Factors Affecting Pollination Activity of Megachile Lanata Lepel

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Factors Affecting Pollination Activity of Megachile Lanata Lepel Proc. Indian Acad. Sci. (Anim. SeL), Vol. 95, No. 6, December 1986, pp. 757-769. © Printed in India. Factors affecting pollination activity of Megachile lanata lepel D P ABROL* and R P KAPIL** Laboratory of Animal Behaviour and Simulated Ecology, Department of Zoology, Haryana Agricultural University, Hisar 125004, India ·Present address: Division of Entomology, S K University of Agricultural Science & Technology, Shalimar Campus, Srinagar (J and K) 191121, India ··Present address: Director, Indian Lac Research Institute (ICAR), Namkum, Ranchi 834010, India MS received 7 September 1985; revised 8 September 1986 Abstract. Foraging activity of Megachile lanata on Crotalaria juncea L. flowers occurred only when minimum threshold of environmental factors was surpassed, while the cessation of activities was governed mainly by the fast decline in values of light intensity and solar radiation. Between the initiation and cessation of field activity, foraging population showed a positive correlation with air temperature, light intensity, solar radiation and nectar-sugar concentration fluctuations, but was negatively correlated with relative humidity, soil temperature and wind velocity. The path coefficient analysis revealed that direct effect of solar radiation and light intensity on foraging population were much pronounced and positive, while the effects of other factors were of very low magnitude, negative or negligible. However, their interrelationships caused accentuation of the overall effects of air temperature, relative humidity and nectar-sugar concentration. The resultant correlation with bee activity were strengthened through their favourable or unfavourable interaction with other factors. Keywords. Environmental factors; Megachile lanata; Crota/aria juncea; pollination; path analysis. 1. Introduction The pollinating effectiveness of bees depends upon their foraging population in the field and their behaviour on a crop. Since the field population as well as individual's foraging behaviour result from their innate and unavoidable responses to various environmental stimuli, ecological investigations on qualitative and quantitative aspects of their foraging on economic crops need to be thoroughly understood. This will help in assessment of the resultant interrelationships for their effective management and utilisation as prospective pollinators. Though pollination effective­ ness of various bee pollinators has extensively been studied in the past, the studies are mainly based on a limited set of environmental conditions. For instance, Cirudarescu (1971) found that the number of insect visitors on lucerne was directly related to temperature and inversely to relative humidity, but the latter authors found it unaffected by relative humidity and vapour pressure. The flower visiting speed of honey bees increased with temperature (Benedek 1972; Burill and Dietz 1981). Wrona (1973) stated that pollination efficiency of honeybees increased with temperature and decreased with wind speed. Szabo and Smith (1972) found that foraging activity was positively correlated with a suitable combination of light intensity and temperature combined but not with the light intensity independent of temperature. Nunez (1977) reported that the morning activity was related to nectar 757 758 D P Abrol and R P Kapil flow and in the evening it W!iS correlated with photoperiod. These reports indicate no fair general pattern of effects of'different environmental factors influencing the pollination activity of bees. The probable reason seems in omission of such contributing factors actually influencing the pollination activity and in random selection of a few convenient ones having either no interaction or working in diverse ways, generating thus inconclusive results. Since environment is a complex of interrelated factors which influence the bee activity, and also plant physiology, a study of a complex phenomenon like pollination shall remain incomplete until a sizeable matrix of factors are taken on ensanable. These were the reasons for the present investigations which include air, temperature, relative humidity, light intensity, solar radiation, nectar-sugar concentration, soil temperature and wind velocity as factors probably influencing bee-flower relationships. 2. Materials and methods This study was conducted during September 1984 in sub-tropical Hissar located in the North Western plains of the country between 28° 59'-29° 46' N (latitude) and 75° 11'-76° 18 E (longitude) at 215·2 m (altitude) on the Plant Breeding Farm of Haryana Agricultural University, Hissar where Crotalaria juncea is grown regularly for seed production. Hourly observations starting from 0800-1800 h on population/ m 2 of Megachile lanata were recorded on C. juncea following Sihag (1982). Concurrent with the forager counts hourly measurements of environmental factors were made in the experimental field. Atmospheric temperature (T) and relative humidity (RH) were measured with a 'dry and wet' bulb thermometer. Soil temperature (ST) was recorded with a soil thermometer at a depth of 25 cm. Light intensity (LI) was recorded with a Luxmeter, model Luxomet-300 manufactured by Mls Research Instrumentation, Naraina Industrial Area, New Delhi. Similarly solar radiation (SR) was recorded by solarimeter, model SM 201, manufactured by MjsCentral Electronics Ltd., Sahibabad, UP. Wind velocity (WV) was recorded with a hand Anemometer manufactured by Mls Research Instrumentation, Naraina Industrial Area, New Delhi held vertically at a height of about 1 meter above the crop surface. Total dissolved solids in the nectais (NSC) were estimated with the pocket refractometers (model 1093, Range, 0-50%; model 312, Range, 40-85%) manufactured by Mls ToshniwalBrothers Pvt. Ltd., New Delhi. The recorded data were analysed on TDC-316 computer for simple correlation and path coefficient analysis following Dewey and Lu (1959). 3. Results 3.1 Commencement and cessation offoraging activity The data in table 1 show the temperature, relative humidity, light intensity, solar radiation, soil temperature and wind velocity in relation to the commencement and cessation of field activity by M. lanata on C. juncea flowers during September 1984. The time at which the commencement of field activity occurred varied from one day to another, which was perhaps dependent upon the attainment of minimum threshold conditions required for the initiation of field activity. ~ ~ ~ ~ ..... ~. '8 §.f ~ .....<;. ~. Table 2. Estimates of correlation coefficients exhibiting interrelationships of different environmental ~ factors influencing pollination activity of M. lanata. Relative Light Solar Nectar-sugar Soil Wind Bee Factors humidity intensity radiation concentration temperature velocity activity f ~ Air temperature -0'359* (}690** 0·0670 0,547** -(}176 -0,264 0,650** is'' Relative humidity -0,0661 0,833** -0'871** (}977** 0'987** -0'357* 5 Light intensity 0,462** 0,364* 0·0632 0·0040 .0'826** s Solar radiation -(}542** (}880** 0,865** 0·1548 Nectar-sugar concentration -0'819** -0'810** 0,584** Soil temperature 0,984** -0,260 i Wind velocity -0,286 *P~0'05, n-2=31 *·P~O·OI, n- 2= 31. .....:I VI\0 760 D P Abrol and R P Kapil Variation in commencement of the field activity, however, could not be explained by anyone factor. A complex combination of various factors was perhaps responsible for initiation of field activity. The studies further revealed that, in general a temperature of 22·5°C, 75% relative humidity, 2100 Ix light intensity, 25 mw/crn 2 solar radiation, 22°C soil temperature and 3·0 kmph wind velocity appeared to be the minimum threshold conditions for initiation of field activity. The cessation of activity was, however, governed mainly by the fast decline in values of light intensity and solar radiation, which were appreciably low than that required for commencement of field activities. It was found that cessation of activities occurred even before the air temperature dropped to the values associated with the commencement of field activity (22·5°C). The critical examination of the data further revealed the occurrence of factor compensatory mechanism for initiation of bee activity within the foraging ranges of the bees, where low values of one factor were compensated by the higher values of others. For instance, on 11 September 1984, foraging flight occurred when air 2 temperature was 22·5°C light intensity 2700 lx and solar radiation 41 mw/cm , while on 14 September 1984, it started at a higher temperature (27'5°C) when values of 2 other factors like light intensity (2100 Ix) and solar radiation (30 mw/crn ) were comparatively lower than those required for the initiation of field activity on 11 September 1984. Similar situation was observed on 19 September 1984, when the foraging flight commenced at 28°C, but the values of light intensity (2600 lx) and solar radiation (25 mw/cm-) were lower than those associated with initiation of field activity on 11 September 1984. Evidently, the observations on 11 September 1984 indicate that low values of air temperature were compensated by higher values of light intensity and solar radiation while on 14 and 19 September, the reverse was true. Thus, existence of factor compensating mechanisms governing initiation of bee activity is a clear possibility. 3.2 Diurnal trends in bee activity in relation to various environmental factors Hourly observations on bee counts showed that their abundance followed air tempe­ rature, light intensity, solar radiation, soil temperature and nectar-sugar
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