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Observations on the Association of Ants with Coccids of Tea

Published online by Cambridge University Press:  10 July 2009

G. M. Das
Affiliation:
Senior Entomologist, Tocklai Experimental Station, Cinnamara P.O., Assam.

Extract

Certain species of COCCIDAE that excrete honeydew and are attended by ants or enclosed in their nests are quite prevalent on tea bushes and seed trees in the plains of Assam and West Bengal but those which are not attended by ants are kept under considerable check by the activities of their natural enemies. In Darjeeling, where the natural enemies are fewer, a number of species occur abundantly and are often responsible for serious damage to tea.

From the studies of the relative population of the ant, Crematogaster dohrni Mayr and the Coccid, Saissetia formicarii (Green), occurring on tea bushes it is doubtful if more than a small portion of the food requirement of the vast ant population in the nests which contain sexual forms could be met from the honeydew excreted by the small number of Coccids enclosed therein. The major part of food must, therefore, come from other sources. Insects attacking or visiting the tea bushes and tea seed trees or even those found on the ground appear to constitute the major part of the food of the ants, C. dohrni and Oecophylla smaragdina (F.).

Several factors are responsible for the decrease in the population or disappearance of the Coccids in the absence of attendant ants. In the plains, Eriochiton theae Green, Coccus hesperidum L. and S. formicarii entirely disappear in the absence of attendant ants either due to the activities of their natural enemies or by contamination with honeydew accumulation or both. Parasitism may be slightly higher in ant-free colonies, but no estimation was possible since, in the absence of ants, the Coccids are quickly destroyed by predators.

The ants do not protect the Coccids from Hymenopterous parasites; but their active movements hinder the parasites in their efforts to oviposit, and this leads to a reduction in the rate of parasitisation.

In the presence of the ants, O. smaragdina and Crematogaster dohrni, predators are rare; they are destroyed as are any other insects or any foreign bodies that happen to be near their nests, whether they constitute food or not. The larvae of predators which have a protective covering or which resemble Coccids, if they happen to have gained access to the Coccid colonies, are not attacked by the ants, because they are not recognised as different from the Coceids.

O. smaragdina does not normally transport Coccids, though young nymphs of E. theae and Coccus hesperidum may be aided in their dispersal, but Crematogaster dohrni and Crematogaster sp. are primarily responsible for the dispersal of S. formicarii and this takes place when an occasion arises to remove the Coccid to more favourable sites.

O. smaragdina does not destroy the nymphs and sedentary form of Coccus hesperidum for food, but sedentary forms which are unable to establish themselves on transfer from withered leaves to a new nest are eaten.

With the control of the attendant ants, the honeydew-producing Coccids disappear or at least they become rare. Conversely, where the Coccids are controlled, the ants automatically disappear.

Type
Research Paper
Copyright
Copyright © Cambridge University Press 1959

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References

Betrem, J. G. (1936). Gegevens omtrent de biologie van de dompolanluis (Pseudococcus citri) en de lamtoroluis (Ferrisiana virgata).—Arch. Koffiecult. Ned.-Ind. 10 pp. 4384. (Rev. appl. Ent. (A) 26 p. 606.)Google Scholar
Corbett, G. H. (1937). Division of Entomology. Annual report for the year 1936.—Gen. Ser. Dep. Agric. S.S. & F.M.S. no. 26 pp. 2948.Google Scholar
Das, G. M. (1954). Ant nests on tea bushes.—Two and a Bud 1 no. 2 pp. 1618.Google Scholar
Dutt, G. R. (1912). Life histories of Indian insects. IV (Hymenoptera).—Mem. Dep. Agric. India Ent. Ser. no. 4 pp. 183267.Google Scholar
Edwards, W. H. (1935). Report of the Government Entomologist.—Rep. Dep. Agric. Jamaica 1934 pp. 2428.Google Scholar
Froggatt, J. L. (1937). Promecotheca antiqua Wse. Leaf pest of coco-nuts.—New Guinea agric. Gaz. 3 no. 2 pp. 2122.Google Scholar
Garcia, C. E. (1935). A field study on the citrus green bug Rhynchocoris serratus Donovan.—Philipp. J. Agric. 6 pp. 311325.Google Scholar
Glover, P. M. (1930). Entomological aspects of lac research in India.—Bull, ent. Res. 21 pp. 261266.CrossRefGoogle Scholar
Groff, G. W. & Howard, C. W. (1925). The cultured citrus ant of south China.—Lingnaam agric. Rev. 2 pp. 108114.Google Scholar
Guenther, K. (1925). Untersuchungen an landwirtschaftlich schädlichen Insekten in Brasilien.—Z. angew. Ent. 11 pp. 400414. (R.A.E. (A) 14 p. 130.)CrossRefGoogle Scholar
Herzig, J. (1937). Ameisen und Blattläuse. (Ein Beitrag zur Ökologie aphidophiler Ameisen.)Z. angew. Ent. 24 pp. 367435. (R.A.E. (A) 26 p. 195.)CrossRefGoogle Scholar
Hough, W. S. (1922). Observations on two mealy bugs, Trionymus trifolii, Forbes, and Pseudococcus maritimus, Ehrh. (Horn., Coccidae).—Ent. News 33 pp. 171176.Google Scholar
Kirkpatrick, T. W. (1927). The common coffee mealy-bug (Pseudococcus lilacinus Ckll.) in Kenya Colony.—Bull. Dep. Agric. Kenya no. 18, 110 pp.Google Scholar
Krishna Ayyar, P. N. (1935). The biology and economic status of the common black ant of South India, Camponotus (Tanaemyrmex) compressus Latr.—Butt. ent. Res. 26 pp. 575585.CrossRefGoogle Scholar
Negi, P. S., Misra, M. P. & Gupta, S. N. (1930). Ants and the lac insect (Laccifer lacca).—J. Bombay nat. Hist. Soc. 34 pp. 182188.Google Scholar
Nixon, G. E. J. (1951). The association of ants with aphids and Coccids.—36 pp. London, Commonw. Inst. Ent.Google Scholar
O'Connor, B. A. (1950). Premature nutfall of coconuts in the British Solomon Islands Protectorate.—Agric. J. Fiji 21 pp. 2142.Google Scholar
Phillips, J. S. (1940). Immature nutfall of coconuts in the Solomon Islands.—Bull. ent. Res. 31 pp. 295316.CrossRefGoogle Scholar
Smith, H. S. & Armitage, H. M. (1931). The biological control of mealybugs attacking citrus.—Bull. Calif, agric. Exp. Sta. no. 509, 74 pp.Google Scholar
Strickland, A. H. (1947). Coccids attacking cacao (Theobroma cacao, L.), in West Africa, with descriptions of five new species.—Bull. ent. Res. 38 pp. 497523.CrossRefGoogle ScholarPubMed
Tunstall, A. C. & Sarmah, K. C. (1947). Notes on stem diseases of tea.—Memor. Tocklai exp. Sta. Indian Tea Ass. no. 16, 77 pp.Google Scholar
Watt, Sir G. & Mann, H. H. (1903). The pests and blights of the tea plant.—2nd edn., 429 pp. Calcutta.Google Scholar
Way, M. J. (1954 a). Studies of the life history and ecology of the ant Oecophylla longinoda (Latreille).—Bull. ent. Res. 45 pp. 93112.CrossRefGoogle Scholar
Way, M. J. (1954 b). Studies on the association of the ant Oecophylla longinoda (Latr.) (Formicidae) with the scale insect Saissetia zanzibarensis Williams (Coccidae).—Bull. ent. Res. 45 pp. 113134.CrossRefGoogle Scholar