Rare click beetlesCleide Costa and Sergio Antonio Vanin
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The family includes three genera and 21 described species, distributed as follows (Costa et al. 2003, 2010): the Holarctic Cerophytum Latreille (western and eastern USA; southern and central Europe and Japan); the Neotropical Brachycerophytum Costa et al. (Mexico, Colombia, Peru and Bolivia) and Phytocerum Costa et al. (Mexico, Costa Rica, Nicaragua, Guatemala, French Guiana, Trinidad, Brazil, Bolivia, Paraguay and Argentina). An undescribed species, up to now represented only by females, is known from Africa.
Adult cerophytids have been collected at light traps or Malaise traps, by beating vegetation, in association with rotten wood or bark, and in leaf litter and underground debris (Steiner, 2000; Costa et al. 2003). Adults are capable of “clicking” by the sudden release of the prothorax in the same manner as Elateridae. It is also possible that the enlarged and modified profemora and the lack of metacoxal plates in Cerophytidae are both connected in some way with escape behavior (Costa et al. 2003).
The larva of Cerophytum is highly unusual and differs from those of all other Elateroidea in having unique mouthparts involving paired sucking grooves, styliform mandibles and maxillae, paired thoracic and abdominal glands and bifurcate pretarsi. The larva of C. elateroides was first described by Rey (1887) based on specimens collected with an adult in the rotten trunk of Sambucus (Caprifoliaceae). Mamaev (1978) redescribed and illustrated the Cerophytum larva based on a series of specimens found in the dark fungus–infested wood (brown rot) of a dead standing Ulmus in association with larvae of Oedemeridae (Costa et al. 2003).
(based on Mamaev 1978; Lawrence 1991; Lawrence et al. 1999a, b; Costa et al. 2003)
- Length 4.3–9.2 mm. Body slightly flattened above, strongly convex below.
- Head deeply inserted into prothorax, slightly declined. Occipital region with weak transverse carina forming short subgenal ridges.
- Frons produced in front of eyes forming median prominence bearing antennal insertions, frontoclypeal region is more or less vertical and mouthparts are ventrally oriented.
- Eyes large, strongly protruding with exocone ommatidia.
- Antennae 11–segmented, serrate to pectinate from antennomeres 3 to 10.
- Labrum free, strongly transverse and truncate.
- Mandibles narrow, strongly curved, unidentate and acute; without mola but with membranous prostheca.
- Maxillae with both galea and lacinia densely setose at apex; apical palpomere more or less expanded and truncate, usually securiform or elongate oval. Ligula membranous, rounded apically; palps approximate, apical palpomere subtriangular.
- Prothorax with posterior angles produced laterally; interlocking device weakly developed.
- Prosternum anterior edge truncate or with ventrally directed chin piece; head rest strongly oblique from lateral perspective
- Prosternal process laterally expanded at middle to form secondary condyle on each side, acute apex fitting into mesoventral cavity.
- Elytra with 9 distinct rows of deep window punctures, sometimes with an additional subhumeral row.
- Legs with metatrochanters more than half as long as metafemora.
- Tarsi 5–5–5; tarsomeres 1 and 5 about equal in length, 2 shorter than 1, 3 and 4 subequals, the latter with a ventral lobe. Pretarsal claws pectinate; empodium not visible.
- Mesoventrite with large, deep mesal cavity, preceded by sclerotized lip, flanked anteriorly by a pair of concave areas and posteriorly by mesocoxal cavities, and extending posteriorly almost to edge of ventrite.
- Hind wing with apical field bearing 2 parallel, oblique, anterior sclerotizations; radial cell elongate; cross–vein r3 extending to RP; medial field with 4 free veins.
- Abdomen with basal four ventrites connate; base of tergite IX and sternite X fused.
- Aedeagus of trilobate type, symmetrical; phallobase Y–shaped; parameres projecting anteriorly, beneath phallobase; parameres divided into proximal sclerotized and distal membranous regions.
- Ovipositor long and narrow; coxites not divided, styli short and terminal, baculi elongate.
- Body elongate, robust but more or less parallel–sided, slightly curved ventrally; vestiture consisting of fine setae only.
- Head prognathous and protracted much narrower than thorax; frontal arms and dorsal endocarinae absent; ventral longitudinal endocarinae present.
- One stemma on each side of head, with well developed lens.
- Antennae short, 3–segmented; subconical sensorium on preapical antennomere, which bears a second conical sensorium.
- Frontoclypeal suture vaguely indicated. Labrum fused to head capsule.
- Sucking mouthparts formed by styliform mandibles and maxillae enclosed in separate lateral channels; mandibles flattened, symmetrical and non–opposable, internal channel extending from near base to apex; galea and lacinia forming slender, blade–like, channelled mala.
- Ventral mouthparts strongly retracted forming maxillolabial complex; labium forming a five–toothed plate
- Prementum and hypopharynx forming 5–dentate sclerome; postmentum subquadrate; labial palps 2–segmented with subacute apical palpomere.
- Paired gland openings present on all thoracic terga and abdominal terga I–VIII.
- Thoracic and abdominal spiracles biforous; closing apparatus present
- Anterior pretarsus bifurcate, with 2 setae.
- Abdominal segments I–VIII each with 3 clearly defined lateral lobes on each side; terga densely clothed with long hairs.
- Abdominal segment IX without urogomphi.
Latreille (1825) placed Cerophytum in the group Sternoxi of Serricornia, along with Buprestidae and most elateroid genera known at the time. In 1834, he proposed a family group based on Cerophytum, and this was recognized by Lacordaire (1857) who suggested a relationship with Eucnemidae. Crowson (1955) considered the family to be part of the Elateroidea (sensu stricto), and this has been followed by most workers. The unusual, apparently plesiomorphic nature of the cerophytid propleurocoxal mechanism prompted Hlavac (1975) to remove the group from Elateroidea and to place it together with two other elateriform families of doubtful affinities, Artematopodidae and Brachypsectridae. In cladograms produced by Lawrence (1988) Cerophytidae formed a clade with Eucnemidae and Throscidae (sensu stricto) or was basal to a clade containing these two families plus Elateridae. A similar association was found in analyses conducted by Calder et al. (1993), Beutel (1995), and Lawrence et al. (1995). In Muona’s (1993) revision of Eucnemidae, Cerophytidae were considered basal to the elateroid complex (Elateroidea sensu Crowson 1955) and in a later cladistic analysis (Muona1995) Cerophytidae and Eucnemidae formed one clade whereas Throscidae (sensu Crowson 1955) represented a derived group within Elateridae (Costa et al.2003, 2010).
(Based on Costa et al., 2003)
- Coleoptera, Polyphaga, Elateriformia, Elateroidea
- Cerophytidae Latreille 1834
- Cerophytum Latreille, 1806 (type species: Elater elateroides Latreille, 1804)
- Brachycerophytum Costa, Vanin, Lawrence & Ide, 2003 (type species: Cerophytum fuscicorne de Bonvouloir, 1870)
- Phytocerum Costa, Vanin, Lawrence & Ide, 2003 (type species: Phytocerum golbachi Costa, Vanin, Lawrence & Ide, 2003)
Costa et al. (2003, 2010) carried out a cladistic analysis of the 21 known species of Cerophytidae, with outgroups from Elateridae, Throscidae and Eucnemidae. Three main clades were recognized: (Cerophytum (Brachycerophytum, Phytocerum)). Synapomorphies for the family include: 1. chin piece ventrally directed; 2. posterior pronotal angles produced laterally; 3. metatrochanters more than half as long as metafemora; 4. base of tergite IX and sternite X fused; 5. parameres divided into proximal sclerotized and distal membranous regions; 6. phallobase Y–shaped; 7. parameres projecting anteriorly, beneath phallobase. Possible larval synapomorphies are: sucking mouthparts formed by styliform mandibles and maxillae enclosed in separate lateral channels; anterior pretarsi bifurcate; and labium forming a five–toothed plate. The Holarctic genus Cerophytum is characterized by having the profemur with a longitudinal carina and the dorsal region of the parameres fringed. Synapomorphies for the Neotropical clade include: posterior angles of pronotum reduced; upper distal angle of profemur acute and produced; and lateroposterior margin of phallobase protruding over the bases of parameres. Brachycerophytum is distinguished by the ninth elytral stria strongly convex, basal portion of penis strongly constricted and bursa copulatrix without smooth and elongate sclerites; while Phytocerum autapomorphies include the lack of a chin piece, presence of an additional row of punctures between stria 8 and 9, and sclerotized spermatheca absent.
Beutel, R. G. (1995). Phylogenetic analysis of Elateriformia (Coleoptera: Polyphaga) based on larval characters. Journal of Zoological Systematics and Evolutionary Research 33: 145–171.
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Costa, C., Vanin, S. A., Lawrence, J. F. & Ide, S. (2003). Systematics and cladistic analysis of Cerophytidae (Elateroidea: Coleoptera). Systematic Entomology 28: 375–407.
Costa, C., Vanin, S. A., Lawrence, J. F. & Ide, S. 2010. 4.4. Cerophytidae Latreille, 1834. p. 54-61. In Leschen, R. A. B., R. G. Beutel & J. F. Lawrence (eds). Coleoptera, Beetles: Morphology and Systematics (Elateroidea, Bostrichiformia, Cucujiformia partim). Volume 2, 786 p. In: N. P. Kristensen & R. G. Beutel (eds). Handbook of Zoology, Arthropoda: Insecta, Walter de Gruyter GmbH & Co.KG, Berlin.
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Steiner, W. E., Jr. (2000). Records and habitats of the ‘rare click beetle’, Cerophytum pulsator (Haldeman), in Virginia and Maryland (Coleoptera: Cerophytidae). Banisteria 15: 43–45.
We thank Kirill V. Makarov (Moscow Pedagogical State University) for permission to use the photographs of Cerophytum elateroides and C. japonicum; Carlos Estevão Simonka for the electronic treatment of figure of Phytocerum minutum; Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) for the Research Grant 302721/2007 – 0 to C. Costa.
Museu de Zoologia, Universidade de São Paulo, Brasil
Correspondence regarding this page should be directed to Cleide Costa at and Sergio Antonio Vanin at
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- First online 02 February 2011
- Content changed 02 February 2011
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Costa, Cleide and Sergio Antonio Vanin. 2011. Cerophytidae. Rare click beetles. Version 02 February 2011. http://tolweb.org/Cerophytidae/9194/2011.02.02 in The Tree of Life Web Project, http://tolweb.org/