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Arctia plantaginis

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destroys the appearance of any outline the object may have. Though the idea of disruptive coloration, which is clearly a camouflage technique, seems counterintuitive in aposematism, it has been demonstrated that the same coloration pattern on a moth can act as either a warning signal or a camouflage depending on the backdrop. Wood tiger moths exhibit a behavior where they essentially 'feign death' by dropping suddenly on to the ground in the presence of a predator and taking on a specific, rigid posture with folded legs. Once on the ground, the moths are much more difficult to detect. This suggests that the hindwing pattern of the wood tiger moth can switch instantly from conspicuous to camouflage, which has obvious adaptive advantages.
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immune variation. A 2013 study demonstrated that male yellow and white larvae saw different survival rates when reared in aggregations; yellow male survived to pupate better in aggregations than white males did, which may reflect different immune investments. In aggregations, white males saw better ability to encapsulate pathogens, while yellow males had higher hemolymph (equivalent to insect 'blood') lytic activity (virus attacking). Thus the two types of wood tiger moth may be maintained in populations because they have different immune investments. This is advantageous in thriving in heterogeneous environments with differential risk factors for immune challenges.
1089: 1065: 582:, meaning their colorations serve to deter predators from attacking. In populations of aposematic species, it is common to have a single coloration phenotype dominate, because predators better learn to avoid the more common phenotype and rare phenotypes suffer higher predation. Rare phenotypes are often selected against because predators are less familiar with their aposematic signal. Thus, other selective pressures exist to perpetuate weaker aposematic signals in exchange for other adaptive benefits. 606: 1031:
across all treatment groups. In groups with higher frequencies of yellow morphs, overall flying activity for both morphs was considerably lower. The data suggest that white male morphs invest less in producing costly warning signals and thus have more energy to invest in flight for both avoiding predation and finding mates. Yellow males, which in previous studies have been shown to be less sexually favored by females than whites, tend to be most active at peak female-calling periods.
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that due to the various climatic conditions of populations of wood tiger moth, there are different costs and benefits to produces more melanin, which serves to maintain the global diversity of warning signals that we see throughout the species. In both yellow and white male phenotypes, individuals with more melanin had a heightened ability to trap heat but an increased predation rate due to its weaker and less effective signal.
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streaks at the margin of the cell and before the anal margin. In the female, the hindwing is red above with the base strongly black. Numerous aberrations have been found and named, which often occur predominantly, and only exceptionally among typical specimens. Major aberrations are listed by Seitz, 1913.
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vary between color morphs and are under frequency dependent selection. In outdoor cage experiments of populations with various frequencies of yellow and white male morphs, researches found that white morphs were significantly more active and had longer periods of sustained activity than yellow morphs
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confers thermoregulatory advantages by increasing a male moth's ability to absorb radiation. This increased melanization comes at a cost, however, as it is costly to produce, and thus male moths with more melanization suffer increased predation as their warning signals are weaker. Thus it is thought
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to secrete two different chemical fluids as defense mechanisms in response to two different types of predators. Along with its colorful, conspicuous hindwing color patterns, these moths secrete defense fluids from their abdomen and thoracic glands. The abdominal fluids deterred ants and not birds,
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Though the aposematic signal of a wood tiger moth is highly conspicuous against vegetative scenery, its patterning is less easy to detect when it drops to the ground. Disruptive coloration is when a pattern creates an illusion that makes discerning the edges of an object difficult. It essentially
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is 32–38 mm. Normally, it has a black forewing in both sexes, with moderately broad, ivory yellow bands. In the male, the hindwing is yellow or white with an irregular marginal band, which is often interrupted, and two or three submarginal spots. The basal portion of the hindwing bears black
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There are populations throughout the globe, but most common in northern latitudes of North America and Eurasia. The North American populations range from Alaska to Manitoba, and south through the Rocky Mountain region to southern New Mexico, with isolated populations occurring in Arizona and the
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A possible explanation for the persistence of white morphs despite their higher predation rates is selection heterogeneity; in other words, due to the wide geographic distribution of the wood tiger moth, different populations experience vastly different selective pressures. One consideration is
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species; it is an adaptive mechanism in which prey produce conspicuous warning signals. In the wood tiger moth, conspicuous coloration patterns communicate a poisonous, toxic, or otherwise unpalatable or unprofitable effect to predators. Typically, aposematic species experience strong selection
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Though it may benefit caterpillars to intake more plant compounds that can help produce defensive chemicals (depending on the plant), this process can be costly and energy intensive for caterpillars. As polyphagous larvae, this process of detoxification and toxin sequestration can be especially
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intake from their diet significantly increases their ability to encapsulate pathogens. Encapsulation is an important, innate immune response that occurs in invertebrates to protect against a variety of parasites and pathogens. The antioxidants serve to protect cells from damage incurred by the
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Selection by predation can impact host immune defense, as demonstrated by an experiment measuring the virulence of a pathogen Serrate marcescens in Arctia plantaginis larvae. Larvae with smaller warning signals had higher survival rates than those with larger warning signals, suggesting that
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Yellow morphs are able to avoid predation more readily than white morphs; however, a laboratory study showed that yellow males had lower mating success compared to white males. This trade-off between reproductive success and predator avoidance could explain why two polymorphisms exist.
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Wood tiger moths have a limited amount of resources to allocate to different life history traits and adaptive strategies; thermoregulation is an important part of their physiology, especially in the cooler climates of North America and Eurasia. As latitude increases, populations of
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populations. Though this extreme gene flow would be thought to lead to fixation of a single morphological phenotype, the differential selective pressures experienced by various populations of the species likely leads to the maintenance of its widespread polymorphism.
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developing a warning signal comes at the expense of immune function. Basically, there is a trade off between immune function and predatory defense. Thus predation is an import factor when considering the evolution of pathogen virulence and host immunity.
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Males are, on average, smaller than females but experience a relatively similar rate of development. Generally a longer development time correlates with a larger pupal mass, and in females, pupal mass correlates with total lifetime eggs produced.
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in adult wood tiger moths. The shapes and patterning of adult warning signals are entirely determined during resource allocation of the larval stage. Once an adult metamorphoses, their warning signal phenotype can no longer change.
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creation of free radicals resulting from the encapsulation reaction. In environments where the pathogen load is likely to be high, the food ingested by an individual moth is important in building its defense mechanisms.
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Lindstedt, Carita; Talsma, Joanneke Hendrika Reudler; Ihalainen, Eira; Lindström, Leena; Mappes, Johanna (2010-01-01). "Diet Quality Affects Warning Coloration Indirectly: Excretion Costs in a Generalist Herbivore".
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and COl results showed little to no differentiation between populations during the two sampling years of 2009 and 2010. This overall high genetic diversity and low differentiation between populations suggests much
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costly if their physiology has to support detoxification processes for different types of plants and compounds. Investing more in detoxification as larvae results in lower reproductive output as adults.
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favoring monomorphic populations. As a specific warning signal phenotype becomes more common in an environment, more and more predators learn to avoid individuals bearing such signals. In
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while thoracic fluids deterred birds but not ants, suggesting that a single species is capable of producing target-specific chemical defense fluids in response to predation threats.
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Johnson, Kelly S.; Felton, Gary W. (2001-12-01). "Plant Phenolics as Dietary Antioxidants for Herbivorous Insects: A Test with Genetically Modified Tobacco".
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prefer slightly moist areas, like meadows with nearby streams. Adults like to spend time close to lupine stands, which are meadows of plants from the genus
1088: 1333:"Multiple Continental Radiations and Correlates of Diversification in Lupinus (Leguminosae): Testing for Key Innovation with Incomplete Taxon Sampling" 2391: 2172: 997:
Females tend to attract males during the day, and they group together at dusk. It has been observed that once attracted to a group of females, male
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are capital breeders, which means that they do not feed as adults, and thus the larval diet is incredibly important component in adult fitness.
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Galarza, Juan A.; Viinikainen, Sari M.; Ashrafi, Roghaieh; Mappes, Johanna (2011-04-01). "First microsatellite panel for the Wood Tiger Moth (
1197: 2555: 813:, a distinct hindwing pattern of bands and splotches of white or yellow on black warns predators of its chemical defenses. Populations of 1636:
Rojas, Bibiana; Burdfield-Steel, Emily; Pakkanen, Hannu; Suisto, Kaisa; Maczka, Michael; Schulz, Stefan; Mappes, Johanna (2017-09-27).
2443: 2352: 2047:"To quiver or to shiver: increased melanization benefits thermoregulation, but reduces warning signal efficacy in the wood tiger moth" 1307: 1980: 2535: 2110: 2550: 2435: 660:
are distributed throughout both montane and lowland habitats, with hugely diverse regions found in North and South America.
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throughout the Alpine regions of Italy, Austria and Switzerland indicated a single whole population. Pairwise Fst values,
619: 2313: 2370: 2115: 2229: 2383: 2284: 2125: 2545: 73: 2540: 2140: 1115:"Putting Parasemia in its phylogenetic place: a molecular analysis of the subtribe Arctiina (Lepidoptera)" 2448: 2318: 981: 605: 188: 1765:"Environment-mediated morph-linked immune and life-history responses in the aposematic wood tiger moth" 1541: 2203: 1709: 1430: 1076: 2295: 2216: 1814:"Warning coloration can be disruptive: aposematic marginal wing patterning in the wood tiger moth" 1331:
Drummond, Christopher S.; Eastwood, Ruth J.; Miotto, Silvia T. S.; Hughes, Colin E. (2012-05-01).
1235: 1615: 1517: 1462: 1277: 218: 68: 2422: 2530: 2502: 2468: 2237: 2084: 2066: 2027: 1986: 1976: 1953: 1904: 1851: 1833: 1794: 1786: 1745: 1727: 1675: 1657: 1607: 1599: 1509: 1501: 1454: 1446: 1370: 1352: 1313: 1303: 1269: 1175: 715: 524: 2458: 2507: 2242: 2120: 2074: 2058: 2017: 1943: 1935: 1894: 1886: 1841: 1825: 1776: 1735: 1717: 1665: 1649: 1591: 1493: 1438: 1360: 1344: 1261: 1165: 1155: 1126: 599: 2489: 595: 1713: 1638:"How to fight multiple enemies: target-specific chemical defences in an aposematic moth" 1434: 55: 2378: 2365: 2079: 2046: 1948: 1923: 1899: 1871:"De novo transcriptome assembly and its annotation for the aposematic wood tiger moth ( 1870: 1846: 1813: 1740: 1697: 1670: 1637: 1365: 1332: 1227: 1170: 1147: 578:
males occur predominantly in two distinct color phenotypes: yellow and white. They are
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Hegna, Robert H.; Nokelainen, Ossi; Hegna, Jonathan R.; Mappes, Johanna (2013-03-22).
1419:"Costs and benefits of plant allelochemicals in herbivore diet in a multi enemy world" 737: 41: 2524: 1924:"Trade-off between Warning Signal Efficacy and Mating Success in the Wood Tiger Moth" 1521: 1497: 532: 205: 17: 1619: 1417:
Reudler, J. H.; Lindstedt, C.; Pakkanen, H.; Lehtinen, I.; Mappes, J. (2015-12-01).
1281: 2163: 1696:; Lindstedt, Carita; Hiltunen, Teppo; Laakso, Jouni; Mappes, Johanna (2009-08-25). 1693: 1466: 1045: 763: 1722: 1698:"Predation on Multiple Trophic Levels Shapes the Evolution of Pathogen Virulence" 2481: 2404: 2278: 2211: 2198: 2185: 1890: 805: 700: 591: 586:
has become a common model for studying the counteracting selective pressures of
125: 2269: 2006:"Frequency-dependent flight activity in the colour polymorphic wood tiger moth" 2022: 2005: 1595: 1442: 1265: 1160: 579: 135: 2357: 2070: 2031: 1837: 1790: 1731: 1661: 1603: 1505: 1450: 1356: 1317: 1273: 779:, to which the moth has both general and specialized defense mechanisms. The 2339: 1781: 1764: 1542:"Diet affects the immune defence and life-history traits of an Arctiid moth 1418: 1389: 1348: 683: 587: 155: 105: 85: 2088: 2062: 1957: 1939: 1908: 1855: 1798: 1749: 1679: 1653: 1611: 1513: 1458: 1374: 1179: 1146:
Schmidt, B. Christian; Lafontaine, J. Donald; Troubridge, James T. (2018).
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diversity and warning signals at the University of Jyväskylä in Finland
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Rojas, Bibiana; Luis-MartĂŤnez, Armando; Mappes, Johanna (2015-08-01).
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Rönkä, Katja; Mappes, Johanna; Kaila, Lauri; Wahlberg, Niklas (2016).
2409: 1390:"Population genetic structure of aposematic alpine wood tiger moths ( 1005:, most likely due to their similar sex pheromones. Similarly, female 548: 165: 115: 95: 2134: 2344: 1763:
Nokelainen, Ossi; Lindstedt, Carita; Mappes, Johanna (2013-05-01).
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Honma, Atsushi; Mappes, Johanna; Valkonen, Janne K. (2015-11-01).
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Proceedings of the Royal Society of London B: Biological Sciences
516: 2138: 539:, Korea and Japan. One subspecies is endemic to North America. 1569:
Comprehensive Insect Physiology, Biochemistry and Pharmacology
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Galarza, Juan A.; Dhaygude, Kishor; Mappes, Johanna (2017).
1302:. Opler, Paul A. Berkeley: University of California Press. 1928:
Proceedings of the Royal Society B: Biological Sciences
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As a polyphagous species, the life history traits of
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will readily mate with females of a related species
2253: 2147: 639:Sierra Nevada mountains of California and Nevada. 775:Birds and ants are the most common predators of 542:This species was formerly a member of the genus 1048:(conversion of resources into melanin). This 8: 1571:. Oxford: Pergamon Press. pp. 453–485. 834:Target specific chemical defense mechanisms 625:This moth is extraordinarily variable. The 552:along with the other species of the genera 2135: 54: 40: 31: 2078: 2021: 1947: 1898: 1845: 1780: 1739: 1721: 1669: 1364: 1169: 1159: 1130: 838:A 2017 study highlighted the ability of 604: 1105: 1060: 535:, northern Iran, Kazakhstan, Mongolia, 523:. Several subspecies are found in the 1631: 1629: 1535: 1533: 1531: 1478: 1476: 324:Parasemia plantaginis passanauriensis 7: 2384:ec6fa786-fb2a-4582-bab8-956e4f57765b 1922:Nokelainen, O.; et al. (2011). 1293: 1291: 1198:"Many Forms of the Wood Tiger Moth ( 1191: 1189: 980:Warning signals show no phenotypic 758:depend on its habitat and diet. In 673:A two-year study of populations of 308:Parasemia plantaginis kamtschadalus 1026:Flight behavior in populations of 795:Protective coloration and behavior 609:Figures 3–7, wood tiger moth forms 25: 618:For a key to the terms used, see 316:Parasemia plantaginis paramushira 1498:10.1111/j.1558-5646.2009.00796.x 1087: 1075: 1063: 959:Arctia plantaginis sachalinensis 719:Lupine, a common host plant for 484:Parasemia plantaginis stoetzneri 288:Parasemia plantaginis carpathica 72: 1254:Conservation Genetics Resources 1232:Die GroĂźschmetterlinge der Erde 1196:Nokelainen, Ossi (March 2013). 895:Arctia plantaginis hesselbarthi 686:and high population density in 464:Parasemia plantaginis macromera 344:Parasemia plantaginis jezoensis 280:Parasemia plantaginis insularum 272:Parasemia plantaginis uralensis 264:Nemeophila plantaginis floccosa 1567:Gotz, P.; Boman, H.G. (1985). 1300:Moths of Western North America 927:Arctia plantaginis melanissima 911:Arctia plantaginis kunashirica 858:Arctia plantaginis plantaginis 804:Aposematism is common in many 364:Parasemia plantaginis japonica 1: 1550:Evolutionary Ecology Research 935:Arctia plantaginis melanomera 903:Arctia plantaginis interrupta 871:Arctia plantaginis carbonelli 863:Arctia plantaginis araitensis 664:Home range and territoriality 476:Parasemia plantaginis altaica 332:Parasemia plantaginis hospita 1975:. New York: Academic Press. 1723:10.1371/journal.pone.0006761 943:Arctia plantaginis nycticans 919:Arctia plantaginis macromera 887:Arctia plantaginis caucasica 787:) is a well known predator. 669:Genetic population structure 620:Glossary of entomology terms 2556:Taxa named by Carl Linnaeus 1891:10.1016/j.gdata.2017.03.008 1584:Journal of Chemical Ecology 1009:are also attracted to male 967:Arctia plantaginis sifanica 367:Inoue & Kobayashi, 1956 2572: 2126:Research group working on 1388:Ashrafi, Roghaieh (2012). 976:Genetics of color patterns 951:Arctia plantaginis petrosa 879:Arctia plantaginis caspica 617: 403:Grote & Robinson, 1868 387:Grote & Robinson, 1868 1971:Jacobson, Martin (1972). 1769:Journal of Animal Ecology 1443:10.1007/s00442-015-3425-0 1298:Powell, Jerry A. (2009). 1266:10.1007/s12686-010-9321-3 1161:10.3897/zookeys.252.28500 224: 217: 194: 187: 69:Scientific classification 67: 62: 53: 48: 39: 34: 2536:Moths described in 1758 2023:10.1093/czoolo/61.4.765 1782:10.1111/1365-2656.12037 1596:10.1023/A:1013691802028 970:(Grum-Grshimailo, 1891) 2551:Moths of North America 2116:Lepidoptera of Belgium 2063:10.1098/rspb.2012.2812 1940:10.1098/rspb.2011.0880 1654:10.1098/rspb.2017.1424 1238:In English translation 742: 723: 610: 372:Nemeophila plantaginis 2296:Parasemia-plantaginis 2285:Parasemia plantaginis 2255:Parasemia plantaginis 2128:Parasemia plantaginis 2106:Wood tiger on UKMoths 1973:Insect sex pheromones 1873:Parasemia plantaginis 1818:Ecology and Evolution 1544:Parasemia plantaginis 1540:Ojala, Katja (2005). 1392:Parasemia plantaginis 1349:10.1093/sysbio/syr126 1250:Parasemia plantaginis 1200:Parasemia plantaginis 1119:Systematic Entomology 740: 718: 699:Wood tiger moths are 608: 492:Parasemia plantaginis 432:Eupsychoma geometrica 424:Nemeophila alascensis 18:Parasemia plantaginis 2379:Fauna Europaea (new) 392:Nemeophila caespitis 384:Nemeophila caespitis 352:Nemeophila macromera 296:Chelonia plantaginis 233:Phalaena plantaginis 1714:2009PLoSO...4.6761F 1694:Friman, Ville-Petri 1435:2015Oecol.179.1147R 785:Cyanistes caeruleus 546:, but was moved to 456:Nemeophila selwynii 448:Platarctia scudderi 408:Nemeophila cichorii 400:Nemeophila cichorii 180:A. plantaginis 2149:Arctia plantaginis 2057:(1755): 20122812. 1648:(1863): 20171424. 1337:Systematic Biology 1132:10.1111/syen.12194 1094:Habitat in Ireland 743: 724: 721:Arctia plantaginis 611: 508:Arctia plantaginis 440:Nemeophila geddesi 416:Platarctia modesta 198:Arctia plantaginis 2518: 2517: 2503:Open Tree of Life 2238:Open Tree of Life 2141:Taxon identifiers 1934:(1727): 257–265. 1830:10.1002/ece3.1736 1824:(21): 4863–4874. 1590:(12): 2579–2597. 1230:in Seitz, A. Ed. 971: 963: 955: 947: 946:(MĂ©nĂ©triès, 1859) 939: 931: 923: 915: 907: 899: 891: 890:(MĂ©nĂ©triès, 1832) 883: 875: 867: 525:Holarctic ecozone 504: 503: 496: 488: 487:O.Bang-Haas, 1927 480: 472: 460: 452: 444: 436: 428: 420: 412: 404: 396: 388: 380: 368: 360: 348: 340: 328: 320: 312: 304: 292: 284: 276: 275:Krulikowsky, 1904 268: 260: 256:Bombyx matronalis 252: 245: 237: 16:(Redirected from 2563: 2511: 2510: 2498: 2497: 2485: 2484: 2482:NBNSYS0000006142 2472: 2471: 2462: 2461: 2452: 2451: 2439: 2438: 2426: 2425: 2413: 2412: 2400: 2399: 2387: 2386: 2374: 2373: 2361: 2360: 2348: 2347: 2335: 2334: 2322: 2321: 2309: 2308: 2299: 2298: 2289: 2288: 2287: 2274: 2273: 2272: 2246: 2245: 2233: 2232: 2220: 2219: 2207: 2206: 2194: 2193: 2181: 2180: 2168: 2167: 2166: 2136: 2093: 2092: 2082: 2042: 2036: 2035: 2025: 2001: 1995: 1994: 1968: 1962: 1961: 1951: 1919: 1913: 1912: 1902: 1866: 1860: 1859: 1849: 1809: 1803: 1802: 1784: 1760: 1754: 1753: 1743: 1725: 1690: 1684: 1683: 1673: 1633: 1624: 1623: 1579: 1573: 1572: 1564: 1558: 1557: 1537: 1526: 1525: 1480: 1471: 1470: 1429:(4): 1147–1158. 1414: 1408: 1407: 1405: 1404: 1385: 1379: 1378: 1368: 1328: 1322: 1321: 1295: 1286: 1285: 1245: 1239: 1225: 1219: 1218: 1216: 1215: 1206: 1193: 1184: 1183: 1173: 1163: 1154:(252): 241–252. 1143: 1137: 1136: 1134: 1110: 1091: 1079: 1067: 1035:Thermoregulation 969: 961: 953: 945: 937: 929: 921: 913: 905: 897: 889: 881: 873: 865: 741:Wood tiger adult 634:Geographic range 600:thermoregulation 495:(Linnaeus, 1758) 494: 486: 478: 470: 459:H. Edwards, 1885 458: 450: 442: 434: 426: 418: 410: 402: 394: 386: 378: 366: 358: 346: 338: 326: 318: 310: 302: 290: 282: 274: 266: 258: 251: 243: 241:Phalaea alpicola 235: 200: 77: 76: 58: 44: 32: 21: 2571: 2570: 2566: 2565: 2564: 2562: 2561: 2560: 2546:Moths of Europe 2521: 2520: 2519: 2514: 2506: 2501: 2493: 2490:Observation.org 2488: 2480: 2475: 2467: 2465: 2457: 2455: 2447: 2442: 2434: 2429: 2421: 2416: 2408: 2403: 2395: 2390: 2382: 2377: 2369: 2364: 2356: 2351: 2343: 2338: 2330: 2325: 2317: 2312: 2304: 2302: 2294: 2292: 2283: 2282: 2277: 2268: 2267: 2262: 2249: 2241: 2236: 2228: 2223: 2215: 2210: 2202: 2197: 2189: 2184: 2176: 2171: 2162: 2161: 2156: 2143: 2102: 2097: 2096: 2044: 2043: 2039: 2010:Current Zoology 2003: 2002: 1998: 1983: 1970: 1969: 1965: 1921: 1920: 1916: 1868: 1867: 1863: 1811: 1810: 1806: 1762: 1761: 1757: 1692: 1691: 1687: 1642:Proc. R. Soc. B 1635: 1634: 1627: 1581: 1580: 1576: 1566: 1565: 1561: 1539: 1538: 1529: 1482: 1481: 1474: 1416: 1415: 1411: 1402: 1400: 1387: 1386: 1382: 1330: 1329: 1325: 1310: 1297: 1296: 1289: 1247: 1246: 1242: 1226: 1222: 1213: 1211: 1204: 1195: 1194: 1187: 1145: 1144: 1140: 1112: 1111: 1107: 1102: 1095: 1092: 1083: 1080: 1071: 1068: 1059: 1037: 1024: 1019: 991: 978: 962:Matsumura, 1930 898:de Freina, 1981 874:de Freina, 1993 866:Matsumura, 1929 854: 849: 836: 827: 802: 797: 773: 748: 729: 709: 697: 671: 666: 645: 636: 623: 616: 596:immune function 500: 499: 471:Matsumura, 1927 443:Neumoegen, 1884 411:Boisduval, 1869 395:Boisduval, 1869 379:Christoph, 1893 339:Schawerda, 1910 303:MĂ©nĂ©triès, 1857 228: 213: 202: 196: 183: 71: 28: 27:Species of moth 23: 22: 15: 12: 11: 5: 2569: 2567: 2559: 2558: 2553: 2548: 2543: 2538: 2533: 2523: 2522: 2516: 2515: 2513: 2512: 2499: 2486: 2473: 2463: 2453: 2440: 2427: 2414: 2401: 2388: 2375: 2366:Fauna Europaea 2362: 2349: 2336: 2323: 2310: 2300: 2290: 2275: 2259: 2257: 2251: 2250: 2248: 2247: 2234: 2221: 2208: 2195: 2182: 2169: 2153: 2151: 2145: 2144: 2139: 2133: 2132: 2123: 2118: 2113: 2111:Fauna Europaea 2108: 2101: 2100:External links 2098: 2095: 2094: 2037: 2016:(4): 765–772. 1996: 1981: 1963: 1914: 1861: 1804: 1775:(3): 653–662. 1755: 1685: 1625: 1574: 1559: 1527: 1472: 1409: 1380: 1343:(3): 443–460. 1323: 1309:978-0520251977 1308: 1287: 1260:(2): 197–199. 1240: 1228:Adalbert Seitz 1220: 1185: 1138: 1125:(4): 844–853. 1104: 1103: 1101: 1098: 1097: 1096: 1093: 1086: 1084: 1081: 1074: 1072: 1069: 1062: 1058: 1055: 1042:P. plantaginis 1036: 1033: 1028:P. plantaginis 1023: 1020: 1018: 1015: 1007:P. plantaginis 999:P. plantaginis 990: 987: 977: 974: 973: 972: 964: 956: 954:(Walker, 1855) 948: 940: 938:(Butler, 1881) 932: 924: 922:(Butler, 1881) 916: 908: 900: 892: 884: 876: 868: 860: 853: 850: 848: 845: 840:P. plantaginis 835: 832: 826: 825:Feigning death 823: 815:P. plantaginis 811:P. plantaginis 801: 798: 796: 793: 777:P. plantaginis 772: 769: 760:P. plantaginis 756:P. plantaginis 747: 744: 732:P. plantaginis 728: 725: 708: 705: 696: 695:Food resources 693: 688:P. plantaginis 675:P. plantaginis 670: 667: 665: 662: 648:P. plantaginis 644: 641: 635: 632: 615: 612: 584:P. plantaginis 576:P. plantaginis 519:of the family 502: 501: 498: 497: 489: 481: 473: 461: 453: 445: 437: 429: 421: 413: 405: 397: 389: 381: 369: 361: 349: 341: 329: 321: 313: 305: 293: 285: 277: 269: 261: 253: 249:Bombyx hospita 246: 238: 236:Linnaeus, 1758 229: 226: 225: 222: 221: 215: 214: 203: 192: 191: 185: 184: 177: 175: 171: 170: 163: 159: 158: 153: 149: 148: 143: 139: 138: 133: 129: 128: 123: 119: 118: 113: 109: 108: 103: 99: 98: 93: 89: 88: 83: 79: 78: 65: 64: 60: 59: 51: 50: 46: 45: 37: 36: 26: 24: 14: 13: 10: 9: 6: 4: 3: 2: 2568: 2557: 2554: 2552: 2549: 2547: 2544: 2542: 2541:Moths of Asia 2539: 2537: 2534: 2532: 2529: 2528: 2526: 2509: 2504: 2500: 2496: 2491: 2487: 2483: 2478: 2474: 2470: 2464: 2460: 2454: 2450: 2445: 2441: 2437: 2432: 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1003:Arctica villa 1000: 995: 988: 986: 983: 975: 968: 965: 960: 957: 952: 949: 944: 941: 936: 933: 928: 925: 920: 917: 912: 909: 904: 901: 896: 893: 888: 885: 880: 877: 872: 869: 864: 861: 859: 856: 855: 851: 846: 844: 841: 833: 831: 824: 822: 818: 816: 812: 807: 799: 794: 792: 788: 786: 782: 778: 770: 768: 765: 761: 757: 752: 745: 739: 735: 733: 726: 722: 717: 713: 706: 704: 702: 694: 692: 689: 685: 680: 676: 668: 663: 661: 659: 655: 654: 649: 642: 640: 633: 631: 628: 621: 613: 607: 603: 601: 597: 593: 589: 585: 581: 577: 573: 571: 567: 563: 559: 555: 551: 550: 545: 540: 538: 534: 533:Transcaucasus 530: 526: 522: 518: 514: 510: 509: 493: 490: 485: 482: 477: 474: 469: 468:sachalinensis 465: 462: 457: 454: 451:Packard, 1864 449: 446: 441: 438: 433: 430: 427:Stretch, 1906 425: 422: 419:Packard, 1864 417: 414: 409: 406: 401: 398: 393: 390: 385: 382: 377: 373: 370: 365: 362: 357: 353: 350: 345: 342: 337: 333: 330: 327:Alberti, 1973 325: 322: 317: 314: 309: 306: 301: 297: 294: 289: 286: 281: 278: 273: 270: 267:Graeser, 1888 265: 262: 257: 254: 250: 247: 244:Scopoli, 1763 242: 239: 234: 231: 230: 223: 220: 216: 211: 207: 201: 199: 193: 190: 189:Binomial name 186: 182: 181: 176: 173: 172: 169: 168: 164: 161: 160: 157: 154: 151: 150: 147: 144: 141: 140: 137: 134: 132:Superfamily: 131: 130: 127: 124: 121: 120: 117: 114: 111: 110: 107: 104: 101: 100: 97: 94: 91: 90: 87: 84: 81: 80: 75: 70: 66: 61: 57: 52: 47: 43: 38: 33: 30: 19: 2254: 2148: 2127: 2121:Lepiforum.de 2054: 2050: 2040: 2013: 2009: 1999: 1972: 1966: 1931: 1927: 1917: 1882: 1878: 1872: 1864: 1821: 1817: 1807: 1772: 1768: 1758: 1708:(8): e6761. 1705: 1701: 1688: 1645: 1641: 1587: 1583: 1577: 1568: 1562: 1556:: 1153–1170. 1553: 1549: 1543: 1492:(1): 68–78. 1489: 1485: 1426: 1422: 1412: 1401:. 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614:Description 592:mate choice 570:Platyprepia 479:Seitz, 1910 435:Grote, 1865 347:Inoue, 1976 283:Seitz, 1910 152:Subfamily: 126:Lepidoptera 35:Wood tiger 2525:Categories 2469:ParasPlant 2164:Q101212772 1403:2017-10-02 1398:jyx.jyu.fi 1214:2021-09-23 1209:jyx.jyu.fi 1100:References 1017:Physiology 982:plasticity 914:Bryk, 1942 852:Subspecies 580:aposematic 566:Platarctia 513:wood tiger 336:interrupta 319:Bryk, 1942 311:Bryk, 1942 136:Noctuoidea 106:Arthropoda 2071:0962-8452 2032:1674-5507 1885:: 71–73. 1838:2045-7758 1791:1365-2656 1732:1932-6203 1662:0962-8452 1604:0098-0331 1522:205782377 1506:1558-5646 1486:Evolution 1451:0029-8549 1423:Oecologia 1357:1063-5157 1318:536166537 1274:1877-7252 684:gene flow 588:predation 562:Parasemia 558:Pararctia 544:Parasemia 527:south to 356:leucomera 174:Species: 156:Arctiinae 92:Kingdom: 86:Eukaryota 2531:Arctiina 2466:MaBENA: 2444:LepIndex 2423:11054336 2327:BugGuide 2303:BioLib: 2293:BAMONA: 2270:Q1070697 2264:Wikidata 2217:2.113604 2178:10160919 2158:Wikidata 2089:23363631 1958:21653589 1909:28386528 1856:26640666 1799:23356667 1750:19707586 1702:PLOS ONE 1680:28954910 1620:11908754 1612:11789960 1514:19659593 1459:26296333 1375:22228799 1282:36128245 1180:30337831 847:Genetics 781:blue tit 627:wingspan 529:Anatolia 521:Erebidae 219:Synonyms 206:Linnaeus 146:Erebidae 142:Family: 102:Phylum: 96:Animalia 82:Domain: 63:Mounted 2397:1808752 2080:3574392 1949:3223681 1900:5374854 1847:4662304 1741:2726984 1710:Bibcode 1671:5627206 1467:2444085 1431:Bibcode 1366:3329764 1236:online 1171:6189224 1152:ZooKeys 1057:Gallery 1050:melanin 771:Enemies 762:, high 658:Lupinus 653:Lupinus 643:Habitat 554:Acerbia 515:, is a 162:Genus: 122:Order: 116:Insecta 112:Class: 2508:983823 2436:939818 2371:447007 2358:309211 2345:PSMAPL 2332:136494 2243:983823 2230:874455 2191:824510 2087:  2077:  2069:  2030:  1991:508233 1989:  1979:  1956:  1946:  1907:  1897:  1854:  1844:  1836:  1797:  1789:  1748:  1738:  1730:  1678:  1668:  1660:  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Index

Parasemia plantaginis


Scientific classification
Edit this classification
Eukaryota
Animalia
Arthropoda
Insecta
Lepidoptera
Noctuoidea
Erebidae
Arctiinae
Arctia
Binomial name
Linnaeus
1758
Synonyms
moth
Erebidae
Holarctic ecozone
Anatolia
Transcaucasus
China
Arctia
aposematic
predation
mate choice
immune function
thermoregulation

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