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    <title>NISCAIR Online Periodicals Repository Collection: IJBT Vol.08(3) [July 2009]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/4733</link>
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      <title>Biodegradation of leaf litter of tree species in presence of cow dung and earthworms</title>
      <link>http://nopr.niscair.res.in/handle/123456789/4751</link>
      <description>Title: Biodegradation of leaf litter of tree species in presence of cow dung and earthworms
&lt;br/&gt;
&lt;br/&gt;Authors: Sannigrahi, A K
&lt;br/&gt;
&lt;br/&gt;Abstract: The dry leaves of &lt;i&gt;Psidium guajava&lt;/i&gt; Linn., &lt;i&gt;Ficus benghalensis&lt;/i&gt; Linn., &lt;i&gt;Codiaeum variegatum&lt;/i&gt; Linn., &lt;i&gt;Polyalthia longifolia&lt;/i&gt; Sonner., &lt;i&gt;Eucalyptus citriodora&lt;/i&gt; Hook., &lt;i&gt;Caesalpinia pulcherrima&lt;/i&gt; Linn., &lt;i&gt;Syzygium cumini&lt;/i&gt; Linn., &lt;i&gt;Artocarpus heterophyllus&lt;/i&gt; Lamk., &lt;i&gt;Musa paradisiaca&lt;/i&gt; Linn., &lt;i&gt;Plumeria rubra&lt;/i&gt; Linn., &lt;i&gt;Litchi chinensis&lt;/i&gt; Gaertn., &lt;i&gt;Pinus insularis&lt;/i&gt; Endl., &lt;i&gt;Elaeocarpus sphaericus&lt;/i&gt; Gaertn., &lt;i&gt;Bombax ceiba&lt;/i&gt; Linn., &lt;i&gt;Streblus asper&lt;/i&gt; Lour. and &lt;i&gt;Dalbergia sissoo&lt;/i&gt; Roxb. were converted to vermicomposts in about 5 to 8 months while those of &lt;i&gt;Mangifera indica&lt;/i&gt; Linn., &lt;i&gt;Terminalia chebula&lt;/i&gt; Retz., &lt;i&gt;Lagerstroemia speciosa&lt;/i&gt; Linn. and &lt;i&gt;Tectona grandis&lt;/i&gt; Linn. took about 10 months. However, &lt;i&gt;Leucaena leucocephala&lt;/i&gt; Lamk. leaves took only 2 months to become vermicompost. These vermicomposts contained: N, 0.9 to 1.9; P, 0.5 to 1.2; K, 0.9 to 2.5; Na, 0.8 to 3.5; Ca, 0.9 to 4.9 and S, 0.9 to 2.2%. The vermicompost of &lt;i&gt;Bombax ceiba&lt;/i&gt; flowers produced in 3.5 months contained: N, 1.2; P, 0.6; K, 1.8; Na, 1.4; Ca, 0.4 and S, 0.9%. Nutritional status of these vermicomposts varied with the variation of tree species. This information would motivate farmers for vermicomposting of dry leaves instead of burning.
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&lt;br/&gt;Page(s): 335-338</description>
      <pubDate>Sun, 28 Jun 2009 22:58:59 GMT</pubDate>
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      <title>Desiccation of callus enhances somatic embryogenesis and subsequent shoot regeneration in sugarcane</title>
      <link>http://nopr.niscair.res.in/handle/123456789/4750</link>
      <description>Title: Desiccation of callus enhances somatic embryogenesis and subsequent shoot regeneration in sugarcane
&lt;br/&gt;
&lt;br/&gt;Authors: Kaur, Ajinder; Gosal, S S
&lt;br/&gt;
&lt;br/&gt;Abstract: Callus cultures were established in three commercial sugarcane varieties, viz., CoJ 64, CoJ 83 and CoJ 86, from spindle leaf segments on Murashige and Skoog (MS) medium supplemented with 2,4-dichlorophenoxyacetic acid (2,4-D; 4 mg/L) and 6-benzylaminopurine (BAP; 0.5 mg/L). The calli were sub-cultured on MS+2,4-D (2 mg/L)+BAP (0.5 mg/L)+agar (0.8% w/v) medium (control) and MS+2,4-D (2 mg/L)+BAP (0.5 mg/L)+agar (1.6% w/v) medium (treatment) to study the effect of desiccation caused by double agar on somatic embryogenesis. Per cent somatic embryogenesis observed in treatment-calli of sugarcane varieties CoJ 64, CoJ 83 and CoJ 86 was 90, 90.63 and 89.66, respectively; while in control-calli the corresponding figures were 66.67, 64.52 and 63.33. Likewise, shoot regeneration from desiccated calli on MS+BAP (0.5 mg/L) medium was also higher over non-desiccated control, i.e., 84.27, 86.52 and 83.13% as compared to 54.35, 56.25 and 50.38%, respectively in CoJ 64, CoJ 83 and CoJ 86. Thus, this fairly simple double agar medium provided an alternative method for improving somatic embryogenesis and, hence, regeneration frequency of sugarcane callus.
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&lt;br/&gt;Page(s): 332-334</description>
      <pubDate>Sun, 28 Jun 2009 22:58:59 GMT</pubDate>
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      <title>An efficient &lt;i&gt;in vitro&lt;/i&gt; protocol for clonal multiplication of Ginger – var. Varada</title>
      <link>http://nopr.niscair.res.in/handle/123456789/4749</link>
      <description>Title: An efficient &lt;i&gt;in vitro&lt;/i&gt; protocol for clonal multiplication of Ginger – var. Varada
&lt;br/&gt;
&lt;br/&gt;Authors: Kavyashree, R
&lt;br/&gt;
&lt;br/&gt;Abstract: An efficient, &lt;i style=""&gt;in vitro &lt;/i&gt;multiplication protocol was developed for &lt;i style=""&gt;Zingiber officinale &lt;/i&gt;Rosc., var. Varada through direct regeneration of vegetative buds. Multiple shoots were induced from vegetative buds on LSBM fortified with BAP (17.76 μ&lt;i style=""&gt;M&lt;/i&gt;) with 96% initiation response. The repeated subculture resulted in rapid shoot multiplication at the average rate of 4-fold per culture. The well-developed multiple shoots formed roots on the same medium after 2-3 passages of subculture, thus eliminating the step of &lt;i style=""&gt;in vitro &lt;/i&gt;rooting. The statistical data pertaining to multiple shoot and root formation revealed highest mean number of 19.1 and 12.3, respectively. The regenerated plantlets were successfully established in the field with 86% survival frequency after few days of indoor acclimatization.
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&lt;br/&gt;Page(s): 328-331</description>
      <pubDate>Sun, 28 Jun 2009 22:58:59 GMT</pubDate>
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    <item>
      <title>Growth and shoot proliferation in &lt;i style=""&gt;Chlorophytum borivilianum &lt;/i&gt;Sant. et Fernand.  &lt;i style=""&gt;in vitro&lt;/i&gt; under different carbon dioxide environment</title>
      <link>http://nopr.niscair.res.in/handle/123456789/4748</link>
      <description>Title: Growth and shoot proliferation in &lt;i style=""&gt;Chlorophytum borivilianum &lt;/i&gt;Sant. et Fernand.  &lt;i style=""&gt;in vitro&lt;/i&gt; under different carbon dioxide environment
&lt;br/&gt;
&lt;br/&gt;Authors: Joshi, N; Dave, A; Vyas, S; Purohit, S D
&lt;br/&gt;
&lt;br/&gt;Abstract: &lt;smarttagtype namespaceuri="urn:schemas-microsoft-com:office:smarttags" name="metricconverter"&gt; &lt;i style=""&gt;In vitro&lt;/i&gt; growth and shoot proliferation in&lt;i style=""&gt; Chlorophytum borivilianum &lt;/i&gt;Sant. et Fernand. were studied in a controlled CO&lt;sub&gt;2&lt;/sub&gt; environment. The cultures were grown on BA supplemented MS medium with or without 3% sucrose. A range of CO&lt;sub&gt;2&lt;/sub&gt; concentrations (0.0, 0.6, 10.0 and 40.0 g m&lt;sup&gt;-3&lt;/sup&gt;) was controlled in small chambers by using solutions of NaHCO&lt;sub&gt;3&lt;/sub&gt;, Na&lt;sub&gt;2&lt;/sub&gt;CO&lt;sub&gt;3&lt;/sub&gt;, KHCO&lt;sub&gt;3&lt;/sub&gt; and K&lt;sub&gt;2&lt;/sub&gt;CO&lt;sub&gt;3&lt;/sub&gt;. In order to maintain a CO&lt;sub&gt;2&lt;/sub&gt;-free environment, a saturated solution of KOH was kept in the chambers. It was observed that the growing shoot cultures required either sucrose in the medium as a carbon source or an environment with controlled CO&lt;sub&gt;2&lt;/sub&gt; concentration. Complete absence of a carbon source caused severe yellowing of shoots and death within 15 d. The growth of shoot cultures at 40.0 g m&lt;sup&gt;-3&lt;/sup&gt; CO&lt;sub&gt;2 &lt;/sub&gt;was comparable to the growth obtained with 3.0% sucrose in the medium. With both CO&lt;sub&gt;2&lt;/sub&gt; and sucrose being available, the best response was obtained at 40.0 g m&lt;sup&gt;-3&lt;/sup&gt; CO&lt;sub&gt;2&lt;/sub&gt; in the chamber. At this concentration the increase in number of shoots was nearly double the standard rate obtained when exposed to the natural CO&lt;sub&gt;2&lt;/sub&gt; level and sucrose supplemented medium. Total fresh and dry wt and shoot number were the maximum under this condition. &lt;/smarttagtype&gt;
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&lt;br/&gt;Page(s): 323-327</description>
      <pubDate>Sun, 28 Jun 2009 22:58:59 GMT</pubDate>
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