Residues of pyrethroid treatments,alone or with foliar urea,on tomato

Phytoparasitica - The effect of foliar urea treatments on the persistence of synthetic pyrethroid residues on tomato was studied. Fenvalerate was found to persist more and deltamethrin less than...     

Spread of phytophthora rot on stored citrus and its prevention by fungicide dips1

Oranges and lemons infected with Phytophthora citrophthora and P. syringae were placed among healthy fruits in boxes kept at 5, 10 and 14°C. The spread of the rot by contact infection was assessed after 3,6,12 and 18 days and again after 7 days' shelf-life at 17°C. P. citrophthora infected adjacent fruits after 12 days at 10°C and 3 days at 14°C. No infection occurred at 5°C. P. syringue infected the fruits at all the temperatures tested. On fruits kept for 6 days at 5°C, the rot developed after shelf-life. The presence of Phytophthora-infected fruits in orange and lemon packing boxes enhanced the development of penicillium rots. Post-harvest dips in metalaxyl at 0.05 and 0.1% concentrations and fosetyl-Al at 0.1,0.2 and 0.3% concentrations prevented the spread of P. citrophthora in packing boxes kept for 30,40 and 60 days at 11°C, but had no effect on penicillium rots. The mixture of the above fungicides with thiabendazole at 0.1%] or imazalil at 0.05%, concentrations gave best control against phytophthora and penicillium rots.     

Chaetotaxy of cercariae of Opisthioglyphe ranae (Fr?lich, 1791) (Trematoda: Plagiorchidae)

A detailed observation of the sensory apparatus of Opisthioglyphe ranae (Fr?lich, 1791) cercariae was carried out. The species was determined on the basis of an experimental study of the life cycle and morphology of sporocysts, cercariae, metacercariae, and adults. In contrast to other species of the family Plagiorchidae, no papillae were present in the positions CId1, CId2, CII0, CII3 and CII4. Papillae with markedly ventral situation on the postacetabular zone were found very rarely. Some of the cercariae possessed ventral papillae variously distributed in the preacetabular zone. A comparative analysis of the chaetotaxy revealed that the cercaria studied by us was very similar to Cercaria 4 of Richard, 1971, with the exception of the number of acetabular papillae and some groups of ventral papillae. Compared to the cercaria of O. ranae studied by Dobrovolskiy (1965). AID papillae and a part of ventral papillae were distributed differently. The chaetotaxy was identical with that of experimentally obtained cercariae of O. ranae from L. stagnalis and of cercariae of the same species obtained from Bulgaria.     

Sleep time following anesthesia in mouse lines selected for resistance or susceptibility to fescue toxicosis

In previous work, a mouse line selected for resistance (R) to fescue toxicosis had higher activities of two hepatic Phase II detoxification enzymes than a mouse line selected for fescue toxicosis susceptibility (S). The primary objective of the present study was to determine whether those same lines also differed in hepatic Phase I enzyme activity, estimated from sleep time (ST) following sodium pentobarbital anesthesia. Additional objectives were to determine whether ST differences between lines were modulated by endophyte-infected fescue in the diet (with or without an enzyme inducer) and whether ST of individual mice was correlated with the effect of a toxin-containing diet on the postweaning growth of those mice. In Exp. I, 24 males from each line were randomly assigned to each of five diets: control (commercial rodent food meal); E+ (50% endophyte-infected fescue seed, 50% control); E+P (the E+ diet supplemented with 1,000 ppm phenobarbital); E- (50% endophyte-free fescue seed, 50% control); and E-P (the E- diet supplemented with 1,000 ppm phenobarbital). After 4 wk on these diets, ST was measured on all the mice. A second ST was recorded on each mouse by randomly sampling one-fourth of the population after 1, 2, 3, or 4 wk on a pelleted rodent food diet. Regardless of diet, R mice had shorter first and second ST than S mice (P < 0.01), suggesting higher hepatic Phase I microsomal enzyme activity. Mice on both phenobarbital-supplemented diets had shorter first ST than mice whose diets did not include that microsomal enzyme inducer (P < 0.01). In Exp. II, ST was measured on male and female R and S mice (n = 280) after they had been fed the E- diet for 2 wk, then the E+ diet for 2 wk, and then a pelleted rodent food diet for 2 wk. Growth response to the E+ diet was the percentage of reduction in gain on the E+ diet compared to gain on the E- diet the previous 2 wk. As in Exp. I, S mice slept longer than R mice (P < 0.01). The residual correlation between ST and gain reduction associated with the E+ diet equaled 0.04. Thus, an animal's apparent Phase I enzyme activity did not predict its growth rate depression on the toxin-containing diet. Based on these and previous studies, divergent selection for toxicosis response in mice was successful partially by causing divergence in activities of hepatic Phase I and II detoxification enzymes.