sp. is described from the siluriform catfish Megalonema platanum (Gunther) (Siluriformes: Pimelodidae) in the Parana River basin, Argentina. The new species is allocated to Monticellia La Rue, 1911 (Proteocephalidae: Monticelliinae) because of the cortical position of the testes, ovary, vitelline follicles and uterus, a globular scolex without a metascolex and uniloculate suckers. The new species differs from all other species of Monticellia (except for M. XMU-MP-1 molecular weight lenha Woodland, 1933) in possessing a vaginal canal opening anterior or posterior to the cirrus-sac.
M. santafesina can be distinguished from M. lenha by the following characteristics: a larger body size; a weakly developed internal longitudinal musculature arranged in 15-35 slim bundles of muscle INCB024360 fibres; vitelline follicles not interrupted at the level of the cirrus-sac and vaginal canal, and with a few paramuscular and/or medullary follicles; the absence of large spinitriches on the anterior margin of the suckers; and the utilisation of Megalonema platanum (in
the Parana River basin) as its host, rather than Sorubimichthys planiceps (Spix & Agassiz) (in the River Amazon). Monticellia santafesina exhibits low values of prevalence (9%) and intensity of infection (1). Megalonema platanum was parasitised by two proteocephalidean cestodes, Rudolphiella cf. lobosa (Riggenbach, 1895) and the new species described in this paper.”
“Sexual size dimorphism (SSD) is a common phenomenon and is a central
topic in Selleck GW4869 evolutionary biology. Recently, the importance of pursuing an ontogenetic perspective of SSD has been emphasized, to elucidate the proximate physiological mechanisms leading to its evolution. However, such research has seldom focused on the critical periods when males and females diverge. Using mark-recapture data, we investigated the development of SSD, sex-specific survivorship, and growth rates in Phrynocephalus przewalskii (Agamidae). We demonstrated that both male and female lizards are reproductively mature at age 10-11 months (including 5 months hibernation). Male-biased SSD in snout-vent length (SVL) was only found in adults and was fully expressed at age 11 months (June of the first full season of activity), just after sexual maturation. However, male-biased SSD in tail length (TL), hind-limb length (LL), and head width (HW) were fully expressed at age 9-10 months, just before sexual maturation. Analysis of age-specific linear growth rates identified sexually dimorphic growth during the fifth growth month (age 10-11 months) as the proximate cause of SSD in SVL. The males experienced higher mortality than females in the first 2 years and only survived better than females after SSD was well developed. This suggests that the critical period of divergence in the sizes of male and female P.