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Heifers were treated with the recommended doses of ivermectin: 0.2 mg/ kg bw by subcutaneous injection or 0.5 mg/kg bw by pour-on. An analytic procedure is described and used for the detection of ivermectin residues excreted in dung. A large amount of the higher pour-on dose was excreted during the first five days after dosing due to a more rapid distribution to intestinal contents. Later faecal concentrations after the pour-on treatment were lower than those found after subcutaneous injection. No degradation of ivermectin was detected in pats exposed in the field for up to 45 days. Ivermectin excreted in dung voided 1–2 days after both treatments significantly reduced the number of dung inhabiting larvae of Aphodius spp. (Coleoptera: Scarabaeidae), but no effect was seen in dung deposited 13–14 days after treatments. Development of cyclorrhaphan larvae was inhibited in dung deposited up to 28–29 days after subcutaneous injection treatment, but only inhibited in dung deposited up to 13–14 days after pour-on treatment. The numbers of Nematocera larvae were not affected. In a laboratory bioassay the Diptera Musca autumnalis DeGeer and Haematobia irritans (Linnaeus) suffered higher mortality in dung from heifers treated by the subcutaneous injection 13–14 days earlier than in dung from heifers treated by pour-on at the same time. After subcutaneous injection, a significant reduction in the rate of decomposition was found in dung from heifers treated 1–2 days earlier, whereas pour-on led to a delayed decomposition in dung collected up to 13–14 days after treatment.

A total of 298 slugs belonging to four species, Arion lusitanicus, A. ater, A. ater rufus and Limax maximus, were collected from six different localities within a radius of 30 km from Copenhagen and examined for naturally acquired Angiostrongylus vasorum infection. Overall, 28 slugs (9%) were infected, but the prevalence varied among the studied localities: Rude Forest (26%), West Amager Forest (18%), Jaegersborg Forest and Deer Park (8%), Frederiksberg Park (4%), Assistens Cemetery Park (0%) and Frederiksberg Botanical Garden (0%). Only third-stage larvae (L3) were recovered from the slugs, in numbers ranging from 1 to 392 per slug. Overall 82% of the infected slugs harboured fewer than 10 larvae and only 14% harboured over 100 larvae.

Biological control of parasitic nematodes of domestic animals can be achieved by feeding host animals chlamydospores of the nematode-trapping fungus Duddingtonia flagrans. In the host faeces, D. flagrans develop traps that may catch nematode larvae. In experiments on agar, D. flagrans had a growth rate between 15 and 60 mm/week at temperatures between 20 and 30°C. The presence of nematodes induces the fungus to produce traps. The rate of trap formation in D. flagrans has an optimum at 30°C, producing 700-800 traps/cm 2 /2 days, when induced by 20 nematodes/cm 2 on agar. Approaching 10 and 35°C the ability to produce traps is gradually reduced. The response of chlamydospore production on agar to changes in temperature is the same as that for trap formation. On agar, at 10, 20 and 30°C D. flagrans loses its trap inducibility after 2-3 weeks. During the ageing process, increasing numbers of chlamydospores are produced up to a certain limit. The time for reaching maximum chlamydospore concentration coincided with the time for loss of induction potential. The implications of these results in relation to biological control in faeces are discussed.

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