ABSTRACT
This study is conducted to determine the population density of mosquitoes in three selected area (Kofar Taramniya, Mabera and Bello Way) in Sokoto metropolis. To identified and count the population of mosquito, different breeding sites were investigated for the preferences of mosquitoes. Mosquito larvae were collected using dipper, ladle spoon from drainages, stagnant water, gutters, open wells, local pots, water tanks and cattle sheds. A total population of 4,764 mosquito larvae were collected and identified From the three (3) selected areas larvae and pupae were encounters in abundance. In Mabera area, a total of 1799 (37.7%) larvae are collected in which 1199 (45.8%) belonging to Anophelesgenera and 600 (27.9%) belong to culexgenera. In kofar Taramniya a total of 1649 (34.6%) larvae are collected in which 1000 (38.2%) belong to Anopheles genera and 649 (30.2%) belong to culexgenera, in Bello Way, A total of 1317 (27.5%) larvae were collected,417 (15.9%) belong to Anophelesgenera and 900 (41.9%)belongto culexgenera. Statistical analysis conducted indicated a significant difference (p<0.05) between the three collections. Mosquitoes encountered belong to two genera of Anophelesand Culex. The predominant genus was Anopheleswith a total of 2,615 larvaewhile Culexhas a total of 2149 larvae in all the three study areas. Considering the medical importance of mosquitoes, the information provided from this study will serve as a basis for understanding the implication of mosquitoes nuisance and provide effective control strategies against the vector and to reduce mosquitoes born disease
ABSTRACT
Objectives of the Study:An Epidemiological Research, a cross-sectional study, was conducted to determine the magnitude of human contamination of irrigation canal perimeter as it relates to the prevalence and intensity of schistosome cercarial infection in snail vectors.Place and Duration of Study:The study was conducted along water canal located within an irrigation area, Kano River Project Phase I, Kadawa, between January and June, 2012.Methodology:The study area was categorized into Zone of Heavy Contamination (ZHC), Zoneof Light Contamination (ZLC) and Zone of Free Contamination (ZFC) based on the density of faecal lumps observed along the canal perimeter using 1m2quadrat sampling technique. Snail vectors of schistosomiasis were collected from these zones, identified and subjected to cercarial shedding. Brevifurcate apharyngeate cercariae were identified as schistosome cercariae.Results:Of the 827 snails collected 28.54% shed schistosome cercariae. The breakdown of infection prevalence was 31.37%, 27.69% and 26.26% for ZHC, ZLC and ZFC respectively. Three snail species recovered in the study area, Bulinus globosus, B. rohlfsi and Biomphalaria pfeifferi had infection intensity of 8.6, 5.67 and 3.94 respectively, with total mean intensity of 4.67. A Chi-squared analysis did not show any significant difference in infection prevalence in the three zones (χ2cal.0.025, χ22, 0.05= 5.99). However, infection intensity was significantly different in the three zones and among the three snail species using analysis of variance (P<0.05). Conclusion:Human environmental contamination with faeces and urine around irrigation canals remains the source of infection to snail hosts and then to humans. It is presumed that contact control through avoidance of defaecation in the open and building of pit latrines near water contact points along irrigation canals will be effective means of drawing a barrier to infection with schistosomes in the study area