A tick assembly pheromone present in the excretory waste product of the soft tick, Ornithodoros porcinus porcinus (Walton), has been separated by high performance liquid chromatography (HPLC). It has been identified as guanine on the basis of absorption and mass spectral data, and bioassays using nymphs of Argas persicus (Oken). Guanine was active at a low concentration of 8 × 10 −12 M/cm 2 of filter paper. Guanine was shown to induce assembly in Amblyomma cohaerens Donitz larvae and Rhipicephalus appendiculatus Neumann adults.Various purines and ammonium salts tested in the assembly bioassay, and with exception of adenine, were shown to be active for A. persicus.
The peripheral nervous system of an ixodid and an argasid tick include the following components: (1) paired optic, cheliceral and pedipalpal nerves and unpaired stomodeal nerve arising from the pre-esophageal portion of the central nervous system (synganglion); (2) 4 pairs of pedal nerve trunks (each with appendicular and hemal branches) and 4 major pairs of opisthosomal nerves (including the paraspiracular, genital, postlateral-myosomal, and ano-myosomal nerves); and (3) the lateral "sympathetic" plexuses formed by contributions of hemal nerves arising from pedal ganglia and from the paraspiracular nerves. The salivary glands are multiply innervated by 4 pairs of nerves. The 1st pair arise from the pedipalpal nerves, the 2nd and 3rd from the lateral sympathetic plexuses, and the 4th from the paraspiracular nerves. Portions of the integument and the majority of non-appendicular muscles are innervated by various fine nerves arising from the lateral sympathetic plexuses and from the 4 pairs of opisthosomal nerves.
Histological observations using specialized techniques reveal neurosecretory cells in 18 centers throughout the rind (cortex) of the central nerve mass or synganglion of Dermacentor variabilis. Many cells contribute to complicated networks of neurosecretory pathways and tracts in pre- and post-esophageal portions of the synganglion. The four types of neurohemal-neuroendocrine associations found in Dermacentor resemble structures found in soft ticks (Argasidae) and in other Arachnida, but are more diverse than those described from any other single species. Neurosecretory terminals are distributed diffusely and in two concentrated associations within the perineurium of the synganglion and major peripheral nerves. Terminals are also distributed in the perineurial layers of lateral segmental organs which lie in the general hemocoel at the level of the pedal nerves. A retrocerebral organ complex surrounds the esophagus at its junction with the midgut. The complex includes dorsal and ventro-lateral lobes (containing neurosecretory terminals and intrinsic secretory cells1 and the proventricular (neurohemal) plexus. This plexus seems to be a modified (concentrated) cardioglial association. Cardioglial associations are also formed by the neurosecretory innervation of vascular walls of the dorsal aorta and circulatory sinuses which envelope the synganglion and major peripheral nerves. Inferential considerations of neurosecretory and endocrine interactions in the Acari are based on these anatomical and histological data which also provide the basis for evolutionary considerations of anatomical relationships and specializations in the neurosecretory systems of other Arachnida.
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