Small tortoiseshell

From Wikipedia, the free encyclopedia
  (Redirected from Aglais urticae)
Jump to: navigation, search
Small tortoiseshell
Aglais urticae LC0310.jpg
Kleine Fuchs, Aglais urticae 6.JPG
Scientific classification
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Lepidoptera
Family: Nymphalidae
Genus: Aglais
Species: A. urticae
Binomial name
Aglais urticae
(Linnaeus, 1758)
Aglais urticae appearance.png
Synonyms

Nymphalis urticae
Vanessa urticae

The small tortoiseshell (Aglais urticae L.) is a colourful Eurasian butterfly in the family Nymphalidae.

Description[edit]

It is a medium-sized butterfly that is mainly reddish-orange in colour, with black and yellow markings on the forewings as well as a ring of blue spots around the edge of the wings. It has a wingspan ranging from 4.5-6.2 cm.[1]

The small tortoiseshell is the National Butterfly of Denmark

Range[edit]

It is found throughout temperate Europe, Asia Minor, Central Asia, Siberia, China, Mongolia, Korea and Japan, wherever Common Nettle which their larvae feed on is found. There are a few records from New York City which, however, are believed to be of introduced insects.

Subspecies[edit]

  • A. u. urticae (Linnaeus, 1758) Europe, W.Siberia - Altai
  • A. u. polaris (Staudinger, 1871) North Europe, Siberia, Russian Far East
  • A. u. turcica (Staudinger, 1871) South Europe, Caucasus, Transcaucasia, Kopet Dagh, Middle Asia
  • A. u. baicalensis (Kleinschmidt, 1929) Sayan, Transbaikalia
  • A. u. eximia (Sheljuzhko, 1919) Amur, Ussuri
  • A. u. stoetzneri (Kleinschmidt, 1929) Szechuan
  • A. u. kansuensis (Kleinschmidt, 1940) North-West China
  • A. u. chinensis Leech, 1893 China Japan Korea
  • A. u. connexa (Butler, [1882]) South Ussuri, South Sakhalin, Kuriles, Japan

The Corsican small tortoiseshell (Aglais ichnusa Hübner, 1819) looks very similar; whether it is a subspecies or a distinct species is yet to be determined. Nymphalis xanthomelas and Nymphalis l-album are also similar in appearance.

Decline in population[edit]

Once among the most common butterflies in Europe and temperate Asia, this butterfly is in very rapid decline, at least in Western Europe. This decline cannot be explained by the decline of its host plant, because the nettle is widespread and even enjoys the general eutrophication of the environment. The chrysalis is sometimes eaten by wasps, but these are also in strong regression. The effect of other phenomena are still poorly understood (environmental degradation, air pollution, contamination by pesticides). Scientific evidence shows that the summer drought is a cause of declining populations, because larvae grow normally on drenched leaves (but hatchlings were even rarer the wet summers of 2007 and 2008). However, before the year 2000, according to data from an English Butterfly monitoring program, there was a good correlation between reproductive success, the abundance of populations of this species and the host plant moisture stress. From 1976 to 1995, the butterfly had more success in summers that were cool and wet at the beginning of summer than when it is was hot and dry. This butterfly may then be sensitive to global warming.

Droughts[edit]

The small tortoiseshell butterfly is severely affected by droughts. During periods of drought, the butterfly experiences a vastly reduced reproductive rate. The drought directly affects the Urtica leaves; the higher the nitrogen and water level in the leaves, the more rapid the growth of the larvae. During a drought, both of these levels drop significantly, leaving the tortoiseshell larvae nothing to feed on. The timing of the rainfall is also a crucial factor. If there is not adequate rainfall in the early summer, then the plants will not be able to fully develop, leaving the larvae without a suitable source of nutrition. These butterflies actively produce smaller broods under these conditions.[2]

Life cycle[edit]

As with several Nymphalid butterflies, the caterpillars feed on stinging nettles (Urtica dioica) and small nettle, Urtica urens. Adults feed on nectar. The species has one of the longest seasons of any Eurasian butterfly, extending from early spring to late autumn. Adults overwinter in hibernation, emerging on the first warm sunny days of the year to mate and breed. In southern parts of the range there may be two broods each year, but northern insects are inhibited by long length of summer days from breeding a second time.[3]

Hatching[edit]

Tortoiseshell butterflies usually began to emerge from their pupa from mid June into August. They began hibernation sometime in October and immediately show territorial behaviour after hibernation.[4] The Tortoiseshell Butterflies that are found in the north usually have one brood a season, whereas further south these butterflies can have two broods. The ability to go through three generations of butterflies in a year is due to the Tortoiseshell Butterflies' decreased thermal requirement. The larvae of this butterfly are social.[5] These larvae can be found on Urtica diocia, which have a high nitrogen content and lots of water in the leaves.[6]

Hibernation[edit]

The small tortoiseshell butterfly tends to enter hibernation by mid to late September.[4] Typically this butterfly will try to hibernate in dark sheltered locations. Because of this hibernation, they need to accumulate a lot of fat to survive the winter. The tortoiseshell needs at least 20% of its body weight in lipids in order to survive, making them much slower.[7] Towards the end of their foraging for hibernation, they are much more susceptible to attacks by birds because of their low muscle to body mass ratio. During the first few weeks of hibernation, Tortoiseshell Butterflies are very susceptible to predator attacks. Up to 50% of the population hibernating in any given area can be eaten. The butterflies that hibernate in areas containing more light, and that are accessible to rodents who can climb, are the most susceptible to this type of predation.[8] During hibernation Tortoiseshell Butterflies are able to supercool in order to keep from freezing. In sheltered areas, these butterflies can stand up to -21 degrees Celsius without freezing. However, they experience rapid weight loss during unusually mild winters.[9]

Developmental stages[edit]

Behaviour[edit]

Predator defence[edit]

The wings of Tortoiseshell Butterflies help conceal them extremely well from predators. When closed, their wings are designed to look like leaves to hide from predators. On the ground, it may take birds up to 30 minutes to see them. In addition to this, when discovered, tortoiseshell butterflies will flick their wings open to reveal bright colours. While they don’t have eyespots like many other butterflies, these bright contrasting colors can often scare a predator, giving the tortoiseshell butterfly ample time to escape.[10] Not only does this colouration tend to frighten birds, it can also act as a warning. The bright red colouration serves as a cautionary sign to the predator about the poor taste of the butterfly. Tortoiseshell butterflies tend to be unpalatable to birds. If a bird sees this bright red colouring, then they will be less likely to eat the butterfly.[11]

The Tortoiseshell Butterfly is particularly fast. When discovered and attacked by a predator, the Tortoiseshell Butterfly will fly away in a straight line in order to outrun the predator.[12]

Territorial defence[edit]

Most butterflies fail to display any territorial behaviour, probably due to selective environmental pressures. The female Tortoiseshell Butterflies generally are found in concentrated areas, so it is advantageous for males to stay in that particular area to increase their mating opportunities. Male butterflies usually bask and feed until mid-day and then display territorial behaviour until roosting. Males typically defend a certain territory for up to 90 minutes, unless they attempt to follow a female or are ousted by another male. The next day they find a new territory to defend. These territories tend to be in direct sunlight in areas that females choose to lay their eggs. More often then not, two or more males may end up sharing territory if the cost of defending the territory is greater than the benefit gained from monopolizing the females.[4]

Male-male interaction[edit]

In order for one male butterfly to gain dominance over the other, he must reach a position slightly above the other butterfly. The non-dominant male will then attempt a series of dives and climbs to escape the pursuer. After a certain distance travelled from the nest, one butterfly will return to the territory while the other flies along in search of another suitable location.[4]

Feeding[edit]

For most butterflies, including the small tortoiseshell butterfly, nectar is one of the main sources of nutrients. In order to obtain the nectar, the butterfly must be able to recognize distinct floral aromas and colours. The small tortoiseshell butterfly is able to differentiate between various flowers through visual signals.[13] Tortoiseshell Butterflies in particular tend to prefer colours at both ends of the visible light spectrum for humans, 400 nm and 600 nm.[14] These correspond to the colours violet and red respectively. This ability comes from their compound eye. The flowers depend on the butterflies for pollination, so it is a mutually beneficial relationship.[13]

Migratory patterns[edit]

During migration, Tortoiseshell Butterflies position themselves in accordance with air currents; they only start migration at certain wind speeds. They are able to do this because of an extra sensory organ in their antennae. These butterflies have a developed Johnston’s organ in their second antennae responsible for determining air currents in a number of other insects.[15] Because their host plants, Urtica diocia, grows in widely distributed areas, tortoiseshell butterflies tend to move around a fair amount as compared to other butterflies. These areas tend to be short thickets and shrubs.[12]

References[edit]

  1. ^ "Small tortoiseshell". Retrieved 30 October 2013. 
  2. ^ Pollard, E., and J. N. Greatorex‐Davies (1997) "Drought reduces breeding success of the butterfly Aglais urticae." Ecological Entomology 22 (3) : 315–318.
  3. ^ E. Pollard and T. J. Yates (1993) Monitoring butterflies for ecology and conservation. Chapman & Hall. ISBN 0 412 63460 0
  4. ^ a b c d R. R. Baker "Territorial behaviour of the Nymphalid butterflies, Aglais urticae (L.) and Inachis io (L.)" Journal of Animal Ecology , 41 (2) 1972, pp. 453–469
  5. ^ Bryant, S., Thomas, C. and Bale, J. (1997), "Nettle-feeding nymphalid butterflies: temperature, development and distribution." Ecological Entomology, 22: 390–398. doi: 10.1046/j.1365-2311 Pollard, E., Greatorex-Davies, J.N. Thomas.1997.00082.x
  6. ^ Pollard, E., Greatorex-Davies, J.N. and Thomas, J.A. (1997), Drought reduces breeding success of the butterfly Aglais urticae. Ecological Entomology, 22: 315–318.
  7. ^ Almbro M, Kullberg C. (2008). Impaired escape flight ability in butterflies due to low flight muscle ratio prior to hibernation. Journal of Experimental Biology 211: 24-48.
  8. ^ Wiklund, Christer, et al. (2008) "Rodent predation on hibernating peacock and small tortoiseshell butterflies." Behavioral Ecology and Sociobiology 62 (3): 379-389
  9. ^ Pullin, A. S., and J. S. Bale. "Effects of low temperature on diapausing Aglais urticae and Inachis io (Lepidoptera: Nymphalidae): Cold hardiness and overwintering survival." Journal of Insect Physiology 35 (4) (1989): 277-281
  10. ^ Vallin, Adrian, Sven Jakobsson, Johan Lind, and Christer Wiklund, (2006) "Crypsis versus Intimidation—anti-predation Defence in Three Closely Related Butterflies." Behavioral Ecology and Sociobiology 59 (3): 455-59
  11. ^ Hagen, S. B., Leinaas, H. P. and Lampe, H. M. (2003), Responses of great tits Parus major to small tortoiseshells Aglais urticae in feeding trials; evidence of aposematism. Ecological Entomology, 28: 503–509
  12. ^ a b Shreeve, T. G. (1981) "Flight Patterns of Butterfly Species in Woodlands." Oecologia 51 (2): 289-93 jstor:4216536
  13. ^ a b Andersson, Susanna. (2003) "Foraging responses in the butterflies Inachis io, Aglais urticae (Nymphalidae), and Gonepteryx rhamni (Pieridae) to floral scents." Chemoecology 13 (1): 1-11
  14. ^ Scherer, Christian, and Gertrud Kolb. (1987) "The influence of color stimuli on visually controlled behavior in Aglais urticae L. and Pararge aegeria L. (Lepidoptera)." Journal of Comparative Physiology A 161 (6): 891-98
  15. ^ Gewecke, Michael, and Monika Niehaus, (1981) "Flight and flight control by the antennae in the small tortoiseshell (Aglais urticae L., Lepidoptera)." Journal of Comparative Physiology A 145 (2) (1981): 249-56