Subscribe Now Subscribe Today
Research Article

Management of Diamondback Moth, Plutella xylostella (Lepidoptera: Plutellidae): a Lesson from South East Asia for Sustainable Integrated Pest Management

Ali H. Sayyed, Mohsin R. Rizvi and Anwaar H. Alvi
Facebook Twitter Digg Reddit Linkedin StumbleUpon E-mail

The diamondback moth, Plutella xylostella (Lepidoptera: Plutellidae) is the greatest threat to crucifer through out the world including Pakistan, sometime causing more than 90% crop loss and estimated cost over US$ 1 billion annually. Prior to the introduction of synthetic insecticides diamondback moths were never reported as the major pests of crucifers, however with widespread use of synthetic insecticides on crucifer important natural enemies were eliminated which led to continue use of synthetic insecticides and eventual insecticide resistance and control failure. This review provides a global overview of the biology and ecology of diamondback moth including past, present and perspective future management strategies with special reference to Pakistan.

Related Articles in ASCI
Similar Articles in this Journal
Search in Google Scholar
View Citation
Report Citation

  How to cite this article:

Ali H. Sayyed, Mohsin R. Rizvi and Anwaar H. Alvi, 2002. Management of Diamondback Moth, Plutella xylostella (Lepidoptera: Plutellidae): a Lesson from South East Asia for Sustainable Integrated Pest Management. Pakistan Journal of Biological Sciences, 5: 234-245.

DOI: 10.3923/pjbs.2002.234.245


Distribution and economic importance: Plutella xylostella is cosmopolitan in distribution (Salinas, 1986) although it is generally thought to have originated in the Mediterranean region (Waterhouse and Norris, 1987). More recently, Kfir (1998) has suggested that P. xylostella might have originated in Southern Africa due to rich and diverse fauna of P. xylostella parasitoids, the large number of indigenous brassicas and the arrhenotokous form of the P. xylostella parasitoid, Diadromus collaris Grav. It has been recorded throughout temperate and tropical zones, as far north as Iceland (60 oN) and far south as Newzealand (45 oS) (Ooi, 1986). Studies have shown that movement of P. xylostella occurs mainly through imported cabbage (Tan and Lim, 1985).

Plutella xylostella is the most destructive pest of cruciferous plants throughout the world (excluding Europe) sometimes causing more than 90% crop loss (Verkerk and Wright, 1996) and inflicts more than US $ one billion in losses per year (FAO, 1992). In the tropics and sub-tropics, P. xylostella can cause damage throughout the year except for a brief period during the rainy season (Talekar and Lee, 1985). The larvae of P. xylostella feed on all above ground parts of the plant thereby reducing yield and quality and thus marketability of the produce (Talekar, 1996).

Lack of natural enemies in many non-indigenous areas, especially of parasitoids, its ability to migrate long distances and its high rate of fecundity are considered to be the major causes of the high pest status of P. xylostella in most parts of the world (Lim, 1986). The widespread use of synthetic insecticides on high value crucifer crops has resulted in high levels of resistance in P. xylostella populations (Talekar and Shelton, 1993).

Host range: The host range for P. xylostella is limited to crucifers that contain mustard oils and their glucosides (Hillyer and Thorsteinson, 1971). Many glucosinolates stimulate feeding in P. xylostella but two of these, 3-butenyl and 2-phenyl ethyl, are toxic at high concentrations (Nayar and Thorsteinson, 1963). The glucosides sinigrin, sinalbin and glucocheirolin act as specific feeding stimulants for P. xylostella and 40 plant species containing one or more of these chemicals serve as hosts, including cabbage, broccoli, cauliflower, collards, rapeseed, mustard and Chinese cabbage. Non-host plants may contain these stimulants but also contain feeding inhibitors or toxins (Gupta and Thorsteinson, 1960a). Certain chemicals such as sulfur-containing glucosinolate or its metabolites, allyl isothio-cyanates act as oviposition stimulants (Gupta and Thorsteinson, 1960b). While Pivnick et al. (1990) reported that male sexual maturation results from exposure to host plants. Alternate weed hosts are especially important in maintaining the P. xylostella populations in temperate countries in spring before cruciferous crops are planted (Talekar and Shelton, 1993).

Biology and ecology: Plutella xylostella adults rest on the host plant during the daytime and become more active just before dusk (Harcourt, 1957). Mating occurs during first 4-15 hours following emergence (Pivnick et al., 1990) with a peak between 1 and 2 hours of scotophase (Ohira, 1979). Mating success of P. xylostella can vary greatly, some males may mate with more than 10 females (Yamada, 1979), and mating success of both sexes may be influenced by age (Yamada, 1979) size (Uematsu, 1992), production of sex pheromone (Chow et. al. 1986) and exposure to host plant (Pivnick et al. 1990). In response to emission of female sex pheromone during the scotophase (Pivnick et al. 1990), the male walks in front of the female, while vigorously fanning its wings (Ashihara, 1977). Male response to female sex pheromone was found to vary among populations in the field but did not differ between susceptible and insecticide resistant populations in the laboratory (Maa, 1986). During mating, the pair faces in opposite directions and hangs downwards, the female above, the male below (Chelliah and Srinivasan, 1986). Females start laying eggs soon after mating (Talekar and Shelton, 1993).

The oviposition rate is the highest in evening, 24 to 48 hours after mating (Abro et al., 1992). The eggs are yellowish white to yellowish green (Chelliah and Srinivasan, 1986), cylindrical to oblong, with average dimensions of 0.48 x 0.25 mm (Bhalla and Dabey, 1986) and are laid mainly on the lower surface of the leaves (Abro et al., 1992). A few eggs are laid on stems and leaf petioles (Harcourt, 1957). The maximum recorded number of eggs laid by a single female is 451 (Marsh, 1917). The period from oviposition to hatching ranges between 2.1 days at 26.4 2.7 oC and 86 14% RH (Wan, 1970) to 11 days at 15-26 oC and 60-90% RH (Kanervo, 1936). Just before hatching the eggs darken (Harcourt, 1957) and soon after emergence neonate larvae start crawling and making "sensing" movements with the head. After stimulation from others, larvae start to feed (Salinas, 1984) and to mine into spongy mesophyll tissue (Harcourt, 1957; Talekar and Shelton, 1993). Isolated larvae tend to starve due to lack of intra-specific stimulus (Salinas, 1984).

The first instar larvae P. xylostella are light green in colour with a dark head and ca 1 to 1.7 mm. in length. (Ho, 1965). The head capsule width is ca 0.16 mm, 0.26 mm 0.38 mm and 0.63 mm for first to fourth instar larvae respectively.

The first instar larvae complete moulting within feeding mines (Talekar and Shelton, 1993). Early second instar larvae emerge and feed from the lower surface of leaves, chewing irregular patches in the leaves and eventually consuming all leaf tissues except the veins and the upper epidermis creating the "window effect" characteristic of P. xylostella (Harcourt, 1957; Talekar and Shelton, 1993). Prior to each moult, the larvae first constructs a loose silken web adhering to leaf surface beneath which larvae moults (Ho, 1965). This also forms a sail for migration on the wind away from source of disturbances or from places where food is scarce (Wu, 1968). The newly moulted second to fourth instar larvae are pale green with a white head (Ho, 1965). Third and fourth instar larvae do the most damage as they consume a greater amount of leaf matter compared with other instars (Salinas, 1972). Fourth instar larvae destined to be males can be distinguished by the fifth abdominal segment as it lighter in colour than adjacent segments due to presence of light coloured, male gonads Liu and Tabashnik, 1997).

Larval development varies from 5-30 days depending on the ambient temperature. It is followed by the pre-pupal and pupal stages, which may last 4-15 days (Harcourt, 1957; Waterhouse and Norris, 1987). When fully grown, the larvae frequently migrate to older and lower leaves nearer the ground (Chua and Lim, 1977) and spin a loose silken cocoon about 9 mm long (Hill, 1983). During the pre-pupal stage, larval coloration often changes from green to pink. The thoracic diameter increases while abdominal length decreases, wing development commences as well as modification to the head appendages (Robertson, 1939). The pre-pupae develop into pupae within 1-3 days at 20 oC (Salinas, 1972). When first formed, the pupa is green but gradually becomes light brown with dark markings. The pupa becomes almost black immediately before emergence. At the pupal stage, the sex of P. xylostella can sometimes be determined by examination of the genital openings (Robertson, 1939). The female pupa also has a greater wet and dry weight (Atwal, 1955).

The adult moth is slender, greyish brown in colour with a wing expanse of 13-17 mm. Wing expansion in male is smaller in size compared with female (Ho, 1965). Each wing has three lobe-like median yellow-white stripes that form a characteristic diamond-shaped pattern giving rise to the common name of the moth. Moths can easily be sexed by the pattern of the "diamond". (Atwal, 1955). The male also has a broad cream coloured dorsal stripe from base to near tornus often edged with black towards disk, whereas in females this stripe is much less distinct and often merged in the general background colour (Robertson, 1939).

Temperature, food availability (Wang, 1983) and rainfall (Talekar and Lee, 1985) are important factors affecting P. xylostella abundance. The development time from egg to adult decreases with increase in temperature (Abro et al., 1992). In Malaysia, for example, P. xylostella takes ca15 days to complete its life cycle in the hotter lowland areas (monthly maximum temperature 26-28oC) compared with ca 26 days in cooler upland areas (monthly maximum temperature 20-24oC) resulting in 24 and 14 generations per annum respectively (Ooi, 1986). The development of P. xylostella is not reported to be greatly affected by fluctuations in relative humidity (Sivapragasam et al., 1984) but food quality affects both the developmental period and fecundity. For example, larvae reared on mature cabbage leaves were observed to spend longer as larval and pupal stages compared with younger leaves (Atwal, 1955). Whereas larvae reared on white or young green cabbage leaves laid significantly more eggs compared with those reared on green mature leaves (Atwal, 1955). Slower development is associated with higher death rates (Atwal, 1955) while higher temperature results in decreased numbers of eggs laid by female (Abro et al., 1992).

Species of Plutella genus: Five economically important species of Plutella (Sch.) have been recorded in the world, all of which are pests of brassicas. Except for P. xylostella, which has become cosmopolitan, the geographic distribution of these species is limited (Kfir, 1998). For example:

P. annulatella (Curt.) in Finland.
P. antiphona (Mey.) in Newzealand.
P. armoraclae (Bus.) in Colorado.
P. porrectella (L.) in Ontario, Canada.
P. balanopis (Mey.) in Southern Africa.

The highest number of Plutella species has been recorded in Americas; in addition to P. xylostella, 7 species in South America mainly Argentina, Chile and Colombia and 9 species in North America, however only 2 species of Plutella have been recorded in Europe (Kfir, 1998).

History of P. xylostella in Malaysia: Plutella xylostella was first recorded in Frasers Hill, Pahang, in 1925 (Ooi, 1986) and by 1941 it had become a major pest in both highland and lowland areas. (Corbett and Pagden, 1941). Since then it has been widely recognized as a serious pest of crucifers. Total losses can reach 70-90% if no control measures are taken (Omar and Mamat, 1997). The history and control of P. xylostella in Malaysia is summarized in Table 1.

The pest status of P. xylostella was exacerbated in Malaysia, as in many other areas where this pest has spread to, by the lack of endemic natural enemies and the presence of extensive cultivation of crucifers, especially varieties of Chinese cabbage, Brassica chinensis var. pekinensis in the Cameron Highlands (Ooi, 1986). Farmers reportedly invested 30% of production costs on the control of P. xylostella in early 1970s but 70% still failed to achieve satisfactory control (Lim, 1974). By the 1980s, pyrethroids failed to control P. xylostella due to high levels of resistance, leading to the increased use of acylurease and Bt. By the late 1980s, the acylurease were also failing due to resistance in both lowland and highland Malaysia (Table 1). The lowland populations of P. xylostella were found to have higher level of resistance to acylurease, probably due to greater number of generations per year compared with the cooler highlands.

Management of Plutella xylostella: In most countries newly introduced pesticides face little registration hurdles, as a result most of which are not registered in the country of origin are readily available at subsidized price. Because of poor enforcement of restrictions on pesticide use, the insecticides registered for rice or cotton are often applied to crucifers which contribute to the overuse and complete dependence on insecticides to control P. xylostella. This sole reliance on pesticides for control facilitates the rapid build up of resistance. The failure of insecticides to control P. xylostella, interest is growing in cultural controls (Talekar and Shelton 1993), which is one of the oldest methods of pest control and since centuries farmers have been using it, for example change in planting date of rice and wheat to prevent them from rice borer and wheat stem maggot damage respectively. Similarly, the disposal of corn residues was recommended in Europe as early as 1897 in order to reduce overwintering populations of European corn borer (Debach and Rosen, 1991). Dent (1991) defined cultural method as a prophylactic method of control and should be considered as the first ditch defense around which to build other control options.

Some of cultural practices and other control methods for P. xylostella are discussed in following sections.

Crop rotation: Since P. xylostella has a narrow host range, the local elimination of the host via crop rotation could prove to be a very effective pest and resistance management tactic.

Table 1:Key events in the history of Plutella xylostella management in Malaysia
Sudderddin and Kok (1978), Ooi (1986), Ooi (1992), Loke et al. (1992), Furlong et al. (1994), Iqbal et al. (1996); Sayyed et al. (2001)

Table 2:A summary of insecticide resistance in Plutella xylostella

A mandatory crucifer-free period has been undertaken for P. xylostella control in regions of at least two countries, Mexico and Australia. After the introduction of a summer break in crucifer production in Southern Queensland during 1990, frequency of resistance to the chemical insecticide permethrin appeared to drop sharply (Roush, 2000).

An important part of the long term and sustainable future of production for some crops may be the establishment of grower cooperatives to produce crucifers (and complementary vegetable crops) in alternate times of the year to defeat pests such the P. xylostella, while stabilizing crop markets. The growers, who do this will remain highly profitable and retain access to relatively cheap and effective insecticides, whereas growers those can not practice host-free periods will probably eventually suffer an economic decline.

Intercropping: The traditional approach to farming is utilization of poly culture which include mixed intercropping, strip intercropping, relay intercropping and alley intercropping. In intercropping plants act as physical barrier by disrupting the chemical or visual communication between pest insects and their host plants (Sheehan, 1986). It also increases parasitoids and predators reproductive potential due to great temporal and spatial distribution of nector and pollen sources (Risch, 1981).The earliest success of P. xylostella control occurred in intercropping of cabbage with tomato which reduce its population in cabbage (Vostrikov, 1915) as the tomato plant contains a volatile compound which acts as a repellent and adversely effect its oviposition (Buranday and Raros, 1973). While Dover (1986) reported the intercropping of brassica with white clover resulting in reduced oviposition by P. xylostella. The dill and garlic have also been reported to act as repellent against P. xylostella (Talekar et al., 1986).

Trap cropping: The use of trap crop has special importance to subsistence farming in developing countries by reducing reliance on pesticides and lowering production costs (Hokkanen, 1991). The pests often show preference for certain plants is the main principle of trap cropping. Indian mustard has been used successfully as a trap crop for P. xylostella control in India (Srinivasan and Moorthy, 1992) however it failed in several other countries like Taiwan, South East Asia and Canada (Talekar, 1996). Similarly, planting collards in field peripheries is a potentially effective trap crop to manage P. xylostella in cabbage (Mitchell et al., 2000). Effective trap cropping may eliminate all insecticides as P. xylostella is retained in trap crop and become heavily parasitized.

Resistant varieties: Resistant plant material is an attractive alternative or supplement to insecticide control (Eckenrode et al., 1981). The dense and easily abraided microscopic wax crystals or waxblooms on the plant surface can interfere with attachment by insects (Juniper, 1995). On the other hand waxblooms by impairing the mobility and effectiveness of predatory insects can increase herbivore populations. For example, the proportion of time spent walking by three generalist predator species is greater on a Brassica oleracea with glossy or reduced-waxbloom mutation than on a normal waxbloom variety (Eigenbrode et al., 1996). As a results these predator species reduce populations of P. xylostella on reduced-waxbloom compared with normal waxbloom varieties. Similar results were reported on glossy B. oleracea P. xylostella population by using Chrysoperla plorabunda and Hippodamia convergens (Eigenbrode and Kabalo, 1999). Glossy leaf waxes apparently elicit non-acceptance behaviour in neonate larvae which result in their failure to successfully establish on these plants (Eigenbrode and Shelton, 1990).

Threshold: Plutella xylostella has developed resistance to every pesticidal group due to indiscriminate use of pesticides. The frequency of chemical application can be reduced by working out the optimal control thresholds (Chen and Sue, 1986). The accepted theory of pest management favoured the application of pesticides when insect pests population approach or exceed on economic threshold which could lead to better and more effective way of pesticide use (Metcalf, 1980). The threshold levels are based upon the larval stage (Kami, 1995). Hartcourt (1957) were the first to establish injury equivalencies for lepidopterous pests of cabbage and was expressed as cabbage looper equivalents (CLE) for example the calculated CLE for P. xylostella larvae is 0.05 (Hartcourt, 1957). Maltais (1994) have shown reduced number of sprays with out endangering yield or quality levels of cabbage based on 0.5-1.0 larvae of P. xylostella per plant threshold.

Insect sterilization: The sterile insect technique has mainly been used against Diptera (Lindquist, 1986). However, the partial sterility or inherited sterility could be used for the control of lepidopterous pests (Omar and Mamat, 1997). The main principle of releasing sterile male insects into the natural population is that these insects mate normally with females which lay infertile eggs (Smith et al., 1964). In order to induce inherited sterility in many insects the ionizing radiation has been used (Omar and Mamat, 1997). The first coordinated attempt to control the P. xylostella in Malaysia was carried out by use of this technique (Ho, 1965). Lepidopterous insects require higher doses of radiation compared with other insects for example Omar and Mamat (1997) reported that a dose between 150 and 200 GY would be suitable for inherited sterility of P. xylostella. Similarly Cook and Hooper (1974) measured the sterilizing effects of an alkylating agent or azirdine compound phenyl metepa on adults of P. xylostella. Males were sterilized after three hours of exposure without effect on the fecundity of females. However these compounds are not recommended as ideal chemosterilants as these have toxicity to mammals. Therefore, more potential chemosterilants have to be evaluated.

Sex pheromones: Sex pheromone are substances produced by the females to attract male for the purpose of mating. Sex pheromones of lepidopterous insects were introduced as biorational chemicals for pest management in the early 1970s (Chow et al., 1974). The evidences for sex Pheromone emission in female adults of P. xylostella was initially reported from Taiwan (Chow et al., 1974). The major component of P. xylostella pheromone are (Z)-11-hexadecenal (Z-11_16:Ald), (Z)-11-hexadecenyl acetate (Z-11-16:Ac), (Z)-11-hexadecenyl alcohol (Z-11-16:oh) (Chow and Lin, 1983). The mixture of Z11-16:Ald and Z11-16: Ac in the range 8+2 to 4+6 has been found to be highly attractive to males in the field (Koshihara et al., 1978), however by adding 1% (Z)-11-hexadecenol (Z-11-16:OH) to the bait could significantly enhance male capture (Koshihara and Yamada, 1981). It was found in later studies that synthetic sex pheromones were effective in attracting same number of adult males as by 10 virgin females (Michereff et al., 2000). Tamaki et al. (1977) have reported that P. xylostella can effectively be controlled by using synthetic pheromones in conjunctions with reduced insecticidal spray application. Similar results were shown by Reddy and Guerrero (2000 and 2001).

Mating disruption with sex pheromones is an alternative to traditional pesticides for insect control (Ridgeway et al., 1990). It has been found that mating disruption can be used to protect cabbage from P. xylostella if pheromones are applied with some supplemental application of insecticides (Mitchell et al., 1997). In contrast, Schroeder et al. (2000) reported that mating disruption of P. xylostella with the present technology was not effective even under very controlled conditions. The sex pheromones have also been found to increase the contact of P. xylostella adults with toxic pathogens (Furlong et al., 1995).

Biological control: Debach and Rosen (1991) defined biological control as the utilization of natural enemies (predators, parasites and pathogens) to reduce the damage caused by noxious organisms to tolerable levels.

Natural enemies can be utilized in three ways:

I) Importation of exotic species and their establishment in a new habitat
ii) Augmentation of established species through direct manipulation of their population.
iii) Conservation through manipulation of the environment.

The history of biological control dates back to 900 and 1200 A.D. when Chinese used predatory ants for control of citrus pests (Debach and Rosen, 1991). Similarly in Arabia, the growers had been using colonies of predatory ants from the mountains to control a pest ant which often destroyed the trees (Sweetman, 1958). However, the first movement of a natural enemy from one country to another occurred in 1762 with the introduction of Mynahbird, Acridotheres tristis from India to Mauritius to use against the red Locust, Nomadacris septemfasciata Serv. (Sweetman, 1958). The modern day example of deliberate manipulation of insect natural enemies to suppress pest population was the importation of the Vedalia lady beetle Rodolia cardinalis Mul. into California in 1888 to control the cotton Cushion Scale, Icery purchasi Mask. on citrus (Dent, 1991). This was an immediate success which generated the support for many other biological control projects.

Biological control when applied successfully to pest problem can provide a relatively permanent and economical solution (Huffaker and Messenger, 1976) and is potentially a cheaper compared with chemical control. Greathead (1984) reported that biological control efforts had resulted in economic success in only 1% of cases and the activity of natural enemies is influenced not only by their direct relationship with their hosts but also by their environmental inter-relationship.

Parasitoids: The term parasitoid was introduced in 1913 (Godfray, 1994) and was defined as " the larva feeds exclusively on its host, eventually killing it. It requires a single host to complete development and are intermediate between predators and parasites.

An insect parasitoid can be characterized as follow

1. The development of the parasitoid results in the death of the host.
2. The host is also an insect.
3. The parasitoid is relatively large in relation to the host.
4. The parasitoid is parasitic at larval stages whereas the adults being free living.
5. The parasitoid does not exhibit heteroecism (passing different stages of life history in different hosts)
6. Their action resembles the predators than parasites

The majority of parasitoids are either members of order Hymenoptera or Diptera (Godfray, 1994). There are about 50000 described species of hymenopterous parasitoids (Gaston, 1991), 15000 described species of dipteran parasitoids while about 3000 species in other orders (Eggleton and Belshaw, 1992). There are 8 millions described species of insects (Gaston, 1991) therefore parasitoids constitutes about 8.5% of all prescribed insects.

The first case of parasitism was recorded from cabbage butterfly Pieris rapae L. which was attacked by a gregarious internal parasitoid Apanteles glomeratus L. and emerged to form a conspicuous cocoon on the integument of its host. Angitia laterallis Grav was the first parasitoid recorded on P. xylostella by Muggeridge (1930) in Newzealand. By 1979 more than 90 species of P. xylostella parasitoids had been catalogued (Goodwin, 1979) and are possible alternative to chemical control (Chua and Ooi, 1986). Historically, indigenous species parasitoids particularly Diadegma semiclausum kept P. xylostella population below economic threshold levels in USA, Europe and Africa (Biever et al., 1992). Because of this potential for control, D. semiclasum and D. collaris were introduced to Newzealand from UK (Thomas and Ferguson, 1989). Diadegma semiclausum as an introduced parasitoid has controlled P. xylostella in certain areas of Malaysia, Taiwan, Philippines, Indonesia, Thailand, Newzealand, Zambia and the Cape Verde Islands (Lim, 1992). In the United States of America P. xylostella was held in check by indigenous parasitoids with D. insulare Cres. (Harcourt, 1986). Similarly in Australia, population of P. xylostella has also been reported to be kept under control by introduced D. eucerophaga Hors., D. rapi. Cam., D. collaris, Apanteles ippeus, Cotesia plutellae kurdg. (Goodwin, 1979). The introduction of D. eucerophaga to Indonesia has led to an average parasitism of over 80% resulting in decline of P. xylostella populations subjected to less insecticidal use (Vos, 1953). In Taiwan C. plutella was regarded as one of the most promising biological control agents of P. xylostella (Chiu and Chien, 1972) but could not give adequate control therefore D. semiclausum was introduced from Indonesia, however it failed to establish (Talekar, 1988). While in Trinidad C. plutellae and Tetrostichus sokolowwskii kurdj. become well established but had not given an effective control of P. xylostella (Yaseen, 1974). While in Hawaii C. plutellae parasitized up to 95% of P. xylostella larvae in the field (Bach and Tabashnik, 1990). In Pakistan T. sokolowwskii kurdj. is well established and have been reported to suppress P. xylostella populations in various climatic conditions of Pakistan (Mushtaque, 1990). In northern Japan the exotic parasitoid, D. semiclausum was introduced and augmented to suppress the density of the P. xylostella in cabbage fields and it was found that percentage parasitism by D. semiclausum reached only up to 53% in the release field in mid June (Noda et al., 2000). In contrast in the Papua New Guinea highlands release and successful establishment of the D. semiclausum reduced crop losses remarkably since 1995 (Saucke et al., 2000).

In the Cameron Highlands of Malaysia, where only one parasitoid Tetrastichus ayyari was present but with out adequate suppression of P. xylostella (Lim, 1982), three species of parasitoids D. semiclausum, D. collaris and the larval parasitoid Macromalon orientale were introduced from Australia, India, Indonesia and Newzealand during 1975-78 (Ooi, 1986), although only D. semiclausum and D. collaris become fully established (Lim, 1982). Further studies conducted during 1988-90 revealed that D. semiclausam had become the dominant parasitoid with C . plutellae becoming less common (Ooi, 1992).The time taken for D. semiclausum to become established may be due to the result of excessive use of insecticides in the region since it is observed to be more susceptible to insecticides compared with C. plutellae (Furlong et al., 1994).

Laboratory studies indicated a temperature range of 20-30 °C as an optimum for parasitization of P. xylostella by C. plutellae and 15-25 °C for D. semiclausum (Talekar and Yang, 1991). As the temperature approaches 30 °C parasitism by D. semiclausum drops sharply (Talekar, 1992). For example in the highland areas of the northern Philippines a single release of D. semiclausum resulted in 64% parasitism of P. xylostella (Poelking, 1992).

Predators: Predatory species have been used for biological control purpose since ancient time and the use of ants in Asia antedates written records. Predators could be an important mortality factor to P. xylostella and cause an average of 90% mortality to first instar larvae (Muckenfuss and Shepard, 1994). While Ullyet (1947) reported that predatory arthropods are an important source of P. xylostella mortality and include Stophylinids, Wasps of genus Polistes, Syrphids, Chrysopids, Hemerobiid and Anthocorrids. However, surprisingly little attention has been given in assessing the role of predators in P. xylostella management but their destruction by insecticides application could contribute to pest resurgence. The glossy plants could enhance the predation as several predators move with difficulty on normal-wax brassica plants. The glossy plant leaves also reduced the mining of first instar larvae of P. xylostella thus expose them to predators (Eigenbrode et al., 1995). For example the predation of P. xylostella larvae by Hippodamia convergens, Orius insidiosus and Chrysopa cornea adult females was significantly greater on glossy types as compared with normal-wax or wild-type counterparts however the later was also effective on normal wax plants (Eigenbrode et al., 1995, Eigenbrode and Kabalo, 1999). Similarly ground dwelling spider, Lycosid spiders are also major biotic mortality agents of immature stages of P. xylostella especially to third and fourth instar larvae (Nemoto, 1993). Among other predators Micraspis discolor, Pardosa pseudoannulata, Cheilomenes sexmaculatus and Episyrphus alterans have been observed as controlling agent of P. xylostella (Karim, 1995).

Virus: Virus disease of insects was first discovered in 1856 A.D. from diseased silkworm larvae, but a plant disease produced by a virus can be traced back 1555 A.D. (Sweetman, 1958). The best-known insect viruses are the baculoviruses, which contain DNA and are either nuclear polyhedral or granulosis viruses (Entwistle and Evans, 1985). Asayama and Osaki (1970) were the first to observe granulosis virus infecting P. xylostella and their potential as control agent for P. xylostella has been reported by Nakahara et al. (1986) and Su (1990). Kadir et al. (1999) have shown that granulosis virus was highly infective against P. xylostella and further suggested that it could be developed as a selective microbial pesticide. The colour of the infected larval body turned to pale green, pale yellow green and to pale yellow in contrast with the dull green of a healthy green. The infected larvae large in size, greater in length and discharged a milky white fluid from its puffy integument (Asayama and Osaki, 1970). The nuclear polyhedrosis virus of Alfalfa looper Autographa californica (AcMNPV) and closely related genomic variants such as Galleria mellonella (MNPV) are also infective to P. xylostella (Farrar and Ridgway, 1999). The nuclear polyhedrosis virus infect the hypodermal tracheal matrix and fat body, whereas the external symptoms are that the larvae become swollen and flucid and the integument become shiny. After death the integument disintegrate and the dead larvae assume the typical melted appearance of larvae with nuclear polyhedrosis.

Entomopathogenic fungi: Fungi is the first microorganism recognized to produce disease among insects (Sweetman, 1958). The infectious nature of fungus disease Beauveria brassiana in Silkworms was first reported in 1835. The entomopathogen fungi mainly belong to order Entomophthorales with about 35 genera infecting insects (Burges and Hussey, 1971). Fungi usually infect insects by penetration of the body cavity via the integument and then proliferate, filling the body with hyphae (Steinhaus, 1973). The larvae and some times pupae of the P. xylostella has been attacked by several species including Erynia blunckii and Zoophthora radican (Wilding, 1986). Zoophthora radicans periodically causes high mortality in P. xylostella population in the countries where it has been recovered. In Newzealand for example, under natural conditions it almost eliminated a population of P. xylostella within 10 days, while in South Africa mortality was so high that hymenopterous parasitoids of the P. xylostella were eliminated through the absence of their hosts (Ullyet, 1947). The larvae killed by the E. blunckii are fixed to the substrate by rhizoids and become covered in a fett-like mate of conidiophores. Roberts (1989) reported that P. xylostella is susceptible to different propagules of Beauveria (B. bassiana and B. brongniartii) and concluded that 6 days after treatment for the experiments to be read is sufficient when the fungal strain is pathogenic to P. xylostella. Vandenberg et al. (1998) have reported the potential B. bassiana to control P. xylostella and Shelton et al. (1998) have shown that P. xylostella larvae appeared to be more susceptible to B. bassiana in later instars.

Entomopathogenic nematodes: The number of nematodes species attacking insects is far greater than generally realized. The great majority have not been described yet (Sweetman, 1958). The nematodes which attack the insects are of Nemathelminthes and include in the classes Nematoda and Nematomorpha, however some members of Acanthocephala spend their larval stage in an insect host and the adult stage in mammals (Debach, 1964). The Entomopathogenic nematodes (Steinernematidae and Heterorhabditidae) have been successfully used to control a number of soil dwelling insect pests (Gaugler and Kaya, 1990). However, their requirements for high humidity, moderate temperature and protection from ultraviolet light have severely limited their utility in foliar application (Gaugler and Kaya, 1990). It has been shown that Steinernema carpocopsae is the most effective nematode against P. xylostella giving 100% mortality after 6 hours of exposure and could cause 40% mortality to immature and mature pupae (Ratnasinghe and Hague, 1998). The foliage application of infective juveniles (IJS) of S. carpocapsae against larvae of P. xylostella with hydraulic nozzles gave 98% mortality (Lello et al., 1996). While the application of infective juveniles (IJS) of Steinernema spp. and Heterorhabditis indicus indicated that the infection of P. xylostella could start within 3 hours postexposure resulting in significant levels of mortality although maximum infection did not occur until 24 hours of exposure (Mason and Wright, 1997).

Chemical control: Insect control using repelling plants (Smith and Secoy, 1981) or natural products such as sulphur combined with religion, ritual and superstition, began with early civilization and continues through the middle ages to the agricultural revolution (Conacher, 1986). As broad scale agriculture emerged, botanical preparations such as nicotine, pyrethrum, hellebore were used more widely (Ordish, 1967).

The P. xylostella feed on highly valued crucifer crops effective control is therefore, necessary, the mainstay of control has been the use of synthetic chemicals. The general use pattern of insecticide vary widely over geographical locations. The most dramatic pattern of insecticide use has been occurred in South East Asia where P. xylostella is the major problem of crucifers. For example in Thailand a dominant product like mevinphos provided excellent control in 1965, fair control in 1974 and poor control in 1984 (Rushtapakornchai and Vattanatangum, 1986). Similar pattern have also been observed in Malaysia (Table 1), Taiwan (Sun et al., 1978), Japan (Hama, 1992) and other parts of the world (Tabashnik et al., 1987).

Bacillus thuringiensis (Bt): represents the major class of microbes used for insect biocontrol (Macintosh et al., 1991). It is a gram-positive soil bacterium distinguished from other bacilli by its production of parasporal crystal proteins (Yamamoto and Powell, 1993). Cry proteins are produced as crystalline inclusions within the bacterium and must be solubilized and cleaved by protease in the insect midgut to form active toxins. The activated toxins then bind to specific receptor sites on insect midgut brush border membranes, leading to the formation of pores and cell lysis (Schnepf et al., 1998).

Development of resistance in Plutella xylostella : Plutella xylostella has a long history of becoming resistant to every insecticide (Talekar and Shelton, 1993). Insecticide resistance in P. xylostella is particularly widespread in South East Asia because of rapid turnover of insect generations, a long and continuous cropping season, the extensive area of crucifers grown, their high value and frequent insecticides application (Magagro and Edelson, 1990; Sun, 1992).

The first report of insecticide resistance in P. xylostella was in 1953 against DDT in Lembang, Indonesia (Ankersmit, 1953). Populations of P. xylostella have since been reported to become resistant to most of other classes of insecticides (Table 2).

Since the first commercial Bt formulations appeared in the late 1930s, they have been used widely as niche products for pest control (Sayyed, 2000). It has been presumed that resistance to Bt toxins was unlikely because of its unique mode of action. However, this was subsequently shown not to be the case and the Plodia interpunctella was the first insect reported to have developed resistance to Bt toxins albeit under laboratory conditions (Tabashnik, 1994). While various other insect species have been subsequently shown to develop resistance under laboratory conditions, the P. xylostella remains the only insect species which has developed resistance in the field (Sayyed et al., 2000a,b). The initial cases of resistance to Bt in P. xylostella was caused by repeated foliar sprays of B. thuringiensis var. kurstaki in Philippines and Hawaii (Tabashnik et al., 1990). Resistance has now been reported in Malaysia, Thailand, Japan, Philippines and the USA (Tabashnik, 1994; Imai and Mori, 1999; Liu et al., 2000; Sayyed et al., 2000a; Sayyed and Wright, 2001). The development of resistance to Bt toxins is seriously threatening their life expectancy as pest control agents, particularly with the introduction of commercially grown transgenic crops expressing insecticidal Bt proteins which increase the risk of resistance by providing a constant selection pressure (Tabashnik et al., 1998; Sayyed et al., 2000a).

Integrated pest management (IPM): Bacillus thuringiensis has become a cornerstone to IPM particularly on some vegetable crops (Marrone, 1994).

The broad definition of IPM, adopted by the FAO panel of experts is: " Integrated pest control is a pest management system that in the context of the associated environment and the population dynamics of the pest species utilizes all suitable techniques and methods in as compatible a manner as possible and maintains the pest population at levels below those causing economic injury level (FAO, 1975). While Kogan (1998) defined IPM as "a decision support system for the selection and use of pest control tactics, single or harmoniously co-ordinated into a management strategy, based on cost/benefit analyses that take into account the interests of an impacts on produce, society and the environment".

The idea of IPM started in the late nineteenth century, when, in the absence of pesticides, crop protection specialists relied on knowledge of pest biology and cultural strategies (Gains, 1957). Interest in IPM declined in the early 1940s with the advent of organochlorine and organophosphate insecticides but by the late 1950s insecticide resistance, resurgence of primary pests, upsurges of secondary pests and overall environmental contamination rekindled interest in more integrated control concepts (Zadoks, 1993). IPM is not a technology package, rather it resembles a "technology basket", intelligent decision have to be made on what techniques in the basket are suitable for a particular location and problem (Teng, 1989). Effective IPM programmes require a holistic and multitactic strategy that enhances the compatibility of pesticides and biological control agents and thus reduces the number and rate of pesticide applications (Sayyed and Arif, 2000). The possibility of integrating microbial agents such as Bt with other biological control agents, culture practices and conventional pesticides has increased considerably with the availability of Bt strains and toxins with broader host ranges, improved formulations and more varied options for their application, including transgenic crops. Bacillus thuringiensis products are far more specific than traditional insecticides and have few direct toxic effects upon specialist and generalist natural enemies (Losey et al., 1999). For example, Cry1Ac expressed in cotton did not produce a toxic effect on several beneficial insects, such as green lacewing, Chrysoperla carnea Steph (Lozzia et al., 1998). The use of NewLeaf® potato containing Cry3A was shown to enhance the population of predators in fields that were protected from the Colorado potato beetle damage without the need for conventional insecticide applications (Feldman and Stone, 1997). Similarly, use of Bt cotton in China resulted in an average increase of 24% in the number of insect predators over what was found in conventional cotton field (Xia et al., 1999).

In Asia, there has been interest in IPM since the late 1970s (Lim, 1990). Planting of trap crops is one of the cultural methods used for pest management of P. xylostella (Metcalf and Luckman, 1994). For example, in India the mustard, Brassica junciais is used to attract P. xylostella, thus reducing the need for insecticides to a maximum of two sprays compared with 10 or more per season using conventional control methods (Srinivasan and Krishna Moorthy, 1992). While in Japan, yellow sticky traps to capture P. xylostella adults plus three sprays of Bt were shown to achieve better control than five sprays of Bt (Rushtapakornchai et al., 1992). In Taiwan, the introduction of two larval parasitoids, pheromone traps and Bt sprays reduced the P. xylostella population density on cauliflower and broccoli to a lower level as compared with neighboring, conventionally sprayed plots (Talekar, 1996). Similarly, Chilcutt and Tabashnik (1999) reported that a combination of parasitoids and Bt generally gave better control of P. xylostella over time than either alone. Ivey and Johnson (1998) reported the greatest yield and value of marketable cabbage when a resistant variety and Bt were incorporated together in an IPM system.

Conclusion: In the last four decades, P. xylostella has become most difficult pest to control because of its intrinsic biology and ecology . The main cause of the failure is the development of resistance by P. xylostella to every group of insecticides used including Bt. However, parasitoids D. semiclausum and C. plutellae have been controlling this pest successfully in highlands and lowlands respectively in South East Asia, which provide the basic model for IPM and use of Bt with these parasitoids could be a success against P. xylostella as Bt has no or minimal effect on beneficial insects (Losey et al., 1999).

The development of insect-resistant Bt crops has been of major significance in the control of insect pests on cotton, maize, potato, rice and a variety of other crops (Hilder and Boulter, 1999). The use of Bt crops have proven successful in several parts of the world because of higher yields and fewer insecticide treatments for target pests (Klotz-Ingram et al., 1999). In a recent study it has been shown that the rapid adoption of this technology is directly tied to benefits of greater effectiveness in pest control technology and very competitive cuts in farmer's costs (Gianessi and Carpenter, 1999; Betz et al., 2000). However, field use of Bt-based spray products has highlighted the problem of evolution of Bt resistant populations of insect pests. In recent reports P. xylostella have also been shown to evolve resistance to Bt crops in the laboratory (Zhao et al., 2000; Sayyed et al., 2001). In Pakistan these crops are at experimental stage therefore a detailed study is required in local ecosystem in order to have their long term role in integrated pest management, before commercializing them.

Fig. 1:
Effect of integrated pest management programs will incorporate multiple tactics. Pesticides should be used only when needed, at the lowest rates possible and in a manner to reduce negative impacts on natural enemies

Previous experiences with P. xylostella management have shown that a single component strategies will fail. Therefore the best solution can be obtained by the use of fully integrated IPM programme, for example host plant resistance, development of new pathogens and insecticides must be available to complement the traditional strategies of biological and cultural control methods (Fig. 1).

There is a need to maintain a source of pesticides because they are powerful and effective pest management tools. However, they should be highly selective, rapid in their impact, adaptable to many situations, relatively economical and compatible to natural enemies. Enhancing the compatibility of pesticides and natural enemies is complex but can reward us with handsome dividends in improved pest control (Metcalf, 1994) and pesticide resistance management (Tabashnik and Croft, 1985).

1:  Abro, G.H., R.A. Soomro and T.S. Syed, 1992. Biology and behaviour of diamondback moth, Plutella xylostella (L.). Pak. J. Zool., 24: 7-10.
Direct Link  |  

2:  Ankersmit, G.W., 1953. DDT resistance in Plutella maculipennis (Curt.) (Lepi) in Java. Bull. Entomol. Res., 44: 421-425.

3:  Asayama, T. and N. Osaki, 1970. A granulosis of the diamondback moth Plutella xylostella . J. Invert. Path., 15: 284-286.

4:  Ashihara, W., 1977. A laboratory bioassay method of the sex pheromone of the diamondback moth Plutella xylostella (L.). Jap. J. Applied Entomol. Zool., 21: 171-172.

5:  Atwal, A.S., 1955. Influence of temperature, photoperiod and food on the speed of development, longevity, fecundity and other qualities of the diamond-back moth Plutella Maculipennis (Curtis) (Lepidoptera: Tineidae). Aust. J. Zool., 3: 185-221.
CrossRef  |  Direct Link  |  

6:  Bach, C.E. and B.E. Tabashnik, 1990. Effects of nonhost plant neighbors on population densities and parasitism rates of the diamondback moth (Lepidoptera: Plutellidae). Environ. Entomol., 19: 987-994.
CrossRef  |  Direct Link  |  

7:  Betz, F.S., B.G. Hammond and R.L. Fuchs, 2000. Safety and advantages of Bacillus thuringiensis-protected plants to control insect pests. Regular Toxicol. Pharmacol., 34: 156-173.
CrossRef  |  Direct Link  |  

8:  Bhalla, O.P. and J.K. Dubey, 1986. Bionomics of the Diamondback Moth in the Northwestern Himalayan. In: Diamondback Moth Management: Proceedings of the First International Workshop, Talekar, N.S. and T.D. Griggs (Eds.). The Asian Vegetable Research and Development Center, Shanhua, Taiwan, pp: 55-62.

9:  Biever, K.D., R.L. Chauvin, G.L. Reed and R.C. Wilson, 1992. Seasonal occurrence and abundance of lepidopterous pests and associated parasitoids on collards in the Northwestern United States. J. Entomol. Sci., 27: 5-18.
Direct Link  |  

10:  Buranday, R.P. and R.S. Raros, 1975. Effects of cabbage-tomato intercropping on the incidence and oviposition of the diamond back moth, Plutella xylostella (L.). Philippines Entomol., 2: 369-374.

11:  Burges, H.D. and N.W. Hussey, 1971. Microbial Control of Insects and Mites. Academic Press, London.

12:  Chelliah, S. and K. Srinivasan, 1986. Bioecology and Management of Diamondback Moth in India. In: Diamondback Moth Management: Proceedings of the First International Workshop, Talekar, N.S. and T.D. Griggs (Eds.). The Asian Vegetable Research and Development Center, Shanhua, Taiwan, pp: 63-76.

13:  Chen, C.N. and W.Y. Su, 1986. Ecology and Control Thresholds of the Diamondback Moth on Crucifers in Taiwan. In: Diamondback Moth Management: Proceedings of the First International Workshop, Talekar, N.S. and T.D. Griggs (Eds.). The Asian Vegetable Research and Development Center, Shanhua, Taiwan, pp: 415-421.

14:  Cheng, E.Y., 1988. Problems of control of insecticide-resistant Plutella xylostella. Pest. Manage. Sci., 23: 177-188.
CrossRef  |  Direct Link  |  

15:  Chilcutt, C.F. and B.E. Tabashnik, 1999. Effects of Bacillus thuringiensis on adults of Cotesia plutellae (Hymenoptera: Braconidae), a parasitoid of the Diamondback moth, Plutella xylostella (Lepidoptera: Plutellidae). Biocontrol Sci. Technol., 9: 435-440.
Direct Link  |  

16:  Chiu, S.C. and C.C. Chien, 1972. Observation on Apanteles plutellae Kurd, a larval parasite of diamondback moth (Plutella xylostella). Plant Prot. Bull., 14: 145-152.

17:  Chow, Y.S. and Y.M. Lin, 1983. Recent advances of sex pheromonal studies of the vegetables pests. Proceedings of the Symposium on Insect Control of Vegetables in Taiwan, (ICVT'83), Department Agriculture and Forestry, Taiwan, pp: 134-143.

18:  Chow, Y.S., Y.M. Lin and H.J. Teng, 1986. Morphological and Biological Evidence for the Presence of a Male Sex Pheromone of the Diamondback Moth. In: Diamondback Moth Management: Proceedings of the First International Workshop, Talekar, N.S. and T.D. Griggs (Eds.). The Asian Vegetable Research and Development Center, Shanhua, Taiwan, pp: 103-108.

19:  Chow, Y.S., S.C. Chiu and C.C. Chien, 1974. Demonstration of a sex pheromone of the diamondback moth (Lepidoptera: Plutellidae). Ann. Entomol. Soc. Am., 65: 510-512.
CrossRef  |  Direct Link  |  

20:  Chua, T.H. and B.H. Lim, 1977. Effect of interplant distance on the distribution pattern of diamondback moth, Plutella xylostella (L.) among host plants. Malays. Applied Biol., 6: 19-23.
Direct Link  |  

21:  Chua, T.H. and P.A.C. Ooi, 1986. Evaluation of three Parasites in the Biological Control of Diamondback Moth in the Cameron Highlands, Malaysia. In: Diamondback Moth Management: Proceedings of the First International Workshop, Talekar, N.S. and T.D. Griggs (Eds.). The Asian Vegetable Research and Development Center, Shanhua, Taiwan, pp: 173-184.

22:  Conacher, J., 1986. Pests, Predators and Pesticides: Some Alternatives to Synthetic Pesticides. Organic Growers Association: Wembley, Western Australia.

23:  Cook, I.M. and G.H.S. Hooper, 1974. Chemosterilization of Plutella maculzpennzs(Curtis) (Lepidoptera: Plutellidae) by exposure to residues of metepa. Aust. J. Entomol., 13: 241-243.
CrossRef  |  Direct Link  |  

24:  Corbett, G.H. and H.T. Padgen, 1941. A review of some recent entomological investigations and observations. Malays. Agric. J., 29: 347-375.

25:  Debach, P., 1964. Biological Control of Insect Pests and Weeds. Chapman and Hall, UK.

26:  Debach, P. and D. Rosen, 1991. Biological Control by Natural Enemies. 2nd Edn., Cambridge University Press, Cambridge, UK., Pages: 408.

27:  Dent, D., 1991. Insect pest management. CAB International, Wallingford, UK.

28:  Dover, J.W., 1986. The effect of labiate herbs and white clover on Plutella xylostella oviposition. Entomol. Exp. Applic., 42: 243-247.
CrossRef  |  Direct Link  |  

29:  Eckenrode, C.J., J.T. Andaloro and A.M. Shelton, 1981. Suppression of lepidopterous larvae in commercial sauerkraut cabbage fields and research plots. J. Econ. Entomol., 74: 276-279.
Direct Link  |  

30:  Eggleton, P. and R. Belshaw, 1992. Insect parasitoids: An evolutionary overview. Philippnies Trans. R. Soc. London, 337: 1-20.
CrossRef  |  Direct Link  |  

31:  Eigenbrode, S.D. and N.N. Kabalo, 1999. Effects of Brassica oleracea waxblooms on predation and attachment by Hippodamia convergens. Entomol. Exp. Applic., 91: 125-130.
CrossRef  |  Direct Link  |  

32:  Eigenbrode, S.D., T. Castagnola, M.B. Roux and L. Steljes, 1996. Mobility of three generalist predators is greater on cabbage with glossy leaf wax than on cabbage with a wax bloom. Entomol. Exp. Applic., 81: 335-343.
CrossRef  |  Direct Link  |  

33:  Eigenbrode, S.D. and A.M. Shelton, 1990. Behaviour of neonate diamondback moth larvae (Lepidoptera, Plutellidae) on glossy-leafed resistant Brassica-oleracea. Enviorn. Entomol., 19: 1566-1571.
Direct Link  |  

34:  Eigenbrode, S.D. and N.N. Kabalo, 1999. Effects of Brassica oleracea waxblooms on predation and attachment by Hippodamia convergens. Entomol. Exp. Applic., 91: 125-130.
CrossRef  |  Direct Link  |  

35:  Eigenbrode, S.D., S. Moodie and T. Castagnola, 1995. Predators mediate host plant resistance to a phytophagous pest in cabbage with glossy leaf wax. Entomol. Exp. Applic., 77: 335-342.
CrossRef  |  Direct Link  |  

36:  Entwistle, P.F. and H.F. Evans, 1985. Viral Control: In Comprehensive Insect Physiology, Biochemistry and Pharmacology. Pergamon Press, Oxford, pp: 347-412.

37:  Farrar, R.R. and R.L. Ridgway, 1999. Relative potency of selected nuclear polyhedrosis viruses against five species of Lepidoptera. J. Agric. Urban Entomol., 16: 187-196.

38:  Fauziah, H.I., O. Dzolkhifl and D.J. Wright, 1992. Resistance to Acylurea Compounds in Diamondback Moth. In: Diamondback Moth Management: Proceedings of the 2nd International Workshop, Talekar, N.S. and T.D. Griggs (Eds.). The Asian Vegetable Research and Development Center, Shanhua, Taiwan, pp: 391-401.

39:  Feldman, J. and T. Stone, 1997. The Development of a Comprehensive Resistance Management Plan for Potatoes Expressing the Cry3A Endotoxin. In: Advances in Insect Control: The Role of Transgenic Plants, Carozzi, N. and Koziel, M. (Eds.). Taylor and Francis, London, UK., pp: 49-61.

40:  FAO., 1975. FAO Panel of Experts on Integrated Pest Control 5th October. Food and Agriculture Organization of United Nations, Rome, Italy, pp: 41.

41:  FAO., 1992. FAO annual report. Food and Agriculture Organization of the United Nations, Rome.

42:  Furlong, M.J., J.K. Pell, O.P. Choo and S.A. Rahman, 1995. Field and laboratory evaluation of a sex-pheromone trap for the autodissemination of the fungal entomopathogen Zoophthora radicans (entomophthorales) by the diamond-back moth, Plutella-xylostella(Lepidoptera: Yponomeutidae). Bull. Entomol. Res., 85: 331-337.

43:  Furlong, M.J., R.H.J. Verkerk and D.J. Wright, 1994. Differential-effects of the acylurea insect growth-regulator teflubenzuron on the adults of 2 endolarval parasitoids of Plutella-xylostella, Cotesia-plutellae and Diadegma-semiclausum. Pest. Sci., 41: 359-364.

44:  Gains, J.C., 1957. Cotton insects and their control in United States. Ann. Rev. Entomol., 2: 319-338.

45:  Gaston, K.J., 1991. How large is a species geographic range. Oikos, 61: 434-438.

46:  Gaugler, R. and H.K. Kaya, 1990. Entomopathogenic Nematodes in Biological Control. CRC Press, Boca Rato.

47:  Gianessi, L.P. and J.E. Carpenter, 1999. Agricultural biotechnology: Insect control benefits. National Center for Food and Agricultural Policy.

48:  Godfray, H.C.J., 1994. Behavioral and Evolutionary Ecology Princeton. University Press, Princeton.

49:  Goodwin, S., 1979. Changes in the numbers in the parasitoid complex associated with diamondback moth, Plutella xylostella L. Aust. J. Zool., 27: 981-981.

50:  Greathead, A.H., 1984. ntegrated pest management of cassava green mite. Proceedings of a Regional Training Workshop in East Africa, April 30-May 4, Commonwealth Institute of Biological Control, Ascot, pp: 25-26.

51:  Gupta, P.D. and A.J. Thorsteinson, 1960. food plant relationships of the diamond-back moth (Plutella maculipennis (Curt.)) II. Sensory regulation of oviposition of the adult female. Entomol. Exp. Applic., 3: 305-314.
CrossRef  |  Direct Link  |  

52:  Lim, G.S., 1982. Effects of parasites on the diamondback moth, Plutella xylostella (L). Ph.D. Thesis, University of London, UK.

53:  Lim, G.S., 1992. Integrated pest management of diamondback moth: practical realities. Proceedings of the 2nd International Workshop on Diamondback Moth and other Crucifer Pests, December 10-14, 1990, Tainan, Taiwan, pp: 565-576.

54:  Lindquist, D.A., 1986. The sterile insect technique and area wise insect control or eradication in the tropics. Proceedings of the International Meeting on Towards a Second Green Revolution from Chemical to New Biological Technologies in Agriculture in the Tropics, September 8-10, 1986, Rome, Italy, pp: 407-414.

55:  Liu, M.Y., Y.J. Tzeng and C. N. Sun, 1982. Insecticide resistance in the diamondback moth. J. Econ. Entomol., 75: 153-155.

56:  Liu, Y.B. and B.E. Tabashnik. 1997. Visual determination of sex of diamondback moth larvae. Can. J. Entomol., 129: 585-586.

57:  Liu, Y-B., B.E. Tabashnik, L. Masson, B. Escriche and J. Ferre, 2000. Binding and toxicity of Bacillus thuringiensis protein Cry1C to susceptible and resistant diamondback moth (Lepidoptera: Plutellidae). J. Econ. Entomol., 93: 1-6.

58:  Loke, W.H., G.S. Lim, A.R. Syed, A.M. Abdul and M.Y. Aziz, et al ., 1992. Management of diamondback moth in Malaysia: Development, implementation and impact. Proceedings of the 2nd International Workshop on Diamondback Moth and other Crucifer Pests, December 10-14, 1990, Tainana, Taiwan, pp: 529-539.

59:  Losey, J.E., L.S. Rayor and M.E. Carter, 1999. Transgenic pollen harms monarch larvae. Nature, 399: 214-214.
CrossRef  |  PubMed  |  Direct Link  |  

60:  Lozzia, G.C., C. Furlanis, B. Manachini and I.E. Rigamonti, 1998. Effects of Bt corn on Rhopalosiphum padi L. (Rhynchota: Aphididae) and on its predator Chrysoperla carena Stephen (Neuroptera: Chrysopidae). Bulll. Zool. Agric. Bachic. Ser. 30: 153-164.

61:  Maa, C.J.W., 1986. Ecological approach to male diamondback moth response to sex pheromone in diamondback moth management. Proceeding of the 1st International Workshop on Diamondback Moth Management, March 11-15, 1985, Tainan, Taiwan, pp: 109-123.

62:  Macintosh, S.C., T.B. Stone, R.S. Jokerst and R.L. Fuchs, 1991. Binding of Bacillus thuringiensis proteins to a laboratory-selected line of Heliothis virescens. Proc. Natl. Acad. Sci. USA., 88: 8930-8933.
PubMed  |  Direct Link  |  

63:  Magagro, J.J. and J.V. Edelson, 1990. Diamondback moth (Lepidoptera: Plutellidae) in South Texas: A technique for resistance monitoring in the field. J. Econ. Entomol., 83: 1201-1206.
Direct Link  |  

64:  Makino, S. and M. Horikiri, 1985. Reduced susceptibility of the diamondback moth, Plutella xylostella L. to pyrethroid insecticides. Proc. Assoc. Plant Prot. Kyushu, 31: 175-178.

65:  Maltais, P.M, J.R. Nuckle and P.V. Leblanc, 1994. Economic threshold for management of lepidopterous larvae on broccoli in Southeastern New-Brunswick. J. Econ. Entomol., 87: 766-774.
Direct Link  |  

66:  Marrone, P.G., 1994. Present and future use of Bacillus thuringiensis in integrated pest management systems: An industrial perspective. Biocontrol Sci. Technol., 4: 517-526.

67:  Marsh, O.H., 1917. The life history of Plutella maculipennis, the diamondback moth. J. Agric. Res., 10: 1-10.

68:  Mason, J.M. and D.J. Wright, 1997. Potential for the control of Plutella xylostella larvae with entomopathogenic nematodes. J. Invertebrate Pathol., 70: 234-242.
Direct Link  |  

69:  Metcalf, R.L. and W.H. Luckman, 1994. Introduction to Insect Pest Management. John Wiley and Sons, New York, Pages: 650.

70:  Metcalf, R.L., 1980. Changing role of insecticides in crop protection. Ann. Rev. Entomol., 25: 219-256.
CrossRef  |  Direct Link  |  

71:  Metcalf, R.L., 1994. Insecticides in Pest Management. In: Introduction to Insect Pest Management, Metcalf, R.L. and W.H. Luckmann (Eds.). John Wiley and Sons, Inc., New York, pp: 245-284.

72:  Michereff, M.F.F., E.F. Vilela, M.M. Filho and A. Mafra-Neto, 2000. Synthetic sex pheromone use for field trapping of diamondback moth males. Pesq. Agropec. Brasil., 35: 1919-1926.
CrossRef  |  Direct Link  |  

73:  Mitchell, E.R., G. Hu and D. Johanowicz, 2000. Management of diamondback moth (Lepidoptera: Plutellidae) in cabbage using collard as a trap crop. HortScience, 35: 875-879.
Direct Link  |  

74:  Mitchell, E.R, G.Y. Hu , J. Okine and J.R. McLaughlin, 1997. Mating disruption of diamondback moth (Lepidoptera: Plutellidae) and cabbage looper (Lepidoptera: Noctuidae) in cabbage using a blend of pheromones emitted from the same dispenser. J. Entomol. Sci., 32: 120-137.
Direct Link  |  

75:  Miyata, T., N. Sinchaisri, B. Sayampal, W. Rushtapakornchai and G.A. Vattanatan, 1988. Toxicological experiments a insecticide resistance patterns. Proceedings of the Meeting of the Joint Research Project on Insect Toxicological Studies on Resistance Insecticides and Integrated Control of the Diamondback Moth, March 9-12, 1988, Bangkok, Thailand, pp: 14-23.

76:  Muckenfuss, A.E. and B.M. Shepard, 1994. Seasonal abundance and response of diamondback moth, Plutella xylostella (L.) (Lepidoptera: Plutellidae) and natural enemies to esfenvalerate and Bacillus thuringiensis subsp. kurstaki Berliner in coastal South Carolina. J. Agric. Entomol., 11: 361-373.
Direct Link  |  

77:  Muggeridge, J., 1930. The diamondback moth its occurrence and control in New Zealand. N. Z. J. Agric., 41: 253-264.

78:  Mushtaque, M., 1990. Some studies on Tetrastichus sokolowskii Kurd (Eulophilidae: Hymenoptera) a parasitoid of diamondback moth in Pakistan. Pak. J. Zool., 22: 37-43.

79:  Nakahara, L.M., J.J.R. Mchugh, C.K. Otsuka, G.Y. Funasaki and P.Y. Lai, 1986. Integrated control of diamondback moth Plutella-xylostella and other insect pests using an overhead sprinkler system an insecticide and biological control agents on a watercress Nasturtium officinale farm in Hawaii USA. Proceedings of the 1st International Workshop on Diamondback Moth Management, March 11-15, 1985, Tainan, Taiwan, pp: 403-414.

80:  Nayar, J.K. and A.J. Thorsteinson, 1963. Further investigations into the chemical basis of insect host plant relationship in an oligophagous insect (Plutella maculipennis Curt): Lepidoptera : Plutellidae). Can. J. Zool., 41: 923-929.
Direct Link  |  

81:  Nemoto, H., 1993. Mechanism of resurgence of the diamondback moth, Plutella xylostella (L.) (Lepidoptera: Yponomeutidae). Jarq-Japan Agric. Res. Q., 27: 27-32.
Direct Link  |  

82:  Noda, T., S. Miyai, K. Takashino and A. Nakamura, 2000. Density suppression of Plutella xylostella (Lepidoptera : Yponomeutidae) by multiple releases of Diadegma semiclausum (Hymenoptera : Ichneumonidae) in cabbage fields in Iwate, Northern Japan. Applied Entomol. Zool., 35: 557-563.
Direct Link  |  

83:  Noppun, V., T. Saito and T. Miyata, 1986. Laboratory selection for resistance with phenthoate and fenvalerate in the diamondback moth, Plutella xylostella L. (Lepidoptera: Yponomeutidae). Crop Prot., 5: 323-327.

84:  Ohira, Y., 1979. Mating behaviour and egg maturation of the diamondback moth, Plutella xylostella L. (Lepidoptera: Plutellidae). Proc. Assoc. Plant Prot. Kyushu, 25: 104-106.

85:  Omar, D. and M.J. Mamat, 1997. The feasibility of using sterile insect technique for the control of diamondback moth on cabbage in Cameron Highlands. Proceedings of the 3rd International Workshop on DBM and its Management, October 29-November 1, 1996, Kuala Lumpur, Malaysia, pp: 130-133.

86:  Ooi, P.A.C., 1986. Diamondback moth in Malaysia in diamondback moth management. Proceedings of the 1st International Workshop on Diamondback Moth Management, March 11-15, 1985, Tainan, Taiwan, pp: 255-265.

87:  Ooi, P.A.C., 1992. Role of parasitoids in managing diamondback moth in the Cameron Highlands, Malaysia. Proceedings of the 2nd International Workshop on Diamondback Moth and other Crucifer Pests, December 10-14, 1990, Tainan, Taiwan, pp: 255-262.

88:  Oppert, B., K.J. Kramer, R.W. Beeman, D. Johnson and W.H. McGaughey, 1997. Proteinase-mediated insect resistance to Bacillus thuringiensis toxins. J. Biol. Chem., 272: 23473-23476.
Direct Link  |  

89:  Ordish, G., 1967. Biological Method in Crop Pest Control. Constable and company Ltd., London.

90:  Gupta, P.D. and A.J. Thorsteinson, 1960. food plant relationships of the diamond-back moth (Plutella maculipennis (Curt.)): I. Gustation and olfaction in relation to botanical specificity of the larva. Entomol. Exp. Applic., 3: 241-250.
CrossRef  |  Direct Link  |  

91:  Hama, H., 1986. Resistance spectrum to various insecticides in the diamondback moth, Plutella xylostella Linne (Lepidoptera: Yponomeutidae). Jpn. J. Applied Entomol. Zool., 30: 277-284.

92:  Hama, H., 1992. Insecticide resistant characteristics of the diamondback moth. Proceedings of the 2nd International Workshop on Diamondback Moth and Orther Crucifer Pests, December 10-14, 1990, Asian Vegetable Research and Development Centre, Taiwan, pp: 455-464.

93:  Harcourt, D.G., 1957. Biology of the diamondback moth, Plutella maculipennis (Curt.) (Lepidoptera: Plutellidae), in Eastern Ontario. II. Life-history, behaviour and host relationships. Can. Entomol., 89: 554-564.
CrossRef  |  Direct Link  |  

94:  Harcourt, D.G., 1986. Population dynamics of the diamondback moth in Southern Ontario. Proceedings of the 1st International Workshop on Diamondback Moth Management, March 11-15, 1986, Tainan, Taiwan, pp: 3-15.

95:  Hilder, V.A. and D. Boulter, 1999. Genetic engineering of crop plants for insect resistance-a critical review. Crop Prot., 18: 177-191.
CrossRef  |  Direct Link  |  

96:  Hill, D.S., 1983. Agricultural Pests of the Tropics and their Control. 2nd Edn., University Press, Cambridge.

97:  Hillyer, R.J. and A.J. Thorsteinson, 1971. Influence of the host plant or males on programming of oviposition in the diamondback moth (Plutella maculipennis (Curt.) Lepidoptera). Can. J. Zool., 49: 983-990.
CrossRef  |  Direct Link  |  

98:  Ho, T.H., 1965. The Life history and control of the diamondback moth in Malaya. Bull. No. 118, Div. of Agriculture, pp: 26.

99:  Hokkanen, H.M.T., 1991. Trap cropping in pest management. Ann. Rev. Entomol., 36: 119-138.
CrossRef  |  Direct Link  |  

100:  Horikiri, M. and S. Makino, 1987. Susceptibility of the diamondback moth, Plutella xylostella L., to insecticides in Kagoshima prefecture. Kyushu Plant Prot. Res., 33: 131-135.
CrossRef  |  Direct Link  |  

101:  Huffaker, C.B. and P.S. Messenger, 1976. Theory and Practice of Biological Control. Academic Press, Inc., New York, USA.

102:  Imai, K. and Y. Mori, 1999. Levels, inheritance and stability of resistance to Bacillus thuringiensis formulation in a field population of the diamondback moth, Plutella xylostella (Lepidoptera: Plutellidae) from Thailand. Applied Entomol. Zool., 34: 23-29.
CrossRef  |  Direct Link  |  

103:  Iqbal, M., R.H.J. Verkerk, M.J. Furlong, P.C. Ong, S.A. Rehman and D.J. Wright, 1996. Evidence for resistance to Bacillus thuringiensis (Bt) subsp. kurstaki HD-1, Bt subsp. aizawai and abamectin in field populations of Plutella xylostella from Malaysia. Pestic. Sci., 48: 89-97.
CrossRef  |  Direct Link  |  

104:  Ivey, P.W. and S.J. Johnson, 1998. Integrating control tactics for managing cabbage looper (Lepidoptera: Noctuidae) and diamondback moth (Lepidoptera: Yponomeutidae) on cabbage. Trop. Agric., 75: 369-374.
Direct Link  |  

105:  Juniper, B.E., 1995. Waxes on Plant Surfaces and their Interactions with Insects. In: Waxes: Chemistry, Molecular Biology and Functions, R.J. Hamilton (Ed.). The Oily Press, Dundee, Scotland, pp: 157-174.

106:  Abdul Kadir, H.B., C.C. Payne, N.E. Crook, J.S. Fenlon and D. Winstanely, 1999. The comparative susceptibility of the diamondback moth Plutella xylostella and some other major lepidopteran pests of brassica crops to a range of baculoviruses. Biocontrol Sci. Technol., 9: 421-433.
CrossRef  |  Direct Link  |  

107:  Kami, V., 1995. Studies in resistance to Bacillus thuringiensis in a field population of Diamondback moth (Plutella xylostella L.) from Tonga. M.Sc. Thesis, University of London, UK.

108:  Kanervo, V., 1936. The diamondback moth (P. maculipennis Curt.) as a pest of cruciferous plants in Finland. Valt. Maatalousk. Julk., 86: 1-86.

109:  Karim, M.A., 1995. Management of insect pests of vegetables. Proceedings of the Vegetable Crops Agribusiness, May 2-4, 1995, Dhaka, Bangladesh, pp: 119-125.

110:  Kfir, R., 1998. Origin of the diamondback moth (Lepidoptera: Plutellidae). Ann. Entomol. Soc. Am., 91: 164-167.
CrossRef  |  Direct Link  |  

111:  Klotz, C.A., S. Jans, J. Fernandez-Cornejo and W.D. McBride, 1999. Farm level production effects related to the adoption of genetically modified cotton for pest management. Agric. Biol. Forum, 2: 73-84.
Direct Link  |  

112:  Kogan, M., 1998. Integrated pest management: historical perspectives and contemporary developments. Ann. Rev. Entomol., 43: 243-270.

113:  Koshihara, T. and H. Yamada, 1981. Female sex pheromone of the diamondback moth, Plutella xylostella Jap. Agri. Res. Quart., 15: 22-28.

114:  Koshihara, T., H. Yamada, Y. Tamaki and T. Ando, 1978. Field attractiveness of the synthetic sex-pheromone of the diamondback moth, Plutella xylostella L. Applied Entomol. Zool., 24: 6-12.

115:  Lello, E.R., M.N. Patel, G.A. Matthews and D.J. Wright, 1996. Application technology for entomopathogenic nematodes against foliar pests. Crop Prot., 15: 567-574.

116:  Lim, G.S., 1986. Biological control of diamondback moth. Proceedings of the 1st Internatoinal Workshop on Diamondback Moth Moth and other Crucifer Pests, March 11-15, 1986, Taiwan, pp: 159-172.

117:  Lim, G.S., 1974. Integrated Pest Control in Developing Countries of Asia. In: Environment and Development, Dworkin, D.M. (Ed.). SCOPE Misc. Publ., UK.

118:  Lim, G.S., 1990. Over view of vegetable IPM in Asia. FAO Plant Prot Bull., 38: 73-87.

119:  Tabashnik, B.E., N.L. Cushing and M.W. Johnson, 1987. Diamondback moth (Lepidoptera: Plutellidae) resistance to insecticides in Hawaii: Intra-island variation and cross-resistance. J. Econ. Entomol., 80: 1091-1099.
CrossRef  |  Direct Link  |  

120:  Talekar, N.S. and J.C. Yang, 1991. Characteristic of parasitism of diamondback moth by two larval parasites. Entomophaga, 36: 95-104.
CrossRef  |  Direct Link  |  

121:  Talekar, N.S., 1996. Biological control of diamondback moth in Taiwan: A review. Plant Prot. Bull., 38: 167-189.
Direct Link  |  

122:  Talekar, N.S., 1992. The Management of Diamondback Moth and other Crucifer Pests. The Asian Vegetable Research and Development Center, Shanhua, Taiwan, Pages: 603.

123:  Talekar, N.S. and A.M. Shelton, 1993. Biology, ecology and management of the diamondback moth. Annu. Rev. Entomol., 38: 275-301.
CrossRef  |  Direct Link  |  

124:  Talekar, N.S. and S.T. Lee, 1985. Seasonality of insect pests of Chinese cabbage and common cabbage in Taiwan. Plant Prot. Bull., 27: 47-52.

125:  Talekar, N.S., 1988. Biological Control of Diamondback Moth on Farmers Field. In: Gardening Nutritious Vegetables, Gershon, J., N.V. llemit and P.J. Lastimosa (Eds.). AVRD Center, Taiwan, pp: 50-54.

126:  Talekar, N.S., S.T. Lee and S.W. Huang, 1986. Intercropping and Modification of Irrigation Method for the Control of Diamondback Moth. In: Diamondback Moth Management: Proceedings of the First International Workshop, Talekar, N.S. and T.D. Griggs (Eds.). The Asian Vegetable Research and Development Center, Shanhua, Taiwan, pp: 145-155.

127:  Tamaki, Y., K. Kawasaki, H. Yalada, T. Kashihara and N.Osaki et al., 1977. Z-11-Hexadecenal and Z-11-hexadecenyl acetate: Sex pheromone components of the diamondback moth (Lepidoptera: Plutellidae). Applied Entomol. Zool., 12: 208-210.
Direct Link  |  

128:  Tan, C.L. and G.S. Lim, 1985. Transnational movement of insect pests (and other invertebrates) via imported cabbages. Proceedings of Regional Conference on Plant Quarantine Support for Agricultural Development, December 10-12, 1985, Kuala Lumpur, Malaysia, pp: 67-73.

129:  Teng, P.S., 1989. Integrated pest management in rice: an analysis of the status que with recommendations for action. Report prepared at task force of the technical advisory committee of the consultative group on international agricultural research (CGIAR) reviewing international activities in IMP.

130:  Thomas, W.P. and A.M. Ferguson, 1989. Plutella xylostella (L.), Diamondback Moth (Lepidoptera: Yponomeutidae). In: A Review of Biological Control of Invertebrate Pests and Weeds in New Zealand 1874-1987, Cameron, P.J., R.L. Hill, J. Bain and W.P. Thomas (Eds.). CAB International, Wallingford, UK., pp: 135-142.

131:  Vandenberg, J.D., M. Ramos and J.A. Altre, 1998. Dose-response and age- and temperature-related susceptibility of the diamondback moth (Lepidoptera: Plutellidae) to two isolates of Beauveria bassiana (Hyphomycetes: Moniliaceae). Environ. Entomol., 27: 1017-1021.
Direct Link  |  

132:  Verkerk, R.H.J. and D.J. Wright, 1996. Multitrophic interactions and management of the diamondback moth: A review. Bull. Entomol. Res., 86: 205-216.
CrossRef  |  Direct Link  |  

133:  Vos, H.C.C.A.A., 1953. Introduction in Indonesia of Angitia cerophaga Grav., a parasitoid of Plutella maculipennis Curt. Contribution of Central Agricultural Research Station No. 134, pp: 1-32.

134:  Vostrikov, P., 1915. Tomatoes as insecticides. The importance of Solanaceae in the control of pests of agriculture. Novotchecherkossk, 10: 9-12.

135:  Wan, M.T.K., 1970. The bionomics and control of the diamondback moth Plutella xylostella L. (P. maculipennis Curt.) (Lep. Plutellidae) in Sarawak (Malaysian Borneo). Sarawak Mus. J., 18: 377-398.

136:  Wang, S.H., 1983. Observation on seasonal occurrence of diamondback moth in vegetable field of Northern Taiwan. Proceedings of the Symposium on Insect Control of Vegetables in Taiwan, (SICVT`83), Taichung, Taiwan, pp: 72-80.

137:  Waterhouse, D.F. and K.R. Norris, 1987. Biological control: Pacific prospects. Inkata Press, Melbourne, pp: 454.

138:  Wilding, N., 1986. The pathogens of diamondback moth and their potential for its control, review diamondback moth management. Proceedings of the 1st International Workshop on AVRDC, March 11-15, 1986, Taiwan, pp: 219-238.

139:  Wu, K.C., 1968. Bionomic study of Plutella maculipenns Curt. Agric. Res., 17: 51-64.

140:  Xia, J.Y., J.J. Cui, L.H. Ma, S.X. Dong and X.F. Cui, 1999. The role of transgenic Bt cotton in integrated insect pest management. Acta Gossypii Sinica, 11: 57-64.

141:  Yamada, M., 1979. Mating habits of the diamondback moth, Plutella xylostella (L.). Jap. J. Applied Entomol. Zool., 23: 43-45.
CrossRef  |  Direct Link  |  

142:  Yamamoto, T. and G.K. Powell, 1993. Bacillus Thuringiensis Crystal Proteins: Recent Advances in Understanding its Insecticidal Activity. In: Advanced Engineered Pesticides, Kim, L. (Ed.). Marcel Dekker Inc., New York, USA, pp: 3-42.

143:  Yaseen, M., 1974. Biology, Seasonal Incidence and Parasitoids of Plutella xylostella L. in Trinidad and the Introduction of Exotic Parasitoids into the Lesser Antilles. In: Crop Protection in the Caribbean, Brathwaite, C.W.D., R.H. Phelpa and F. Bennett, (Eds.). University of West Indies, India pp: 237-244.

144:  Zadoks, J.C., 1993. Crop Protection: Why and How. In: Crop Protection and Sustainable Agriculture, Chadwick, D.J. and J. Marsh (Eds.). John Wiley and Sons, Chichester, UK., pp: 48-60.

145:  Uematsu, H., 1992. Effects of Age and Body Size on the Mating Success of Diamondback Moth. In: Diamondback Moth Management: Proceedings of the 2nd International Workshop, Talekar, N.S. and T.D. Griggs (Eds.). The Asian Vegetable Research and Development Center, Shanhua, Taiwan, pp: 37-41.

146:  Ullyet, G.C., 1947. Mortality factors in populations of Plutella maculipennis (Curtis) (Tineidae: Lepidoptera) and their relation to the problem of control. Entomol. Memographs Union South Africa Department Agric. Forestry, 2: 75-202.

147:  Zhao, J.Z., H.L. Collins, J.D. Tang, J. Cao and E.D. Earle et al., 2000. Development and characterization of diamondback moth resistance to transgenic broccoli expressing high levels of Cry1C. Applied Environ. Microbiol., 66: 3784-3789.
CrossRef  |  Direct Link  |  

148:  Pivnick, K.A., B.J. Jarvis, G. P. Slater, C. Gillot and E.W. Underhill, 1990. Alternation of diamondback moth (Lepidoptera: Plutellidae) to volatile of oriental mustard: the influence of age, sex, and prior exposure to males of host plants. Environ. Entomol., 19: 704-709.

149:  Poelking, A., 1992. Diamondback moth in the Philippines and its control with Diadegma semiclausum. Proceedings of the Second International Workshop on the Management of Diamondback Moth and other Crucifer Pests, December, 10-14, 1990, Tainan, Taiwan, pp: 271-278.

150:  Ratnasinghe, G. and N.G.M. Hague, 1998. The invasion, development and reproduction of Steinernema carpocapsae (Rhabditida: Steinernematidae) in the diamondback moth, Plutella xylostella. (Lepidoptera: Yponomeutidae). Nematropica, 28: 1-6.

151:  Reddy, G.V.P. and A. Guerrero, 2001. Optimum timing of insecticide applications against diamondback moth Plutella xylostella in cole crops using threshold catches in sex pheromone traps. Pest Manage. Sci., 57: 90-94.
Direct Link  |  

152:  Reddy, G.V.P. and A. Guerrero, 2000. Pheromone-based integrated pest management to control the diamondback moth Plutella xylostella in cabbage fields. Pest Manage. Sci., 56: 882-888.
Direct Link  |  

153:  Ridgeway, R.L., R.M. Silverstein and M.N Inscoe, 1990. Behaviour-Modifying Chemicals for Insect Management. Marcel Dekker, Inc., New York.

154:  Risch, S.J., 1981. Insect herbivore abundance in tropical monocultures and polycultures. An experimental test of two hypotheses. Ecology, 62: 1325-1340.

155:  Roberts, D.W., 1989. World picture of biological control of insects by fungi. Memorias Inst. Oswaldo Cruz, 84: 89-100.
Direct Link  |  

156:  Robertson, O.L., 1939. Diamondback moth investigation in New zealand. Newzealand J. Sci. Technol., 20: 330-340.

157:  Roush, R.T., 2000. Resistance Management for Agricultural Pests. In: Entomopathogenic Bacteria: From Laboratory to Field Application, Charles, J.F., A. Delecluse and C. Nielsen-Le Roux (Eds.). Kluwer Academic Publishers, London, pp: 399-417.

158:  Rushtapakornchai, W. and T. Vettabatangum, 1986. Present Status of Insecticidal Control of Diamondback Moth in Thailand. In: Diamondback Moth Management, Proceeding of the First International Workshop, Taiwan, 11-15 March 1986, Talekar, N.S. and T.D. Griggs (Eds.). Asian Vegetable Research and Development Center, Taiwan, pp: 307-312.

159:  Rushtapakornchai, W., A. Vattanatangum and T. Saito, 1992. Development and Implementation of the Yellow Sticky Trap for Diamondback Moth Control in Thailand. In: Diamondback Moth and other Crucifer Pests Proceedings of the Second International Workshop, Taiwan, Talekar, N.S. and T.D. Griggs (Eds.). Vegetable Research and Development Center, Tainan, Taiwan, pp: 523-528.

160:  Salinas, P.J., 1972. Studies on the ecology and behaviour of the larvae of Plutella xylostella (Linnaus) (Lepidoptera: Plutellidae). Ph.D. Thesis, University of London, London.

161:  Salinas, P.J., 1984. Studies on the behaviour of the larvae of Plutella xylostella (L.) (Lepidoptera: Plutellidae) a world pest of cruciferous crops. Normal spacing behav. Turrialba, 34: 77-84.

162:  Salinas, P.J., 1986. Studies on the Diamondback Moth in Venezuela with Reference to Other Latinamerican Countries. In: Diamondback Moth Management. Proceeding of the First International Workshop, Tainan Taiwan, 11-15 March 1986, Talekar, N.S. and T.D. Griggs (Eds.). Asian Vegetable Research and Development Center, Taiwan, pp: 17-24.

163:  Saucke, H., F. Dori and H. Schmutterer, 2000. Biological and integrated control of Plutella xylostella (Lep., Yponomeutidae) and Crocidolomia pavonana (Lep., Pyralidae) in Brassica crops in Papua New Guinea. Biocontrol Sci. Tech., 10: 595-606.
Direct Link  |  

164:  Sayyed A.H. and D.J. Wright, 2001. Cross-resistance and inheritance of resistance to Cry1Ac toxin in diamondback moth, Plutella xylostella from lowland Malaysia. Pest. Manage. Sci., 57: 413-421.
PubMed  |  

165:  Sayyed, A.H., R. Haward, S. Herrero, J. Ferre and D.J. Wright, 2000. Genetic and Biochemical approach for characterization of resistance to Bacillus thuringiensis toxin Cry1Ac in a field population of the Diamondback moth. Applied Environ. Microbiol., 66: 1509-1516.
Direct Link  |  

166:  Sayyed, A.H., J. Ferre and D.J. Wright, 2000. Mode of inheritance and stability of resistance to Bacillus thuringiensis to Plutella xylostella populations from Malysia. Pest. Manage. Sci., 56: 743-748.
Direct Link  |  

167:  Sayyed, A.H., T.H. Schuler and D.J. Wright, 2001. Resistance to Bt canola expressing Cry1Ac is incompletely dominant in field-derived populations of Plutella xylostella. Sci.,

168:  Sayyed, H.A. and M.J. Arif, 2000. Studies on physiological response of FH-682 cotton to various dosage of dimecron 100SCW. Pak. J. Biol. Sci., 3: 1865-1867.
CrossRef  |  Direct Link  |  

169:  Sayyed, H.A., 2000. Resistance mechanisms to Bacillus thuringiensis and its specific Cry toxins in the diamondback moth, Plutella xylostella L. Ph.D. Thesis, University of London, pp: 187.

170:  Schnepf, E., N. Crickmore, J. van Rie, D. Lereclus and J. Baum et al., 1998. Bacillus thuringiensis and its pesticidal crystal proteins. Microbiol. Mol. Biol. Rev., 62: 775-806.
Direct Link  |  

171:  Schroeder, P.C., A.M. Shelton, C.S. Ferguson, M.P. Hoffmann and C.H. Petzoldt, 2000. Application of synthetic sex pheromone for management of diamondback moth, Plutella xylostella, in cabbage. Entomol. Exp. Applic., 94: 243-248.
CrossRef  |  Direct Link  |  

172:  Shelton, A.M., J.D. Vandenberg, M. Ramos and W.T. Wilsey, 1998. Efficacy and persistence of Beauveria bassiana and other fungi for control of diamondback moth (Lepidoptera :Plutellidae) on cabbage seedlings, J. Entomol. Sci., 33: 142-151.

173:  Sheehan, W., 1986. Response of specialist and generalist natural enemies to agroecosystem diversification: A selective review. Environ. Entomol., 15: 456-461.
Direct Link  |  

174:  Sivapragasam, A., G.S. Lim and M. Ruwaida, 1984. Experimental trials on integrated pest management programme for Plutella xylostella (L). Proceedings of the Seminar on Integrated Pest Management Kuala Lumpur, January 1984, Malaysia, pp: 11-23.

175:  Smith, C.N. and D.M. Secoy, 1981. Plants used for agricultural pest control in Western Europe before 1850. Chem. Ind., 1: 12-17.
Direct Link  |  

176:  Smith, C.N., G.C. LaBreque and A.B. Borkovec, 1964. Insect chemosterilants. Ann. Rev. Entomol., 9: 269-284.
CrossRef  |  Direct Link  |  

177:  Srinivasan, K. and P.N.K. Moorthy, 1992. Development and Adoption of Integrated Pest Management for Major Pests of Cabbage Using Indian Mustard as a Trap Crop. In: Diamondback Moth Management: Proceedings of the 2nd International Workshop, Talekar, N.S. and T.D. Griggs (Eds.). The Asian Vegetable Research and Development Center, Shanhua, Taiwan, pp: 511-521.

178:  Steinhaus, E.A., 1973. Microbial Diseases of Insects. In: Biological Control of Insects Pests and Weeds, Debach, P. (Ed.). Chapman and Hall, London, pp: 515-547.

179:  Su, C.Y., 1990. Microbial control of the diamondback moth Plutella xylostella using Bacillus thuringiensis and granulosis virus. Plant Prot. Bull., 32: 10-23.

180:  Sudderuddin, K.I. and P.F. Kok, 1978. Insecticide resistance in Plutella xylostella collected from Cameron Highlands of Malaysia. FAO Plant Bull., 26: 54-57.

181:  Sun, C.N., H. Chi and N.T. Feng, 1978. Diamondback moth resistance to diazinon and methomyl in Taiwan. J. Econ. Entomol., 71: 551-554.
Direct Link  |  

182:  Sun, C.N., 1992. Insecticide Resistance in Diamondback Moth. In: Proceedings of the Second International Workshop, Tainan Taiwan, Talekar, N.S. and T.D. Griggs (Eds.)., Asian Vegetable Research and Development Center, Tainan, Taiwan, pp: 419-426.

183:  Sweetman, H.L., 1958. The Principles of Biological Control: Interrelation of Hosts and Pests and Utilization in Regulation of Animal and Plant Populations. Dubuque, Iowa.

184:  Tabashnik, B.E., 1994. Evolution of resistance to Bacillus thuringiensis. Ann. Rev. Entomol., 39: 47-79.
CrossRef  |  Direct Link  |  

185:  Tabashnik, B.E. and B.A. Croft, 1985. Evolution of pesticide resistance in apple pests and their natural enemies. Entomophaga, 30: 37-49.
CrossRef  |  Direct Link  |  

186:  Tabashnik, B.E., Y.B. Liu, T. Malvar, D.G. Heckel, L. Masson and J. Ferre, 1998. Insect resistance to Bacillus thuringiensis: Uniform or diverse? Philos. Trans. R. Soc. Lond., 353: 1751-1756.
CrossRef  |  Direct Link  |  

187:  Tabashnik, B.E., N.L. Cushing, N. Finson and M.W. Johnson, 1990. Field development of resistance to Bacillus thuringiensis in diamondback moth (Lepidoptera: Plutellidae). J. Econ. Entomol., 83: 1671-1676.
CrossRef  |  Direct Link  |  

©  2021 Science Alert. All Rights Reserved