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Paper Type | : | Research Paper |
Title | : | Analysis of field-aged pheromone lures in cotton field |
Country | : | United Kindom |
Authors | : | Ibrahim Salihu Koko, Prof. Alan Cork |
: | 10.9790/2380-0110107 |
ABSTRACT: The purpose of the paper is to determine the longevity, half life and the release rates of Pheromone lures from three commercial companies in India for the Spodoptera litura. Pheromone lures was extracted and examine by the use of Gas chromatography (GC). The major component was detected as ZE-9, 12: 14Ac. Lures from Natural Resource Institute (NRI), Basarass, Agriland as well as PCI lure for the use on Spodoptera litura was aged in cotton field in India in various dispensers like polyethylene vials, rubber tubes, and rubber septum. The result of this research work shows that the standard NRI lures had their lure impregnated with 0.89mg as initial dose and 5.63% remaining life at the 6th week. Basarass pheromone company lure had 0.1mg as initial dose and 12.88% at the end of 6th week, PCI company lure had -0.01mg as initial dose and 7.84% remaining life at the end of the 6th week, Agriland company lure was impregnated with 0.05mg as initial dose and 48.02% remaining life at 6th week respectively. The conclusion that was drawn is that companies like Basarass and Agriland do not put enough milligram (mg) of the major component and the release rates fluctuates on the field due to impurities and this had given the cure some measure of longevity with adverse effect on the performance. Among the recommendations that have been made in this paper companies should endeavor to increase the amount of milligrams impregnated in the lure and find the means and ways of increasing longevity without compromising on the fast release of the major component.
Key words: Pheromone, lures, cotton
Key words: Pheromone, lures, cotton
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[5] Downham, M.C.A., Moawad, G.M. and Mc Veigh, L.J.: Field investigation of an attracticide control technique using the sex pheromone of the Egyptian cotton leaf worm, Spodoptera lituralis (Lepidoptera: Noctuidae) in Bulleting of Entomological Research, 85, 463-472 (1995).
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[7] Miller, E., Staten, R.T.,Nowel, C.and Gourd, J.: "pink bollworm (Lepidoptera: Gelichiidae): point source destiny and its relationship to efficacy in attraticide formulations of Gossyplure" in journal of economic entomology, 83 (4) (1990).
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[10] Van Emden, H.F. Pest control, Edward Arnold, London, 2nd Edition, 42-43 (1989). http://ro.unctad.org/infocomm/ang/als/cotton/market.htm
[2] Crithcley, B.R., Campion, D.G. and Mc Veigh, L.J.: "Pheromone control in the integrated pest management of cotton" in Green, M.B. de, D.J. and Lyon, B. (eds) pest management in cotton, Ellis Horwood Limited, Chichester, 83-87 (1989).
[3] David G.G.: Field comparison of spruce budworm pheromone lures, United State Department of Agriculture, Northeastern Forest Experiment Station research note NE-339 (2) (1986).
[4] De Souza, K.R., Mc Veigh, L.J. and Wright D.J.: "Selection of insecticides for lure and kill studies against Spodoptera lituralis (Lepidoptera: Noctuidae) in journal of economic entomology, 85 (6): 2100 (1992).
[5] Downham, M.C.A., Moawad, G.M. and Mc Veigh, L.J.: Field investigation of an attracticide control technique using the sex pheromone of the Egyptian cotton leaf worm, Spodoptera lituralis (Lepidoptera: Noctuidae) in Bulleting of Entomological Research, 85, 463-472 (1995).
[6] Kranthi, K.R., Banerjee, S.K., Sheo R., Mayee, C.D and Russell, D.A.: New vistas in IRM based cotton IPM in India World research conference3, Cape Town, South Africa (2004). Extracted from http//Whalolab.msu.edu/rpmnews/vol.14.no.i/globe/rpm-g-Kranthi-et al .htm-2lk
[7] Miller, E., Staten, R.T.,Nowel, C.and Gourd, J.: "pink bollworm (Lepidoptera: Gelichiidae): point source destiny and its relationship to efficacy in attraticide formulations of Gossyplure" in journal of economic entomology, 83 (4) (1990).
[8] Munro, J.M. cotton and its production in G.A. Mathews and J.P. Tustall, insect pests of cotton, cab international, Oxon. P 3 (1994).
[9] Narayanamoorthy A. and Kalamkar S.S.: Is Bt cotton cultivation economically viable for Indian farmers? An empirical Analysis, economic and political weekly, 41, (26) Pp 2716-2717, (2006).
[10] Van Emden, H.F. Pest control, Edward Arnold, London, 2nd Edition, 42-43 (1989). http://ro.unctad.org/infocomm/ang/als/cotton/market.htm
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Abstract : In the present study, rabies was confirmed by Nested RT-PCR on saliva of 24 animals suspected to be rabid. Amplification with first round primers (Rab N1 and Rab N5) yielded a 1477 bp product, while primers used for second round amplification (RabNfor and RabNrev) yielded a 762 bp product. By nested RT-PCR, viral RNA could be detected in 9/24 (36.0%) saliva samples. Confirmatory diagnosis by Immunofluorescence performed on brain sample revealed 17 true positive cases. Sensitivity of 68.0% was recorded by application of Nested RT-PCR on saliva samples. It was concluded that Nested RT-PCR applied on saliva of rabies suspected animal can help in intravitam diagnosis of rabies. Keywords: Immunofluorescence, Intravitam, Nested RT-PCR, Rabies, Saliva.
[1] T. Nagaraj, P. V. Joel, A. Desai, A. Kamat, S. N. Madhusudana and V. Ravi. Ante mortem diagnosis of human rabies using saliva samples: Comparison of real time and conventional RT-PCR techniques, Journal of Clinical Virology, 36, 2006, 17–23
[2] M. K. Sudarshan, S. N. Madhusudana, B. J. Mahendra, N. S. Rao, D. H. Narayana and S. A. Rahman. Assessing burden of human rabies in India: results of a national multi-centre epidemiological survey. International Journal of Infectious Diseases, 11, 2007, 29-35.
[3] T. Hemachudha. Human rabies: clinical aspects, pathogenesis, and potential therapy, In (edn.): Lyssaviruses, edited by Rupprecht CE, Dietzschold B, and Koprowski H, 1994 Springer-Verlag, Berlin, Germany.
[4] R. W. Emmons. Rabies diagnosis and rabies vaccine. Northern England Journal of Medicine, 301, 1991, 331–332.
[5] D. B. Fishbein, J. S. Smith, C. E. Rupprecht and K. Clark. Unexplained rabies in three immigrants in the United States. A virologic investigation. Northern England Journal of Medicine, 324, 1991, 205-11.
[6] L. G. Schneider. Spread of virus from the central nervous system. In: Baer, G.M. (Ed.),The Natural History of Rabies. Academic Press, 1975, New York, 273–301.
[7] S. A. Nadin-Davis, Polymerase chain reaction protocols for rabies virus discrimination. Journal of Virological Methods, 75, 1998, 1-8.
[8] A. Kaw, C. K. Singh, B. S. Sandhu, N. K. Sood, Ramneek, D. Deka and S. Awahan, Diagnosis of rabies in animals by Nested RT-PCR, Indian Journal of Animal Sciences, 81(4), 2011, 367-369.
[9] A. C. Hanlon, S. J. Smith and R. G. Anderson. Article II: Laboratory diagnosis of rabies, Journal of American Veterinary Medical Association, 215, 1999, 1444-1447.
[10] P. Crepin, L. Audry, Y. Rotivel, A. Gacoin, C. Caroff and H. Bourhy. Intravitam diagnosis of human rabies by PCR using saliva and cerebrospinal fluid. Journal of Clinical Microbiology, 36, 1998, 1117–1121.
[2] M. K. Sudarshan, S. N. Madhusudana, B. J. Mahendra, N. S. Rao, D. H. Narayana and S. A. Rahman. Assessing burden of human rabies in India: results of a national multi-centre epidemiological survey. International Journal of Infectious Diseases, 11, 2007, 29-35.
[3] T. Hemachudha. Human rabies: clinical aspects, pathogenesis, and potential therapy, In (edn.): Lyssaviruses, edited by Rupprecht CE, Dietzschold B, and Koprowski H, 1994 Springer-Verlag, Berlin, Germany.
[4] R. W. Emmons. Rabies diagnosis and rabies vaccine. Northern England Journal of Medicine, 301, 1991, 331–332.
[5] D. B. Fishbein, J. S. Smith, C. E. Rupprecht and K. Clark. Unexplained rabies in three immigrants in the United States. A virologic investigation. Northern England Journal of Medicine, 324, 1991, 205-11.
[6] L. G. Schneider. Spread of virus from the central nervous system. In: Baer, G.M. (Ed.),The Natural History of Rabies. Academic Press, 1975, New York, 273–301.
[7] S. A. Nadin-Davis, Polymerase chain reaction protocols for rabies virus discrimination. Journal of Virological Methods, 75, 1998, 1-8.
[8] A. Kaw, C. K. Singh, B. S. Sandhu, N. K. Sood, Ramneek, D. Deka and S. Awahan, Diagnosis of rabies in animals by Nested RT-PCR, Indian Journal of Animal Sciences, 81(4), 2011, 367-369.
[9] A. C. Hanlon, S. J. Smith and R. G. Anderson. Article II: Laboratory diagnosis of rabies, Journal of American Veterinary Medical Association, 215, 1999, 1444-1447.
[10] P. Crepin, L. Audry, Y. Rotivel, A. Gacoin, C. Caroff and H. Bourhy. Intravitam diagnosis of human rabies by PCR using saliva and cerebrospinal fluid. Journal of Clinical Microbiology, 36, 1998, 1117–1121.
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Abstract : Milk sample was obtained from 17 lactating animals suspected to be rabid. An attempt was made by employing advanced molecular approach Nested RT-PCR and TaqMan real time PCR on milk samples with an aim to detect the presence of rabies viral RNA. Confirmatory diagnosis of rabies was made by applying conventional techniques; Immunofluorescence on brain tissue. This study depicts the presence of rabies viral RNA in 2/17 milk sample with a sensitivity of 54.54% by Nested RT-PCR and 4/17 milk samples with a sensitivity of (60%) by TaqMan real time PCR when compared with FAT applied on brain tissue. This study confirms the presence of rabies viral RNA in milk. Keywords: Immunofluorescence, Intravitam, Nested RT-PCR, Rabies, Saliva.
[1] T. Nagaraj, P. V. Joel, A. Desai, A. Kamat, S. N. Madhusudana and V. Ravi. Ante mortem diagnosis of human rabies using saliva samples: Comparison of real time and conventional RT-PCR techniques, Journal of Clinical Virology, 36, 2006, 17–23
[2] S. Jogai, B. D. Radotra, A. K. Banerjee. Rabies viral antigen in extracranial organs: a post-mortem study. Neuropathology and Applied Neurobiology, 28(4), 2002, 334-338.
[3] M. K. Sudarshan, S. N. Madhusudana, B. J. Mahendra, N. S. Rao, D. H. Narayana and S. A. Rahman. Assessing burden of human rabies in India: results of a national multi-centre epidemiological survey. International Journal of Infectious Diseases, 11, 2007, 29-35.
[4] S. Wacharapluesadee and T. Hemachudha. Urine as a source of rabies RNA detection in human rabies diagnosis. Clinical Infectious Diseases, 34, 2002, 874-5.
[5] W. Saengseesom, C. Mitmoonpitak, S. Kasempimolporn and V. Sitprija. Real-time PCR analysis of dog cerebrospinal fluid and saliva samples for ante-mortem diagnosis of rabies. Southeast Asian Journal of Tropical Medicine and Public Health, 38(1), 2007, 53-57.
[6] S. A. Nadin-Davis, Polymerase chain reaction protocols for rabies virus discrimination. Journal of Virological Methods, 75, 1998, 1-8.
[7] A. Kaw, C. K. Singh, B. S. Sandhu, N. K. Sood, Ramneek, D. Deka and S. Awahan, Diagnosis of rabies in animals by Nested RT-PCR, Indian Journal of Animal Sciences, 81(4), 2011, 367-369.
[8] A. C. Hanlon, S. J. Smith and R. G. Anderson. Article II: Laboratory diagnosis of rabies, Journal of American Veterinary Medical Association, 215, 1999, 1444-1447.
[9] G. J. Hughes, J. S. Smith, C. A. Hanlon and C. E. Rupprecht. Evaluation of a Taq-Man PCR assay to detect rabies virus RNA: influence of sequence variation and application to quantification of viral loads. Journal of Clinical Microbiology, 42, 2004, 299–306.
[2] S. Jogai, B. D. Radotra, A. K. Banerjee. Rabies viral antigen in extracranial organs: a post-mortem study. Neuropathology and Applied Neurobiology, 28(4), 2002, 334-338.
[3] M. K. Sudarshan, S. N. Madhusudana, B. J. Mahendra, N. S. Rao, D. H. Narayana and S. A. Rahman. Assessing burden of human rabies in India: results of a national multi-centre epidemiological survey. International Journal of Infectious Diseases, 11, 2007, 29-35.
[4] S. Wacharapluesadee and T. Hemachudha. Urine as a source of rabies RNA detection in human rabies diagnosis. Clinical Infectious Diseases, 34, 2002, 874-5.
[5] W. Saengseesom, C. Mitmoonpitak, S. Kasempimolporn and V. Sitprija. Real-time PCR analysis of dog cerebrospinal fluid and saliva samples for ante-mortem diagnosis of rabies. Southeast Asian Journal of Tropical Medicine and Public Health, 38(1), 2007, 53-57.
[6] S. A. Nadin-Davis, Polymerase chain reaction protocols for rabies virus discrimination. Journal of Virological Methods, 75, 1998, 1-8.
[7] A. Kaw, C. K. Singh, B. S. Sandhu, N. K. Sood, Ramneek, D. Deka and S. Awahan, Diagnosis of rabies in animals by Nested RT-PCR, Indian Journal of Animal Sciences, 81(4), 2011, 367-369.
[8] A. C. Hanlon, S. J. Smith and R. G. Anderson. Article II: Laboratory diagnosis of rabies, Journal of American Veterinary Medical Association, 215, 1999, 1444-1447.
[9] G. J. Hughes, J. S. Smith, C. A. Hanlon and C. E. Rupprecht. Evaluation of a Taq-Man PCR assay to detect rabies virus RNA: influence of sequence variation and application to quantification of viral loads. Journal of Clinical Microbiology, 42, 2004, 299–306.
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Paper Type | : | Research Paper |
Title | : | Molecular Detection of Rabies by SYBR Green Real Time PCR |
Country | : | India |
Authors | : | A Kaw, C K Singh, B S Sandhu, K Bansal, N K Sood |
: | 10.9790/2380-0111618 |
Abstract : The present study was envisaged to compare the sensitivity of SYBR Green real time PCR with immunofluorescence PCR for diagnosis of rabies. SYBR Green real time PCR technique was applied on brain samples collected from 39 rabies suspected animals. Sensitivity of SYBR Green technique was compared in accordance with WHO recommended gold standard test viz. Fluorescent Antibody Technique (FAT) applied on brain samples. SYBR Green real time PCR applied on brain samples had successfully confirmed rabies in 16/39 with a Sensitivity of 80% . It was concluded that SYBR Green real time PCR is a useful, specific, sensitive and better molecular approach for diagnosis of rabies from brain of rabid suspected cases and can be used as confirmatory test for rabies diagnosis. Keywords: Brain, Molecular, Rabies, Real time PCR, SYBR Green.
[1] D. L. Knobel, S. Cleaveland, P. G. Coleman, E. M. Fevre, M. I. Meltzer, M. E. G. Miranda, A. Shaw, J. Zinsstag and F. X. Meslin. Re-evaluating the burden of rabies in Africa and Asia. Bulletin World Health Organisation, 83, 2005, 360-368.
[2] E. M. Black, J. P. Lowings, J. Smith, P. R. Heaton and L. M. McElhimney, L.M. A rapid RT-PCR method to differentiate six established genotypes of rabies and rabies-related viruses using TaqMan technology. Journal of Virological Methods, 105, 2002, 25-35.
[3] E. Picard-Meyer, V. Bruyére, J. Barrat, E. Tissot, M. J. Barrat and F. Cliquet. Development of a hemi-nested RT-PCR method for the specific determination of European Bat Lyssavirus 1. Comparison with other rabies diagnostic methods.Vaccine, 22, 2004, 1921-1929.
[4] P. R. Wakeley, N. Johnson, L. M. McElhinney, D. Marston, J. Sawyer and A. R. Fooks. Development of a real-time, differential RT-PCR TaqMan® assay for lyssavirus genotypes 1, 5 and 6. Development in Biologicals (Basel), 126, 2006, 227- 236.
[5] T. Nagaraj, P. V. Joel, A. Desai, A. Kamat, S. N. Madhusudana and V. Ravi. Ante mortem diagnosis of human rabies using saliva samples: Comparison of real time and conventional RT-PCR techniques, Journal of Clinical Virology, 36, 2006, 17–23
[6] P. R. Heaton, L. M. McElhinney, J. H. A. Bowen-Davies and J. P. Lowings. Heminested PCR assay for detection of six genotypes of rabies and rabies-related viruses, Journal of Virological Methods, 81(1-2), 1999, 63-69. [7] A. Ermine, D. Larzul, P. E. Ceccaldi, J. L. Guesdon and H. Tsiang. Polymerase chain reaction amplification of rabies virus nucleic acids from total mouse brain RNA. Molecular and Cell Probes, 4, 1989, 189-191.
[8] K. A. McColl, A. R. Gould, P. W. Seeck, P. T. Hooper, H. A. Westbury and J. S. Smith. Polymerase chain reaction and other laboratory techniques in the diagnosis of long incubation rabies in Australia. Australian Veterinary Journal, 70, 1993, 84-89.
[9] S. A. Nadin-Davis, Polymerase chain reaction protocols for rabies virus discrimination. Journal of Virological Methods, 75, 1998, 1-8.
[10] G. J. Hughes, J. S. Smith, C. A. Hanlon and C. E. Rupprecht. Evaluation of a Taq-Man PCR assay to detect rabies virus RNA: influence of sequence variation and application to quantification of viral loads. Journal of Clinical Microbiology, 42, 2004, 299–306.
[2] E. M. Black, J. P. Lowings, J. Smith, P. R. Heaton and L. M. McElhimney, L.M. A rapid RT-PCR method to differentiate six established genotypes of rabies and rabies-related viruses using TaqMan technology. Journal of Virological Methods, 105, 2002, 25-35.
[3] E. Picard-Meyer, V. Bruyére, J. Barrat, E. Tissot, M. J. Barrat and F. Cliquet. Development of a hemi-nested RT-PCR method for the specific determination of European Bat Lyssavirus 1. Comparison with other rabies diagnostic methods.Vaccine, 22, 2004, 1921-1929.
[4] P. R. Wakeley, N. Johnson, L. M. McElhinney, D. Marston, J. Sawyer and A. R. Fooks. Development of a real-time, differential RT-PCR TaqMan® assay for lyssavirus genotypes 1, 5 and 6. Development in Biologicals (Basel), 126, 2006, 227- 236.
[5] T. Nagaraj, P. V. Joel, A. Desai, A. Kamat, S. N. Madhusudana and V. Ravi. Ante mortem diagnosis of human rabies using saliva samples: Comparison of real time and conventional RT-PCR techniques, Journal of Clinical Virology, 36, 2006, 17–23
[6] P. R. Heaton, L. M. McElhinney, J. H. A. Bowen-Davies and J. P. Lowings. Heminested PCR assay for detection of six genotypes of rabies and rabies-related viruses, Journal of Virological Methods, 81(1-2), 1999, 63-69. [7] A. Ermine, D. Larzul, P. E. Ceccaldi, J. L. Guesdon and H. Tsiang. Polymerase chain reaction amplification of rabies virus nucleic acids from total mouse brain RNA. Molecular and Cell Probes, 4, 1989, 189-191.
[8] K. A. McColl, A. R. Gould, P. W. Seeck, P. T. Hooper, H. A. Westbury and J. S. Smith. Polymerase chain reaction and other laboratory techniques in the diagnosis of long incubation rabies in Australia. Australian Veterinary Journal, 70, 1993, 84-89.
[9] S. A. Nadin-Davis, Polymerase chain reaction protocols for rabies virus discrimination. Journal of Virological Methods, 75, 1998, 1-8.
[10] G. J. Hughes, J. S. Smith, C. A. Hanlon and C. E. Rupprecht. Evaluation of a Taq-Man PCR assay to detect rabies virus RNA: influence of sequence variation and application to quantification of viral loads. Journal of Clinical Microbiology, 42, 2004, 299–306.
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Abstract : Agricultural activities are link with many other activities. Any sector of an economy cannot function in isolated manner. Rather how it integrates with other sectors determines its efficiency. In fact, we are very obsessed with systems concept. In a bigger system, every subsystem of it is not only interlinked but also interdependent. Agriculture is no exception. Agricultural productivity largely depends on irrigation system, communication network, power supply, marketing facilities, banking system and other infrastructural facilities. Ultimately outcome from agriculture would depend on how these elements are interlinked. Not only several factors but also their derivatives (linkage) also influence productivity. In this paper, we identify and explain different types of agricultural derivatives to enhance agricultural productivity of land i.e. effect of interlinkage on productivity.
Key Words: Interlinked, Agricultural Sector, Value Productivity, HIV Seeds, Derivatives, Respondent farmers, Dominant factors, Chemical Fertilizer Intensity, Cropping Intensity.
Key Words: Interlinked, Agricultural Sector, Value Productivity, HIV Seeds, Derivatives, Respondent farmers, Dominant factors, Chemical Fertilizer Intensity, Cropping Intensity.
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[2] Gangopadhyay, S. and Sengupta, K. (1987) " Small Farmers, Money Lender and Training Activity" Oxford University Papers, 333-342.
[3] Bardhan, P.K. and Rudra. (1978), Bhaduri (1973)," Interlinkage on Land, Labour and Credit relations", An analysis of village survey data in East India, Economic and Political Weekly, 13, Annual Number, February..
[4] (4)Gangopadhyay, S. and Sengupta, K. (1987) " Small Farmers, Money Lender and Training Activity" Oxford University Papers, 333-342.
[5] Bardhan, P. K. (ed): "The Economic Theory of Agrarian Institutions", Clarendon Press Oxford, 1989.
[6] Basu. K. (1984):"The Less Developed Economy", A critique Contemporary Theory, Oxford Economic Press.
[7] Bharadwaj, K. (1975): "Production Condition in Indian Agriculture", Cambridge University Press.
[8] Dutta, Santosh Kumar.(2002): " A Study of the Interlinkage in Agriculture",Naya Udyog, Kolkata.
[9] Rudra, A. (1975): "Loans as a of Agrarian Relations", Some Results of a Preliminary Survey in West Bengal , Economic and Political Weekly,July 12.
[10] Shafi, M. (1965): "Approaches to the Measurement of Agricultural Efficiency", Department of Geography, A.M.U., Aligarh.
[2] Gangopadhyay, S. and Sengupta, K. (1987) " Small Farmers, Money Lender and Training Activity" Oxford University Papers, 333-342.
[3] Bardhan, P.K. and Rudra. (1978), Bhaduri (1973)," Interlinkage on Land, Labour and Credit relations", An analysis of village survey data in East India, Economic and Political Weekly, 13, Annual Number, February..
[4] (4)Gangopadhyay, S. and Sengupta, K. (1987) " Small Farmers, Money Lender and Training Activity" Oxford University Papers, 333-342.
[5] Bardhan, P. K. (ed): "The Economic Theory of Agrarian Institutions", Clarendon Press Oxford, 1989.
[6] Basu. K. (1984):"The Less Developed Economy", A critique Contemporary Theory, Oxford Economic Press.
[7] Bharadwaj, K. (1975): "Production Condition in Indian Agriculture", Cambridge University Press.
[8] Dutta, Santosh Kumar.(2002): " A Study of the Interlinkage in Agriculture",Naya Udyog, Kolkata.
[9] Rudra, A. (1975): "Loans as a of Agrarian Relations", Some Results of a Preliminary Survey in West Bengal , Economic and Political Weekly,July 12.
[10] Shafi, M. (1965): "Approaches to the Measurement of Agricultural Efficiency", Department of Geography, A.M.U., Aligarh.
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Abstract : An experiment was carried out at Department of Zoology and Aquaculture, Acharya Nagarjuna University, India from July to August 2010 to assess the effect of feed on larval survival of Macrobrachium rosenbergii. Three experiments viz. Artemia nauplii plus egg custard (E-1), Artemia nauplii only (E-2) and Egg custard only (E-3) were taken for the study each with two replicates. The experiment was conducted in fiber tanks with Macrobrachium rosenbergii larvae at a density of 100 no/ lt of water. Highest average survival rate (42%) was found in E-1 and the lowest survival rate was obtained in E-3. The results obtains that there is a immense potentiality for increasing freshwater prawn seed production through closed water system by using Artemia nauplii plus egg custard as feed.
Key Words: Macrobrachium rosenbergii, Artemia nauplii, Egg custard, larval growth
Key Words: Macrobrachium rosenbergii, Artemia nauplii, Egg custard, larval growth
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[10] Islam, M. S. A Khan nd S. U. Ahmad., 2000. Observations on the larval rearing of Macrobrachium rosenbergii by using different types of feed n Bangladesh costal environment. Pakistan J. Bio. Sci 3 (10): 1790-1792.
[2] Ahmad, M. K and N. Mahmood. 1978. On the early embryonic development and hatching of the giant prawn Macrobrachium reosenbergii(de man). Chittagong University studies, part 2: 97-101.
[3] Bhuiyan, A.L., K. S. Islam and Kar, P. R., 1983. Development and transfer of technology of culture of seed s of the giant prawn Macrobrachium rosenbergii (de man) for distributing to prawn farmers. Annual report of BARC research project, Dhaka. Bangladesh. 16 pp.
[4] Das. S. M., 1989. Hand book of limnology and water pollution. South Asian Publishers pvt. Ltd.36 Netaji Subhash Marg. New Delhi.
[5] Fuzimura, T., 1966. Notes on the development of mass culturing techniques of giant prawn Macrobrachium rosenbergii (de man). Proc. IPFC. 12th sess.
[6] Fuzimura. T., 1972. Development of rearing techniques for the giant prawn Macrobrachium rosenbergii (de man). Nat. Mar. Fish. Ser. USA.
[7] Fuzimura. T and H. Okamoto, 1972. Notes on progress made in developing mass culture techniques for prawn Macrobrachium rosenbergii in Hawaii. In Coastal Aquaculture in the Indio- pacific Region. ; Edited by T.V.R Pillay. West Byflect, England, Fishing News Books Ltd., for IPFC/FAO. 313-327 PP.
[8] Islam, K. S., A. L. Bhuiyan and Kar, P. R., 1983. Factor affecting seed culture of Macrobrachium rosenbergii with special reference to salinity tolerance. Chattagang University Studies, Part II 7: 85-89.
[9] Islam, K. S., and Y. S. A. Khan, 1990. Mass production of post larvae of Macrobrachium rosenbergii at the prawn Hatchery and Research Centre. Cox's Bazar, Bangladesh. Bangladesh J. Zoo., 18: 53-59.
[10] Islam, M. S. A Khan nd S. U. Ahmad., 2000. Observations on the larval rearing of Macrobrachium rosenbergii by using different types of feed n Bangladesh costal environment. Pakistan J. Bio. Sci 3 (10): 1790-1792.
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Abstract : Indian major carp Labeo rohita was induced breeding in eco-carp hatchery with 3 different inducing agents, viz. ovaprim, ovatide, Carp pituitary extract at fish breeding center at Amloh Distt. Fathegarh Sahib (Punjab) India. Total ten trial doses of ovaprim, ovatide and Carp Pituitary Extract (CPE) used for induced breeding in Labeo rohita. The fertilization was found 61.30% with ovaprim, 58.50% with ovatide and 55.96% with carp pituitary extract treatment. The percentage hatchling was 72.20% with ovaprim, 66.37 % with ovatide and 59.25% with carp pituitary extract treatment.A comparison was carried out for fecundity, fertilization, and hatching rate during the induced spawning of Labeo rohita administered single dose of ovaprim and ovatide while carp pituitary extract double dose to female brooder. Ovaprim performed much better than Ovatide and pituitary gland extract.
Key Words: Labeo rohita (Rohu); Induced breeding; ovatide; ovaprim; Carp pituitary extract.
Key Words: Labeo rohita (Rohu); Induced breeding; ovatide; ovaprim; Carp pituitary extract.
[1] Agarwal, S.C. 1999. Aquaculture in Punjab. National workshop on sustainable aquaculture in Punjab, 21–22 Jan 1999, PAU, Ludhiana.
[2] Billard, R., K. Alagarawami, R. E. Peter and B. Breton. 1983. Potentialisation per le pimozide des effects du LH-RH-A sur la secretion gonadotrope hypophyaire l'ovulation et la spermiation chez la carpe commune (Cyprinus carpio). C. R. Acad. Sci. Paris 296:181-184
[3] Chaudhari, H. and K.H. Alikunhi: Observations on the spawning in Indian carps by hormone injection. Curr. Sci., 26,381-382 (1957).
[4] Chondar, S. L.: HCG a better substitute for pituitary gland for induced breeding of silver carp on commercial scale. In: Proceedings of the second International conference on warm water aquaculture. finfish, Hawaii, G.S.A., pp. 521-534 (1985).
[5] Dehadrai, P. V. 1986: Carp seed production in India, p. 33
[6] Harvey, B. J. and W. S. Hoar. 1979. The theory and practice of induced breeding in fish. IDRC-TX 21e. 48p.
[7] Jhingran, V.G. and R. S. V. Pullin: A hatchery manual for the common chinese and Indian major carps. Asian development bank and International centre for living aquatic resources management, Manila, Philippines. pp. 191 (1985).
[8] Nandeesha, M.C. and K.G. Rao: Recent developments in carp culture technology in India with special reference to the state of Andhra Pradesh. In: Proceedings of the workshop on fish culture management techniques and nutrition, (Eds: Huisman et al.) 14- 19 November, Malang pp. 203-210 (1989).
[9] Nandeesha, M.C., K.G. Rao, R. Jayanna, N.C. Parker, T.J. Varghese, P. Keshavanath and H.P.C. Shetty: Induced spawning of Indian major carps through single application of Ovaprim In: The second asian fisheries forum, (Eds: R. Hirano and M. Hanyu). Asian Fisheries Society, Manila, Philippines. pp. 581-585 (1990)
[10] Peter, R. E., J. P. Chang, C. S. Nahorniak, R. J. Omeljaniuk, M. Sokolowska, S. R. Shih and R. Billard. 1986. Interaction of catecholamines and sGnRH in regulation of gonadotropin secretion in teleost fish. Recent Prog. Horm. Res. 42:513-548.
[2] Billard, R., K. Alagarawami, R. E. Peter and B. Breton. 1983. Potentialisation per le pimozide des effects du LH-RH-A sur la secretion gonadotrope hypophyaire l'ovulation et la spermiation chez la carpe commune (Cyprinus carpio). C. R. Acad. Sci. Paris 296:181-184
[3] Chaudhari, H. and K.H. Alikunhi: Observations on the spawning in Indian carps by hormone injection. Curr. Sci., 26,381-382 (1957).
[4] Chondar, S. L.: HCG a better substitute for pituitary gland for induced breeding of silver carp on commercial scale. In: Proceedings of the second International conference on warm water aquaculture. finfish, Hawaii, G.S.A., pp. 521-534 (1985).
[5] Dehadrai, P. V. 1986: Carp seed production in India, p. 33
[6] Harvey, B. J. and W. S. Hoar. 1979. The theory and practice of induced breeding in fish. IDRC-TX 21e. 48p.
[7] Jhingran, V.G. and R. S. V. Pullin: A hatchery manual for the common chinese and Indian major carps. Asian development bank and International centre for living aquatic resources management, Manila, Philippines. pp. 191 (1985).
[8] Nandeesha, M.C. and K.G. Rao: Recent developments in carp culture technology in India with special reference to the state of Andhra Pradesh. In: Proceedings of the workshop on fish culture management techniques and nutrition, (Eds: Huisman et al.) 14- 19 November, Malang pp. 203-210 (1989).
[9] Nandeesha, M.C., K.G. Rao, R. Jayanna, N.C. Parker, T.J. Varghese, P. Keshavanath and H.P.C. Shetty: Induced spawning of Indian major carps through single application of Ovaprim In: The second asian fisheries forum, (Eds: R. Hirano and M. Hanyu). Asian Fisheries Society, Manila, Philippines. pp. 581-585 (1990)
[10] Peter, R. E., J. P. Chang, C. S. Nahorniak, R. J. Omeljaniuk, M. Sokolowska, S. R. Shih and R. Billard. 1986. Interaction of catecholamines and sGnRH in regulation of gonadotropin secretion in teleost fish. Recent Prog. Horm. Res. 42:513-548.
'
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- Abstract
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Abstract : In Vitro trial was conducted to evaluate the binding ability of commercial high grade bentonite (HGB), on aflatoxin (AF) in broiler diets at pH 4.5 and 6.5. Contaminated substrate containing AF was added to broilers chicken diets to get the desired level of 0.5 ppm. A high grade bentonite was added at 0.5, 0.75 and 1.0 per cent levels to the contaminated diet and incubated for three hours. At 4.5 pH, 84.90, 88.47 and 92.90 per cent binding of AF was recorded at 0.5, 0.75 and 1.0 per cent inclusion levels of HGB respectively (P<0.05). At 6.5 pH, 87.60, 91.47 and 96.80 per cent binding of AF was recorded at 0.5, 0.75 and 1.0 per cent inclusion levels of HGB respectively (P<0.05). In the present trial it was evident that both at pH 4.5 and 6.5 the binding ability of HGB at the inclusion level of one percent was significantly higher.
Key words: Aflatoxin, High grade bentonite, pH, In Vitro binding.
Key words: Aflatoxin, High grade bentonite, pH, In Vitro binding.
[1] Manafi, M., Narayana Swamy, H. D. and Pirany, N. 2009a. In vitro Binding Ability of Mycotoxin Binder in Commercial Broiler Feed. African J. Agr. Res., 4(2):141-143.
[2] Mohamadi, H. and Alizadeh, M. 2010. A Study of the Occurrence of Aflatoxin M1 in Dairy Products Marketed in Urimia, Iran. J. Agr. Sci. Tech., 12: 579-583
[3] Devegowda, G., 2002. Mycotoxins: Economic risks and their control. In: Handbook of Poultry Nutrition. Published by American Soybean Association, pp. 246-260.
[4] Eralsan, G., Essz, D., Akdogan, M., Sahindokuyucu, F. and Altrintas, L. 2005. The effects of Aflatoxin and Sodium Bentonite and Alone on Some Blood Electrolyte Levels in Broiler Chickens. Turk Vet. Hayvanclk Dergisi., 29: 601- 605.
[5] Hagler, W. M., Tyczkowska, K. and Hamilton, P. B. 1984. Simultaneous Occurrence of Deoxynivalenol, Zearalenone and Aflatoxin in 1982 Scabby Wheat from Midwestern United States. Appl. Environ.Microbiol., 47: 151-154.
[6] Santurio, J. M., Mallmannl, C. A., Rosa, A. P., Appel, G., Heer, A., Dageforde, S. and Bottcher, M. 1999. Effect of Sodium Bentonite on the Performance and Blood Variables of Broiler Chickens Intoxicated with Aflatoxin. Brit. Poultry Sci., 40: 115- 119.
[7] Vieira, S.L. 2003. Nutritional implication of mould development in feed stuffs and alternatives to reduce the mycotoxin problem in poultry feeds. World's Poultry Science Journal, Vol.59. March 2003. pp.111-122.
[8] Shotwell, O.L., Hesseltine, C.W., Stubblefield,R.D. and Sorenson,W.G.,1966.Production of aflatoxin on rice. Appl.Micrbial.,14:425-428 .
[9] Romer, T.R., 1975, Screening method for the detection of aflatoxins in mixed feeds and other agricultural commodities with subsequent confirmation and quantitative measurement of aflatoxins in positive samples. J.A.O.A.C., 58: 500-506.
[10] AOAC, 1995. Official Methods of Analysis. 16th Ed., Association of Official Analytical Chemists, Washington, D.C.
[2] Mohamadi, H. and Alizadeh, M. 2010. A Study of the Occurrence of Aflatoxin M1 in Dairy Products Marketed in Urimia, Iran. J. Agr. Sci. Tech., 12: 579-583
[3] Devegowda, G., 2002. Mycotoxins: Economic risks and their control. In: Handbook of Poultry Nutrition. Published by American Soybean Association, pp. 246-260.
[4] Eralsan, G., Essz, D., Akdogan, M., Sahindokuyucu, F. and Altrintas, L. 2005. The effects of Aflatoxin and Sodium Bentonite and Alone on Some Blood Electrolyte Levels in Broiler Chickens. Turk Vet. Hayvanclk Dergisi., 29: 601- 605.
[5] Hagler, W. M., Tyczkowska, K. and Hamilton, P. B. 1984. Simultaneous Occurrence of Deoxynivalenol, Zearalenone and Aflatoxin in 1982 Scabby Wheat from Midwestern United States. Appl. Environ.Microbiol., 47: 151-154.
[6] Santurio, J. M., Mallmannl, C. A., Rosa, A. P., Appel, G., Heer, A., Dageforde, S. and Bottcher, M. 1999. Effect of Sodium Bentonite on the Performance and Blood Variables of Broiler Chickens Intoxicated with Aflatoxin. Brit. Poultry Sci., 40: 115- 119.
[7] Vieira, S.L. 2003. Nutritional implication of mould development in feed stuffs and alternatives to reduce the mycotoxin problem in poultry feeds. World's Poultry Science Journal, Vol.59. March 2003. pp.111-122.
[8] Shotwell, O.L., Hesseltine, C.W., Stubblefield,R.D. and Sorenson,W.G.,1966.Production of aflatoxin on rice. Appl.Micrbial.,14:425-428 .
[9] Romer, T.R., 1975, Screening method for the detection of aflatoxins in mixed feeds and other agricultural commodities with subsequent confirmation and quantitative measurement of aflatoxins in positive samples. J.A.O.A.C., 58: 500-506.
[10] AOAC, 1995. Official Methods of Analysis. 16th Ed., Association of Official Analytical Chemists, Washington, D.C.
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Abstract : This study was conducted in Timergara District Dir (Lower) Pakistan to estimate the cost of milk production. The methodology used for this study is mainly quantitative. Data was collected through questionnaire from a sample size of 80 farmers in the town of Timergara. The cubic cost function model was used to analyze the collected data. The study shows that average values of dry and milking buffaloes were 2 and 42 respectively while the average milk production per buffalo was 0.11 mounds (5.5 kg). The major cost components of milk production were green fodder, dry fodder, concentrates, medicines, management, equipment, building and other miscellaneous. The total fixed cost (TFC) and average variable cost (AVC) per farm was 39761 and 468.51 rupees respectively. The marginal cost (MC) was minimum at output level 680 and the average variable cost (AVC) was minimum at i.e. Rs.468. The optimal level of milk production was 1232 mounds (61600 kg). The results show that none of the sampled farmers operated at the optimum level of operation.
Keywords: Cost, Milk, Pakistan, Production, Return, Timergara,
Keywords: Cost, Milk, Pakistan, Production, Return, Timergara,
[1] Govt: of Pakistan. (2009-10) Economic Survey of Pakistan Bureau of Statistics Economic Affair Division, Ministry of Food
Agriculture and Livestock, Islamabad, Pakistan, pp.2 4.
[2] Muhammad,.M.A. (1997) 'Economic analysis of milk production in district Okara' Pakistan Veterinary Journal, pp. 135-148.
[3] Khan, M. (1999) 'Economics of Milk production and marketing in the Development of Pakistan-With special reference to Peshawar
District' Unpublished Ph.D Thesis, University of Wales, Aberystwyth, UK.
[4] Khan,.M, Kanes K. Rajah and Michael Haines. (1998) 'An analysis of strategies and efficiency in the milk production systems in
Peshawar District KPK, Pakistan", Journal of the University of Wales Agricultural Society, P.49-70.
[5] Bouquiaux, J.M and R.Hellemans. (1998) Economic analysis of milk production in Belgium. Brussels, Centrum-economics
[7] Kalra, K.K., Rajvir. S, .Anil., Singh, R. and Chauhan,.R. (1995) 'Economic analysis of milk production and disposal in rural areas
of Haryana', Indian Journal of Dairy Science. Pp.546-555
[8] Singh, R.P.,Bhatnagar and Singh,B. (1995) 'Economic efficiency of milk production system under rural conditions', Indian Journal
of Animal Research. pp.27-32
[9] Sharma, J.P and .Singh, R.V. (1994) 'An economic analysis of milk production by different breeds of milch animals in humidtemperate
zone of Himachal Pradesh Indian Journal-of-Dairy-Science.pp.24-47.
[10] Dev,. R..Gupta and Raj, D. (1994) 'An economic analysis of milk production in Churu district of Rajasthan'. Indian-
Journal-of-Dairy-Science. Pp.749-755.
Agriculture and Livestock, Islamabad, Pakistan, pp.2 4.
[2] Muhammad,.M.A. (1997) 'Economic analysis of milk production in district Okara' Pakistan Veterinary Journal, pp. 135-148.
[3] Khan, M. (1999) 'Economics of Milk production and marketing in the Development of Pakistan-With special reference to Peshawar
District' Unpublished Ph.D Thesis, University of Wales, Aberystwyth, UK.
[4] Khan,.M, Kanes K. Rajah and Michael Haines. (1998) 'An analysis of strategies and efficiency in the milk production systems in
Peshawar District KPK, Pakistan", Journal of the University of Wales Agricultural Society, P.49-70.
[5] Bouquiaux, J.M and R.Hellemans. (1998) Economic analysis of milk production in Belgium. Brussels, Centrum-economics
[7] Kalra, K.K., Rajvir. S, .Anil., Singh, R. and Chauhan,.R. (1995) 'Economic analysis of milk production and disposal in rural areas
of Haryana', Indian Journal of Dairy Science. Pp.546-555
[8] Singh, R.P.,Bhatnagar and Singh,B. (1995) 'Economic efficiency of milk production system under rural conditions', Indian Journal
of Animal Research. pp.27-32
[9] Sharma, J.P and .Singh, R.V. (1994) 'An economic analysis of milk production by different breeds of milch animals in humidtemperate
zone of Himachal Pradesh Indian Journal-of-Dairy-Science.pp.24-47.
[10] Dev,. R..Gupta and Raj, D. (1994) 'An economic analysis of milk production in Churu district of Rajasthan'. Indian-
Journal-of-Dairy-Science. Pp.749-755.
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Abstract : The seeds of horsegram (Macrotyloma uniflorum (Lam.) Verdc) cv. Dapoli Kulthi- 1 were subjected to gamma radiation (100, 200, 300 and 400Gy), EMS (0.2, 0.3, 0.4 and 0.5 %) and combination treatments. The mutations affecting gross morphological changes in plant habit, leaf and pod morphology, and maturity were scored as viable mutations. These mutants were characterized and named on the basis of specific characters constantly observed in them throughout the course of investigation. Effect of mutagens on the frequency and spectrum of different types of viable mutations in M2 generation were recorded. The high frequency of mutations in terms of mutants per 1000 M2 plant population was observed in low doses of EMS (0.2%), gamma radiation (100Gy) as well as in their combination (400Gy +0.4% EMS). The range of viable mutations in gamma radiation, EMS and their combinations was 0.61 to 2.16%, 0.62 to 2.98% and 0.21 to 1.81% respectively. Spectrum of viable mutations included desirable characters like early maturity, tall and dwarf habit, profuse branching, increased leaf area, higher number of pods, grains and grain weight were used to select desirable mutants.
Key words: Horsegram, EMS, Gamma radiation, frequency, viable mutations.
Key words: Horsegram, EMS, Gamma radiation, frequency, viable mutations.
[1] D. S. Virk, M. Chakraborty, J. Ghosh and D. Harris. Participatory evaluation of horsegram (Macrotyloma uniflorum) varieties and their on-station responses to on-farm seed priming in eastern India. Expl Agric., 42, 2006, 411–425.
[2] A. D. Barnabas, G. K. Radhakrishnan and U. Ramakrishnan. Characterization of a begomovirus causing horsegram yellow mosaic disease in India. Eur. J. Plant Pathol., 127, 2010, 41–51.
[3] C. S. Wang, S. V. Mohamed, J. M. Sung and T. L. Jeng. Optimization of somatic embryogenesis in suspension cultures of horsegram (Macrotyloma uniflorum (Lam.) Verdc) a hardy grain legume. Scientia Horticulturae, 106, 2005, 427–439.
[4] B. S. Keshava, A. S. Halepyati, B. T. Pujari and B. K. Desai. Yield and economics of horsegram (Macrotyloma uniflorum (Lam.) Verdc) as influenced by genotypes, plant densities and phosphorus levels. Karnataka J. Agric. Sci., 20(3), 2007, 589-591.
[5] S. N. Bolbhat. Studies on induced mutations in horsegram (Macrotyloma uniflorum (Lam.) Verdc). doctoral diss., University of Pune, Pune (MS), India, M.Sc., 2011.
[6] K. N. Dhumal and S. N. Bolbhat. Induction of genetic variability with gamma radiation and its applications in improvement of horsegram, in Feriz Adrovic (Ed.), Gamma Radiation, (Croatia: In Tech Publisher, 2012) 207-228.
[7] M. C. Kharkwal. Induced mutations in chickpea (Cicer arietinum L.) IV. Types of macro-mutations induced. Indian J. Genet., 60 (3), 2000, 305-320.
[8] P. M. Gaur and V. K. Gour. A gene inhibiting flower colour in chickpea (Cicer arietinum L.). Indian J. Genet., 62 (3), 2001, 273-274.
[9] R. Kartika and B. Subba Lakshmi. Effects of gamma-rays and EMS on two varieties of soybean. Asian J. Plant Sci., 5 (4), 2006, 721-724.
[10] S. G. Auti and B. J. Apparao. Induced mutagenesis in mungbean (Vigna radiata (L.) Wilczek): Proc. Induced Plant Mutations in the Genomics Era. Food and Agricultural Organization of the United Nations. Italy, Rome, 2009, 107-110
[2] A. D. Barnabas, G. K. Radhakrishnan and U. Ramakrishnan. Characterization of a begomovirus causing horsegram yellow mosaic disease in India. Eur. J. Plant Pathol., 127, 2010, 41–51.
[3] C. S. Wang, S. V. Mohamed, J. M. Sung and T. L. Jeng. Optimization of somatic embryogenesis in suspension cultures of horsegram (Macrotyloma uniflorum (Lam.) Verdc) a hardy grain legume. Scientia Horticulturae, 106, 2005, 427–439.
[4] B. S. Keshava, A. S. Halepyati, B. T. Pujari and B. K. Desai. Yield and economics of horsegram (Macrotyloma uniflorum (Lam.) Verdc) as influenced by genotypes, plant densities and phosphorus levels. Karnataka J. Agric. Sci., 20(3), 2007, 589-591.
[5] S. N. Bolbhat. Studies on induced mutations in horsegram (Macrotyloma uniflorum (Lam.) Verdc). doctoral diss., University of Pune, Pune (MS), India, M.Sc., 2011.
[6] K. N. Dhumal and S. N. Bolbhat. Induction of genetic variability with gamma radiation and its applications in improvement of horsegram, in Feriz Adrovic (Ed.), Gamma Radiation, (Croatia: In Tech Publisher, 2012) 207-228.
[7] M. C. Kharkwal. Induced mutations in chickpea (Cicer arietinum L.) IV. Types of macro-mutations induced. Indian J. Genet., 60 (3), 2000, 305-320.
[8] P. M. Gaur and V. K. Gour. A gene inhibiting flower colour in chickpea (Cicer arietinum L.). Indian J. Genet., 62 (3), 2001, 273-274.
[9] R. Kartika and B. Subba Lakshmi. Effects of gamma-rays and EMS on two varieties of soybean. Asian J. Plant Sci., 5 (4), 2006, 721-724.
[10] S. G. Auti and B. J. Apparao. Induced mutagenesis in mungbean (Vigna radiata (L.) Wilczek): Proc. Induced Plant Mutations in the Genomics Era. Food and Agricultural Organization of the United Nations. Italy, Rome, 2009, 107-110