The causes of seasonal changes in numbers of the yellow dung fly, Scathophaga stercoraria (Diptera: Scathophagidae)

ABSTRACT. 1. Counts of adult Scathophaga stercoraria (L.) on cow pats were made in Houghall, County Durham, in 1964 and 1965.
2. A spring peak of numbers was due to adults (overwintered mainly as pupae or larvae) maturing and going to dung to breed. Numbers then dropped, rising to one or more peaks in late June—early July. In 1964 there was then a summer drop in numbers until late September. In 1965 high numbers persisted in summer associated with cooler, wetter weather. Autumn peaks in both years persisted until severe frosts or snow.
3. Mature adults, developed from eggs laid during the spring peak, form the first generation when breeding in mid-late June. No clear generations can be identified after this, due to eggs being laid daily (females have successive gonotrophic cycles). Changes in adult numbers breeding reflects survival of eggs and newly-hatched larvae 5–6 weeks earlier, and lower survival rates of adults in mid-summer compared with spring and autumn.
4. Adult Scathophaga numbers in vegetation rose as numbers on dung dropped. Females dissected to count ovariole tunica dilatations showed that most flies in vegetation were immature, with some parous flies hunting insects to develop the next batch of eggs.
5. Females on dung were dissected and found to range from immature to seven-parous. Those gravid for the first time were grossly under-represented, possibly due to wider dispersal.
6. It is suggested that seasonal changes in this r-strategist cannot be explained simply in terms of generations nor by the occurrence of adult diapause.     

Sex and immunity in the yellow dung fly Scathophaga stercoraria

The immune system is of increasing interest to evolutionary biologists. Immunity may trade-off against other fitness components, with recent work suggesting reproduction in particular impinges on immune defence. There may also be sex differences in the immune system. Additionally, while life history traits typically have low heritability, little is known about additive genetic variance of immunity. An insect's major defence against multicellular pathogens is to encapsulate the invader. Phenoloxidase (PO) is a key enzyme in the cascade resulting in the melanized capsule, and is often used to estimate resistance to an immune insult. We examined the effects of copulation, egg laying, sex and age on PO in Scathophaga stercoraria. We also measured the heritability of PO activity. The sexes differed in haemolymph PO activity and PO was significantly affected by age, but not by copulation or egg laying. There was significant heritable variation for haemolymph PO.     

On the copulation duration of the yellow dung fly (Scathophaga stercoraria)

We model the optimal copulation duration in the yellow dungflyScathophaga stercoraria, assuming that males optimize their reproductive success per day. The independent state-variables of a male are the actual sperm reserves, the female encounterrate and the time of the day. We used stochastic dynamic programming to predict the optimal copulation duration. The model predicts that copulation duration should increase (i) for larger males, (ii) for males with a better previous diet (iii) for males accepting more females (iv) for males staying away from the dung during a whole day. It also predicts that (v) males on a restricted diet should accept fewer matings, (vi) testes size should shrivel during the day, (vii) the correlation coefficient between copulation duration and sequence number should decrease with increasing initial sperm reserve and with increasing number of copulations performed on a given day.There are two essential differences between our model and a model of Parker (1992). (i) Our model assumes that males optimize per day. Parker's model assumes that males optimize per mating bout, one bout comprising many days. (ii) Since all the important state variables depend only on the moment of the copulation, our model does not assume a long-time memory in dungflies, and it is more flexible than Parker's model. Overall, both models explain the data available equally well.     

Size-dependent alternative male mating tactics in the yellow dung fly,Scathophaga stercoraria

Whenever males can monopolize females and/or resources used by females, the opportunity for sexual selection will be great. The greater the variation among males in reproductive success, the greater the intensity of selection on less competitive males to gain matings through alternative tactics. In the yellow dung fly, Scathophaga stercoraria, males aggressively compete for access to receptive, gravid females on fresh dung. Larger males are better able to acquire mates and to complete copulation successfully and guard the female throughout oviposition. Here we demonstrate that when an alternative resource is present where females aggregate (i.e. apple pomace, where both sexes come to feed), smaller males will redirect their searching for females from dung to the new substrate. In addition, we identify a class of particularly small males on the alternative substrate that appears never to be present searching for females on or around dung. Smaller males were found to have a mating ‘advantage’ on pomace, in striking contrast to the pattern observed on dung, providing further support for the existence of an alternative male reproductive tactic in this species.     

The heritability of sexually dimorphic traits in the yellow dung fly Scathophaga stercoraria (L.)

A precise method was used for estimating the proportion of heritable variation in two life history parameters of the yellow dung fly, whereby environmental components of variance were minimized. Significant heritable variation for body size was revealed for father to son and mother to daughter relationships. Variation in development time was not significantly heritable. There is a marked sexual dimorphism in body size in this species which is discussed in the light of the observed sex-genotype interaction in heritabilities and low genetic correlation for size between the sexes. It is suggested that opposing pressures of sexual and natural selection and/or genetic pleotropy may be responsible for the maintenance of heritable variation, and the evolution of sexual dimorphism in these two traits.     

Heteropopulation males have a fertilization advantage during sperm competition in the yellow dung fly (Scathophaga stercoraria)

Sexual conflict occurs whenever there is not strict genetic monogamy. The sexually antagonistic coevolution that potentially occurs because of this conflict involves adaptation by one sex followed by the counter-adaptation by the other, and may be thought of as an evolutionary arms-race. As a result of these cycles of antagonistic coevolution, females from one population may be less resistant to heteropopulation males, at least after short periods of allopatry, as they will not have evolved any resistance to them. We tested this prediction in yellow dung fly (Scathophaga stercoraria) populations from the UK and Switzerland. Males from each population mated as first and second males to females from each population, and the mean numbers of offspring sired by the last male to mate in each situation were compared. We also compared the fertility and fecundity of single females mated to males from both populations, as well as the fertility and fecundity of the F(1) crosses. Both crosses produced viable and fertile offspring and the offspring sex ratios were not skewed. However, the fecundity of F(1)-cross females was greater than that of the parentals. In the sperm-competition experiment, there was a significant interaction between male and female origin influencing the proportion of offspring sired by the second male to mate, with heteropopulation males always outcompeting conpopulation males. This effect was independent of copula duration and the delay between copulations. In a separate experiment, we tested to see whether this was due to female preference for genetically dissimilar males but found no evidence for paternity biasing based on genetic similarity. Our results therefore seem to be best explained by sexually antagonistic coevolution as females appear less resistant to males with which they have not coevolved.     

Temperature effects on egg size and their fitness consequences in the yellow dung fly Scathophaga stercoraria

Organisms and parts of an organism like eggs or individual cells developing in colder environments tend to grow bigger. A unifying explanation for this Bergmann's rule extended to ectotherms has not been found, and whether this is an adaptive response or a physiological constraint is debated. The dependence of egg and clutch size on the mother's temperature environment were investigated in the yellow dung fly Scathophaga stercoraria. Smaller eggs were laid at warmer temperatures in the field and the laboratory, where possible confounding variables were controlled for. As clutch size at the same time was unaffected by temperature, this effect was not due to a trade-off between egg size and number. Temperature-dependent egg sizes even persisted within individuals: when females were transferred to a cooler (warmer) environment, they laid third-clutch eggs that were larger (smaller) than their first-clutch eggs. The fitness consequences of these temperature-mediated egg sizes were further investigated in two laboratory experiments. Neither egg and pre-adult survivorship nor larval growth rate were maximized, nor was development time minimized, at the ambient temperature corresponding to the mother's temperature environment. This does not support the beneficial acclimation hypothesis. Instead, this study yielded some, but by no means conclusive indications of best performance by offspring from eggs laid at intermediate temperatures, weakly supporting the optimal temperature hypothesis. In one experiment the smaller eggs laid at 24 °C had reduced survivorship at all ambient temperatures tested. Smaller eggs thus generally performed poorly. The most parsimonious interpretation of these results is that temperature-mediated variation in egg size is a maternal physiological response (perhaps even a constraint) of unclear adaptive value. This revised version was published online in November 2006 with corrections to the Cover Date.     

Some effects of rearing the yellow dung fly Scatophaga stercoraria in cattle dung containing invermectin

Invermectin was added to cattle dung in controlled concentrations like those found in the pats of injected cattle, and the medium was used to rear larvae of the dung fly Scatophaga stercoraria. Ivermectin at 0.036 ppm (wt/wet weight) debilitates 50% of the larvae within 48 h. At 0.015 ppm, 50% of the larvae are unable to pupariate, while at 0.001 ppm, 50% of the larvae fail to reach the adult stage. Adults produced from larvae reared in pats containing 0.0005 ppm invermectin show high levels of fluctuating asymmetry in wing characteristics as well as deformities in the wing veins themselves. The data are discussed in relation to the effects of excreted ivermectin on pastureland biology.     

Copula in yellow dung flies (Scathophaga stercoraria): investigating sperm competition models by histological observation

While sperm competition has been extensively studied, the mechanisms involved are typically not well understood. Nevertheless, awareness of sperm competition mechanisms is currently recognised as being of fundamental importance for an understanding of many behavioural strategies. In the yellow dung fly, a model system for studies of sperm competition, second male sperm precedence appears to result from a combination of sperm displacement and sperm mixing. Displacement was until recently thought to be directly from the female's sperm stores, the spermathecae (i.e. males were thought to ejaculate directly into these stores), and under male control. However, recent work indicates displacement is indirect (i.e. males do not ejaculate directly into the sperm stores) and that it is female-aided, although the evidence was not based on direct observation. Here, we used histological techniques to directly determine interactions during copula and sperm transfer. Our results are consistent with inference and clearly show that males ejaculate into the bursa copulatrix. Our data are also consistent with active female involvement in sperm displacement, which is indirect, and indicate the aedeagus may remove some spermatozoa from the bursa at the end of copula. In addition, evidence suggests females aid sperm transport to and from the spermathecae, possibly by muscular movement of a spermathecal invagination.     

Developmental stability in yellow dung flies (Scathophaga stercoraria): fluctuating asymmetry,heterozygosity and environmental stress

The genetic basis for developmental stability, the ability of an organism to withstand genetic and environmental disturbance of development, is poorly understood. Fluctuating asymmetry (FA: small random deviations from symmetry in paired, bilateral traits) is the most widely used measure of developmental stability, and evidence suggests FA is weakly and negatively associated with genome‐wide heterozygosity. We investigated the genetic basis of developmental stability in the yellow dung fly. Fly lines were inbred for 16 generations at which time they were homozygous at the phosphoglucomutase (PGM) loci and PGM appears to influence FA in at least one other taxon. After 16 generations of inbreeding, lines homozygous for different PGM alleles were crossed and levels of FA for four metric traits were compared in the inbred and crossed flies. We also compared FA levels in these flies with previously gathered data on wild‐type (second generation outcrossed) flies, and additionally looked at the effects of two environmental stresses (larval food limitation and increased temperature) on FA. There were no significant differences in any measure of FA, nor in mean FA, in any trait when inbred and crossed flies were compared. Comparison of FA in these and wild flies also revealed no significant differences. Food limitation had no influence on FA, whereas heat stress increased FA of naturally, but not sexually, selected traits. Our results do not show a negative relationship between heterozygosity and FA, but support the notion that FA levels are stress, trait and taxon specific.     

Temporal and microspatial variation in the intensities of natural and sexual selection in the yellow dung fly Scathophaga stercoraria

Studies of phenotypic selection in natural populations often concentrate only on short time periods and do not quantify selection intensities. We quantified temporal and microspatial variation in the intensities of natural and sexual selection for body size in the yellow dung fly over 2 years. Female fecundity selection intensity remained approximately constant over the season with an overall mean ± SE of 0.187 ± 0.014. Selection intensity for male reproductive success, defined as eggs obtained by mating males, did not differ from zero, indicating there was no assortative mating by size. Sexual selection intensity for male mating success favouring large males was variable but overall strong in the two years (0.499 ± 0.053 and 0.510 ± 0.051). As theoretically expected for male–male competition, sexual selection intensity increased with competitor density and reached an asymptote at about 250 males per pat; it also decreased with time in spring and increased again in autumn as a function of density. Small males had the best chance of obtaining a female at very low male densities. Greater selection intensity for large size in males than females is consistent with, and might be responsible for, the observed sexual size dimorphism in this species, as males are larger. The seasonal pattern of mean male body size (smallest at the beginning and end of the season) most likely reflects mere environmental (primarily temperature) influences on phenotypic size.     

Taxonomy of the genus Scathophaga Meigen (Diptera: Scathophagidae) in Korea

Three species of the genus Scathophaga–S. mellipes (Coquillet), S. scybalaria (Linnaeus) and S. stercoraria (Linnaeus) – are treated in this study. Of these, S. scybalaria (Linnaeus) is reported for the first time from Korea. A key to the Korean species, their domestic localities and some illustrations are given.     

Effects of horn fly and house fly (Diptera: Muscidae) larvae on the development of parasitic nematodes in bovine dung

Laboratory studies were conducted to determine the effects of horn fly, Haematobia irritans (L.), and house fly, Musca domestica L., larvae on the development of a mixed population of parasitic nematodes in compressed and crumbled bovine dung. Fresh dung (100 g per sample) from a single calf passing trichostrongyle type eggs was infested with 150 horn fly or 150 house fly eggs. After 14-15 d, more horn flies and house flies had emerged from the compressed dung than from the crumbled dung, but more third stage parasitic nematode larvae were recovered from the crumbled dung containing either fly species than from dung containing no flies.     

The effect of sperm storage and timing of mating on offspring sex ratios in the yellow dung fly Scatophaga stercoraria

1. Offspring sex ratios in the yellow dung fly Scatophaga stercoraria were examined in the laboratory. 2. Previous work indicated that females using previously stored sperm to fertilise their eggs produced male‐biased sex ratios. This result may have been due to female influences or the effects of sperm storage per se. 3. This pattern was not reproduced in the study presented here. Females that were allowed to mate just prior to oviposition produced similarly male‐biased sex ratios to those females that used previously stored sperm to fertilise their clutch. 4. Captive‐reared females may have perceived a lack of males in the population and thus produced a male‐biased offspring sex ratio. Alternatively, gamete ageing or extra‐chromosomal sex ratio distorters may have produced the male bias.     

Oviposition of the dung beetle Aphodius ater in relation to the abundance of yellow dungfly larvae (Scatophaga stercoraria)

1. The dung beetle Aphodius ater and the yellow dungfly Scatophaga stercoraria are temporally co-occurring species in sheep dung, which they use for reproduction and nutrition ( A. ater ) or for reproduction only ( S. stercoraria ) during the spring in northern Germany. Scatophaga stercoraria uses fresh sheep dung pellets a few hours old for oviposition, whereas A. ater lays eggs into 2–10-day-old pellets. In the present study, the egg laying behaviour of A. ater in sheep dung in relation to the presence of larvae of S. stercoraria was investigated experimentally.
2. Choice experiments, based on examining the egg laying behaviour of beetles in 2- and 4-day-old pellets with and without high and low densities of fly larvae, showed the following. In 2-day-old pellets, the beetles did not distinguish between pellets without fly larvae or with fly larvae at low larval density but avoided laying eggs into pellets with a high larval density. In 4-day-old pellets, the beetles always preferred to lay their eggs into pellets without fly larvae, regardless of larval density.
3. The influence of different densities of larvae of S. stercoraria on dung depletion was examined by measuring the dry weight, organic matter content and organic nitrogen content of the remaining dung after larval development. The presence of the larvae led to a reduction in all three parameters.
4. The beetles' behaviour of laying eggs into older pellets, and their awareness of the presence of high densities of fly larvae, enables them to avoid egg laying into pellets that will have been depleted by fly larvae before the beetle larvae have finished their development.     

Effects of ivermectin and doramectin faecal residues on the invertebrate colonization of cattle dung

Abstract: The effects of avermectin [ivermectin (IVM) and doramectin (DRM)] faecal residues on dung colonization and degradation by invertebrates were evaluated during late spring in the east of La Pampa province, Argentina. The study was conducted after collection of faecal material from animals (10 steers per group) allocated to the following groups: untreated control group (CG) and groups treated subcutaneously (200 μg/kg) with either DRM (DG) or a long‐acting formulation of IVM (IG). Fifty pats (550 g each) per group were collected, prepared and deposited on the field on days 3, 7, 16 and 29 post‐treatment (pt). Eight pats per group were recovered after 7, 14, 21, 42, 100 and 180 days post‐deposition (pd) on the field. The weight, percentage of dry matter, number of arthropods and nematodes from faeces were determined. The faecal concentrations of IVM and DRM were measured by high performance liquid chromatography (HPLC) throughout the trial period to correlate the pattern of drug degradation in dung with pd time. The total number of arthropods in dungs from CG was higher (P < 0.05) than those counted between days 3 and 29 pt in IG and DG. A decrease in the number of Coleoptera larvae (P < 0.05) between days 21 and 42 days pd was observed in both treated groups. Diptera larvae counts in CG pats were significantly higher (P < 0.05) than those obtained in treated groups in the 7‐ and 14‐day‐old pats. A lower number (P < 0.05) of Collembola, compared with pats from CG, was recovered from IG and DG pats deposited at days 3 and 7 pt and exposed from day 42. The counts of Acari in pats from treated animals were lower (P < 0.05) than those observed in CG pats at 3, 8 and 16 days pt. There were no differences neither in adult Scarabaeidae recovered nor in the proportions of dung buried and destroyed by great dung beetles. Dung specific nematodes were reduced (P < 0.05) in IG and DG pats from 3 and 7 days pt compared with those of CG pats. The comparative results shown here demonstrate that the negative effects of both IVM and DRM on dung colonization are similar. The pattern of drug degradation in the environment was very slow. High residual concentrations of both active parent compounds were recovered in dungs exposed in the field for up to 180 days pd. Concentrations as high as 13 ng/g (IVM) and 101 ng/g (DRM) were measured in faeces obtained from pats deposited on day 27 pt and exposed to the environment during 180 days. The results show a decrease in invertebrate colonization of dung recovered from IVM‐ and DRM‐treated cattle, which is in agreement with the large drug residual concentrations measured in faeces.     

Effects of the veterinary antiparasitic drug eprinomectin on dung beetles (Coleoptera: Scarabaeidae), the non-pest fly Neomyia cornicina and pest fly Haematobia irritans (Diptera: Muscidae) in Japan

Effects of the antiparasitic drug eprinomectin were studied in the laboratory and field experiments in Hokkaido, Japan, by pour-on administrations (500 μg/kg) on the pest fly Haematobia irritans (Linnaeus), nontarget coprophagous fly Neomyia cornicina (Fabricius), and the dung beetles Caccobius jessoensis Harold and Liatongus minutus (Motschulsky). Eprinomectin excreted into cattle dung was highest at 3 days post-treatment in both experiments, then it declined rapidly at 7 days and was not detected on or after day 14 post-treatment. In laboratory experiments, pupation and emergence rates of H. irritans and N. cornicina were hampered from 1 to 14 days post-treatment. There were no significant differences in the numbers of brood balls constructed by C. jessoensis in dung from treated and control cattle. Adult emergence rates of C. jessoensis were significantly reduced on days 1 and 3 post-treatment in dung from treated cattle. There were no significant differences in the numbers of brood balls constructed by L. minutus in dung from treated and control cattle, but survival rates of larvae were significantly reduced on days 1 and 3 post-treatment. In field experiments, the numbers of brood balls by L. minutus recovered from beneath dung pats were significantly larger in number in dung from treated cattle, suggesting that adult beetles are attracted to dung pats from treated cattle. Survival rates of larvae in these brood balls of L. minutus were significantly reduced 1 day post-treatment in dung pats from treated cattle, and equivalent levels to the control were restored 7 days post-treatment. The results are discussed in relation to the effects of endectocides on nontarget insects in grazing pastures.