Total organic carbon distribution and budget through the Strait of Gibraltar in April 1998

In order to investigate total organic carbon (TOC) exchange through the Strait of Gibraltar, samples were taken along two sections from the western (Gulf of Cádiz) and eastern (Western Alboran Sea) entrances of the Strait and at the middle of the Strait in April 1998. TOC was measured by using a high-temperature catalytic oxidation method. The results referenced here are based on a three-layer model of water mass exchange through the Strait, which includes the Atlantic inflow, Mediterranean outflow and an interface layer in between. All layers were characterised by a decrease of TOC concentrations from the Gulf of Cádiz to the Western Alboran Sea: from 60–79 to 59–66 μM C in the Atlantic inflow and from 40–60 to 38–52 μM C in the Mediterranean waters, respectively. TOC concentrations in the modified North Atlantic Central Water varied from 43 to 55 μM C. Intermediate TOC values were measured in the interface layer (43–60 μM C). TOC concentrations increased from the middle of the Strait towards continents indicating a contribution of organic carbon of photosynthetic origin along Spain and Morocco coasts or TOC accumulation due to upwelling in the northeastern part of the Strait. Our results indicate that the short-term variability caused by the tide greatly impacts the TOC distribution, particularly in the Gulf of Cádiz. The TOC input from the Atlantic Ocean to the Mediterranean Sea through the Strait of Gibraltar varies from 0.9×10⁴ to 1.0×10⁴ mol C s⁻¹ (or 0.28×10¹² to 0.35×10¹² mol C year⁻¹, respectively). This estimate suggests that the TOC inflow and outflow through the Strait of Gibraltar are two and three orders of magnitude higher than reported via the Turkish Straits and Mediterranean River inputs.     

Cadmium,copper and lead in the western Mediterranean Sea

The results of determinations of cadmium, copper and lead in western Mediterranean waters collected during the PHYCEMED 81 cruise are discussed in this paper. The analyses were carried out according to two different methods: flameless atomic absorption and anodic stripping voltammetry. Very strict conditions of sampling and treatment were maintained in order to reduce the chance of contamination. The concentrations found are considerably lower than those usually reported for Mediterranean waters. The distributions are homogeneous, both vertically and from one station to another. The average concentrations are 8 ng 1^?1 for Cd, 90 ng 1^?1 for Cu and 30–40 ng^?1 for Pb. This homogeneity, as well as the concentrations of cadmium and lead, may be explained by the hydrological conditions of the Mediterranean Sea.     

Comparison of the biology, dynamics, and secondary production of Talorchestia brito (Amphipoda, Talitridae) in Atlantic (Portugal) and Mediterranean (Tunisia) populations

The biology, population dynamics, and production of Talorchestia brito were studied at two sandy beaches located on the Atlantic (Portugal) and on the Mediterranean (Tunisia) coasts, respectively. The seasonal variation in abundance and the overall densities were similar in both populations. Reproduction occurred from February to September in the Atlantic, and from March to early November in the Mediterranean. The sex ratio was male biased in the Atlantic, and female biased in the Mediterranean. Based on data from the Atlantic population, both abundance and the proportion of reproductive females were positively correlated with temperature, while the proportion of juveniles in the population was positively correlated with temperature and sediment moisture. On average, individuals from the Atlantic were larger than the ones from the Mediterranean. Life span was estimated at six to nine months in the Atlantic, and five to eight months in the Mediterranean. Talorchestia brito was shown to be a semiannual species, with iteroparous females producing two broods per year, and exhibited a bivoltine life cycle. The minimum age required for males' and females' sexual differentiation and for female sexual maturation was shorter in the Mediterranean. Growth production (P) was estimated at 0.19 g m⁻² y⁻¹ ash free dry weight (AFDW; 4.3 kJ m⁻² y⁻¹) in the Atlantic population, and 0.217 g m⁻² y⁻¹ AFDW (4.9 kJ m⁻² y⁻¹) in the Mediterranean one. Elimination production (E) was estimated at 0.35 g m⁻² y⁻¹ AFDW (7.9 kJ m⁻² y⁻¹) in the Atlantic, and 0.28 g m⁻² y⁻¹ AFDW (6.3 kJ m⁻² y⁻¹) in the Mediterranean. The average annual biomass ( ) (standing stock) was estimated at 0.032 g m⁻² in the Atlantic beach, and 0.029 g m⁻² in the Mediterranean one, resulting, respectively, in ratios of 5.9 and 7.5 and ratios of 10.8 and 9.6. Like other talitrids, T. brito exhibited geographic variation in morphometrical characteristics, sex ratio, growth rates, life span, and reproduction period, with the Atlantic population presenting a slower life history.     

Le phosphore et l'azote en mer Mediterranee,bilans et fertilite potentielle

The UNEP (1977) study concerning the terrestrial discharges of phosphorus and nitrogen into the Mediterranean Sea is used in this work, along with the calculated values of the water fluxes (Bethoux, 1979, 1980). Owing to the phosphorus concentrations in the deep waters and the terrestrial discharges, the balance of this element requires low concentrations in the surface layers (< 0.1 μg P l^?1) which appear to be in agreement with the measured phosphate concentrations in the Strait of Gibraltar and in the Strait of Sicily. The phosphorus cycle in the Mediterranean Sea is characterised by the transfer of the terrestrial and Atlantic influxes from the surface layer to the intermediate and deep layers.The geographic distribution of the terrestrial discharges is highly asymmetric, and the vertical movements of the water masses in certain regions induce an important hydrologic recycling of phosphorus. The potential fertility (linked to the assimilation of the available phosphorus) is estimated from the local surface phosphorus flows and from the hydrologic recycling. Its values range, in the Western basin, between 9 and 86 g C m^?2y^?1 in the Southern and Northern parts of this basin, respectively. In addition to biological reasons, the nitrogen budget in the Mediterranean Sea should be comparable to that of phosphorus because the geographical variations of the nitrate concentrations in the deep waters and the distribution of terrestrial discharges are similar to those of phosphorus. However, the relatively low values of terrestrial discharges of nitrogen proposed by UNEP (compensating about 28% of the outflowing nitrate fluxes in the Strait of Gibraltar) do not allow a balance of this nutrient unless we introduce a high concentration (too high in the author's opinion) in the Atlantic surface waters.     

Mercury levels in the dissolved and particulate fractions of the Tyrrhenian sea

Determination of the actual mercury concentration in Mediterranean basin seawater was achieved by means of an instrument based on fluorescence spectrometry developed for this purpose, during a field study aboard the oceanographic ship “L.F. Marsili”, between August 1980 and May 1982.Dissolved ·total’ and ·reactive’ mercury and mercury associated with particulate matter were determined on surface and subsurface waters in the Tyrrhenian Sea from La Spezia to Sicily.Concentrations in the range 1.4–19.7 ng l⁻¹ for ·total dissolved mercury’, 0.5–5.9 ng l⁻¹ for ·reactive dissolved mercury’ and 0.3–8.0 ng l⁻¹ for mercury associated with the particulate matter, were measured on surface and subsurface waters in the Tyrrhenian Sea from La Spezia to Sicily.Even if the mean value of the total mercury concentration (dissolved + particulate) was found to be about twice as high as those observed for the oceans, the difference does not seem to be as high as predicted by the model proposed by Buffoni and co-workers to explain the large difference of mercury levels between tunas caught, respectively, in the Mediterranean and in the Oceans.     

Chromium(VI) distributions in the Arctic and the Atlantic Oceans and a reassessment of the oceanic Cr cycle

Chromium(VI) concentrations ranging between 3.0 and 6.1 nmol l⁻¹ and 3.1 and 7.3 nmol l⁻¹ were found in the Arctic and Atlantic Oceans, respectively. The vertical profiles show modest depletion of chromium(VI) in surface waters, but poor overall correlations between Cr(VI) and nutrient profiles. Given that Cr(VI) is the dominant oxidation state of chromium in open-ocean waters, these data are combined with literature data to reassess the distribution of Cr in oceanic waters. It is concluded that while Cr shows some characteristics of both “recycled” and “accumulated” vertical profiles, it does not fall clearly within either group.     

Detailed current structures in the Eastern Channel of the Tsushima Strait in summer

We discussed the detailed current structures in the Eastern Channel of the Tsushima Strait, using four sets of acoustic Doppler current profiler (ADCP) data, which were taken by the quadrireciprocal method (Katoh, 1988), for removing tidal currents, in summers of 1987–1989. In the Eastern Channel, diurnally averaged currents balanced almost geostrophically. In the upper layer of the deepest part of the Eastern Channel, there existed a current core which corresponded to one branch of the Tsushima Current. The current direction in this core was between NE and ENE in all observations but the magnitude of velocity in 1987 differed largely from that in 1988. Another current core with lower velocities was found near the north coast of Kyushu. Near the bottom at the deepest part of the Eastern Channel, the velocity was more or less 0.3 kt (15 cm s^–1). Along the east coast of Tsushima and in waters northeast of it, countercurrents were observed. The continuity of these countercurrents was interpreted as follows: A part of the current flowing from the Western Channel of the Tsushima Strait into the Japan Sea turns clockwise in waters northeast of Tsushima, and flows southwestward along the east coast of Tsushima. The southwestward current along Tsushima was correlated with the northeastward current in the central part of the Eastern Channel. The transport through the Eastern Channel was between 0.59 and 1.30 Sv (1 Sv=10⁶ m³s^–1). The baroclinic component, which was defined as the transport based on calculations of geostrophic current with assuming zero velocity near the bottom, was very small.     

Evaluation of atmospheric transport as a nonpoint source of polycyclic aromatic hydrocarbons in marine sediments of the Eastern Mediterranean

Coastal marine sediment, air and seawater samples were collected at six sampling stations in the Eastern Mediterranean Sea distant from pollutant point sources. All sediment samples were analyzed to determine polycyclic aromatic hydrocarbon (PAH), black carbon (BC) and organic carbon (OC) contents. The PAH contents of gaseous and seawater samples of the study were determined in order to evaluate the role of air–sea exchange as PAH nonpoint source to the marine sediments. The average concentration of the total PAHs (∑PAHs) in the sediments varied from 2.2 to 1056.2 ng g⁻¹ dry weight. The average BC and OC contents varied from 0.3 to 5.6 and from 2.9 to 21.4 mg g⁻¹ dry weight, respectively. ∑PAH concentration in the marine atmosphere varied from 20.0 to 83.2 ng m⁻³. Air–water exchange flux (F_A–W) estimation has indicated air transport as a significant source of PAHs to pristine marine sediments of Eastern Mediterranean. In addition, the significant correlation between the PAHs and the organic and soot carbon content further suggests the importance of atmospheric input of PAHs to the sediments.     

Cretan deep water outflow into the Eastern Mediterranean

A simple hydraulic model is used to estimate the deep water fluxes of Cretan Deep Water (CDW), through the Cretan Arc Straits and into the Eastern Mediterranean Basins. The input to the model consists of the height of the deep water reservoir above sill depth and its density difference from the overlying water masses. Data from four hydrographic cruises, which took place in 1995, 1991 and 1987, are used to estimate the depth of the reservoir above the sill and the density difference. The results show a significant CDW outflow of 0.75×10⁶ m³ s⁻¹ in early 1995. The outflow of CDW through Kassos Strait, in the east, is 0.53×10⁶ m³ s⁻¹, while 0.22×10⁶ m³ s⁻¹ outflows through the Antikithira Strait in the west. The model results agree with fluxes estimated from current meter observations.The CDW outflow has been neither steady nor uniform during the period 1987–95. In the Kassos Strait, the outflow commenced in 1987 and increased rapidly until 1991; since then, it appears to have stabilised. In the Antikithira Strait, in contrast, the outflow has increased steadily since 1987. Such modifications in the CDW outflow are associated with changes in its hydrographic characteristics. The salinity of CDW increased constantly, by approximately 0.1, between 1987 and 1995 while its temperature warmed, between 1987 and 1991, and then cooled.     

Trace metal fronts in Scottish coastal waters

Dissolved cadmium and copper concentrations have been determined in 76 surface water samples in coastal and ocean waters around Scotland by anodic stripping voltammetry (ASV). A trace metal/salinity ‘front’ is observed to the west, north and north-east of Scotland separating high salinity ocean water (>35 × 10⁻³) with low concentrations of dissolved Cd and Cu from lower salinity (<35 × 10⁻³) coastal water containing higher concentrations of Cd and Cu. Mean Cd concentrations in ocean and coastal waters are 7 ng dm⁻³ (0·06 n ) and 11 ng dm⁻³ (0·10 n ) respectively; for Cu the respective levels are 60 ng dm⁻³ (0·95 n ) and 170 ng dm⁻³ (2·68 n ). The observed distribution is attributed principally to freshwater runoff and the advection of contaminated Irish Sea water into the study area.     

Dissolved organic carbon, nitrogen and phosphorus in the N-E Atlantic and the N-W Mediterranean with particular reference to non-refractory fractions and degradation

Dissolved organic carbon (DOC), dissolved organic nitrogen (DON) and dissolved organic phosphorus (DOP) measured in deep profiles in the N-E Atlantic and in the N-W Mediterranean in the period 1984–2002 are described. After accurate validation, they show close agreement with those previously published.Classic profiles were obtained, with concentrations decreasing in deep waters. In the Mediterranean and in the Atlantic comparable concentrations were found in the 1500–2000 m waters, 44–46 μmol l⁻¹ DOC, 2.6–2.8 μmol l⁻¹ DON and 0.02–0.03 μmol l⁻¹ DOP. In the surface layers, DOC concentrations were higher, but DON and DOP concentrations lower, in the Mediterranean than in the Atlantic, leading to higher element ratios in the Mediterranean. In autumn, values were, respectively, DOC:DON 17 vs. 14, DOC:DOP 950 vs. 500 and DON:DOP 55 vs. 35. The data suggest an increase in DOC and DON in the North Atlantic Central Water over 15 years, which may be linked to the North Atlantic climatic oscillations.Refractory DOM found in the 1500–2000 m layer exhibited C:N:P ratios of 1570:100:1. The labile+semi-labile (=non-refractory) DOM (nrDOM) pool was computed as DOM in excess of the refractory pool. Its contribution to total DOM above the thermocline in the open sea amounted to 25–35% of DOC, 30–35% of DON, and 60–80% of DOP. Element ratios of the nrDOM varied among stations and were lower than those of refractory DOM, except for C:N in the Mediterranean: nrDOC:nrDON 10–19, nrDOC:nrDOP 160–530 and nrDON:nrDOP 15–38. The specific stoichiometry of DOM in the Mediterranean led us to postulate that overconsumption of carbon is probably a main process in that oligotrophic sea.By coupling non-refractory DOM stoichiometry and relationships between the main DOM elements in the water column, the relative mineralization of C, N and P from DOM was studied. Below the thermocline, the preferential removal of phosphorus with regard to carbon from the semi-labile DOM can be confirmed, but not the preferential removal of nitrogen. In the ocean surface layers, processes depend on the oceanic area and can differ from deep waters, so preferential carbon removal seems more frequent. Bacterial growth efficiency data indicate that bacteria are directly responsible for mineralization of a high proportion of DON and DOP in the deep water.     

Iodine chemistry in deep anoxic basins and overlying waters of the Mediterranean Sea

Iodate (IO₃⁻) is the predominant dissolved species of iodine in the oxygenated waters of the Mediterranean Sea. Iodide (I⁻) is present in significant quantities (up to 65 nM) in oxygenated waters in the photic zone and near the interface above the anoxic and saline Bannock Basin. Lesser quantities of I⁻ (< 10 nM) are found throughout the rest of the oxic water column. An additional unidentified dissolved iodine species is present immediately above the anoxic interface.Total dissolved iodine (ΣI) increases dramatically across the seawater/brine interface. Part of this increase is undoubtedly the result of the dissolution of iodine-rich evaporites during formation of the brine bodies at the Tyro and Bannock Basins. The vertical distribution of ΣI and other dissolved chemical species (particularly PO₄³⁻) in the Bannock Basin brine, however, suggests an additional, present-day, diagenetic source of dissolved iodine to the brine. Based on the increase in the concentration of the most soluble major ions across the seawater/brine interface, 5–7 μM of the 11.5-μM increase in ΣI concentration must be attributed to diagenesis.     

Reactive mercury in the central North Atlantic Ocean

The level of reactive mercury in pelagic waters near the Mid Atlantic Ridge, south of the Azores, and in the Sargasso Sea, north of Bermuda, was studied. The reactive Hg concentration in both locations was shown to be fairly uniform with depth at a level of 2.5 ± 0.5 pmol l⁻¹. The profiles show no indication of a simple Hg-nutrient relationship. The deep water from the Famous area was also sampled and showed no elevated Hg levels.     

Spatio-temporal distribution of dissolved inorganic carbon and net community production in the Chukchi and Beaufort Seas

As part of the 2002 Western Arctic Shelf–Basin Interactions (SBI) project, spatio-temporal variability of dissolved inorganic carbon (DIC) was employed to determine rates of net community production (NCP) for the Chukchi and western Beaufort Sea shelf and slope, and Canada Basin of the Arctic Ocean. Seasonal and spatial distributions of DIC were characterized for all water masses (e.g., mixed layer, halocline waters, Atlantic layer, and deep Arctic Ocean) of the Chukchi Sea region during field investigations in spring (5 May–15 June 2002) and summer (15 July–25 August 2002). Between these periods, high rates of phytoplankton production resulted in large drawdown of inorganic nutrients and DIC in the Polar Mixed Layer (PML) and in the shallow depths of the Upper Halocline Layer (UHL). The highest rates of NCP (1000–2850 mg C m⁻² d⁻¹) occurred on the shelf in the Barrow Canyon region of the Chukchi Sea and east of Barrow in the western Beaufort Sea. A total NCP rate of 8.9–17.8×10¹² g for the growing season was estimated for the eastern Chukchi Sea shelf and slope region. Very low inorganic nutrient concentrations and low rates of NCP (<15–25 mg C m⁻² d⁻¹) estimated for the mixed layer of the adjacent Arctic Ocean basin indicate that this area is perennially oligotrophic.     

On the oxidation and burial of organic carbon in sediments of the Iberian margin and Nazaré Canyon (NE Atlantic)

As a contribution to the EC-OMEX-II program, sediment carbon and nitrogen budgets are presented for the Iberian Margin (northeastern Atlantic). The budgets for degradable organic carbon and associated nitrogen were calculated from sediment and pore water properties, using a steady-state version of a numerical coupled diagenetic model, OMEXDIA. Data were collected throughout the major upwelling period along five transects, four of which were located on the open margin and one positioned in a major submarine canyon, the Nazaré Canyon.A comparison of in situ oxygen profiles measured with monocathodic microelectrodes and with Clark type microelectrodes showed that monocathodic electrodes overestimate the oxygen concentration gradient near the sediment–water interface. This artifact probably results from the loss in sensitivity of the monocathodic microelectrode during profiling. Shipboard time course measurements with Clark type electrodes demonstrated transient conditions upon sediment retrieval on deck and indicated enhanced rates of oxygen consumption in the surface sediment, presumably as a result of lysis or exudation of oxidisable substrates by infauna. As a result, oxygen fluxes calculated from shipboard oxygen profiles overestimated in situ fluxes by up to a factor of 5 for water depths >1000 m.The sediments from the canyon and from a depositional area on the shelf were enriched in organic carbon (3–4.5 wt%) relative to the open margin stations (0.5–2 wt%) and showed C/N ratios exceeding Redfield stoichiometry for marine organic matter, indicating there was deposition of organic carbon of terrestrial origin in these areas. The oxidation of organic carbon on the open margin declined from ˜11 gCm⁻²y⁻¹ on the shelf to 2 gCm⁻²y⁻¹ at 5000 m water depth, and was dominated by aerobic oxidation. The reactivity of the degradable organic carbon at the time of deposition was <2.5 y⁻¹ on the shelf, and declined to <0.5 y⁻¹ offshore. The burial of refractory organic carbon at the stations along the open margin transects also declined with increasing water depth from ˜5 gCm⁻²y⁻¹ on the shelf to <1 gCm⁻²y⁻¹ at 2000 m depth, whereas the burial of particulate inorganic carbon declined from ˜20 gCm⁻²y⁻¹ to <5 gCm⁻²y⁻¹. A comparison of the estimated total organic carbon deposition and predicted delivery for the shelf suggest that 58 to 165 gCm⁻²y⁻¹ is oxidized in the water column, laterally advected, or focused into one of the canyons.Anaerobic oxidation, denitrification and, therefore, total oxidation of organic carbon was enhanced within the canyon relative to the open margin. Total organic carbon oxidation decreased with water depth from 22 gCm⁻²y⁻¹ at the head of the canyon to 3 gCm⁻²y⁻¹ over its fan. The reactivity of the organic carbon deposited in the canyon was lower than those of the shelf stations, suggesting that the canyon is being enriched in older, laterally advected organic matter. The burial of refractory organic carbon in sediments from the Nazaré Canyon was considerably higher than in the sediments from the open margin; it also decreased with depth from 20 gCm⁻²y⁻¹ at 343 m to ˜2.5 gCm⁻²y⁻¹ at 4298 m water depth. The burial of particulate inorganic carbon was slightly lower than that of refractory organic carbon.The burial of refractory organic carbon and the deposition of degradable organic carbon were both positively correlated with the sedimentation rates for the Iberian Margin, and indicated burial efficiencies were 0.6 to 48%. A single trend for burial efficiency versus sedimentation rate for both the canyon and the open margin indicates that the sedimentation rate was the master variable for the geographical distribution of organic carbon oxidation and carbon preservation on the NW Iberian Margin.     

The behaviour of dissolved Cd, Co, Zn, and Pb in North Atlantic near-surface waters (30°N/60°W–60°N/2°W)

In September 1993 (M26) and June/July 1996 (M36), a total of 239 surface samples (7 m depth) were collected on two transects across the open Atlantic Ocean (224 samples) and northwest European shelf edge area. We present an overview of the horizontal variability of dissolved Cd, Co, Zn, and Pb in between the northwest and northeast Atlantic Ocean in relation to salinity and the nutrients. Our data show a preferential incorporation of Cd relative to P in the particulate material of the surface ocean when related to previously published parallel measurements on suspended particulate matter from the same cruise. There is a good agreement with results recently estimated from a model by Elderfield and Rickaby (Nature 405 (2000) 305), who predict for the North Atlantic Ocean a best fit for α_Cd/P=[Cd/P]_POM/[Cd/P]_SW of 2.5, whereas the approach of our transect shows a α_Cd/P value of 2.6. The Co concentrations of our transects varied from <5 to 131 pmol kg⁻¹, with the lowest values in the subtropical gyre. There were pronounced elevations in the low-salinity ranges of the northwest Atlantic and towards the European shelf. The Co data are decoupled from the Mn distribution and support the hypothesis of marginal inputs as the dominant source. Zinc varied from a minimum of <0.07 nmol kg⁻¹ to a maximum of 1.2 and 4.8 nmol kg⁻¹ in regions influenced by Labrador shelf or European coastal waters, respectively. In subtropical and northeast Atlantic waters, the average Zn concentration was 0.16 nmol kg⁻¹. Zinc concentrations at nearly three quarters of the stations between 40°N and 60°N were <0.1 nmol kg⁻¹. This suggests that biological factors control Zn concentrations in large areas of the North Atlantic surface waters. The Pb data indicated that significant differences in concentration between the northwest and northeast Atlantic surface waters presently (1996) do not exist for this metal. The transects in 1993 and 1996 exhibited Pb concentrations in the northeast Atlantic surface waters of 30 to 40 pmol kg⁻¹, about a fifth to a quarter of the concentrations observed in 1981. This decline is supported by our particle flux measurements in deep waters of the same region.     

Manganese in the Western North Atlantic Ocean

Dissolved and total dissolvable manganese concentrations have been measured at four stations in the western North Atlantic Ocean. Total dissolvable manganese concentrations are high in surface waters, decrease to uniformly low levels throughout the bulk of the water column, and increase in the bottom nepheloid layer. Dissolved Mn (Mn_d) concentrations follow the total dissolvable concentrations throughout the surface and deep waters but do not increase in the near-bottom waters.Deep water concentrations of Mn_d decrease from 30 ng l^?1 in the Newfoundland Basin to 20 ng l^?1 in the Sargasso Sea. This change and other features of the deep water distribution of dissolved manganese could be associated with the slow oxidation of Mn²⁺ to MnO₂. There is also evidence at one station of scavenging of manganese from the dissolved phase in the near-bottom layer which may again be related to the kinetics of manganese oxidation.     

Responses of marine phytoplankton in iron enrichment experiments in the northern North Sea and northeast Atlantic Ocean

Short-term iron enrichment experiments were carried out with samples collected in areas with different phytoplankton activity in the northern North Sea and northeast Atlantic Ocean in the summer of 1993. The research area was dominated by high numbers of pico-phytoplankton, up to 70,000 ml⁻¹. Maximum chlorophyll a concentrations varied from about 1.0 μg l⁻¹ in a high-reflectance zone (caused by loose coccoliths, remnants from a bloom of Emiliania huxleyi) and about 3.5 μg l⁻¹ in a zone in which the phytoplankton were growing, to about 0.5 μg l⁻¹ in the northeast Atlantic Ocean. From the high-reflectance zone to the northeast Atlantic Ocean, nitrate concentrations increased from 0.5 μM to 6.0 μM. Concentrations of reactive iron in surface water showed an opposite trend and decreased from about 2.6 nM in the high-reflectance zone to <1.0 nM in the northeast Atlantic Ocean. In the research area, no signs of true iron deficiency were found, but iron enrichments in the high-reflectance zone, numerically dominated by Synechococcus sp., resulted in increased nitrate uptake. Ammonium uptake was hardly affected. Strong support for the effect of Fe on cell physiology is given by the increase in the f-ratio. Net growth rates of the phytoplankton (changes in cell numbers over 24 h) were almost unchanged. Phytoplankton collected from the northeast Atlantic Ocean, did not show changes in the nitrogen metabolism upon addition of iron. Net growth rates in these incubations were low or negative, with only slightly higher values with additional iron.     

Transient Eastern Mediterranean deep waters in response to the massive dense-water output of the Aegean Sea in the 1990s

We present a detailed account of the changing hydrography and the large-scale circulation of the deep waters of the Eastern Mediterranean (EMed) that resulted from the unique, high-volume influx of dense waters from the Aegean Sea during the 1990s, and of the changes within the Aegean that initiated the event, the so-called ‘Eastern Mediterranean Transient’ (EMT). The analysis uses repeated hydrographic and transient tracer surveys of the EMed in 1987, 1991, 1995, 1999, and 2001/2002, hydrographic time series in the southern Aegean and southern Adriatic Seas, and further scattered data. Aegean outflow averaged nearly 3 × 10⁶ m³ s⁻¹ between mid-1992 and late 1994, and was largest during 1993, when south and west of Crete Aegean-influenced deep waters extended upwards to 400 m depth. EMT-related Aegean outflow prior to 1992, confined to the region around Crete and to 1800 m depth-wise, amounted to about 3% of the total outflow. Outflow after 1994 up to 2001/2002, derived from the increasing inventory of the tracer CFC-12, contributed 20% to the total, of 2.8 × 10¹⁴ m³. Densities in the southern Aegean Sea deep waters rose by 0.2 kg/m³ between 1987 and 1993, and decreased more slowly thereafter. The Aegean waters delivered via the principal exit pathway in Kasos Strait, east of Crete, propagated westward along the Cretan slope, such that in 1995 the highest densities were observed in the Hellenic Trench west of Crete. Aegean-influenced waters also crossed the East Mediterranean Ridge south of Crete and from there expanded eastward into the southeastern Levantine Sea. Transfer into the Ionian mostly followed the Hellenic Trench, largely up to the trench’s northern end at about 37°N. From there the waters spread further west while mixing with the resident waters. Additional transfer occurred through the Herodotus Trough in the south. Levantine waters after 1994 consistently showed temperature–salinity (T–S) inversions in roughly 1000–1700 m depth, with amplitudes decreasing in time. The T–S distributions in the Ionian Sea were more diverse, one cause being added Aegean outflow of relatively lower density through the Antikithira Strait west of Crete. Spreading of the Aegean-influenced waters was quite swift, such that by early 1995 the entire EMed was affected. and strong mixing is indicated by near-linear T–S relationships observed in various places. Referenced to 2000 and 3000 dbar, the highest Aegean-generated densities observed during the event equaled those generated by Adriatic Sea outflow in the northern Ionian Sea prior to the EMT. A precarious balance between the two dense-water source areas is thus indicated. A feedback is proposed which helped triggering the change from a dominating Adriatic source to the Aegean source, but at the same time supported the previous long-year dominance of the Adriatic. The EMed deep waters will remain transient for decades to come.