JOURNAL OF AGRICULTURAL SCIENCE IN FINLAND Maataloustieteellinen Aikakauskirja Vol. 58: 221—237, 1986 Blossom beetle (Meligethes aeneus Fab.) as a yield factor in turnip rape (Brassica campestris L.) UNTO TULISALO Öljynpuristamo Oy, SF-00810 HELSINKI, Finland TUOMO WUORI Ritokalliontie II C, SF-00330 HELSINKI, Finland Abstract. Over the period from 1972—1982 the incidence of blossom beetles and their effect on yield formation in rape were studied in field trials and cage experiments at the Agri- cultural Research Centre, Vantaa, near Helsinki. The beetles migrated to the winter rape stands in May, when maximum daily temperaturesrose above + I5°C, and the migration to the spring rape stands occurred about three weeks later. The population peak in both winter and spring rapes occurred just before flowering. During the 1970’s the diminishing cultivation of winter turnip rape, the chief host of the blossom beetle, together with an increase in the extent of spring rapes resulted in the reduction of beetle populations to such low levels that intensive control measures were not required until 1981. It appears that the blossom beetles are gradually adapting themselves to the develop- mental rhytm of spring turnip rape. In the cage experiments beetles were maintained on the plants a) from the seedling stage to flowering, b) from flowering to maturity and c) from the seedling stage to maturity, start- ing with populations of 5, 15 or 25 beetles/plant. In the first treatment the beetles had no sig- nificant effect upon yields, as the plants were able to compensate for the injuries. In the other treatments even the lowest population density reduced yields. The larvae, too, contributed to the yield loss. Apparently a vigorous stand can tolerate large numbers of beetles up to a few days before flowering, provided they are promptly destroyed after that. In the field trials, yield losses caused by natural populations of beetles ranged from 0 —34 °7o. Even lower incidences than 2 beetles/plant caused measurable losses in yield. The injured plants produced fewer siliquas than the control plants, but tended to compensate by increas- ing seed number and seed weight. The trial results confirm that the threshold level, 1 beetle/plant at the early bud stage, should be followed. On the other hand they clearly demonstrate that the threshold level is es- sentially dependent upon the growing conditions and time of injury. For fully effective con- trol generally two applications of insecticide are needed. The best control strategy in the future will probably involve a comprehensive regional application eg. in two to three year sequences in order to prevent the beetle populations from building up to excessive levels. Index words: Blossom beetles, rapeseed, threshold levels for control, yield 221 https://www.c-info.fi/en/info/?token=tedVSs2x7BnOMoUU.BemkPltJajOgOvlinFIsyg.DKCWaGA4hEwzDJK1IbeAiyQrxkcLBg5FZpVH1LeHw_80asQvULDIsNRfawFz-eplozr2-4iX2OXbN45j7HSLGnRFRrfb18XA4z2Qk1KbHBgnknKYS-hyCyPIVir1w3SK7OHU0VKALEb-6NH_YHl3aetyuxDXBI3FYAphbkH6BZVt-q0NYC0W0w Introduction The blossom beetle (.Meligethes aeneus) is a permanent pest throughout the entire cultiva- tionarea of rapeseed in Europe. The damage caused by blossom beetles to rapeseed is a very complicated question and no simple numeri- cal data can be given to quantify it. The re- sponse of oilseed rape to pests is influenced greatly by a complex of several environmen- tal factors: water consumption, nitrogen nut- rition, temperature etc. (Winfield 1961, Pal- lot et ai. 1984). In addition, the ability of the rape plant to compensate for injuries plays a key role in yield formation (Winfield 1961, Williams & Free 1979, McGregor 1981). The effect of minor factors depends on the optimum balance among the major factors. Seed yield per rape plant is determined by the number of pods, seeds per pod and seed weight. Of these components the number of pods per plant has the greatest impact on yield (Olsson 1960) and thus the blossom beetle has a direct effect on yield by reducing the number of flower initials. Recent studies with spring rape have shown, however, that of the flowers that open only 45 % develop into pods (Tayo & Morgan 1975). Therefore provided the damage occurs early in the flowering stage, rape plants can possibly lose a proportion of their flowers without loss of seed yield (Mendham & Scott 1975). The capacity for compensating for such losses by retention of flowers varies under different growing condi- tions. Since the nineteenth century considerable research has been carried out on blossom bee- tles. As early as 1854 Heeger described them as pests. A few years later Gallus (1866) gave a good description of thebiology of this group and of the injuries they cause. Among others Wolf & Krause (1925) disputed the blossom beetle’s status as a pest and Kalt (1918) even regarded Meligethes as a benefi- cial insect. Later studies, however, explored the biology of the blossom beetle more thor- oughly (Burkhardt & Lengerken 1920, Nol- te 1954, Frizsche 1957, Blazejevska 1960). After the first controversial studies by Faber et al. (1920) the agronomic importance of Meli- gethes aeneus as a permanent pest of crucif- erous plants was clarified and by the end of the 1940’s its status as a pest was well accept- ed, when the acreage of various forms of oil- seed rape began to increase greatly. Many de- tailed aspects of its life cycle have been studied since then, e.g. natural enemies (Osborn 1960), temperature and humidity preferences (Nolte 1959), overwintering (Nolte 1954), colour vision (Nolte 1959) and host plants (Pruffer 1958). The chemical control of the blossom beetle is well documented in the literature. However, studies on the abundance of M. aeneus and its effect on the yield of the host plant or eco- nomic threshold levels of control are not so numerous. As well as describing injuries (cf. Maurer & Menche 1940), Winfield (1961) has studied control measures for Trowse mustard (Brassica juncea) and Gould (1975) for win- ter and spring rape (B. napus). It was not un- til the 1970’s that Free and Williams (1978, 1979 a) investigated in considerable depth the yield losses caused by blossom beetles in Trowse mustard and spring rape. The ability of rape plants to compensate for pest dama- ge is well illustrated in their studies. In Finland the blossom beetle is a common insect throughout the country (Vappula 1962). It has been known as a pest of swede, turnip and cabbage since 1897 (Reuter 1898). The beetle has also been found to injure flowering sprouts of cauliflower and brocco- li (Vappula 1962). It became a really harm- ful pest during the 1950’s and 1960’s as the cultivation of winter turnip rape became pre- valent. After the gradual introduction of spring oilseed brassicas a little rape but mainly turnip rape the mean annual num- ber of beetles decreased right up till 1977. It was not until 1981 that the beetles started once again to cause significant losses in several areas. The aim of the present study was to assess the effect of Meligethes aeneus on rapeseed 222 yields in field trials and cage experiments. This paper reports the results collected since 1972 and also some frequency figures from 1952 onwards. Materials and methods /. Open field trials Over the period from 1972—1982 a total of 35 field trials were carried out on spring and winter turnip rape. From 1972 to 1973 the field plot size was 25 x 25 m. This large size was designed to minimize the effect of bee- tles migrating from plot to plot. During the next three years theplots were made even lar- ger (50 X 50 m) and the replicates were lo- cated several kilometres apart. In 1977 a ran- domized block design was adopted with five replicates and a plot size of 4 X 25 m. Between 1972 and 1975 winter turnip rape, cv. Gruber, spring turnip rape, cv. Torpe and spring swede rape, cv. Oro were grown in the trials. From 1976 to 1977 spring turnip rape, cv. Torch and winter turnip rape, cv. Gruber were planted and from 1978 onwards only spring turnip rape, cv. Torch was grown. The seeding rates were 24 kg/ha for winter turnip rape, 10 kg/ha for spring turnip rape and 12 kg/ha for spring swede rape. Recommended fertilizer rates, 100 kg N/ha, were applied. Tok E 25, nitrofen, was applied as a herbi- cide in most of the trials. The insecticide used in the experiments was fenitrothion in 1972—75 and permethrin in 1976—82. The treated plots were sprayed at the early bud stage and again just before flowering. Pest incidence Sampling was started when the first blos- som beetles were migrating to therape plants. At each sampling date, every third day on average, the growth stage of the rape plants was recorded as well. The number of beetles was estimated in the field trials by two different methods. The number of beetles per 10 plants was counted in each of the blocks every third day. The first plants of the sample were selected at random from the rows after which every third was taken into the count. The beetles were count- ed on both sides of the yield block. In addi- tion, a netted sample was always taken from the same block. The beetles were netted on warm, dry days between 10.30 and 15.30with one sample consisting of 25 sweeps. The number of eggs and larvae in the stands was counted on inflorescence samples taken twice a week, starting from the flower bud stage. In addition, soil samples were taken using an auger and the number of pupae in the samples was counted. Insect damage Plant samples for determining the number of damaged pods were taken at the stage when flowering was completed but when the plants were still green. At this stage it was still pos- sible to count the number of blind stalks fair- ly accurately. Later, some of the blind stalks would have been lost and it would also have been difficult to differentiate between injuries caused by the blossom beetle and those aris- ing from physiological pod abortion or other such causes. However, as a high proportion of the primordial flower buds at the tip of each raceme had set fruit, a large degree of error was possible in estimating injuries in the tips of the shoots. Also the total number of healthy pods was counted to give a more reli- able picture of the amount of damage. “Tip- drop” damage caused by larvae was recorded in those rare cases where it occurred. The following parameters were measured on the plant samples of 25/block: plant height, number of branches, number of pods on the main raceme and branches, number of seeds in the pods and thousand seed weight. The first plant was selected at random from the rows and every third plant after that. 2. Cage experiments The cage experiments were carried out dur- ing the summer of 1973. The cages used in the 223 experiments consisted of wooden frames cov- ered with fibre netting of a mesh size small enough to prevent the passage of blossom beetles (Fig. 1). The basal area of the cages was 0.6 m 2. The cages were set out in the spring rape field after seedling emergence. The experimen- tal units consisted of 5, 15 and 25 bee- tles/plant, introduced at three different dates, and a control. The beetles were kept in the cages as follows: the first treatment from the seedling stage to the flowering stage, the second treatment from the flowering stage to maturity and the third treatment from the seedling stage to maturity. The experiments were carried out with four replicates making a total of 40 experimental units. The control cages were treated with fenitrothion. The first treatment was terminated by applying feni- trothion before the start of flowering. The beetles were collected from a neighbouring ra- peseed field the day before being placed in the cages. The parameters measured in the cage expe- riments were yield/cage, number of branches, total number of pods, number of pods on the main raceme and branches and thousand seed weight. Results and discussion The coincidence between rape plants and the blossom beetle On average, the first blossom beetles were observed on winter turnip rape from the first week of May onwards. When the spring was early, as for instance in 1974, the first blos- som beetles could already be observed on the plants by the end of April. These beetles had obviously overwintered on the crop. The ac- tual migration of the beetles to the crop did not begin until maximum daily temperatures had exceeded + 15°C for several days in suc- cession (Fig 2). In 1982 the first beetles only started to appear on plant stands, mainly Ta- raxacum officinale, during the latter half of May. The migration and swarming of the beetles thus followed the same temperature de- velopment in our study as in other studies (Nolte 1959, Free & Williams 1979 b). After overwintering the beetles can migrate directly onto winter turnip rape. Spring oil plants, however, do not serve as food and re- production sites until early June (Fig 3). Thus, for the first two or three weeks, the beetles need other food plants (Fig 4). During the 1970’s when both winter and spring rapes were grown within the same area, the beetles first migrated to winter turnip rape in spring, then to spring turnip rape and finally to spring swede rape (Fig 5). The maximum population densities were observed on winter rape just before or at the beginning of flowering of the main raceme, ie. in the middleof May (Fig 2). The peak den- sities on spring rape were observed during the same growth stage, which occurred one month Fig. 1, The cages in cage experiments were covered with fibre netting. 224 225 no. of Fig. 2. The frequency of blossom beetles in the winter rape stand and maximum daily temperatures in 1975. Fig. 3. The frequency of blossom beetles in a spring rape stand and maximum daily temperatures in 1975. later (Fig 3). This is due to the fact that the beetles lay their eggs on rape buds but not on open flowers. The work of Williams & Free (1978) among others confirms this observa- tion. 226 The abundance and population growth of blossom beetles Blossom beetles feed on the pollen of many different plant species (Pruffer 1958), but in Fig. 4. The flowering time of the food plants of blos- som beetles in early summer. Fig. 5. Blossom beetle numbers observed on winter and spring rapes during the summer of 1977. Finland they reproduce only on cultivated cru- cifers and a number of wild brassicas (Saalas 1943). In Finland most wild cruciferous plants flower relatively late. As a result the beetle pop- ulation living on them is rather sparse, even though the blossom beetle presumably occurs throughout the country (Vappula 1962). The population growth and mass reproduction of the beetle are dependent on cultivated cruci- fers. Reproduction on winter rape is close to the optimum, while on spring oil crops it is normally lower. Following the gradual phasing out of the cultivation of winter turnip rape and the slow introduction of spring rapes, the mean annual number of beetles decreased right up till 1977 (Fig 6). Thereafter the steadily increasing field area of spring rapes did not need to be sprayed for many years. It was not until 1981, by which time the cultivation of these crops had reached considerable proportions that the beetles started to cause losses in several regions. The reduction in size of the beetle popula- tion associated with the change in oil crop spe- cies can be partly explained by the fact that the reproduction of the beetles is more effec- tive on winter rape than on spring rape. A considerable proportion of the beetles appa- rently die before theirmigration to their main regenerative source, i.e. spring oil plants. This explanation is further supported by the obser- vation that when the spring is cool, the abun- dance of the beetles and their reproductive rate on spring rape appears to be higher be- cause the migration of thebeetles occurs later when spring rape serves better as a food source. The variations in the numbers of larvae on winter and spring rape during 1977 are pre- sented in Fig 7. Predators and parasites reduce the size of the larvalpopulation on the plants relatively little. Really significant population losses occur only when the larvae migrate into the soil to pupate (Nilsson 1985). In Nils- son’s study the losses at this stage were esti- mated to rise to a maximum of 40 % of the whole population. The reduction of popula- tion size during the winter has not been studied quantitatively, but is likely to be rath- er small. The overall growth of the blossom beetle population depends mainly upon the availa- bility of the regenerative host and is otherwise fairly constant. Apparently there is no weak point at any individual development stage, for example a specific parasite or disease, which in epidemic proportions could wipe out the population. The blossom beetle is thus a per- manent pest possessing a stong reproductive capacity. This was clearly seen in the steady Fig. 6. Changes in the mean annual number of blossom beetles in winter and spring rapes in 1975—82. 227 228 Fig. 7. The number of larvae/plant in winter and spring rape during the summer of 1977. Fig. 8. Yearly variations in the number of larval pro- geny of blossom beetles and the effect of con- trol measures in 1977—81. 3 population growth after 1977. The changes in the number of adult beetles (Fig 6) and the gradual increase in the number of progeny on the plant stands after 1977 (Fig 8) serve as examples of this. The netted sample figures over a long pe- riod are presented in Figs 9 and 10 to depict the abundance of blossom beetles. Quite apart from annual variations in population abun- dance, one can observe that the time of peak occurrence varies over the years by almost a month. It would seem that during the twenty- five years from 1952 to 1977, as winter rape displaced wild crucifers as the main food plant of blossom beetles, the population peak gra- dually shifted almost three weeks earlier. These observations clearly show that the blossom beetle has been able to adapt itself to new plant species rather well. In the long run it remains to be seen whether the blossom beetle will be able to change its reproduction cycle to exploit spring oil plants more effec- tively. On the other hand, the seed weevil (Ceutorhynchus assimilis Payk.), previously an abundant pest on winter rape, has disap- peared almost completely. The effect on yield I. The cage experiments When the blossom beetles were kept on the plants for about one week at the bud stage, which corresponds approximately to field con- ditions, they did not have enough time to cause any significant decrease in yield (Table 1). However, all the beetle levels used reduced the number of siliquas on the main racemes, Fig. 9. Blossom beetle numbers in the netted samples collected from winter rape in 1952—77. Fig. 10. Blossom beetle numbers in the netted samples collected from spring rape in 1977—81. 229 Table 1. The effect of blossom beetles on yield and yield components of spring turnip rape in cage experiments in 1973. Beetles/ Yield/cage No. of No. of healthy pods 1 000 plant g branches ~ ; ; ~ " Z ; seed weightTerminal Branches Total no. raceme X S; X S; X S; X S; X S; X S; Control 100.10 5.31 6.82 0.27 37.05 1.19 68.68 1.83 105.72 2.33 3.02 0.01 5 A 83.95 6.31 7.67 0.25 30.30 1.56 71.30 5.30 101.60 4.23 3.22 0.03 5 B 70.98 10.99 9.02 0.19 26.45 1.55 59.00 12.81 85.45 12.53 3.20 0.08 5 C 53.25 4.89 8.48 0.90 15.07 1.93 35.25 5.46 50.32 6.10 3.23 0.08 15 A 104.86 9.11 7.82 0.63 25.30 1.21 79.97 7.56 105.27 6.72 3.04 0.09 15 B 60.50 8.80 7.35 0.35 24.58 2.63 29.38 3.69 57.05 6.14 3.08 0.03 15 C 24.47 3.24 9.00 0.32 11.20 1.75 29.47 3.41 40.68 3.47 3.13 0.13 25 A 108.57 7.62 8.85 0.40 23.22 1.08 105.02 14.04 128.25 14.98 3.03 0.02 25 B 28.12 6.67 8.88 0.34 17.80 2.47 25.10 2.76 42.90 5.05 3.06 0.10 25 C 12.38 2.41 9.80 0.46 3.80 0.85 87.32 11.45 91.13 11.34 2.78 0.02 A = Beetles present in the cages from the seedling to the flowering stage B = Beetles present in the cages from the flowering stage to maturity C = Beetles present in the cages from the seedling stage to maturity while at the same time increasing the number of siliquas on the axillary racemes. This com- pensation explains the increase in yields when the larger numbers of beetles were present. The lowest beetle level used in the cage ex- periments may also occur under natural field conditions, but the two highest levels would be abnormally high. In the other treatments the blossom beetles and their offspring remained on the plants ei- ther from the start of the flowering stage or throughout the whole growing season starting from the bud stage. With such long periods of exposure, even the lowest number of bee- tles introduced caused considerable damage. The presence of blossom beetles throughout the flowering period was sufficient to cause considerable yield loss. The flowering period lasts rather long, and part of the yield loss was caused by the larvae. During this stage the plants were no longer able to compensate for the damage by means of extra growth. Al- though the plants still formed new shoots, new siliquas failed to develop on them. This situa- tion does not, however, correspond to field conditions, as blossom beetle densities are highest at the beginning of flowering and de- crease rather quickly thereafter. Contrary to former suppositions it was clearly seen that even small blossom beetle numbers during the flowering stage caused yield decreases. According to previous ac- counts, the presence of blossom beetles during the flowering stage should not cause any los- ses in yield (Williams & Free 1978). Proba- bly the growing larvae rather effectively cur- tailed the flowering of the plant by destroying not only flowers of the upper floral axis, but also by attacking the growing apex of both the main stem and its branches. In addition, it is obvious that the larvae, especially in great numbers, also strain the plants much and de- crease their ability to compensate. Although it is mere speculation to draw di- rect conclusions concerning the results of the cage experiments, they did at least give new information on one important aspect. A stand in good condition can probably carry rather high numbers of beetles for a few days before flowering without any yield losses resulting, provided the beetles are destroyed after that. The plants may compensate for flower buds injured or destroyed by blossom beetles by producing new racemes, extra buds on exist- ing racemes, or by increasing the size of seeds in the remaining pods as Winfield (1961) has 230 231 also noticed. However, the plant’s ability to compensate decreases quickly as the flowering advances towards the side stems. When great numbers of blossom beetles occur in the field, the onset of flowering is de- layed and the colour of the flowering field is much lighter than in healthy vegetation. Seri- ous blossom beetle damage can thus be seen by the colour of the vegetation from a dis- tance. 2. Open field trials Studies were carried out from 1976 to 1982 to clarify how naturally varying populations of blossom beetles affected rape yields under field conditions. An attempt was made to keep the control plots free of beetles with insec- ticides, but due to the mobility of the insects it was practically impossible to eliminate them entirely. Thus slight injuries were observed also in the control plots. Likewise, the in- secticides caused slight phytotoxic symptoms on rape. Insecticide applications nonetheless gave effective control of blossom beetle peaks during the bud stage. Only in 1978 was the degree of control poor, owing to bad weather. Blossom beetle numbers over the trial pe- riod were very low, only during the 1976 and 1981 seasons did they exceed 2 beetles/plant. In 1981 the development of the rape stands was hampered by drought as well as by large number of beetles, and yields fell to a very low level. The results of the trials are given in Ta- ble 2. Even though the effects of the blossom beet- le populations on yield formation in spring ra- pe varied considerably from year to year, it is quite evident that numbers of beetles even lower than 2 beetles/plant can result in yield losses. Actual yield losses in the trials ranged from 0—34 %, with the largest numbers of insects, as expected, causing the highest levels of damage. In 1977, when few beetles oc- curred, the untreated stands produced higher yields than the stands kept free of beetles. The implication here is that within certain limits, a blossom beetle population will not necessa- rily result in a yield loss; it may even increase the yield. Slight injuries during the early stages of yield formation may stimulate the plant to compensate by means of additional growth. On the other hand, when beetle numbers are low, the effects of insecticides may be nega- tive due to their phytotoxicity. The yield losses caused by blossom beetles are related mainly to a reduction in the num- ber of healthy pods producing seed, both in the main raceme and in side branches. None- theless, this loss was partly compensated for by the fact that the remaining pods carried a larger number of heavier seeds. The injuries inflicted by the beetles also stimulated the pro- duction of side branches, but for the most part these new branches did not bear productive pods. The beetles had no effect upon the height of the rape stands (Table 2). The impact of blossom beetle populations upon yield formation in rape depends not only upon the degree and time of injury, but very decisively upon the prevailing growing condi- tions. Provided the conditions are otherwise favourable, even extensive injury to the main stem will not necessarily reduce yields, as a stand in good condition will be able to com- pensate for the injury by means of side bran- ches. This compensative ability does fall off, though, as flowering progresses. The most se- vere losses are incurred in a situation where the plants are suffering from drought and lack of nitrogen. Under such conditions even small numbers of beetles can cause yield losses. It would appear that the larvae contribute to these losses to a greater extent than previous- ly thought, which again becomes manifest eg. during a drought. This idea is supported by the results of the cage experiments, in which a large population of beetles at the early bud stage did not cause yield losses, provided the plants were kept free of the beetles and their larvae thereafter. Chemical control and threshold levels At the present time, the only realistic way of controlling blossom beetles is by the use of 232 Table 2. The effect of blossom beetles on yield and yield componentsof spring turnip rapein field trials conducted at different sites (I— V) at the Agr. Research Centre in 1976—82. Year, Yield 1 000 No. of seeds/pod Healthy pods/ Damaged pods/ Number Plant No. of Site seed of height beetles/ k g/ha ">" wtg tr br total tr br tr br branches cm plant 1976 I A 1428 100 2.81 9.3 21.3 14.8 28.3 4.2 89 2.0 B 1 532 107 2.76 19.0 26.2 8.4 13.4 3.8 95 II A 1 460 100 2.83 20.0 15.3 8.2 7.0 2.9 92 2.2 B 1680 115 2.69 28.5 23.4 3.8 3.2 2.7 98 IV A 1 130 100 2.82 8.5 25.1 18.0 37.0 4.0 78 3.9 B 1299 115 2.56 26.8 39.3 7.6 11.9 3.7 81 1977 I A 1466* 100 2.24 14.2 12.4 13.2 26.3 33.7 7.4 20.0 2.8 113 0.6 B 1227 84 2.21 14.5 12.3 13.7 26.6 30.0 7.1 22.1 2.9 113 II A 1754 100 2.64 15.4 12.6 14.2 22.2 17.2 7.7 11.2 2.6 97 0.5 B 1 884 107 2.54 14.2 12.4 13.3 21.7 27.6** 9.0 14.9* 2.3 104 HI A 1230 100 2.44 14.0 11.7 13.0 21.9 16.9 9.6 16.5 2.5 93 0.2 B 1 169 95 2.38 15.2 13.5 14.3 20.8 20.0 8.4 20.9 2.7 105* IV A 1 421 100 2.40 16.3 14.4 15.3 15.0 26.7* 14.0 26.3 3.5 98*** 0.8 B 1362 96 2.18 14.2 12.9 13.5 14.1 18.4 13.3 32.4 3.3 78 1978 I A 1 789 100 17.0 14.0 15.6 21.7 21.9* 12.7* 25.3*** 3.3 96 2.0 B 1935 108 15.0 11.9 14.2 24.4 13.3 8.9 12.3 2.8 97 II A 1410 100 15.4 11.6 13.8 14.9 6.7 8.2 7.3 2.2 87 0.9 B 1 848** 131 16.7 12.7 14.9 27.4*** 18.2** 6.2 11.3* 3.3 96 111 A 2 113 100 18.3* 13.2 16.0 28.2 31.4* 6.8 18.7* 3.7 93 1.4 B 2 110 100 16.0 12.1 14.2 28.2 18.1 6.5 11.8 2.9 87 IV A 1 851 100 16.9 14.6 15.7 31.5* 42.5 7.2 21.3 3.2 95* 1.8 B 1923 104 18.1 14.0 16.0 25.2 25.8 7.3 19.7 2.8 87 A = No insect control, B = Insecticide sprayed, tr = terminal recame,br = branches. * Significant at the 5