https://www.selleckchem.com/products/imd-0354.html Rhopalovalva chidorinoki Nasu, sp. nov. is described from Japan, with the photographs of the adult and genitalia. The diagnostic characters of the new species are given with comparison with the allied species, R. exartemana (Kennel, 1901).Cryptotermes Banks, 1906 is the third most diverse kalotermitid genus worldwide after Glyptotermes Froggatt, 1897 and Neotermes Holmgren, 1911, with its greatest diversity found in the Neotropics (Krishna et al. 2013a). Furthermore, the greatest number of species of Cryptotermes are known from the Caribbean Basin (Scheffrahn Křeček 1999, Casala et al. 2016, Scheffrahn 2019). Although Araujo (1977) and Bacchus (1987) list Cryptotermes domesticus (Haviland, 1898) from Trinidad (treated as mainland) and Panama, respectively, Scheffrahn Křeček (1999) and Scheffrahn et al. (2009) doubt the existence of this Asian species in the New World. Without C. domesticus, the total extant Neotropical diversity of Cryptotermes is 29 endemic and three exotic species (Constantino 2020).The Anaphothrips genus-group is a complex of 40 genera of Thripinae that share the condition of "no long pronotal setae". In traditional Thysanoptera classifications this absence of long pronotal setae was interpreted as a plesiomorphy by comparison to the condition in Aeolothripidae. Thus Jacot-Guillarmod (1974) catalogued all Thripinae genera with species showing this condition in a sub-tribe Aptinothripina Karny, a long-established arrangement that had been adopted by many authors. However, a study by Buckman et al. (2013) confirmed that taxa in the families Merothripidae and Melanthripidae share an important number of structural plesiomorphies, and these taxa all have long pronotal setae. From this it is concluded that absence of long pronotal setae is a derived condition, and moreover this loss apomorphy has arisen independently within several unrelated genera, such as Dichromothrips, Trichromothrips and Thrips (M