The bionomics of swift moths. I.—The ghost swift moth, Hepialus humuli (L.)

1964 ◽  
Vol 55 (1) ◽  
pp. 147-160 ◽  
Author(s):  
C. A. Edwards

The larvae of two species of swift moths, Hepialus humuli (L.) and H. lupulinus (L.), live in the soil and are common under grass in the British Isles, but do not usually have any obvious effect upon the grass. The larvae of H. humuli are polyphagous and when they occur under agricultural or horticultural crops they may cause damage by feeding on the roots. Lettuce, strawberry and chrysanthemum are most frequently damaged.The adults, which are described, fly at dusk, the female seeking the male. The female lays between 200 and 1,600 eggs, with a mean of about 600, over a period of four days. Sweep-net catches showed the ratio of the sexes to be approximately equal, and mercury-vapour light-trap catches showed that the flight period in southern England is principally in June.In the laboratory, never less than 80 per cent, of eggs hatched, even in dry air, and the shortest incubation period, between 11 and 24 (mean 18) days, was at 20°C. At 5°C. they did not hatch, but remained viable for at least six months.The larvae were reared in small cells drilled in blocks of plaster of Paris, which were stood in a tray of water, or in vials containing a layer of moist plaster of Paris, and were fed on pieces of carrot.The growth of the larval head capsules was geometric and allowed 12 instars to be distinguished at 15°C.; at higher temperatures there may be more.The growth curve of the larvae was S-shaped with a very distinct fall in weight in each instar for several days before moulting. The daily intake of food was weighed, and the conversion rate shown to be small, ranging from 0·00058 to 0·04, as compared with 0·205 to 0·49 recorded for other Lepidopterous larvae.At 5°C., larvae did not develop beyond the second instar, nor beyond the fourth at 10°C. The optimum temperature for their development (mean period 224 days) was 15°C., although mortality was high. They developed at 20°C. more rapidly (mean 197 days) but more died. Larvae kept in a container sunk in the soil outdoors developed more slowly than those at 15°C. and had only reached the eighth instar by February (239 days after hatching). This evidence, together with that from an artificially infested plot in the field and general field observations, suggests that the usual life-cycle lasts two years.

1981 ◽  
Vol 71 (4) ◽  
pp. 621-629 ◽  
Author(s):  
John Bowden

AbstractAnalysis of catches of Chrysoperla carnea (Steph.) in a light-trap and a suction trap at Rothamsted, southern England, showed that the light-trap catch varied as predicted from a model proposed to describe the functioning of a light-trap: catch = constant × , where W = trap illumination and I = background illumination. After adjustment to allow for changes in illumination during the flight period of C. carnea, the light-trap catch was very similar to the suction-trap catch. For C. carnea, a light-trap provides as unbiased a sample as a suction trap, but because of variation in trap effectiveness with variation in illumination, light-trap catches obscure changes in activity and abundance. Although similar studies are desirable to confirm this for other species, it is suggested that in light-trap studies catches should be adjusted to allow for changes in illumination during flight or trapping periods.


1989 ◽  
Vol 79 (2) ◽  
pp. 185-192 ◽  
Author(s):  
W. J McGeachie

AbstractA Robinson 125-W mercury-vapour light-trap was operated at an exposed site near Cranfield aerodrome, south-eastern England. The effects of moon-light, temperature and wind speed on light-trap catch were investigated. The dependent variable, In (catch +1), was compared with the independent variables moonlight illuminance, air temperature and wind speed, using multiple regression analysis. An algorithm was developed and used to estimate moonlight illuminance. Increases in mean illuminance and mean wind speed were associated with a decreased light-trap catch. Increases in mean temperature were associated with an increased catch. When the moth catch was broken down into individual families and species, other trends became apparent. Catches of noctuid moths were unaffected by variation in mean illuminance, although they were influenced by variation in mean temperature and mean wind speed. On the other hand, catches of crambine moths were very sensitive to fluctuations in mean illuminance and mean wind speed although unaffected by changes in mean temperature. The multiple regression equations were used to predict future light-trap catches. The correlations between observed and predicted In (catch +1) for (a) all moths, (b) noctuid moths and (c) crambine moths, were very good. It is suggested that the observed moonlight trend for crambine moths is a consequence of changing behaviour as moonlight illuminance changes rather than the alternative of changing light-trap effectiveness.


1975 ◽  
Vol 65 (2) ◽  
pp. 303-348 ◽  
Author(s):  
John Bowden ◽  
Marjory G. Morris

AbstractUsing the inverse square law, estimates can be made of the distances at which illumination from a light-trap is equal to that from background sources. From these distances an index of trap radius can be constructed which can be considered as a measure of trap potential. Between new moon and full moon trap radii vary, depending upon the times of the night at which the trap may be operating, in ratios from about 10:1 to 15:1. A comparable index of light-trap catches can be calculated which allows catches to be examined in relation to changing radius of the trap. Analysis of a series of catches in Uganda and Ghana shows that many species are more abundant than expected in periods of moonlight, particularly at and near full moon, the biggest difference between new moon and full moon being about 10:1 for Marasmia trapezalis (Gn.), whereas the Isoptera, Bostrychidae and Spodoptera triturata (Wlk.) are 3–4 times more frequent at full moon. The ratios between catch at new moon and catch at full moon suggest that the primary determinant of catch is the frequency with which insects cross the boundary of a region of influence whose size is determined by a radius of equal energy. Deductions about the pattern of insect activity through a lunation, and nightly, and the general agreement between curves describing the change in radius of the trap and those of trap catches suggest that changes in catch over a lunation can be explained by changes in the effectiveness of the trap. When corrections are made to allow for such changes, all taxa show some increase in numbers in moonlit periods and in many taxa this increase is substantial. Correction of catches should take account of flight periodicity and this periodicity should, if possible, be confirmed by methods independent of light-traps.


1968 ◽  
Vol 58 (2) ◽  
pp. 279-294 ◽  
Author(s):  
D. G. Gibbs ◽  
A. D. Pickett ◽  
Dennis Leston

Pupulations of the West African cocoa capsids Distantiella theobroma (Dist.) and Sahlbergella singularis Hagl. were sampled in 1966–67 by several methods: fast knockdown over sheets with pyrethrum, mercury-vapour light-trap, direct counts in a small artificially established area of high population, and observations of presence or absence in randomly selected inspection squares.A population build-up in mature cocoa accompanies and probably directly depends on development of the main crop from July or August to October. When pods become scarce after harvesting there is in S. singilaris a period of dispersal in which the species becomes more widespread as feeding is transferred to vegetative tissues, and in D. theobroma a more local change of feeding sites.Subsequent events vary greatly between areas and between years. It is suggested that the extent to which capsids are able to utilise vegetative tissues varies and depends on nutritional changes in the external parenchymatous tissues from which their food is obtained.Low humidities during spells of harmattan in January and February almost certainly kill larvae in exposed situations, but feeding conditions following such periods may be particularly favourable to capsids as large rapid population increases can occur locally. The factors involved are obscure but may be related to processes of regeneration stimulated by leaf loss and other damage in dry conditions.The densities and seasonal patterns found are discussed in relation to results of previous workers and some implications for control briefly considered.


1983 ◽  
Vol 90 (2) ◽  
pp. 177-193 ◽  
Author(s):  
K. A. J. Herniman ◽  
J. P. T. Boorman ◽  
W. P. Taylor

SUMMARYNewborn calves were bled at monthly intervals and examined for serum antibodies to bluetongue virus (BTV). Maternal immunity persisted for 3 months and it was possible to calculate decay rates for virus neutralizing antibody. Calves were subclinically infected with BTV within a few months of becoming susceptible and neutralization tests were used to deduce the serotype responsible. A profile of virus activity was built up over a 12 month period. Frequent light trap catches were used to examine the population dynamics of suspected Culicoides vector species. Two species, imicola and schultzei were present throughout the wet and dry seasons and survival rates were sufficiently long to account for virus transmission at any time of the year.


1978 ◽  
Vol 29 (2) ◽  
pp. 107-115
Author(s):  
Hiroyuki TAKAOKA ◽  
Sinichi NODA ◽  
Susumu YAMAMOTO
Keyword(s):  

1973 ◽  
Vol 66 (3) ◽  
pp. 757-760 ◽  
Author(s):  
Augustine Day ◽  
J. M. Stanley ◽  
J. C. Webb ◽  
J. G. Hartsock
Keyword(s):  

1993 ◽  
Vol 83 (1) ◽  
pp. 59-65 ◽  
Author(s):  
Kiyomitsu Ito ◽  
Hachiro Sugiyama ◽  
Nik Mohd. Noor b. Nik Salleh ◽  
Chang Poon Min

AbstractDaily light trap catches of Scotinophara coarctata (Thunberg) were analysed from mid-September 1986 to December 1990 and the physiological status of the trapped adults was examined. The catch size fluctuated synchronously with the lunar phase; large catches occurred around the full moon period and very few adults were trapped around the new moon period. Seasonally, the catches were large from January to March and from July to September, while they were small from May to June and October to November. The seasonal fluctuations of the catches seemed to be related to the growth stages of the rice plants on which the adults multiplied. The sex ratio of trapped adults was biased toward males, unlike that of the cage-reared insects which was 1:1. Most of the trapped females showed undeveloped ovaries and some of these females appeared to have oviposited previously. Light-attracted adults showed a considerable tolerance to starvation and survived for 20–30 days when they were given water, but for only two days in the absence of water. When the light-attracted females were supplied with food, their ovaries developed rapidly and females with mature eggs were produced after nine days. When the starvation period was prolonged, the ovaries remained immature and the fat bodies reduced in size. The nocturnal take-off of the adults was not triggered simply by the full moon illumination. Adult eclosion did not synchronize with the moon cycle.


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