Determining head capsule width of the mayfliesDeleatidiumspp. from labia lengths (note)

1987 ◽  
Vol 21 (1) ◽  
pp. 151-152 ◽  
Author(s):  
Michael S. Field‐Dodgson
1990 ◽  
Vol 38 (4) ◽  
pp. 347 ◽  
Author(s):  
GR Allen

A field study was undertaken to determine the phenologies of the solitary larval endoparasitoids Cotesia urabae and Dolichogenidea eucalypti in relation to that of their bivoltine host Uraba lugens. C. urabae had two generations within both the summer and the winter generation of U. lugens, and D. eucalypti had two generations in the summer but only one generation in the winter. D. eucalypti parasitised a narrower range of host sizes in the field. Both parasitoids attacked recently hatched (typically 1st instar) or 'small hosts' at the beginning at each host generation. In summer D. eucalypti was the first to emerge from hosts, but both D. eucalypti and C. urabae, emerged from hosts which had modes of 0.85-1.05 mm in head capsule width and 0.9-1.5 mg in dry weight (mid hosts). In winter, C. urabae emerged from hosts which had modes of 1.15 mm in head capsule width and 2.7 mg in dry weight (large hosts). Both species in summer, and C. urabae in winter, then proceeded to parasitise hosts of around these sizes to commence second parasitoid generations. In its second generation in summer and its first generation in winter, D. eucalypti typically emerged after most unparasitised hosts had pupated. Both species of parasitoid overwintered within the larval stage of their host. Levels of parasitisation appeared to be low, and dropped between first and second generations within each host generation. It was concluded that C. urabae and D. eucalypti displayed continuity of generations and a high level of synchronisation with U. lugens in the Adelaide region.


1975 ◽  
Vol 107 (9) ◽  
pp. 927-934 ◽  
Author(s):  
Gerard F. Iwantsch ◽  
Zane Smilowitz

AbstractThe effects of parasitism by Hyposoter exiguae (Viereck) on certain developmental parameters of Trichoplusia ni (Hübner) were influenced by host age at parasitism.Head-capsule growth increments for parasitized Trichoplusia ni became smaller with each successive molt during parasitism so that determination of instar on the basis of head-capsule width became impossible.Parisitized T. ni showed a proportionately smaller gain in weight from time of stinging until parasitoid emergence the older they were when stung (6 times for 3rd instars; 2 times for 4th instars; and no gain for 5th instars). This retardation was evident 24 h after parasitism. Essentially the same results were obtained for dry weight.Percentage dry weight of parasitized larvae tended to increase over control values until the 5th stadium when controls abruptly increased. Values for parasitized 5ths remained below the controls. Values found on the last days reflected those of the parasitoid which composed most of the mass inside the host cuticle.Hemolymph specific gravity in controls and parasitized 3rd instars oscillated with a frequency of one stadium in the 3rd, 4th, and early 5th stadia. Specific gravity of controls then rose to a maximum of 1.0501 in the prespinning phase and dropped by the pharate–pupal phase. Values for parasitized larvae in the 5th stadium rose slightly before leveling off, and parasitized 5th instars rose to a maximum on the next-to-last day. Maximum values attained for hosts parasitized as 3rd and 5th instars never reached that for controls on day 11. This may be related to the complete unacceptability or unsuitability of T. ni larvae for parasitism from day 11 on.


1977 ◽  
Vol 34 (2) ◽  
pp. 254-261 ◽  
Author(s):  
David M. Rosenberg ◽  
Allen P. Wiens ◽  
Ole A. Sæther

Cricotopus (Cricotopus) bicinctus (Meigen) and C. (C.) mackenziensis Oliver, two common species of Chironomidae in the Fort Simpson area, N.W.T., were examined for changes resulting from experimental field exposure to Norman Wells crude oil. Larvae of both species were always present in higher numbers on oiled than unoiled artificial substrates but numbers of C. bicinctus increased more quickly than C. mackenziensis in response to the oil. Cricotopus mackenziensis larvae occurred in higher numbers than C. bicinctus larvae on unoiled artificial substrates. Cricotopus bicinctus tended to dominate C. mackenziensis on oiled artificial substrates. Size of larvae, as measured by head capsule width, was unaffected by increased food supply during periods of maximum algal biomass on oiled artificial substrates. Larvae on oiled artificial substrates apparently produced part of another generation when compared to larvae on unoiled artificial substrates.


2016 ◽  
Vol 107 (4) ◽  
pp. 487-492 ◽  
Author(s):  
C.F. Farder-Gomes ◽  
M.A. Oliveira ◽  
P.L. Gonçalves ◽  
L.M. Gontijo ◽  
J.C. Zanuncio ◽  
...  

AbstractThe leaf-cutting ant Atta sexdens Forel (Hymenoptera: Formicidae) is one of the most damaging agricultural pests in the Neotropics. Management strategies predominantly rely on the use of general insecticides. What is needed are more species-specific and environmentally friendly options. Parasitioids such as phorid flies (Diptera: Phoridae) may be one such option, but a greater understanding of the ecology of the flies and their ant hosts is essential to devise biological control strategies. Here we report parasitism rates, ant host size, parasitoid abundance per host and resultant sex ratios of two phorid species Apocephalus attophilus Borgmeier and Eibesfeldtphora tonhascai Brown parasitizing A.sexdens. The two species achieved parasitism rates of 1.48 and 1.46%, respectively and the pupal period was 14.7 ± 1.1 days and 22.1 ± 2.8 days, respectively. There was no significant difference between the head capsule width of ants parasitized by either A. attophilus or E. tonhascai. Likewise, there was no significant effect between the head capsule width of parasitized and unparasitized ants for both species. A significant positive correlation was found between the head capsule width of the parasitized ants and the number of adult parasitoids A. attophilus emerged. Ants parasitized by E. tonhascai survived significantly longer than those parasitized by A. attophilus. There was no significant effect of ant head width on the sex ratio of the offspring of either parasitoid species and no significant difference in the sex ratio (male: female) of their offspring. In summary, these data addressed here are important steps when considering natural enemies for biological control. Studying survival of the parasitized ants, parasitoid offspring sex ratio and host size preference allows for a better understanding of ant natural biological control in the field and can help in rearing of A. attophilus and E. tonhascai in laboratory.


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