scholarly journals Morphological characterization of local and introduced finger millet (Elusine coracana (L.) Gaertn) germplasm in Sri Lanka

2018 ◽  
Vol 29 (2) ◽  
pp. 167
Author(s):  
W. M. R. Kumari ◽  
D. K. N. G. Pushpakumara ◽  
W. M. W. Weerakoon ◽  
D. M. J. B. Senanayake ◽  
H. D. Upadhyaya
Planta Medica ◽  
2010 ◽  
Vol 76 (05) ◽  
Author(s):  
APPR Amarasinghe ◽  
RP Karunagoda ◽  
DSA Wijesundara

Phytotaxa ◽  
2021 ◽  
Vol 513 (3) ◽  
pp. 265-270
Author(s):  
DUILIO IAMONICO ◽  
SINDHU ARYA ◽  
VENUGOPALAN NAIR SARADAMMA ANIL KUMAR

Indobanalia thyrsiflora is an endemic species occurring in peninsular India (Andhra Pradesh, Karnataka, Kerala and Tamil Nadu States) and Sri Lanka. A nomenclatural study of the basionym Banalia thyrsiflora, published by Moquin-Tandon in Candolle’s Prodromus (year 1849), is carried out and the name is lectotypified on a specimen deposited at P (barcode P00609924); isolectotypes are traced at K and CAL. A preliminary morphological characterization of the species is also given, based on field surveys and examination of herbarium specimens. We noted that I. thyrsiflora is highly variable. However, we prefer to avoid, for the moment, taxonomic conclusions about the various morphotypes found, waiting the complete results of this ongoing morphological and molecular investigations.


2015 ◽  
Vol 24 (4) ◽  
pp. 362 ◽  
Author(s):  
S.M.P.C. Padmini ◽  
D.K.N.G. Pushpakumara ◽  
R. Samarasekera

2018 ◽  
Vol 113 (2) ◽  
pp. 96-105
Author(s):  
H.P.T. Sasanka HEWATHILAKE ◽  
N.W.B. BALASOORIYA ◽  
Yoshihiro NAKAMURA ◽  
H.M.T.G.A. PITAWALA ◽  
H.W.M. Athula Chandana WIJAYASINGHE ◽  
...  

2015 ◽  
Vol 25 (1) ◽  
pp. 127
Author(s):  
T.A.B.D. Sanjeewa ◽  
D.K.N.G. Pushpakumara ◽  
U.R. Sangakkara

Author(s):  
B. L. Soloff ◽  
T. A. Rado

Mycobacteriophage R1 was originally isolated from a lysogenic culture of M. butyricum. The virus was propagated on a leucine-requiring derivative of M. smegmatis, 607 leu−, isolated by nitrosoguanidine mutagenesis of typestrain ATCC 607. Growth was accomplished in a minimal medium containing glycerol and glucose as carbon source and enriched by the addition of 80 μg/ ml L-leucine. Bacteria in early logarithmic growth phase were infected with virus at a multiplicity of 5, and incubated with aeration for 8 hours. The partially lysed suspension was diluted 1:10 in growth medium and incubated for a further 8 hours. This permitted stationary phase cells to re-enter logarithmic growth and resulted in complete lysis of the culture.


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