Beetle, Cheilomenes Lunata Fab.(Coleoptera: Coccinelidae) on Aphis Craccivora Koch Was Studied Under Fluctuating Laboratory Condition of 25 - 32°C and 33 - 73° RH
Total Page:16
File Type:pdf, Size:1020Kb
- 18 Life Cycle of the Ladybird Beetle, Ch eilomenes lunata Fab. (Coleoptera: Coccinellidae), A Potential Biocontrol Agent of the Cowpea Aphid, Aphis Craccivora (Koch) (Homoptera:Aphididae) ODEBIYI, 1. A. and KEMABONTA, K. A. I' Department of Crop Protection and Environmental Biology, University of Ibadan, Ibadan, Nigeria. Niger. J. Entomo!' 23: 18 - 21 (2006) ABSTRACT. The life cycle of the ladybird beetle, Cheilomenes lunata Fab.(Coleoptera: Coccinelidae) on Aphis craccivora Koch was studied under fluctuating laboratory condition of 25 - 32°C and 33 - 73° RH. The average incubation period was 3.2 days with a hatchability of 93.1 %. There were four larval instal's with nd developmental duration averaging 3.0, 2.2, 2.2 and 4.2 days for the 1'\ 2 , 3 rd and 4th larval instars, respectively. The total larval developmental period ranged from 9.7 - 13.5 days and the pupal period lasted for 4.8 days. Mortality at these stages were 37.6 and 7.5% respectively. Pre-oviposition period averaged 3.7 days. The mean number of eggs per female was 1257.4 and the mean oviposition period was 47.0 days. The longevity of mated males and females averaged 87.9 and 72.1 days, respectively, while those of unmated males and females averaged 80.8 and 61.5 days, respectively. The male to female ratio was 1: 1. Information were given on the moulting process and copulation of the ladybird beetle. INTRODUCTION Aphis craccivora (Koch) (Homoptera: the efficacy and efficiency of the ladybirds as a Aphididae) is a minor pest of cowpea [f'igna predator evaluated, factors limiting abundance of unguiculatai (L.) Walp.] in Africa. It is however an the ladybird beetle understood, and a cheap mass- important vector of cowpea aphid-borne mosaic rearing technique under controlled conditions virus, which causes resetting, stunting, and mosaic developed. of the plants, (Berks and Corti, 1975; lIT A, 1776, The objective of this study was therefore to 1977). Singh and Allen (1979) reported that under study the life cycle of C. lunata on A. craccivora. unfavourable conditions a generation might take only 3 days. The adults live for 6 to 15 days and MATERIALS AND METHODS may produce more than 100 progenies. In Nigeria, Site of the Experiment the fecundity and developmental rate of A. The experiment was carried out in the craccivora varied widely with changes III laboratory of the Department of Crop Protection temperature (Ansari, 1978). Under suitable climatic and Environmental Biology, University of lbadan, conditions, the development of one generation under fluctuating laboratory conditions of 25 - takes 6 to 8 days and has a fecundity of about 100 32°C and 33 - 73% RH. progenies. With each generation, the degree of infestation of affected plant increases five to eight Culture of Prey (A. craccivora) and Predator fold. This may cause stunting of plants and poor (C. lu nata) nodulation of the roots which affect the yield; in A culture of A. craccivora was established on extreme cases, the plant dies (Heinze, 1977; Singh non-infested cowpea (Ife brown) planted in 5cm and Van Enden, 1979). diameter plastic pots containing field soil in order Methods used to control vl craccivora include to ensure a continuous and sufficient supply of all chemical, cultural, resistant varieties and biological developmental stages. There were two plants per contro!' It has been observed that the coccinelid pot which were watered regularly and maintained beetle, Cheil omenes lunata Fab., indigenous to weed-free. The plants were infested with adult A. Nigeria and many countries in tropical Africa, can craccivora at the podding stage using camel's hair be used effectively as a bio-control agent. brush moistened in water. To use this lady beetle in hie-control, the life C. lunata (males and females) were collected cycle of the ladybird beetle on cowpea aphid must from cowpea field at the Agricultural Biology farm be studied, and released on A craccivora infested potted plants in rectangular wooden cages (59 x 44 x 45cl11) with * Corresponding Author. nylon mesh on the sides. Three cages each 'Present address: Nigerian Stored Products Research containing three potted plants infested with A. Institute, P.M.B. 21543, Lagos, Nigeria. craccivora and C lunata were maintained. e-mail: [email protected] - ODEBIYI: THE LIFE CYCLE OF THE LADYBIRD BEETLE 19 Rearing Unit Larval Stage Plastic Petri dishes, 8.5cm in diameter, were The number of observed moults (three) used as rearing units. The lids of the dishes were indicatd that C. lunata passed through four larval bored with a hot iron pipe three-centimeter in instars (Table 2). From measurement of head diameter. The holes so made on the lids were capsule width a mean growth ratio of 1.3 was covered with fine nylon mesh glued with Evostic® calculated. st to allow for adequate ventilation. A moistened 1 Instar filter paper, 8.5cm in diameter, was placed at the Newly emerged l " instar larvae were tiny and bottom of each Petri dish and a leaf or two broad translucent. They did not move for about 24 hr. leaves of cowpea were placed on the filter paper to until the colour deepened. The larvae were provide food for the aphids. conspicuously co loured with patches of pale yellow on the black background. The antennae and Life Cycle of C. lunata labial palps were not very visible. The maxillae and Egg stage mandibles though relatively small, were Eggs removed from the rearing units after conspicuous. Setae were observed on all parts of oviposition by female C. lunata were transferred to the body but more on the dorso-lateral aspects. The st. I a new rearing unit containing only moistened filter 1 mstar arva measured 2.5 mrn in length and had paper. The incubation period of 250 newly laid 2.0m head capsule width of 0.44mm, duration 111 eggs was determined. the instar 2.9 days and mortality was 15.1 %. Larval and pupal stages Moulting Process Following larval ecIosion from egg, Moulting in the 1st, and subsequent instars, development was followed to the adult stage by was preceded by a short period of inactivity during daily observation. The number of larval instars was which the larva glued itself by the anal extremety determined by direct counting of larval moults. to the inner surface of the rearing unit or on a leaf. The widths of the head capsules were measured It remained still in this position with the skin using a micrometer eyepiece mounted on a tightly stretched and the whole body appeared to be binocular microscope at varying magnification. overstuffed under the skin. The skin then split The larvae were fed with A. craccivora. across the dorsal surface from the head down to the third thoracic segment. The head got pulled out Adult Stage from the head capsule and the new larva got out of Ten newly emerged females and 10 newly the exuvia. The whole moulting process took few emerged males were kept separately in a rearing minutes. The larva moved briefly after moulting unit and fed with A craccivora ad lihitum to obtain and then rested. rd the longevity of unmated adults. Newly emerged 211d, 3 and 4th instal's males and females (10 each) were paired to obtain The newly hatched larvae were translucent but the fecundity, oviposition period, post-oviposition the colour got deepened to black background with period and the longevity of mated adults. some white spots. The antennae and labial palps became more conspicuous as the larva got older. In th. I Test of Parthenogenesis in C. lunata tIre «4 mstar, t tree antennal segments were evident To know if parthenogenesis takes place in C. and mandibles and maxillae were very well lunata, 20 virgin females were confined singly and developed. All the larval instars emitted brownish fed ad libitum with all the life stages of A. drops when slightly pressed. Table 1 shows the size craccivora in the rearing units. Observations on and the duration of each larval instar. Mortality in ')nd ~ rd d 4th . oviposition were made over a period of 30 days. the ~ ,.J an mstars were 7.5, 9.5 and 5.5%, respectively. RESULTS Egg Stage Pupal Stage Two days before entering into the pupal stage, When laid, the eggs of C. lunata were 1.5± the 4th instar larvae became less active, and less 0.0 I rnrn long (n=20), brightly co loured but 24 hr sensitive to disturbance. They became shortened in before hatching, they became translucent, making length an attached to the Petri dish at the caudal black young larvae, visible through the chorion. extrern ity. Incubation period averaged 3.2 days. At eclosion, the chorion cracked at the side and tiny ant-like The pupa was of bright golden colour that later larva wriggled out head first, leaving a transparent became light orange with crescent shaped black chorion. Interval between the 1st and the last larval marking that jointed end to end. Nine segments eclosure from eggs in a batch was never more than were visible, the remaining being covered up by 3 hr. Percentage viability of the eggs averaged the last larval exuviae. The pupa, when disturbed, 98. I %. (Table I). had a curious habit of lifting the body into a - NIGERIAN JOURNAL OF ENTOMOLOGY VOL. 23, 2006 20 Table l. Developed durntion, body length and mortality of Eggs were deposited near aphid colonies. This life cycle stages of C lunutu reared on A cracciovoru may be an important factor for the survival of the Stage Length Developmental eXt) ( + SO (mm) duration (days) Mortality newly hatched larvae which do not have to search Egg 15±001 3.2±0.36 1.9 for food.