Inhibition of development of Ostertagia ostertagi – effect of temperature on the infective larval stage

Parasitology ◽  
1982 ◽  
Vol 85 (1) ◽  
pp. 27-32 ◽  
Author(s):  
M. G. Smeal ◽  
A. D. Donald

SUMMARYPopulations of Ostertagia ostertagi established from fresh larvae and from larvae stored at 4 °C for up to 12 weeks contained about 10% inhibited early 4th-stage larvae. This value rose to 21% after 16 weeks, due to an increase in numbers of inhibited larvae while adult numbers remained unchanged. Storage at 15 °C had no effect. In the case of larvae stored at 4 °C for 8 weeks, increasing the larval dose to 90000 had no significant effect on the proportion of the dose which was inhibited. The response to low temperature storage was much weaker than in previously reported studies on British populations, which accords with our earlier conclusion that low temperature cannot be the effective stimulus for inhibition in Australia.

Alloy Digest ◽  
1964 ◽  
Vol 13 (8) ◽  

Abstract USS 9% Nickel Steel was specifically developed for low-temperature storage vessels operating down to minus 320 F. It is recommended for cryogenic service. This datasheet provides information on composition, physical properties, elasticity, and tensile properties as well as fracture toughness. Filing Code: SA-166. Producer or source: United States Steel Corporation.


2006 ◽  
Vol 75 (3) ◽  
pp. 209-212 ◽  
Author(s):  
Kodthalu Seetharamaiah Shivashankara ◽  
Seiichiro Isobe ◽  
Hiroshi Horita ◽  
Makiko Takenaka ◽  
Takeo Shiina

2020 ◽  
Vol 147 ◽  
pp. 01015
Author(s):  
Dimas Fendy Pradana ◽  
Ignatius Hardaningsih ◽  
Dini Wahyu Kartika Sari

The objectives of this study were to evaluate the sperm viability of Najawa carp (Cyprinus carpio L.) in cryopreservation pre-conditions at 4°C. The design used in this study was Complete Randomized Design with 4 treatments, BSS as a control, 10% DMSO, 0,2 M Sucrose, and 5% DMSO + 0,1 M Sucrose; each consist of three replications. The parameters observed were progressive motility of fresh sperm, diluted sperm before low temperature storage, and 2 hours; 3 hours; 4 hours; 5 hours; one day; one week; a month after 4°C storage. The data were analyzed by ANOVA. The data showed that there was no significant difference between treatment (P>0.05). The best viability was 40.56% of sperm motility which survive for one week, it was achieved by 5% DMSO + 0,1 M Sucrose.


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