogen (8–20%) being proportionally less on this tropical shelf compared with other non-deltaic shelves. Differences in carbon and nitrogen mineralization among stations related best to water depth and proximity to river basins, with rates of mineralization based on net ∑CO2 production ranging from 17 to 39 ( mean=23) mmol C m−2 d−1. The overall ratio of O2:CO2 flux was 1.3, close to the Redfield ratio, implying that most organic matter mineralized was algal. Sulfate reduction was estimated to account for ≈30% (range: 6–62%), and denitrification for ≈5% (range: 2–13%), of total C mineralization; there was no measurable CH4 production. Discrepancies between ∑CO2 production across the sediment–water interface and sediment incubations suggest that as much as 5 mmol m−2 d−1 (≈25% of ∑CO2 flux) was involved in carbonate mineral formation. Most microbial activity was in the upper 20 cm of sediment. Rates of net NH4+ production ranged from 1.6 to 2.7 mmol N m−2 d−1, with highly variable N2 fixation rates contributing little to total N input. Ammonification and nitrification rates were sufficient to support rapid rates of denitrification (range: 0.1–12.4 mmol N m−2 d−1). On average, nearly 50% of total N input to the shelf sediment was denitrified. The average rates of sedimentation, mineralization, and burial of C and N were greater in the northern section of the shelf than in the far northern section, presumably due to higher rainfall and river discharge, as plankton production was similar between regions. The relative proportion of plankton primary production remineralized at the seafloor was in the range of 30–50% which is at the high end of the range found on other shelves. The highly reactive nature of these sediments is attributed to the deposition of high-quality organic material as well as to the shallowness of the shelf, warm temperatures year-round, and a variety of physical disturbances (cyclones, trawling) fostering physicochemical conditions favorable for maintaining rapid rates of microbial metabolism. The rapid and highly efficient recycling of nutrients on the inner and middle shelf may help to explain why the coral reefs on the outer shelf have remained unscathed from increased sediment delivery since European settlement.  相似文献   

19.
The 26.5 ka Oruanui eruption, from Taupo volcano in the central North Island of New Zealand, is the largest known ‘wet’ eruption, generating 430 km3 of fall deposits, 320 km3 of pyroclastic density–current (PDC) deposits (mostly ignimbrite) and 420 km3 of primary intracaldera material, equivalent to 530 km3 of magma. Erupted magma is >99% rhyolite and <1% relatively mafic compositions (52.3–63.3% SiO2). The latter vary in abundance at different stratigraphic levels from 0.1 to 4 wt%, defining three ‘spikes’ that are used to correlate fall and coeval PDC activity. The eruption is divided into 10 phases on the basis of nine mappable fall units and a tenth, poorly preserved but volumetrically dominant fall unit. Fall units 1–9 individually range from 0.8 to 85 km3 and unit 10, by subtraction, is 265 km3; all fall deposits are of wide (plinian) to extremely wide dispersal. Fall deposits show a wide range of depositional states, from dry to water saturated, reflecting varied pyroclast:water ratios. Multiple bedding and normal grading in the fall deposits show the first third of the eruption was very spasmodic; short-lived but intense bursts of activity were separated by time breaks from zero up to several weeks to months. PDC activity occurred throughout the eruption. Both dilute and concentrated currents are inferred to have been present from deposit characteristics, with the latter being volumetrically dominant (>90%). PDC deposits range from mm- to cm-thick ultra-thin veneers enclosed within fall material to >200 m-thick ignimbrite in proximal areas. The farthest travelled (90 km), most energetic PDCs (velocities >100 m s−1) occurred during phase 8, but the most voluminous PDC deposits were emplaced during phase 10. Grain size variations in the PDC deposits are complex, with changes seen vertically in thick, proximal accumulations being greater than those seen laterally from near-source to most-distal deposits. Modern Lake Taupo partly infills the caldera generated during this eruption; a 140 km2 structural collapse area is concealed beneath the lake, while the lake outline reflects coeval peripheral and volcano–tectonic collapse. Early eruption phases saw shifting vent positions; development of the caldera to its maximum extent (indicated by lithic lag breccias) occurred during phase 10. The Oruanui eruption shows many unusual features; its episodic nature, wide range of depositional conditions in fall deposits of very wide dispersal, and complex interplay of fall and PDC activity.  相似文献   

20.
Fluid inclusion leachates obtained from vug and vein quartz samples from an Archean (3.23 Ga) Fe-oxide hydrothermal deposit in the west-central part of the Barberton greenstone belt, South Africa, were analyzed by ion chromatography for chloride, bromide, and iodide. The deposit, known as the ironstone pods, formed by seafloor hydrothermal activity and fluid discharge. Quartz is dominated by type I liquid-vapor, aqueous inclusions with a bimodal salinity distribution (0–0.25 MCl− and 0.9–1.8 MCl−). Bulk analytical salinities range from 0.45 to 0.99 MCl− represent averages of type I inclusions. Bulk fluid inclusion bromide and iodide concentrations are 1.44–3.32 mM and 0.01–0.12 mM, respectively. For comparison, modern seawater has halogen contents of 590 mM chloride, 0.9 mM bromide, and 0.5 μM total iodine. In the fluids from the ironstone pods, bromide and iodide are enriched relative to chloride, when compared with modern seawater.Approximate Br−Cl− and I−Cl− ratios of 3.2 Ga Barberton seawater are 2.5 × 10−3 and 40 × 10−6, respectively. Dispersion to higher values was caused principally by reaction with organic sediments whose trends are similar to those seen for modern vent fluids at unsedimented and sedimented ridges, relative to modern seawater. These halide ratios are greater than those of modern seawater, suggesting a change in the halide ratios of seawater over geological time. The analytical data are consistent with a model in which marine organic sedimentation has fractionated bromine and iodine out of seawater relative to chloride, thereby causing the halide ratios of seawater to decrease from high early and mid-Archean values towards their present day values.  相似文献   

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