Introduction. Cytokinins enhance axillary shoots, which helps prolific shoot multiplication in vitro. Very few reports are available on biochemical changes associated with this in vitro proliferation of Citrus. The present study was undertaken to find out the influence of two widely used cytokinins on various morphological and biochemical constituents of in vitro proliferated shoots of Citrus species. Materials and methods. Shoots of (0.5 to 1.0) cm long from in vitro proliferated shoots of five Citrus species were cultured on MS medium supplemented with eight increasing levels of benzylaminopurine (BAP) or kinetin spread from (0.25 to 2) mg$\cdot$L-1. After 6 weeks of culture, morphogenetic characters were observed, and shoot samples were crushed with 5 mL of hot ethanol; the extract collected was used for the estimation of reducing sugars, total phenols, ortho dihydric (OD) phenol, amino nitrogen and protein percentages. Results and discussion. For all the morphogenetic characters studied, except the shoot number, there were significant interactions between the Citrus species and the different concentrations of BAP and kinetine. Increased concentration of cytokinins reduced the amount of total phenol, OD phenol and total protein. Calamondin recorded the lowest percent of reducing sugar and protein. The maximum amount of reducing sugars was recorded for C. volkameriana. Supplementation of BAP resulted in the highest amount of total and OD phenols, whereas kinetin improved the reducing sugar and amino nitrogen.

Larvae of Cirina forda (Westwood) (Lepidoptera: Saturniidae), a popular food insect in the southern parts of Nigeria were raised in the laboratory on cut foliage as well as on a growing Vittelaria paradoxa tree at the University of Ilorin, Nigeria. Comparative observations were made on the insect's biology and behaviour in both rearing systems in order to ascertain if the larvae could be reared in captivity on cut foliage. Egg eclosión began 24–48 hours after egg-laying and lasted 10 days. First instars initially aggregated after egg hatch, then migrated in single file to feed after approximately 12 hours after emergence. The first and second instars fed as an aggregate, while the third and subsequent instars fed separately. The first two instars did not exhibit any defensive response when disturbed, but the subsequent four instars emitted a green fluid which may act as a repellant to potential predators. High mortalities were suffered by the first and the penultimate instars. Results have shown that Cirina larvae could be easily reared artificially on V. paradoxa to serve as source of food for humans.