Significance of Trianthema portulacastrum L. in sustenance of Apis florea colonies during dearth period

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Research Paper 01/07/2015
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Significance of Trianthema portulacastrum L. in sustenance of Apis florea colonies during dearth period

Ujjwal Layek, Prakash Karmakar, Pankaj Kumar Pal
Int. J. Biosci. 7(1), 22-29, July 2015.
Copyright Statement: Copyright 2015; The Author(s).
License: CC BY-NC 4.0

Abstract

The paper reports flowering phenology, floral visitors of Trianthema portulacastrum and melissopalynological analyses of 8 honey samples and 374 pollen loads of Apis florea, collected during May to August from Bankura district, West Bengal. T. portulacastrum flowers during April to October. Flowers open at 6.30-7.00 am in the morning. Anther dehiscence takes place after 30 minutes from flower opening. Closing of the flower takes place at about 11.30 am – 12.15 pm. During the opening phase of the flower, a number of visitors viz. Apis cerana, A. florea, Augochloropsis metallica, Halictus sp., Pseudoborbo bevani and Trigona iridipennis visit the flower for nectar or pollen. Melissopalynological analyses revealed that all the honey samples were multifloral in origin and T. portulacastrum present in all the honey samples. Regarding the pollen foraging scenario of the bee species, T. portulacastrum also played an important role during those months. The overall result reflects the importance of T. portulacastrum as a major source of both nectar and pollen grains for A. florea colonies during dearth period.

Adamson RS. 1962. The South African species of Aizoaceae XII. Sesuvium, Trianthema, Zaleya. Journal of South African Botany 28, 243-253.

Balyan RS, Bham VM. 1986. Emergence, growth and reproduction of horse purslane (Trianthema portulacastrum) as influenced by Environmental Conditions. Weed Science 34, 516-519.

Duthie JF. 1960.  Flora  of  Upper  Gangetic  plain. Delhi, India. Periodical experts 500.

Erdtman G. 1960. The acetolysis method. A revised description. Svensk Botanisk Tidskrift 54, 561-564.

Holm L, Doll J, Holm E, Pancho J, Herberger J. 1997. World Weeds: Natural Histories and Distribution. John Wiley and Sons, New York. 1129 p.

Jeffrey C. 1960. Notes on tropical African Aizoaceae, Kew Bull. 14, 235-238.

Jones GD, Bryant VM. 1996. Melissopalynology. In: Jansonius, J; (Mc Gregor, D. C. Eds.). Palynology, principles and applications salt lake city: AASP Found, 933-938.

Kifle TB, Hora KW, Merti AA. 2014. Screening of potential herbaceous honey plants for beekeeping development. Agriculture, Forestry and Fisheries 3(5), 386-391. http://dx.doi.org/10.11648/j.aff.20140305.19

Kumar G, Banu GS, Pappa V, Sundararajan M, Pandian MR. 2004. Hepatoprotective activity of Trianthema portulacastrum L. against paracetamol and thioacetamide intoxication in albino rats. Journal of Ethnopharmacology 92, 37-40. http://dx.doi.org/10.1016/j.jep.2003.12.009

Louveaux J, Maurizio A, Vorwohl G. 1978. Methods of Melissopalynology. Bee World 59, 139-157.

Maurizio A. 1951. Pollen analysis of honey. Bee World 32, 1-5.

Rattanata N, Daduang S, Phaetchanla S, Bunyatratchata W, Promraksa B, Tavichakorntrakool R, Uthaiwat P, Boonsiri P, Daduang J. 2014. Antioxidant and antibacterial properties of selected thai weed extracts. Asian Pacific Journal of Tropical Biomedicine 4(11), 890-895. http://dx.doi.org/10.12980/APJTB.4.2014APJTB-2014-0422

Shanmugam SK, Bama S, Kirthiga N, Kumar RS, Sivakumar T, Dhanabal P. 2007. Investigation of analgestic activity of leaves part of the Trianthema portulacastrum (L) in standard experimental animal models. International Journal of Green Pharmacy 1(1), 39-41.

Shymsunder A, Rajyalakshmi G, Bharath A, Rajeshwar Y. 2009. Antihyperglycemic activity of Trianthema portulacastrum plant in streptozotocin induced Diabetic Rats. Pharmacologyonline 1, 1006-11.

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