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Despite the potentials and contributions of guinea fowls to economic and social life in Ghana, accurate sex identification in these birds is still a major problem. Three hundred and sixty guinea fowls (180 birds per sex) were used in determining a more accurate and farmer friendly sexing technique. The sexing methods explored were vent, biometric, and molecular techniques. Vent sexing was accomplished by measuring phalli in 28 and 32-week-old birds, while biometric sexing involved the measurement of morphometric traits and data analyzed using discriminant function analysis. Molecular sexing was carried out by DNA extraction and subsequent PCR using the 2550F/2718R primer set. Females had a wider (P<0.05) pelvic inlet than male birds from first week of age until the end of the study, while the opposite was true for wattle length. However, wattle length differed (P<0.05) between both sexes after 4 weeks of age. Combining the biometric variables in a discriminant function, males could be distinguished from females with an accuracy of 94%. During molecular sexing, the P2/P8 primer set was not effective in sexing guinea fowls because it amplified a single band in both sexes and in the same manner. The sex of guinea fowls was properly determined using the primer set 2550F/2718R. Females produced 2 bands of 396 bp and 344 bp, while males only produced the larger band. Phallus size in the 2 sexes were distinguishable from 8 weeks of age, with males having longer and thicker (P<0.05) phalli than their female counterparts. Combining the 2 variables in a discriminate function, males and females could be distinguished with 98.3% accuracy. While the molecular method remains the most accurate sexing technique, the biometric method emerged as the most farmer friendly approach to sexing guinea fowls.

The physiological basis of seasonal breeding in the guinea fowl (Numida meleagris) still remains unknown, despite the socioeconomic importance of these birds, particularly in Ghana. A study involving a total of 50 local guinea cocks was conducted, and documented gross anatomical and histological differences in the reproductive organs of breeding and non-breeding male guinea fowls. The study also compared peripheral testosterone concentrations in breeding and non-breeding cocks. Seasonal differences in variables measured were determined using two-tailed t-test/Mann-Whitney U-test. All comparisons were made at 5% level of significance. Breeding males had significantly (P = 0.000) higher anatomical biometric parameters than their non-breeding counterparts. Also, breeding birds had thicker (P = 0.000) phalli than their non-breeding counterparts. Histologically, regressing testis was characterized by the presence of sloughed off cells and increased debris in the tubular lumen and within the excurrent duct system, collapsed tubules and reduction in tubular lumen. Germ and Sertoli cell populations and nuclear diameters and actual seminiferous tubular diameter and length in regressing testes were significantly (P = 0.000) lower than in active testes. Leydig cell nuclear diameters and populations were also significantly (P = 0.000) reduced. Relative volume of seminiferous tubules in the testis, testicular sperm production/mg testis and per testis and peripheral testosterone concentrations were all higher (P < 0.05) in breeding than non-breeding testis. The ducts in the epididymal region also saw significant (P < 0.05) reductions in luminal diameters in non-breeding birds. Significant regression in anatomical and histological structures of the guinea cock reproductive tract occurred during the non-breeding season, and lower peripheral testosterone concentrations may be responsible for this phenomenon.