Differential parasitism by four species of phorid flies when attacking three worker castes of the leaf-cutting ant Atta laevigata (Smith, 1858).

Certain species of parasitic flies belonging to the Phoridae are known to attack Atta spp. workers foraging along trails, near nest openings used by the ants to supply the colony with plant material, and in the areas where the ants are actively cutting plant material. However, there have been no previous studies of phorid parasitism of non-foraging worker ants, for example excavators and soldiers. Excavators can be found on the surface around specialized nest openings, carrying and dumping soil on characteristic mounds. Soldiers can be found on the trails protecting foragers or guarding the different types of nest openings. The current study was performed to investigate the differential parasitism rates of Atta laevigata (Smith, 1858) worker castes by four species of phorids. Ants of all castes on trails and at nest entrances were collect from 18 mature colonies in the field. A total of 21,254 ants were collected from trails and 14,649 collected from the mounds of loose soil near nest openings. The captured workers were maintained under controlled laboratory conditions to evaluate the rate of parasitism. Of the ants collected from trails, 1,112 (5.23%) were found to have been parasitized, of which 1,102 were foragers and only 10 were soldiers. Of the ants collected from the soil mounds near the nest openings, only 27 (0.18%) were found to have been parasitized, of those 25 were excavators and 2 were soldiers. When evaluating parasitism of ants on the trails, 46.2% were attacked by Apocephalus attophilus Borgmeier, 1928, 22.6% by Myrmosicarius grandicornis Borgmeier, 1928, 16.6% by Eibesfeldtphora erthali (Brown, 2001) and 14.6% by Apocephalus vicosae Disney, 2000. Only two species of phorid, M. grandicornis and E. erthali, were observed parasitizing excavators, whilst only E. erthali parasitized soldiers. This is the first time that Atta spp. excavators and soldiers have been shown to be parasitized by phorids. The low rates of parasitism and specificity of certain phorid species for excavators and soldiers is discussed in relation to the behavioral interactions of hosts and their parasitoids, as well as the relationship between host and parasitoid size.

Novel Mucoralean Fungus From a Repugnant Substrate: Mucor merdophylus sp. nov., Isolated From Dog Excrement.

The repeated observation of dog dung covered by abundant white cottony mycelium in a private garden in the city of Rio de Janeiro, state of Rio de Janeiro (Brazil) prompted an investigation to clarify the identity of the fungus involved. Three different species of mucoralean fungi (together with some ascomycete asexual morphs) were present. Two were identified as belonging to Mycotypha sp. and Thamnostylum sp., and the third belonged to Mucor sp. This publication deals with the full taxonomic elucidation of the latter. Based on morphological, physiological, and molecular data (ITS and LSU rDNA regions), it was recognized that this Mucor differed from all other species. It produces strongly sympodially circinate branched sporangiophores (some with up to four septa) with numerous swellings resembling abortive sporangia. It also has cylindrical, obovoid, pyriform, or ovoid columellae and its sporangiospores are mostly ellipsoid, although some are subglobose and others are irregular. Based on the evidence of the analyzed datasets, the new species Mucor merdophylus is hereby proposed.

The geographical region of origin determines the phagocytic vulnerability of Lichtheimia strains.

Mucormycoses are life-threatening infections that affect patients suffering from immune deficiencies. We performed phagocytosis assays confronting various strains of Lichtheimia species with alveolar macrophages, which form the first line of defence of the innate immune system. To investigate 17 strains from four different continents in a comparative fashion, transmitted light and confocal fluorescence microscopy was applied in combination with automated image analysis. This interdisciplinary approach enabled the objective and quantitative processing of the big volume of image data. Applying machine-learning supported methods, a spontaneous clustering of the strains was revealed in the space of phagocytic measures. This clustering was not driven by measures of fungal morphology but rather by the geographical origin of the fungal strains. Our study illustrates the crucial contribution of machine-learning supported automated image analysis to the qualitative discovery and quantitative comparison of major factors affecting host-pathogen interactions. We found that the phagocytic vulnerability of Lichtheimia species depends on their geographical origin, where strains within each geographic region behaved similarly, but strongly differed amongst the regions. Based on this clustering, we were able to also classify clinical isolates with regard to their potential geographical origin.

Reproductive biology of Rhaphiodon vulpinus (Ostariophysi: Cynodontidae) in the Tocantins River Basin, Brazil

In order to evaluate aspects of the reproductive biology of Rhaphiodon vulpinus in the Upper and Middle Tocantins River, samples were taken monthly from October, 1999 through September, 2001, by means of gill nets. Males, which were more abundant than females (chi2 146.87: df=1: p<0.05), matured at a smaller size. The reproductive period of the species extended essentially from November through January, with a peak of activity in November. Fecundity, with an estimated mean value of 98,185 oocytes, varied from 38,177 to 215,841 oocytes, and it did not correlate with the length of the individual female analyzed (r=0.4663: p=0.206). Relative fecundity was 130.6 oocytes/g total weight. Mature oocytes had a mean diameter of 0.98 mm, corresponding to a volume of 0.50 mm³

Visando avaliar aspectos da biologia reprodutiva de Rhaphiodon vulpinus, foram realizadas coletas mensais no período de outubro de 1999 a setembro de 2001, no alto e médio rio Tocantins utilizando redes de espera. Os machos foram mais abundantes que as fêmeas (chi2 146,87: gl=1: p<0,05) e alcançaram o tamanho de primeira maturação em comprimentos menores. O período reprodutivo da espécie se estendeu, essencialmente, de novembro até janeiro, com pico de atividade no primeiro mês. A fecundidade, com valor médio estimado de 98185 ovócitos, variou de 38177 a 215841. A correlação entre o comprimento padrão das fêmeas e a fecundidade não foi significativa (r=0,4663: p=0,206). A fecundidade relativa foi de 130,6 ovócitos/g de peso total. O diâmetro médio dos ovócitos maduros foi 0,98 mm, correspondendo a volume de 0,50 mm³