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    <title>NISCAIR Online Periodicals Repository Collection: IJEB Vol.49(10) [October 2011]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/12849</link>
    <description />
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        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/12869" />
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        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/12867" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/12866" />
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    <title>The Collection's search engine</title>
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  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/12869">
    <title>Sodium selenite attenuated cisplatin-induced toxicity in rats: Role of electrolytes homeostasis</title>
    <link>http://nopr.niscair.res.in/handle/123456789/12869</link>
    <description>Title: Sodium selenite attenuated cisplatin-induced toxicity in rats: Role of electrolytes homeostasis
&lt;br/&gt;
&lt;br/&gt;Authors: Noori, Shafaq; Mahboob, Tabassum
&lt;br/&gt;
&lt;br/&gt;Abstract: Sodium selenite (1 mg/kg body weight, ip) for&#xD;
10 consecutive days treatment showed marked increase in intra-erythrocytes K&lt;sup&gt;+&lt;/sup&gt;&#xD;
and plasma Na&lt;sup&gt;+&lt;/sup&gt; level while slight increase in Na&lt;sup&gt;+ &lt;/sup&gt;K&lt;sup&gt;+&lt;/sup&gt;&#xD;
ATPase level. No mortality was observed at this dose of sodium selenite.&#xD;
However, sodium selenite pretreatment partially restored the Na&lt;sup&gt;+&lt;/sup&gt; K&lt;sup&gt;+&lt;/sup&gt;&#xD;
ATPase and intra-erythorcytes and plasma sodium level, while completely&#xD;
restored the intra-erythrocytes K&lt;sup&gt;+ &lt;/sup&gt;and plasma Mg&lt;sup&gt;2+ &lt;/sup&gt;level.&#xD;
No change was observed in plasma Ca&lt;sup&gt;2+&lt;/sup&gt; level. Thus sodium selenite&#xD;
successively attenuated the Cisplatin-induced electrolytes alterations and&#xD;
toxicity by exerting the stress response of sodium.
&lt;br/&gt;
&lt;br/&gt;Page(s): 791-794</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/12868">
    <title>Effect of mating and parasitism regimes on progeny production and sex-ratio of &lt;i&gt;Campoletis chlorideae&lt;/i&gt; Uchida</title>
    <link>http://nopr.niscair.res.in/handle/123456789/12868</link>
    <description>Title: Effect of mating and parasitism regimes on progeny production and sex-ratio of &lt;i&gt;Campoletis chlorideae&lt;/i&gt; Uchida
&lt;br/&gt;
&lt;br/&gt;Authors: Dhillon, M K; Sharma, H C
&lt;br/&gt;
&lt;br/&gt;Abstract: The ichneumonid parasitoid,&lt;i&gt; C&lt;/i&gt;.&lt;i&gt; chlorideae&lt;/i&gt; is an important&#xD;
natural enemy of pod borer/bollworm, &lt;i&gt;Helicoverpa armigera&lt;/i&gt; (Hubner) in&#xD;
different agro-ecosystems. The sex-ratio of parasitoids has an important bearing on the population build up of the natural&#xD;
enemies for biological control of insect&#xD;
pests. Therefore, the present studies were conducted to gain an understanding&#xD;
of the influence of mating behaviour and abundance of the insect host on fecundity and sex-ratio of the&#xD;
parasitoid, &lt;i&gt;C. chlorideae&lt;/i&gt;. There was no significant influence of number of matings&#xD;
and abundance of the insect host on&#xD;
cocoon formation, adult emergence, and larval and pupal periods of &lt;i&gt;C.&#xD;
chlorideae&lt;/i&gt;. However, fecundity and female longevity were significantly influenced by mating&#xD;
and abundance of the insect host.&#xD;
There was a significant and positive correlation &#xD;
(r = 0.84**) between longevity and fecundity of &lt;i&gt;C. chlorideae&lt;/i&gt; females.&#xD;
The unmated &lt;i&gt;C. chlorideae&lt;/i&gt; females produced only males. Nearly 20% of the&#xD;
females that had mated twice were able to parasitize the &lt;i&gt;H. armigera&lt;/i&gt;&#xD;
larvae successfully. The sex-ratio of the progeny from females that had mated&#xD;
twice was male biased. Females mated with males from the unmated females&#xD;
produced significantly less numbers of females than those mated with males from&#xD;
the fertilized females, indicating genetic regulation of sex-ratio in &lt;i&gt;C.&#xD;
chlorideae&lt;/i&gt;.
&lt;br/&gt;
&lt;br/&gt;Page(s): 786-790</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/12867">
    <title>Non-exhaustive test for aerobic capacity determination in running rats</title>
    <link>http://nopr.niscair.res.in/handle/123456789/12867</link>
    <description>Title: Non-exhaustive test for aerobic capacity determination in running rats
&lt;br/&gt;
&lt;br/&gt;Authors: Manchado-Gobatto, FB; Gobatto, CA; Contarteze, RVL; Mello, MAR
&lt;br/&gt;
&lt;br/&gt;Abstract: A simple and&#xD;
applicable method for non-exhaustive aerobic evaluation in running rats is&#xD;
described. Wistar rats were submitted to running test at different velocities&#xD;
(10, 15, 20, 25 m/min) with 48 h recovery among them. At each velocity, the rats&#xD;
ran two bouts of 5 min with 2 min of rest between bouts. Blood samples were&#xD;
collected at the end of each bout for lactate determination. For each&#xD;
intensity, delta lactate was calculated and using deltas obtained by four&#xD;
tests, an individual linear interpolation was plotted. The y-intercept of&#xD;
linear interpolation was the “null delta lactate” equivalent to the critical&#xD;
velocity (CV). To verify the lactate stabilization at CV, the animals were&#xD;
submitted to 25 min of continuous exercise &#xD;
(15, 20, 25 m/min), with blood collection every 5 min. The estimated CV was&#xD;
16.6±0.7 m/min, with significant linear regressions (R=0.90±0.03). The rats&#xD;
presented maximal lactate steady state (MLSS) at 3.9±0.4 mmol/L, at 20 m/min.&#xD;
The CV was less than MLSS but significantly correlated with this parameter&#xD;
(r=0.78). This non-exhaustive test seems to be valid for the aerobic evaluation&#xD;
of sedentary rats and this protocol underestimates the MLSS in 20%. This test&#xD;
seems to be the interesting method for the evaluation of rats submitted to&#xD;
acute exercise or physical training.
&lt;br/&gt;
&lt;br/&gt;Page(s): 781-785</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/12866">
    <title>Novel substrate (algal protein) for cultivation of &lt;i style=""&gt;Rhodospirillum rubrum&lt;/i&gt;</title>
    <link>http://nopr.niscair.res.in/handle/123456789/12866</link>
    <description>Title: Novel substrate (algal protein) for cultivation of &lt;i style=""&gt;Rhodospirillum rubrum&lt;/i&gt;
&lt;br/&gt;
&lt;br/&gt;Authors: Vatsala, T M; Rekha, R; Srividhya, R
&lt;br/&gt;
&lt;br/&gt;Abstract: &lt;i style=""&gt;Rhodospirillum&#xD;
rubrum&lt;/i&gt; was grown under light anaerobic conditions&#xD;
with phycocyanin (C-pc) extracted from &lt;i style=""&gt;Spirulina&#xD;
platensis &lt;/i&gt;as the sole source of carbon and nitrogen&lt;i style=""&gt;.&lt;/i&gt; When grown under these conditions cellular components like&#xD;
lipids, carbohydrates, protein, carotenoids, bacteriochlorophyll were similar&#xD;
to the one grown with malic acid and ammonium chloride. Growth of &lt;i style=""&gt;R. rubrum&lt;/i&gt; increased with increase in&#xD;
concentration of C-pc (200 to 1000 mg/l). &lt;i style=""&gt;R.&#xD;
rubrum&lt;/i&gt; also utilized C-pc under dark anaerobic condition. With both malic&#xD;
acid and C-pc as carbon sources C-pc was consumed only after exhaustion of&#xD;
malic acid under light anaerobic condition. No aberration of cell morphology&#xD;
was seen under scanning electron microscope (SEM). &lt;i style=""&gt;R. rubrum&lt;/i&gt; utilized both phycocyanobilin and phycoprotein individually&#xD;
as well as in combination. When grown with 1000 mg/l of phycoprotein 450 mg/l&#xD;
of biomass was obtained, and with combination of phycocyanobilin (75 mg/l) and&#xD;
phycoprotein (925 mg/l) 610 mg/l of biomass was obtained. Phycocyanobilin alone&#xD;
did not inhibit the growth of &lt;i style=""&gt;R. rubrum&lt;/i&gt;.&#xD;
Utilization of C-pc with protease like activity was observed in plate assay.&#xD;
Protease like activity was also observed as zones around the colonies in plates&#xD;
containing sterilized casein, gelatin and filter sterilized bovine serum&#xD;
albumin. No amino acids were detected in the supernatant when analyzed with&#xD;
ninhydrin. Extracellular protease like activity was highest when C-pc was used&#xD;
as substrate (2.8 U/ml). Intracellular protease like activity was not detected&#xD;
in cell free extracts.
&lt;br/&gt;
&lt;br/&gt;Page(s): 773-780</description>
  </item>
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