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| Q55982681 | Adoption of lycaenidNiphanda fusca(Lepidoptera: Lycaenidae) caterpillars by the host antCamponotus japonicus(Hymenoptera: Formicidae) |
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| Q27332122 | Ants use partner specific odors to learn to recognize a mutualistic partner |
| Q38661083 | Arthropods Associate with their Red Wood ant Host without Matching Nestmate Recognition Cues. |
| Q64084122 | Bacterial communities within caterpillars are shifted following transition from solitary living to social parasitism of ant colonies |
| Q54553082 | Basal subtribes of the Nymphidiini (Lepidoptera: Riodinidae): phylogeny and myrmecophily |
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| Q40265591 | Chemical Strategies of the Beetle Metoecus Paradoxus, Social Parasite of the Wasp Vespula Vulgaris |
| Q42005651 | Comparative study of the morphology of stridulatory organs of the Iberian lycaenid butterfly pupae (Lepidoptera). |
| Q22305438 | Corruption of ant acoustical signals by mimetic social parasites: Maculinea butterflies achieve elevated status in host societies by mimicking the acoustics of queen ants |
| Q34158406 | Cuckoos versus hosts in insects and birds: adaptations, counter-adaptations and outcomes |
| Q35842880 | Cuticular Hydrocarbons as Potential Close Range Recognition Cues in Orchid Bees. |
| Q28079807 | Cuticular Lipids as a Cross-Talk among Ants, Plants and Butterflies. |
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| Q50969343 | Evidence for passive chemical camouflage in the parasitic mite Varroa destructor. |
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| Q57247109 | Habitat use of the endangered parasitic butterflyPhengaris arionclose to its northern distribution limit |
| Q57247098 | Host ant use of the Alcon blue butterfly at the northern range margin |
| Q28601027 | Host plant use drives genetic differentiation in syntopic populations of Maculinea alcon |
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| Q56926872 | Host-Specific Myrmecophily and Myrmecophagy in the Tropical Coccinellid Diomus thoracicus in French Guiana |
| Q30370182 | Host-ant specificity of endangered large blue butterflies (Phengaris spp., Lepidoptera: Lycaenidae) in Japan. |
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| Q24672922 | Increased genetic diversity as a defence against parasites is undermined by social parasites: Microdon mutabilis hoverflies infesting Formica lemani ant colonies |
| Q57577458 | Influence of host plant phenology and oviposition date on the oviposition pattern and offspring performance of the butterfly Phengaris alcon |
| Q30358734 | Lock-picks: fungal infection facilitates the intrusion of strangers into ant colonies. |
| Q51566108 | Male-specific (Z)-9-tricosene stimulates female mating behaviour in the spider Pholcus beijingensis. |
| Q51544490 | Mimetic host shifts in an endangered social parasite of ants. |
| Q38875443 | Mimicry for all modalities |
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| Q98946156 | Nonaggressive behavior: A strategy employed by an obligate nest invader to avoid conflict with its host species |
| Q33196305 | Parasitic exploitation as an engine of diversity |
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| Q57577447 | Phengaris (Maculinea) teleius butterflies select host plants close to Myrmica ants for oviposition, but P . nausithous do not |
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| Q51862547 | Testing the adjustable threshold model for intruder recognition on Myrmica ants in the context of a social parasite. |
| Q64935217 | The Microbiome of the Maculinea-Myrmica Host-Parasite Interaction. |
| Q58789099 | The habitat vegetational structure and the success of the blue alcon,Maculinea alcon(Denis & Schiffermüller) |
| Q21189459 | The re-discovered Maculinea rebeli (Hirschke, 1904): Host ant usage, parasitoid and initial food plant around the type locality with taxonomical aspects (Lepidoptera, Lycaenidae) |
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