Effect of temperature on predation of Chilocorus bipustulatus L. (Col.: Coccinellidae) feeding on Agonoscena pistaciae (Hem.: Psyllidae)

Chilocorus bipustulatus L. (Col.: Coccinellidae) is a predatory coccinellid with a wide geographical distribution. Biological control programs should have a good understanding of the capacity of a predator to kill the target prey. Therefore, the age-stage specific predation rate and functional response of C. bipustulatus feeding on Agonoscena pistaciae (Hem.: Psyllidae) were studied at 18, 25, and 32 °C (65?±?5%RH and 16 L: 8D) to confirm its potential as a biological control agent of common pistachio psylla. The functional response at 18 and 25 °C were described by type II and type III at 32 °C. The estimated maximum attack rate (T/Th) was at 25 °C. Moreover, the highest net feeding (C₀) was observed at 25 °C (3271.5 psyllids). This laboratory study, thus, suggested that the predatory coccinellid C. bipustulatus reacted to the rise of temperature by enhancing the predation rate on A. pistaciae.

     

Investigation and prediction spatial variability in chemical properties of agricultural soil using geostatistics

Determination of the chemical characteristics of soil for balanced fertilization on large scales is an important factor in achieving a precision agriculture. Laboratory analyses of soil properties are usually expensive and time consuming. Surmounting these problems is possible using geostatistics. Therefore, this research aims at selecting a proper interpolation method using 213 soil samples for alfalfa farmland in Hamadan Province, Iran. Various factors such as pH, EC, , , K, P, Fe, Zn, B and Co were measured. Ordinary kriging and co-kriging were assessed to derive maps of soil physico-chemical properties, using mean absolute error (MAE), mean bias error (MBE), root mean squared error (RMSE) and average kriging standard error (AKSE) as statistical criteria. Variography analysis indicated that the ranges of influence for pH, EC, , , K, P, Zn, Fe, B and Co were 65, 55, 78, 79, 75, 60, 50, 65, 70 and 30 km, respectively, and the measuring error varied between 0.366 and 0.843. The results revealed that, based on precision criteria, co-kriging was the best method for interpolating the chemical properties of soil. Finally, using to the co-kriging for each determined variable, a related zoning map for fertility management of the study area was prepared.     

Effect of chronic intracerebroventricluar administration of lipopolysaccharide on connexin43 protein expression in rat hippocampus

Background: Hippocampal damages, which are accompanied by inflammation, are among the main causes of epilepsy acquisition. We previously reported that chronic intracerebroventricular (i.c.v.) injection of lipopolysaccharide (LPS) modulates epileptogenesis in rats. There is a network of gap junction channels in the hippocampus that contribute to epileptogenesis. Gap junction channels are formed by oligomeric protein subunits called connexins (Cx). Astrocytic Cx43 and neuronal Cx36 are expressed in the hippocampus. In order to find out the possible role of gap junctions in seizure-modulating effect of LPS and neuroinflammation, we studied the effect of central administration of LPS on expression of Cx36 and Cx43 in rat hippocampus. Methods: LPS, 2.5 µg/rat/day, was injected i.c.v. to male Wistar rats for 14 days. mRNA and protein abundance of Cx36, Cx43 and IL1-β were measured in rat hippocampus by real time-PCR, Western blot and ELISA techniques, at the beginning, in the middle, and at the end of the treatment period. Results: IL1-β protein level was significantly increased 6 h after first injection of LPS. Cx36 and Cx43 mRNA expression did not alter during chronic administration of LPS. A selective decrease in Cx43 protein expression was observed after 7 injections of LPS. Conclusion: It is suggested that Cx43 containing gap junctions in the hippocampus is down-regulated in response to chronic injection of LPS. This event can inhibit propagation of toxic and noxious molecules to neighboring cells and modulate hippocampal excitability and epileptogenesis. Key Words: Connexin36 (Cx36), Connexin43 (Cx43), Interleukin-1β (IL1-β )