** Attention Valued Customers,
In March 2013, we made a minor modification to our ez-Malaise trap. The mesh size of its white netting is 108 x 32 mesh/square inch (changed from 96 x 26 mesh/square inch). Please note this change before making purchases.
This headless emergence trap is a simplified version of our soil emergence traps. Instead of collecting bottles, it has a small loop sewn on ceiling from which to suspend objects, such as a tray or sticky trap.
The front panel of the headless emergence trap is of clear plastic for observation of insect activity; the three side panels are of white Polyester netting (108 x 32 mesh) for ventilation. The headless emergence trap has two openings: an 18-cm sleeve opening in the clear panel for removal of insects and a large dome-shaped zipper opening in the opposite mesh panel for easy access to inside.
Headless emergence trap is floorless. Like the amphibious emergence trap, the headless emergence trap has flaps around the base that can be covered with soil (60 X 60 cm) to keep insects inside. Loops at each corner are for tent pegs (not included) needed to stake down the trap in windy conditions.
Improvise an insect rearing cage by staking over plants.
Pack Contents
x1 Fabric Trap Body
x8 Fiberglass Rods (Ø4 mm, L55 cm, 2 spares)
x4 ABS Plastic Joints (2-Way)
x4 ABS Plastic Feets
Click to Search for Studies Using This Product Line
Collection of related articles from the last 10 years:
Silverleaf nightshade (Solanum elaeagnifolium), a reservoir host for ‘Candidatus Liberibacter solanacearum’, the putative causal agent of zebra chip disease of potato. Thinakaran et al. (2015). Plant Disease, 99(7), 910-915.
Avian malaria infection intensity influences mosquito feeding patterns. Jiayue et al. (2018). International Journal for Parasitology, 48(3-4), 257-264.
A new species of Contarinia Rondani (Diptera: Cecidomyiidae) that induces flower galls on canola (Brassicaceae) in the Canadian prairies. Mori et al. (2019). The Canadian Entomologist, 151(2), 131-148.
Host plant resistance promotes a secondary pest population. Straub et al. (2020). Ecosphere, 11(3), e03073.
Disentangling the mechanisms linking dispersal and sociality in supergenemediated ant social forms. Amaranta et al. (2021). Proceedings of the Royal Society B: Biological Sciences, 288(1949), 20210118.
Choice and No-Choice Feeding Assays of Cotton Fleahoppers (Pseudatomoscelis seriatus) on Cotton Expressing the Mpp51Aa2 Protein. Arthur et al. (2024). Agronomy, 14(1), 84.
