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        <title>Saline Systems - Most accessed articles</title>
        <link>http://www.salinesystems.org</link>
        <description>The most accessed research articles published by Saline Systems</description>
        <dc:date>2010-02-24T00:00:00Z</dc:date>
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                                <rdf:li rdf:resource="http://www.salinesystems.org/content/4/1/3" />
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        <item rdf:about="http://www.salinesystems.org/content/4/1/3">
        <title>Chemical and physical properties of some saline lakes in Alberta and Saskatchewan</title>
        <description>Background:
The Northern Great Plains of Canada are home to numerous permanent and ephemeral athalassohaline lakes. These lakes display a wide range of ion compositions, salinities, stratification patterns, and ecosystems. Many of these lakes are ecologically and economically significant to the Great Plains Region. A survey of the physical characteristics and chemistry of 19 lakes was carried out to assess their suitability for testing new tools for determining past salinity from the sediment record.
Results:
Data on total dissolved solids (TDS), specific conductivity, temperature, dissolved oxygen (DO), and pH were measured in June, 2007. A comparison of these data with past measurements indicates that salinity is declining at Little Manitou and Big Quill Lakes in the province of Saskatchewan. However salinity is rising at other lakes in the region, including Redberry and Manito Lakes.
Conclusion:
The wide range of salinities found across a small geographic area makes the Canadian saline lakes region ideal for testing salinity proxies. A nonlinear increase in salinity at Redberry Lake is likely influenced by its morphometry. This acceleration has ecological implications for the migratory bird species found within the Redberry Important Bird Area.</description>
        <link>http://www.salinesystems.org/content/4/1/3</link>
                <dc:creator>Jeff Bowman</dc:creator>
                <dc:creator>Julian Sachs</dc:creator>
                <dc:source>Saline Systems 2008, 4:3</dc:source>
        <dc:date>2008-04-22T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1746-1448-4-3</dc:identifier>
        <prism:publicationName>Saline Systems</prism:publicationName>
        <prism:issn>1746-1448</prism:issn>
        <prism:volume>4</prism:volume>
        <prism:startingPage>3</prism:startingPage>
        <prism:publicationDate>2008-04-22T00:00:00Z</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/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>
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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/1/1/8">
        <title>Endospores of halophilic bacteria of the family Bacillaceaeisolated from non-saline Japanese soil may be transported by Kosa event (Asian dust storm)</title>
        <description>Background:
Generally, extremophiles have been deemed to survive in the extreme environments to which they had adapted to grow. Recently many extremophiles have been isolated from places where they are not expected to grow. Alkaliphilic microorganisms have been isolated from acidic soil samples with pH 4.0, and thermophiles have been isolated from samples of low temperature. Numerous moderately halophilic microorganisms, defined as those that grow optimally in media containing 0.5&#8211;2.5 Molar (3&#8211;15%) NaCl, and halotolerant microorganisms that are able to grow in media without added NaCl and in the presence of high NaCl have been isolated from saline environments such as salterns, salt lakes and sea sands. It has tacitly been believed that habitats of halophiles able to grow in media containing more than 20% (3.4 M) are restricted to saline environments, and no reports have been published on the isolation of halophiles from ordinary garden soil samples.
Results:
We demonstrated that many halophilic bacteria that are able to grow in the presence of 20% NaCl are inhabiting in non-saline environments such as ordinary garden soils, yards, fields and roadways in an area surrounding Tokyo, Japan. Analyses of partial 16S rRNA gene sequences of 176 isolates suggested that they were halophiles belonging to genera of the family Bacillaceae, Bacillus (11 isolates), Filobacillus (19 isolates), Gracilibacillus (6 isolates), Halobacillus (102 isolates), Lentibacillus (1 isolate), Paraliobacillus (5 isolates) and Virgibacillus (17 isolates). Sequences of 15 isolates showed similarities less than 92%, suggesting that they may represent novel taxa within the family Bacillaceae.
Conclusion:
The numbers of total bacteria of inland soil samples were in a range from 1.4 &#215; 107/g to 1.1 &#215; 106/g. One tenth of the total bacteria was occupied by endospore-forming bacteria. Only very few of the endospore-forming bacteria, roughly 1 out of 20,000, are halophilic bacteria. Most of the halophilic bacteria were surviving as endospores in the soil samples, in a range of less than 1 to about 500/g soil. Samples collected from seashore in a city confronting Tokyo Bay gave the total numbers of bacteria and endospores roughly 1000 time smaller than those of inland soil samples. Numbers of halophilic bacteria per gram, however, were almost the same as those of inland soil samples. A possible source of the halophilic endospore originating from Asian dust storms is discussed.</description>
        <link>http://www.salinesystems.org/content/1/1/8</link>
                <dc:creator>Akinobu Echigo</dc:creator>
                <dc:creator>Miki Hino</dc:creator>
                <dc:creator>Tadamasa Fukushima</dc:creator>
                <dc:creator>Toru Mizuki</dc:creator>
                <dc:creator>Masahiro Kamekura</dc:creator>
                <dc:creator>Ron Usami</dc:creator>
                <dc:source>Saline Systems 2005, 1:8</dc:source>
        <dc:date>2005-10-20T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1746-1448-1-8</dc:identifier>
        <prism:publicationName>Saline Systems</prism:publicationName>
        <prism:issn>1746-1448</prism:issn>
        <prism:volume>1</prism:volume>
        <prism:startingPage>8</prism:startingPage>
        <prism:publicationDate>2005-10-20T00:00:00Z</prism:publicationDate>
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                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.salinesystems.org/content/4/1/2">
        <title>Microbial life at high salt concentrations: phylogenetic and metabolic diversity</title>
        <description>Halophiles are found in all three domains of life. Within the Bacteria we know halophiles within the phyla Cyanobacteria, Proteobacteria, Firmicutes, Actinobacteria, Spirochaetes, and Bacteroidetes. Within the Archaea the most salt-requiring microorganisms are found in the class Halobacteria. Halobacterium and most of its relatives require over 100&#8211;150 g/l salt for growth and structural stability. Also within the order Methanococci we encounter halophilic species. Halophiles and non-halophilic relatives are often found together in the phylogenetic tree, and many genera, families and orders have representatives with greatly different salt requirement and tolerance. A few phylogenetically coherent groups consist of halophiles only: the order Halobacteriales, family Halobacteriaceae (Euryarchaeota) and the anaerobic fermentative bacteria of the order Halanaerobiales (Firmicutes). The family Halomonadaceae (Gammaproteobacteria) almost exclusively contains halophiles. Halophilic microorganisms use two strategies to balance their cytoplasm osmotically with their medium. The first involves accumulation of molar concentrations of KCl. This strategy requires adaptation of the intracellular enzymatic machinery, as proteins should maintain their proper conformation and activity at near-saturating salt concentrations. The proteome of such organisms is highly acidic, and most proteins denature when suspended in low salt. Such microorganisms generally cannot survive in low salt media. The second strategy is to exclude salt from the cytoplasm and to synthesize and/or accumulate organic &apos;compatible&apos; solutes that do not interfere with enzymatic activity. Few adaptations of the cells&apos; proteome are needed, and organisms using the &apos;organic-solutes-in strategy&apos; often adapt to a surprisingly broad salt concentration range. Most halophilic Bacteria, but also the halophilic methanogenic Archaea use such organic solutes. A variety of such solutes are known, including glycine betaine, ectoine and other amino acid derivatives, sugars and sugar alcohols. The &apos;high-salt-in strategy&apos; is not limited to the Halobacteriaceae. The Halanaerobiales (Firmicutes) also accumulate salt rather than organic solutes. A third, phylogenetically unrelated organism accumulates KCl: the red extremely halophilic Salinibacter (Bacteroidetes), recently isolated from saltern crystallizer brines. Analysis of its genome showed many points of resemblance with the Halobacteriaceae, probably resulting from extensive horizontal gene transfer. The case of Salinibacter shows that more unusual types of halophiles may be waiting to be discovered.</description>
        <link>http://www.salinesystems.org/content/4/1/2</link>
                <dc:creator>Aharon Oren</dc:creator>
                <dc:source>Saline Systems 2008, 4:2</dc:source>
        <dc:date>2008-04-15T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1746-1448-4-2</dc:identifier>
        <prism:publicationName>Saline Systems</prism:publicationName>
        <prism:issn>1746-1448</prism:issn>
        <prism:volume>4</prism:volume>
        <prism:startingPage>2</prism:startingPage>
        <prism:publicationDate>2008-04-15T00:00:00Z</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/1/1/5">
        <title>Organic compatible solutes of halotolerant and halophilic microorganisms</title>
        <description>Microorganisms that adapt to moderate and high salt environments use a variety of solutes, organic and inorganic, to counter external osmotic pressure. The organic solutes can be zwitterionic, noncharged, or anionic (along with an inorganic cation such as K+). The range of solutes, their diverse biosynthetic pathways, and physical properties of the solutes that effect molecular stability are reviewed.</description>
        <link>http://www.salinesystems.org/content/1/1/5</link>
                <dc:creator>Mary Roberts</dc:creator>
                <dc:source>Saline Systems 2005, 1:5</dc:source>
        <dc:date>2005-08-04T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1746-1448-1-5</dc:identifier>
        <prism:publicationName>Saline Systems</prism:publicationName>
        <prism:issn>1746-1448</prism:issn>
        <prism:volume>1</prism:volume>
        <prism:startingPage>5</prism:startingPage>
        <prism:publicationDate>2005-08-04T00:00:00Z</prism:publicationDate>
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                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <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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                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.salinesystems.org/content/1/1/10">
        <title>Saline systems of the Great Plains of western Canada: an overview of the limnogeology and paleolimnology</title>
        <description>In much of the northern Great Plains, saline and hypersaline lacustrine brines are the only surface waters present. As a group, the lakes of this region are unique: there is no other area in the world that can match the concentration and diversity of saline lake environments exhibited in the prairie region of Canada and northern United States. The immense number of individual salt lakes and saline wetlands in this region of North America is staggering. Estimates vary from about one million to greater than 10 million, with densities in some areas being as high as 120 lakes/km2.Despite over a century of scientific investigation of these salt lakes, we have only in the last twenty years advanced far enough to appreciate the wide spectrum of lake types, water chemistries, and limnological processes that are operating in the modern settings. Hydrochemical data are available for about 800 of the lake brines in the region. Composition, textural, and geochemical information on the modern bottom sediments has been collected for just over 150 of these lakes. Characterization of the biological and ecological features of these lakes is based on even fewer investigations, and the stratigraphic records of only twenty basins have been examined.The lake waters show a considerable range in ionic composition and concentration. Early investigators, concentrating on the most saline brines, emphasized a strong predominance of Na+ and SO4-2 in the lakes. It is now realized, however, that not only is there a complete spectrum of salinities from less than 1 ppt TDS to nearly 400 ppt, but also virtually every water chemistry type is represented in lakes of the region. With such a vast array of compositions, it is difficult to generalize. Nonetheless, the paucity of Cl-rich lakes makes the northern Great Plains basins somewhat unusual compared with salt lakes in many other areas of the world (e.g., Australia, western United States). Compilations of the lake water chemistries show distinct spatial trends and regional variations controlled by groundwater input, climate, and geomorphology. Short-term temporal variations in the brine composition, which can have significant effects on the composition of the modern sediments, have also been well documented in several individual basins.From a sedimentological and mineralogical perspective, the wide range of water chemistries exhibited by the lakes leads to an unusually large diversity of modern sediment composition. Over 40 species of endogenic precipitates and authigenic minerals have been identified in the lacustrine sediments. The most common non-detrital components of the modern sediments include: calcium and calcium-magnesium carbonates (magnesian calcite, aragonite, dolomite), and sodium, magnesium, and sodium-magnesium sulfates (mirabilite, thenardite, bloedite, epsomite). Many of the basins whose brines have very high Mg/Ca ratios also have hydromagnesite, magnesite, and nesquehonite. Unlike salt lakes in many other areas of the world, halite, gypsum, and calcite are relatively rare endogenic precipitates in the Great Plains lakes. The detrital fraction of the lacustrine sediments is normally dominated by clay minerals, carbonate minerals, quartz, and feldspars.Sediment accumulation in these salt lakes is controlled and modified by a wide variety of physical, chemical, and biological processes. Although the details of these modern sedimentary processes can be exceedingly complex and difficult to discuss in isolation, in broad terms, the processes operating in the salt lakes of the Great Plains are ultimately controlled by three basic factors or conditions of the basin: (a) basin morphology; (b) basin hydrology; and (c) water salinity and composition. Combinations of these parameters interact to control nearly all aspects of modern sedimentation in these salt lakes and give rise to four &apos;end member&apos; types of modern saline lacustrine settings in the Great Plains: (a) clastics-dominated playas; (b) salt-dominated playas; (c) deep water, non-stratified lakes; and (d) deep water, &quot;permanently&quot; stratified lakes.</description>
        <link>http://www.salinesystems.org/content/1/1/10</link>
                <dc:creator>William Last</dc:creator>
                <dc:creator>Fawn Ginn</dc:creator>
                <dc:source>Saline Systems 2005, 1:10</dc:source>
        <dc:date>2005-11-18T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1746-1448-1-10</dc:identifier>
        <prism:publicationName>Saline Systems</prism:publicationName>
        <prism:issn>1746-1448</prism:issn>
        <prism:volume>1</prism:volume>
        <prism:startingPage>10</prism:startingPage>
        <prism:publicationDate>2005-11-18T00:00:00Z</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>
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        <title>Proteomics with a pinch of salt: a cyanobacterial perspective</title>
        <description>Cyanobacteria are ancient life forms and have adapted to a variety of extreme environments, including high salinity. Biochemical, physiological and genetic studies have contributed to uncovering their underlying survival mechanisms, and as recent studies demonstrate, proteomics has the potential to increase our overall understanding further. To date, most salt-related cyanobacterial proteomic studies have utilised gel electrophoresis with the model organism Synechocystis sp. PCC6803. Moreover, focus has been on 2&#8211;4% w/v NaCl concentrations within different cellular compartments. Under these conditions, Synechocystis sp. PCC6803 was found to respond and adapt to salt stress through synthesis of general and specific stress proteins, altering the protein composition of extracellular layers, and re-directing control of complex central intermediary pathways. Post-transcriptional control was also predicted through non-correlating transcript level data and identification of protein isoforms.In this paper, we also review technical developments with emphasis on improving the quality and quantity of proteomic data and overcoming the detrimental effects of salt on sample preparation and analysis. Developments in gel-free methods include protein and peptide fractionation workflows, which can increase coverage of the proteome (20% in Synechocystis sp. PCC6803). Quantitative techniques have also improved in accuracy, resulting in confidence in quantitation approaching or even surpassing that seen in transcriptomic techniques (better than 1.5-fold in differential expression). Furthermore, in vivo metabolic labelling and de novo protein sequencing software have improved the ability to apply proteomics to unsequenced environmental isolates. The example used in this review is a cyanobacterium isolated from a Saharan salt lake.</description>
        <link>http://www.salinesystems.org/content/4/1/1</link>
                <dc:creator>Jagroop Pandhal</dc:creator>
                <dc:creator>Phillip Wright</dc:creator>
                <dc:creator>Catherine Biggs</dc:creator>
                <dc:source>Saline Systems 2008, 4:1</dc:source>
        <dc:date>2008-04-15T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1746-1448-4-1</dc:identifier>
        <prism:publicationName>Saline Systems</prism:publicationName>
        <prism:issn>1746-1448</prism:issn>
        <prism:volume>4</prism:volume>
        <prism:startingPage>1</prism:startingPage>
        <prism:publicationDate>2008-04-15T00:00:00Z</prism:publicationDate>
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