Adult triatomines occasionally fly into artificially lit premises in Amazonia. This can result in Trypanosoma cruzi transmission to humans either by direct contact or via foodstuff contamination, but the frequency of such behaviour has not been quantified. To address this issue, a light-trap was set 45 m above ground in primary rainforest near Manaus, state of Amazonas, Brazil and operated monthly for three consecutive nights over the course of one year (432 trap-hours). The most commonly caught reduviids were triatomines, including 38 Panstrongylus geniculatus, nine Panstrongylus lignarius, three Panstrongylus rufotuberculatus, five Rhodnius robustus, two Rhodnius pictipes, one Rhodnius amazonicus and 17 Eratyrus mucronatus. Males were collected more frequently than females. The only month without any catches was May. Attraction of most of the known local T. cruzi vectors to artificial light sources is common and year-round in the Amazon rainforest, implying that they may often invade premises built near forest edges and thus become involved in disease transmission. Consequently, effective Chagas disease prevention in Amazonia will require integrating entomological surveillance with the currently used epidemiological surveillance

16.9 km 2 is the main island (Lopes and Ulbrich, 2015), and the remaining area is distributed among 20 smaller islands, of which Rata Island is the largest with 0.8 km 2. The archipelago has suffered major ecological disturbances due to several human interventions. In 1737, fortifications were built, and the archipelago was transformed into a penal colony for almost 200 years. During this period, a large part of the native vegetation was devastated while exotic plants and animals were introduced to serve as food (Teixeira et al., 2003; Serafini et al., 2010). The human population in the archipelago increased significantly in 1942 through military occupation (i.e., World War II). Afterwards, significant changes were observed in the archipelago due to: • Several insecticide applications campaigns (i.e., DDT) for mosquito-control; • Wild animal introductions, such as the Teju lizard (Salvator merianae Duméril & Bibron) and the Mocó cavy (Kerodon rupestris Wied-Neuwied); • Release of birds seized in trade fairs and public markets of Recife (i.e., Saffron finch (Sicalis flaveola (Linnaeus)), House Sparrow (Passer domesticus (Linnaeus)), and the White-bellied seedeater (Sporophila leucoptera (Vieillot));

São apresentados resultados da coleta de ectoparasitos em cães e gatos entre agosto de 2001 e maio de 2002 em diferentes bairros da cidade Manaus. No cão foram encontrados: Ctenocephalides f. felis (Bouché, 1835) (Siphonaptera, Pulicidae), Heterodoxus spiniger (Enderlein, 1909)(Phthiraptera, Boopidae), Trichodectes canis (De Geer, 1778) (Phthiraptera, Trichodectidae) e Rhipicephalus sanguineus (Latreille,1806) (Acari, Ixodidae). No gato foi coletado C. f. felis. A prevalência de ectoparasitos foi de 80,8% para cães e 72,7% para gatos. Para a pulga C. f. felis foi de 28,7% para cães e 72,7% para gatos. Para o piolho H. spiniger foi de 12,3% para cães. Para o piolho T. canis foi de 0,1% para cães e para o carrapato R. sanguineus foi de 63% para cães. A média de infestaçãode pulga foi de 1,26 para cães e 1,27 para gatos. A proporção sexual fêmea/macho foi de 1,96:1 no cão e de 3,66:1 no gato. A pulga C. canis (Curtis, 1826), registrada em 1922, não foi coletada.

Triplocania Roesler, 1940 has a high rate of endemism per country, with only five species out of a total of 118 described species, occurring in more than one country. Brazil is the second most diverse country in terms of Triplocania species, with 34 species recorded. In this paper, Triplocania furcatoides González-Obando, Carrejo-Gironza & García Aldrete, 2017 was recorded for Brazil and new records of Triplocania furcata New, 1972 made for four Brazilian states (Amazonas, Pará, Roraima and Tocantins), thus decreasing Wallace shortfall of these two species.

Two new species of Triplocania Roesler, based on male specimens, were here described and illustrated for Ecuador, increasing the number of Ecuadorian species of Triplocania to seven. The first identification key to Triplocania species from Ecuador is presented. The Ecuadorian Triplocania species here described increase the diversity of Triplocania in Ecuador to seven species, making it the third most diverse country in Triplocania.