Peter V. Vršanský

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Bioluminescence is a common feature of the communication and defence of marine organisms, but this phenomenon is highly restricted in the terrestrial biota. Here, we present a geographical distribution of only the third order of luminescent insects—luminescent cockroaches, with all 13 known and/or herein reported new living species (based on deposited(More)
Morphna paleo sp. n., the earliest winged representative of any living cockroach genus and the earliest representative of the family Blaberidae, is described from the Danian Arkhara-Boguchan coal mine in the Amur River region (Russian Far East). The branched Sc and A suggest Ectobiidae (=Blattellidae) probably is not the ancestral family because Blaberidae(More)
The presence of bioluminescent system in cockroaches (Zompro and Fritzche 1999) and in Lucihormetica luckae in particular has been contested in reply byMerritt (2013), based on the absence of direct evidence of bioluminescence in the original article (Vršanský et al. 2012). Main counterarguments were based on (1) a single anecdotal reference to the presence(More)
Viviparity evolved in bacteria, plants, ˃141 vertebrate lineages (ichthyosaurs, lizards, fishes, mammals, and others), and in 11 of 44 insect orders. Live-birth cockroaches preserved with brood sac (3D recovered two times optically) included Diploptera vladimir, Diploptera savba, Diploptera gemini spp.n., D. sp.1–2, and Stegoblatta irmgardgroehni from Green(More)
The new, small cavernicolous species Helmablatta louisrothi gen. et sp. n. (Nocticolidae) from the Tan-Phu cave (Vietnam) is one of the most morphologically interesting cockroaches. The extremely modified upstanding tergal gland composite from three tergites and may serve for gripping the female head during copulation. This presumption is supported by the(More)
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