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        <title>Saline Systems - Latest Articles</title>
        <link>http://www.salinesystems.org</link>
        <description>The latest research articles published by Saline Systems</description>
        <dc:date>2010-02-24T00:00:00Z</dc:date>
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        <item rdf:about="http://www.salinesystems.org/content/6/1/2">
        <title>Distribution of picophytoplankton communities from brackish to hypersaline waters in a South Australian coastal lagoon</title>
        <description>Background:
Picophytoplankton (i.e. cyanobacteria and pico-eukaryotes) are abundant and ecologically critical components of the autotrophic communities in the pelagic realm. These micro-organisms colonized a variety of extreme environments including high salinity waters. However, the distribution of these organisms along strong salinity gradient has barely been investigated. The abundance and community structure of cyanobacteria and pico-eukaryotes were investigated along a natural continuous salinity gradient (1.8% to 15.5%) using flow cytometry.
Results:
Highest picophytoplankton abundances were recorded under salinity conditions ranging between 8.0% and 11.0% (1.3x106 to 1.4x106 ml-1). Two populations of cyanobacteria (Synechococcus sp. and Prochlorococcus sp.) and 5 distinct populations of pico-eukaryotes were identified along the salinity gradient. The picophytoplankton cytometric-richness decreased with salinity and the most cytometrically diversified community (4 to 7 populations) was observed in the brackish-marine part of the lagoon (i.e. salinity below 3.5%). One population of pico-eukaryote dominated the community throughout the salinity gradient and was responsible for the bloom observed between 8.0% and 11.0%. Finally only this halotolerant population and Prochlorococcus sp. were identified in hypersaline waters (i.e. above 14.0%). Salinity was identified as the main factor structuring the distribution of picophytoplankton along the lagoon. However, nutritive conditions, viral lysis and microzooplankton grazing are also suggested as potentially important players in controlling the abundance and diversity of picophytoplankton along the lagoon.
Conclusions:
The complex patterns described here represent the first observation of picophytoplankton dynamics along a continuous gradient where salinity increases from 1.8% to 15.5%. This result provides new insight into the distribution of pico-autotrophic organisms along strong salinity gradients and allows for a better understanding of the overall pelagic functioning in saline systems which is critical for the management of these precious and climatically-stress ecosystems.</description>
        <link>http://www.salinesystems.org/content/6/1/2</link>
                <dc:creator>Mathilde Schapira</dc:creator>
                <dc:creator>Marie-Jeanne Buscot</dc:creator>
                <dc:creator>Thomas Pollet</dc:creator>
                <dc:creator>Sophie Leterme</dc:creator>
                <dc:creator>Laurent Seuront</dc:creator>
                <dc:source>Saline Systems 2010, 6:2</dc:source>
        <dc:date>2010-02-24T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1746-1448-6-2</dc:identifier>
        <prism:publicationName>Saline Systems</prism:publicationName>
        <prism:issn>1746-1448</prism:issn>
        <prism:volume>6</prism:volume>
        <prism:startingPage>2</prism:startingPage>
        <prism:publicationDate>2010-02-24T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>PDF</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.salinesystems.org/content/6/1/1">
        <title>Culture independent molecular analysis of bacterial communities in the mangrove sediment of Sundarban, India</title>
        <description>Background:
Sundarban is the world&apos;s largest coastal sediment comprising of mangrove forest which covers about one million hectares in the south-eastern parts of India and southern parts of Bangladesh. The microbial diversity in this sediment is largely unknown till date. In the present study an attempt has been made to understand the microbial diversity in this sediment using a cultivation-independent molecular approach.
Results:
Two 16 S rRNA gene libraries were constructed and partial sequencing of the selected clones was carried out to identify bacterial strains present in the sediment. Phylogenetic analysis of partially sequenced 16 S rRNA gene sequences revealed the diversity of bacterial strains in the Sundarban sediment. At least 8 different bacterial phyla were detected. The major divisions of detected bacterial phyla were Proteobacteria (alpha, beta, gamma, and delta), Flexibacteria (CFB group), Actinobacteria, Acidobacteria, Chloroflexi, Firmicutes, Planctomycetes and Gammatimonadates.
Conclusion:
The gammaproteobacteria were found to be the most abundant bacterial group in Sundarban sediment. Many clones showed similarity with previously reported bacterial lineages recovered from various marine sediments. The present study indicates a probable hydrocarbon and oil contamination in this sediment. In the present study, a number of clones were identified that have shown similarity with bacterial clones or isolates responsible for the maintenance of the S-cycle in the saline environment.</description>
        <link>http://www.salinesystems.org/content/6/1/1</link>
                <dc:creator>Abhrajyoti Ghosh</dc:creator>
                <dc:creator>Nirmalya Dey</dc:creator>
                <dc:creator>Amit Bera</dc:creator>
                <dc:creator>Amit Tiwari</dc:creator>
                <dc:creator>Sathyaniranjan Kb</dc:creator>
                <dc:creator>Kalyan Chakrabarti</dc:creator>
                <dc:creator>Dhrubajyoti Chattopadhyay</dc:creator>
                <dc:source>Saline Systems 2010, 6:1</dc:source>
        <dc:date>2010-02-17T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1746-1448-6-1</dc:identifier>
        <prism:publicationName>Saline Systems</prism:publicationName>
        <prism:issn>1746-1448</prism:issn>
        <prism:volume>6</prism:volume>
        <prism:startingPage>1</prism:startingPage>
        <prism:publicationDate>2010-02-17T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.salinesystems.org/content/5/1/9">
        <title>Biodiversity of poly-extremophilic Bacteria: Does combining the extremes of high salt, alkaline pH and elevated temperature approach a physico-chemical boundary for life?</title>
        <description>Bacterial microorganisms that grow optimally at Na+ concentrations of 1.7 M, or the equivalent of 10% (w/v) NaCl, and greater are considered to be extreme halophiles. This review focuses on the correlation between the extent of alkaline pH and elevated temperature optima and the extent of salt tolerance of extremely halophilic eubacteria; the focus is on those with alkaline pH optima, above 8.5, and elevated temperature optima, above 50&#176;C. If all three conditions are required for optimal growth, these microorganisms are termed &quot;poly-extremophiles&quot;. However, only a very few extreme halophiles able to grow optimally under alkaline conditions as well as at elevated temperatures have been isolated so far. Therefore the question is: do the combined extreme growth conditions of the recently isolated poly-extremophiles, i.e., anaerobic halophilic alkalithermophiles, approach a physico-chemical boundary for life? These poly-extremophiles are of interest, as their adaptive mechanisms give insight into organisms&apos; abilities to survive in environments which were previously considered prohibitive to life, as well as to possible properties of early evolutionary and extraterrestrial life forms.</description>
        <link>http://www.salinesystems.org/content/5/1/9</link>
                <dc:creator>Karen Bowers</dc:creator>
                <dc:creator>Noha Mesbah</dc:creator>
                <dc:creator>Juergen Wiegel</dc:creator>
                <dc:source>Saline Systems 2009, 5:9</dc:source>
        <dc:date>2009-11-23T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1746-1448-5-9</dc:identifier>
        <prism:publicationName>Saline Systems</prism:publicationName>
        <prism:issn>1746-1448</prism:issn>
        <prism:volume>5</prism:volume>
        <prism:startingPage>9</prism:startingPage>
        <prism:publicationDate>2009-11-23T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.salinesystems.org/content/5/1/8">
        <title>A systems biology approach to investigate the response of Synechocystis sp. PCC6803 to a high salt environment</title>
        <description>Background:
Salt overloading during agricultural processes is causing a decrease in crop productivity due to saline sensitivity. Salt tolerant cyanobacteria share many cellular characteristics with higher plants and therefore make ideal model systems for studying salinity stress. Here, the response of fully adapted Synechocystis sp. PCC6803 cells to the addition of 6% w/v NaCl was investigated using proteomics combined with targeted analysis of transcripts.
Results:
Isobaric mass tagging of peptides led to accurate relative quantitation and identification of 378 proteins, and approximately 40% of these were differentially expressed after incubation in BG-11 media supplemented with 6% salt for 9 days. Protein abundance changes were related to essential cellular functional alterations. Differentially expressed proteins involved in metabolic responses were also analysed using the probabilitistic tool Mixed Model on Graphs (MMG), where the role of energy conversion through glycolysis and reducing power through pentose phosphate pathway were highlighted. Temporal RT-qPCR experiments were also run to investigate protein expression changes at the transcript level, for 14 non-metabolic proteins. In 9 out of 14 cases the mRNA changes were in accordance with the proteins.
Conclusion:
Synechocystis sp. PCC6803 has the ability to regulate essential metabolic processes to enable survival in high salt environments. This adaptation strategy is assisted by further regulation of proteins involved in non-metabolic cellular processes, supported by transcriptional and post-transcriptional control. This study demonstrates the effectiveness of using a systems biology approach in answering environmental, and in particular, salt adaptation questions in Synechocystis sp. PCC6803</description>
        <link>http://www.salinesystems.org/content/5/1/8</link>
                <dc:creator>Jagroop Pandhal</dc:creator>
                <dc:creator>Josselin Noirel</dc:creator>
                <dc:creator>Phillip Wright</dc:creator>
                <dc:creator>Catherine Biggs</dc:creator>
                <dc:source>Saline Systems 2009, 5:8</dc:source>
        <dc:date>2009-09-07T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1746-1448-5-8</dc:identifier>
        <prism:publicationName>Saline Systems</prism:publicationName>
        <prism:issn>1746-1448</prism:issn>
        <prism:volume>5</prism:volume>
        <prism:startingPage>8</prism:startingPage>
        <prism:publicationDate>2009-09-07T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.salinesystems.org/content/5/1/7">
        <title>Molt-inhibiting hormone stimulates vitellogenesis at advanced ovarian developmental stages in the female blue crab, Callinectes sapidus 1: an ovarian stage dependent involvement</title>
        <description>To understand the hormonal coordination of the antagonism between molting and reproduction in crustaceans, the terminally anecdysial mature female Callinectes sapidus was used as a model. The regulatory roles of crustacean hyperglycemic hormone (CHH) and molt-inhibiting hormone (MIH) in vitellogenesis were examined. A competitive specific RIA was used to measure the levels of MIH and CHH in the hemolymphs of mature females at pre- and mid- vitellogenic stages, and their effects on vitellogenesis at early (early 2, E2) and mid vitellogenesis (3) stages were determined in vitro. A hepatopancreas fragments incubation system was developed and the levels of vitellogenin (VtG), as well as VtG mRNA and heterogeneous nuclear (hn)VtG RNA were determined using RIA or QPCR, respectively. MIH titers were four times higher at mid-vitellogenesis than at pre-vitellogenesis, while CHH levels in the hemolymph were constant. In the in vitro incubation experiments, MIH increased both VtG mRNA levels and secretion at ovarian stage 3. At stage E2, however, MIH resulted in a mixed response: downregulation of VtG mRNA and upregulation of hnVtG RNA. CHH had no effect on any of the parameters. Actinomycin D blocked the stimulatory effects of MIH in stage 3 animals on VtG mRNA and VtG, while cycloheximide attenuated only VtG levels, confirming the MIH stimulatory effect at this stage. MIH is a key endocrine regulator in the coordination of molting and reproduction in the mature female C. sapidus, which simultaneously inhibits molt and stimulates vitellogenesis.</description>
        <link>http://www.salinesystems.org/content/5/1/7</link>
                <dc:creator>Nilli Zmora</dc:creator>
                <dc:creator>John Trant</dc:creator>
                <dc:creator>Yonathan Zohar</dc:creator>
                <dc:creator>J. Sook Chung</dc:creator>
                <dc:source>Saline Systems 2009, 5:7</dc:source>
        <dc:date>2009-07-07T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1746-1448-5-7</dc:identifier>
        <prism:publicationName>Saline Systems</prism:publicationName>
        <prism:issn>1746-1448</prism:issn>
        <prism:volume>5</prism:volume>
        <prism:startingPage>7</prism:startingPage>
        <prism:publicationDate>2009-07-07T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.salinesystems.org/content/5/1/6">
        <title>Molt-inhibiting hormone stimulates vitellogenesis at advanced ovarian developmental stages in the female blue crab, Callinectes sapidus 2: novel specific binding sites in hepatopancreas and cAMP as a second messenger</title>
        <description>The finding that molt-inhibiting hormone (MIH) regulates vitellogenesis in the hepatopancreas of mature Callinectes sapidus females, raised the need for the characterization of its mode of action. Using classical radioligand binding assays, we located specific, saturable, and non-cooperative binding sites for MIH in the Y-organs of juveniles (J-YO) and in the hepatopancreas of vitellogenic adult females. MIH binding to the hepatopancreas membranes had an affinity 77 times lower than that of juvenile YO membranes (KD values: 3.22 &#215; 10-8 and 4.19 &#215; 10-10 M/mg protein, respectively). The number of maximum binding sites (BMAX) was approximately two times higher in the hepatopancreas than in the YO (BMAX values: 9.24 &#215; 10-9 and 4.8 &#215; 10-9 M/mg protein, respectively). Furthermore, MIH binding site number in the hepatopancreas was dependent on ovarian stage and was twice as high at stage 3 than at stages 2 and 1. SDS-PAGE separation of [125I] MIH or [125I] crustacean hyperglycemic hormone (CHH) crosslinked to the specific binding sites in the membranes of the J-YO and hepatopancreas suggests a molecular weight of ~51 kDa for a MIH receptor in both tissues and a molecular weight of ~61 kDa for a CHH receptor in the hepatopancreas. The use of an in vitro incubation of hepatopancreas fragments suggests that MIH probably utilizes cAMP as a second messenger in this tissue, as cAMP levels increased in response to MIH. Additionally, 8-Bromo-cAMP mimicked the effects of MIH on vitellogenin (VtG) mRNA and heterogeneous nuclear (hn) VtG RNA levels. The results imply that the functions of MIH in the regulation of molt and vitellogenesis are mediated through tissue specific receptors with different kinetics and signal transduction. MIH ability to regulate vitellogenesis is associated with the appearance of MIH specific membrane binding sites in the hepatopancreas upon pubertal/final molt.</description>
        <link>http://www.salinesystems.org/content/5/1/6</link>
                <dc:creator>Nilli Zmora</dc:creator>
                <dc:creator>Amir Sagi</dc:creator>
                <dc:creator>Yonathan Zohar</dc:creator>
                <dc:creator>J. Sook Chung</dc:creator>
                <dc:source>Saline Systems 2009, 5:6</dc:source>
        <dc:date>2009-07-07T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1746-1448-5-6</dc:identifier>
        <prism:publicationName>Saline Systems</prism:publicationName>
        <prism:issn>1746-1448</prism:issn>
        <prism:volume>5</prism:volume>
        <prism:startingPage>6</prism:startingPage>
        <prism:publicationDate>2009-07-07T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.salinesystems.org/content/5/1/5">
        <title>DNA fingerprinting differentiation between B-carotene 
hyperproducer strains of Dunaliella from around the world</title>
        <description>Background:
Dunaliella salina is the most important species of the genus for &#946;-carotene production. Several investigations have demonstrated that D. salina produces more than 10% dry weight of pigment and that the species grows in salt saturated lagoons. High plasticity in the green stage and the almost indistinguishable differences in the red phase make identification and differentiation of species and ecotypes very difficult and time consuming.
Results:
In this work, we applied our intron-sizing method to compare the 18S rDNA fingerprint between D. salina (CCAP 19/18), D. salina/bardawil (UTEX LB2538) and &#946;-carotene hyperproducing strains of Dunaliella isolated from salt saturated lagoons in Baja, Mexico. All hyperproducer strains reached &#946;-carotene levels of about 10 pg/cell. Optical microscopy did not allow to differentiate between these Dunaliella strains; however, 18S rDNA fingerprinting methodology allowed us to differentiate D. salina from D. salina/bardawil.
Conclusion:
In Baja Mexico we found D. salina and D. salina/bardawil species by using intron-sizing-method. The National Center for Biotechnology Information (NCBI) Dunaliella 18S rDNA gene sequences were analyzed with our methodology and extraordinary correlation was found with experimental results.</description>
        <link>http://www.salinesystems.org/content/5/1/5</link>
                <dc:creator>Jorge Olmos</dc:creator>
                <dc:creator>Leonel Ochoa</dc:creator>
                <dc:creator>Jesus Paniagua</dc:creator>
                <dc:creator>Rosalia Contreras</dc:creator>
                <dc:source>Saline Systems 2009, 5:5</dc:source>
        <dc:date>2009-06-30T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1746-1448-5-5</dc:identifier>
        <prism:publicationName>Saline Systems</prism:publicationName>
        <prism:issn>1746-1448</prism:issn>
        <prism:volume>5</prism:volume>
        <prism:startingPage>5</prism:startingPage>
        <prism:publicationDate>2009-06-30T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.salinesystems.org/content/5/1/4">
        <title>Molecular characterization and the effect of salinity on cyanobacterial diversity in the rice fields of Eastern Uttar Pradesh, India</title>
        <description>Background:
Salinity is known to affect almost half of the world&apos;s irrigated lands, especially rice fields. Furthermore, cyanobacteria, one of the critical inhabitants of rice fields have been characterized at molecular level from many different geographical locations. This study, for the first time, has examined the molecular diversity of cyanobacteria inhabiting Indian rice fields which experience various levels of salinity.
Results:
Ten physicochemical parameters were analyzed for samples collected from twenty experimental sites. Electrical conductivity data were used to classify the soils and to investigate relationship between soil salinity and cyanobacterial diversity. The cyanobacterial communities were analyzed using semi-nested 16S rRNA gene PCR and denaturing gradient gel electrophoresis. Out of 51 DGGE bands selected for sequencing only 31 which showed difference in sequences were subjected to further analysis. BLAST analysis revealed highest similarity for twenty nine of the sequences with cyanobacteria, and the other two to plant plastids. Clusters obtained based on morphological and molecular attributes of cyanobacteria were correlated to soil salinity. Among six different clades, clades 1, 2, 4 and 6 contained cyanobacteria inhabiting normal or low saline (having EC &lt; 4.0 ds m-1) to (high) saline soils (having EC &gt; 4.0 ds m-1), however, clade 5 represented the cyanobacteria inhabiting only saline soils. Whilst, clade 3 contained cyanobacteria from normal soils. The presence of DGGE band corresponding to Aulosira strains were present in large number of soil indicating its wide distribution over a range of salinities, as were Nostoc, Anabaena, and Hapalosiphon although to a lesser extent in the sites studied.
Conclusion:
Low salinity favored the presence of heterocystous cyanobacteria, while very high salinity mainly supported the growth of non-heterocystous genera. High nitrogen content in the low salt soils is proposed to be a result of reduced ammonia volatilization compared to the high salt soils. Although many environmental factors could potentially determine the microbial community present in these multidimensional ecosystems, changes in the diversity of cyanobacteria in rice fields was correlated to salinity.</description>
        <link>http://www.salinesystems.org/content/5/1/4</link>
                <dc:creator>Ashish Srivastava</dc:creator>
                <dc:creator>Poonam Bhargava</dc:creator>
                <dc:creator>Arvind Kumar</dc:creator>
                <dc:creator>Lal Rai</dc:creator>
                <dc:creator>Brett Neilan</dc:creator>
                <dc:source>Saline Systems 2009, 5:4</dc:source>
        <dc:date>2009-04-06T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1746-1448-5-4</dc:identifier>
        <prism:publicationName>Saline Systems</prism:publicationName>
        <prism:issn>1746-1448</prism:issn>
        <prism:volume>5</prism:volume>
        <prism:startingPage>4</prism:startingPage>
        <prism:publicationDate>2009-04-06T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.salinesystems.org/content/5/1/3">
        <title>Egg banks in hypersaline lakes of the South-East Europe </title>
        <description>The cyst banks of 6 coastal hypersaline lakes of South-East Europe have been investigated. The study concerned the bottom sediments of Khersonesskoe and Koyashskoe lakes in the Crimea (Ukraine), Nart&#235; saltworks (Albania), Vecchia Salina at Torre Colimena (Apulia, Italy), Pantano Grande and Pantano Roveto at Vendicari (Sicily, Italy). A total of 19 cyst types were recognised. The cyst banks of lakes were found to be well separated in the representation derived from a statistical multivariate data analysis. For all the lakes examined a comparison was possible between the resting community in sediments (cyst bank) and the active one in the water. The cyst banks contained more species than those recorded over a multi-year sampling effort in the water column. The study of cyst hatching, performed on 5 cyst types under lab conditions, demonstrated that cysts do not hatch under the same conditions. Furthermore, each cyst type shows a wide range of preferential hatching conditions, which allow us to confirm the ecological generalism of salt lake species.</description>
        <link>http://www.salinesystems.org/content/5/1/3</link>
                <dc:creator>Salvatore Moscatello</dc:creator>
                <dc:creator>Genuario Belmonte</dc:creator>
                <dc:source>Saline Systems 2009, 5:3</dc:source>
        <dc:date>2009-03-17T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1746-1448-5-3</dc:identifier>
        <prism:publicationName>Saline Systems</prism:publicationName>
        <prism:issn>1746-1448</prism:issn>
        <prism:volume>5</prism:volume>
        <prism:startingPage>3</prism:startingPage>
        <prism:publicationDate>2009-03-17T00:00:00Z</prism:publicationDate>
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                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.salinesystems.org/content/5/1/2">
        <title>Long-term surveillance of sulfate-reducing bacteria in highly saline industrial wastewater evaporation ponds
</title>
        <description>Abundance and seasonal dynamics of sulfate-reducing bacteria (SRB), in general, and of extreme halophilic SRB (belonging to Desulfocella halophila) in particular, were examined in highly saline industrial wastewater evaporation ponds over a forty one month period. Industrial wastewater was sampled and the presence of SRB was determined by quantitative real-time PCR (qPCR) with a set of primers designed to amplify the dissimilatory sulfite reductase (dsrA) gene. SRB displayed higher abundance during the summer (106&#8211;108 targets ml-1) and lower abundance from the autumn-spring (103&#8211;105 targets ml-1). However, addition of concentrated dissolved organic matter into the evaporation ponds during winter immediately resulted in a proliferation of SRB, despite the lower wastewater temperature (12&#8211;14&#176;C). These results indicate that the qPCR approach can be used for rapid measurement of SRB to provide valuable information about the abundance of SRB in harsh environments, such as highly saline industrial wastewaters. Low level of H2S has been maintained over five years, which indicates a possible inhibition of SRB activity, following artificial salination (&#8776;16% w/v of NaCl) of wastewater evaporation ponds, despite SRB reproduction being detected by qPCR.</description>
        <link>http://www.salinesystems.org/content/5/1/2</link>
                <dc:creator>Eitan Ben-Dov</dc:creator>
                <dc:creator>Ariel Kushmaro</dc:creator>
                <dc:creator>Asher Brenner</dc:creator>
                <dc:source>Saline Systems 2009, 5:2</dc:source>
        <dc:date>2009-02-18T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1746-1448-5-2</dc:identifier>
        <prism:publicationName>Saline Systems</prism:publicationName>
        <prism:issn>1746-1448</prism:issn>
        <prism:volume>5</prism:volume>
        <prism:startingPage>2</prism:startingPage>
        <prism:publicationDate>2009-02-18T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
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