首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 374 毫秒
1.
We present evidence for strong hydrothermal activity in the eastern Manus Basin (depth: 1700–2100 m), the existence of large scale triple-layered buoyant plumes at depths of 1100 m (“shallow plume”), 1700 m (“deep plume”), and 1400 m (“middle plume” with less extent than the other two plumes) that were revealed from water column anomalies of CH4, Mn, Al and pH observed in November to December 1990. Judging from the horizontal distribution of these parameters, the deep plume seems to originate from two distinct hydrothermal sites (eastern and western sites) in the research area, the eastern site being visually ascertained with deep-tow observations at the same time. The CH4/Mn ratio (mol mol−1) of the deep plume (0.02–0.05) is the lowest yet observed in hydrothermal plumes. The order of magnitude difference of CH4/Mn ratios between the shallow plume and the deep plume suggests that different kinds of fluid-rock interaction occurred to make the hydrothermal end members for the deep and shallow plumes. The shallow plume, which had an areal extent of more than 50 km, may be an episodic “megaplume”, because it was not recognized in the previous CH4 profiles in 1986, and because it has a similar CH4/Mn ratio as the megaplume observed in the North Fiji Basin. We found that the eastern deep plume is characterized by enormously high aluminium concentrations (0.6– 1.5 μmol kg−1), pH anomalies (0.1) and high Al/Mn ratios (10–17). The endmember fluid for the eastern deep plume may have an unusually low pH value to dissolve this much aluminum during fluid-rock interaction, or this plume may originate from an eruption-influenced fluid.  相似文献   

2.
We sampled hydrothermal plumes over the N. Gorda Ridge four times between March and August 1996 to document Mn and Fe discharge resulting from a magmatic intrusion/seafloor eruption. Two separate event plumes, EP96A and B, and chronic hydrothermal emissions lasting 6 months were characterized. Shipboard time-series measurements of an event plume sample were used to calibrate an Fe phase clock useful for estimating sample age up to 6 days after fluid discharge. Samples collected from EP96A and B had Mn/heat (<0.15 nmol J-1) and Fe/Mn (>2 mol mol-1) ratios similar to historical event plume observations. We suggest these “signature” ratio values are generally characteristic of event plumes and hypothesize that Mn and Fe may be supplied to event plumes by different processes: Mn by entrainment of fluids from an extant shallow subseafloor reservoir, and Fe by short-lived, high-temperature water-rock reaction coincident with dike emplacement. Calculations based on the Fe phase clock indicate that the two event plumes were released more than a month apart. The largest event plume, EP96A (2.3×106 M Mn and 13×106 M Fe), formed 7 March soon after seismic activity began. The smaller EP96B (0.49×106 M Mn and 3.5×106 M Fe) was not discharged until 11 April, 3 weeks after the cessation of seismic activity detectable by SOSUS T-phase monitoring. We hypothesize that the subseafloor disturbance that triggered EP96B also resulted in the episodic flushing of a reservoir of chronic-plume-like fluids. Total event plume inventories of Mn and Fe at N. Gorda Ridge are much smaller than those associated with the 1986 event at N. Cleft segment of the Juan de Fuca Ridge, but comparable to event plume inventories at N. Cleft segment in 1987 and CoAxial segment in 1993. Mn/heat values for chronic plumes over the eruption site underlying EP96A evolved from moderate (0.25 oonmol J-1, reflecting probable admixture with event plume formation fluids) to high (0.7 nmol J-1, typical of chronic plumes) to low (0.1 nmol J-1, similar to diffuse vent fluid values), marking a complete episode of intrusion/eruption-induced hydrothermal discharge.  相似文献   

3.
The amount of metabolic energy available for primary production by chemolithoautotrophic microorganisms in a submarine hydrothermal plume is evaluated using geochemical models. Oxidation of elemental sulfur and metal sulfides precipitated in the hydrothermal plume represent the largest potential sources of metabolic energy in the plume (∼600 cal/kg vent fluid from each source). Among dissolved substrates, oxidation of H2 potentially provides the greatest amount of energy (∼160 cal/kg). Smaller, but still significant, amounts of energy are also available from sulfate reduction (54 cal/kg), methanogenesis (17 cal/kg), and methanotrophy (13 cal/kg). Only negligible amounts of energy are available from oxidation of Fe(II) or Mn(II) compounds or Fe3+ reduction (<1 cal/kg vent fluid). The models suggest that most primary production in the plume should occur in the early stages of plume development from sulfur- and H2-oxidizers entrained in the plume or colonizing the surfaces of minerals settling from the plume. The total primary productivity potential in the plume is estimated to be about 50 mg dry wt biomass/kg vent fluid. This translates to a global annual biomass production in hydrothermal plumes on the order of 1012 g dry wt/yr, which represents only a small fraction of the total photosynthetic biomass production in the oceans (∼1017 g dry wt/yr). Nevertheless, biomass generated in hydrothermal plumes may represent a significant fraction of the organic matter in the deep ocean as well as that deposited in sediments in ocean basins.  相似文献   

4.
Total heat, salt, and other tracer masses released during a hydrothermal event are shown to be proportional to, but not necessarily equal to, volume integrals of resulting water column anomalies. Proportionality coefficients depend on anomaly definition, on background hydrographic and tracer profiles, on expansion coefficients of the equation of state at an appropriate pressure, and on tracer to heat anomaly ratios at the venting source. For Gorda Ridge event plumes, which are described in other papers of this issue, volume integrals of conventionally defined heat anomalies underestimate actual released heat by a factor of 2.4 if the discharge is not anomalously saline. Under certain combinations of hydrographic and source anomaly conditions, not unlike those found on the East Pacific Rise at 10°N, the apparent total heat released during an event can be deceivingly zero. This analysis also establishes a linear relationship between the ratio of tracer anomaly to heat anomaly at any point in the plume to the same ratio at the source. One consequence is that the ratio of anomalous 3He to heat in Gorda Ridge event plumes is approximately 2.4 larger in the water column than it is at the source. Results are independent of the entrainment process involved in event plume formation, and they are shown to hold true even for background hydrographic profiles that do not vary linearly with depth.  相似文献   

5.
Event plumes form as episodic discharges of large volumes of hydrothermal solutions in response to magmatic diking/eruptive events. In consequence, event plumes represent the sudden injection of exploitable reduced chemical substrates, as well as inhibitory constituents, and likely induce successional changes in the microbial community structure and activity within event plume waters. In response to a major seismic event detected beginning 28 February 1996 at the northern Gorda Ridge, a series of three rapid response and follow-up cruises (GREAT 1, 2 and 3) were mounted over a period of three months. This report focuses on time-series measurements of manganese geomicrobial parameters in the two event plumes found in association with this seismic event.Scanning transmission electron microscopy, elemental microanalysis, and radioisotope (54Mn) uptake experiments were employed on samples collected from vertical and tow-yo casts from the three cruises. Numbers of bacteria and ratios of metal precipitating capsuled bacteria to total bacteria were greatest in the youngest (days old) plume, EP96A, found during GREAT 1; however, when normalized to the hydrothermal temperature anomaly, the greatest values were found in a second event plume, EP96B, discovered during GREAT 2 (up to 1 month old). Early capsule bacteria and particulate Mn distributions may have been influenced by entrainment of resuspended sediment, while those of the oldest (2–3 months) plume sample may have been subjected to preferential aggregation and particle settling.  相似文献   

6.
Results of the chemical investigation on the Bannock and Tyro Basins are reported.Both basins were found to be hypersaline ( 10 times higher than salinity of normal seawater) and anoxic. In all investigated basins a region of transition, a few meters thick, was identified at depths > 3327 dbar. It is characterized by a sharp gradient of salinity, and all concentrations of analysed species increase strongly except for dissolved oxygen and nitrate, which immediately drop to zero. This region appears as a sharp boundary that prevents mixing. As a result, in the presence of organic matter, an anoxic condition developed with the complete depletion of dissolved oxygen. At the same time, hydrogen sulphide and ammonium accumulated within the brine. Between the Bannock and the Tyro brines differences occur in the measured concentrations of H2S, SO2−4, Ca2+ and NH3. There are some differences also within the Bannock area sub-basins.The Libeccio sub-basin, in the Bannock area, contains a double-layered brine: the upper layer is 140 dbar thick and the lower layer is 300 dbar thick. A second interface between upper and lower brines develops at a depth of 3500 dbar. Nearly all of the measured concentrations vs. depth show the double layer, with the exception of ammonium, the concentration of which remains nearly constant throughout the anoxic column. Profiles of the other species analyzed show remarkable differences on passing from the upper to the lower brine. Hydrogen sulphide, sulphate and fluoride concentrations appear constant and then increase at the second interface. The calcium concentration is also constant in the upper brine, but decreases at the second interface. Total alkalinity and phosphate concentrations show a maximum peak just below the first interface. However, after passing through the second interface all the chemical parameters exhibit an almost constant behaviour down to the bottom.Hypersaline conditions are attributed to the dissolution of Messinian evaporite, and anoxia is suggested to originate from the oxidation of organic matter present in sediments and from the absence of bottom water circulation in such a deep and enclosed environment.The chemical conditions can be summarized as follows: in the Libeccio Basin the values for the species analysed have the ranges: 39–321 psu for ‘salinity’, 8.2−6.5 for pH, 2.7–4.0 mM for total alkalinity, 0.2-0 mM for dissolved oxygen, 0–1669 μM for hydrogen sulphide, 0–198 μM for thiol, 31–99 mM for sulphate, 11–21 mM for calcium, 7–100 μM for fluoride, 0.2–3080 μM for ammonium, 5.8-0 μM for nitrite, 0.2–12 μM for phosphate and 8–130 μM for silicate.  相似文献   

7.
This publication considers the probing data on aquatic anomalies (hydrothermal plumes) in the areas of 26° and 29° N of the Mid-Atlantic Ridge (MAR). The mass of the hydrothermal iron supply and the intensity of the iron sedimentation onto the bottom were estimated by means of sediment traps. It was found that the plume of the TAG hydrothermal vent 6 km3 in volume contained about 67 t of suspended Fe; the plume of the Broken Spur field (up to 8.24 km3 in volume) contained 23.5 t or less because of the lower concentration. The data on the sedimentary matter fluxes showed that 0.3–0.5% of the hydrothermal iron was precipitated immediately from a plume of neutral buoyancy onto the bottom; the bulk of the iron was dissipated into the environment. From the dimensions of the plumes, the flow dynamics, the iron concentrations in the plumes, and the amounts of iron supplied by hydrothermal vents, it was found that the resident time of the plumes considered was from 5 to 10 days.  相似文献   

8.
Methane is a useful tracer for studying hydrothermal discharge, especially where the source fluids are of low temperature and lack metal precipitates. However, the dual origins of deep-sea methane, both chemical and biological, complicate the interpretation of methane observations. Here, we use both the concentration and stable carbon isotopic composition (δ13C) of dissolved methane to trace hydrothermal plumes and identify the source and behavior of methane at two sites of newly discovered hydrothermal activity on the Central Indian Ridge (11–13°S). At both sites, methane and optical anomalies between 2500 and 3500 m at all stations indicate active hydrothermal discharge. We compared methane concentrations and δ13C at three stations, two (CTIR110136 and CTIR110208) with the most prominent anomalies at each site, and a third (CTIR110140) with near-background methane values. At stations CTIR110136 and CTIR110208, the concentration and δ13C of methane in distinct plumes ranged from 3.3 to 42.3 nmol kg−1 and −30.0 to −15.4‰, respectively, compared to deep-water values of 0.5 to 1.2 nmol kg−1 and −35.1 to −28.9‰ at the station with a near-background distal plume (CTIR110140). δ13C was highest in the center of the plumes at CTIR110136 (−15.4‰) and CTIR110208 (−17.8‰). From the plume values we estimate that the δ13C of methane in the hydrothermal fluids at these stations was approximately −19‰ and thus the methane was most likely derived from magmatic outgassing or the chemical synthesis of inorganic matter. We used the relationship between δ13C and methane concentration to examine the behavior of methane at the plume stations. In the CTIR110208 plume, simple physical mixing was likely the major process controlling the methane profile. In the CTIR110136 plume we interpret a more complicated relationship as resulting from microbial oxidation as well as physical mixing. We argue that this difference in methane behavior between the two areas stems from a distinct bathymetric dissimilarity between the two stations. The location of CTIR110208 on the open slope of a ridge allowed rapid plume dispersion and physical mixing, whereas the location of CTIR110136 in a small basin surrounded by wall structures inhibited physical mixing and enhanced microbial oxidation.  相似文献   

9.
High-temperature microbes were present in two hydrothermal event plumes (EP96A and B) resulting from the February–March 1996 eruptions along the North Gorda Ridge. Anaerobic thermophiles were cultured from 17 of 22 plume samples at levels exceeding 200 organisms per liter; no thermophiles were cultured from any of 12 samples of background seawater. As these microorganisms grow at temperatures of 50–90°C, they could not have grown in the event plume and instead most probably derived from a subseafloor environment tapped by the event plume source fluids. Event plumes are thought to derive from a pre-existing subseafloor fluid reservoir, which implies that these thermophiles are members of a native subseafloor community that was present before the eruptive event. Thermophiles also were cultured from continuous chronic-style hydrothermal plumes in April 1996; these plumes may have formed from cooling lava piles. To better understand the nutritional, chemical, and physical constraints of pre-eruptive crustal environments, seven coccoidal isolates from the two event plumes were partially characterized. Results from nutritional and phylogenetic studies indicate that these thermophiles are heterotrophic archaea that represent new species, and probably a new genus, within the Thermococcales.  相似文献   

10.
 Hydrothermal vent fields south of the Garret Fracture zone were sampled for the isotope composition of helium and oxygen ([18O]H2O/[16OH2O). The helium isotopes end-member (3He / 4He=8.3×R a and [4He]≈1.2–2.4×10-5 cm3 STP g-1) is quite similar to other known hydrothermal sites pointing to the homogeneous helium composition of the upper mantle. The δ18O end-member value (δ18O≈0.5–0.6‰) confirms previous suggestions from other sites and from isotope modeling, that hydrothermal fluids are slightly enriched in 18O relative to the ocean as a result of water–rock interactions at high temperature. Received: 11 December 1995/Revision received: 20 December 1996  相似文献   

11.
Bio-acoustic surveys and associated zooplankton net tows have documented anomalously high concentrations of zooplankton within a 100 m layer above the hydrothermal plumes at Endeavour Segment, Juan de Fuca Ridge. These and other data suggest that congregating epi-plume zooplankton are exploiting a food substrate associated with the hydrothermal plume. Ascending, organic-rich particles could provide a connection. Consequently, two paired sequentially sampling ascending and descending particle flux traps and a current meter were deployed on each of three moorings from July 1994 to May 1995. Mooring sites included an on-axis site (OAS; 47°57.0′N, 129°05.7′W) near the main Endeavour vent field, a “down-current” site 3 km west of the main vent field (WS), and a third background station 43 km northeast of the vent field (ES). Significant ascending and descending particle fluxes were measured at all sites and depths. Lipid analyses indicated that ascending POC was derived from mid-depth and deep zooplankton whereas descending POC also contained a component of photosynthetically derived products from the sea surface. Highest ascending POC fluxes were found at the hydrothermal plume-swept sites (OAS and WS). The limited data available, however, precludes an unequivocal conclusion that hydrothermal processes contribute to the ascending flux of organic carbon at each site. Highest ascending to descending POC flux ratios were also found at WS. Observed trends in POC, PMn/PTi, and PFe/PTi clearly support a hydrothermal component to the descending flux at the plume-swept WS site (no descending data was recovered at OAS) but not at the background ES site. Alternative explanations for ascending particle data are discussed. First-order calculations for the organic carbon input (5–22 mg C m−2 d−1) required to sustain observed epi-plume zooplankton anomalies at Endeavour are comparable both to measured total POC flux to epi-plume depths (2–5 mg C m−2 d−1: combined hydrothermal and surface derived organic carbon) and to estimates of the total potential in situ organic carbon production (2–9 mg C m−2 d−1) from microbial oxidation of hydrothermal plume H2, CH4 and NH4+.  相似文献   

12.
A computational fluid dynamics (CFD) model was developed to simulate the turbulent flow and species transport of deep-sea high temperature hydrothermal plumes. The model solves numerically the density weighted unsteady Reynolds-averaged Navier–Stokes equations and energy equation and the species transport equation. Turbulent entrainment and mixing is modeled by a k–ε turbulence closure model. The CFD model explicitly considers realistic vent chimney geometry, vent exit fluid temperature and velocity, and background stratification. The model uses field measurements as model inputs and has been validated by field data. These measurements and data, including vent temperature and plume physical structure, were made in the ABE hydrothermal field of the Eastern Lau Spreading Center. A parametric sensitivity study based on this CFD model was conducted to determine the relative importance of vent exit velocity, background stratification, and chimney height on the mixing of vent fluid and seawater. The CFD model was also used to derive several important scalings that are relevant to understanding plume impact on the ocean. These scalings include maximum plume rise height, neutrally buoyant plume height, maximum plume induced turbulent diffusivity, and total plume vertically transported water mass flux. These scaling relationships can be used for constructing simplified 1-dimensional models of geochemistry and microbial activity in hydrothermal plumes. Simulation results show that the classical entrainment assumptions, typically invoked to describe hydrothermal plume transport, only apply up to the vertical level of ~0.6 times the maximum plume rise height. Below that level, the entrainment coefficient remains relatively constant (~0.15). Above that level, the plume flow consists of a pronounced lateral spreading flow, two branches of inward flow immediately above and below the lateral spreading, and recirculation flanking the plume cap region. Both turbulent kinetic energy and turbulence dissipation rate reach their maximum near the vent; however, turbulent viscosity attains its maximum near the plume top, indicating strong turbulent mixing in that region. The parametric study shows that near vent physical conditions, including chimney height and fluid exit velocity, influence plume mixing from the vent orifice to a distance of ~10 times the vent orifice diameter. Thus, physical parameters place a strong kinetic constraint on the chemical reactions occurring in the initial particle-forming zone of hydrothermal plumes.  相似文献   

13.
This study presents first-time observations of bacterial and viral abundances in hydrothermal event plumes. Two water-column event plumes were formed in conjunction with seismic events and seafloor volcanic eruptions on the northern Gorda Ridge in February–March 1996. Epifluorescence counts of bacteria and viruses were performed on water samples from 3 successive cruises staged in the 10–90 days that followed the onset of seismicity. Relative to background seawater at these 1800–3200 m depths, bacterial abundance was enhanced by 2–3 fold within both event plumes. In contrast, viral numbers were below background seawater values in the younger and more intense of the two event plumes (EP96A), and enhanced in the other (EP96B). Changes in viral abundance may be a secondary response to that of plume bacteria as well as being influenced by particle formation and precipitation within the plumes. Lower bacteria/heat, virus/heat and virus/bacteria ratios in EP96A versus EP96B confirm distinct differences in the microbial response to event plume formation, possibly related to observed differences in plume chemistry.  相似文献   

14.
Chemoautotrophic production in seafloor hydrothermal systems has the potential to provide an important source of organic carbon that is exported to the surrounding deep-ocean. While hydrothermal plumes may export carbon, entrained from chimney walls and biologically rich diffuse flow areas, away from sites of venting they also have the potential to provide an environment for in-situ carbon fixation. In this study, we have followed the fate of dissolved and particulate organic carbon (DOC and POC) as it is dispersed through and settles beneath a hydrothermal plume system at 9°50′N on the East Pacific Rise. Concentrations of both DOC and POC are elevated in buoyant plume samples that were collected directly above sites of active venting using both DSV Alvin and a CTD-rosette. Similar levels of POC enrichment are also observed in the dispersing non-buoyant plume, ∼500 m downstream from the vent-site. Further, sediment-trap samples collected beneath the same dispersing plume system, show evidence for a close coupling between organic carbon and Fe oxyhydroxide fluxes. We propose, therefore, a process that concentrates POC into hydrothermal plumes as they disperse through the deep-ocean. This is most probably the result of some combination of preferential adsorption of organic carbon onto Fe-oxyhydroxides and/or microbial activity that preferentially concentrates organic carbon in association with Fe-oxyhydroxides (e.g. through the microbial oxidation of Fe(II) and Fe sulfides). This potential for biological production and consumption within hydrothermal plumes highlights the importance of a multidisciplinary approach to understanding the role of the carbon cycle in deep-sea hydrothermal systems as well as the role that hydrothermal systems may play in regulating global deep-ocean carbon budgets.  相似文献   

15.
Vertical gas profiles of N2, N2O and O2were obtained in intact sediment cores from a Tagus estuary salt marsh using membrane inlet mass spectrometry. This technique allows direct measurements of dissolved gas concentrations with minimal disturbance. O2concentrations decreased sharply with depth, becoming undetectable below 14mm. Denitrification products (N2and N2O) occurred in the surface layer of the sediment where O2was present. Diffusion of N2and N2O from the anaerobic zone, denitrification in anaerobic microsites and aerobic denitrification are possible explanations for this observation. N2was the sole product of denitrification in control sediment cores probably because of the great demand for electron acceptors in this sediment. The addition of NO3 − and CH3CO2 − increased the concentrations of N2and N2O in the sediment. Significantly higher concentrations in treated cores occurred between 1·5 and 2·0cm for N2and between 0·5 and 1·5cm for N2O. The peak in N2concentration occurred in the anaerobic zone of the sediment, close to the aerobic–anaerobic interface while the peak in N2O concentration occurred above this interface where concentrations of O2were approximately 10μM. This is indicative that, in this sediment, production of N2O is less sensitive to the presence of O2than reduction of N2O to N2.  相似文献   

16.
Vertical profiles of dissolved and particulate 210Po and 210Pb were measured across the redox transition zone at Station F1 in Framvaren Fjord, Norway. In this fjord, a sharp decrease in pH above the O2/H2S interface facilitates the aerobic dissolution of MnO2. In contrast, Fe(II) concentrations begin to increase only at the O2/H2S interface depth. Activity profiles reveal that dissolved 210Po and 210Pb are sequestered efficiently by particulates in surface waters. As polonium-210 and lead-210 activities descend down into the aerobic manganese reduction (AMR) zone, they are remobilized during the reductive dissolution of the carrier phase oxyhydroxides. Both 210Po and 210Pb are highly enriched at the O2/H2S interface where an active community of microbes, such as anoxygenic phototrophs (e.g., Chromatium, Chlorobium sp.), thrives. The coincident peaks in 210Po, 210Pb and microbial biomass suggest a strong biological influence on the behavior of these radionuclides. There is a strong covariance between the vertical distribution of Mn and Pb, indicating that their redox cycling is closely coupled and is likely microbially mediated.  相似文献   

17.
A new hydrothermal vent site in the Southern Mariana Trough has been discovered using acoustic and magnetic surveys conducted by the Japan Agency for Marine-Earth Science and Technology's (JAMSTEC) autonomous underwater vehicle (AUV), Urashima. The high-resolution magnetic survey, part of a near-bottom geophysical mapping around a previously known hydrothermal vent site, the Pika site, during the YK09-08 cruise in June–July 2009, found that a clear magnetization low extends ∼500 m north from the Pika site. Acoustic signals, suggesting hydrothermal plumes, and 10 m-scale chimney-like topographic highs were detected within this low magnetization zone by a 120 kHz side-scan sonar and a 400 kHz multibeam echo sounder. In order to confirm the seafloor sources of the geophysical signals, seafloor observations were carried out using the deep-sea manned submersible Shinkai 6500 during the YK 10-10 cruise in August 2010. This discovered a new hydrothermal vent site (12°55.30′N, 143°38.89′E; at a depth of 2922 m), which we have named the Urashima site. This hydrothermal vent site covers an area of approximately 300 m×300 m and consists of black and clear smoker chimneys, brownish-colored shimmering chimneys, and inactive chimneys. All of the fluids sampled from the Urashima and Pika sites have chlorinity greater than local ambient seawater, suggesting subseafloor phase separation or leaching from rocks in the hydrothermal reaction zone. End-member compositions of the Urashima and Pika fluids suggest that fluids from two different sources feed the two sites, even though they are located on the same knoll and separated by only ∼500 m. We demonstrate that investigations on hydrothermal vent sites located in close proximity to one another can provide important insights into subseafloor hydrothermal fluid flow, and also that, while such hydrothermal sites are difficult to detect by conventional plume survey methods, high-resolution underwater geophysical surveys provide an effective means.  相似文献   

18.
This paper evaluates the simultaneous measurement of dissolved gases (CO2 and O2/Ar ratios) by membrane inlet mass spectrometry (MIMS) along the 180° meridian in the Southern Ocean. The calibration of pCO2 measurements by MIMS is reported for the first time using two independent methods of temperature correction. Multiple calibrations and method comparison exercises conducted in the Southern Ocean between New Zealand and the Ross Sea showed that the MIMS method provides pCO2 measurements that are consistent with those obtained by standard techniques (i.e. headspace equilibrator equipped with a Li–Cor NDIR analyser). The overall MIMS accuracy compared to Li–Cor measurements was 0.8 μatm. The O2/Ar ratio measurements were calibrated with air-equilibrated seawater standards stored at constant temperature (0 ± 1 °C). The reproducibility of the O2/Ar standards was better than 0.07% during the 9 days of transect between New Zealand and the Ross Sea.The high frequency, real-time measurements of dissolved gases with MIMS revealed significant small-scale heterogeneity in the distribution of pCO2 and biologically-induced O2 supersaturation (ΔO2/Ar). North of 65°S several prominent thermal fronts influenced CO2 concentrations, with biological factors also contributing to local variability. In contrast, the spatial variation of pCO2 in the Ross Sea gyre was almost entirely attributed to the biological utilization of CO2, with only small temperature effects. This high productivity region showed a strong inverse relationship between pCO2 and biologically-induced O2 disequilibria (r2 = 0.93). The daily sea air CO2 flux ranged from − 0.2 mmol/m2 in the Northern Sub-Antarctic Front to − 6.4 mmol/m2 on the Ross Sea shelves where the maximum CO2 influx reached values up to − 13.9 mmol/m2. This suggests that the Southern Ocean water (south of 58°S) acts as a seasonal sink for atmospheric CO2 at the time of our field study.  相似文献   

19.
Mesoscale distribution of the density and productivity of bacterioplankton at representative geological locations in the rift ecosystem of the North Fiji Basin were clarified by sampling using a mannedShinkai 6500 submersible. The bacterioplankton density inside the hot and warm fluids of hydrothermal vents was one order magnitude greater than that in the deep water outside the vent plume. The bacterial production was highest inside the hot and warm vent fluids, and was higher just outside the hot and warm vent fluids than further outside in the deep water surrounding the vent plume, respectively. Productivity from outside to inside the vent fluid varied from 0.01 to 0.71 gC m–3 day–1.  相似文献   

20.
To understand the source and nature of the ore-forming fluids of the Edmond hydrothermal field on the Central Indian Ridge, we studied the He-Ar isotope composition and fluid inclusions of the hydrothermal precipitates.Our results show that the sulfide samples contain noble gases He, Ne, Kr, and Xe with their abundances in between those of air-saturated water(ASW) and mid-ocean ridge basalt(MORB). The ~3He/~4He ratio varies from1.3 to 8.7 R_a(n=10, average: 5.1 R_a), whereas the ~(40)Ar/~(36) Ar ratio is from 285.3 to 314.7(n=10, average: 294.8). These results suggest that the He was derived from a mixture of MORB with variable amounts of seawater, but the Ar in the ore-forming fluids trapped in the sulfides is predominantly derived from seawater. The fluid inclusions of barite have a wide range of homogenization temperatures and salinities varying from 163°C to 260°C and 2.6 wt%to 8.5 wt% Na Cl equiv., respectively. It is suggested that the ore-forming fluids were produced by phase separation, which agreed with the present-day vent fluid study.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号