Phosphorus limitation of primary productivity in the eastern Mediterranean Sea

Although NO3- is generally considered to limit primary productivity in most of the world’s oceans, previous studies have suggested the Mediterranean Sea may be an exception. In this study of the southeastern Mediterranean, we found that all the PO43- was removed from the upper water column during the winter phytoplankton bloom in the core and boundary of a warm-core eddy, while measurable (0.3-0.6 µM) NO3- remained. The N:P (NO3-: PO43-) ratio in the core and boundary of the Cyprus eddy was 27.4 and the slope of the linear portion of the N vs. P scattergram with 25.5 with a positive intercept of 0.5 µM on the NO3- axis. A similar N:P ratio (28-29), slope (21-23), and intercept (0.9-1.1) was found for the water column across much of the southern Levantine basin. These data, taken together with the results of incubation experiments, lead us to conclude that the southeastern Mediterranean is strongly P limited. The degree of P limitation increases from west to east across the entire basin. We suggest that removal of PO43 by adsorbtion on Fe- rich dust particles may be an important process controlling the concentration of P in the water column

Atmospheric input of nitrogen and phosphorus to the Southeast Mediterranean: Sources, fluxes, and possible impact

Estimates of the sources and wet deposition fluxes of inorganic nutrients (PO43-, NO3-, NO2-, NH4+) have been made using a long-term wet atmospheric deposition measurement at three sites along the Mediterranean coast of Israel. The nutrient composition in rainwater indicated a dominant anthropogenic source for NO, and NH: and a continental, natural, and anthropogenic, rock/soil source for PO43-. The calculated long-term dissolved inorganic N (IN) and inorganic P (IP) fluxes were 0.28 and 0.009 g m(-2) yr(-1) to the coastal zone and estimated as 0.24 and 0.008 g m(-2) yr(-1) to the Southeast (SE) Mediterranean, with a possible increasing pattern of the annual dissolved IN fluxes. Concentration of total and seawater leachable LP (LIP) from dust was examined on 20 Whatman 41 filters collected during 1996. The mean total IP concentration in dust was 0.13 +/- 0.11% (geomean = 0.09%), with a mean of 387 +/- 205 mu g IP per g of dust leached by seawater. LIP from dust varies between 6 and 85% (mean of 38%) of the dry total IF. Dust of desert-type (Saharan) events exhibited lower LIP solubility in seawater (similar to 25%, median) than air masses of European origin (similar to 45%, median). The calculated ratio of wet deposition to total (wet and dry) deposition here of 0.2 showed the importance of dry deposition of P in the SE Mediterranean basin compared to atmospheric inputs into the northwestern basin. The total IP and seawater LIP fluxes from dry deposition were estimated as 0.04 and 0.01 g m(-2) yr(-1), respectively. Atmospheric inputs of bioavailable N and P represent an imbalanced contribution to the new production of 8-20 and 4-11%, respectively, and reinforce the unusual N: P ratios (similar to 27) and possible P limitation in the SE Mediterranean

Anoxic nitrification in marine sediments

Nitrate peaks are found in pore-water profiles in marine sediments at depths considerably below the conventional zone of oxic nitrification. These have been interpreted to represent nonsteady- state effects produced by the activity of nitrifying bacteria, and suggest that nitrification occurs throughout the anoxic sediment region. In this study, ΣNO3 peaks and molecular analysis of DNA and RNA extracted from anoxic sediments of Loch Duich, an organic-rich marine fjord, are consistent with nitrification occurring in the anoxic zone. Analysis of ammonia oxidiser 16S rRNA gene fragments amplified from sediment DNA indicated the abundance of autotrophic ammonia-oxidising bacteria throughout the sediment depth sampled (40 cm), while RT-PCR analysis indicated their potential activity throughout this region. A large non-steady-state pore-water ΣNO3 peak at ~21 cm correlated with discontinuities in this ammonia-oxidiser community. In addition, a subsurface nitrate peak at ~8 cm below the oxygen penetration depth, correlated with the depth of a peak in nitrification rate, assessed by transformation of 15N-labelled ammonia. The source of the oxidant required to support nitrification within the anoxic region is uncertain. It is suggested that rapid recycling of N is occurring, based on a coupled reaction involving Mn oxides (or possibly highly labile Fe oxides) buried during small-scale slumping events. However, to fully investigate this coupling, advances in the capability of high-resolution pore-water techniques are required

Bacterially mediated removal of phosphorus and cycling of nitrate and sulfate in the waste stream of a "zero-discharge" recirculating mariculture system

Simultaneous removal of nitrogen and phosphorus by microbial biofilters has been used in a variety of water treatment systems including treatment systems in aquaculture. In this study, phosphorus, nitrate and sulfate cycling in the anaerobic loop of a zero-discharge, recirculating mariculture system was investigated using detailed geochemical measurements in the sludge layer of the digestion basin. High concentrations of nitrate and sulfate, circulating in the overlying water (~15 mM), were removed by microbial respiration in the sludge resulting in a sulfide accumulation of up to 3 mM. Modelling of the observed S and O isotopic ratios in the surface sludge suggested that, with time, major respiration processes shifted from heterotrophic nitrate and sulfate reduction to autotrophic nitrate reduction. The much higher inorganic P content of the sludge relative to the fish feces is attributed to conversion of organic P to authigenic apatite. This conclusion is supported by: (a) X-ray diffraction analyses, which pointed to an accumulation of a calcium phosphate mineral phase that was different from P phases found in the feces, (b) the calculation that the pore waters of the sludge were highly oversaturated with respect to hydroxyapatite (saturation index = 4.87) and (c) there was a decrease in phosphate (and in the Ca/Na molar ratio) in the pore waters simultaneous with an increase in ammonia showing there had to be an additional P removal process at the same time as the heterotrophic breakdown of organic matter

Nutrient budget for the Eastern Mediterranean: Implications for phosphorus limitation

The eastern Mediterranean has a high nitrate to phosphate (N : P) ratio (~28 : 1) in the deep water and a highly unusual P limitation of the primary productivity. We present a detailed nutrient budget of inputs to the basin, which shows that there is a high N: P ratio (>16 : 1) in all the input sources, particularly from the atmospheric source, where the N: P ratio was 117 : 1. The high N: P ratio is retained within the system because there is no significant denitrification in either the sediments or intermediate water. This is because of the extreme oligotrophic nature of the system, which is caused by the unusual anti-estuarine flow at the Straits of Sicily. Support for this conclusion is provided by the observation that the only area of the eastern Mediterranean where the N: P ratio in deeper water is ~16 : 1 is the northern Adriatic, which is also the only area with significant denitrification. The N budget (total input to basin vs. net output at the straits of Sicily) balances closely. This N balance suggests that N fixation is an insignificant process in this P-limited system. The unusually light 15N values in the deep water nitrate and particulate organic nitrogen can be explained by processes other than nitrogen fixation. These processes include a lack of significant denitrification in the basin and by particulate organic matter exported from surface waters during the Plimited winter plankton bloom

Sources and timing of trace metal contamination to sediments in remote sealochs, NW Scotland

Sediment cores from a transect of sealochs, Etive, Sunart, Nevis, Duich, Broom and Torridon in N.W. Scotland were analysed for the trace metals lead, copper, and zinc. In addition, sediment cores from the Clyde Sea Basin (Loch Fyne, the Gareloch, Clyde dumpsite) and from the Irish and Celtic Seas were analysed as possible source areas for contaminated particles. The sediment cores were dated using excess 210Pb and 137Cs, and Al normalisation was used to correct for sediment compositional effects. All cores showed increased concentrations of all trace metals (and M/Al) towards the surface, with a maximum of 280–500% above background being observed in Loch Etive. Only cores from Duich and Torridon (Zn/Al and Pb/Al) and Etive (Zn/Al) did not continue to show an increase in trace metals to the uppermost samples. The burden of atmospherically derived trace metals accumulated over the past 100 years was compared with similar published burdens from a series of freshwater lochs adjacent to the sealochs. Plots of excess 210Pb (used to correct for sediment focusing) against atmospherically derived Pb showed a series of linear relationships of systematically decreasing gradient towards the north-west, away from potential urban sources of lead. It was calculated that 49% (15–77%) of the Pb but only 3% (1–4%) of the Zn and 2% (0–3%) of the Cu reached the sealochs from atmospheric sources. The remaining trace metals deposited in the sealochs came from marine particles. Using trace metal ratios as an indicator of pollutant provenance, it was shown that the trace metals came predominantly from the Irish Sea. There was no evidence of trace metals derived from the Firth of Clyde basin. It was concluded that trace metal contamination from the Clyde and the surrounding industrialised urban area was mainly deposited in the estuary and the Clyde Sea basin with its adjoining sealochs, such as the Gareloch and Loch Fyne

Impact of atmospheric deposition on N and P geochemistry in the southeastern Levantine basin

Aeolian dust was collected from 2001 to 2003, as part of a longer-term study, to estimate the nutrient input to the Levantine basin from atmospheric deposition. Adsorption experiments, using dust samples from six individual dust storms, showed insignificant adsorption of phosphate onto dry deposited Saharan dust. Thus adsorption onto dust can be discounted as a reason for the high nitrogen:phosphorus (N:P) ratio in the deep water of the eastern basin. A single dust storm sample from the Western Mediterranean was able to adsorb some phosphate from seawater, and it is speculated that this may be linked to the action of acid aerosols on the dust during cloud formation, or to the varying chemical composition in different sources of dust. Dry atmospheric deposition is an important net supplier of both N and P to the eastern basin. Leachable inorganic nitrogen concentrations and fluxes are higher in background (non-storm) samples than in storm samples, probably due to the smaller grain size and aerosol source. Total P is supplied naturally with the dust, as shown by the close correlation between total P and Al (r2=0.95). However, there is a poor correlation between leachable inorganic P (LIP) and Al (r2=0.20), which may be related to grain-size effects and/or recycling processes in the atmosphere. Even so, the supply of LIP to surface waters is greatest during dust storms due to comparatively high deposition of aerosol material. While atmospheric input of P during dust storms does not produce significant in situ increases in chlorophyll, probably due to rapid microbial grazing, it does represent an important proportion of the long-term nutrient input to the basin. This may be increasing as the frequency of dust storms increases