2012
DOI: 10.1134/s1995425512040099
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Comparison of nutrition range in Dreissena polymorpha and Dreissena bugensis mussels by biochemical markers

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Cited by 13 publications
(4 citation statements)
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“…The combined lipid extracts were filtered, dried by passing through anhydrous Na 2 SO 4 layer, and evaporated at 35 °C. FA methyl esters (FAMEs) were prepared in a mixture of methanol:sulfuric acid (20:1, v/v) at 90 °C for 2 h as previously described (Makhutova et al 2012). FAMEs were analyzed on a gas chromatograph (GC) equipped with a mass spectrometer detector (model 6890/5975C, Agilent Technologies, Santa Clara, CA, USA) and a 30 m long × 0.25 mm internal diameter HP-FFAP capillary column (Agilent Technologies, Santa Clara, CA, USA).…”
Section: Fatty Acid Analysismentioning
confidence: 99%
“…The combined lipid extracts were filtered, dried by passing through anhydrous Na 2 SO 4 layer, and evaporated at 35 °C. FA methyl esters (FAMEs) were prepared in a mixture of methanol:sulfuric acid (20:1, v/v) at 90 °C for 2 h as previously described (Makhutova et al 2012). FAMEs were analyzed on a gas chromatograph (GC) equipped with a mass spectrometer detector (model 6890/5975C, Agilent Technologies, Santa Clara, CA, USA) and a 30 m long × 0.25 mm internal diameter HP-FFAP capillary column (Agilent Technologies, Santa Clara, CA, USA).…”
Section: Fatty Acid Analysismentioning
confidence: 99%
“…Hence, the quagga mussel can allocate more energy into growth and reproduction, which has been suggested as the major difference in life strategy between the two dreissenids (Ram et al, 2012). While different allocation of energy budget in both species seems to contribute substantially to the shift of dominance, only Makhutova et al (2012) compared the nutrient range (by analytical detection of lipids) between the two dreissenids to determine their energy budget. By contrast, a number of earlier studies on zebra mussel revealed that the body composition of this species contains 5%–10% carbohydrates, 5%–20% lipids, and 60%–70% proteins (Bruner et al, 1994; Nalepa et al, 1993; Smolders et al, 2004; Sprung, 1995; Sprung & Borcherding, 1991; Voets et al, 2006; Walz, 1979).…”
Section: Introductionmentioning
confidence: 99%
“…The column temperature program was as follows: from 100°C to 190°C at 3°C/min, 5 min isothermally, then to 230°C at 10°C/min, and 20 min isothermally. Other instrument conditions were as described elsewhere (Makhutova et al 2012). FAME peaks were identified by their mass spectrum compared to those in a database (NIST-2005, Gaithersburg, MD, USA) and to those of available authentic standards (Sigma-Aldrich, St. Louis, MO, USA).…”
Section: Fa Analysismentioning
confidence: 99%
“…The combined lipid extracts were filtered, dried by passing through an anhydrous Na 2 SO 4 layer, and evaporated at 35°C. FA methyl esters (FAMEs) were prepared in a mixture of methanol/sulfuric acid (20: 1, v/v) at 90°C for 2 h as previously described (Makhutova et al 2012). FAMEs were analyzed on a gas chromatograph equipped with a mass spectrometer detector (model 6890/5975C, Agilent Technologies, Santa Clara, CA, USA) and a 30-m-long × 0.25-mm internal diameter HP-FFAP capillary column (Agilent Technologies, Santa Clara, CA, USA).…”
Section: Fa Analysismentioning
confidence: 99%