Temperature impact on the phenology of Nesidiocoris tenuis feeding on Tetranychus urticae: simulation through life cycle modelling

Author(s):  
O. Gavkare ◽  
P. L. Sharma ◽  
R. S. Chandel ◽  
S. C. Verma ◽  
B. B. Fand ◽  
...  
2019 ◽  
Vol 47 (5) ◽  
pp. 683-692 ◽  
Author(s):  
Dimitris M. Papadimitriou ◽  
Eleftherios A. Petrakis ◽  
Konstantina A. Arvaniti ◽  
Athanasios C. Kimbaris ◽  
Moschos G. Polissiou ◽  
...  

2021 ◽  
pp. 304-342
Author(s):  
Lynn E. Long ◽  
Gregory A. Lang ◽  
Kaiser Clive

Abstract This chapter provides information on the various economically important insect and arthropod pests causing damage to cherry production, such as Rhagoletis indifferens, Drosophila suzukii, Choristoneura rosaceana, Tetranychus urticae and Caliroa cerasi, among others. Notes on their life cycle, damage and management methods are also presented.


1970 ◽  
Vol 16 ◽  
pp. 109-114 ◽  
Author(s):  
Najmoon Naher ◽  
Md Wahedul Islam ◽  
M Khalequzzaman ◽  
Mohd Mainul Haque

The duration of developmental stages of Tetranychus urticae Koch was studied in different months of a year at room temperature. In addition fecundity of this mite was also observed in winter, autumn and summer seasons. T. urticae eggs hatched to larvae in the shortest duration of 1.07 ± 0.26 days and the longest duration of 11.67 ± 2.33 days in April and January, respectively. The larval period of T. urticae took the shortest time of 0.55 ± 0.50 days in May and 2.93 ± 1.07 days in December. The protonymph transformed to deutonymph in 0.89 ± 0.32 day in May and 3.71 ± 1.94 in December and January. The deutonymph required the shortest duration of 0.92 ± 0.41 days in August and the longest of 10.26 ± 1.48 days in January. The temperature played significant (P<0.001) role on the duration of developmental stages of T. urticae. The high temperature accelerated the developmental rate and reduced the duration of developmental periods. Its life cycle completed within 4.22 ± 0.46 days at 28.53 ± 3.17°C but 28.33 ± 2.36 days at 13.78 ± 2.36°C. A female T. urticae deposited 82.46 ± 4.11 eggs in autumn, 62.96 ± 12.09 eggs in summer and 58.21 ±1 3.65 eggs in winter. Key words: Developmental stages, Tetranychus urticae, temperature, fecundity   DOI:10.3329/jbs.v16i0.3751 J. bio-sci. 16: 109-114, 2008


Author(s):  
Betty Ruth Jones ◽  
Steve Chi-Tang Pan

INTRODUCTION: Schistosomiasis has been described as “one of the most devastating diseases of mankind, second only to malaria in its deleterious effects on the social and economic development of populations in many warm areas of the world.” The disease is worldwide and is probably spreading faster and becoming more intense than the overall research efforts designed to provide the basis for countering it. Moreover, there are indications that the development of water resources and the demands for increasing cultivation and food in developing countries may prevent adequate control of the disease and thus the number of infections are increasing.Our knowledge of the basic biology of the parasites causing the disease is far from adequate. Such knowledge is essential if we are to develop a rational approach to the effective control of human schistosomiasis. The miracidium is the first infective stage in the complex life cycle of schistosomes. The future of the entire life cycle depends on the capacity and ability of this organism to locate and enter a suitable snail host for further development, Little is known about the nervous system of the miracidium of Schistosoma mansoni and of other trematodes. Studies indicate that miracidia contain a well developed and complex nervous system that may aid the larvae in locating and entering a susceptible snail host (Wilson, 1970; Brooker, 1972; Chernin, 1974; Pan, 1980; Mehlhorn, 1988; and Jones, 1987-1988).


Author(s):  
J. W. Horn ◽  
B. J. Dovey-Hartman ◽  
V. P. Meador

Osmium tetroxide (OsO4) is a universally used secondary fixative for routine transmission electron microscopic evaluation of biological specimens. Use of OsO4 results in good ultrastructural preservation and electron density but several factors, such as concentration, length of exposure, and temperature, impact overall results. Potassium ferricyanide, an additive used primarily in combination with OsO4, has mainly been used to enhance the contrast of lipids, glycogen, cell membranes, and membranous organelles. The purpose of this project was to compare the secondary fixative solutions, OsO4 vs. OsO4 with potassium ferricyanide, and secondary fixative temperature for determining which combination gives optimal ultrastructural fixation and enhanced organelle staining/contrast.Fresh rat liver samples were diced to ∼1 mm3 blocks, placed into porous processing capsules/baskets, preserved in buffered 2% formaldehyde/2.5% glutaraldehyde solution, and rinsed with 0.12 M cacodylate buffer (pH 7.2). Tissue processing capsules were separated (3 capsules/secondary fixative.solution) and secondarily fixed (table) for 90 minutes. Tissues were buffer rinsed, dehydrated with ascending concentrations of ethanol solutions, infiltrated, and embedded in epoxy resin.


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