Structure of a bat assemblage (Mammalia, Chiroptera) in Serra do Caraça Reserve, South-east Brazil

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Abstract

The Serra do Caraça Reserve is situated in the southern portion of the Espinhaço Mountain Range, and contains areas of "campos de altitude", "cerrado" and atlantic forest. This study had as its objective the registering of the bats species that occur in the reserve. The data collection was carried out in one year through monthly samplings, using mist nets set on trails, and also through hand capture. A total of 246 individuals were collected (0.72 bats/net-hour), distributed across 15 species, belonging to the families Phyllostomidae (83.0%; nine species), Vespertilionidae (12.5%; three species) and Molossidae (4.5%; three species). The most abundant species were Sturnira lilium (E. Geoffroy, 1810) (n = 121, 60.5%), Myotis nigricans (Schinz, 1821) (n = 21, 10.5%) and Platyrrhinus lineatus (E. Geoffroy, 1810) (n = 10, 5.0%), and less represented were Lasiurus blossevilli (Lesson y Garnot, 1826) (n = 2, 1.0%), Eumops perotis (Schinz, 1821) (n = 2, 1.0%) e Vampyressa pusilla (Wagner, 1843) (n = 1, 0.5%). The richness of species found and the non-occurrence of phyllostomines in the reserve could be indicative of some level of forest disturbance.

Related collections

Most cited references 22

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Guillain-Barré syndrome.

F. Hahn (1998)

Guillain-Barré syndrome (GBS) is viewed as a reactive, self-limited, autoimmune disease triggered by a preceding bacterial or viral infection. Campylobacter jejuni, a major cause of bacterial gastroenteritis worldwide, is the most frequent antecedent pathogen. It is likely that immune responses directed towards the infecting organisms are involved in the pathogenesis of GBS by cross-reaction with neural tissues. The infecting organism induces humoral and cellular immune responses that, because of the sharing of homologous epitopes (molecular mimicry), cross-react with ganglioside surface components of peripheral nerves. Immune reactions against target epitopes in Schwann-cell surface membrane or myelin result in acute inflammatory demyelinating neuropathy (85% of cases); reactions against epitopes contained in the axonal membrane cause the acute axonal forms of GBS (15% of cases). Care for such patients may be challenging, yet the prognosis overall is favourable. Optimal supportive care and anticipation and prevention of complications are the mainstay of therapy. Admission to the intensive-care unit is necessary in 33% of patients who require intubation and assisted ventilation. Immunomodulation with infusions of IgG or plasma exchange treatments foreshorten the disease course.