The larvae of the Old World genera Leucinodes Guenée, 1854 and Sceliodes Guenée, 1854 are internal feeders in the fruits of Solanaceae, causing economic damage to cultivated plants like Solanum melongena and Solanum aethiopicum. In sub-Saharan Africa five nominal species of Leucinodes and one of Sceliodes occur. One of these species, the eggplant fruit and shoot borer Leucinodes orbonalis Guenée, 1854, is regarded as regularly intercepted from Africa and Asia in Europe, North and South America and is therefore a quarantine pest on these continents. We investigate the taxonomy of African Leucinodes and Sceliodes based on morphological characters in wing pattern, genitalia and larvae, as well as mitochondrial DNA, providing these data for identification of all life stages. The results suggest that both genera are congeneric, with Sceliodes syn. n. established as junior subjective synonym of Leucinodes. Leucinodes orbonalis is described from Asia and none of the samples investigated from Africa belong to this species. Instead, sub-Saharan Africa harbours a complex of eight endemic Leucinodes species. Among the former nominal species of Leucinodes (and Sceliodes) from Africa, only Leucinodes laisalis (Walker, 1859), comb. n. (Sceliodes) is confirmed, with Leucinodes translucidalis Gaede, 1917, syn. n. as a junior subjective synonym. The other African Leucinodes species were unknown to science and are described as new: Leucinodes africensis sp. n., Leucinodes ethiopica sp. n., Leucinodes kenyensis sp. n., Leucinodes malawiensis sp. n., Leucinodes pseudorbonalis sp. n., Leucinodes rimavallis sp. n. and Leucinodes ugandensis sp. n. An identification key based on male genitalia is provided for the African Leucinodes species. Most imports of Leucinodes specimens from Africa into Europe refer to Leucinodes africensis, which has been frequently imported with fruits during the last 50 years. In contrast, Leucinodes laisalis has been much less frequently recorded, and Leucinodes pseudorbonalis as well as Leucinodes rimavallis only very recently in fruit imports from Uganda. Accordingly, interceptions of Leucinodes from Africa into other continents will need to be re-investigated for their species identity and will likely require, at least in parts, revisions of the quarantine regulations. The following African taxa are excluded from Leucinodes: Hyperanalyta Strand, 1918, syn. rev. as revised synonym of Analyta Lederer, 1863; Analyta apicalis (Hampson, 1896), comb. n. (Leucinodes); Lygropia aureomarginalis (Gaede, 1916), comb. n. (Leucinodes); Syllepte hemichionalis Mabille, 1900, comb. rev., Syllepte hemichionalis idalis Viette, 1958, comb. rev. and Syllepte vagans (Tutt, 1890), comb. n. (Aphytoceros). Deanolis iriocapna (Meyrick, 1938), comb. n. from Indonesia is originally described and misplaced in Sceliodes, and Leucinodes cordalis (Doubleday, 1843), comb. n. (Margaritia) from New Zealand, Leucinodes raondry (Viette, 1981), comb. n. (Daraba) from Madagascar as well as Leucinodes grisealis (Kenrick, 1912), comb. n. (Scelio...
Emitting ultrasound upon hearing an attacking bat is an effective defence strategy used by several moth taxa. Here we reveal how Yponomeuta moths acquire sophisticated acoustic protection despite being deaf themselves and hence unable to respond to bat attacks. Instead, flying Yponomeuta produce bursts of ultrasonic clicks perpetually; a striated patch in their hind wing clicks as the beating wing rotates and bends. This wing structure is strikingly similar to the thorax tymbals with which arctiine moths produce their anti-bat sounds. And indeed, Yponomeuta sounds closely mimic such arctiine signals, revealing convergence in form and function. Because both moth taxa contain noxious compounds, we conclude they are mutual Müllerian acoustic mimics. Yponomeuta’s perpetual clicking would however also attract bat predators. In response, their click amplitude is reduced and affords acoustic protection just as far as required, matching the distance over which bat biosonar would pick up Yponomeuta echoes anyway – advanced acoustic defences for a deaf moth.
We provide a comprehensive overview of those Lepidopteran invasions to Europe that result from increasing globalisation and also review expansion of species within Europe. A total of 97 non-native Lepidoptera species (about 1% of the known fauna), in 20 families and 11 superfamilies have established so far in
JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact support@jstor.org.. British Ecological Society is collaborating with JSTOR to digitize, preserve and extend access to Journal of Animal Ecology. Summary 1. Two leaf-mining moths in the genus Phyllonorycter colonized Great Britain in the mid-1980s, both feeding on introduced garden and amenity plants: P. leucographella on Pyracantha spp., and P. platani on Platanus spp. 2. Systematic surveys of the distribution and spread of the two species were carried out spanning a period of 5 and 3 years. The effect of humans in dispersing the two moths was also studied. 3. The relationship between the square root of the range and time was in both cases remarkably linear, suggesting that the spread of the moths can be viewed as a simple travelling wave. The velocity of this wave was 10-3 km year-' for P. leucographella and 8-6 km year-' for P. platani. 4. There were slight deviations from the predicted pattern of spread as a series of concentric circles. For P. leucographella these are partially explained by variations in urbanization, which is correlated with the density of host plants. 5. Several foci of colonization outside the main range were detected, due to human activities. There was also evidence of artificial spread in the vicinity of the main advance, but this was not sufficient to obscure the simple pattern detected.
We studied the spread of a small leaf-mining moth [Phyllonorycter leucographella (Zeller), Gracillariidae] after its accidental introduction into the British Isles. At large geographical scales, previous work had shown the spread to be well described by a travelling weve of constant velocity. Here, we report the pattern of spread at scales of 1 km. By locating all bushes of the insect's foodplant (Pyracantha spp.) within 1-km quadrats, the precise pattern of colonisation at finer spatial scales could be established. Where the 1-km site was colonised by moths from the main advancing front, no spatial pattern in the order that bushes were infested was found. If the source of colonisation was a single or small group of infested plants within the site, there was some evidence that nearby plants were colonised first. We found no evidence of population turnover after colonisation. We interpret the results in terms of a two-stage model of invasion that produces different patterns at small and large geographical scales.
The species of Acentropinae recorded from Africa are listed and described with illustrations of the adults and genitalia.Ten new synonymies are established. The following species are described new to science: Parapoynx zambiensis,Argyrophorodes angolensis, A. suttoni, Elophila acornutus, E. ealensis, E. minima, Nymphicula hexaxantha, Eoophylabelladotae, E. cameroonensis, E. carcassoni, E. citrialis, E. dentisigna, E. euprepialis, E. grandifuscalis, E. interopalis,E.kingstoni, E. piscatorum, E. platyxantha, E. principensis, E. ruwenzoriensis, E. stepheni, E. tanzanica. E. nyasalis kenyalis is described as a new subspecies.
Abstract. Water ferns (Azolla spp., Azollaceae) are reported for the first time as host plants for the larvae of the small China-mark moth Cataclysta lemnata (Linnaeus) (Lepidoptera: Crambidae: Acentropinae) in rice fields and waterways of northern Iran. Cataclysta lemnata is a semi-aquatic species that has been recorded to feed on Lemnaceae and a few other aquatic plants. However, it has not been reported before on Azolla spp. Larvae use water fern as food source and shelter and, at high population density in the laboratory, they completely wiped water fern from the water surface. Feeding was confirmed after rearing more than eight continual generations of C. lemnata on water fern in the laboratory. Adults obtained this way are darker and have darker fuscous markings in both sexes compared with specimens previously reported and the pattern remains unchanged after several generations.
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