Mastophora hutchinsoni

Mastophora are widely distributed throughout the world in temperate climates except for Euro Asia and South Africa. The M. hutchinsoni primarily reside in the northeastern regions of North America near areas of a more temperate climate. The range of locations in North America are from Minnesota to New Hampshire.

M. hutchinsoni primarily nest and feed in shrubs or short trees, where they hunt and build their webs. These spiders will often utilize nearby leaves and twigs as a location to place their egg sacs.[7] Due to the limited range of prey affected by the female’s aggressive mimicry technique, the predator frequently moves to different locations according to prey availability. They do so by riding a silken thread that travels with the direction of the wind.

Lacinipolia renigera

As a result of a highly specialized hunting technique that mimics the disparate chemical compositions of its prey, the hunting range for the M. hutchinsoni is limited to a couple families of male moths. The females typically hunt either Noctuidae moths consisting of the bristly cut-worm, bronzed cutworm, and smoky tetanolita or the bluegrass worm of the Pyralidae family during prime activity hours in the evening, which results in nocturnal hunting patterns.[6][7] In particular, the Lacinipolia renigera (bristly cut-worm) constitutes two-thirds of total prey biomass and, together with the Tetanolita mynesalis (smoky tetanolita), makes up to ninety percent of the overall diet of M. hutchinsoni.[3] Adult females will often capture more than one moth per night.[7]

Female M. hutchinsoni employ a specialized hunting tactic where they aggressively mimic the pheromones of moths to attract male moths near their bolas trap. Female moths produce a complex pheromone typically combining two compounds in a ratio specific to the species. This allows male moths to easily distinguish between mates of different species. The periods of activity for each moth are also different. For instance, the bristly cut-worm is active earlier in the night than the smoky tetanolita. Thus, the female spiders must adjust the level of chemicals produced to accommodate for different moths.[6][8]

Instead of producing bolas like adult females to capture their prey, spiderlings remain motionless in the margins of leaves in shrubs or trees and wait to quickly ambush small flies that pass. In preparation for capture, the early-instar spiders extend both of their front legs which contain small bristles that aid in capture. These immature spiders also seem to attract male Psychoda using a mechanism near to or the same as aggressive chemical mimicry.[7][8]

The males do not construct a bolas to capture. Although females lose the strong bristles on their front legs after maturation, the males retain these features. Accordingly, it seems that they reserve hunting tactics similar to juvenile spiders. Thus, the male spiders have a similar diet to spiderlings--psychodid flies .[7][8]

Bolas Web Design

Unlike many of the web designs constructed by its closely related species in the family of orb weavers, M. hutchinsoni do not form the typical two-dimensional orb web. Instead, the females primarily reside in a nearby leaf or plant while producing a single horizontal thread which they stay on and travel across during times of predation. At the terminal end, the spider forms an extremely adhesive orb which it quickly hurls in a circular pattern to capture flying prey.[1][7] The bolas is much more efficient at capturing moths as it prevents the prey from escaping through shedding its scales--an escape mechanism that would otherwise work on typical orb webs.[3] If there is no prey captured after a short while, the Mastophora brings the orb back and consumes it--preparing to form another one to replace the former. Such behavior has been attributed to the short-term efficacy of the orb’s stickiness. Accordingly, after a single use of the bolas, the female must form another if intending to hunt more prey.[2]

Spiderlings will hatch during the spring. The rate of development between the two sexes will differ as males develop much more quickly than females. While the males fully develop during the summer months, the females mature around the fall season.[7] During this gap, the mature males often leave their webs and reside in the webs of developing females awaiting to mate.[5]

The pheromone compositions are unique to their respective species of moth--this differentiation helps male moths recognize the correct mating partner. Accordingly, the pheromones usually contain a blend of multiple chemical components. The bristly cutworm which makes up the majority of the diet of the M. hutchinsoni emits a pheromone with (Z)-9-tetradecenyl acetate (Z9-14: Ac) and 3.8 percent (Z,E)-9,12-tetradecenyl acetate (ZE-9, 12-14: Ac). M. Meanwhile, Tetanolita mynesalis, the other main food source, emits a blend with two parts (3Z, 9Z)-(6S, 7R)-epoxy heneocosadiene and one part (3Z, 6Z, 9Z)-heneicosatrience). Nephelodes minians (the bronzed cutworm) holds a chemical composition consisting of a blend of (Z)-11-hexadecenal and (Z)-11- hexadecenyl acetate. M. hutchinsoni is not only able to synthesize the components of different chemical blends but also mimic the exact ratios.[3][9]

Despite being nocturnal hunters, M. hutchinsoni have poor vision and rather rely on prey wing vibrations to trigger bolas construction.[2] The female has tiny hairs on her legs that are sensitive to such vibrations. Using a cabbage looper moth as an intermediate wing vibration rate for the L.renigera and T. mynelasis, the bolas spider constructs a bolas a few minutes after being exposed to wing vibrations.[6]