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<title>Volume 20 Year 2016</title>
<link>http://dr.lib.sjp.ac.lk/handle/123456789/6898</link>
<description/>
<pubDate>Wed, 07 Jan 2026 05:57:16 GMT</pubDate>
<dc:date>2026-01-07T05:57:16Z</dc:date>
<item>
<title>Novel member of Ras family proteins from Disk Abalone (Haliotis discus discus): Structural profiling and its transcriptional modulation under host pathologic conditions</title>
<link>http://dr.lib.sjp.ac.lk/handle/123456789/6936</link>
<description>Novel member of Ras family proteins from Disk Abalone (Haliotis discus discus): Structural profiling and its transcriptional modulation under host pathologic conditions
Elvitigala, D. A. S.; Premachandra, H. K. A; Wan, Q.; Lim, B.; Jung, H.; Choi, C. Y.; Lee, J.
Among small GTPases, the Ras family proteins capture a remarkable place in dictating&#13;
cellular proliferation, differentiation and survival in development of an organism. Major&#13;
members of the Ras family include Ras (H-Ras, K-Ras, N-Ras), Rap1, and Rap2, all of&#13;
which can act as oncogenes upon mutation. In the present study, a novel Ras family&#13;
protein (AbRFP) was characterized from Disk Abalone (Haliotis discus discus), an&#13;
economically important, edible marine gastropod; further analyzing its transcriptional&#13;
profile in healthy and immune-challenged animals. The full-length cDNA of AbRFP is&#13;
2704 bp and it consists of an open reading frame of 552 bp, encoding a 184 amino acid&#13;
peptide with a calculated molecular mass of ~21 kDa and isoelectric point of 8.63. The&#13;
amino acid sequence resembles the characteristic features of typical Ras family proteins,&#13;
including GTP/Mg2+ binding sites and guanine nucleotide exchange factor (GEF)&#13;
interaction sites, as predicted by the NCBI-conserved domain database server.&#13;
Phylogenetic study of AbRFP showed the generally accepted relationships, with AbRFP&#13;
exhibiting highest proximity to a Ras protein from Portuguese oyster. Quantitative realtime&#13;
PCR detected ubiquitous AbRFP mRNA expression, with strongest levels in muscle&#13;
along with mantle and the lowest level in hepatopancreas. The AbRFP transcriptional&#13;
profile in gills of Abalone challenged with Vibrio parahaemolyticus or viral hemorrhagic&#13;
septicemia virus (VHSV) demonstrated significant up-regulations (p &lt; 0.05) at 12 h and&#13;
24 h post-injection (p.i.), respectively. Moreover, significant elevation (p &lt; 0.05) of&#13;
mRNA expression was detected in hemocytes at 72 h p.i. with V. parahaemolyticus.&#13;
These findings suggest that AbRFP may play a role under pathological conditions in Disk&#13;
Abalone.
</description>
<pubDate>Fri, 01 Jan 2016 00:00:00 GMT</pubDate>
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<dc:date>2016-01-01T00:00:00Z</dc:date>
</item>
<item>
<title>Towards a Steady State Economy in Sri Lanka</title>
<link>http://dr.lib.sjp.ac.lk/handle/123456789/6935</link>
<description>Towards a Steady State Economy in Sri Lanka
Wijeratne, A. T.; Dias, P.; Adhikari, N.
In general, it is desired that Sri Lankan economy shows growth. A growing economy&#13;
brings waste production which leads environmental pollutions such as air pollution water&#13;
pollution etc. At present, increasing population in Sri Lanka requires more natural&#13;
resources to meet the market demand. The ultimate result is an imbalance in the&#13;
biological cycles, and an irreversible change in both economic process and environment.&#13;
An irreversible economic process increases entropy. Ultimately, the entropy will reach its&#13;
maximum value. Then everything will become standstill since there would not exist more&#13;
energy to continue the economic process. As a solution, the concept of a steady state&#13;
economy is structured.Sri Lankan economy was assessed within steady state economics&#13;
to evaluate the present economic situation of Sri Lanka. A statistical analysis was carried&#13;
out on Gross Domestic Product (GDP), population, energy use, CO2 emission through&#13;
time series analysis and regression analysis,to identify the extent to which Sri Lankan&#13;
economy has deviated from a steady state economy. Regression analysis indicates a&#13;
strong relationship between GDP and CO2 emission. Total population size in Sri Lanka is increased from 9.9 million in 1960 to 20.48 million in 2013. CO2 emission per capita is&#13;
increased from 0.25 metric tons in 1960 to 0.65 metric tons in 2010. CO2 emission is&#13;
increased from 2259 kiloton in 1960 to 12831 kiloton in 2010. Rapid growth rates, CO2 emissions, population growth rates reveal that Sri Lankan&#13;
economy is far apart from the concept of steady state.Transition to a steady state&#13;
economy would require the implementation of new policies to restrict the utilization of&#13;
nonrenewable resources. On the other hand it is mandatory to have legal regulations&#13;
encouraging renewable resource use, energy efficiency, and reuse and recycling.
</description>
<pubDate>Fri, 01 Jan 2016 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://dr.lib.sjp.ac.lk/handle/123456789/6935</guid>
<dc:date>2016-01-01T00:00:00Z</dc:date>
</item>
<item>
<title>Nucleotide Sequence and Secondary Structure Variations in ITS2-rDNA Region of the Members of Anopheles culicifacies (Diptera: Culicidae) Species Complex</title>
<link>http://dr.lib.sjp.ac.lk/handle/123456789/6934</link>
<description>Nucleotide Sequence and Secondary Structure Variations in ITS2-rDNA Region of the Members of Anopheles culicifacies (Diptera: Culicidae) Species Complex
Shanika, K.H.S.; Harischandra, I.N.; De Silva, B.G.D.N.K.
Anopheles culicifacies, major vector of malaria in Sri Lanka is a five member species&#13;
complex. Differences of the vector competence of siblings, is still poorly delineated.&#13;
Therefore, the current study was carried out to observe any relationship of the variations&#13;
in vector competence to ITS2 nucleotide sequences and secondary structure&#13;
characteristics of the species complex. DNA was extracted from sibling species B and E,&#13;
the ITS2 region was amplified and sequenced. Sequences for A, C and D siblings were&#13;
retrieved from NCBI GenBank. The complex divided into two groups, AD and BCE&#13;
based on primary and secondary structure of the ITS2 sequences. Secondary structures of&#13;
all species had three helices where pyrimidine-pyrimidine mismatch in Helix II and a&#13;
UUUGG motif at 5‘ of Helix III were displayed only for B, C and E. Among five types of&#13;
loops, interior and exterior loops were more conserved than other loop types. Results&#13;
showed the major vector sibling E and poor or non vector sibling B shares identical&#13;
nucleotide sequence and secondary structure. Therefore, ITS2 secondary structure is&#13;
independent of the vector competence of the sibling species.
</description>
<pubDate>Fri, 01 Jan 2016 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://dr.lib.sjp.ac.lk/handle/123456789/6934</guid>
<dc:date>2016-01-01T00:00:00Z</dc:date>
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<item>
<title>Android Application: Sound Pressure Level Meter and Frequency Spectrum Analyzer</title>
<link>http://dr.lib.sjp.ac.lk/handle/123456789/6933</link>
<description>Android Application: Sound Pressure Level Meter and Frequency Spectrum Analyzer
Bandara, N. D. N. C.; Wanniarachchi, W. K. I. L.
In this paper we present the development of Sound Pressure Level Meter and Frequency&#13;
Spectrum Analyzer application for Android based devices. The developed application can&#13;
visualize real time waveform and frequency spectrum of an input audio signal in both&#13;
linear and dB scale. The GPS location, current date and time are also embedded to the&#13;
application for convenience. A comparison was carried out with currently available&#13;
smartphone apps of similar type and the results are in good agreement with the app&#13;
developed in this project. The current version of the app is capable of capturing signal of&#13;
maximum frequency up to 4000Hz. Therefore, analysis of frequency spectrum of the&#13;
voice transmission which range between 300Hz to 3400Hz can be carried out&#13;
successfully.
</description>
<pubDate>Fri, 01 Jan 2016 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://dr.lib.sjp.ac.lk/handle/123456789/6933</guid>
<dc:date>2016-01-01T00:00:00Z</dc:date>
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