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1.
226Ra data on eleven vertical profiles taken during the GEOSECS program from the Antarctic Ocean and its vicinity in both the Atlantic and the Pacific are presented. Replicate measurements were made on each sample using the Rn-emanation method. The precision (1 σ) based on triplicate analyses averages about ±2.5%. Waters all around the Antarctic continent below 2 km depth appear to exhibit a uniform226Ra concentration of 21.5 ± 1dpm/100kg, except perhaps locally such as the Ross Sea and the Drake Passage where small variations may be present. Higher in the water column, the226Ra contents decrease toward the surface with gradients which vary as a function of the influence exerted by the Antarctic Convergence. Across this oceanic front, a north-to-south increase of226Ra occurs (the increase being the largest near the surface: from 8 to 18 dpm/100 kg), reflecting the combining effect of deep-water upwelling and meridional water mixing. The core layer of the Antarctic Intermediate Water contains about 14 dpm/100 kg of226Ra and that of the Circumpolar Intermediate Water (O2 minimum and local T maximum) about 18 dpm/100 kg. To a first approximation,226Ra covaries with Si in the circumpolar waters.  相似文献   

2.
228Ra concentrations were measured in 12 subsurface water samples collected during August–September 1970 in the North Atlantic at the Second Geosecs Intercalibration Station.228Ra concentrations ranged from 1.5 to 2.1 dpm/100 kg in the water layer between 100 and 600 m depth, above the main thermocline, but decreased with increasing depth to less than 0.5 dpm/100 kg at 1.5 km, below the main thermocline. The two deepest samples, collected below 4 km depth, indicated that the228Ra concentration increased again to at least 1.2 dpm/100 kg as the interface with the sea floor sediments was approached. Above the 4 km level, the228Ra profile was roughly similar to the tritium profile measured by Roether and Münnich.  相似文献   

3.
We report here on particulate and dissolved210Pb profiles at 16 stations, and on total210Pb profiles at 3 stations, all occupied during the Pacific GEOSECS expedition. Comparison with measurements at Yale on GEOSECS library samples indicates that during separation of particulate lead from dissolved lead, our filtered water samples suffered some loss of210Pb in the filtration system; this effect appears to have reduced the dissolved210Pb activities by ～ 20% in stations where the water was filtered. However, for these first Pacific data on the210Pb distribution between the two phases, this effect does not significantly interfere with our recognition of the major features of both particulate and dissolved210Pb distributions.The dissolved210Pb profiles in general vary geographically, following the226Ra profiles. In deep water,226Ra increases northward and eastward from the southwest Pacific, from ～ 22dpm/100kg, to over 40 dpm/100 kg in the northeast Pacific. Our dissolved210Pb profiles show a similar increase in deep water, varying from about 10 to 20 dpm/100 kg along this line, and are commonly characterized by a mid-depth maximum. This210Pb maximum reflects the mid-depth226Ra maximum of the Pacific Deep Water observed along the western boundary current.In surface water at low latitudes there is a significant210Pb flux from the atmosphere, which produces a210Pb/226Ra activity ratio generally greater than unity. This flux penetrates as deep as 600 m, as indicated by an “induced”210Pb minimum caused by the surface maximum. The surface water210Pb excess decreases toward high southern latitudes and vanishes in the Circumpolar region.The particulate210Pb profiles show a general increase with depth, from ～ 0.3dpm/100kg in subsurface water to ～ 1.5dpm/100kg in bottom water, with or without a mid-depth maximum that reflects the226Ra or dissolved210Pb maximum. The particulate210Pb normally comprises about 2% of the total210Pb in subsurface water, and this fraction increases to about 10% near the bottom. As the filtration loss is not taken into account, the fraction of particulate210Pb quoted here is an upper limit. Since the particulate matter concentrations are quite uniform in the water column below a few hundred meters, the210Pb activity of the particulate matter also increases with depth. The particulate matter has a210Pb concentration of ～ 100dpm/g in subsurface water, but the concentration increases to ～ 500dpm/g or more toward the bottom. This indicates that there is a cumulative adsorption of Pb onto the suspended particles as they are sinking through the water column.  相似文献   

4.
We present the distribution of226Ra in eight vertical profiles from the eastern Pacific. The profiles are located along a meridional trend near 125°W, from 43°S to 29°N. Surface226Ra concentrations are about 7 dpm/100 kg, except for the two stations south of 30°S where the higher values are due to the Antarctic influence. Deep waters show a distinctive south-to-north increase in the226Ra content, from about 26 to 41 dpm/100 kg near the bottom. Unlike in the Atlantic and Antarctic Oceans, the effect of226Ra injection from bottom sediments is clearly discernible in the area. The presence of this primary226Ra can be traced up to at least 1–1.5 km above the ocean floor, making this part of the sea bed among the strongest source regions for the oceanic226Ra. Numerical solutions of a two-dimensional vertical advection-diffusion model applied to the deep (1.2–4 km)226Ra data give the following set of best fits: upwelling velocity(Vz) = 3.5m/yr, vertical eddy diffusivity(Kz) = 0.6cm2/s, horizontal (north-south) eddy diffusivity(Ky) = 1 × 107cm2/s, and water-column regeneration flux of226Ra(J) = 3.3 × 10?5dpmkg?1yr?1 as an upper limit. These parametric values are in general agreement with one-dimensional (vertical) model fits for the Ra-Ba system. However, consideration of226Ra balance leads us to suspect the appropriateness of describing the vertical exchange processes in the eastern Pacific with constantVz and Kz. If future modeling is attempted, it may be preferable to treat the area as a diffusion-dominant mixing regime with depth-dependent diffusivities.  相似文献   

5.
Seven vertical profiles of226Ra have been measured along an east-west traverse at about 30°N from San Diego to northwest of Hawaii. These profiles show that there is a distinct core of Ra maximum spreading westward as a tongue in the northeast Pacific deep water. This core starts in the east with 21.1 Ra units (1Ra unit= 10?14g/kg) at 3.9 km depth at about 130°W, and deepens westward to 4.1 km with its Ra reduced to 18.3 units at 150°W. A similar core with some uncertainty due to possible sampling errors extends westward near the bottom at 5.2 km depth from 19.4 Ra units at 150°W to 15.9 units at about 180° longitude. In addition, these profiles appear to be correlated with each other in structure above the cores of Ra maximum. These cores indicate that the Ra input depends locally on the type and composition of sediments and so the flux varies over the ocean bottom. On the basis of a one-dimensional diffusion-decay model, a horizontal diffusion coefficient of 106 cm2/sec has been computed along these cores. Although this value appears to be slightly lower, it is not inconsistent with those derived from other physical methods.  相似文献   

6.
The water retention curve (θ(ψ)), which defines the relationship between soil volumetric water content (θ) and matric potential (ψ), is of paramount importance in characterizing the hydraulic behaviour of soils. However, few methods are so far available for estimating θ(ψ) in undisturbed soil samples. We present a new design of TDR‐pressure cell (TDR‐Cell) for estimating θ(ψ) in undisturbed soil samples. The TDR‐Cell consists of a 50‐mm‐long and 50‐mm internal diameter stainless steel cylinder (which constitutes the outer frame of a coaxial line) attached to a porous ceramic disc and closed at the ends with two aluminium lids. A 49‐mm‐long and 3‐mm‐diameter stainless steel rod, which runs longitudinally through the centre of the cylinder, constitutes the inner rod of a coaxial TDR probe. The TDR‐Cell was used to determine the θ(ψ) curves of a packed sand and seven undisturbed soil samples from three profiles of agricultural soils. These θ(ψ) curves were subsequently compared to those obtained from the corresponding 2‐mm sieved soils using the pressure plate method. Measurements of bulk electrical conductivity, σa, as a function of the water content, σa(θ), of the undisturbed soil samples were also performed. An excellent correlation (R2 = 0·988) was found between the θ values measured by TDR on the different undisturbed soils and the corresponding θ obtained from the soil gravimetric water content. A typical bimodal θ(ψ) function was found for most of the undisturbed soil samples. Comparison between the θ(ψ) curves measured with the TDR‐Cell and those obtained from the 2‐mm sieved soils showed that the pressure plate method overestimates θ at low ψ values. The σa(θ) relationship was well described by a simple power expression (R2 > 0·95), in which the power factor, defined as tortuosity, ranged between 1·18 and 3·75. Copyright © 2011 John Wiley & Sons, Ltd.  相似文献   

7.
Two ocean profiles from the Peru Basin from regions with different surface productivities were analyzed for total210Pb and201Po to evaluate the influence of particulates in the water column on their distribution. Comparison with a published226Ra profile for the region was made. The profile closest to the coast, where upwelling and productivity are high, shows depletion of210Pb relative to226Ra at all depths, with particularly marked excursions from radioactive equilibrium at the surface and in the bottom water.210Po appears to be deficient relative to210Pb at depth as well. Mean residence times in the deep water, relative to particulate removal from the water column to the sediments, of about 100 years for210Pb and about two years for210Po are indicated. The profile northwest of the upwelling region shows the226Ra210Pb210Po system close to equilibrium at all depths to 1500 m (except for the effect of atmospheric210Pb input seen at the surface.  相似文献   

8.
The surface water of the Japan Sea contained226Ra of70 ± 4dpm m−3 which was nearly equal to that of the surface water in the North Pacific. The concentration of226Ra in the Japan Sea deep water below 500 m was151 ± 8dpm m−3, showing a vertically and regionally small variation. This concentration of226Ra in the deep water is unexpectedly high, because the Japan Sea deep water has a higher Δ14 C value by about 50‰ than the Atlantic deep water containing the same226Ra. One of the causes to be considered is larger contribution of226Ra from biogenic particles dissolving in the Japan Sea deep water, but the Japan Sea is not so fertile in comparison to the Bering Sea. The other more plausible cause is the internal ventilation of the Japan Sea water, which means that the residence time of the Japan Sea Proper water is considerably long although the water is vertically mixed fairly well especially in winter. The ventilation may supply some amounts of radiocarbon and oxygen but does not change the inventory of226Ra. The residence times of the Japan Sea deep water and of water within the Japan Sea are calculated by solving simultaneous equations for226Ra and14C with a three-box model to be 300–400 years and 700–1000 years, respectively.  相似文献   

9.
Recent radium measurements from the near-surface Caribbean Sea are presented. The surface horizontal and vertical distributions of226Ra are essentially the same as reported by Szabo et al. (1967) for the early 1960's. The226Ra activity at the surface is relatively uniform across the Caribbean, with an average of8.2±0.4dpm/100kg. The subsurface distribution to ～200 m averages7.8±0.4dpm/100kg and increases slowly below 200 m. reaching ～9.5 dpm/100 kg at 560 m. In contrast to226Ra, the surface concentration of228Ra was much more variable in both time and space. An average increase of 33% was found between 1968 and 1976 in the western Caribbean and during both years an anomalously high228Ra activity was found in the eastern Caribbean. These data support previous hypotheses that water entering the eastern Caribbean has been enriched in228Ra prior to entry and that variable mixing of the Atlantic water masses found to the northeast and southeast of the Lesser Antilles may produce temporal variations in the near-surface228Ra activity. Scatter plots of228Ra vs. salinity and sigma-t indicate that the near-surface vertical distribution of228Ra in the Caribbean Sea is predominantly influenced by advection. Thus228Ra cannot be used to study near-surface vertical mixing rates in this region.  相似文献   

10.
226Ra and210Pb were measured in sections and profiles collected in the Weddell Sea during the International Weddell Sea Oceanographic Expedition in 1973. The results can be correlated with the circulation and mixing schemes deduced from hydrographic observations. Along the surface cyclonic gyre the Ra activities are fairly uniform at about 17 dpm/100 kg, quite similar to those of the Circumpolar surface water south of the Antarctic Convergence. The210Pb activities in the northern flank of the gyre, probably influenced by the high210Pb-bearing Circumpolar Deep Water in the north, are as high as 12 dpm/100 kg. At the central gyre and its southern flank, the surface water210Pb activities are about 7 dpm/100 kg. The warmer surface water at the central gyre has a Ra activity of about 19 dpm/100 kg, slightly higher than the colder surface water at the flanks. Thus lower210Pb/226Ra activity ratios are observed in the central gyre, and higher ratios in its flanks. Similar relationships between Ra and Pb are noted in the Weddell Sea Bottom Water (WSBW): lower Pb associated with higher Ra in the center; higher Pb with slightly lower Ra in the flanks.Vertical profiles along the cyclonic gyre show lower Ra and Pb activities in the southwestern Weddell Basin where lower temperature and lower silicate are observed. Similar to Ba, both Ra and Si are non-conservative in the Weddell Sea, with significant input from the bottom sediments and particulate dissolution during subsurface mixing.Each water mass or type in the Weddell Sea is well characterized by its Ra content, but not well by its Pb content. Ra and Si are crudely correlated with a slope of about 7 × 10?4 dpm Ra per μmole of Si. The fact that the WSBW values fall on the slope suggests that the net input rate for Ra (corrected for the decay rate) is proportional to that of Si. The linear extrapolation to zero Si gives a Ra value of 13 dpm/100 kg. These relationships are quite similar to those observed in the Circumpolar waters.  相似文献   

11.
青海湖是青藏高原的重要组成部分,它是维系青藏高原东北部生态安全的重要水体.其沿岸地下水的排放直接影响了青海湖的水文生物地球化学过程,然而对该问题的研究仍然不充分.本研究于2014年对青海湖泉湾湖水、河水和地下水进行223Ra和224Ra活度的测定分析,并对泉湾湖水水平向和垂直向的Ra活度分布进行深入分析,最后估算并探讨了泉湾水体的停留时间和布哈河口沿岸地下水的排放通量.表层湖水、河水、地下水不同端元的水体223Ra和224Ra活度值分别为0.441和0.026 dpm/100 L、0.22和0.016 dpm/100 L以及0.061和1.30 dpm/100 L,最高值为地下水,其次湖水,河水最小;总体上泉湾湖水223Ra和224Ra活度随离岸距离增加分别由0.047到0.011 dpm/100 L和1.4到0.2 dpm/100 L的减小,垂向上Ra活度呈楔形分布,Ra活度在不同方向上的非保守性分布主要受到悬浮颗粒物解析的影响;通过水体滞留时间模型计算获得青海湖泉湾水体的平均停留时间为1.8天,进一步分析泉湾水体Ra的源汇项,应用镭同位素质量平衡模型获得泉湾布哈河口沿岸地下水排放通量为0.054～0.109 m3/(m2·d).  相似文献   

12.
A14C balance for the Eastern Caribbean deep water indicates the average inflow of Atlantic water into the basin to be 2.3 × 105 m3/sec (±30%), or about 2–4 times the values estimated previously. The balance uses a model representation of the deep-water turnover, and is based on14C concentrations at a station in the Venezuelan Basin which average Δ14C= 89‰ below 800 m depth with a total range of only 9‰, as well as on a14C concentration of the Atlantic inflow of Δ14C= ?71%. as obtained from measurements outside the Antilles Arch. The turnover time of the basin water below 2500 m depth is 55 years, which corresponds to an average upwelling velocity at this depth of about 35 m/year. With such upwelling, the temperature profile below 1800 m (the depth of the sill determining the inflow of new water) requires a vertical eddy diffusivity of about 5 cm2/sec. The oxygen consumption, and silica and CO2 regeneration, rates below 2500 m depth are obtained as ?0.18, + 0.08, and + 0.2 μmole kg?1 yr?1, respectively. The CO2 regeneration has but a negligible effect on the14C balance.  相似文献   

13.
A fiber extraction technique is used to concentrate Ra and Th isotopes from 1000 liters or more of seawater. Natural226Ra and234Th are used as yield tracers. In the equatorial Pacific the228Ra activity of surface water varies from 20 to 1 dpm/1000 kg and generally decreases away from continental shelf areas. Across the Peru Current System, this decrease is modeled as one-dimensional diffusion and indicates the possibility of two flow regimes with distinct characteristic mixing lengths and apparent eddy diffusivities of 105 and 107 cm2/s. The perturbing effects of advection and equatorial upwelling west of the Galapagos Islands are noted. Off the coast of Southern California a vertical228Ra distribution gives an apparent diffusivity of 1.6 cm2/s for the upper thermocline.226Ra concentrations near the coast appear to be higher than the open ocean values at comparable depths, which may reflect supply of this isotope from continental shelf sediments and/or upwelling. The insoluble daughter/soluble parent activity ratios228Th/228Ra and234Th/238U in the equatorial Pacific surface water display latitudinal trends which may be correlated with productivity variations. Near the coast of California these ratios reflect the differing oceanographic conditions north and south of Pt. Conception indicating a mean chemical removal time constant on the order of 4 months for Th and other highly reactive elements within the Southern California Bight. The232Th content of seawater sampled is less than 0.1 μg/1000 1; most of the published values for seawater232Th could well be too high. A comparison of the two methods of determining228Ra (via228Ac and via228Th) made on 64 seawater samples shows that the time delay required by the228Th method is more than compensated by its better analytical simplicity and precision.  相似文献   

14.
The eastern Pontides orogenic belt is one of the most complex geodynamic settings in the Alpine–Himalayan belt due to the lack of systematical geological and geophysical data. In this study, 1D crustal structure and P-wave velocity distribution obtained from gravity modeling and seismological data in the area has been used for the development of the thermal model of the eastern Pontides orogenic belt. The computed temperature-depth profiles suggest a temperature of 590?±?60°C at a Moho depth of 35?km indicates the presence of a brittle-ductile transition zone. This temperature value might be related to water in the subducted crust of the Tethys oceanic lithosphere. The Curie temperature depth value of 29?km, which may correspond to the crustal magma chambers, is found 5–7?km below the Moho depth. Surface heat flow density values vary from 66.5 and 104.7?mW?m?2. High mantle heat flow density value of 48?mW?m?2 is obtained for the area should be related to melting of the lithospheric mantle caused by upwelling of asthenosphere.  相似文献   

15.
The progressive weakening and final disappearance (in 1979) of the long-term meromictic structure of the Dead Sea are clearly reflected in the depth profiles of210Pb and210Po. In 1977/78, prior to overturn, dissolved210Pb (35–50 dpm kg?1) predominated over particulate210Pb (1–2 dpm kg?1) in the oxic upper waters, whereas the reverse was true in the anoxic deep waters (16–20 dpm kg?1 particulate vs. 2–5 dpm kg?1 dissolved). The exact extent of the disequilibrium between210Pb and226Ra is hard to evaluate in the upper oxic layers, because the progressive deepenings resulted in mixing with deep waters. By contrast, one can estimate the residence time of dissolved210Pb in the unperturbed anoxic deepest layers, because these remained isolated, at about 3 years. Following the overturn of 1979, dissolved210Pb exceeded particulate210Pb at all depths. The210Po profiles of the stratified lake resembled in shape those of its grandparent210Pb, but with distinct characteristics of their own in the oxic upper waters where particulate210Po (8–12 dpm kg?1) was greatly in excess over particulate210Pb, while dissolved210Po (25–40 dpm kg?1) was slightly deficient. Immediately following the overturn, dissolved and particulate210Po were similar (about 15 dpm kg?1), at all depths. The destruction of the lake's meromictic structure was accompanied by a reduction of its210Pb inventory, while that of210Po was almost unaffected. Thus, at overturn a transient state was created with the inventory of210Po exceeding that of210Pb.  相似文献   

16.
226Ra profiles have been measured in the western Indian Ocean as part of the 1977–1978 Indian Ocean GEOSECS program. These profiles show a general increase in deep and bottom water Ra concentration from the Circumpolar region to the Arabian Sea. A deep Ra maximum which originates in the Arabian Sea and in the Somali basin at about 3000 m depth spreads southward into the Mascarene basin and remains discernible in the Madagascar and Crozet basins. In the western Indian Ocean, the cold Antarctic Bottom Water spreads northward under the possibly southward-flowing deep water, forming a clear benthic front along the Crozet basin across the Southwest Indian Ridge into the Madagascar and Mascarene basins. The Antarctic Bottom Water continues to spread farther north to the Somali basin through the Amirante Passage at 10°S as a western boundary current. The benthic front and other characteristic features in the western Indian Ocean are quite similar to those observed in the western Pacific where the benthic front as a distinctive feature was first described by Craig et al. [15]. Across the Mid-Indian Ridge toward the Ceylon abyssal plain near the triple junction, Ra profiles display a layered structure, reflecting the topographic effect of the mid-ocean ridge system on the mixing and circulation of the deep and bottom waters. Both Ra and Si show a deep maximum north of the Madagascar basin. Linear relationships between these two elements are observed in the deep and bottom water with slopes increasing northward. This suggests a preferential input of Ra over Si from the bottom sediments of the Arabian Sea and also from the flank sediments of the Somali basin.  相似文献   

17.
The flux of226Ra from bottom sediments has been determined from patterns of226Ra/230Th disequilibrium in ten deep-sea cores from the world oceans. Values range from ? 0.0015 dpm/cm2 yr (in the Atlantic) to 0.21 dpm/cm2 yr (in the north equatorial Pacific). The flux is poorly related to sediment type, but is inversely correlated in a non-linear fashion with sediment accumulation rate. There is a direct relationship between the production rate of226Ra near the sediment-water interface (i.e. the integrated230Th activity in the biologically mixed zone) and the226Ra flux. The226Ra concentration in near-bottom water follows the geographic variation in the226Ra flux. The high flux from north equatorial Pacific sediments especially is reflected in the high bottom water226Ra concentrations in that area. The data suggest that both rate of circulation and the magnitude of the radium flux influence the near-bottom226Ra concentration.  相似文献   

18.
Based on results obtained during the GEOSECS program the primary features of the distribution of226Ra in the Atlantic Ocean can be defined. Outside the Antarctic no significant variation has been found in the226Ra content of surface waters. Eighty samples yield an average of 7.4 dpm/100 kg (normalized to a salinity of 35.00‰). Deep waters in the central Atlantic have226Ra contents several dpm/100 kg higher than expected from the mixing of Antarctic Bottom Water (21.3 dpm/100 kg) and basal North Atlantic Deep Water (10.3 dpm/100 kg). These excesses correlate well with deficiencies in O2 and excesses in SiO2. The intermediate water226Ra maximum in the South Atlantic is associated with the inflow of low-oxygen Circumpolar Intermediate Water beneath the Antarctic Intermediate Water.  相似文献   

19.
Three ferromanganese nodules handpicked from the tops of 2500 cm2 area box cores taken from the north equatorial Pacific have been analysed for their U-Th series nuclides.230Thexc concentrations in the surface 1–2 mm of the top side of the nodules indicate growth rates of 1.8–4.6 mm/106 yr. In two of the nodules a significant discontinuity in the230Thexc depth profile has been observed at ～0.3 m.y. ago, suggesting that the nodule growth has been episodic. The concentration profiles of231Paexc (measured via227Th) yield growth rates similar to the230Thexc data. The bottom sides of the nodules display exponential decrease of230Thexc/232Th activity ratio with depth, yielding growth rates of 1.5–3.3 mm/106 yr.The230Thexc and231Paexc concentrations in the outermost layer of the bottom face are significantly lower than in the outermost layer of the top face. Comparison of the extrapolated230Thexc/232Th and230Thexc/231Paexc activity ratios for the top and bottom surfaces yields an “age” of (5?15) × 104 yr for the bottom relative to the top. This “age” most probably represents the time elapsed since the nodules have attained the present orientation.The210Pb concentration in the surface ～0.1 mm of the top side is in large excess over its parent226Ra. Elsewhere in the nodule, up to ～1 mm depth in both top and bottom sides,210Pb is deficient relative to226Ra, probably due to222Rn loss. The absence of210Pbexc below the outermost layer of the top face rules out the possibility of a sampling artifact as the cause of the observed exponentially decreasing230Thexc and231Paexc concentration profiles. The flux of210Pbexc to the nodules ranges between 0.31 and 0.58 dpm/cm2 yr. The exhalation rate of222Rn, estimated from the226Ra-210Pb disequilibrium is ～570 dpm/cm2 yr from the top side and >2000 dpm/cm2 yr from the bottom side.226Ra is deficient in the top side relative to230Th up to ～0.5–1 mm and is in large excess throughout the bottom. The data indicate a net gain of226Ra into the nodule, corresponding to a flux of (24?46) × 10?3 dpm/cm2 yr. On a total area basis the gain of226Ra into the nodules is <20% of the226Ra escaping from the sediments. A similar gain of228Ra into the bottom side of the nodules is reflected by the high228Th/232Th activity ratios observed in the outermost layer in contact with sediments.  相似文献   

20.
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   

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