Development and reproduction of Stratiolaelaps scimitus (Acari: Laelapidae) with fungus gnat larvae (Diptera: Sciaridae), potworms (Oligochaeta: Enchytraeidae) or Sancassania aff. sphaerogaster (Acari: Acaridae) as the sole food source.

Stratiolaelaps (=Hypoaspis) miles (Berlese) (Acari: Mesostigmata: Laelapidae) is a polyphagous soil-dwelling predatory mite that is widely marketed for use in greenhouse production systems to manage populations of dark-winged fungus gnats, Bradysia spp. (Diptera: Sciaridae) and for supplemental control of thrips. The suggestion by Walter and Campbell (2003, Biol. Control 26: 253-269) that North American commercial cultures of S. miles may actually be S. scimitus was confirmed. The development and reproduction at 21-23 degrees C of S. scimitus provided ad libidum with one of three different prey--the fungus gnat Bradysia aff. coprophila (Lintner), potworms (Enchytraeidae), or Sancassania aff. sphaerogaster (Zachvatkin, 1937) (Acari: Astigmata: Acaridae)--were compared. Developmental duration of the egg and non-feeding larval stages were 2.47 and 1.11 days, respectively; mortalities were 8.3 and 5.5%. Stratiolaelaps scimitus failed to develop beyond the protonymphal stage when provided with S. aff. sphaerogaster alone, although some feeding was observed. Development and reproduction of S. scimitus was successful on both fungus gnat larvae and enchytraeids, with no influence of prey on protonymphal duration (4.70 days) and mortality (8.3%), or on deutonymphal duration (4.61 days) and mortality (6.1%). Adult female S. scimitus feeding on potworms, compared to those feeding on fungus gnat larvae, had a significantly shorter pre-oviposition period (2.69 vs. 4.59 days). However, diet did not influence other adult female developmental or reproductive characteristics (oviposition period, 18.6 days; post-oviposition period, 6.2 days; total adult longevity, 27.3 days; total number of eggs, 26.5). S. scimitus reared on potworms tended (p = 0.06) to have a higher intrinsic rate of increase, a higher finite rate of increase and a shorter doubling time (rm = 0.142 day(-1), lambda = 1.153, Dt = 4.85 days) than those reared on fungus gnat larvae (rm = 0.105 day(-1), lambda = 1.110, Dt = 6.58 days), but differences in net reproductive rate (R0) and generation time (G) were not significant.

Effects of greenhouse pesticides on the soil-dwelling predatory mite Stratiolaelaps scimitus (Acari: Mesostigmata: Laelapidae) under laboratory conditions.

Knowledge of the effects of pesticides on biological control agents is required for the successful implementation of integrated pest management (IPM) programs in greenhouse production systems. Laboratory assays were conducted to assess the effects of an acaricide (dicofol), two insecticides (chlorpyrifos and pyriproxyfen), and two fungicides (fosetyl-Al and mefenoxam) on Stratiolaelaps scimitus (Womersley), a soil-dwelling predatory mite widely marketed in North America under the name Hypoaspis miles (Berlese) as a biological control agent of dark-winged fungus gnats (Bradysia spp.). Eggs, larvae, protonymphs, deutonymphs, and adult male and female mites were first assayed using dicofol, an acaricide used in the experiments as a positive control, applied to filter paper in an enclosed arena. Protonymphs were assayed for lethal and sublethal effects against the remaining pesticides at maximum label-recommended rates applied to filter paper, by using dicofol as a positive control and water as a negative control. The larva and protonymph were the life stages most susceptible to dicofol, with estimated 24-h LC50 values of 9 and 26 mg m(-2), respectively. Chlorpyrifos was highly toxic to the protonymphs of S. scimitus, causing >95% mortality after 24-h exposure and 100% mortality after 48 h. In contrast, the insect growth regulator (IGR) pyriproxyfen was much less toxic to protonymphs of S. scimitus; pyriproxyfen caused no significant mortality, compared with <5% mortality in the water control. Mortality caused by the fungicides was also relatively low; 72-h exposure to fosetyl-Al and mefenoxam resulted in 17.4 and 27.5% mortality, respectively. The IGR and fungicides increased the duration of the protonymphal stage by 1.2-1.8-fold, but they had no effect on the duration of subsequent life stages, nor on the duration of preoviposition, oviposition, and postoviposition periods of adult females. Total numbers and viability of eggs laid by mites exposed to the IGR and fungicides did not differ from the negative control, although the average rate of egg production during the oviposition of mites exposed to fosetyl-Al was increased. Pyriproxyfen, fosetyl-Al, and mefenoxam are likely to be compatible with S. scimitus under field conditions, because these pesticides caused little mortality of protonymphs, and they did not negatively affect the development and reproduction of S. scimitus under extreme laboratory conditions. In contrast, the use of chlorpyrifos in conjunction with S. scimitus is not recommended unless more comprehensive testing under semifield or field conditions demonstrates compatibility.

Fungus gnats, Bradysia spp. (Diptera: Sciaridae), and other arthropods in commercial bagged soilless growing media and rooted plant plugs.

Fungus gnats, Bradysia spp., in greenhouses cause economic losses to horticultural producers by damaging young root systems during plant propagation, by spreading soilborne diseases, and by reducing the marketability of the crop. In a greenhouse cage study, our observations suggested that bagged soilless growing media or rooted plant plugs from wholesale distributors may be sources for the introduction of fungus gnats into commercial greenhouse facilities. To evaluate these possibilities, carefully collected samples of bagged soilless growing media stored in the greenhouse, as well as bagged soilless growing media and rooted plant plugs delivered from midwestern wholesale distributors, were incubated under controlled conditions in the laboratory. Fungus gnats emerged from soilless media stored in the greenhouse, soilless media delivered from wholesale distributors, and from rooted plant plugs delivered from wholesale distributors. These results demonstrate that pasteurization of even bagged soilless media may be essential to effectively managing greenhouse populations of fungus gnats. However, pasteurization is not an option for responding to contamination of rooted plant plugs. Preliminary evidence is provided that application of entomopathogenic nematodes may offer potential as a method for managing fungus gnats in plant plugs, so long as treatment is early. Other arthropods found contaminating soilless media and rooted plant plugs included the western flower thrips, Frankliniella occidentalis (Pergande), Collembola, Acari, Formicidae, Staphylinidae, Psychodidae, and other Diptera.

Method for quantitative sampling of fungus gnat larvae in soilless growing media.

A simple method is described for separating fungus gnat larvae from soilless growing media. Samples are first fractionated by water flotation with an inverted flask procedure and then the sediment is degassed under reduced air pressure and fractionated in magnesium sulfate (MgSO4) solution (density of 1.12 g cm(-3)). Fungus gnat larvae with only a small amount of contaminating debris are recovered from the surface of the MgSO4 solution for immediate counting or for preservation in alcohol. In evaluations of different commercial soilless growing media with a range of components, two repetitions of the water flotation step eliminated 20-40% of the dry weight of samples and virtually all of the perlite from further processing. Repeating both the water and MgSO4 flotations a third time only marginally improved the recovery of larval fungus gnats, Bradysia sp. nr. coprophila, added to pasteurized media. Extraction efficiency differed between instars and, to a lesser extent, between different types of media. Across three commercial soilless media tested, recovery was 24-33% for first, 68-85% for second, 85-95% for third, and 98-100% for fourth instars. Within combinations of media and instar, recovery was consistent. With this method, a 400-cm3 sample can be processed and be ready for counting in 1-1.5 h; samples can also be processed in batches or in assembly-line manner to process many samples per day. The method may also prove useful for quantitative recovery of shore fly larvae, thrips pupae, and other arthropods from soilless growing media.