Resurrection and redescription of Clepsinepallida Verrill, 1872 (Hirudinida, Glossiphoniidae) with a phylogeny of the genus Alboglossiphonia.

Alboglossiphoniapallida (Verrill, 1872) comb. nov. is resurrected and redescribed based on morphological and molecular data from specimens of the type locality (New Haven County, Connecticut, USA) that demonstrate it is distinct from North American Alboglossiphoniaheteroclita, European Alboglossiphoniaheteroclita, and Alboglossiphoniapapillosa. Alboglossiphoniapallida is characterized by having dark chromatophores on the dorsal surface arranged lateral to patrilaterally and medially as a thin line or interrupted thin line along with three pairs of eye spots (with the first pair closest together), six pairs of crop ceca, and a united gonopore. Additional sampling of specimens of the genus Alboglossiphonia is needed to understand its phylogeny especially as many species have not been collected since their description.

Sucking of human blood by Placobdella costata (O. F. Müller, 1846) (Hirudinida: Glossiphoniidae): Case study with notes on body form.

Four events of Placobdella costata sucking human blood are described.Human blood was sucked by both adult and juvenile specimens of P. costata.The feeding strategies of juveniles under parental care are presented.New data on juvenile specimens' body form are presented.Information on the potential role of mammals in dispersion and habitat preferences of leeches P. costata is considered.

Parasitism of Placobdelloides siamensis (Oka, 1917) (Glossiphoniidae: Hirudinea) in Snail-eating Turtles, Malayemys spp., and the effects of host and aquatic environmental factors.

The Siam Shield Leech, Placobdelloides siamensis, is a common leech found on Malayemys turtles in Thailand. Sixty Snail-eating Turtles (29 Malayemys macrocephala and 31 M. subtrijuga) were caught over twelve months (February 2017 - January 2018) to determine host characteristics (body size, weight and sex), parasitism (prevalence, intensity and density) and seasonal aquatic environmental factors (conductivity, nitrate nitrogen, dissolved oxygen, pH, salinity and total dissolved solids). There was no significant difference of infection rate between species and sex in both turtle species. Leech prevalence indicated that all turtle individuals were infected throughout year, while the infection rate was significantly higher in larger and heavier turtles mainly on the carapace with an average number of leech approximately 474.80 ± 331.38 individuals for individual host infection and 76.53 ± 20.27 individuals for infection per 100 g body weight. The high level of leech parasitism also caused a rot wound and shell hole which caused the host to die. Aquatic environmental factors did not influence the infection of leeches in both turtle species. Therefore, the factors that influenced the infection rate of P. siamensis were based on only host body size and weight without effect from season. In addition, this study also showed two new hosts, including Cyclemys oldhamii and Heosemys grandis and the widespread distribution from northern, north-eastern, western, central and southern Thailand were reported.

Low genetic diversity in Ozobranchus jantseanus (Hirudinida: Ozobranchidae) in Japan: Possibility of introduction with their host turtles.

Leeches belonging to the genus Ozobranchus are ectoparasitic on sea and freshwater turtles. The freshwater species O. jantseanus has been recorded from China and Japan. Ozobranchus jantseanus inhabiting Japan is considered to be a non-indigenous species, because their primary host, the Reeves' pond turtle, Mauremys reevesii, is thought to have been introduced in the last few centuries from adjacent Asian countries. To assess whether the Japanese populations of O. jantseanus were likely to have been introduced, their genetic diversity was investigated using mitochondrial cytochrome c oxidase subunit I sequences. The very low sequence diversity as well as the historical record of this species from Japan suggest that Japanese populations of O. jantseanus may have been artificially introduced along with their host turtles. Molecular phylogenies of COI showed that two marine Ozobranchus species formed a clade together with the freshwater O. jantseanus.