BDS Logo

British Dragonfly Society

Draft Management Fact File

Please note: These MFFs are still draft versions.
Any comments sent to the Conservation Officer would be most welcome.

The Common Club-tail - Gomphus vulgatissimus (L.)

Identification

Gomphus habitat

Teneral Gomphus vulgatissimus © C. Murray

The Common Club-tail (Gomphus vulgatissimus) is a medium sized species with a distinctively club-shaped abdomen as suggested by its common name. Females and teneral males are mainly black1 with extensive yellow markings on the thorax and abdomen. The shape of the hind wing differs between the male and female and can be used to help distinguish the sex of insects even while they are immature. As the male matures most of the yellow markings turn green although the spots on the sides of abdominal segments 7-9 remain bright yellow2. Unlike most dragonflies the eyes are separate and do not meet at the top of the head, which aids identification, and in mature adults the eyes are dull green2. This dragonfly is elusive as an adult, but can be seen most frequently during emergence or as a teneral insect. Once it has settled in the vegetation or upon stones, its cryptic colouration makes is difficult to observe3. It can be mistaken for the Golden-ringed Dragonfly Cordulegaster boltonii, but it is much smaller and the pattern of pale markings is very different4.

Larvae of the Common Club-tail are unique, and unlike other British species have short bulbous antennae. The shape of the exuvial case is diagnostic2 and easy to identify with the head appearing triangular due to the way the antennae always form an apex at the front of the head.

Status

The Common Club-tail is a nationally notable species (Nb), being found in less than 100 10km-squares in Britain. It is an extremely local insect, but where suitable habitats occur it can be found in very large numbers2. It is the subject of three local Biodiversity Action Plans, in Worcestershire (this county having more 1km-square records than any other nationwide), Shropshire and Cheshire.

Distribution

The Common Club-tail is the most widespread Gomphid species in Europe1, inhabiting many central and northern countries. It occurs from Southern Scandinavia, eastward to Russia and South to France and Northern Italy. However, it is scarce in the Mediterranean4.

In Britain it is confined to Midland and Southern counties5 with the River Dee supporting the most northerly population6. It is found on the mature stages of seven river systems and their tributaries; five of these rise in the Welsh Uplands (the Dee, Severn, Wye, Tywi and Teifi) and two in Southern England (Thames and Arun)4.

Distribution map from the National Biodiversity Network Gateway website.

Ecology and Habitat Requirements

In Britain the Common Club-tail is a riverine species typically associated with moderate to slow flowing water5. It breeds in unpolluted, meandering rivers, which have a depositional nature4. Silty substrates are favoured over stretches with rock beds5 as the larvae are burrowers, living in the mud and silt. Inhabited reaches are typically adjacent to woodland, as it provides cover for the adults2, rather than more open habitats5. Common Club-tails spend most of their adult life away from water7 perching on the ground, on bushes1 and in treetops2. They are often found in woodland and use the tree canopy more than most species1, 2. They are elusive insects and consequently knowledge about their terrestrial requirements is limited.

Mature males are territorial, preferring to fly low over open water rather than along the shoreline, to defend territories or to hunt8, 9. They appear to show a preference for stretches where the banks are steep and where there is some tree cover2.

Copulation is rarely seen, but has been witnessed some distance from water2, 10. It can be seen in woodland glades, where males will display over bracken to encourage females to fly down to mate.

Females oviposit alone, favouring quieter stretches in an attempt to avoid male attention4, 5. They fly low over the water, dipping their abdomen below the surface several times before disappearing2.

The larvae of the Common Club-tail live within the silt and mud on the riverbed for 3 to 5 years2, foraging actively in the sediment at night11. Research suggests that they prefer clumps of emergent vegetation9, although it is not a necessity. This explains why the species continues to thrive along the Thames regardless of the tremendous build up of pleasure boat traffic12. The larvae are usually found on meanders where silt deposition is greatest2 and research indicates that they favour the inside of these9. Research also suggests that the larvae prefer gentle banksides and require water at least 20cm deep which is slow flowing9. It has been suggested that both the eggs2 and larvae may be carried a short way downstream during their development5. It is likely that the preference for slow flowing water prevents them from being washed too far downstream2 and they appear reluctant to wander, except at low current speeds13. Ole Müller14 found that the angle of the front of the head adopted by Gomphids helps to prevent the larvae from being dislodged.

Gomphus habitat

Gomphus vulgatissimus habitat - the River Severn in Shropshire © BDS/ C. Daguet

The Common Club-tail is a spring species with a tightly synchronised emergence4 triggered by increasing day length and rising water temperature in May and June15. The larvae wait for the sun to come up before leaving the water and may travel some distance to find a suitable emergence site16. Distances of 20m or more have been recorded16, 17 and observations on the continent suggest that in some situations stones are chosen in preference to plants on lake margins18, 19. This probably reflects the anatomy of the larvae as the legs, which are widely spread, are not adapted for climbing reeds12, 20. Unlike most British Dragonflies, Common Club-tails can emerge in a horizontal position, although observations suggest that the numbers of larvae actually doing this is very low15. Collision with overhanging vegetation at the beginning of the maiden flight can knock teneral adults into the water13. Common Club-tails are famous along reaches of the Thames, Severn, Wye and Arun, where mass emergence occurs. There is a tendency for dense concentrations of emerging individuals to occur at well-spaced sites, with small number of exuviae found in between5. One survey carried out in Worcestershire over the last 18 years has shown that emergence rates at the same location can vary from 1.5 to 6.0 per metre per year (M. Averill, pers. comm.).

Gomphus habitat

Immature female Gomphus vulgatissimus © BDS/ C. Daguet

Following emergence, the maiden flight of teneral insects aims away from water, usually into vegetation at the top of the riverbank. Thus, woodland or scrub within close proximity of inhabited rivers provides a local source of food and shelter for adults, particularly during their maturation period5. Dispersal is invariably away from the river and adults can be seen flying in woodland rides or along hedgerows often several kilometres away from the breeding site. Maturing insects can be found feeding in woodland clearings up to 10km from the river2.

Summary of the Main Habitat Requirements

The Common Club-tail inhabits and breeds in moderate to slow-flowing river systems in which there is sufficient silt deposited for the larvae to burrow. Bankside tree cover and adjacent woodland are important requirements for adults2.

Flight period: early May to end of June/early July

Current Threats

Management

General Guidelines

Best Management Practice

Habitat Restoration and Recreation

Case Study

-

References

  1. Askew, R. R. (1988). The Dragonflies of Europe. Harley Books, Colchester.
  2. Vick, G. (1997). Field Guide to the Dragonflies and Damselflies of Great Britain and Ireland. Eds Brooks, S. & Lewington, R., British Wildlife, Hook.
  3. Hammond, C. O. (1983). The Dragonflies of Great Britain and Ireland. (2nd Edition revised by R. Merrit). Harley Books, Colchester.
  4. Merritt, R., Moore N. W., & Eversham, B. C. (1996). Atlas of the Dragonflies of Britain and Ireland. Centre for Ecology and Hydrology, Peterborough, pp. 108-109.
  5. Kemp, R. G., & Vick, G. S. (1983). Notes on observation on Gomphus vulgatissimus (Linnaeus) on the River Severn and River Thames. Journal of the British Dragonfly Society 1(2), pp. 22-25.
  6. Duff, R. (2002). English Nature, Cheshire to Lancashire Team, 2002, River Dee SSSI Cheshire/Shropshire Notification under section 28c the Wildlife and Countryside Act 1981, Management Statement.
  7. Averill, M. (2002). Club-tailed Dragonfly Gomphus vulgatissimus Action Plan. In: Worcester Biodiversity Action Plan, available at: http://worcestershire.whub.org.uk/home/wcc-bio-action-plans-club-tailed-dragonfly.pdf
  8. Vallee - In: Hinterman (1983) - see below.
  9. Hinterman, U. (1983). The Influence of River Management on Four Dragonfly Species on the River Arun (Sussex). M.Sc. Dissertation, University College London.
  10. Moore, N. W. (1991). Where do adult Gomphus vulgatissimus (L.) go during the middle of the day? Journal of the British Dragonfly Society, 5 (2), pp. 40-43.
  11. Foidl, J., Buchwald, R., Heitz, A., and Heitz, S. (1993). Untersuchungen zum Larvenbiotop von Gomphus vulgatissimus Linné 1758 (Gemeine Keiljungfer, Gomphidae, Odonata). Mitt. Bad. Landesver. Naturk. Naturschutz, N. F., 15: 637 - 660 [OdA 9266]. In: Corbet (1999). Dragonflies - Behaviour and Ecology of Odonata
  12. Goodyear, K. G. (1994). Gomphus vulgatissimus (Linnaeus) in Oxfordshire and Hampshire. Journal of the British Dragonfly Society 10(1), pp. 19.
  13. Corbet, P.S. (1999). Dragonflies - Behaviour and Ecology of Odonata. Harley Books, Essex.
  14. Müller O. (1995). Ökologische Untersuchungen an Gomphiden (Odonata: Gomphidae) unter besonderer Berücksichtigung ihrer Larvenstadien. DrT, Humboldt Univ., Berlin [OdA 10590].
  15. Averill, M. T. (1989). Emergence attitudes in Gomphus vulgatissimus. Journal of the British Dragonfly Society 5(2) pp. 37-39.
  16. Silsby, J. (1993). Wildlife Reports Dragonflies, British Wildlife 4(6) pp. 388-389.
  17. Martin, R. (1895). Une éclosion de libellules. Feuill. Jeun. Nat. 25: pp141-142.
  18. Wesenberg-Lund, C. (1913). Odonaten-Studien. Int. Rev. Hydrobiol. 6:155-228; 373-422.
  19. Corbet, P.S. (1962). A Biology of Dragonflies. H.F & G. Witherby Ltd, London.
  20. Longfield, C. (1937). The Dragonflies of the British Isles. Frederick Warne & Co. Ltd, London.
  21. National Rivers Authority. (1994). The quality of rivers and canals in England and Wales (1990 to 1992). Water Quality Series No. 19. HMSO, London.
  22. Schmidt, E. (1984). Gomphus vulgatissimus L. an einem belasteten Havelsee, dem Tegeler See (Insel Scharfenberg) in Berlin (West). Libellula, 3(3/4):35-51. In: Corbet (1999). Dragonflies - Behaviour and Ecology of Odonata.
  23. Tobias, A. (1996). Einfluss von Feinsandüberschichtigungen auf grabende Libellenlarven (Gomphidae). TagBer. Dtsch. Ges. Limnol. 1995: 435 - 439. (OdA 11034). In: Corbet (1999). Dragonflies - Behaviour and Ecology of Odonata
  24. Silsby, J. (1985). Emergence of Gomphus vulgatissimus. Oral presentation at meeting of the British Dragonfly Society, Leeds, October 1985.
  25. Williamson, E. B. (1903). Spiders as enemies of dragonflies. Entomology News 14, pp 160-161. In: Corbet (1962) A biology of Dragonflies.
  26. World Wildlife Fund website (2002). Wümmewiesen Restoration Project, Wise Use of Floodplains.
  27. Kemp, R. G. K. (1988). Is Gomphus vulgatissimus (L.) exclusively a riverine species in the British Isles? Journal of the British Dragonfly Society 4(1) pp. 8-9.
  28. Dufour, C. (1978). Etude faunistique des odonates de Suisse Romande. Conservation de la faune et section protection de la nature et des sites du Canton de Vaud, Switzerland.

Management file updated on 17 April 2007