Bioremediation of Phenanthrene by Mycoplana sp. MVMB2 Isolated from Contaminated Soil

The effect of nutrient and surfactant addition on the biodegradation of phenanthrene was studied in a batch scale soil–slurry system using isolated Mycoplana sp. MVMB2strain. The study was conducted using an artificially phenanthrene spiked and as well as contaminated soil from petrochemical industrial site. Maximum phenanthrene degradation and subsequent high microbial growth were observed at optimum pH (pH 6) and C/N/P ratio (100:20:3). To investigate maximum substrate degradation potential of Mycoplana sp. MVMB2, very high concentrations of phenanthrene (50–200 mg/kg soil) were used. The organism was capable of degrading >60% for a concentration below 20 mg/kg soil and >40% for concentrations up to 200 mg/kg within 8 days. Further the influence of five different surfactants namely Span 80, Tween 20, Triton X‐100, cetyl trimethyl ammonium bromide, and sodium dodecyl sulfate were tested at their critical micelle concentration (CMC) levels for phenanthrene degradation in the soil. The addition of surfactant enhanced the biodegradation and a maximum of 84.49% was obtained for Triton X‐100. Complete phenanthrene degradation by Mycoplana sp. MVMB2 was observed at 3 CMC concentration of Triton X‐100. The optimized parameters obtained were used for the degradation of phenanthrene present in the contaminated soil and 98.6% biodegradation was obtained. Thus, the results obtained in the study suggested that biodegradation of phenanthrene by Mycoplana sp. MVMB2 appeared to be feasible to remediate phenanthrene rich contaminated sites.     

Use of Chrysotile Fibres in the Degradation of Cationic and Nonionic Surfactants in Aqueous Solutions

It was previously observed that sodium dodecylbenzenesulfonate (SDBS) is degraded in the presence of chrysotile fibres. A higher catalytic efficiency was obtained than the reported values for TiO₂ under the same conditions. Chrysotile, a clay mineral fibre of low cost and relatively abundant, probably acts as a catalyst through an Advanced Oxidative Process (AOP) involving free radical formation. In this work, experiments with non‐ionic – Triton X‐45 (octil‐phenoxy polyethoxy ethanol) – and cationic – Herquat 3500 (alkyl dimethyl benzyl ammonium chloride) – surfactants were carried out. Diluted aqueous solutions (50 ppm) of these surfactants were kept in contact with chrysotile (4.0 g) in the dark at room temperature. The aromatic ring disappearance was followed through the absorbance peaks at 224 nm (Triton X‐45) and 208 nm (Herquat 3500) in the UV spectra. After 4 h, reductions in the surfactant solution concentration of 65.0% and 35.0% were observed for the Triton X‐45 and the Herquat 3500 surfactants, respectively. In both cases, reactions carried out without aeration showed a lower reduction of the aromatic ring concentration (30.0% less) when compared to the values obtained for the systems with airflow. The system containing the non‐ionic surfactant seems to achieve equilibrium after 2 h, what is not observed for the cationic surfactant system.     

Influence of Surfactants on Degradation of 1‐(2‐Chlorobenzoyl)‐3‐(4‐chlorophenyl) Urea by Nanoscale Zerovalent Iron

Nanoscale zerovalent iron (NZVI) has been proved to be effective in the degradation of environmental pollutants and exhibits advantages in the removal of 1‐(2‐chlorobenzoyl)‐3‐(4‐chlorophenyl) urea (CCU), an analog of diflubenzuron. This present study focused on the influence of surfactants in the degradation procedure with NZVI in order to provide a simple and rapid removal method for CCU. Triton X‐100, Tween 20, Tween 80, sodium dodecyl sulfonate (SDS), and cetyltrimethylammonium bromide (CTAB) were investigated under anaerobic conditions. The experimental results demonstrated that the degradation rate increased sharply with the presence of SD during the first 15 min, up to 99.97% with addition of 0.01 g L^?1 SDS, whereas the presence of Triton X‐100, Tween 80, and Tween 20 resulted in a slight enhancement of the degradation of CCU. The enhancement strength of them was in the order Tween 20, Triton X‐100, and Tween 80. However, addition of the cationic surfactant CTAB resulted in a significant inhibitive effect. In contrast, the mixed surfactants did not result in the expected performance, and the performance was lower than that using some certain single surfactant among the mixed surfactants.     

Scum in Nutrient Removal Plants: The Role of Carbon Sources in “Microthrix parvicella” Growth

Scum formation is a widespread problem in activated sludge nutrient removal plants. It often comes along with an excessive development of the filamentous bacterium “Microthrix parvicella” stabilizing the flotation process. As “M. parvicella” was found to depend on long‐chain fatty acids (LCFA) as sole carbon source not only in vitro but also in situ, some options of in‐situ substrate supply are discussed. Wastewater concentrations of fatty acids in the range of 2 to 15 mg L^‐1 and homologue concentrations from synthetic surfactant degradation below 10 mg L^‐1 rule out these substrates as source for excessive biomass production. They might, however, well be suitable for start‐up of a “M. parvicella” population. Build‐up of excessive biomass might rely on fatty acid supply originating in cell walls of lysed stationary phase bacteria of long residence time sludge fractions such as scum layers. Moreover, biogenic surfactants such as rhamnolipids have been proved to be an excellent carbon source for excessive biomass production in vitro.     

Naphthalene Degradation Kinetics of Micrococcus sp., Isolated from Activated Sludge

Biodegradation of naphthalene by Micrococcus sp., isolated from the effluent of an activated sludge plant, was studied. The effects of pH (5–8), glucose concentration (100–1000 mg/L) and inoculum concentrations (1–5%) on the growth and naphthalene degradation potential of Micrococcus sp. were investigated. Maximum naphthalene degradation and subsequent high microbial growth were observed at optimum pH (pH 7), glucose concentration (500 mg/L) and inoculum concentration (3%). To investigate the maximum naphthalene tolerance potential of Micrococcus sp., very high concentrations of naphthalene (500–5000 mg/L) were used in the presence of non‐ionic surfactants. The examined surfactants (Triton X‐100 and Tween‐80) increased the bioavailability of naphthalene to the microbes and Complete naphthalene degradation by Micrococcus sp. was observed at an initial naphthalene concentration of 500 mg/L. However, the degradation potential decreases as the naphthalene concentration increases. Very high naphthalene concentrations also affected the growth of microbes and the corresponding substrate inhibition kinetics was described using four models (Haldane, Webb, Edward and Aiba). Based on correlation coefficient and percentage error values, all four substrate kinetic models were able to describe the dynamic behavior of naphthalene biodegradation by Micrococcus sp.     

Screening of surfactants for harmful algal blooms mitigation

Screening experiments were conducted in order to find promising synthetic surfactants for harmful algal blooms (HABs) mitigation. The chemically synthesized surfactant cocamidopropyl betaine (CAPB) showed characteristics of relatively high inhibition efficiency, high biodegradability and low cost. The motility inhibition ratios of 10 mg/L CAPB on Cochlodinium polykrikoides and Alexandrium tamarense were about 60% after 5 min. The biodegradation test indicated that the half-life of CAPB in seawater was shorter than one day and 90% was biodegraded after five days under the initial concentration of 100 mg/L at 25 degrees C. Further cell lysis experiments revealed the selective lysis effect of CAPB on different HAB organisms. More than 90% of C. polykrikoides lysed at the concentration of 10 mg/L CAPB after 24 h and at 15 mg/L CAPB after 4 h, whereas the lysis effect of CAPB on A. tamarense was slight, no more than 10% after 2 h interaction with 50 mg/L CAPB. This research provided preliminary data for CAPB as a candidate in harmful algal blooms mitigation and pointed out unresolved problems for its practical application in the meantime.     

Activation of Persulfate by Surfactants under Acidic and Basic Conditions

Activated persulfate is a commonly used oxidant source used for in situ chemical oxidation (ISCO) for remediation of subsurface contamination. Surfactants are sometimes used in ISCO to desorb contaminants and dissolve nonaqueous phase liquids (NAPLs). The potential activation of persulfate by such surfactants was investigated, and the reactive oxygen species generated by persulfate in the presence of anionic, nonionic, and cationic surfactants were determined. Twenty surfactants were screened; most activated persulfate to generate reductants + nucleophiles at acidic and basic pH. The most reactive anionic, nonionic, and cationic surfactants (Lankropol 4500, polyethylene glycol 400, and Ethoduomeen T/25) were investigated in more detail. All three surfactants activated persulfate; however, the cationic surfactant showed the most potential for persulfate activation with high fluxes of hydroxyl radical and reductants + nucleophiles. The results of this research demonstrate that surfactants added to ISCO systems often activate persulfate to generate reductants at both acidic and basic pH, and hydroxyl radical at basic pH. These findings provide a new paradigm for persulfate activation in surfactant in situ chemical oxidation (SISCO) systems; pH regimes >11 may not be necessary for persulfate activation resulting in cost savings and potentially more effective activation of persulfate.     

Copper speciation survey from UK marinas, harbours and estuaries

The use of copper in antifouling paints has increased in the UK in the last 20 years as TBT and several other organic biocides have been phased out. To assess the probable impact of copper on estuarine systems a survey was undertaken to measure the different fractions of copper present in the water column at current usage. The different fractions measured were; labile copper, (LCu) considered as both the free copper ions and inorganically bound copper, the total dissolved copper (TDCu) present, and the difference between them taken as the organically bound likely non-toxic copper fraction. The survey considered sites with different levels of boat use, namely marinas, harbours and estuaries, differing physical parameters of suspended and dissolved organic matter, different seasons of the year and different depths in the water column all of which control speciation behaviour. Suspended particulate matter (SPM) values were measured at all sites and increased from West to East coast locations (5.7-34.4 mg/l). Dissolved organic matter (DOM) values ranged from 0.58 to 2.2mg/l C. The total dissolved copper concentrations ranged from 0.30 to 6.68 microg/l, with labile fraction ranging from 0.02 to 2.69 microg/l, and most labile copper concentrations below 1 microg/l. None of the yearly mean copper measurements exceeded the 76/464/EEC EQS of 5 microg/l. Of the 306 measurements, only one dissolved copper value in one season was above 5 microg/l. This ratio of labile to total copper was between 10 and 30%. The results from this survey suggest that if toxicity of copper is due to the labile fraction then using the total dissolved copper concentrations as an indicator of impact overestimate the risk by a factor of four times.     

Surfactant‐Enhanced Electroosmotic Flushing in a Trichlorobenzene Contaminated Clayey Soil

Remediation of the sites contaminated with organic contaminants, such as chlorobenzenes, remains a challenging issue. Electroosmotic flushing can be a promising approach which is based on mechanism of electrokinetic remediation for removal of organic contaminants from fluids in low‐permeability soil. To select an optimum surfactant that can effectively enhance electroosmotic flushing, three common surfactants, Triton X‐100 (EK2), Tween 80 (EK3), and a mixture of sodium dodecyl sulfate and Triton X‐100 (EK4) buffered with Na₂HPO₄/NaH₂PO₄ solution, were tested. The efficiency of each kind of surfactant was evaluated using a three‐dimensional box filled with a clayey soil spiked with 1,2,4‐trichlorobenzene, and compared with a test (EK1) without surfactant. The results demonstrated that the buffer solutions efficiently neutralized H⁺ and OH^? produced by electrolysis. EK3 with Tween 80 added in the flushing solution reached the highest electroosmotic permeability of 10^?4 cm²/v/s and achieved a notably high cumulative electroosmotic flow (EOF) of 5067 mL within 6 d, which was 6.3, 3.4, and 4.2 times higher than that in EK1, EK2, and EK4, respectively. There were 420 mL more cumulative EOF obtained after 50 h of electrical application in EK4 than in EK2. The introduction of nonreactive ions can increase the current, thereby benefiting the EOF. Both the higher pH caused by the buffer and the application of nonionic surfactants can make the zeta potential more negative, thereby increasing the EOF. Tween 80 can be recommended as the best flushing solution for removing organic contaminants from sites when electrokinetic remediation is applied.     

On the ecology of Azolla filiculoides Lam. in Damietta district, Egypt

Azolla filiculoides Lam. is a tiny aquatic fern growing as free floating mats covering the stagnant water of the irrigation and drainage canals of Damietta district, Egypt. Ecological characteristics and distribution of the fern were investigated and results were discussed.Vegetation analysis of Azolla indicate that the most common associated species with Azolla are: Phragmites australis [presence (P) = 93.3%], Echinochloa stagnina (P = 70%), Eichhornia crassipes (P = 57%), Pluchea dioscoridis (P = 56.7%), Persicaria salicifolia (P = 26.7%), Phylla nodiflora (P = 13.3%) and Ludwigia stolonifera (P = 10%). Submerged species, e.g. Ceratophyllum spp. and Potamogeton spp. are completely absent in the stands dominated with solid mats of Azolla. This could be explained by that these mats prevent light penetration and oxygen which are required to submerged plants which in turn are decayed.The pH of the water where Azolla was recorded ranged from 7.1 to 9.0 (mean = 7.8), total dissolved salts ranged from 280 to 2600 mg/l (mean = 880 mg/l). The total phosphorus showed the range from 0.01 to 0.82 mg/l (mean = 0.22 mg/l). The ammonia-N is relatively high, varying from 2 to 18 mg/l (mean = 7.0 mg/l), however, the nitrate-N varied from 2.1 to 54.1 mg/l with a mean value of 20.5 mg/l.The fresh biomass of Azolla ranged from 114 to 4280 g/m² in irrigation canals and from 506 to 2760 g/m² in drainage canals. The dry biomass varied from 16 to 23 g/m² in irrigation canals. The range from 26 to 320 g/m² was obtained for drainage canals.     

Mercury in wahoo, Acanthocybium solandri, from offshore waters of the southeastern United States and the Bahamas

Wahoo, Acanthocybium solandri, are predatory oceanic fish that occur and are harvested in all tropical and subtropical oceans. Total mercury concentrations analyzed in dorsal muscle tissue of 208 wahoo from offshore waters of the southeastern United States and the Bahamas ranged from 0.021 to 3.4 mg/kg (wet weight), with a mean of 0.50 mg/kg (± 0.595 SD). Analyses indicated significant positive linear relationships between mercury and length, as well as, age of wahoo. The piscivorous nature, generally high trophic position, fast growth rate, and associated high metabolism of wahoo within tropical offshore pelagic environments may lead to comparatively higher concentrations of mercury over relatively short time periods. Mercury in wahoo, a highly mobile species consisting of one world-wide population, is regionally influenced by large-scale spatial differences in available mercury in selected prey fish species - many of which have been found to contain relatively high concentrations of mercury.     

Sorption-desorption kinetics and toxic cell concentration in marine phytoplankton microalgae exposed to Linear Alkylbenzene Sulfonate

Linear Alkylbenzene Sulfonates (LAS) are ubiquitous surfactants. Traces can be found in coastal environments. Sorption and toxicity of C₁₂-LAS congeners were studied in controlled conditions (2-3500 μg C₁₂LAS/L) in five marine phytoplanktonic species, using standardized methods. IC₅₀ values ranged from 0.5 to 2 mg LAS/L. Sorption of ¹⁴C₁₂-6 LAS isomer was measured at environmentally relevant trace levels (4 μg/L) using liquid scintillation counting. Steady-state sorption on algae was reached within 5 h in the order dinoflagellate > diatoms > green algae. The sorption data, fitted a L-type Freundlich isotherm, indicating saturation. Desorption was rapid but a low LAS fraction was still sorbed after 24 h. Toxic cell concentration was 0.38 ± 0.09 mg/g for the studied species. LAS toxicity results from sorption on biological membranes leading to non-specific disturbance of algal growth. Results indicate that LAS concentrations in coastal environments do not represent a risk for these organisms.     

A Cloud Point Extraction Approach Developed for Analyzing Pesticides Prometryne and Isoproturon from Multi‐media

A new analytic methodology based on the cloud point extraction coupled with HPLC (CPE‐HPLC) was developed and successfully applied to determination of the pesticides isoproturon (IPU) and prometryne (PRO) from multi‐media (contaminated water, soil, and food vegetable). Several non‐ionic surfactants including poly ethylene glycol 6000 (PEG‐6000), TritonX‐114, and Triton X‐100 were comparatively analyzed as extraction solvents. Other parameters such as surfactant concentration, ionic strength, and equilibration temperature, and duration were also investigated. The optimal conditions for CPE were presented with 2.4% w/v PEG‐6000, 11% w/v Na₂SO₄ and heating assistance at 50°C for 25 min. The calibration curves for the two analytes were linear ranging from 0.001 to 10.0 mg L^?1, with correlation coefficients being 0.99 determined by a HPLC–UV detector. Under the condition, the average recoveries were 85.4–90.6% for water, 84.4–92.7% for soil, and 84.4–92.1% for vegetable. Thus, the method presented here was proved to be rapid, efficient, and green for extraction and determination of isoproturon and prometryne residues from food and multi‐environmental media.     

Hydrogeochemistry of seepage water collected within the Youngcheon diversion tunnel,Korea: source and evolution of SO4‐rich groundwater in sedimentary terrain

In the Youngcheon Diversion Tunnel area, South Korea, 46 samples of tunnel seepage water (TSW) and borehole groundwater were collected from areas with sedimentary rocks (mainly sandstone and shale) and were examined for hydrogeochemical characteristics. The measured SO₄ concentrations range widely from 7·7 to 942·0 mg/l, and exceed the Korean Drinking Water Standard (200 mg/l) in about half the samples. The TDS (total dissolved solid) content generally is high (171–1461 mg/l) from more shale‐rich formations and also reflects varying degrees of water–rock interaction. The water is classified into three groups: Ca? SO₄ type (61% of the samples collected), Ca? SO₄? HCO₃ type (15%) and Ca? HCO₃ type (24%). The Ca? HCO₃ type water (mean concentrations=369 mg/l Ca, 148 mg/l HCO₃ and 23 mg/l SO₄) reflected the simple reaction between CO₂‐recharged water and calcite, whereas the more SO₄‐rich nature of Ca? SO₄ type water (mean concentrations=153 mg/l Ca, 66 mg/l HCO₃ and 416 mg/l SO₄) reflected the oxidation of pyrite in sedimentary rocks and fracture zones. Pyrite oxidation resulted in precipitation of amorphous iron hydroxide locally within the tunnel as well as in high concentrations of Ca (mean 153 mg/l) and Na (mean 49 mg/l) for TSW, and is associated with calcite dissolution resulting in pH buffering. The pyrite oxidation required for the formation of Ca? SO₄ type water was enhanced by the diffusion of oxygenated air through the fractures related to the tunnel's construction. The subsequent outgassing of CO₂ into the tunnel resulted in precipitation of iron‐bearing carbonate. Copyright © 2001 John Wiley & Sons, Ltd.     

Biological effects of anthropogenic salt-load on the aquatic Fauna: A synthesis of 17 years of biological survey on the rivers Werra and Weser

The reduction and the smoothened amplitudes of the chloride concentrations since 2000 have resulted in a gradual positive development of the aquatic fauna in the River Werra. In the salinized section of the river increasing species numbers have been determined along the salinity gradient, which shows maximum chloride concentrations of about 2500 mg/l, maximum potash concentrations at approximately 200 mg/l, and magnesia concentrations peaked at 320 mg/l. As an immediate consequence of the reduction in salt concentration the immigration of various caddis fly species into the lower River Werra was observed. The Number of taxa per sample rose from 5 to more than 30 in the lower Werra region. Changes in species-richness could be seen more frequently in river sections where chloride concentrations fluctuated around 1500 mg/l.     

Surfactant-Induced Reductions in Soil Hydraulic Conductivity

Surfactant solutions are being proposed for in situ flushing of organic contaminants from soils and aquifers. The feasibility of surfactant additives in remediation may depend in large part on how these chemicals affect the hydraulic conductivity of the porous media. While there is evidence in the literature of conductivity loss during surfactant flushing (Miller et al. 1975; Nash et al. 1987), there has been little research on quantifying the process for unconsolidated sediments. Surfactant-affected hydraulic conductivity reductions were measured in two soils (Teller loam and Daugherty sand). Testing was done with eight surfactants at a variety of concentrations (10^-5 to 10^-l mole/kg), surfactant mixtures, and added solution electrolytes. The Teller was also tested with its organic matter removed. Maximum hydraulic conductivity decreases were 47 percent for the sand and more than two orders of magnitude for the loam. Surfactant concentrations, surfactant mixtures, soil organic content, and added solution electrolytes all affected the degree of conductivity reduction. Results indicate that surfactant-affected hydraulic conductivity losses should be considered prior to in situ remediation and may preclude surfactant use in some fine grain soils.     

On the Toxicity and Biodegradation of Cationic Surfactants Über die Toxizität und den biologischen Abbau kationischer Tenside

Three ammonium halide type surfactants were tested under standard laboratory condition for biodegradability and acute toxicity to Daphnia magna and in the Microtox test with the luminescent bacterium Photobacterium phosphoreum. The tested compounds are dimethyldistearylammonium chloride (DSDMAC), cetyltrimethylammonium bromide (HTMAB) and cetylbenzyldimethylammonium chloride (HBDMAC). The results indicate DSDMAC is less toxic than the other two surfactants and that it biodegrades rapidly at both lower (2.5 mg/L) and higher (10 mg/L) concentrations.     

Nitrate and herbicide loading in two groundwater basins of Illinois'' sinkhole plain

This investigation was designed to estimate the mass loading of nitrate (NO₃⁻) and herbicides in spring water discharging from groundwater basins in an agriculturally dominated, mantled karst terrain. The loading was normalized to land use and NO₃⁻ and herbicide losses were compared to estimated losses in other agricultural areas of the Midwestern USA. Our study area consisted of two large karst springs that drain two adjoining groundwater basins (total area of 37.7 km²) in southwestern Illinois' sinkhole plain, USA. The springs and stream that they form were monitored for almost 2 years. Nitrate–nitrogen (NO₃–N) concentrations at three monitoring sites were almost always above the background concentration (1.9 mg/l). NO₃–N concentrations at the two springs ranged from 1.08 to 6.08 with a median concentration of 3.61 mg/l. Atrazine and alachlor concentrations ranged from <0.01 to 34 μg/l and <0.01 to 0.98 μg/l, respectively, with median concentrations of 0.48 and 0.12 μg/l, respectively. Approximately 100,000 kg/yr of NO₃–N, 39 kg/yr of atrazine, and 2.8 kg/yr of alachlor were discharged from the two springs. Slightly more than half of the discharged NO₃⁻ came from background sources and most of the remainder probably came from fertilizer. This represents a 21–31% loss of fertilizer N from the groundwater basins. The pesticide losses were 3.8–5.8% of the applied atrazine, and 0.05–0.08% of the applied alachlor. The loss of atrazine adsorbed to the suspended solid fraction was about 2 kg/yr, only about 5% of the total mass of atrazine discharged from the springs.     

Floodplain connection buffers seasonal changes in urban stream water quality

Urban streams in the Northeastern United States have large road salt inputs during the winter, increased nonpoint sources of inorganic nitrogen and decreased short‐term and permanent storage of nutrients. Restoration activities that re‐establish connection between streams and riparian environments may be effective for improving urban stream water quality. Meadowbrook Creek, a first‐order stream in Syracuse, NY, provides a unique setting to explore impacts of stream–floodplain connection because it flows along a negative urbanization gradient, from channelized and armoured headwaters to a broad, vegetated floodplain with a riparian aquifer. In this study, we investigated how reconnection to groundwater and introduction of riparian vegetation impacted urban surface water chemistry by making biweekly longitudinal surveys of stream water chemistry in the creek from May 2012 until June 2013. We used multiple methods to measure groundwater discharge rates along the creek. Chloride concentrations in the upstream, disconnected reach were influenced by discharge of road salt during snow melt events and ranged from 161.2 to 1440 mg/l. Chloride concentrations in the downstream, connected reach had less temporal variation, ranging from 252.0 to 1049 mg/l, because of buffering by groundwater discharge, as groundwater chloride concentrations ranged from 84.0 to 655.4 mg/l. In the summer, there was little to no nitrate in the disconnected reach because of limited sources and high primary productivity, but concentrations reached over 1 mg N/l in the connected reach because of the presence of riparian vegetation. During the winter, when temperatures fell below freezing, nitrate concentrations in the disconnected reach increased to 0.58 mg N/l but were still lower than the connected reach, which averaged 0.88 mg N/l. Urban stream restoration projects that restore floodplain connection may impact water quality by storing high salinity road run‐off during winter overbank events and discharging that water year‐round, thereby attenuating seasonal fluctuations in chloride. Contrary to prior findings, we observed that floodplain connection and riparian vegetation may alter nitrate sources and sinks such that nitrate concentrations increase longitudinally in connected urban streams. Copyright © 2014 John Wiley & Sons, Ltd.     

Characteristics of the Ecosystems of Water Bodies Separating from Kandalaksha Bay of the White Sea

The coastal water bodies that separate from White Sea water area due to Kandalaksha coast rise are examined. The hydrological and hydrochemical characteristics of these water bodies are found to notably differ from these in the bays and straits connected with them. Extreme values of water temperature and salinity were recorded. High concentrations of oxygen (>20 mg/l) were recorded in the near-surface water layers and high concentrations of hydrogen sulfide (>90 mg/l) in bottom waters. The species composition of phyto- and zooplankton was found to be poor. The characteristics of enzymatic destruction in subsurface waters of lakes are an order of magnitude greater than those in White Sea open areas.