Five species are recognized in this genus, all from the Old World (Mound and Nickle 2009), but only C. brunneus has been found in Malaysia. A closely related species, C. claratris, has been reported as a pest (Murai 2000) and vector of tospoviruses on tomatoes in Thailand (Halaweh and Poehling 2009). This species was not detected in our collections, nor was it reported during earlier surveys (Mound and Azidah 2009). The species C. brunneus is from Africa, but has been found recently in Peninsular Malaysia on a range of different plant species (Table 1).

Recognition: Ceratothripoides brunneus is a large brown species; body largely brown except fore tibiae and antennal segment III paler brown, forewing uniformly brown; abdominal segment VIII posterior margin with complete comb of microtrichia; mesonotum and metanotum without pair of campaniform sensilla; male abdominal sternites III–VII with many small pore plates; male abdominal tergite IX without drepanae. This species is similar in structure to the species of Megalurothrips, Pezothrips, Odontothrips, and Odonthripiella, and these share many characteristics including a pair of dorso-apical setae on the first antennal segment. In this paper, this species and the legume-flower thrips (Megalurothrips) are distinguished based on the microtrichial comb on abdominal tergite VIII. Recognition of Ceratothripoides is easy if males are available, because the sternites have numerous pore plates (Mound and Nickle 2009).

Species of the genus Dichromothrips are usually found on orchids. In Peninsular Malaysia, only two species have been recorded so far, although three further species are recorded from western Malaysia - D. borneensis, D. nigricornis and D. major. The species D. corbetti originated from the Oriental Region but is now introduced worldwide via cultivated orchids. It was described from Vanda joaquim in Kuala Lumpur (Mound 1976), but is known from a wide range of Orchidaceae including Dendrobium spp., Arundina spp., Cattelya spp., and Vanda spp. from various localities in lowland Malaysia (Table 1).

Recognition: Large and dark brown species, forewing base paler, tarsi and tibial apex yellow; antennal segments brown, segment III and IV with apices elongate. Pronotum without long posteroangular setae, and metafurcal spinula diffuse or weakly defined. These characters are useful in distinguishing the species from the other members of the genus.

The original material of this species is apparently lost (Mound 1976), and the species is recognized based on female specimens from Taiwan identified by H. Priesner. Recently, it has been reported as an invasive species in US on bamboo orchids (Arundina spp.) from Malaysia, Thailand and Taiwan (Department of Agriculture and Plant Industry Division 2010), and as a pest of orchids in Korea (Lee et al. 2002). There are specimens in the CSIRO collection, Canberra, Australia labelled as being associated with damage to Vanilla plants in India. In Malaysia, this species has been taken only from Arundina graminifolia (Bamboo orchid) from Pahang and Sarawak with its distribution restricted to highlands.

Recognition: This large, dark brown species is similar in body colour to D. corbetti. It is distinguished by the fore wing with the subapical area paler, the pronotum with long posteroangular setae, and the metafurcal spinula well developed.

This species is known as the European Flower Thrips, due to its wide distribution in Europe, but it causes less damage to horticulture than F. occidentalis. Both species share many morphological characteristics, but F. intonsa can be recognized by the shorter postocular setae, and the absence of paired campaniform sensilla on the metanotum. Both species also seem to share similar habitats, such that they have been recorded in Peninsular Malaysia only from highlands, but from a wide range of flowers in various plant families, including Plantaginaceae, Alliaceae, Verbenaceae, Orchidaceae, and Asteraceae.

Recognition: Body colour brown, tibiae and tarsi yellow; antennal segments III and IV yellow; forewing pale with dark setae. All species of Frankliniella have the forewing first and second veins with complete setal rows, the head with ocellar setae pair I present, and the pronotum with four pairs of long major setae. Tergite VIII posterior margin with comb of microtrichia in females but not in males.

This species is known as the Western Flower Thrips, and although originally from the South Western states of the USA it is now found worldwide (Moritz et al. 2001). Frankliniella is the largest genus in the family Thripidae, with 230 species mostly from Central and South America. F. occidentalis has been collected commonly in the Cameron Highlands on many different flower hosts, including roses, orchids, daisy, and chrysanthemum. However, two specimens were collected from Gerbera sp. at Penang Butterfly Farm. The species is an important vector of Tomato Spotted Wilt Virus (TSWV) and Impatiens Necrotic Spot Virus (INSV). However, there are very few or perhaps no records of these viruses being transmitted among Malaysian crops.

Recognition: Body length about 1.5 mm (female), male is smaller about 1.0 mm in length. Body colour varies from yellow to brown, abdomen sometimes shaded medially in specimens from Malaysia, forewing pale yellow, femora and tibiae yellow; antennal segments III, IV and V basal half pale, segments II and VI–VIII dark brown. Pronotum anterior margin with two pairs of long setae, metanotal campaniform sensilla present. Tergite VIII posterior margin with comb of microtrichia in females but not in males.

This species is widespread in tropical and sub-tropical countries. It is commonly collected in the lowlands of Peninsular Malaysia, breeding on flowers and leaves of many host plants. It has been sampled from flowers of Bougainvillea sp., Jatropha integerrima, and Plumbago auriculata. Frankliniella schultzei is an important vector of Tomato Spotted Wilt Virus (TSWV), although occasionally, it is a useful predator of mites on cotton (Milne and Walter 1997).

Recognition: This species apparently exists as two very different colour forms, with the body either brown or yellow. According Gikonyo et al. (2017) from the field surveys in Kenya indicate that the two colour forms of F. schultzei could be different species, of which, both showed distinct host preferences, lack of interbreeding and molecular differences. In general, F. schultzei is distinguished by the lack of ctenidia on abdominal tergite V, the position of ocellar setae pair III between the posterior ocelli, and the absence from the posterior margin of tergite VIII of a comb of microtrichia.

This is the most common and widespread species of the genus in the Oriental area. It breeds in legume flowers and is an important pest on bean crops through feeding in the flowers in south China (Tang et al. 2015).

Recognition: Body colour brown; fore tibiae, apices of mid and hind tibiae yellow; antennal segment III slightly yellow, segment IV and V brown; antennal segments III and IV with apical constriction, segment VI unusually elongate; abdominal sternite VII posteromarginal setae S1 situated in front of posterior margin

There are 13 species currently listed in Megalurothrips, but these are difficult to identify due to variation both within and between species. Correct identification of species in this genus requires morphological study and comparison of both sexes. In Peninsular Malaysia, only three species are reported: M. typicus, M. mucunae, and M. usitatus, and the latter species is the one most commonly collected on crops in both highlands and lowlands. Adults of M. typicus have been taken from Moraceae, Passifloraceae and Fabaceae, but with no reliable record of the host on which it breeds.

Recognition: This species is similar to M. sjostedti, the only species in this genus from Africa, but the colour of the forewing and antennae are different (Palmer 1987). Megalurothrips typicus is easy to distinguish from the other oriental Megalurothrips species, because all three pairs of posteromarginal setae on abdominal sternite VII arise at the posterior margin.

This sunflower thrips is widespread worldwide, and is the only species in the genus Microcephalothrips. In Peninsular Malaysia, adults of this species have been collected largely from the plant family Asteraceae from Tagetes patula, Cosmos caudatus, Chrysanthemum indicum, Tridax procumbens, and Sphagneticola trilobata. Other plant families from which adults have been taken include Heliconiaceae, Orchidaceae, and Acanthaceae.

Recognition: Body largely brown except fore tibiae, tarsi, and antennal segment III slightly paler. Based on morphology, it is related to the Thrips genus-group, because of the presence of a pair of ctenidia on abdominal segments V–VIII, but no other member of this group has setae on the prosternum (Figure 13). The triangular lobed craspedum on the abdominal tergites is very distinctive character of this species. Pronotum without any long setae, surface smooth without any fine transverse lines. Forewing usually curved and vein setae small.

This species is widespread from Pakistan to Japan, Taiwan, and northern Australia (Hoddle and Mound 2003), and is now introduced to the Caribbean area and Florida. S. dorsalis is known as a vector of Tospovirus, the species often becomes a pest of many different crops including vegetables and cut-flowers in Southeast Asia. It was also found infesting young leaves of ‘Berembang’ tree (Sonneratia caseolaris) in UKM’s green house. This mangrove tree is the host to firefly, Pteroptyx tener from Peninsular Malaysia.

Recognition: This is amongst the smallest of species in the subfamily Thripinae, with the body of both sexes usually less than 1mm. Body yellow, with all femora, tibiae, and tarsi yellow; antennal segment I pale, segment II variable pale or slightly shaded, segments III–VIII brown; forewings pale yellow to light brown, with apex paler. Abdominal tergites and sternites IV–VII with median brown marking. An identification key to the species of this genus is available in Ng et al. (2014).

This Oriental rice thrips breeds on grasses including paddy, on which crop it is a pest in Philippines and Thailand. However, such infestation has not been reported in Malaysia. This thrips usually lives in moist places like in paddy field and grasses by the pond site.

Recognition: Body uniformly brown; antennal segments I–II dark, II paler at apex, III pale, IV slightly shaded, V–VII dark; all tibiae and tarsi pale; fore wing uniformly shaded. Metanotum with closely spaced striations, campaniform sensilla absent, median setae arising behind the anterior margin but varying in position. Meso- and metafurca each without a spinula. Male abdominal sternites III–VII with a transverse pore plate.

Identification of this species from its close relative, T. hawaiiensis, is not easy, and a third related species, T. razanii, was described recently from Peninsular Malaysia (Ng et al. 2010). For correct identification of these species it is essential that specimens are well-mounted onto slides. Thrips florum has not been reported as a severe pest in Malaysia’s agriculture sector, but it has been collected from a wide range of flowers.

Recognition: Body colour brown; antennae brown except segment III yellow; legs yellow; forewing brown pale at base. Ocellar setae III arising outside ocellar triangle; postocular seta II much shorter than setae I and III. Mesonotum without sculpture lines near campaniform sensilla; metanotum with many lines at the anterior and laterally. Forewing clavus apical seta usually shorter than subapical seta. This species is very similar to both T. hawaiiensis and T. razanii, and comparisons are given in Ng et al. (2010). More discussion is available in Palmer (1999).

This is the most common and abundant species of the genus Thrips in Peninsular Malaysia, and is found on a wide range of cultivated plants in various families including Asteraceae, Apocynaceae, and Fabaceae. It is considered the pollinator of oil palm trees, but is reported as a pest of roses in Georgia, citrus in India, coffee and mangoes in Thailand, and banana in Australia (Palmer 1999).

Recognition: Body colour brown or bicoloured with head and pronotum paler than brown abdomen. Antennal segment III yellow, segments IV and V usually brown or paler at base; legs yellow; forewing paler at base. More discussion about the variation of this species is available in Palmer (1999) and Ng et al. (2010). A key to the species of Thrips genus from Peninsular Malaysia was published by Mound and Azidah (2009).

This species is a common pest in Malaysia and also many other Southeast Asian countries. It is a vector of plant tospovisuses, but it can also cause severe feeding damage to the leaves of crops such as eggplant and capsicum (Tan et al. 2016).

Recognition: Body colour pale yellow; antennae 7-segmented, segments I and II pale yellow, other segments light brown. The species is easy to distinguish from most Thrips species because of the complete posteromarginal comb on abdominal tergite VIII and the lack of discal setae on abdominal sternites. In Malaysia, the species has been taken from crops including Capsicum, Cucumis and Solanum (Mound & Azidah, 2009), as well as species of Rubiaceae.