Resource utilisation by thrips
As a result of extensive field work over the past 50 years, various patterns of resource utilisation by thrips in Australia have become clearer, including flowers, leaves, grasses, fungi and predation on other arthropods.
Thrips and flowers
In much of the southern half of Australia the flower-habitat is dominated by the plague thrips,
Thrips imaginis, although north of Brisbane this species is replaced by the closely related
Thrips safrus. In the eastern rainforests the most common flower thrips is
Thrips setipennis, but in the flowers of
Eucalyptus across much of the continent
Thrips australis predominates. The genera
Cranothrips,
Odontothripiella and
Thrips have each developed a range of host-specific species, although some species in each of these genera are oligophagous. Similarly, a few of the species of
Pseudanaphothrips seem to be host-specific, but the biological significance of some of the named species in this genus remains in doubt due to lack of field work on host specificity and structural variation (Mound & Palmer, 1981).
Cycadothrips includes three described species that breed only in the male cones of
Macrozamia cycads in eastern, western and central Australia, and the genus
Anaphothrips and its relatives involve at least 50 species that live in flowers from a wide range of plant families (Mound & Masumoto, 2009). Similarly, the flowers of native Poaceae support an interesting diversity of specialist thrips taxa (Mound, 2011b).
Kirk (1997) summarised the available information on pollination by thrips species and indicated that the importance of these insects as pollinators had probably been overlooked. Since then other studies have emphasised the significance of thrips, including Williams
et al. (2001) for a rainforest tree,
Wilkiea huegeliana, in eastern Australia, also Mound & Terry (2001), Terry
et al. (2004) and Brookes
et al. (2015) for
Macrozamia cycads, and in Southeast Asia
Macaranga trees are pollinated by thrips (Moog
et al., 2002). The close association of particular thrips species with particular flowers, coupled with the mobility of these insects, suggests that pollination by thrips is more general than has been proven experimentally. For example,
Thrips knoxi is abundant in the flowers of various
Lomandra species,
Thrips wellsae is abundant in the flowers of certain Epacridaceae in the south-eastern mountains (Mound & Masumoto, 2005), and
Oxythrips australopalmae is abundant in the flowers of two palm trees in northern Queensland,
Normanbyia and
Arch¬ontophoenix (Mound & Tree, 2011). However, precise demonstrations of pollination by Thysanoptera, such as that on
Macrozamia cycads, and by
Thrips antiaropsidis on
Antiaropsis decipiens (Moraceae) in New Guinea, remain unusual (Zerega
et al., 2004).
Thrips and leaves
In the moist tropics and eastern coastal regions of Australia, many species of Phlaeothripidae are known to feed on green leaves or apical buds (Mound, 2008). Moreover, there are many such species in the dry areas, particularly on the foliage of
Casuarina and
Acacia species (Mound, 1970; Crespi
et al., 2004). Leaf-feeding Phlaeothripidae are often host-specific, and thus members of this family are rarely considered pests. In contrast, some leaf-feeding species of Thripidae are polyphagous, with many introduced species being pests of non-native cultivated plants. Particularly noteworthy is the absence of any Thysanoptera from the leaves of
Eucalyptus species, the solitary exception being a polyphagous panchaetothripine species,
Australothrips bicolor. Members of the Thripidae subfamily Panchaetothripinae are all leaf-feeders, but these are primarily tropical in distribution, with few species occurring in southern Australia (Mound, 2009). Members of another thripid subfamily, the Dendrothripinae, are also leaf-feeding, and there are several endemic species and genera (Mound, 1999; Mound & Tree, 2016). The fourth thripid subfamily, the Sericothripinae, is also well represented in Australia, with both native and introduced species feeding primarily on leaves (Mound & Tree, 2009b), with one significant in the biological control of the noxious weed,
Ulex europeaus (Ireson
et al., 2008). Minimising water loss is an essential survival strategy for small insects in dry areas, and many Phlaeothripidae species achieve this by inducing galls. One native species of Thripidae,
Cyrilthrips cecidis, is particularly interesting as it is one of the few members of this family worldwide that has been demonstrated to induce leaf galls (Tree & Mound, 2009).
Thrips and grasses
Plants of the family Poaceae, and to a much lesser extent Cyperaceae, support a particularly wide diversity of Thysanoptera. Among the Aeolothripidae,
Desmothrips reedi and
Gelothrips cinctus are predators on small arthropods at the base of grasses. But it is amongst the Thripinae that Poaceae have been particularly adopted as hosts (Mound, 2011b). Most Thripinae that breed on Poaceae feed on leaves, with only a few breeding in the florets, such as members of the genus
Chirothrips. Several species associated with pasture grasses in the South of the continent are clearly European immigrants, whereas in the North many species are shared with Southeast Asia. However, there are several endemic radiations of Thripinae on native Poaceae, and a number of endemic genera are now recognised.
Thrips and fungi
Fungus-feeding thrips in Australia are all members of the Tubulifera family Phlaeothripidae. The abundance of such thrips is higher in dry sclerophyll leaf litter than in rainforest leaf litter, and
Eucalyptus leaf litter appears to support a richer thrips fauna than
Acacia leaf litter (Tree & Walter, 2012).
Thrips as predators
A few species of thrips, in all three major families, act as predators, and the range of prey includes thrips larvae, mites and their eggs, scale-insects and whitefly nymphs (Palmer & Mound, 1991). These thrips are generally facultative predators, taking prey as well as feeding on plant tissues (Mound & Teulon, 1995). This behaviour is found in various species of Aeolothripidae and also the pest species,
Thrips tabaci and
Frankliniella occidentalis. However, several groups of thrips are obligate predators, such as members of the Thripidae genus
Scolothrips that feed on mites (Mound, 2011a), including
Scolothrips ochoa that feeds on
Raoiella mites on
Eucalyptus leaves (Mound
et al., 2010).
References
Brookes DR, Hereward JP, Terry LI & Walter GH (2015) Evolutionary dynamics of a cycad obligate pollination mutualism – Pattern and process in extant Macrozamia cycads and their specialist thrips pollinators. Molecular Phylogenetics and Evolution 93: 83 – 93
Crespi BJ, Morris DC & Mound LA (2004) Evolution of Ecological and Behavioural Diversity: Australian Acacia Thrips as Model Organisms. Canberra: Australian Biological Resources Study & CSIRO Entomology 328 pp.
Ireson JE, Holloway RJ & Chatterton WS (2008) Phenology and development of the gorse thrips, Sericothrips staphylinus Haliday (Thysanoptera: Thripidae), a biological control agent for gorse, Ulex europeus L. (Fabaceae), in Tasmania. Biological Control 45: 65 – 71.
Kirk WDJ (1997) Feeding, pp. 119 – 174. In Lewis, T (ed.), Thrips as Crop Pests. CAB International, Wallingford.
Moog UB, Fiala B & Federle WM (2002) Thrips pollination of the dioecious ant plant Macaranga hullettii (Euphorbiaceae) in Southeast Asia. American Journal of Botany 89: 50 – 59.
Mound LA (1970) Convoluted maxillary stylets and the systematics of some Phlaeothripine Thysanoptera from Casuarina trees in Australia. Australian Journal of Zoology 18: 439 – 463.
Mound LA (1999) Saltatorial leaf-feeding Thysanoptera (Thripidae: Dendrothripinae) from Australia and New Caledonia, with newly recorded pests of ferns, figs and mulberries. Australian Journal of Entomology 38: 257 – 273.
Mound LA (2008) Identification and host associations of some Thysanoptera Phlaeothripinae described from Australia pre-1930. Zootaxa 1714: 41 – 60. http://www.mapress.com/zootaxa/2008/f/zt01714p060.pdf
Mound LA (2009) New taxa and new records of Australian Panchaetothripinae (Thysanoptera, Thripidae). Zootaxa 2292: 25 – 33. http://www.mapress.com/zootaxa/2009/f/zt02292p033.pdf
Mound LA (2011a) Species recognition in the genus Scolothrips (Thysanoptera, Thripidae), predators of leaf-feeding mites. Zootaxa 2797: 45 – 53. http://www.mapress.com/zootaxa/2011/f/zt02797p053.pdf
Mound LA (2011b) Grass-dependent Thysanoptera of the family Thripidae from Australia. Zootaxa 3064: 1 – 40. http://www.mapress.com/zootaxa/2011/f/zt03064p040.pdf
Mound LA & Masumoto M (2005) The genus Thrips (Thysanoptera, Thripidae) in Australia, New Caledonia and New Zealand. Zootaxa 1020: 1 – 64. http://www.mapress.com/zootaxa/2005f/zt01020p064.pdf
Mound LA & Masumoto M (2009) Australian Thripinae of the Anaphothrips genus-group (Thysanoptera), with three new genera and thirty-three new species. Zootaxa 2042: 1 – 76.
Mound LA & Palmer JM (1981) Phylogenetic relationships between some genera of Thripidae (Thysanoptera). Entomologica Scandinavica. Supplementum 15: 153 – 170.
Mound LA & Terry I (2001) Pollination of the central Australian cycad Macrozamia macdonnellii, by a new species of basal clade thrips. International Journal of Plant Sciences 162(1): 147 – 154.
Mound LA & Teulon DAG (1995) Thysanoptera as phytophagous opportunists. pp. 3 – 20 in Parker B.L., Skinner M. & Lewis T. (eds). Thrips Biology and Management. New York : Plenum Publishing Co.
Mound LA & Tree DJ (2009b) Identification and host-plant associations of Australian Sericothripinae (Thysanoptera, Thripidae). Zootaxa 1983: 1 – 22.
Mound LA & Tree DJ (2011) New records and four new species of Australian Thripidae (Thysanoptera) emphasise faunal relationships between northern Australia and Asia. Zootaxa 2764: 35 – 48. http://www.mapress.com/zootaxa/2011/f/zt02764p048.pdf
Mound LA & Tree DJ (2016a) Genera of the leaf-feeding Dendrothripinae (Thysanoptera, Thripidae), with new species from Australia and Sulawesi, Indonesia Zootaxa 4109 (5):569 – 582.
Mound LA, Tree DJ & Goldarazena A (2010) A new species of predatory Scolothrips (Thysanoptera, Thripidae) feeding on Raoiella mites (Tenuipalpidae) in Australia. Zootaxa 2620: 63 – 68.
Palmer JM & Mound LA (1991) Thysanoptera. pp. 67 – 76 in Rosen D (ed.). The Armoured Scale Insects, Their Biology, Natural Enemies andControl. Amsterdam: Elsevier Vol. B.
Terry I, Moore CJ, Walter GH, Forster PI, Roemer RB, Donaldson JD & Machin PJ (2004) Association of cone thermogenesis and volatiles with pollinator specificity in Macrozamia cycads. Plant Systematics and Evolution 243: 233 – 247.
Tree DJ & Mound LA (2009) Gall-induction by an Australian insect of the family Thripidae (Thysanoptera: Terebrantia). Journal of Natural History 43: 1147 – 1158.
Tree DJ & Walter GH (2012) Diversity and abundance of fungivorous thrips (Thysanoptera) associated with leaf-litter and bark across forest types and two tree genera in subtropical Australia. Journal of Natural History 46: 2897 – 2918.
Williams G, Adams P & Mound LA (2001) Thrips (Thysanoptera) pollination in Australian subtropical rainforests, with particular reference to pollination of Wilkiea huegeliana. (Monimiaceae). Journal of Natural History 35: 1 – 21.
Zerega NJC, Mound LA & Weiblen GD (2004) Pollination in the New Guinea endemic Antiaropsis decipiens (Moraceae) is mediated by a new species of thrips, Thrips antiaropsidis sp. nov. (Thysanoptera: Thripidae). International Journal of Plant Sciences 165: 1017 – 1026.