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1.
The Flemish Pass Basin is a deep-water basin located offshore on the continental passive margin of the Grand Banks, eastern Newfoundland, which is currently a hydrocarbon exploration target. The current study investigates the petrographic characteristics and origin of carbonate cements in the Ti-3 Member, a primary clastic reservoir interval of the Bodhrán Formation (Upper Jurassic) in the Flemish Pass Basin.The Ti-3 sandstones with average Q86.0F3.1R10.9 contain various diagenetic minerals, including calcite, pyrite, quartz overgrowth, dolomite and siderite. Based on the volume of calcite cement, the investigated sandstones can be classified into (1) calcite-cemented intervals (>20% calcite), and (2) poorly calcite-cemented intervals (porous). Petrographic analysis shows that the dominant cement is intergranular poikilotopic (300–500 μm) calcite, which stared to form extensively at early diagenesis. The precipitation of calcite occured after feldspar leaching and was followed by corrosion of quartz grains. Intergranular calcite cement hosts all-liquid inclusions mainly in the crystal core, but rare primary two-phase (liquid and vapor) fluid inclusions in the rims ((with mean homogenization temperature (Th) of 70.2 ± 4.9 °C and salinity estimates of 8.8 ± 1.2 eq. wt.% NaCl). The mean δ18O and δ13C isotopic compositions of the intergranular calcite are −8.3 ± 1.2‰, VPDB and −3.0 ± 1.3‰, VPDB, respectively; whereas, fracture-filling calcite has more depleted δ18O but similar δ13C values. The shale normalized rare earth element (REESN) patterns of calcite are generally parallel and exhibit slightly negative Ce anomalies and positive Eu anomalies. Fluid-inclusion gas ratios (CO2/CH4 and N2/Ar) of calcite cement further confirms that diagenetic fluids originated from modified seawater. Combined evidence from petrographic, microthermometric and geochemical analyses suggest that (1) the intergranular calcite cement precipitated from diagenetic fluids of mixed marine and meteoric (riverine) waters in suboxic conditions; (2)the cement was sourced from the oxidation of organic matters and the dissolution of biogenic marine carbonates within sandstone beds or adjacent silty mudstones; and (3) the late phases of the intergranular and fracture-filling calcite cements were deposited from hot circulated basinal fluids.Calcite cementation acts as a main controlling factor on the reservoir quality in the Flemish Pass reservoir sandstones. Over 75% of initial porosity was lost due to the early calcite cementation. The development of secondary porosity (mostly enlarged, moldic pores) and throats by later calcite dissolution due to maturation of organic matters (e.g., hydrocarbon and coals), was the key process in improving the reservoir quality.  相似文献   

2.
Diagenetic analysis based on field and petrographic observations, isotope and microthermometric data was used to reconstruct the fluid flow history of the Cretaceous shallow water limestones from the Panormide platform exposed in north-central Sicily. Analysis focused on diagenetic products in cavities and dissolution enlarged fractures of the karstified limestones that occur just below a regional unconformity. The fluid flow history could be broken down into five stages that were linked to the kinematic and burial history of the region. (1) Petrography (zoned cathodoluminescence and speleothem textures) and stable isotopes (6.5 < δ18OV-PDB < ?3.5‰ and 0 < δ13CV-PDB < ?14‰) indicate that the earliest calcite phase was associated with karstification during emergence of the platform. Limestone dissolution at this stage is important with regard to possible reservoir creation in the Panormide palaeogeographic domain. (2) Fine-grained micrite sedimentation, dated as latest Cretaceous by nannopalaeontology and its 87Sr/86Sr isotope ratio (0.7078), marks replacement by marine fluids during subsequent submergence of the karstified platform. (3) The following calcite cement was still precipitated by marine-derived fluids (?7.0 < δ18OV-PDB < ?5.0‰ and ?3.0 < δ13CV-PDB < 0.5‰/Tm = ?2 to ?5 °C), but at increasingly higher temperatures (Th = 60–120 °C). This has been interpreted as precipitation during Oligocene foredeep burial. (4) Hot (Th = 130–180 °C), low saline (Tm < ?2.5 °C) fluids with increasingly higher calculated δ18OSMOW signatures (+6 to +14‰) subsequently invaded the karst system. These fluids most likely migrated during fold and thrust belt development. The low salinity and relatively high δ18OSMOW signatures of the fluids are interpreted to be the result of clay dewatering reactions. The presence of bitumen and associated fluorite with hydrocarbon inclusions at this stage in the paragenesis constrains the timing of oil migration in the region. (5) Finally, high saline fluids with elevated 87Sr/86Sr (0.7095–0.7105) signatures invaded the karst system. This last fluid flow event was possibly coeval with localized dolomitization and calcite cementation along high-angle faults of Pliocene age, as suggested by identical radiogenic signatures of these diagenetic products.  相似文献   

3.
Poor biostratigraphic control for some Triassic-Jurassic successions in the North Sea Basin and sub-basins necessitates the use of alternative correlation methods. This study examines the use of diagenetic signatures to distinguish continenetal from marine sandstone successions (Triassic-Jurassic) in the UK Central Graben. The key diagenetic alterations encountered in these successions include kaolinitization of the framework grains and the development of sphaerosiderite and pyrite. The δ 13CV-PDB values of siderite (−8.1 to −8.5‰) and of ankerite (−10.8 to −9.2‰), indicate a strong contribution of dissolved carbon from the decay of plant material in soil. However, marine water likely influenced diagenesis during periods of relative sea level rise by providing the dissolved sulfate (SO42−) required for the precipitation of pyrite. The presence of diagenetic alterations such as kaolinitization of framework grains and cementation by sphaerosiderite could indicate that the sediments were deposited in an overall continental setting. However, the occurrence of pyrite and scattered grains of deep-green colored glauconite suggests occasional marine influence. Such information on the changes of the diagenetic realm provides important clues for establishing a framework for stratigraphic correlations. Caution should be exercised when interpreting petrographic data as subsequent episodes of telodiagenesis can complicate petrographic interpretations.  相似文献   

4.
The Esino Limestone of the western Southern Alps represents a differentiated Ladinian-Lower Carnian (?) carbonate platform comprised of margin, slope and peritidal inner platform facies up to 1000 m thick. A major regional subaerial exposure event lead to coverage by another peritidal Lower Carnian carbonate platform (Breno Formation). Multiphase dolomitization affected the carbonate sediments. Petrographic examinations identified at least three main generations of dolomites (D1, D2, and D3) that occur as both replacement and fracture-filling cements. These phases have crystal-size ranges of 3–35 μm (dolomicrite D1), 40–600 μm (eu-to subhedral crystals D2), and 200 μm to 5 mm (cavity- and fracture-filling anhedral to subhedral saddle dolomite D3), respectively.The fabric retentive near-micritic grain size coupled with low mean Sr concentration (76 ± 37 ppm) and estimated δ18O of the parent dolomitizing fluids of D1 suggest formation in shallow burial setting at temperature ∼ 45–50 °C with possible contributions from volcanic-related fluids (basinal fluids circulated in volcaniclastics or related to volcanic activity), which is consistent with its abnormally high Fe (4438 ± 4393 ppm) and Mn (1219 ± 1418 ppm) contents. The larger crystal sizes, homogenization temperatures (D2, 108 ± 9 °C; D3, 111 ± 14 °C) of primary two-phase fluid inclusions, and calculated salinity estimates (D2, 23 ± 2 eq wt% NaCl; D3, 20 ± 4 eq wt% NaCl) of D2 and D3 suggest that they formed at later stages under mid-to deeper burial settings at higher temperatures from dolomitizing fluids of higher salinity, which is supported by higher estimated δ18O values of their parent dolomitizing fluids. This is also consistent with their high Fe (4462 ± 4888 ppm; and 1091 ± 1183 ppm, respectively) and Mn (556 ± 289 ppm and 1091 ± 1183 ppm) contents, and low Sr concentrations (53 ± 31 ppm and 57 ± 24 ppm, respectively).The similarity in shale-normalized (SN) REE patterns and Ce (Ce/Ce*)SN and La (Pr/Pr*)SN anomalies of the investigated carbonates support the genetic relationship between the dolomite generations and their calcite precursor. Positive Eu anomalies, coupled with fluid-inclusion gas ratios (N2/Ar, CO2/CH4, Ar/He), high F− concentration, high F/Cl and high Cl/Br molar ratios suggest an origin from diagenetic fluids circulated through volcanic rocks, which is consistent with the co-occurrence of volcaniclastic lenses in the investigated sequence.  相似文献   

5.
Different methods have been used to examine minerals and/or solid bitumens in three adjacent Carpathian regions of Poland, Ukraine and Slovakia. The minerals fill smaller and larger veins and cavities, where they occur either together or separately. They usually co-occur with the solid bitumens. All δ13CPDB values measured for calcite lie in a relatively wide interval between −6.25‰ and +1.54‰, while most values fall into the narrower interval from below 0 to about −3‰. The general range of calcite δ18O results for the whole studied region is between +17.13‰ and +25.23‰ VSMOW or from about −11 to −5‰ VPDB, while the majority of these values are between +20.0 and 23.5‰ VSMOW (−10.53 and −8.00‰ PDB, respectively). δ18OVSMOW results for quartz vary between +23.2 and 27.6. The carbonate percentage determined in some samples falls between from <2% CaCO3 to >90% CaCO3, while the TOC values changes from 0.09% to over 70%.The aliphatic fraction predominates in all studied samples, mainly in bitumens and oils. The composition of the aliphatic fraction is relatively homogeneous and points to a strong aliphatic, oil-like paraffin character of the bitumens. Such a composition is characteristic of the Carpathian oils and different from the rocks studied that contain the higher percentage of a polar fraction. The content of the aliphatic fraction in bitumens is only slightly higher than that in two oils used for comparison. The distribution of n-alkanes is variable in rocks, solid bitumens as well as inclusions in quartz and calcite. Two groups of bitumens may be distinguished. Those with a predominance of long-chain n-alkanes in the C25–C27 interval (in some cases from C23–C25 and without or with a very low concentration of short-chain n-alkanes in the interval of C14–C21) show also a high content of isoprenoids i.e. of pristane (Pr) and phytane (Ph). In all but one bitumen samples, Pr predominates over Ph. The second group comprises oils and rock samples with a characteristic predominance of short-chain n-alkanes in the interval from C13–C19 and a low percentage of the long-chain n-alkanes from the n-C27–n-C33 interval. Pristane and phytane exhibit a concentration comparable to that of C17 and C18 n-alkanes with a Pr predominance over Ph. Due to high maturity, only small amounts of the most stable compounds from the hopane group have been observed in the samples, also oleanane in one case. Among the aromatic hydrocarbons, phenanthrene and its methyl- and dimethyl-derivatives are dominant in bitumens, source rocks and inclusions in calcite and quartz. Occurrence of cyclohexylbenzene and its alkyl-derivatives as well as cyclohexylfluorenes in solid bitumens suggest that they formed from oil accumulations under the influence of relatively high temperatures in oxidizing conditions.Homogenization temperatures for aqueous/brine inclusions in quartz within the Dukla and Silesian units (Polish and Ukrainian segments) are between 125 and 183.9 °C, while salinities are low in the interval of 0.2–5.5 wt% NaCl eq. The inclusions in calcite homogenize at higher temperatures of almost 200 °C and the brine displays higher salinity than the fluid in the quartz. Two quartz generations may be distinguished by inclusion and isotope characteristics and the macroscopic diversity. Oil inclusions homogenize at 95 °C. One phase inclusions in quartz contain methane, CO2 and nitrogen in variable proportions.  相似文献   

6.
Sea-ice and water samples were collected at 14 stations on the shelves and slope regions of the Chukchi and Beaufort Seas during the spring 2002 expedition as part of the Shelf–Basin Interaction Studies. Algal pigment content, particulate organic carbon and nitrogen, and primary productivity were estimated for both habitats based on ice cores, brine collection and water samples from 5-m depth. The pigment content (0.2–304.3 mg pigments m−2) and primary productivity (0.1–23.0 mg C m−3 h−1) of the sea-ice algae significantly exceeded water-column parameters (0.2 and 1.0 mg pigments m−3; <0.1–0.4 mg C m−3 h−1), making sea ice the habitat with the highest food availability for herbivores in early spring in the Chukchi and Beaufort Seas. Stable isotope signatures for ice and water samples did not differ significantly for δ15N, but for δ13C (ice: −25.1‰ to −14.2‰; water: −26.1‰ to −22.4‰). The analysis of nutrient concentrations and the pulse-amplitude-modulated fluorescence signal of ice algae and phytoplankton indicate that nutrients were the prime limiting factor for sea-ice algal productivity. The estimated spring primary production of about 1–2 g C m−2 of sea-ice algae on the shelves requires the use of substantial nutrient reservoirs from the water column.  相似文献   

7.
Ancient hydrocarbon seepage occurred in the Hrabůvka quarry at the boundary between the basement of the Bohemian Massif (represented by folded Lower Carboniferous siliciclastics of the Culm facies) and Tertiary sedimentary cover of the Carpathian Foredeep (formed by Lower Badenian siliciclastics and calcareous clays). The unconsolidated Lower Badenian sediments contain lithified domains composed of limestone and breccias with limestone cement, whereas the basement rocks are cut by subvertical neptunic dykes filled up by limestone and calcite-marcasite-pyrite veinlets representing sealed fluid conduits. The deeply negative δ13C values of both vein calcite and limestone (down to −38.1‰ V-PDB) indicate that oxidation of hydrocarbons was the major source of carbon for authigenic mineralization. A fluid inclusion study suggests low fluid temperatures (<50 °C) and low and variable salinities of aqueous fluids associated with hydrocarbons (0.7–6.7 wt. % NaCl eq.). The variability of δ18O values of authigenic carbonates (−1.7 to −8.2‰ V-PDB) could reflect either slight changes in temperature of escaping fluids (mostly within 15 °C), and/or some mixing with meteoric waters. The low δ34S values of vein marcasite (∼–20‰ V-CDT) are consistent with bacterial reduction of sulfate in the hydrothermal system. Low C1/(C2+C3) ratios in hydrocarbon gas extracted from authigenic carbonates (9.9 and 5.8) as well as the high δ13C values of methane (−31.8 and −32.4‰ V-PDB) are compatible with a thermogenic source of hydrocarbons. REE data indicate sequestration of REE from finely dispersed detrital material in the apical part of the hydrothermal system. The available data are compatible with two possible scenarios of fluid origin. The hydrocarbons could have been leached from underlying Paleozoic sedimentary sequence by aqueous fluids that infiltrated into the basement after Tertiary tectonic reactivation. Alternatively, an external source of hydrocarbon-bearing fluids can be found in the adjacent Outer Western Carpathians flysch nappes containing petroleum-producing lithologies. Nevertheless, a regional flow of hydrocarbon-bearing fluids is evidenced by the occurrence of very similar hydrocarbon-bearing vein mineralizations in a wider area.  相似文献   

8.
Deeply buried (4500–7000 m) Ordovician carbonate reservoirs in the Tazhong area, Tarim Basin, NW China show obvious heterogeneity with porosity from null in limestones and sweet dolostones to 27.8% in sour dolostones, from which economically important oils, sour gas and condensates are currently being produced. Petrographic features, C, O, Sr isotopes were determined, and fluid inclusions were analyzed on diagenetic calcite, dolomite and barite from Ordovician reservoirs to understand controls on the porosity distribution. Ordovician carbonate reservoirs in the Tazhong area are controlled mainly by initial sedimentary environments and eo-genetic and near-surface diagenetic processes. However, vugs and pores generated from eogenetic and telogenetic meteoric dissolution were observed to have partially been destroyed due to subsequent compaction, filling and cementation. In some locations or wells (especially ZG5-ZG7 Oilfield nearby ZG5 Fault), burial diagenesis (e.g. thermochemical sulfate reduction, TSR) probably played an important role in quality improvement towards high-quality reservoirs. C2 calcite and dolomite cements and barite have fluid inclusions homogenization temperatures (Ths) from 86 to 113 °C, from 96 to 128 °C and from 128 to 151 °C, respectively. We observed petrographically corroded edges of these high-temperature minerals with oil inclusions, indicating the dissolution must have occurred under deep-burial conditions. The occurrence of TSR within Ordovician carbonate reservoirs is supported by C3 calcite replacement of barite, and the association of sulfur species including pyrite, anhydrite or barite and elemental sulfur with hydrocarbon and 12C-rich (as low as −7.2‰ V-PDB) C3 calcite with elevated Ths (135–153 °C). The TSR may have induced burial dissolution of dolomite and thus probably improved porosity of the sour dolostones reservoirs at least in some locations. In contrast, no significant burial dissolution occurred in limestone reservoirs and non-TSR dolostone reservoirs. The deeply buried sour dolostone reservoirs may therefore be potential exploration targets in Tarim Basin or elsewhere in the world.  相似文献   

9.
Nutrient inputs associated with coastal population growth threaten the integrity of coastal ecosystems around the globe. In order to assess the threat posed by rapid growth in tourism, we analyzed the nutrient concentrations as well as the δ15N of NO3− and macrophytes to detect wastewater nitrogen (N) at 6 locations along a groundwater-dominated coastal seagrass bed on the Caribbean coast of Mexico. We predicted that locations with greater coastal development would have higher concentrations of dissolved inorganic nitrogen (DIN) and phosphorus (P), as well as δ15N of NO3−, reflecting wastewater sources of N. However, concentrations of NO3− were not significantly different between developed (3.3 ± 5.3 μM NO3−) and undeveloped (1.1 ± 0.7 μM) marine embayments. The most important control on DIN concentration appeared to be mixing of fresh and salt water, with DIN concentrations negatively correlated with salinity. The δ15N of NO3− was elevated at an inland pond (7.0 ± 0.42‰) and a hydrologically-connected tide pool (7.6 ± 0.57‰) approximately 1 km downstream of the pond. The elevated δ15N of NO3− at the pond was paralleled by high δ15N values of Cladophora sp., a ubiquitous green alga (10 ± 1‰). We hypothesize that inputs of nitrogen rich (NO3− > 30 μM) groundwater, characterized by 15N enriched signatures, flow through localized submarine groundwater discharges (SGD) and contribute to the elevated δ15N signatures observed in many benthic macrophytes. However, changes in nitrogen concentrations and isotope values over the salinity gradient suggest that other processes (e.g. denitrification) could also be contributing to the 15N enrichments observed in primary producers. More measurements are needed to determine the relative importance of nitrogen transformation processes as a source of 15N to groundwaters; however, it is clear that continued inputs of anthropogenic N via SGD have the potential to severely impact ecologically and economically valuable seagrass meadows and coral reefs along the Caribbean coast of Mexico.  相似文献   

10.
The effects of chronic hypoxia and low salinity on anti-predatory responses of the green-lipped mussel Perna viridis were investigated. Dissolved oxygen concentrations ranged from hypoxic to normoxic (1.5 ± 0.3 mg l−1, 3.0 ± 0.3 mg l−1 and 6.0 ± 0.3 mg l−1), and salinities were selected within the variation during the wet season in Hong Kong coastal waters (15‰, 20‰, 25‰ and 30‰). The dissolved oxygen and salinity significantly affected some anti-predatory responses of mussel, including byssus production, shell thickness and shell weight, and the adductor diameter was only significantly affected by salinity. Besides, interactive effects of dissolved oxygen and salinity on the byssus production and shell thickness were also observed. In hypoxic and low salinity conditions, P. viridis produced fewer byssal threads, thinner shell and adductor muscle, indicating that hypoxia and low salinity are severe environmental stressors for self-defence of mussel, and their interactive effects further increase the predation risk.  相似文献   

11.
The fluxes of total mass, organic carbon (OC), biogenic opal, calcite (CaCO3) and long-chain C37 alkenones (ΣAlk37) were measured at three water depths (275, 455 and 930 m) in the Cariaco Basin (Venezuela) over three separate annual upwelling cycles (1996–1999) as part of the CARIACO sediment trap time-series. The strength and timing of both the primary and secondary upwelling events in the Cariaco Basin varied significantly during the study period, directly affecting the rates of primary productivity (PP) and the vertical transport of biogenic materials. OC fluxes showed a weak positive correlation (r2=0.3) with PP rates throughout the 3 years of the study. The fluxes of opal, CaCO3 and ΣAlk37 were strongly correlated (0.6<r2<0.8) with those of OC. The major exception was the lower than expected ΣAlk37 fluxes measured during periods of strong upwelling. All sediment trap fluxes were significantly attenuated with depth, consistent with marked losses during vertical transport. Annually, strong upwelling conditions, such as those observed during 1996–1997, led to elevated opal fluxes (e.g., 35 g m−2 yr−1 at 275 m) and diminished ΣAlk37 fluxes (e.g., 5 mg m−2 yr−1 at 275 m). The opposite trends were evident during the year of weakest upwelling (1998–1999), indicating that diatom and haptophyte productivity in the Cariaco Basin are inversely correlated depending on upwelling conditions.The analyses of the Cariaco Basin sediments collected via a gravity core showed that the rates of OC and opal burial (10–12 g m−2 yr−1) over the past 5500 years were generally similar to the average annual water column fluxes measured in the deeper traps (10–14 g m−2 yr−1) over the 1996–1999 study period. CaCO3 burial fluxes (30–40 g m−2 yr−1), on the other hand, were considerably higher than the fluxes measured in the deep traps (∼10 g m−2 yr−1) but comparable to those obtained from the shallowest trap (i.e. 38 g m−2 yr−1 at 275 m). In contrast, the burial rates of ΣAlk37 (0.4–1 mg m−2 yr−1) in Cariaco sediments were significantly lower than the water column fluxes measured at all depths (4–6 mg m−2 yr−1), indicating the large attenuation in the flux of these compounds at the sediment–water interface. The major trend throughout the core was the general decrease in all biogenic fluxes with depth, most likely due to post-depositional in situ degradation. The major exception was the relatively low opal fluxes (∼5 g m−2 yr−1) and elevated ΣAlk37 fluxes (∼2 mg m−2 yr−1) measured in the sedimentary interval corresponding to 1600–2000 yr BP. Such compositions are consistent with a period of low diatom and high haptophyte productivity, which based on the trends observed from the sediment traps, is indicative of low upwelling conditions relative to the modern day.  相似文献   

12.
New petrographic and fluid inclusion data from core samples of Upper Permian dolomitic limestone (Hauptdolomit, Zechstein group, Stassfurt carbonate sequence) from a gas field located at the northern border of the Lower Saxony Basin (LSB) essentially improve the understanding of the basin development. The gas production at the locality is characterized by very high CO2 concentrations of 75–100% (with CH4 and N2).Samples consist of fine grained, mostly laminated and sometimes brecciated dolomitic limestone (mudstone/wackestone) from the transition zone between the shallow water zone (platform) and the upper slope. The study focuses on migration fluids, entrapped as fluid inclusions in diagenetic anhydrite, calcite, and fluorite, and in syn-diagenetic microfractures, as well as on the geochemistry of fluorite fracture mineralizations, obtained by LA-ICP-MS analysis. Fluid inclusion studies show that the diagenetic fluid was rich in H2ONaClCaCl2. Recrystallized anhydrite contains aqueous inclusions with homogenization temperatures (Th) of ca. 123 °C, but somewhat higher Th of ca. 142 °C was found for calcite cement followed by early Fluorite A with Th of 147 °C. A later Fluorite B preserves gas inclusions and brines with maximum Th of 156 °C. Fluorite B crystallized in fractures during the mobilization of CO2-bearing brines. Crossing isochores for co-genetic aqueous-carbonic and carbonic inclusions indicate fluid trapping conditions of 180–200 °C and 900–1000 bars. δ13C-isotopic ratios of gas trapped in fluid inclusions suggest an organic origin for CH4, while the CO2 is likely of inorganic origin.Basin modelling (1D) shows that the fault block structure of the respective reservoir has experienced an uplift of >1000 m since Late Cretaceous times.The fluid inclusion study allows us to, 1) model the evolution of the LSB and fluid evolution by distinguishing different fluid systems, 2) determine the appearance of CO2 in the geological record and, 3) more accurately estimate burial and uplift events in individual parts of the LSB.  相似文献   

13.
Atmospheric dry deposition of nitrogen (N) and dinitrogen (N2) fixation rates were assessed in 2004 at the time-series DYFAMED station (northwestern Mediterranean, 43°25′N, 7°52′E). The atmospheric input was monitored over the whole year. Dinitrogen fixation was measured during different seasonal trophic states (from mesotrophy to oligotrophy) sampled during nine cruises. The bioavailability of atmospherically deposited nutrients was estimated by apparent solubility after 96 h. The solubility of dry atmospheric N deposition was highly variable (from ∼18% to more than 96% of total N). New N supplied to surface waters by the dry atmospheric deposition was mainly nitrate (NO3−) (∼57% of total N, compared to ∼6% released as ammonium (NH4+)). The mean bioavailable dry flux of total N was estimated to be ∼112 μmol m−2 d−1 over the whole year. The NO3− contribution (70 μmol NO3− m−2 d−1) was much higher than the NH4+ contribution (1.2 μmol NH4+ m−2 d−1). The N:P ratios in the bioavailable fraction of atmospheric inputs (122.5–1340) were always much higher than the Redfield N:P ratio (16). Insoluble N in atmospheric dry deposition (referred to as “organic” and believed to be strongly related to anthropogenic emissions) was ∼40 μmol m−2 d−1. N2 fixation rates ranged from 2 to 7.5 nmol L−1 d−1. The highest values were found in August, during the oligotrophic period (7.5 nmol L−1 at 10 m depth), and in April, during the productive period (4 nmol L−1 d−1 at 10 m depth). Daily integrated values of N2 fixation ranged from 22 to 100 μmol N m−2 d−1, with a maximum of 245 μmol N m−2 d−1 in August. No relationship was found between the availability of phosphorus or iron and the observed temporal variability of N2 fixation rates. The atmospheric dry deposition and N2 fixation represented 0.5–6% and 1–20% of the total biological nitrogen demand, respectively. Their contribution to new production was more significant: 1–28% and 2–55% for atmospheric dry deposition and N2 fixation, respectively. The dry atmospheric input was particularly significant in conditions of water column stratification (16–28% of new production), while N2 fixation reached its highest values in June (46% of new production) and in August (55%).  相似文献   

14.
Diagenesis is of decisive significance for the reservoir heterogeneity of most clastic reservoirs. Linking the distribution of diagenetic processes to the depositional facies and sequence stratigraphy has in recent years been discipline for predicting the distribution of diagenetic alterations and reservoir heterogeneity of clastic reservoirs. This study constructs a model of distribution of diagenetic alterations and reservoir heterogeneity within the depositional facies by linking diagenesis to lithofacies, sandstone architecture and porewater chemistry during burial. This would help to promote better understanding of the distribution of reservoir quality evolution and the intense heterogeneity of reservoirs. Based on an analogue of deltaic distributary channel belt sandstone in Upper Triassic Yanchang Formation, 83 sandstone plug samples were taken from 13 wells located along this channel belt. An integration of scanning electron microscopy, thin sections, electron microprobe analyses, rate-controlled porosimetry (RCP), gas-flow measurements of porosity and permeability, and nuclear magnetic resonance (NMR) experiments, together with published data, were analysed for the distribution, mineralogical and geochemical characteristics of detrital and diagenetic components and the distribution of reservoir quality within the distributary channel belt.Distribution of diagenetic alterations and reservoir heterogeneity within the distributary channel belt sandstones include (i) formation of high quality chlorite rims in the middle part of thick sandstones with coarser grain sizes and a lower content of ductile components resulted from the greater compaction resistance of these sandstones (providing larger pore spaces for chlorite growth), leading to formation of the intergranular pore – wide sheet-like throat and intergranular pore - intragranular pore – wide sheet-like throat (Φ>15%, k>1mD) in the middle part of thick sandstones; (ii) formation of thinner chlorite rims in the middle part of thinner sandstones is associated with the intergranular pore - intragranular pore – narrow sheet-like throat (9%<Φ<14%, 0.2mD<k<0.8mD); (iii) strong cementation by kaolinite in the more proximal sandstones of distributary channel owing to the strong feldspar dissolution by meteoric water, resulting in the intragranular pore - group of interstitial cement pores – narrow sheet-like throat/extremely narrow sheet-like throat (8%<Φ<11%, 0.1mD<k<0.3mD) due to the pore-filling kaolinite occluding porosity; (iv) formation of dense ferrocalcite zones (δ18OVPDB = −23.4‰ to −16.6‰; δ13 CVPDB = −4.0‰ to −2.3‰) favoured in the top and bottom of the channel sandstone which near the sandstone-mudstone bouding-surface, destroying pore space (Φ<8%, k<0.1mD); (v) strong compaction in sandstone of distributary channel edge laterally as a result of fine grain size and high content of ductile components in those sandstones, forming the group of interstitial cement pores – extremely narrow sheet-like throat with porosity values less than 8%.  相似文献   

15.
Denitrification, anammox (Anx) and di-nitrogen fixation were examined in two mangrove ecosystems- the anthropogenically influenced Divar and the relatively pristine Tuvem. Stratified sampling at 2 cm increments from 0 to 10 cm depth revealed denitrification as the main process of N2 production in mangrove sediments. At Divar, denitrification was ∼3 times higher than at Tuvem with maximum activity of 224.51 ± 6.63 nmol N2 g−1 h−1 at 0–2 cm. Denitrifying genes (nosZ) numbered up to 2 × 107 copies g−1 sediment and belonged to uncultured microorganisms clustering within Proteobacteria. Anammox was more prominent at deeper depths (8–10 cm) mainly in Divar with highest activity of 101.15 ± 87.73 nmol N2 g−1 h−1 which was 5 times higher than at Tuvem. Di-nitrogen fixation was detected only at Tuvem with a maximum of 12.47 ± 8.36 nmol N2 g−1 h−1. Thus, in these estuarine habitats prone to high nutrient input, N2-fixation is minimal and denitrification rather than Anx serves as an important mechanism for counteracting N loading.  相似文献   

16.
At Matienzo (Basque–Cantabrian Basin, northern Spain), a large stratabound HTD body (4 by 2 km2 and 80–400 m thick) delimited by two parallel sinistral strike-slip faults is exposed in Aptian carbonates. The margins of the HTD body are characterised by dolomite “tongues” indicating that some limestone beds were more prone to dolomitisation. However, no clear relationship between HTD occurrence and precursor limestone facies can be established. Massive limestone beds, as found at the top of the HTD body, act as barriers to hydrothermal processes, since no dolomite is present in or above these beds. Three types of dolomites have been differentiated, i.e. 1) matrix, 2) coarse crystalline and 3) zebra dolomite. The distribution of the dolomite types is attributed to ascending fluid flow and changing degree of dolomite oversaturation.The dolomite body was formed by two dolomitisation phases under burial conditions. No indications for a synsedimentary/early diagenetic dolomitisation have been observed. The first dolomitisation phase is characterized by ferroan dolomite and the second by non-ferroan dolomite. The two HTD phases are characterised by depleted δ18O-values (ranging between −10‰ and −16‰ V-PDB), δ13C-values similar to the Aptian–Albian marine signature and homogenisation temperatures of primary fluid inclusions between 120 °C and 150 °C. The dolomitising fluid was enriched in 87Sr compared to Aptian seawater, excluding the latter as an unmodified fluid source for dolomitisation. Microthermometry of primary fluid inclusions indicates that the dolomitising fluid evolved from a moderate saline (9.7 – 14.0 wt% NaCl) to a more saline (10.9 – 21.0 wt% NaCl) H2O–NaCl brine. The dolomitising fluid likely originated from evaporated seawater. Fluid circulation through the dolomitised strata is inferred to have taken place during the tectonically active period of the late Albian throughout which important sinistral-strike slip movements along basement faults occurred.  相似文献   

17.
Organic carbon fluxes through the sediment/water interface in the high-latitude North Atlantic were calculated from oxygen microprofiles. A wire-operated in situ oxygen bottom profiler was deployed, and oxygen profiles were also measured onboard (ex situ). Diffusive oxygen fluxes, obtained by fitting exponential functions to the oxygen profiles, were translated into organic carbon fluxes and organic carbon degradation rates. The mean Corg input to the abyssal plain sediments of the Norwegian and Greenland Seas was found to be 1.9 mg C m−2 d−1. Typical values at the seasonally ice-covered East Greenland continental margin are between 1.3 and 10.9 mg C m−2 d−1 (mean 3.7 mg C m−2 d−1), whereas fluxes on the East Greenland shelf are considerably higher, 9.1–22.5 mg C m−2 d−1. On the Norwegian continental slope Corg fluxes of 3.3–13.9 mg C m−2 d−1 (mean 6.5 mg C m−2 d−1) were found. Fluxes are considerably higher here compared to stations on the East Greenland slope at similar water depths. By repeated occupation of three sites off southern Norway in 1997 the temporal variability of diffusive O2 fluxes was found to be quite low. The seasonal signal of primary and export production from the upper water column appears to be strongly damped at the seafloor. Degradation rates of 0.004–1.1 mg C cm−3 a−1 at the sediment surface were calculated from the oxygen profiles. First-order degradation constants, obtained from Corg degradation rates and sediment organic carbon content, are in the range 0.03–0.6 a−1. Thus, the corresponding mean lifetime of organic carbon lies between 1.7 and 33.2 years, which also suggests that seasonal variations in Corg flux are small. The data presented here characterize the Norwegian and Greenland Seas as oligotrophic and relatively low organic carbon deep-sea environments.  相似文献   

18.
JGOFS-KERFIX (KERguelen point FIXe) time-series station, located south of the polar front in the Indian sector of the Antarctic Ocean, was occupied monthly between January 1990 and March 1995. Annual cycles of dissolved inorganic carbon (DIC), total alkalinity (TALK), oxygen (O2) and nutrients (nitrate, silicate, phosphate and ammonia) in the upper ocean are presented for this site. From seasonal drawdown of nutrients and DIC, we estimate a spring–summer net community production of 3.2±0.5 mol m−2 and C/N/P ratios of 100/16/1. The Si/N ratio varies between 1.8 and 3, suggesting low iron concentrations. The spring–summer biogenic silicon export derived from silicate drawdown is 1.18 mol m−2, consistent with model estimates of silicate export at this site. Seasonal and interannual variations of oxygen, nitrate and DIC due to physical and biological processes are quantified using a simple month-to-month budget formulation. From these budgets, an annual net community production of 5.7±3.3 mol m−2 yr−1 is estimated, about twice the averaged spring–summer production, indicating that, at KERFIX, there is a positive net community production throughout the year. Air–sea CO2 fluxes show that KERFIX is a strong CO2 sink for the atmosphere of 2.4–5.1 mol m−2 yr−1 in 1993, depending on the gas exchange formulation used. A 2.1–3.3 mol m−2 yr−1 outgassing of O2 is observed at KERFIX except in 1993 and 1994 where a decreasing trend of temperature induces an increase of O2 solubility.  相似文献   

19.
Previous work has shown that methane anomalies frequently occur within the rift valley of the Mid-Atlantic Ridge (MAR). The plumes appear confined within the high, steep walls of the valley, and it is not known whether methane may escape to the open ocean outside. In order to investigate this question, the concentration and 13C/12C ratio of methane together with CCl3F concentration were measured in the northeastern Atlantic including the rift valley near 50°N. This segment contained methane plumes centered several 100 m above the valley floor with δ13C values mostly between –15‰ and –10‰. A limited number of helium isotope measurements showed that δ3He increased to 17% at the bottom of the valley, which suggests the helium and methane sources may be spatially separated. In the eastern Atlantic away from the ridge (48°N, 20°W), the methane concentration decreased monotonically from the surface to the bottom, but the methane δ13C exhibited a mid-water maximum of about –25‰. The bottom water methane contained a significantly lower δ13C of about –36‰. Thus, it appears that isotopically heavy methane escapes from the MAR into North Atlantic Deep Water (NADW) that contacts the ridge crest while circulating to the east. The formation of NADW supplies isotopically light methane that dilutes the input of heavy carbon from the ridge. We employed a time-dependent box model to calculate the extent of isotope dilution and thereby the flux of MAR methane into the NADW circulation. The degree of methane oxidation, which affects the 13C/12C of methane through kinetic isotope fractionation, was estimated by comparing methane and CFC-11 model results with observations. The model calculations indicate a MAR methane source of about 0.06×10−9 mol L−1 yr−1 to waters at the depth of the ridge crest. Assuming this extends to a 500 m thick layer over half of the entire Atlantic, the amount of methane escaping from the MAR to the open ocean is estimated to be about 1×109 mol yr−1. The total production of methane within the rift valley is likely much greater than the flux from the valley to the outside because of local oxidation. This implies that serpentinization of ultramafic rocks supports much of methane production in the rift valley because the amount expected from basalt degassing in association with mantle helium (<0.6×109 mol CH4 yr−1) is less than even the net amount escaping from the valley. The model results also indicate the methane specific oxidation rate is about 0.05 yr−1 in open waters of the northern Atlantic.  相似文献   

20.
The total organic carbon (TOC) and total inorganic carbon (CT) exchange between the Atlantic Ocean and the Mediterranean Sea was studied in the Strait of Gibraltar in September 1997. Samples were taken at eight stations from western and eastern entrances of the Strait and at the middle of the Strait (Tarifa Narrows). TOC was analyzed by a high-temperature catalytic oxidation method, and CT was calculated from alkalinity–pHT pairs and appropriate thermodynamic relationships. The results are used in a two-layer model of water mass exchange through the Strait, which includes the Atlantic inflow, the Mediterranean outflow and the interface layer in between. Our observations show a decrease of TOC and an increase of CT concentrations from the surface to the bottom: 71–132 μM C and 2068–2150 μmol kg−1 in the Surface Atlantic Water, 74–95 μM C and 2119–2148 μmol kg−1 in the North Atlantic Central Water, 63–116 μM C and 2123–2312 μmol kg−1 in the interface layer, and 61–78 μM C and 2307–2325 μmol kg−1 in the Mediterranean waters. However, within the Mediterranean outflow, we found that the concentrations of carbon were higher at the western side of the Strait (75–78 μM C, 2068–2318 μmol kg−1) than at the eastern side (61–69 μM C, 2082–2324 μmol kg−1). This difference is due to the mixing between the Atlantic inflow and the Mediterranean outflow on the west of the Strait, which results in a flux of organic carbon from the inflow to the outflow and an opposite flux of inorganic carbon. We estimate that the TOC input from the Atlantic Ocean to the Mediterranean Sea through the Strait of Gibraltar varies from (0.97±0.8)104 to (1.81±0.90)104 mol C s−1 (0.3×1012 to 0.56×1012 mol C yr−1), while outflow of inorganic carbon ranges from (12.5±0.4)104 to (15.6±0.4)104 mol C s−1 (3.99–4.90×1012 mol C yr−1). The high variability of carbon exchange within the Strait is due to the variability of vertical mixing between inflow and outflow along the Strait. The prevalence of organic carbon inflow and inorganic carbon outflow shows the Mediterranean Sea to be a basin of active remineralization of organic material.  相似文献   

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