Rare earth elements distribution in seawater and suspended particulate of the Central Mediterranean Sea

Rare earth element (REE) content in suspended and dissolved phases from the Strait of Sicily (Central Mediterranean Sea) has been measured. Vertical profiles of several dissolved REEs along the water column reflect the 3-D oceanographic features of the studied area and identifies the different water masses present there. Shale-normalized REE distribution patterns and derived parameters calculated for the suspended particulate show different atmospheric dust-surface inputs and their interactions with seawater. Finally, combined information from [La/Yb]_N, ratios, REE/La ratios and Eu anomalies measured in the suspended particulate suggest an important contribution of volcanic materials from the Etna volcano and Saharan dust to the lithogenic fraction of the suspended particulate.     

Recognition of water masses according to geochemical signatures in the Central Mediterranean sea: Y/Ho ratio and rare earth element behaviour

This study reports the results of geochemical investigations carried out in the Strait of Sicily (Central Mediterranean Sea) during the oceanographic cruise BANSIC 2000, focusing on the area around the Pantelleria Island. We evaluate the interface processes between dissolved phase and suspended particulate matter in the water columns on the basis of Y/Ho ratio and rare earth elements and yttrium distributions that are suitable to trace the occurrence of different water layers in Central Mediterranean Area. The main source of trace elements to the sea water system was recognized in the atmospheric fallout, while different scavenging mechanisms among Y and rare earth elements occur. Cation exchange at the dissolved phase-suspended media interface is driven by their external electronic configurations as monitored through the Y/Ho ratios, shape, and amplitude of the tetrad effects calculated along the water columns. The shape and amplitude of the tetrad effects in bottom waters suggest that the preferential Y scavenging from deep water layers depends on the hydrothermal activity in the seafloor. Here, Y is surface-complexed through the formation of inner-sphere complexes; Ho and other heavy rare earth elements are sorbed onto suspended particulate matter surfaces as weak outer-sphere complexes; these materials have a montmorillonite like nature; and preferential incorporation medium rare earth elements in crystal structures of biogenic carbonates is suggested by the relationship between the Eu anomaly and the nutrient contents of water masses.     

Species and distribution of rare earth elements in the Baotou section of the Yellow River in China

This paper analyses the contents and species distributions of rare earth elements (REEs) in the water-suspended particulate-sediment system of the Baotou section of the Yellow River, China, with known anthropogenic REE input from industrial discharges. The major forms of REEs were suspended and dissolved in the mainstream and the tributaries of the Baotou section, respectively. The concentrations of the dissolved and suspended REEs had the same trends in the overlying water along the mainstream, which increased from the Seqi section (site A) to the mouth of the Sidaosha River (site D), reaching a maximum value at site D, and tending to decrease thereafter. The contents of REEs in sediment cores showed enrichment with light rare earth elements (LREEs). The bound to carbonates and to Fe–Mn oxides are the major forms of REE in the secondary phase and the REE exhibited LREE enrichment pattern and moderate Eu depletion in suspended particulates and surface sediments. The contents and species distributions of REEs in the water-suspended particulate-sediment system of the Baotou section suggest that the anthropogenic source of REEs from Baotou city have enhanced REE accumulation to the Baotou section. This information is important for predicting possible pollution resulting from anthropogenic REE input into rivers.     

Determination of polyfluoroalkyl compounds in water and suspended particulate matter in the river Elbe and North Sea, Germany

The distribution of polyfluoroalkyl compounds (PFCs) in the dissolved and particulate phase and their discharge from the river Elbe into the North Sea were studied. The PFCs quantified included C₄-C₈ perfluorinated sulfonates (PFSAs), 6:2 fluorotelomer sulfonate (6:2 FTS), C₆ and C₈ perfluorinated sulfinates (PFSiAs), C₄-C₁₂ perfluorinated carboxylic acids (PFCAs), perfluoro-3,7-dimethyl-octanoic acid (3,7m₂-PFOA), perfluorooctane sulfonamide (FOSA), and n-ethyl perfluroctane sulfonamidoethanol (EtFOSE). PFCs were mostly distributed in the dissolved phase, where perfluorooctanoic acid (PFOA) dominated with 2.9–12.5 ng/L. In the suspended particulate matter FOSA and perfluorooctane sulfonate (PFOS) showed the highest concentrations (4.0 ng/L and 2.3 ng/L, respectively). The total flux of ΣPFCs from the river Elbe was estimated to be 802 kg/year for the dissolved phase and 152 kg/year for the particulate phase. This indicates that the river Elbe acts as a source of PFCs into the North Sea. However, the concentrations of perfluorobutane sulfonate (PFBS) and perfluorobutanoic acid (PFBA) in the North Sea were higher than that in the river Elbe, thus an alternative source must exist for these compounds.     

Chromium geochemistry in coastal environment of the Western Harbour,Egypt: water column,suspended matter and sediments

The distribution of Cr between water, total suspended matter (TSM) and sediments in the maine harbour in Egypt (Western Harbour), has been studied in two surveys. Dissolved Cr displayed a negative association with salinity, indicating land sources outlets as a major source of inputs for it. The Harbour presents higher Cr concentrations in dissolved form above the background (0.17 μg/L) concentration for total dissolved Cr. The most important factors controlling the distribution of particulate Cr in the Western Harbour are the depositional from several activities inside the Harbour, as well as different charges from several landbased sources along its southern edge. Chromium was associated in decreasing amount in the: residual >oxidizable-organic >acid reducible >exchangeable fractions of the analyzed sediments. Therefore, the results indicate that Cr in sediments from W.H is not available for exchange and/or release into the marine environment.     

Modeling the carbon dynamics of the La Grande hydroelectric complex in northern Quebec

A mechanistic semi-empirical carbon cycle model of the La Grande reservoir complex in northern Quebec, Canada was conceived in order to investigate the climate impact of such a large alteration of the continental water cycle. The model includes inputs from the drainage basin, organic matter release from flooded soils, CO₂ emissions across the water-atmosphere interface and sedimentation. Most input data stems from previous research by our group on those ecosystems. The model includes the seven reservoirs of the La Grande complex and was run for periods of 50 and 100 years. Terrigeneous dissolved, particulate and suspended soil carbon fluxes and concentrations were computed. Over 100 years, 31.3 × 10¹² g C are released from flooded soils, equivalent to 28-29% of inputs from the drainage basin. 40-74% of dissolved organic carbon is mineralized. CO₂ fluxes over 100 years are 50.5-79.8 × 10¹² g C, 46.4-67.9 × 10¹² g C more than in the absence of reservoirs. The increase in mineralization of organic matter and in CO₂ emissions is a result of the increase in cumulated water residence time due to the creation of the reservoirs. Changes in other carbon sinks and sources likely offset a part of this additional carbon flux to the atmosphere. In the first years following flooding of the reservoir, organic carbon release from flooded soils exceeds CO₂ emissions, implying the downstream export of large quantities of eroded soil organic carbon. After this initial period, CO₂ emissions are fuelled by organic carbon originating from the drainage basin.     

Origin and Distribution of Suspended Organic Matter As Inferred From Carbon Isotope Composition in A Mediterranean Semi-Enclosed Marine System

The origin and distribution of suspended organic matter, the trophic features and the stable carbon isotopic composition of particulate organic carbon (POC) were studied monthly in a Western Mediterranean semi-enclosed basin. Sampling stations were selected as a function of wind-exposure and the degree of vegetation cover and then compared with an adjacent unvegetated site. the predominant vegetation was seagrass (Posidonia oceanica and Cymodocea nodosa) and Caulerpa prolifera. Water samples were analyzed for total suspended matter (inorganic and organic fractions), photosynthetic pigments (chlorophyll-a and phaeopigments), dissolved organic carbon, particulate organic carbon and their isotopic composition. Temperature and salinity were also measured at the same sampling sites within range of Mediterranean limits. the suspended organic matter concentration was 1.77 ± 1.55 mg l^-1; the chlorophyll-a concentration was low (0.35 ± 0.24 μg l^-1); the disolved organic carbon concentration was 2,140 ± 2,010 μg l^-1; the particulate organic carbon concentration was 212 ± 106 μg l^-1 and the isotopic composition was 18.77 ± 2.51%_°. There were significant temporal differences except for phaeopigments, POC and its POC isotopic composition, and there were no spatial differences other than for δ¹³C. This picture highlighted a general seasonal trend and trophical features similar to adjacent sea.

Spatial differences in δ¹³C showed that the source of suspended organic matter was different between stations as that between sources and wind-hydrodynamic constraints. In     

Mineralization of particulate organic matter derived from coral-reef organisms in reef sediments of the Gulf of Aqaba

In situ and laboratory incubation experiments in a fringing reef in the Gulf of Aqaba were performed to study degradation rates of particulate organic matter in reef sediments. Coral mucus, clam eggs, and zooxanthellae were used as model particulate organic compounds for these experiments. Aerobic and anaerobic mineralization rates were calculated by dissolved inorganic carbon (DIC) and O₂ fluxes from the sediments under different particulate organic matter additions. Fast enhancement (approximately twofold) of O₂ and DIC fluxes were found with the addition of coral mucus and clam eggs compared with control incubations without addition. Most of the degradation is believed to have occurred anaerobically rather than aerobically (DIC:O₂ ratios were 4.3–28.1). Higher degradation rates of coral mucus and clam eggs were estimated in carbonate sediment than in silicate sediment (1.2–1.6-fold), which was attributed to the different physical and chemical properties of both sediments. Our study shows the significance of the reef sediment as a suitable site for microbial degradation of particulate organic material excreted from different reef community organisms. This may increase the regeneration of nutrients in the reef environment necessary to sustain high biological productivity.     

天然湖水表面微层砷,磷酸盐,悬浮颗粒物及藻类富集现象的研究

本文利用自制的玻璃板表面微层水采样器采集并分析了天津水上公园湖水表面微层中砷的四种不同形态：亚砷酸盐、砷酸盐、一甲基刖酸盐、二甲基刖酸盐，以及溶解态总磷、总磷、县浮颗粒物和藻类的富集情况，初步探讨了它们在湖水表面微层富集的原因，结果表明，它们在湖水表面微层中均有不同程度的富集现象，其中以总磷、悬浮颗粒物和藻类尤为明显，它们在湖水表面微层的富集除了也大气物理运动过程的生物活动有关外，还与采样站位有关     

Biomass of suspended bacteria over coral reefs

The biomass of bacteria suspended in water flowing over coral reefs at Lizard Island and Yonge Reef (Northern Great Barrier Reef) was estimated by measurement of muramic acid. Values ranged from 20 mg C m^-3 in the open water up to about 60 mg C m^-3 over the reef flat. Direct counts of total numbers of free bacteria were made for comparison. Values of around 2.0x10⁹ cells g^-1 muramic acid showed that there was a good agreement between direct counts and muramic acid content of free bacteria in the open water. In samples containing suspended particulate matter, ratios of direct counts to muramic acid concentration were lower, because bacteria on particles could not be counted. Thus, these ratios were used to indicate the proportions of bacteria attached to particles. Changes in the biomass and numbers of bacteria were determined in water masses identified either by a drogue or fluorescein, as they moved across the reefs. In the zone on the outside of the reef, the number of free bacteria decreased compared to open sea water, but total biomass increased, showing that particulate matter containing bacteria was thrown up into suspension. About 50% of bacteria were attached to particles. Water flowing over the reef flats contained much particulate material with bacteria attached. Bacteria constituted between about 5 and 20% of particulate organic carbon.     

Origin and Distribution of Suspended Organic Matter As Inferred From Carbon Isotope Composition in A Mediterranean Semi-Enclosed Marine System

Abstract

The origin and distribution of suspended organic matter, the trophic features and the stable carbon isotopic composition of particulate organic carbon (POC) were studied monthly in a Western Mediterranean semi-enclosed basin. Sampling stations were selected as a function of wind-exposure and the degree of vegetation cover and then compared with an adjacent unvegetated site. the predominant vegetation was seagrass (Posidonia oceanica and Cymodocea nodosa) and Caulerpa prolifera. Water samples were analyzed for total suspended matter (inorganic and organic fractions), photosynthetic pigments (chlorophyll-a and phaeopigments), dissolved organic carbon, particulate organic carbon and their isotopic composition. Temperature and salinity were also measured at the same sampling sites within range of Mediterranean limits. the suspended organic matter concentration was 1.77 ± 1.55 mg l^?1; the chlorophyll-a concentration was low (0.35 ± 0.24 μg l^?1); the disolved organic carbon concentration was 2,140 ± 2,010 μg l^?1; the particulate organic carbon concentration was 212 ± 106 μg l^?1 and the isotopic composition was 18.77 ± 2.51%_°. There were significant temporal differences except for phaeopigments, POC and its POC isotopic composition, and there were no spatial differences other than for δ¹³C. This picture highlighted a general seasonal trend and trophical features similar to adjacent sea.

Spatial differences in δ¹³C showed that the source of suspended organic matter was different between stations as that between sources and wind-hydrodynamic constraints. In     

Metals in Zooplankton from the Baltic Sea, 1980-84

Between 1980 and 1984, plankton was collected for metal analysis during four expeditions in the Baltic Sea. for comparison, samples from adjacent areas of the northeastern Atlantic Ocean were also taken. the mixed net-plankton samples were analyzed by AAS for metals (Al, Cd, Co, Cr, Cu. Fe, Mn, Ni, Pb, and Zn). the results are discussed with regard to spatial and temporal trends and for comparison with data from other authors. Correlations among the contents of the different metals and between the metal contents and 'external factors' including salinity, season, percentage of co-collected phytoplankton, and concentration of dissolved and particulate metals in the water are considered.

There is a tendency for higher metal contents in plankton from the brackish Baltic Sea (Al, Mn and Hg), while other metals (e.g. Cd) show higher levels in samples taken from the marine environment. Except for mercury, no clear correlations could be found between the metal content in plankton and the dissolved concentration of the same metal in the ambient water. Otherwise, the contents of aluminium, iron, manganese and zinc in the suspended particulate matter and in the plankton seem to be partly related to each other.     

Relationship between the zooplankton,phytoplankton, particulate matter and dissolved free amino acids in the Celtic Sea

Estimates of the biomass of zooplankton, phytoplankton and particulate matter collected in the Celtic Sea during mixed-water conditions (on 8 and 9 April 1983) were compared to the concentration and diversity of sixteen dissolved free amino acids (DFAA) measured in seawater and in particles. During a day profile, variations of dissolved amino acids with depth reflected the feeding activity of copepods. The relationship was not apparent in a night profile and other processes, such as heterotrophic utilization of dissolved nitrogen by microorganisms, were thought to be involved. The ratios of total DFAA concentration (nM litre^-1) in the particulate phase over the concentration in seawater ranged from 1 to 200 within the water column. Of the sixteen amino acids measured, ornithine, a decomposition product of arginine, was responsible for more than 70% of the total concentration of DFAA in seawater. In the particles, phenylalanine ranged from 30 to 88% of total DFAA. In seawater this amino acid occurred in the 20 to 40 m depths (1.3 to 9.9% of total DFAA) in the day profile and at 5 m (12.4%) and 80 m (6.4%) in the night profile. Previously it has only been found in very low concentrations (<5%) in seawater, and its presence is considered to be the result of zooplankton feeding.     

Influence of some abiotic environmental factors on acute toxicity of inorganic lead to Cyprinus carpio var communis (Linn.) and Catla catla (Ham.) in simulated toxic aquatic environment

With the increase of water hardness from 60 to 720?mg/L CaCO₃, total alkalinity from 32 to 376?mg/L CaCO_3, pH from 7.6 to 7.9 and chloride from 28 to 350?mg/L, 96?h LC₅₀ on the basis of total lead increased from 8.2 to 1291?mg/L for Cyprinus carpio and 5.3 to 865?mg/L for Catla catla, when soil sediments were included these values were further raised to 1356 and 874?mg/L, respectively. The dissolved lead LC₅₀ values in all the treatments of soil and water was consistent with fixed amount of dissolved lead (1.04–1.78?mg/L) being needed for median lethal toxicity. Total lead toxicity also decreased with increase in pH from 6.3 to 11.3. 96?h LC₅₀ values increased for common carp 15 to 631?mg/L and for catla, 8 to 355?mg/L. But dissolved lead toxicity was found to increase with the increase of pH from 6.3 to 11.3 for both common carp (LC₅₀, 3.53 to 0.24?mg/L) and catla (LC₅₀, 2.21 to 0.09?mg/L). Removal of dissolved Pb with increasing carbonate content, particulate matter and pH due to adsorption, precipitation or coprecipitation reaction, reduced the dissolved lead concentration and thus the total lead toxicity. Increase in toxicity of lead with increase of exposure time was the biological response of longer contact time and decrease in dissolved lead toxicity with decrease in pH was due to increase H⁺ ion competition.     

Sources and biochemical composition of suspended particulate material in a submarine cave with sulphur water springs

Sources, biochemical composition and nutritional value of suspended particulate material were investigated from February 1994 to February 1995 in a submarine cave (Grotta Azzurra, Capo Palinuro, southwestern Italy) with hot sulphur springs and associated mats of chemolithoautotrophic bacteria in its innermost dark part (Snow Hall). Concentrations of total suspended material (TSM), particulate inorganic material (PIM), organic carbon (POC), organic nitrogen (PON), chlorophyll a (Chl a), phaeopigments (Phaeo), carbohydrates (TCH), proteins (TPR) and lipids (TLI) were measured at four stations along an outside–inside transect, in order to address whether the quantity and quality of suspended particles varied over time with increasing distance from the entrance of the cave and estimate the relative contribution of chemosynthesis versus photosynthesis in supplying POC to cave heterotrophs. The abundance and biochemical composition of suspended material available to filter-feeders varied over time, but no significant quantitative or qualitative differences were detected along the outside–inside transect. Concentrations of TSM and of its different compounds (PIM, POC, PON, Phaeo, TCH, TPR, TLI) were homogeneous among the four stations or fluctuated without any consistent trend, with no apparent ageing and degradation of organic material in the innermost dark station. Conversely, concentrations of Chl a significantly decreased from outside to inside the cave at all sampling periods. It is suggested that suspended POC in Grotta Azzurra consists of mixed assemblages of particles coming from advection of photosynthetic material from the open sea and local inputs of carbon by sulphur-oxidizing bacteria. Based on POC/Chl a ratios, the relative contributions of chemosynthesis versus photosynthesis in supplying POC to benthic heterotrophs was estimated to be 31 and 69%, respectively. Received: 9 December 1996 / Accepted: 14 January 1997     

The flux of particulate carbon in an estuary

The major sources and sinks of suspended particulate carbon are identified for northern Chesapeake Bay, Maryland, USA. The area of the bay under consideration was divided into two sections. The northernmost section (upper bay), from the head of the bay to the vicinity of Baltimore, was characterized by a high input of particulate carbon from upland drainage. The section from Baltimore to the mouth of the Potomac River (middle bay) was dominated by an internal supply of particulate carbon from primary production. The northernmost section was characterized by major particulate carbon losses to the bottom and to benthic respiration, with slightly less than half (43%) of the particulate carbon respired in the water column or converted to dissolved organic matter. In contrast, respiration in the water column or conversion to dissolved organic matter was responsible for the loss of about 65% of the particulate carbon in the middle section of the bay, while losses to the bottom and to benthic respiration totaled only 12%. Even though the supply of particulate carbon to the upper bay was about 1.5 times the supply to the middle bay, the loss of carbon due to biological activity (biological efficiency) in each area was similar, and amounted to about 70% of the supply of particulate carbon.The research reported here was partially supported by the University of Maryland and by the U. S. Bureau of Sport Fisheries and Wildlife under Contract No. 14-16-0005-2096. Contribution No. 471 of the Natural Resources Institute, University of Maryland, USA.     

Elemental composition of surface waters in the Antarctic Peninsula and interactions with the environment

The fast changes in chemical and biological properties of many coastal and inland waters in the last decades reflect the pressure of man on the environment. The surface waters of the Antarctic Peninsula, located far from industrial or populated areas, could eventually be used as background lines. Surface water samples were taken from five lagoons of King George Island, Antarctic Peninsula, and from the Kitiesh Lake. Sample pH and electrical conductivity were analysed in situ and in the laboratory, respectively. The dissolved fractions were analysed in 1997 and 1998. Total concentrations only for 1998 were determined in another fraction adjusted to pH 2. Aluminium, Ca, Cr, Mn, Co, Ni, Cu, Zn, As, Se, Sr, Cd, Sn, Sb, Ba, Bi, and Pb were quantified in all samples by means of inductively coupled plasma-mass spectrometry (ICP-MS). Total and dissolved elemental concentrations were discussed considering the composition of particulate material suspended in the waters removed by streams or by water runoff, or from atmospheric aerosols. Concentrations of dissolved elements change from one lagoon to another. Total and dissolved elemental concentrations could be related to water movement by windstorms, to chemical mechanisms in water and/or to natural and anthropogenic atmospheric factors.     

Influences of Suspended Particles on the Runoff of Pesticides from an Agricultural Field at Askim, SE-Norway

Field and laboratory experiments were conducted to study the loss of particles from agricultural fields, and the role of suspended particles in carrying pesticides in surface runoff and drainage water. Propiconazole, a widely used fungicide was applied to experimental fields located at Askim, SE-Norway. Samples from surface runoff and drainage water were collected and analyzed for sediment mass, pesticides, particulate and dissolved organic carbon through a whole year. The surface soil and the runoff material were characterized by its particle size distribution, organic carbon content in size fractions and its ability to bind propiconazole. The results show that (1) particle runoff mostly occurred during the rainfall event shortly after harrowing in autumn. The highest particle concentration observed in the surface runoff water was 4600 mg l^–1, and in the drainage water 1130 mg l^–1; (2) the erosion of surface soil is size selective. The runoff sediment contained finer particle/aggregates rich in organic matter compared to its original surface soil; (3) the distribution coefficient (K _d) of propiconazole was significantly higher in the runoff sediment than in the parent soil. According to our calculation, particle-bound propiconazole can represent up to 23% of the total amount of propiconazole in a water sample with a sediment concentration of 7600 mg l^–1, which will significantly influence the transport behavior of the pesticide.     

WATER QUALITY IN THE RED SEA COASTAL WATERS (EGYPT): ANALYSIS OF SPATIAL AND TEMPORAL VARIABILITY

In order to provide a background picture of the water quality of the Egyptian Red Sea a number of hydrological and chemical parameters have been measured bimonthly in 2000. Few data are available on this area, which is apparently subjected to an increasing human impact due to recreational (swimming and diving), industrial (mainly phosphate shipping and industry) and fishing/harbor activities. The results of the present study indicate that changes in the salinity and pH were not significant with highly oxygenated seawaters. The levels of suspended solids (as total suspended matter, TSM) and chlorophyll-a (Chl-a) were generally low and showed an homogeneous distribution in the study region. The ratio of chlorophyll-a to total suspended matter concentrations increased between November and March and decreased from May to September. Chlorophyll-a was significantly correlated with transparency and total suspended matter concentrations in July, September and November. Nitrogen, phosphorus and reactive silicate concentrations were generally low, and allowed classifying the Egyptian Red Sea coastal water as oligotrophic to mesotrophic. The middle region of the study area, which was located between Safaga and Qusair displayed relatively high phosphate contents when compared with other coastal areas. The high values of N:P ratios indicate that PO 4 -P is the limiting factor for phytoplankton growth in the Red Sea coastal waters, with the possible exception of the middle region. Significant relationships were found between chlorophyll-a concentrations and nutrient levels in different sampling periods. Spatial distribution patterns of the studied variables revealed that productivity of the Red Sea coastal waters is mostly controlled by phosphate concentrations, salinity, temperature and dissolved oxygen.     

Water quality in the Red Sea coastal waters (Egypt): Analysis of spatial and temporal variability

In order to provide a background picture of the water quality of the Egyptian Red Sea a number of hydrological and chemical parameters have been measured bimonthly in 2000. Few data are available on this area, which is apparently subjected to an increasing human impact due to recreational (swimming and diving), industrial (mainly phosphate shipping and industry) and fishing/harbor activities. The results of the present study indicate that changes in the salinity and pH were not significant with highly oxygenated seawaters. The levels of suspended solids (as total suspended matter, TSM) and chlorophyll-a (Chl-a) were generally low and showed an homogeneous distribution in the study region. The ratio of chlorophyll-a to total suspended matter concentrations increased between November and March and decreased from May to September. Chlorophyll-a was significantly correlated with transparency and total suspended matter concentrations in July, September and November. Nitrogen, phosphorus and reactive silicate concentrations were generally low, and allowed classifying the Egyptian Red Sea coastal water as oligotrophic to mesotrophic. The middle region of the study area, which was located between Safaga and Qusair displayed relatively high phosphate contents when compared with other coastal areas. The high values of N:P ratios indicate that PO 4 -P is the limiting factor for phytoplankton growth in the Red Sea coastal waters, with the possible exception of the middle region. Significant relationships were found between chlorophyll-a concentrations and nutrient levels in different sampling periods. Spatial distribution patterns of the studied variables revealed that productivity of the Red Sea coastal waters is mostly controlled by phosphate concentrations, salinity, temperature and dissolved oxygen.