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<title>Basic and Applied Sciences</title>
<link>https://ir.kdu.ac.lk/handle/345/6719</link>
<description/>
<pubDate>Mon, 06 Apr 2026 10:53:16 GMT</pubDate>
<dc:date>2026-04-06T10:53:16Z</dc:date>
<item>
<title>Estimation of Phenolic Content, Flavonoid Content, and Antioxidant Activities of Selected Fruits in Sri Lanka</title>
<link>https://ir.kdu.ac.lk/handle/345/6915</link>
<description>Estimation of Phenolic Content, Flavonoid Content, and Antioxidant Activities of Selected Fruits in Sri Lanka
Dharmasiri, PGNH; Samarakoon, KW; Ranasinghe, P; Jayasooriya, PT
The aim of this study was to evaluate the Total Phenolic Content (TPC), Total Flavonoid&#13;
Content (TFC), and in vitro antioxidant activity, of six underutilized fruits in Sri Lanka.&#13;
The selected fruits are Elaeocarpus angustifolius L (Ceylon blue olive), Elaeocarpus serratus&#13;
L (Veralu), Manikara zapota L (Sapadilla), Ziziphus mauritiana L (Masan), Flacourtia&#13;
indica L (Ugurassa) , and Garcinia xanthochymus L (Ratagoraka). The fruit extracts&#13;
were prepared with 100% methanol, and crude extract (CE) of fruit was fractionated into&#13;
hexane (HX), ethyl acetate (EA), and aqueous (AQ ). TFC and TPC of each fraction were&#13;
determined by aluminium chloride colourimetric and Folin-ciocalteu methods using 96&#13;
well microplates respectively. Antioxidant activities were determined using Ferric reducing&#13;
power (FRAP), and Oxygen radical absorbance capacity (ORAC) assay methods. Among&#13;
different fractions, the highest TPC and TFC were found in AQ of veralu (377.57 ± 65.65&#13;
mg GAE/ g of extract), CE of Masan (357.04 ± 9.63 mg GAE/ g of extract), EA of&#13;
Ugurassa (173.47 ± 18.891 mg GAE/ g of extract), and EA of Ceylon blue olive (49.14 ±&#13;
1 .60 mg QE / g of extract). The highest FRAP was found in AQ of Ugurassa (745.90 ±&#13;
23.06 mg TE/ g of extract), CE of Veralu (668.75 ± 7.7 mg TE/ g of extract), and EA of&#13;
Ratagoraka (650.51 ± 6.88 mg TE/ g of extract). The highest ORAC was shown in AQ&#13;
of Ratagoraka (113.72 ± 17.78 mg TE/ g of extract), CE of Veralu (31.38 ± 0.25 mg TE/&#13;
g of extract), and EA of Ratagoraka (143.24 ± 3.09 mg TE/ g of extract). In conclusion,&#13;
Sapadilla, Ratagoraka, and Veralu possessed the highest antioxidant capacity compared&#13;
to other fruit types. Thus, the CE fraction of Masan, the AQ fraction of Ugurassa, and&#13;
the EA fractions of Ratagoraka will be good sources of antioxidants for the formulation&#13;
of food supplements.
</description>
<pubDate>Fri, 01 Sep 2023 00:00:00 GMT</pubDate>
<guid isPermaLink="false">https://ir.kdu.ac.lk/handle/345/6915</guid>
<dc:date>2023-09-01T00:00:00Z</dc:date>
</item>
<item>
<title>Application of the Peak-to-Valley Method for in-situ Gamma Spectroscopy Using NaI(Tl) Detector</title>
<link>https://ir.kdu.ac.lk/handle/345/6914</link>
<description>Application of the Peak-to-Valley Method for in-situ Gamma Spectroscopy Using NaI(Tl) Detector
Rodrigo, Y; Sumithrarachchi, CS; Lamabadusuriya, MR
The depth distribution in soil is required to quantify the radioactivity in environment&#13;
using in-situ gamma spectroscopy. The conventional approach to determining depth&#13;
distribution is the core sampling method, which requires samples from several depths&#13;
in the soil and is a time-consuming process. In-situ gamma spectroscopy can be used&#13;
as a rapid and e cient way to quantify radioactivity in large areas. The Peak-to-Valley&#13;
(PTV) method which is based on the attenuation of gamma rays through matter, emerges&#13;
as a novel approach, enabling the derivation of depth distribution information from insitu&#13;
gamma spectra without having core samples. The present study aimed to validate&#13;
the PTV method using the NaI(Tl) detector and obtained a correlation between the PTV&#13;
ratio and depth distribution. Water was used as the attenuation medium to create different&#13;
depths and 137Cs and 40K sources were kept at different depths. The NaI(Tl) detector was&#13;
used to measure spectra at each depth and calculated the PTV ratios. The results show&#13;
a higher correlation of 2nd order between the PTV ratio and the depth for both 137Cs&#13;
and 40K. It reveals that the PTV ratio of the in-situ gamma spectrum can be used to&#13;
derive the depth distribution parameter. The relationship between the PTV ratio and&#13;
the depth distribution parameter was obtained for several locations. This relationship is&#13;
used for calibrating in-situ gamma detector which can be used in a similar environment&#13;
to determine radioactivity.
</description>
<pubDate>Fri, 01 Sep 2023 00:00:00 GMT</pubDate>
<guid isPermaLink="false">https://ir.kdu.ac.lk/handle/345/6914</guid>
<dc:date>2023-09-01T00:00:00Z</dc:date>
</item>
<item>
<title>Identification of Pathogenic Bacteria (Escherichia coli) in Drinking Water Sources and Detection of their Antibiotic Resistant Genes in Gampaha District, Sri Lanka</title>
<link>https://ir.kdu.ac.lk/handle/345/6913</link>
<description>Identification of Pathogenic Bacteria (Escherichia coli) in Drinking Water Sources and Detection of their Antibiotic Resistant Genes in Gampaha District, Sri Lanka
Wijesooriya, R; Perera, ODK; Bodhinayaka, VA
Water plays a critical role on Earth, and its significance is particularly evident in relation&#13;
to human beings. The present study aimed to identification of Escherichia coli and&#13;
detection of their antibiotic resistant genes in drinking water sources of five different&#13;
regions Gampaha district, Sri Lanka. Five resources of randomly collect drinking water&#13;
samples (n = 50) from every 10 samples from five different regions were used for analysis.&#13;
The pathogenic microorganisms were isolated via membrane filtration technique (0.45&#13;
µm) and identified via conventional standard biochemical keys including Indole, Citrate,&#13;
MRVP, TSI, Motility and Chromogenic culture and Gram stain. The DNA extraction&#13;
was performed via column-based method. The disk diffusion method was performed to&#13;
access the antibiotic sensitivity of the isolated Escherichia coli following CLSI guidelines&#13;
via Ampicillin, Gentamicin and Tetracycline antibiotics (10 mg). From total sample 18%&#13;
were positive with Escherichia coli in unprotected well, protected well and tap line samples.&#13;
All nine samples exhibit resistance to Ampicillin (&lt; 13 mm), sensitive to the Gentamicin&#13;
(&gt; 15 mm) and resistant to Tetracycline (&lt; 11 mm). Molecular determination, 2% agarose&#13;
gel image, confirmed the presence of E. coli DNA as evidenced by the presence 400&#13;
base pairs (bp) band size and UidA gene found in one sample confirmed the presence of&#13;
different strains of isolated E. coli. The specific antibiotic resistant genes were analyzed&#13;
and all three samples were negative for the tet (a), tet (C), tet (m) and blaTEM antibiotic&#13;
resistant genes which confirms that isolated E. coli were not resistant for the Tetracycline&#13;
and Ampicillin due to mentioned genes.
</description>
<pubDate>Fri, 01 Sep 2023 00:00:00 GMT</pubDate>
<guid isPermaLink="false">https://ir.kdu.ac.lk/handle/345/6913</guid>
<dc:date>2023-09-01T00:00:00Z</dc:date>
</item>
<item>
<title>Morphological, Vocal, and Genetic Characterization of Motacilla flava – tschutschensis Allospecies Complex in Sri Lanka</title>
<link>https://ir.kdu.ac.lk/handle/345/6912</link>
<description>Morphological, Vocal, and Genetic Characterization of Motacilla flava – tschutschensis Allospecies Complex in Sri Lanka
Samarasinghe, RMNS; Allport, G; Weerakkody, SN; Gunasekara, VR; Seneviratne, SS
Yellow wagtail complex was long considered a single species (Motacilla flava). Recent&#13;
phylogenetic studies however, split this species into two; the Western Yellow Wagtail&#13;
(Motacilla flava) and the Eastern Yellow Wagtail (Motacilla tschutschensis). Until 2020, there&#13;
were no records of the Eastern Yellow Wagtail in Sri Lanka. Nonetheless, using several&#13;
vocal, plumage, and a single genetic marker, a study in 2021 indicated that the Eastern&#13;
Yellow Wagtail is wintering in Sri Lanka. In the present study, the yellow wagtail complex&#13;
in Sri Lanka was critically evaluated using an assortment of phenotypic and genetic&#13;
characteristics obtained from live-caught birds. The phylogenetic affinities of yellow&#13;
wagtails wintering in Sri Lanka were constructed using Maximum likelihood inference and&#13;
Bayesian inference using the mitochondrial ND2 gene region as the genetic marker. The&#13;
morphological and vocal variations between Eastern (n = 15) and Western (n = 11) yellow&#13;
wagtails were analyzed through the ANOVA test and the principal component analysis&#13;
(PCA). The molecular phylogenetic trees and the number of peaks at the downstroke of&#13;
the first flight call (p = 0.00015) of the yellow wagtail reveal that both Eastern and Western&#13;
yellow wagtails are wintering in Sri Lanka. However, the morphological characteristics&#13;
failed to separate the two species into two distinct clusters (Fn=26 = 3.9816, p = 0.0147).&#13;
Our study revealed the migratory occurrence of both the Western Yellow and the Eastern&#13;
Yellow wagtails in Sri Lanka. The studied Eastern Yellow Wagtails clustered to the North&#13;
Asian tschutschensis clade.
</description>
<pubDate>Fri, 01 Sep 2023 00:00:00 GMT</pubDate>
<guid isPermaLink="false">https://ir.kdu.ac.lk/handle/345/6912</guid>
<dc:date>2023-09-01T00:00:00Z</dc:date>
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