The thrips (thysanoptera) liothrips xanthocerus (phlaeothripidae) and Neohydatothrips catenatus (thripidae) inhabit leaf clusters on Pluchea sericea (Asteraceae).
Article Type: Report
Subject: Thrips (Distribution)
Insect-plant relationships (Research)
Author: Wiesenborn, William D.
Pub Date: 09/01/2011
Publication: Name: Florida Entomologist Publisher: Florida Entomological Society Audience: Academic Format: Magazine/Journal Subject: Biological sciences Copyright: COPYRIGHT 2011 Florida Entomological Society ISSN: 0015-4040
Issue: Date: Sept, 2011 Source Volume: 94 Source Issue: 3
Topic: Event Code: 690 Goods & services distribution; 310 Science & research Advertising Code: 59 Channels of Distribution Computer Subject: Company distribution practices
Geographic: Geographic Scope: United States Geographic Code: 1USA United States
Accession Number: 298614275
Full Text: Liothrips xanthocerus Hood is the only thrips that has been collected from Pluchea sericea (Nutt.) Cov. (Asteraceae) leaves in California (Cott 1956; Bailey 1957; Hoddle et al. 2008). Collections have only found adults, also taken from willow (Salicaceae, Salix sp.) and creosote bush (Larrea tridentata [DC.] Cov.) (Cott 1956). Pluchea sericea, or arrowweed, is an erect, slender-stemmed, willow-like shrub that grows to 4 m in height, frequently in wet soils, and produces silvery leaves 1-4 cm long and 3-6 mm wide (Munz 1974). It occurs at elevations below 1000 m from California to Texas, north into Nevada and Utah and south into northern Mexico (Nesom 2006). Cott (1956) commented that collected L. xanthocerus adults may be strays, because larvae of the species have not been found. Here I describe the eggs and larvae of L. xanthocerus on P. sericea and report a second thrips species, Neohydatothrips catenatus (Hood), which also inhabits the plant's leaf clusters.

I collected thrips from P. sericea at 3 localities during 28 Apr-15 Sep 2010. One locality (34[degrees]46'N 114[degrees]32'W, 140 m elevation) was near Topock in Mohave County, Arizona. The second locality (33[degrees]17'N 114[degrees]41'W, 67 m) was 135 km south along the river near Cibola in La Paz County, Arizona. The third locality (35[degrees]10'N 114[degrees]41'W, 571 m) was at Hiko Springs near Laughlin in Clark County, Nevada. The first two, floodplain localities lie within the Sonoran Desert, whereas the third locality intersects the Sonoran and Mojave Deserts. All 3 sites contain moist soils from shallow groundwater or irrigation. Terminal leaf-clusters on apical and lateral stems were plucked and examined for all life stages of thrips. I mounted adults on slides and identified them as L. xanthocerus (Cott 1956; Mound & Kibby 1998) and N. catenatus (Hood 1957 [as Sericothrips catenatus], Mound & Kibby 1998; Hoddle et al. 2008) with the latter verified by S. Nakahara (USDA-ARS-SEL, Beltsville Maryland; lot no. 1102723). Vouchers of adults of both species and second-instar larvae of L. xanthocerus were deposited at the Entomology Museum, University of California, Riverside.

Eggs of L. xanthocerus were found on top of the dense trichomes that cover P. sericea leaves (Fig. 1B). They were oviposited parallel to the leaf surface. Eggs (n = 10) are 0.35-0.39 mm long and 0.15-0.17 mm wide. The chorion is sculptured with the 4- or 5-sided polygons (Fig. 1D) characteristic of Tubulifera (Heming 1991).

Larvae of L. xanthocerus were found within terminal leaf-clusters on apical and lateral stems. Second-instar larvae (Fig. 1C) were differentiated from first instars (Fig. 1A) by their longer antennal segments. First instars (n = 28) are 0.7-1.1 mm long, and second instars (n = 36) are 1.2-2.2 mm long. Both larval instars are mostly yellowish-white with darker sclerotization visible dorsally on the antennae, head, anterior pronotum (in paired plates), legs, and abdominal segments IX-X (Fig. 1A, C). Small, lateral plates on abdominal segment VIII also are sclerotized in second-instar larvae (Fig. 1C). The head, mouth cone, and coxae are sclerotized in ventral view. The mouth cone, coxae, and small sclerotized-plates above the middle and hind coxae are translucent. Remaining sclerotization is brown in first instars and blackish brown in second instars. Black malpighian-tubules are visible in both larval instars (Fig. 1A, C). Overall patterns of sclerotization in first and second instars resemble those on the phlaeothripid Haplothrips verbasci (Osborn), and sclerotization on the head and prothorax resembles that on Liothrips sp. (Figs. 28.5, 28.10 and 28.94; Heming 1991).

Antennae are 7-segmented in both larval instars of L. xanthocerus. The terminal segment on first instars is darkened. The completely dark antennae on second instars (Fig. 1C) contrast with the yellow coloration of segments III-VII on adults (see Hoddle et al. 2008). Antennal sense-cones on second instar larvae, examined on cleared specimens with phase contrast, are arranged similar to those on other tubuliferans (Figs. 28.97-28.99; Heming 1991). They occur apically on the outside, inside, outside, and outside-top of segments III-VI, respectively, with a second, shorter sense cone on the outside of segment IV. The sense cones are straight (Fig. 1E), similar to Liothrips mikaniae (Priesner) (Cock 1982) but differing from Liothrips russelli (Hood) (Fig. 28.98; Heming 1991).

Larvae and adults of L. xanthocerus were observed at Topock on 14 May & 15 Sep 2010, indicating at least 2 generations per year. The absence of life stages within leaf clusters at Hiko Springs on 26 Jan 2011 suggests the species does not overwinter on plants.


Larvae and male and female adults of the terebrantian N. catenatus were also found in P. sericea leaf clusters. The species was distinctive due to grey patches on the pronota of adult females (Hood 1957; Hoddle et al. 2008). Second instar N. catenatus and first instar L. xanthocerus larvae were similar in size. Larvae of the 2 species were distinguished by the prominent setae on the terminal abdominal segments in Phlaeothripidae but not Thripidae (Figs. 28.4-28.5 and 28.9-28.10; Heming 1991).

Quiescent instars of L. xanthocerus and N. catenatus were not found within leaf clusters. Berlesefunnel samples of soil beneath P. sericea at Hiko Springs yielded 1 second-instar pupa, recognized by its long wing pads (Fig. 28.17; Heming 1991), of L. xanthocerus on 31 May 2010 and abundant second-instar larvae, pupae, and adults of N. catenatus on 16 Jun 2010. Pluchea sericea may be the primary, if not the only, host of L. xanthocerus. The record on willow may have been a misidentification of arrow-weed, and development on the co-occurring but dissimilar L. tridentata seems unlikely. Liothrips species generally are phytophagous (Cott 1956). Neohydatothrips catenatus was first recorded on unspecified desert-shrubs in southern Arizona (Hood 1957) and has been collected on Hyptis emoryi Torrey (Lamiaceae) (Hoddle et al. 2008). This Sonoran desert shrub borders the lower Colorado River north into southern Nevada (Turner et al. 1995), and scattered H. emoryi occur at Hiko Springs. Both P. sericea and H. emoryi produce leaves densely covered with trichomes. Different life-histories between thrips species, such as methods of oviposition, may facilitate their coexistence as herbivores within P. sericea leaf clusters.


Larvae of the tubuliferan thrips Liothrips xanthocerus Hood and larvae and adults of the terebrantian thrips Neohydatothrips catenatus (Hood) are reported for the first time inhabiting terminal leaf clusters on apical and lateral stems of Pluchea sericea, a desert riparian plant of southwestern North America. Eggs and first and second instar larvae of L. xanthocerus are photographed and described.


BAILEY, S. F. 1957. The Thrips of California. Part I: Suborder Terebrantia. Bull. California Insect Surv. 4: 143-220.

COCK, M. J. W. 1982. The biology and host specificity of Liothrips mikaniae (Priesner) (Thysanoptera: Phlaeothripidae), a potential biological control agent of Mikania micrantha (Compositae). Bull. Entomol. Res. 72: 523-533.

COTT, H. E. 1956. Systematics of the suborder Tubulifera (Thysanoptera) in California. University of California Publications in Entomology, vol. 13. University of California Press, Berkeley, California, 210 pp + 4 plates.

heming, B. S. 1991. Order Thysanoptera, pp. 1-21 In F. W. Stehr [ed.], Immature Insects, vol. 2. Kendall/Hunt Publishing, Dubuque, Iowa, 975 pp.

HODDLE, M. S., MOUND, L. A., AND PARIS, D. L. 2008. Thrips of California. CBIT Publishing, Queensland, Australia ( Thrips_of_California.html. Accessed 19 January 2011).

HOOD, J. D. 1957. Fifteen new Thysanoptera from the United States. Proc. Biol. Soc. Washington 70: 49-60.

MOUND, L. A., AND KIBBY, G. 1998. Thysanoptera: an Identification Guide, 2nd ed. CAB International, Wallingford, UK.

MUNZ, P. A. 1974. A Flora of Southern California. University of California Press, Berkeley, California, 1086 pp.

NESOM, G. L. 2006. Pluchea, pp. 478-484 In Flora of North America, North of Mexico, vol. 19. Oxford University Press, New York, New York, xxiv + 579 pp.

TURNER, R. M., BOWERS, J. E., AND BURGESS, T. L. 1995. Sonoran Desert Plants: an Ecological Atlas. University of Arizona Press, Tucson, Arizona, 504 pp.


Boulder City, Nevada

Gale Copyright: Copyright 2011 Gale, Cengage Learning. All rights reserved.