Large copper

From Seitz C. dispar Haw. (76). Very variable in size, many specimens [of dispar dispar] being smaller than large rutilus [now subspecies] ; differs from the latter in the larger spots of the underside, especially in the female. In the male an additional black spot appears frequently, but not always, in the centre of the cell on the upperside, this spot being in the female usually more than twice as large as in rutilus— ab. cuneigera Tutt are individuals in which the spot in the cell of the forewing is enlarged to a streak which occupies the greater part of the cell. ab. alba Tutt are albinotic specimens, such as occur in all species of coppers, bearing usually asymmetrical and irregular light patches on the wings in variable position. — rutilus Wernb. (= hippothoe Hbn.) (761, g) is the continental form of dispar; the forewing always without cell-spot, the discocellular spot smaller, or absent, the ocelli considerably smaller on the underside of both sexes and in the female also on the upperside. The springform of rutilus, vernalis Hormuz., rather closely resembles dispar in certain districts (e. g. Bordeaux, etc.), while the summer-form is considerably smaller. The dark spots are sometimes enlarged to streaks, which happens especially often on the underside; this is ab. sagittifera Hormuz. (76g). In ab. radiata Oberth. these streaks are also present on the hindwing, which is likewise the case in ab. nigrolineata Verity, whose redgolden upperside is said to be densely dusted with red. — In the east of the Region two forms are known: a reddish golden one in which the discal spots on the hindwing beneath are absent or obsolescent, while the row of submarginal spots on the forewing is very evenly developed and regular, dahurica Graes. [now subspecies(76g), from Amurland. — The second form is more yellowish golden — auratus Leech [now subspecies]76 ¢) —, the upperside of the male does never bear a discocellular spot, while the underside is distinctly spotted; the female of this form is recognized by the underside being ashy grey instead of blue-grey; from Corea, North China and Tibet. Both these last-Asiatic forms have been united by Leech as well as Staudinger and Rebel, but some specimens agree better with Graeser’s description and others with Leech’s. As Alpheraky records auratus from June and Graeser his dahurica from the middle of July to August, the two insects may possibly be seasonal forms. — borodowskyi Gr.-Grsh.[ Lycaena dispar ssp. borodowskyi Grum-Grshimailo, 1900[ is a further form, from Manchuria; it is large, brilliantly coloured and prominently spotted. — The larva of the rutilus-forms is dark green with paler lateral stripe. It hibernates young and feeds in May on various species of Rumex and on Polygonum bistorta. There are one or two broods according to the district, the butterflies being found in swampy meadows which are occasionally flooded. The species, though plentiful in some places, occurs in most localities in single specimens only and also not every year. By the application of low temperatures Standfuss obtained females in which the black markings of the upperside were modified.[4]

• 
  Lycaena dispar ♂
• 
  Lycaena dispar ♂ △
• 
  Lycaena dispar ♀
• 
  Lycaena dispar ♀ △

Armenia, Austria, Azerbaijan, Belarus, Belgium, Bulgaria, Czech Republic, Estonia, Finland, France, Georgia, Germany, Greece, Hungary, Italy, Kazakhstan, Latvia, Lithuania, Luxembourg, Moldova, Mongolia, Montenegro, Poland, Switzerland, Turkey, Ukraine, and Uzbekistan.[1]

It is regionally extinct in the United Kingdom, due to habitat loss.[1] As well it has been extinct in the British Isles, since the 1860s, with declining numbers occurring across numerous, other western European countries.[2]

• L. d. dispar (Haworth, 1802) − England − extinct
• L. d. batava (Oberthür, 1923) – Netherlands
• L. d. rutila (Werneberg, 1864) − Europe, Caucasus, Transcaucasia, N. Tien-Shan, W. Tien-Shan, Dzhungarsky Alatau, Ghissar
• L. d. festiva Krulikowsky, 1909 − Ural, W. Siberia
• L. d. dahurica (Graeser, 1888) − Transbaikalia, W.Amur
• L. d. aurata Leech, 1887 − Siberia, E. Amur, Ussuri.
• L. d. borodowskyi Grum-Grshimailo, 1900 Manchuria

Lycaena dispar was first recorded in 1749, from the Huntingdonshire fens,[5] England.[6] Documentation of the large copper was done by the Committee appointed by the Entomological Society of London for the Protection of British Lepidoptera.[6] "The butterfly occurred formerly in England, but is now extinct. The eggs were laid on Rumex hydrolapathum, the larva was green like the leaves of Rumex, with dark dorsal line. Pupa at first green, later grey with a dark dorsal line and two abbreviated pale stripes. — Early last century the species was still plentiful in several swampy districts of England, for instance at Whittlesea-Mere and other places, but did not occur in Ireland. On account of the intense cultivation of the soil in England these swamps were drained and the land employed for agriculture. In 1820 fifty or even more specimens of dispar could still be obtained in a short time. At that period 3 to 4 shillings the dozen were paid in England. In 1845 a rapid decrease was noticed in Cambridgeshire. In 1847 five specimens were caught in Huntingdonshire, since when no further captures have been recorded. In the [eighteen] seventies the commercial value had already increased to 20 shilling. In 1893, in the auction-room in London 31 specimens were sold which realized about £ 139, i. e. nearly 90 shillings the specimens. At another sale, in 1902, an average price of £ 5. was paid for dispar, a specially fine female realizing as much as £ 7."

Lycaena dispar, is widely distributed in central Europe, as far north as southern Finland, extending across temperate Asia to the Amur region and to Manchuria Korea.[2][1] Occurring throughout much of mainland Europe, L. dispar, is found between 40° and 60° latitudes.[2]

The British subspecies of this butterfly (L. d. dispar) was first described in 1759 in Huntingdonshire,[7] and was declared extinct in 1864 after the last populations in East Anglia were lost.[8] Most of our knowledge of its life cycle and ecology comes from studies of the similar subspecies (L. d. batava') found in the Netherlands. The species can be identified by the silvery hindwing undersides, from the large specimens of the related, more common, drier habitat species Caena virgaureae and Lycaena hippothoe.

Female

Egg

Lycaena dispar is a wetland species in decline throughout Europe.[9] The primary habitat of this butterfly has been drained for agricultural and other land usage, limiting their habitat.[9] When it can, L. dispar will utilize plants growing away from watersides and among reed-fen vegetation.[10] In this way L. dispar can avoid possible flooding that can occur in lower lying areas closer to the water's edge.[9] The species prefers undisturbed grasslands along the riverbanks and stream banks, where its larval food plant, the greater water dock, (R. hydrolapathum) can be found.[3]

Warmer microclimates, as well as warmer regions in general are preferred by L. dispar, allowing for faster growth time of larvae.[3]

Land disturbances through agriculture, primarily the mowing of grass, and other foliage has a negative influence on populations of L. dispar, such that mowing shortly after egg-laying, will result in disastrous losses due to the eggs being destroyed and the newly hatched larvae being deprived of host plants, for food: L. dispar lays its eggs on host food plants, commonly low-lying, with larval migration limited to the area around their birth, host plant.[3] For conservation purposes, it is highly recommended that L. dispar habitats be closely managed, with promotion in increased habitat heterogeneity, being most important: this strategy has proven beneficial for many other species of butterfly.[3]

Lycaena dispar has a bivoltine life cycle, throughout most of its European distribution, stretching from May to June, and from the end of July to early September, with peak flight occurring in July.[2] Two generations of L. dispar are standard, the first is characterized by fewer numbers, with the second generation producing more offspring that overwinter, as half-grown, third instar larvae.[2][10] In the warmer parts (southern distribution) of its European habitat range, L. dispar can be capable of third generations.[2] During the winter months, larvae enter diapause, a period of metabolic inactivity, that is characterized by the development of physiological tolerance to various environmental stressors: cold temperatures, starvation, in order to survive winter conditions.[10] Overwinter survival can be greatly reduced due to flooding for prolonged periods of time, resulting in high mortality of L. dispar larvae in diapause.[9]

Lycaena dispar larvae have three characteristic stages: pre-diapause in the autumn, winter diapause and post-diapause in the spring.[9] Heavy mortality is common between oviposition (when females lay their eggs) in the late summer and the resumption of larval feeding in late spring: larvae begin feeding again in early may.[9] In order to enter diapause, L. dispar uses temperature and photoperiodic indicators to determine when to start the overwinter process: entering diapause at low temperatures (<15°C) [10] As well as temperature, environmental and endogenous factors also determine when larvae terminate diapause: generally when ambient temperature is high (>25°C).[10]

Lycaena dispar females are capable of producing on average 32 chorionated eggs per egg load with an average of 714 eggs being laid in their lifetime.[11] Ovipositing females are specific about the quality of host plant they chose to lay their larvae on with plants preferably lacking flowering or fruiting stems and having inflorescences.[3] Plants that receive greater sunlight allow for larvae to grow faster and develop within a shorter period. Females, for this reason prefer warmer microclimates where host plant conditions are optimal.[10] Notably herbivore leaf damage and fungal infections of host plants, are not significant in reducing egg densities, laid by females.[10] In late June, the L. dispar larvae leave their host, food plant, migrating to vegetation no further than 25cm away from their original host and roughly 10cm above ground.[11] Once there larvae begin to change color, from bright green to pale yellow-brown, allowing them to blend in better with their surroundings during pupation, which lasts between 10 and 14 days.[11][10]

Lycaena dispar is subject to predation from invertebrate species as well as parasitoids (Phryxe vulgaris).[9] During pre-diapause invertebrate predation is responsible for a large proportion of mortality.[9] Parasitoids are commonly found in post-diapause larvae, and results in the death of late, instar larvae.[9] Vertebrate predators often include reed-nesting birds amphibians and small mammals.[9]

Illustration from John Curtis's British Entomology Volume 5

This species was formerly classified as a priority for protection and re-introduction in the UK under its national Biodiversity Action Plan. The species was driven to extinction in Britain by drainage and consequently great reduction of fen habitat. In the rest of the Western Europe, the draining of wetlands and building and agricultural activity on shallow riverbanks has caused a strong decline. In eastern Europe, undeveloped riverbanks and deltas are a habitat for the species, though even there it is somewhat threatened due increasing human influence on these areas.

There have been several reintroduction attempts to sites in both Britain and Ireland, but these have all ultimately failed. This is largely due to L. dispar stock being raised in captivity for long periods of time, before being released into the wild, resulting in adults that are maladapted to their natural environment, and ultimately do not survive.[9] Research is now being conducted to see whether a further attempt is worthwhile in more extensive habitats available in the Great Fen project and the Norfolk Broads.

Today, L. dispar is a near threatened species in some regions, leading to a growing concern over its conservation.[10] It is listed in the Bern Convention on the Conservation of European Wildlife and Natural Habitats, and is protected via Annexes II and IV of the European Community Habitats Directive.[2] In order to boost population numbers, mass rearing would be beneficial, therefore further research is needed to improve survivorship of mass-reared, L. dispar individuals.[10] Conservation efforts need to address the species' high sensitivity to climate and land usage, such as reclamation of wetlands for agricultural purposes and intensive management of grasslands through mowing of vegetation, having a negative influences on population numbers of L. dispar.[2]

• Images of male and female specimens of the extinct British (nominate) race Lycaena dispa dispar