POPULATION SUPPRESSION BY TRANSMISSION OF INHERITED STERILITY TO PROGENY OF IRRADIATED CABBAGE LOOPERS, TRICHOPLUSIA NI

1969 ◽  
Vol 101 (5) ◽  
pp. 513-520 ◽  
Author(s):  
David T. North ◽  
Gerald G. Holt

AbstractLaboratory population experiments and theoretical calculations are presented that demonstrate effective population suppression by the introduction of partially sterile cabbage loopers into a native population. The use of partially sterile males is advantageous because they are highly competitive with native moths, and since their progeny are sterile provides for population suppression over at least three generations. It is projected, based on experimental results, that 92% control can be obtained for three generations through a single release of partially sterile males. This modification of the sterile-male technique for Lepidoptera could result in control and sizeable savings in cost. Insecticide and other forms of control can be used simultaneously without any effect on the efficiency of the release program.

1964 ◽  
Vol 96 (1-2) ◽  
pp. 143-143 ◽  
Author(s):  
M. D. Proverbs

Chemicals must be used to control the codling moth, Carpocapsa pomonella (L.), in most apple and pear growing areas throughout the world. Unfortunately, this practice has caused or contributed to greatly increased mite populations, decimation of many beneficial insects, insecticide resistance, soil poisoning, and other problems. Successful use of the sterile male technique against the codling moth would eliminate or alleviate a number of these problems. This technique consists essentially in the sustained over-flooding of the native population with sexually sterile males. The main prerequisites for its use include: (1) a method of inducing sterility or dominant lethality in the sperm without affecting normal behaviour or longevity of the male, (2) the released insects themselves must not be injurious or noxious, ( 3 ) the method of release should permit intimate mingling of the sterile males with the native population, and (4) the availability of an economical method of mass culturing the insect. Photographs illustrate how these prerequisites were investigated for the codling moth.


2016 ◽  
Vol 99 (sp1) ◽  
pp. 87-94 ◽  
Author(s):  
Cynthia L. Cagnotti ◽  
Andrea V. Andorno ◽  
Carmen M. Hernández ◽  
Leonela Carabajal Paladino ◽  
Eduardo N. Botto ◽  
...  

2003 ◽  
Vol 29 ◽  
pp. 424-434 ◽  
Author(s):  
Cheryl A. Kaye ◽  
John W. Heinrich ◽  
Lee H. Hanson ◽  
Rodney B. McDonald ◽  
Jeffrey W. Slade ◽  
...  

2020 ◽  
Author(s):  
Brendan J. Trewin ◽  
Daniel Pagendam ◽  
Brian J. Johnson ◽  
Chris Paton ◽  
Nigel Snoad ◽  
...  

AbstractRapid advances in biological and digital technologies are revolutionizing the population control of invasive disease vectors such as Aedes aegypti. Methods such as the sterile and incompatible insect techniques (SIT/IIT) rely on modified males to seek out and successfully mate with females, and in doing so outcompete the wild male population for mates. Currently, these interventions infer the success of mating interactions between male and female insects through area-wide population surveillance and observations of mating competitiveness are rare. Furthermore, little is known about male Ae. aegypti behaviours and biology in field settings. In preparation for a large, community scale IIT program, we undertook a series of mark-release-recapture experiments using rhodamine B to mark male Ae. aegypti sperm and measure mating interactions with females. We also developed the Spatial and Temporally Evolving Isotropic Kernel (STEIK) framework to assist researchers to estimate the movement of individuals through space and time. Results showed that ~40% of daily females captured were unmated, suggesting interventions will need to release males regularly to be effective at suppressing Ae. aegypti populations. Males moved rapidly through the landscape, particularly when released during the night. Although males moved further than what is typically observed in females of the species, survival was considerably lower. These unique insights will lead to a greater understanding of mating interactions in wild insect populations and lay the foundation for robust suppression strategies in the future.Author SummaryModern scientific techniques for controlling populations of the dengue vector, Aedes aegypti, utilize the mating biology of adult male mosquitoes to achieve suppression through a sterilization process. As the study of Ae. aegypti control has typically focused on adult female mosquitoes, knowledge on male movement, survival and mating interactions in the field is lacking. Here we undertook several mark-release-recapture experiments on adult male Ae. aegypti in Innisfail, Australia, and measured important biological parameters. For the first time in large field experiments, we employed rhodamine B as a marker that when fed to adult males, identified both marked males and the wild females they mated with. We observed males moving further through the landscape, but surviving for a shorter period, than previous measurements undertaken on females in a field setting. A high proportion (~40%) of unmated females suggests individuals are constantly available for mating. As such, sterile male strategies may need to release at regular intervals to achieve effective population suppression. The unique insights provided by this study will assist in designing future sterile male field interventions.


2011 ◽  
Vol 104 (6) ◽  
pp. 1999-2008 ◽  
Author(s):  
Rajendra Soopaya ◽  
Lloyd D. Stringer ◽  
Bill Woods ◽  
Andrea E. A. Stephens ◽  
Ruth C. Butler ◽  
...  

1988 ◽  
Vol 102 ◽  
pp. 71-73
Author(s):  
E. Jannitti ◽  
P. Nicolosi ◽  
G. Tondello

AbstractThe photoabsorption spectra of the carbon ions have been obtained by using two laser-produced plasmas. The photoionization cross-section of the CV has been absolutely measured and the value at threshold, σ=(4.7±0.5) × 10−19cm2, as well as its behaviour at higher energies agrees quite well with the theoretical calculations.


Author(s):  
R. H. Morriss ◽  
J. D. C. Peng ◽  
C. D. Melvin

Although dynamical diffraction theory was modified for electrons by Bethe in 1928, relatively few calculations have been carried out because of computational difficulties. Even fewer attempts have been made to correlate experimental data with theoretical calculations. The experimental conditions are indeed stringent - not only is a knowledge of crystal perfection, morphology, and orientation necessary, but other factors such as specimen contamination are important and must be carefully controlled. The experimental method of fine-focus convergent-beam electron diffraction has been successfully applied by Goodman and Lehmpfuhl to single crystals of MgO containing light atoms and more recently by Lynch to single crystalline (111) gold films which contain heavy atoms. In both experiments intensity distributions were calculated using the multislice method of n-beam diffraction theory. In order to obtain reasonable accuracy Lynch found it necessary to include 139 beams in the calculations for gold with all but 43 corresponding to beams out of the [111] zone.


Author(s):  
H. S. Kim ◽  
S. S. Sheinin

The importance of image simulation in interpreting experimental lattice images is well established. Normally, in carrying out the required theoretical calculations, only zero order Laue zone reflections are taken into account. In this paper we assess the conditions for which this procedure is valid and indicate circumstances in which higher order Laue zone reflections may be important. Our work is based on an analysis of the requirements for obtaining structure images i.e. images directly related to the projected potential. In the considerations to follow, the Bloch wave formulation of the dynamical theory has been used.The intensity in a lattice image can be obtained from the total wave function at the image plane is given by: where ϕg(z) is the diffracted beam amplitide given by In these equations,the z direction is perpendicular to the entrance surface, g is a reciprocal lattice vector, the Cg(i) are Fourier coefficients in the expression for a Bloch wave, b(i), X(i) is the Bloch wave excitation coefficient, ϒ(i)=k(i)-K, k(i) is a Bloch wave vector, K is the electron wave vector after correction for the mean inner potential of the crystal, T(q) and D(q) are the transfer function and damping function respectively, q is a scattering vector and the summation is over i=l,N where N is the number of beams taken into account.


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