Friday, 20 May 2016
Friday, 15 April 2016
Scarlet bean (Phaseolus coccineus L.): a potential bean for India
Citation:
Singh BK, Gyan GP, Tiwari SK and Singh
B. 2016. Scarlet bean (Phaseolus coccineus
L.): a potential bean for India. In: National Symposium on Vegetable
Legumes for Soil and Human Health (Singh B, Singh M, Rai AB, Singh PM, Prasad
RN, Mishra GP, Singh BK, Ranjan JK, Devi J, Seth T, Nagendran K., Chaukhande P,
Kumar R, Gautam KK, Gujjar RS and Kumar YB Eds). ICAR-IIVR, Varanasi, 12-14
February 2016, pp 162-170.
Email: bksinghkushinagar@yahoo.co.in
Botanically,
the Scarlet bean is Phaseolus coccineus (fay-see-OH-lus
koh-SIN-ee-us), which in Greek meaning “Red Bean”; though the seeds are
multi-colored (In Greek it is: fah-SO-lee KOH-kee-no). It is also
known as Scarlet runner beans, a term that reflects the growth habit and
scarlet/red flowers. The other names by which it is known include, fire-bean,
mammoth, red-giant, scarlet-emperor, runner-bean, multiflora-bean, haricot
d’Espagne, Oregon Lima Bean, Aycoctl by the Aztecs, Ayocote by the Spanish,
case knife bean in England, and Feija da Espanha, feijaescarlata and
feijatrepador in Portugal. The vines are perennial, but not frost hardy, and
are usually grown as a half-hardy annual. It is generally climbing or trailing
type, often grown as an annual crop for dry seeds, immature pods, shelled beans
or as an ornamental plant. The vines may grow to 5-6 m or more in length. It
belongs to the Fabaceae or legume family, and economically occupies the second
position after P. vulgaris because of its highly nutritive
value for humans and animals. The vine bears large
green heart shaped leaves; attractive cluster of bright scarlet flowers,
followed by numerous slender pods of about 10-12 cm long and 2.5-3.0 cm wide
during January through March. The knife-shaped pods are normally green; however, there are very rare varieties
bred by amateurs that have very unusual purple pods. An example of such a
purple-podded runner bean is 'Aeron Purple Star'. The beans are as attractive
as the vines and flowers themselves. Most varieties have
red flowers and multicolored seeds (though some have white
flowers and white seeds), and they are often grown as ornamental plants.
Wednesday, 30 March 2016
Snap bean (Phaseolus vulgaris L.): advances in genetic improvement
Citation:
Singh BK, Lal H, Ranjan JK and Singh B.
2016. Snap bean (Phaseolus vulgaris
L.): advances in genetic improvement. In: National Symposium on Vegetable
Legumes for Soil and Human Health (Singh B, Singh M, Rai AB, Singh PM, Prasad
RN, Mishra GP, Singh BK, Ranjan JK, Devi J, Seth T, Nagendran K., Chaukhande P,
Kumar R, Gautam KK, Gujjar RS and Kumar YB Eds). ICAR-IIVR, Varanasi, 12-14
February 2016, pp 125-136.
E-mail: bksinghkushinagar@yahoo.co.in
Common bean (Phaseolus
vulgaris L.), an important legume, is a rich source of protein, vitamins,
minerals and fibre. The main categories of common beans, on the basis of uses, are
dry beans (seeds harvested at complete maturity), snap beans (tender pods with
reduced fibre harvested before the seed development phase) and shell beans (seeds
harvested at physiological maturity) and. Snap bean is also known as French
bean, garden bean, green bean, edible podded bean, string bean, fresh bean or vegetable
bean. As the name implies, snap beans break easily
when the pod is bent, giving off a distinct audible snap sound. The pods of snap beans (green, yellow and purple in colour) are harvested when they are
rapidly growing, fleshy, tender (not tough and stringy), bright in colour, and
the seeds are small and underdeveloped (8 to 10 days after flowering). After
that period, excessive seed development reduces quality and the pod becomes fibrous,
pithy and tough, and loses its bright colour. Snap bean seeds may also be used in dry static like the dry bean types. In
that case pinto, kidney, pink, small red, etc. terms are used. In India, the
dry bean type varieties are known as rajmash/rajmah, and snap bean named as
rajmah phali in Hindi. Common beans display a wide range of growth habits from
bush determinate to pole indeterminate types. Bush types are the most widely
grown and are a relatively short duration crop; but on the other hand, in
smallholder agriculture or in kitchen garden where land is scarce,
labour-intensive high-yielding climbing beans getting popularity now-a-days. Dry
bean is the largest pulse crop in the world with 23.60 mt of annual production
grown on 29.29 mha area; and the top ten producing countries are Mayanmar (3.90
mt), India (3.63 mt), Brazil (2.79 mt), China (1.46 mt), USA (1.45 mt), Tanzania
(1.20 mt), Mexico (1.08 mt), Kenya (0.61 mt), Ethiopia (0.46 mt) and Rawanda
(0.43 mt). Moreover, snap beans’ global annual production and area is about 20.74
mt and 1.54 mha, respectively with maximum production in China (16.20 mt)
followed by Indonesia (0.87 mt), India (0.62 mt), Turkey (0.61 mt), Thailand
(0.31 mt), Egypt (0.25 mt), Spain (0.17 mt), Italy (0.14 mt), Morocco (0.13 mt)
and Bangladesh (0.09 mt) [FAOSTAT 2012]. In
India, it is grown on an area of about 1 lakh ha mainly in the states of
Maharashtra, Jammu and Kashmir, Himachal Pradesh, Uttarakhand, North-East
hills, Nilgiri (Tamil Nadu), hills of central India, Palni hills (Kerala)
Chickmagalur (Karnataka) and Darjeeling hills (West Bengal). The tender pods of
snap bean are good source of ascorbic acid (vitamin
C), phylloquinone (vitamin K), β-carotene (vitamin A), riboflavin
(vitamin B2), niacin (vitamin B3), Mn, K, Ca, P, Fe and omega-3 fatty acid. It
is a legume crop, do fix some nitrogen but the N fixing bacteria are not active
as with other legumes; therefore there is need to fertilize the field with
nitrogenous fertilizer to harness the yield potential.
References
Acosta-Gallegos JA, Kelly JD and Gepts P. 2007.
Pre-breeding and genetic diversity in common bean (Phaseolus vulgaris). Crop Science 47 (Supplement 3): S44–S59.
Ali MA. 1950. Genetics of resistance to the common
bean mosaic virus in the bean (Phaseolus
vulgaris L.). Phytopathology 40: 69–79.
Andrews
SA. 2013. Snapping green beans.
http://humanelivingnet.net/2013/12/17/snapping-green-beans (accessed on
22.09.2014).
Arumuganathan
K and Earle ED.1991. Nuclear DNA content of some important plant species. Plant
Molecular Biology Reporters 9 (3): 208–218.
Beebe
S, Gonzalez AV and Rengifo J. 2000. Research on trace minerals in the common
bean. Food and Nutrition Bulletin 21: 387–391.
Bellucci
E, Bitocchi E, Rau D, Rodriguez M, Biagetti E, Giardini A, Attene G, Nanni L
and Papa R. 2014. Genomics of origin, domestication and
evolution of Phaseolus vulgaris. In:
Genomics of Plant Genetic Resources- Volume 1 (Tuberosa R, Graner A and Frison E eds.). Springer:
Dordrecht, The Netherlands, pp. 483–507.
Bennett MD and Leitch
IJ. 2010. Plant DNA C-values Database (Release 5.0, Dec. 2010).
Chacon SMI, Pickersgill B and Debouck DG. 2005.
Domestication patterns in common bean (Phaseolus
vulgaris L.) and the origin of the Mesoamerican and Andean cultivated
races. Theoretical and Applied Genetics 110: 432–444.
Debouck
DG, Toro O, Paredes OM, Johnson WC and Gepts P. 1993. Genetic diversity and
ecological distribution of Phaseolus
vulgaris in north-western South America. Economic Botany 47: 408–423.
Delgado-Salinas
A, Bibler R and Lavin M. 2006. Phylogeny of the genus Phaseolus (Leguminosae): A recent diversification in an ancient
landscape. Systematic Botany 31: 779–791.
Drijfhout E, Silbernagel MJD and Burke W. 1978.
Differentiation of strains of bean common mosaic virus. Netherlands Journal of
Plant Pathology 84: 13–26.
Drijfhout E. 1978. Inheritance of temperature-dependent
string formation in common bean (Phaseolus
vulgaris L.). Netherlands Journal of Agricultural Science 26: 99–105.
FAO
2010. The Second Report on the State of the World’s Plant Genetic Resources for
Food and Agriculture. Rome, Italy, pp. 251–252.
FAOSTAT
2012. http://faostat.fao.org/site/567/DesktopDefault.aspx?PageID=567#ancor
(accessed on 28 February 2014).
Federici CT, Ehdaie B and
Wanes JAG. 1990. Domesticated and wild tepary bean: field performance with and
without drought-stress. Agronomy Journal 82: 896–900.
Freytag
GF and Debouck DG. 2002. Taxonomy, Distribution, and Ecology of the Genus Phaseolus (Leguminosae-Papilionoideae)
in North America, Mexico and Central America. Botanical Research Institute of
Texas, Ft. Worth, Texas, USA.
Genchev
D and Kiryakov I. 2002. Inheritance of resistance to white mold disease (Sclerotinia
sclerotiorum (Lib.) de Bary) in A 195 (Phaseolus vulgaris L.). Bulgarian Journal of Agricultural Science 8:
181–187.
Gepts
P and Bliss FA. 1985. F1 hybrid weakness in the common bean: differential
geographic origin suggests two gene pools in cultivated bean germplasm. Journal
of Heredity 76: 447–450.
Gepts P, Kmiecik K, Pereira P and Bliss FA. 1988.
Dissemination pathways of common bean (Phaseolus
vulgaris, Fabaceae) deduced from phaseolin electrophoretic variability I.
The Americas Economic Botany 42: 73–85.
Gepts
P, Osborn TC, Rashka K and Bliss FA. 1986. Phaseolin-protein variability in
wild forms and landraces of the common bean (Phaseolus vulgaris): Evidence for multiple centers of
domestication. Economic Botany 40: 451–468.
Gepts
P. 1998. Origin and evolution of common bean: Past events and recent trends.
HortScience 33: 1124–1130.
Islam
FMA, Basford KE, Jara C, Redden RL and Beebe S. 2002. Seed compositional and
disease resistance differences among gene pools in cultivated common bean.
Genetic Resources and Crop Evolution 49: 285–293.
Kami
J, Velásquez VB, Debouck DG and Gepts P. 1995. Identification of presumed
ancestral DNA sequences of phaseolin in Phaseolus
vulgaris. Proceeding of the National Academy of Sciences of the USA 92:
1101–1104.
Kelly
JD and Vallejo VA. 2004. A comprehensive review of the major genes conditioning
resistance to anthracnose in common bean. HortScience 39: 1196–1207.
Kelly JD. 2004. Advances in common bean improvement: some
case histories with broader applications. Acta Horticulturae 637: 99–122.
Koenig
R, Singh SP and Gepts P. 1990. Novel phaseolin types in wild and cultivated
common bean (Phaseolus vulgaris,
Fabaceae). Economic Botany 44: 50–60.
Kolkman
JM and Kelly JD. 2003. QTL conferring resistance and avoidance to white mold in
common bean. Crop Science 43: 539–548.
Kwapata
K, Nguyen T and Sticklen M. 2012. Genetic transformation of common bean (Phaseolus vulgaris L.) with the Gus
color marker, the Bar herbicide resistance, and the barley (Hordeum vulgare) HVA1 drought tolerance
genes. International Journal of Agronomy Vol. 2012: 1–8.
Leakey
CLA. 1988. Genotypic and phenotypic markers in common bean. In: Genetic
Resources of Phaseolus Beans (Gepts P
ed.). Kluwer Academic Publishers, Boston, USA, pp. 245–327.
Méndez-Vigo
B, Rodríguez-Suárez C, Pañeda A, Ferreira JJ and Giraldez R. 2005. Molecular
markers and allelic relationships of anthracnose resistance gene cluster B4 in
common bean. Euphytica 141: 237–245.
Miklas
PN, Kelly JD, Beebe SE and Blair MW. 2006. Common bean breeding for resistance
against biotic and abiotic stresses: from classical to MAS breeding. Euphytica
147: 106–131.
Myers
JR and Baggett JR. 1999. Improvement of snap bean. In: Common Bean Improvement
in the Twenty-first Century (Singh SP ed.). Kluwer Academic Press, Dordrecht,
The Netherlands, pp. 289–329.
Paredes
M and Gepts P. 1995. Extensive introgression of Middle American germplasm into
Chilean common bean cultivars. Genetic Resources and Crop Evolution 42: 29–41.
Prakken
R. 1934. Inheritance of colors and pod characters in Phaseolus vulgaris L. Genetica 16: 177–294.
Ram
HH. 2005. Vegetable breeding: principle and practices. 2nd Revision,
Kalyani Publishers, Ludhiana, India, pp 256–273.
Schmit
V, Jardin P, Baudoin JP and Debouck DG. 1993. Use of chloroplast DNA
polymorphisms or the phylogenetic study of seven Phaseolus taxa including P.
vulgaris and P. coccineus.
Theoretical and Applied Genetics 87: 506–516.
Sicard D, Michalakis Y, Dron M
and Neema C. 1997. Genetic diversity and pathogenic variation of Colletotrichum lindemuthianum in the
three centers of diversity of its host, Phaseolus
vulgaris. Phytopathology 87: 807–813.
Silbernagel
MJ. 1986. Snap bean breeding. In: Breeding Vegetable Crops (Bassett MJ Ed.).
AVI Publication Co., Westport, Connecticut, USA, pp. 243–282.
Singh
BK, Deka BC and Ramakrishna Y. 2014. Genetic variability, heritability and
interrelationships in pole-type French bean (Phaseolus vulgaris L.). Proceedings of the National Academy of
Sciences, India Section B: Biological Sciences 84(3): 587–592.
Singh BK, Pathak KA, Ramakrishna Y, Verma VK and Deka BC.
2011. Purple-podded French bean with high antioxidant content. ICAR News: A
Science and Technology Newsletter 17 (3): 9.
Singh BK, Ramakrishna Y, Verma VK and Singh SB.
2013. Vegetable cultivation in Mizoram: status, issues and sustainable
approaches. Indian Journal of Hill Farming 26 (1): 1–7.
Singh BK, Sharma SR and Singh B. 2009. Combining
ability for superoxide dismutase, peroxidase and catalase enzymes in cabbage
head (Brassica oleracea var. capitata L). Scientia Horticulturae
122 (2): 195–199.
Singh BK, Sharma SR and Singh B. 2010. Heterosis
for superoxide dismutase, peroxidase and catalase enzymes in the heads of
cabbage (Brassica oleracea var. capitata L). Journal of Genetics
89 (2): 217–221.
Singh BK. 2014. VRFBB-91: A French bean (Phaseolus
vulgaris) germplasm for earliness. Vegetable Newsletter 1 (1): 5.
Singh
SP, Gepts P and Debouck DG. 1991a. Races of common bean (Phaseolus vulgaris, Fabaceae). Economic Botany 45: 379–396.
Singh SP, Gutierrez JA, Molina A, Urrea C and Gepts P.
1991b. Genetic diversity in cultivated common bean. II. Marker-based analysis
of morphological and agronomic traits. Crop Science. 31: 23–29.
Singh SP, Nodari R and Gepts P. 1991c. Genetic diversity
in cultivated common bean. I. Allozymes. Crop Science 31: 19–23.
Singh
SP. 2001. Broadening genetic base of common bean cultivars: A review. Crop
Science 41: 1659–1675.
Skroch
PW and Nienhuis J. 1995. Qualitative and quantitative characterization of RAPD
variation among snap bean genotypes (Phaseolus
vulgaris L.). Theoretical and Applied Genetics 91: 1078–1085.
Sofkova
S, Poryazov I and Kiryakov I. 2010. Breeding green beans (Phaseolus vulgaris L.) for complex disease resistance. Genetics and
Breeding 38 (3): 77–88.
Yu K, Chun S and Zhang BL. 2012. Development and
application of molecular markers to breed common bean (Phaseolus vulgaris L.) for resistance to common bacterial blight
(CBB)–current status and future directions. In: Applied Photosynthesis (Najafpour
M ed.). Shanghai, China, pp 365-388.
http://cdn.intechopen.com/pdfs-wm/30614.pdf.
Advances in genetic improvement of cauliflower (Brassica oleracea L. var. botrytis L.).
Citation:
Singh BK. 2015. Advances in genetic improvement of cauliflower (Brassica
oleracea L. var. botrytis
L.). In: Novel Genomic Tools and Modern Genetics and Breeding Approaches for
Vegetable Crops Improvement (Pandey S, Singh
B, Mishra GP, Karkute SG Eds). ICAR-IIVR Training Manual No. 66, ICAR-IIVR,
Varanasi, India, pp 101-115.
E-mail: bksinghkushinagar@yahoo.co.in
Cauliflower (Brassica
oleracea L. var. botrytis
L.), an important member of cole crops (Brassica
oleracea), is one of the most popular vegetables worldwide. The word Cole seems
to come from the abbreviation of the word ‘caulis’ meaning stem, and it was
variously spelt as Kale (English), Kohl (German), Kool (Dutch), Kal
(Scandinavian), Kaali (Finnish), Kaol and Kol (Breton), Chou (French), Col (Spanish),
Cal (Irish), Cavolo (Italian), and Couve (Portuguese).
The Cole crops are a group of highly differentiated plants and these are
generally grown all over the world from tropical to arctic climatic conditions.
The present concept of curd “pre-floral fleshy apical meristem” consists
of a shoot system with short internodes, branch apices and bracts. Globally, cauliflower
grows at the latitude 11-60 °N with average temperature ranging from 5-8 °C to
25-28 °C. In its vegetative growth period, it may withstand temperature as low
as –10 °C and as high as 40 °C for a few days. Both in world as well as India,
cauliflower follows cabbage in importance with regard to area (1258 and 433.9
thousand ha), production (22840 and 8573 thousand Mt) and productivity (18.2
and 19.8 Mt/ha), respectively (NHB 2014). In India, cauliflower is grown in the
hills and the plains at altitude ranged from 11-35 °N and temperature ranged
from 5-40 °C. Important states producing cauliflowers in India are West Bengal,
Bihar, Maharashtra, Madhya Pradesh, Odisha, Gujarat, Haryana, Chhatishgarh,
Jharkhand, Assam and Uttar Pradesh (NHB 2014). It is also grown in northern
Himalayas and in Nilgiri hills. The curds of cauliflower are harvested from
September to February in northern Indian plains and from March to November in
the hills of North and South India. Over the last 15 years, cauliflower’s
acreage and production in India is increased continuously by 60.7% & 75.3%,
respectively; but its productivity increased only 9.1%.
References:
Ahluwalia
KS, Swarup V and Chatterjee SS. 1977. Inheritance of qualitative characters in
Indian cauliflower. Veg Sci 4: 67–80.
Chakrabarty
R, Viswakarma N, Bhat SR, Kirti PB, Singh BD and Chopra VL. 2002. Agrobacterium mediated transformation of
cauliflower: optimization of protocol and development of Bt-transgenic
cauliflower. J Biosciences 27: 495–503.
Chatterjee
SS and Kabir J. 2002. Cole crops. In: Vegetable Crops vol.-I (Bose TK, Kabir J,
Maity TK, Parthasarthy VA and Som MG Eds). Naya Prokash, 206 Bidhan Sarani,
Kolkata.
Crisp
P and Tapsell CR. 1993. Cauliflower- Brassica oleracea L. In: Genetic
Improvement of Vegetable Crops (Kalloo G and Bergh BO Eds). Pergamon Press,
Oxford, New York, USA, pp 157–178.
Dias JS and Ortiz R (2014). Advances in transgenic
vegetable and fruit breeding. Agril
Sci 5: 1448–1467.
Dickson MH, Lee CY and Bramble AE. 1988. Orange-curd
high carotene cauliflower inbreds, NY156, NY163, and NY165. HortScience 23:
778–779.
Gill
HS. 1993. Improvement of Cole crops. In: Advances in Horticulture
vol.5-Vegetable Crops: Part I (Chadha KL and Kalloo G Eds). Malhotra Publishing
House, New Delhi, pp 287–303.
Gray
AR and Crisp P. 1976. Breeding system, taxonomy and breeding strategy in
cauliflower (Brassica oleracea var. botrytis L.). Euphytica 26: 369–375.
Kachroo
A, Schopfer CR, Nasrallah ME and Nasrallah JB. 2001. Allele-specific
receptor-ligand interactions in Brassica
self-incompatibility. Science 293: 1824–1826.
Mariani C, De Beuckeleer M, Truettner J, Leemans J and
Goldberg RB. 1990. Induction of male sterility in plants by a chimaeric
ribonuclease gene. Nature 347: 737–741.
Metwali EMR, Fuller MP and Jellings AJ. 2012. Agrobacterium mediated transformation of anti-stress genes
into cauliflower (Brassica oleracea var. botrytis L.)- transformation and confirmation of
stress tolerance. Aust J Basic Appl Sci 6(5): 31–39.
Nasrallah
JB and Nasrallah ME. 1993. Pollen-stigma signaling in the sporophytic
self-incompatibility response. Plant Cell 5: 1325–1335.
Nieuwhof
N. 1969. Cole crops. Leonard Hill, London, UK.
Ogura H. 1968. Studies on the new male-sterility in
Japanese radish, with special reference to the utilization of this sterility
towards the practical raising of hybrid seeds. Mem Fac Agric Kagoshima Univ. 6:
39–78.
Pearson OH. 1972. Cytoplasmically inherited male
sterility characters and flavor components from the species cross Brassica
nigra (L) Koch × B. oleracea L.
J Amer Soc Hort Sci 97
(3): 397–402.
Prakash S, Wu XM and Bhat SR. 2011. History,
evolution, and domestication of Brassica
crops. In: Plant Breeding Reviews vol. 35 (Janick
J Ed). John
Wiley & Sons, Inc., New Jersey, pp 19–84.
Ram HH. 2000. Vegetable breeding- principles and
practices. Kalyani Publishers, Ludhiana.
Sato
K, Nishio T, Kimura R, Kusaba M, Suzuki T, Hatakeyama K, Ockendon DJ and Satta
Y. 2002. Co-evolution of the S-locus genes SRK, SLG and SP11/SCR in Brassica oleracea and B. rapa. Genetics 162: 931–940.
Sharma
RP. 1998. Role of biotechnological options for vegetable breeding. In: Advanced
Technologies in Improvement of Vegetable Crops including Cole Crops
(Chakraborty AK and Singh N Eds). Division of Vegetable Crops, IARI, Pusa, New
Delhi, pp 48–51.
Sidki
S. 1962. Morphology of curd of cauliflower. Amer J Bot 49: 290–297.
Singh BK and Devi J. 2015. Improved production
technology for Cole crops (Brassica
oleracea). In: Improved Production Technologies in Vegetable Crops (Singh
N, Roy S, Karmakar P, Chaurasia SNS, Gupta S and Singh B Eds.). IIVR Training
Manual No. 59, Indian Institute of Vegetable Research, Varanasi, pp 102–119.
Singh BK, Sharma SR and Singh B. 2010. Heterosis
for superoxide dismutase, peroxidase and catalase enzymes in the heads of
cabbage (Brassica oleracea var. capitata L). J Genetics 89 (2):
217–221.
Swarup
V and Chatterjee SS. 1972. Origin and genetic improvement of Indian
cauliflower. Eco Bot 26: 381–393.
U N. 1935. Genome analysis in Brassica with special reference to the experimental formation of B. napus and peculiar mode of fertilization. Jpn J Bot 7: 389–452.
U N. 1935. Genome analysis in Brassica with special reference to the experimental formation of B. napus and peculiar mode of fertilization. Jpn J Bot 7: 389–452.
Tuesday, 26 May 2015
Meghalaya Local: A Natural CMS based hybrid of cauliflower grown in Meghalaya
VK Verma, AK Jha and BK Singh
Vegetable
Newsletter 1 (1): 6, 2014
E-mail:
bksinghkushinagar@yahoo.co.in
Meghalaya Local
a long duration high yielding local cultivar of cauliflower is widely grown by
the farmers in the East Khasi Kills, West Khasi Hills, Jaintia Hills and part
of Ribhoi district in Meghalaya. Being a cross pollinated crop heterosis
breeding is very popular in this crop. To produce the quality hybrid seed, the
uses of male sterile line is very important. Two type of male sterile lines
i.e. MS-I (with non-viable pollen) and MS-II (without stamen) were identified
and tested from the local collection (Table 1).
Table 1. Yield and related traits
of CMS lines
|
Traits
|
MS-I
|
MS-II
|
|
Days to curd
initiation
|
115.3
|
117.0
|
|
Days to curd
maturity
|
140.0
|
148.0
|
|
No. of leaves
|
23.7
|
26.0
|
|
Leaf weight
(kg)
|
1.30
|
1.50
|
|
Leaf length
(cm)
|
53.8
|
55.0
|
|
Leaf dia (cm)
|
25.0
|
28.2
|
|
Stalk wt.(g)
|
12.1
|
11.6
|
|
Marketable curd
wt. (kg)
|
0.920
|
1.100
|
|
Gross plant
weight (kg)
|
2.290
|
2.670
|
|
Harvest index
(%)
|
40
|
41
|
VRFBB-91: A French bean (Phaseolus vulgaris) germplasm for earliness
BK Singh
Vegetable
Newsletter 1 (1): 5, 2014
E-mail:
bksinghkushinagar@yahoo.co.in
French bean varieties
developed by different organizations generally start pod setting during
February to mid-March and very sparsely during first fortnight of December in
North Indian plains. IIVR has recently identified a new genotype ‘VRFBB-91’
whose pods are ready to harvest during first fortnight of December. It has been collected from Jhum land of Kolasib, Mizoram. Plant
growth is bush type, height ranged from 45-60 cm and bears pink colour flowers at
35-40 days after sowing. The pods of VRFBB-91 are green
and bright in colour, fleshy, tender, straight, cylindrical, free from
parchment and harvested usually about 9-12 days after flowering. The pod sieve size
i.e. pods width (measuring through ventral to dorsal sutures) and pods thickness
(measuring through sidewall to sidewall) both ranged from 0.82-0.88 cm, hence
pod cross-sectional shape is round, a desirable trait of vegetable French bean.
On an average, the weight and length of each tender pod is 6.6 g and 15.4
cm, respectively. The line bears 20-22
pods/plant and yields 140-150 g tender pods/plant in crop duration of 80-85
days. A pod contains about 6.7 seeds which is kidney shape, black in colour and
100 seeds’ weight is approximately 23.85. The yield potential (tender pods) of VRFBB-91 is 115-120 q/ha which is better than released
varieties such as Kashi Sampann, Arka Komal, Arka Suvidha, Swarnaprya, Pant
Anupma and Arka Anoop (25-50 q/ha).
Monday, 25 May 2015
Indian collections of turmeric (Curcuma longa L.): Genetic variability, inheritance, character association and performance
BK Singh and Y
Ramakrishna
Indian Journal of Plant Genetic Resources 27 (3): 263-270, 2014
E-mail:
bksinghkushinagar@yahoo.co.in
Abstract
Twenty-seven genotypes of turmeric (Curcuma longa L.) were evaluated to estimate the
variability and inheritance pattern, to suggest suitable
breeding strategies and to identify productive genotypes.
Highly significant mean squares for all the
traits indicated large variation among
genotypes. High genetic gain through selection is expected for shoot length, leaf area, rhizome yield and dry matter yield because of additive
gene inheritance; while curcumin accumulation in rhizome could be improved by
selecting the heterotic seedlings as it is governed by non-additive gene.
Furthermore, leaf length and curcumin content could be the most effective and
reliable selection indices, as indicated by correlation and path coefficients, in identifying the curcumin-rich productive
genotypes. A variety of North East India ‘Megha Turmeric-1’ excelled
for the traits of commercial importance (dry matter recovery and curcumin
yield). Conclusively, the genotypes of North East India were superior to other
parts of India for most of the economic traits and potentially useful for genetic enhancement as well as for varietal
improvement of turmeric.
Key Words: Curcumin; Heritability; North East India
(NEI); Turmeric (Curcuma longa); Variability; Yield.
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