Predation by Achaearanea tepidariorum (Koch 1841) on mealybugs Planococcus citri (Risso 1813) is facilitated by the design of its web, which features a tangle of sticky gumfooted lines, and wrap attacks as well as the ability to handle the prey, whose body is covered with a waxy secretion, via silk. Crawling, i.e., wingless, mealybugs (in particular those in the nymphal stages and adult females and, to a lesser extent, winged males) are caught by means of the gumfooted lines, covered with globules of an adhesive secretion. The process of wrap attack and subsequent handling of the captured prey is a series of the following consecutive events: (1) confining and immobilising the mealybugs with sticky silk; (2) biting with chelicerae and paralyzing the prey with a toxin; (3) detaching the confined prey, attached to the tense threads, from the plant surface and catapulting it toward the central section of the web; (4) wrapping the catapulted prey in viscid silk emitted by the spinning apparatus; (5) transporting the wrapped prey to the central section of the web; (6) wrapping the prey in the central section of the web in nonsticky silk, whose tufts are present in this part of the web even before the attack; (7) filling the prey with digestive fluid; (8) sucking the prey empty; and (9) cleaning the chelicerae and mouth parts. The process of silk tuft wrapping was described for the first time. The described ability to hunt mealybugs implies the possibility of using A. tepidariorum spiders for biological control of these pests.
Cocoons of Theridiosoma gemmosum consist of two main parts, the egg sac case and the stalk. The inner space of the egg sac case is filled with nonsticky flocculent silk. Measuring 600-800 nm in diameter, the flocculent threads are never made up of bundles of longitudinally oriented nanofibrils. The egg case wall consists of a lower layer of highly ordered threads and an upper layer of cover silk. The lower, permanently white layer consists of threads in a mesh-like arrangement, the thicker threads being 4-6 microm and the thinner threads being 2-3 microm in diameter. Each thread is a bundle of parallel nanofibrils, with a diameter between 150 and 300 nm. The silk secretions of these fibers, emitted from spigots, are processed by legs. The upper layer of the egg case is applied to the threads of the lower layer by direct rubbing against its surface, i.e. without the use of legs. In the lower and middle part of the egg case, the accumulated secretion forms a virtually compact encrustation, whereas in the upper, conically shaped, part of the egg case where it becomes the stalk, this secretion becomes substantially scarcer. The stalk is a continuation of the egg case, its proximal part made of fibers similar to those forming the inner layer of the egg case wall. The distal part of the stalk continues towards the suspension area either as a compact bundle of parallel fibers, or the stalk forks into two bundles of roughly the same thickness, which continue towards the suspension area separately. On the surface of objects onto which cocoons are attached, the secretion of the piriform glands acts as an adhesive sheet.
Scanning electron microscopy and atomic force microscopy were used to study the silk spinning apparatus and silks of Harpactea rubicunda spiders. Three types of silk secretions that are produced by three kinds of silk spinning glands (ampullate, piriform, and pseudaciniform) and released through three types of spigots, were confirmed for both adult and juvenile spiders. Silk secretions for the construction of spider webs for shelter or retreat are produced by the pseudaciniform silk glands. Silk secretions that are released from spigots in the course of web construction are not processed by the legs during the subsequent process of hardening. Pairs of nanofibril bundles seemed to be part of the basic microarchitecture of the web silk fibers as revealed by AFM. These fiber bundles frequently not only overlap one another, but occasionally also interweave. This structural variability may strengthen the spider web. High-resolution AFM scans of individual nanofibrils show a distinctly segmented nanostructure. Each globular segment is ∼30-40 nm long along the longitudinal axis of the fiber, and resembles a nanosegment of artificial fibroin described by Perez-Rigueiro et al. (2007).
The mating of Theridiosoma gemmosum consists of a series of successive copulations. In the interval between two consecutive copulations, the females unwind the silken threads released by the male spinning organs; these threads are known as draglines or lifelines. The silk thus obtained is rolled up by the females into bundles, which they ingest prior to the next copulation. In other words, the mating of T. gemmosum involves the transfer of nutrients from the male to the female via silk. The silk provided by the male during copulation and eaten by the female, can be considered a nuptial gift
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