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Clusiodes

Owen Lonsdale and Steve Marshall
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Containing group: Clusiidae

Introduction

Caloren & Marshall (1998) described the behaviour, biology and faunistics of the New World Clusiodes, and Rohácek (1995) described that for species in the Czech and Slovak Republics. The most recent treatment was by Lonsdale & Marshall (2007), who redefined the genus, restricting it to only 31 of the 64 species previously treated as Clusiodes. The remaining 33 species were transferred to its sister genus Hendelia Czerny, rendering Clusiodes almost entirely north temperate in distribution, and Hendelia almost entirely tropical and south temperate in distribution.

European species of Clusiodes and Hendelia beckeri have been reared from puparia collected in numerous species of rotting deciduous tree trunks including aspen, ash, birch, poplar and alder (Caloren & Marshall, 1998; Rohácek, 1995); several puparia and larvae of Clusiodes ruficollis have also been collected from under the bark of felled hornbeam in Britain (Withers, 1985). North American Clusiodes have been reared from dead tulip trees  and likely develop in elm and maple (Caloren & Marshall, 1998). Clusiodes species overwinter as puparia or late-instar larvae in the larval habitat (Caloren & Marshall, 1998).

Adults of both genera are found predominantly on hardwood, but several Clusiodes species have been collected off of softwood trees such as pine, hemlock and fir (Caloren & Marshall, 1998; Rohácek, 1995; Withers, 1985). North American Clusiodes have also been found in association with rotting fungus (Caloren & Marshall, 1998). Small dung baits also regularly attract these species, particularly those baits placed on fallen wood that is bare and exposed. Sasakawa (1998) notes that Clusiodes and Sobarocephala have been collected with Malaise traps or fruit fly traps baited with putrid pork.

Fallen trunks are usually the most reliable microhabitat at which to collect adult Hendelia and Clusiodes, since they are often used as lek sites. Rohácek (1995) noted that pale, conspicuous trunks (generally fallen trunks without bark) were selected by males of several Clusiodes species to attract females. Rohácek (1995) also observed numerous teneral specimens of C. ruficollis emerging from a moist, rotten beech trunk; these newly emerged adults were seen to search for new logs to use them as mating places; males patrolled these logs defending territory, but females visited the mating sites only briefly to copulate, then searched for similar, but more rotten logs to oviposit in. North American Clusiodes have been noted to prefer treefalls (both new and old) in sunspots, where males perform wing-flicking displays (alone or with conspecifics) and 'ambush-style attacks', in addition to the territorial patrolling and head-to-head confrontations previously noted in European species (Caloren & Marshall, 1998).

Characteristics

Clusiodes, like its sister-genus Hendelia, can be characterized by reduced anterior and posterior fronto-orbitals, well developed interfrontal and median genal bristles, swollen spermathecal ducts, a large subapical disc on the ventral receptacle, a longitudinal desclerotization on the female seventh sternite, a crested fin-like phallapodeme, a distiphallus that is rod-like basally with a membranous distal section, and an elongate pregonite that is perpendicular to the long axis of the hypandrium (Lonsdale & Marshall, 2007).

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Figure. Top: External male terminalia of select European taxa, left lateral and posterior (left to right): Clusiodes pictipes (Zetterstedt); C. geomyzinus (Fallen); C. freyi Tuomikoski; C. apicalis (Zetterstedt); C. caledonicus (Collin); C. gentilis; C. verticalis (Collin). Bottom: C. apicalis (Zetterstedt), hypandrial complex, left lateral. © Owen Lonsdale.

Head bristles of Clusiodes melanostomus. © Owen Lonsdale

Clusiodes can be separated from Hendelia by having a pubescent arista, evenly spaced fronto-orbitals, one pair of lateral white stripes on the shoulders, and large parallel surstyli that sometimes have an anterodistal process (Lonsdale & Marshall, 2007). Clusiodes species are sometimes black in colouration, but a number of species have a yellow vittate scutum. Most Clusiodes, particularly the smaller ones, are generally matt, setulose and rounder in appearance than other Clusiidae. Species of Clusiodes also have shorter legs (usually thin and cylindrical) and heads that are generally rounded with a broadly curved frons, narrow face and blunt features.

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Habitus of Clusiodes gracilolobus (top) & C. ater (bottom). © Owen Lonsdale

Discussion of Phylogenetic Relationships

Hendelia and Clusiodes are sister genera, supported by the synapomorphies listed above. They form a clade with Heteromeringia Czerny in the Clusiodinae on the basis of telescoped and darkly pigmented spermathecae.

Clusiodes and Hendelia show a clear north/south division, with Clusiodes almost entirely north temperate and Hendelia almost entirely tropical and south temperate in distribution.  Most Clusiodes clades include widely separated sister species that often occur on separate continents; this diverse aggregate of Nearctic and Palaearctic species support the theory that trans-oceanic speciation events have been frequent in the genus (Caloren & Marshall, 1998). 

Clusiodes can be divided into two well-supported Holarctic clades, the C. albimanus and C. geomyzinus species groups, which largely overlap each other's distributions.  The C. albimanus group is most obviously characterized by bicoloured fore tarsi, and the C. geomyzinus group is characterized by two well-developed dorsocentral bristles, a large bulging gena and short hypandrial bristles on a swollen basal lobe. 

A discussion of the phylogeny and biogeography of Clusiodes was provided in detail by Lonsdale & Marshall (2007).

References

Caloren, D.C. & S.A. Marshall. 1998. A revision of the New World species of Clusiodes Coquillett (Diptera: Clusiidae). Studia Dipterologica 5:261-321.

Lonsdale, O. & S.A. Marshall. 2007. Redefinition of the genera Clusiodes and Hendelia (Diptera: Clusiidae: Clusiodinae), with a review of Clusiodes. Studia Dipterologica 14: 117-159.

Rohacek, J. 1999. Clusiidae. Folia Fac. Sci. Nat. Univ. Masaryk. Brun., Biol. 100: 291-293.

Withers, P. 1985. Notes on some British Clusiidae and reduction of Clusiodes facialis (Coll.) to synonymy. Proceedings of the Transactions of the British Entomological Natural History Society 18: 63-64.

Sasakawa, M. 1998. Family Clusiidae. In. Contributions to a Manual of Palaearctic Diptera; Volume 3: Higher Brachycera. L. Papp & B. Darvas (eds.), pp. 219-225. Science Herald, Budapest.

Title Illustrations
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Scientific Name Clusiodes ater Melander & Argo
Specimen Condition Live Specimen
Life Cycle Stage Adult
Copyright © Steve Marshall
Scientific Name Clusiodes apiculatus Malloch
Specimen Condition Live Specimen
Sex Female
Life Cycle Stage Adult
Copyright © Steve Marshall
Scientific Name Clusiodes melanostomus complex
Specimen Condition Live Specimen
Life Cycle Stage Adult
Copyright © Steve Marshall
About This Page

Owen Lonsdale
Canadian National Collection of Insects, Arachnids & Nematodes

Steve Marshall
University of Guelph, Canada

Correspondence regarding this page should be directed to Owen Lonsdale at and Steve Marshall at

Page: Tree of Life Clusiodes. Authored by Owen Lonsdale and Steve Marshall. The TEXT of this page is licensed under the Creative Commons Attribution-NonCommercial License - Version 3.0. Note that images and other media featured on this page are each governed by their own license, and they may or may not be available for reuse. Click on an image or a media link to access the media data window, which provides the relevant licensing information. For the general terms and conditions of ToL material reuse and redistribution, please see the Tree of Life Copyright Policies.

Citing this page:

Lonsdale, Owen and Steve Marshall. 2009. Clusiodes. Version 24 November 2009 (under construction). http://tolweb.org/Clusiodes/27684/2009.11.24 in The Tree of Life Web Project, http://tolweb.org/

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