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    <title>DSpace Collection:</title>
    <link>http://repository.fuoye.edu.ng:80/handle/123456789/804</link>
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        <rdf:li rdf:resource="http://repository.fuoye.edu.ng:80/handle/123456789/1355" />
        <rdf:li rdf:resource="http://repository.fuoye.edu.ng:80/handle/123456789/1347" />
        <rdf:li rdf:resource="http://repository.fuoye.edu.ng:80/handle/123456789/1335" />
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    <dc:date>2026-04-16T04:42:07Z</dc:date>
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  <item rdf:about="http://repository.fuoye.edu.ng:80/handle/123456789/1355">
    <title>VARIATION IN THE PROTEIN LEVEL OF DIFFERENT ACCESSIONS OF PIGEON PEA (Cajanus cajan L. Millspaugh)</title>
    <link>http://repository.fuoye.edu.ng:80/handle/123456789/1355</link>
    <description>Title: VARIATION IN THE PROTEIN LEVEL OF DIFFERENT ACCESSIONS OF PIGEON PEA (Cajanus cajan L. Millspaugh)
Authors: OLAIYA, Aderonke Eunice; Agbolade, J. O.
Abstract: Ten accessions of Pigeon pea (Cajanus cajan) obtained from National Centre for&#xD;
Genetic Resources and Biotechnology (NACGRAB), Ibadan, Oyo state, were&#xD;
assessed for their genetic and phylogenic relatedness through electrophoretic&#xD;
analysis of the seed proteins. 0.2g of the seeds were weighed and macerated with&#xD;
mortar and pestle in 0.2M phosphate buffer containing 0.133M of acid (NaH2PO4)&#xD;
and 0.067 of base (Na2HPO4) at Ph 6.5.Protein characterization with standard&#xD;
marker revealed that the seeds of the 10 accessions contained proteins (B.S.A,&#xD;
Oval Albumin, Pepsinogen, Trypsinogen and Lysozyme) with molecular weights&#xD;
ranging from 66 and above kda, 45 – 65 kda, 44 – 33 kda, 32-24 kda and 23-14 kda&#xD;
respectively.
Description: All the accessions had at least two proteins and two major bands in&#xD;
common. The study revealed intraspecific similarities and genetic diversity in&#xD;
protein contents among the ten accessions of pigeon pea (Cajanus cajan).</description>
    <dc:date>2015-10-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://repository.fuoye.edu.ng:80/handle/123456789/1347">
    <title>ESTABLISHING A METHOD FOR THE MASS PROPAGATION OF Piper guineense (Schumach) VIA TISSUE CULTURE</title>
    <link>http://repository.fuoye.edu.ng:80/handle/123456789/1347</link>
    <description>Title: ESTABLISHING A METHOD FOR THE MASS PROPAGATION OF Piper guineense (Schumach) VIA TISSUE CULTURE
Authors: Ogechi Tope, OKAFOR; PROF. S.V.A., UZOCHUKWU
Abstract: Piper guineense (Schumach) has great potentials for economic exploration because of the&#xD;
proven use of its medicinal content in human health. The plant material is usually&#xD;
obtained from thick forests by women who have to walk long distances in the bush to&#xD;
reach it. A technique that improves its propagation and domestication, such as tissue&#xD;
culture, becomes necessary. This study was therefore initiated to develop a method for&#xD;
the mass propagation of Piper guineense seedlings using in vitro regeneration. Plants&#xD;
react differently to media concentrations and constituents for their in vitro regeneration.&#xD;
Comparative growth of Piper guneensee inoculated on Murashige and Skoog(MS)&#xD;
medium supplemented with some growth regulators were investigated. Mature nodes&#xD;
were collected from the medicinal garden of National Centre for Genetic Resources and&#xD;
Biotechnology (NACGRAB) Ibadan. Nodes of the species were inoculated onto MS&#xD;
media.
Description: The MS media was supplemented with the following concentrations of growth&#xD;
regulators 0.25, 0.50, 0.75, 1.0mg/l. BAP, the same concentration for KIN and 0.05mg/l&#xD;
of NAA for all replicate. After two weeks of inoculation it was observed that, the plant let&#xD;
with BAP 0.50mg/l +NAA 0.05mg/l were found contamination-free and sprouted, while&#xD;
other treatments showed contamination including control. Furthermore, after 7 days the&#xD;
sprouted, plantlets with treatment of BAP 0.50mg/l +NAA 0.05mg/l were also&#xD;
contaminated, thereby yielding no positive result. Many repeats of the experiment also&#xD;
yielded contaminated products.</description>
    <dc:date>2015-10-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://repository.fuoye.edu.ng:80/handle/123456789/1335">
    <title>COMPARATIVE STUDY OF VEGETATIVE AND FRUIT MOPHOLOGY OF FOUR VARIETIES OF OKRA (Abelmoschus escululentus(L.) moench)</title>
    <link>http://repository.fuoye.edu.ng:80/handle/123456789/1335</link>
    <description>Title: COMPARATIVE STUDY OF VEGETATIVE AND FRUIT MOPHOLOGY OF FOUR VARIETIES OF OKRA (Abelmoschus escululentus(L.) moench)
Authors: MONSURAT OMOTOLA, IYIOLA; Prof. B.O., Akinyele
Abstract: Comparative study of vegetative and fruit morphology of four varieties of okra (Abelmoschus&#xD;
esculentus (L.)Moench was investigated in the screen house of the Department of plant science&#xD;
and biotechnology, Federal University of Oye-Ekiti. Two seeds of each okra variety were sown&#xD;
in a 5L plastic bucket, each treatment was replicated five times. Seedlings were thinned to one&#xD;
plant per stand four weeks after sowing. The growing plants were adequately watered at an&#xD;
interval of three days. At the stage of flower and fruit production, the leaf length, leaf width,&#xD;
plant height, length of leaf stalk, leaf stalk girth, stem girth were measured with a tape graduated&#xD;
in centimeters. Stem thickness was measured with meter rule and the number of leaves per stand&#xD;
was counted. Pods were harvested at full maturity and the pod length was measured using a tape&#xD;
graduated in centimeters. Pod thickness was measured with meter rule; the number of seeds per&#xD;
pod was counted.
Description: Pod weight and seed weight were taken using a weighing balance. Data&#xD;
collected were subjected to analysis of variance (ANOVA) and means were separated using the&#xD;
Duncan multiple range test (DMRT). Seven (7) of the eleven characters investigated were found&#xD;
to be significantly different that is they are not stable while the remaining four (4) has no&#xD;
significant difference indicating their stability</description>
    <dc:date>2015-10-01T00:00:00Z</dc:date>
  </item>
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