helminths and arthropods collected from warthogs at monthly intervals, prevalence, rainfall and temperature data, clear patterns of seasonal abundance could be determined only for Physocephalus sexalatus and Haematopinus phacochoeri

There is increasing alarm and awareness about the health dangerposed by the arthropod vector causing Onchocerciasis. This study was carried out with the aim to throw more light on the prevalence of the arthropod vector, Simulun damnosum. This research enabled us toproffer preventive advice to government and citizens. In carrying out this study, villages around flowing waters were used as sample sites. The method applied was direct observation, coupled with efficientrecording. Atmospheric temperature readings were periodically taken along with the density of the insect population observed under such temperature. The same was done for relative humidity (%), solar radiation (gm-ca/cm2, lum) and luminescence (cd/m2) in relation to the insect population of available FMH at every given period (fly per man hour). Our findings showed that climate conditions influence the reproductive level and numbers of the vector. The wet season is most conducive for the arthropod vector to reproduce and multiply. The humidity is high and temperature seems to be at the average. It is during this period that greater preventive measures need to beintentionally heightened to subdue the dangerous activities of the vector.

The Malaysian Pangolin (Manis javanica) is an endangered species,
but is widely hunted for its medicinal value in body parts. A total of sixteen pangolins were screened for blood protozoa and six
pangolins were confi rmed to be positive for eperythrozoonosis infection based on morphology from blood smears stained with 8% Giemsa. The causative organism, Eperythrozoon sp., with a size of 0.3 μm were observed under a compound microscope at 100× magnification on the surface of red blood cells as blue coloured dots. This is the fi rst report of Eperythrozoon infection from pangolins in Malaysia. Further identifi cation using polymerase chain reaction (PCR) is necessary to confi rm E. ovis or wenyonii,
which is uncultivatable in artifi cial media.