Comparative morphology and ultrastructure of the mouthparts in unfed larvae of <Emphasis Type="Italic">Platytrombidium fasciatum</Emphasis> and <Emphasis Type="Italic">Camerotrombidium pexatum</Emphasis> (Acariformes: Microtrombidiidae)

The mouthparts of unfed larvae of Platytrombidium fasciatum (C. L. Koch, 1836) and Camerotrombidium pexatum (C. L. Koch, 1837) (Acariformes: Microtrombidiidae) were studied using both light optical (whole-mounted specimens, toluidine blue stained semi-thin sections) and electron microscope (TEM, SEM) methods. The mouth apparatus incorporated within the gnathosoma occupies an axial position and is covered from above by the arched dorsal shield, or scutum. The chelicerae are comparatively long and separated, and the lateral lips form a permanent apomorphic sucker provided with an internal cuticular sclerite. The pharynx is extremely wide and totally fused with the bottom of the infracapitulum. The pharyngeal dilators originate on the posterior portions of the cervix (epistome) and on the capitular apodemes and run nearly parallel to the cervix to the dorsal pharyngeal wall. Comparatively short sigmoid pieces serve as origin of the muscles—cheliceral levators inserting on the posterior wall of the basal cheliceral segments. There are two sets of the extrinsic gnathosomal muscles originating on the posterior portion of the scutum: retractors of chelicerae inserting on the posterior portions of the basal cheliceral segments, and retractors of the gnathosoma inserting on the very posterior parts of the capitular apodemes. The labrum and the cervix delimit the pharynx and the subcheliceral space. The labrum and the cervix for the most part are weakly sclerotized cuticular plates and do not have own muscles. The larval mouth apparatus, in comparison with that of adult microtrombidiid mites, is simply organized and more specialized for ingestion of large masses of liquid food.     

The anatomy of the adult uropodid Fuscouropoda agitans (Arachnida; Acari), with comparative observations on other Acari

A thin, compressible, lateral suture and ventral plate overlap permit limited movement of the thick and rigid dorsal and ventral plates of Fuscouropoda agitans. Seven pairs of large dermal glands debouch onto the surface. Trochanteral rotation permits defensive leg adpresion and an insectan type of ambulation. The complex hypopharynx-pedipalpal-coxae has a buccal and cheliceral cavity separated by an atriculated epipharynx. The pharynx is Y-shaped in cross section. Extensive paired salivary glands lie above the very long and dexterous 3-segmented chelicerae, and a large pair of coxal glands debouch on coxae 1. From four blunt-ended tracheae, bundles of unbranching tracheoles extend in specific tracts to all organs. The ventriculus is small with three pairs of large caeca; a tightly packed single layer of digestive cells individually enlarged to absorb-phagocytize and digest the food. A typical mesostigmatid excretory tube is present. A typical acarine synganglion is present; mixed nerves have a basal swelling. A postulated neurosecretory organ arises from the pedipalpal nerve. The oocytes enlarge within funicular stalks from the walls of the small median ovary. A large spermatophore is stored in the seminal vesicle; fertilization occurs during oviposition. A tension hinge partially opens both male and female genital plates; closure effected by muscles acting on very long genital plate apodemes. Within sequentially produced spermatogonial cysts of the testes, meiosis is completely synchronous. A large, multilobed male accessory gland produces a large volume of seminal fluid; a mixture of at least four secretions. The origins and msertions of the body wall, genital organ, digestive tract, mouthpart and leg muscles are listed and illustrated. A comparison of anactinotrichid and actinotrichid mites indicates fundamental and consistent morphological differences in aspects of the cuticle, leg articulations, digestive system, excretory system, reproductive system and coxal glands.     

Functional morphology and ultrastructure of mouthparts in unfed water mite larvae Piona carnea (Koch, 1836) (Acariformes: Pionidae)

Mouthparts of unfed larvae Piona carnea (Koch, 1836) (Acariformes: Pionidae) were studied on whole-mount preparations, semi-thin sections and with TEM and SEM methods. The mouth apparatus is incorporated within the pseudotagma, gnathosoma, composed of the infracapitulum and of the chelicerae resting on the roof of the latter. The gnathosoma inclines to the long axis of the body and is inserted at its base into the idiosoma by the circumcapitular fold. The basal cheliceral segments are long and fused. An anterior projection, the proposed fused fixed digits, protrudes from the distal end of the basal cheliceral segment forward between the movable digits. The movable digits are always found in protruded position, strongly curved upward and show a groove on their inner sides. The ventral wall of the infracapitulum is made of the mentum posterior and the malapophyses anterior to the palp articulation. The malapophyses are squeezed between the large palps and envelope the distal portion of the chelicerae from the sides. The ventral portion of the fused malapophyses are provided with a characteristic ventral cuticular fork of unknown function. Each malapophysis terminates by a flexible lateral lip provided by several rigid jags looking posterad. The palps face downward and backward, and bear on the tibia the large curved palpal claws turned laterad. The palp femur bears on the ventral aspect a characteristic wide spade-like projection provided with its own muscles originating on the dorsal wall of the femur. The labrum is a thick cuticular arrow-like structure protruding forward into the preoral cavity, whereas the cervix is a thin weakly sclerotized plate. The particular labral valve projects forward from the dorsal basis of the labrum into the preoral cavity. The labrum and the cervix are provided by their own small labral and cervical muscles originating on the cervical apodemes. The pharynx is totally separated from the ventral wall of the infracapitulum and is devoid of ventral dilators. The dorsal pharyngeal dilators originate on the thick and sclerotized capitular apodeme and, posteriorly, on the paired cuticular branches, capitular apodemes, which end freely in the body cavity and are combined with the common salivary duct. The short sigmoid pieces serve for origin of the levator muscles of the chelicerae. Retraction of the gnathosoma and the chelicerae is mediated by several sets of muscles originating on the dorsal plate.     

Mouthparts in Leptotrombidium larvae (Acariformes: Trombiculidae)

Mouthparts of Leptotrombidium larvae (Acariformes: Trombiculidae), potential vectors of tsutsugamushi disease agents, were studied in detail using light microscopy, scanning electron microscopy, and transmission electron microscopy. The mouthparts incorporated within the pseudotagma gnathosoma are composed of the infracapitulum ventrally and the chelicerae dorsally. The ventral wall of the infracapitulum is formed by a wide mentum posteriorly and a narrowed malapophysis anteriorly. The malapophysis firmly envelops the distal cheliceral portions by its lateral walls. The lateral lips of the malapophysis are flexible structures hiding the cheliceral blades in inactive condition and turning back forming a type of temporary sucker closely applied to the host skin during feeding. The roof of the infracapitulum is formed by a weakly sclerotized labrum anteriorly and a cervix with the capitular apodemes extending posteriorly. The labral muscles are lacking. The capitular apodemes serve as origin for pharyngeal dilators running to the dorsal wall of the pharynx fused with the bottom of the infracapitulum. The basal cheliceral segments are separated from each other besides the very posterior portions where they are movably joined by the inner walls. The sigmoid pieces serve for insertion of the cheliceral elevators originating at the posterior portions of the basal segments. The movable digits reveal the solid basal sclerite and the cheliceral blade curved upward with a tricuspid cap on its tip. Dendrites of nerve cells run along the digits to their tips. The ganglia are placed within the basal segments just behind the movable digits. The chelicerae also reveal well developed flexible fixed digits overhanging the basal portions of the blades. The gnathosoma possesses several sets of extrinsic muscles originating at the scutum and at the soft cuticle behind it. Laterally, the gnathosoma bears five‐segmented palps with a trifurcate palpal claw. J. Morphol. 277:424–444, 2016. © 2016 Wiley Periodicals, Inc.     

Scanning electron microscopic observation of the pretarsal suckers of the honey-bee ectoparasite,Varroa jacobsoni (Gamasida: Dermanyssina)

The pretarsus of the female miteVarroa jacobsoni Oudemans (1904) consists of two main parts, a cuticular basal stalk and an extrudable, membranous ambulacral pad, the caruncle. The caruncle, when fully extruded and expanded, becomes a bilobed sucker, and when deflated, the entire caruncle is retracted into the basal stalk. The basal stalk of the pretarsus with the sucker fully retracted into it resembles an inverted cone with its narrow portion attached to the apex of the tarsus. The basal stalk consists of three large plates; two lateral and one median. The proximal end of each lateral plate bears a sclerotized claw-like structure which functions to support the expanded caruncle. The median plate possesses a long, narrow ridge process connecting the basal stalk with the caruncle, and functions to control retraction and protraction of the caruncle. The morphology and function of the basal stalk suggest that the claw-like structure are the ungues; the median plate is the unguifer, and the median ridge is the tendon of the retractor/depressor muscles of the pretarsus. The significance of the pretarsal suckers to the control of the mite is also discussed.     

Musculature of Notholca acuminata (Rotifera: Ploima: Brachionidae) revealed by confocal scanning laser microscopy

Abstract. The body-wall and visceral musculature of Notholca acuminata was visualized using phalloidin-linked fluorescent dye under confocal laser scanning microscopy. The body-wall musculature includes dorsal, lateral, and ventral pairs of longitudinally oriented body retractor muscles, two pairs of head retractors, three pairs of incomplete circular muscles, which are modified into dorso-ventral muscles, and a single pair of dorsolateral muscles. The visceral musculature consists of a complex of thick muscles associated with the mastax, as well as several sets of delicate fibers associated with the corona, stomach, gut, and cloaca, including thin longitudinal gut fibers and viscero-cloacal fibers, never before reported in other species of rotifers. The dorsal, lateral, and ventral retractor muscles and the incomplete circular muscles associated with the body wall appear to be apomorphies for the Rotifera. Muscle-revealing staining shows promise for providing additional information on previously unrecognized complexity in rotifer musculature that will be useful in functional morphology and phylogenetic analyses.     

Integument and sensory nerve differentiation ofDrosophila leg and wing imaginal discs in vitro

Summary An ultrastructural analysis is presented of the cuticular and neural structures formed by the prothoracic leg and wing imaginal discs of maleDrosophila melanogaster larvae during culture in vitro with 0.2 g/ml of -ecdysone. A pupal cuticle, and subsequently an imaginal cuticle with a well-defined epicuticle and a laminated endocuticle is formed. The ultrastructure of the epidermis and of cuticular structures such as bristles, trichomes, apodemes, and tracheoles is very similar to that found in situ. Dendrites and nerve cell bodies are formed in vitro, and sensory axons form nerve bundles similar to those of normal appendages in situ, despite their isolation from the central nervous system. It is concluded that at the ultrastructural level, differentiation in vitro closely parallels the normal course of development.     

Anatomy and function of the ptychoid defensive mechanism in the mite Euphthiracarus cooki (Acari: Oribatida)

Ptychoidy is a defensive adaptation of several groups of oribatid mites in which legs and coxisternum can be fully retracted into the opisthosoma and protected by a ventrally deflected prodorsum, resulting in a seed-like appearance. Using Euphthiracarus cooki as a model, we examined details of exoskeletal and muscular anatomy in combination with studies of live individuals to provide the first functional analysis of ptychoidy. There are two main functional components: the first is a set of exoskeletal and muscular adaptations, mostly of the podosoma and prodorsum, that combine to effect leg withdrawal and prodorsal deflection; the second comprises adaptations of the opisthosoma that allow control of hydrostatic pressure during the large hemocoel volume adjustments associated with ptychoidy. Adaptations important in the closing process (enptychosis) are found in four body regions. Much of the podosomal exoskeleton (especially pleural) is unsclerotized, which facilitates leg retraction and prodorsal deflection during enptychosis. The coxisternum has several flexible furrows along which it folds in order to bring legs into a tightly parallel arrangement. The prodorsum has specialized attachment surfaces (manubrium and inferior retractor process) for retractor muscles and a paired bothridial scale that participates in prodorsal alignment during enptychosis. The subcapitulum has a prominent capitular apodeme on which important retractor muscles insert. The mineralized notogaster has an anterior "collar" that accommodates the retracted prodorsum; it includes paired notches and receptacles that accommodate the bothridial scales, thereby creating a temporary fixed axis for rotation of the prodorsum in a "lazy hinge" mechanism. Specialized muscles form the retractor system; most conspicuous are the large coxisternal retractors and prodorsal retractors, both of which originate on the notogaster. Other components have adjustor roles; among them are muscles of the endosternal system that control retraction of the subcapitulum and assist leg retraction, and the dorsoventral muscles which adjust the folded coxisternum. Hemolymph pressure control is a function of the opisthosoma, where the principle exoskeletal elements form a pleated venter, having a cross-sectional shape like an inverted "W." Paired holoventral plates (each representing fused genital, aggenital, anal, and anal plates) form the inner angle and are flanked by paired plicature plates. The holoventral plates are connected medially in two ways : 1) by three permanent bridges of sclerotized cuticle that include an anterior phragmatal bridge and two widely spaced, hollow apodemes (preanal, postanal); 2) by temporary zipper-like closures of two different types. Lateral compression of the pleats is effected by a series of transversely arranged, lateral compressor muscles that run from plicature to holoventral plate edges, and from holoventral plate edges to the medial apodemes. Compression increases hydrostatic pressure in the opisthosoma and stores energy in both the slightly deformed, mineralized notogaster and in the three holoventral bridges. During normal activity the compressor system is active and the inflated podosomal region provides support for the extended legs. When the mite is irritated, the prodorsum is hydraulically ejected from its active position in the notogastral collar, then relaxation of the compressors causes a fall in hemolymph pressure and return of the notogaster to an undeformed condition. Muscles of the retractor system then act in specific sequence to retract and adjust the coxisternum and prodorsum until they are precisely positioned at the completion of enptychosis. The process takes between 0.5 and 1 sec. When irritation ceases, partial opening allows sensory leg hairs to "test" the environment. Resumption of normal, active posture (ecptychosis) involves activation of the lateral compressor system and hydraulic inflation of the podosoma, through which legs are extended and the prodorsum is reflected.     

Postemergence Growth in the Fly <Emphasis Type="Italic">Sarcophaga falculata</Emphasis> initiated by Neurosecretion from the Ocellar Nerve

THE formation of the endocuticle and growth of skeletal muscles which takes place in the fly after eclosion is termed the postemergence growth. An increase in volume of skeletal muscles was observed in Glossina¹ and the deposition of cuticular growth layers described for some orders of both Exopterygota² and Endopterygota³. The postemergence growth which was shown to be induced by some blood-borne factor from the head⁴, hitherto considered to be the tanning hormone bursicon⁵, is initiated by neurosecretion from the ocellar nerve of the pharate adult. Experiments have been performed which indicate that neurosecretion induces the growth of the endocuticle. The process of postemergence growth was assessed by measuring the size of the longitudinal skeletal apodemes. This begins after eclosion and is correlated with the growth in thickness of the cuticle. The enlargement of the surface of the apodemes also indicates the growth of the skeletal muscles, which spread over the newly deposited cuticle. This phenomenon is a constant feature of this species since more than 2,000 specimens were examined at different periods of the year and none were found in which postemergence growth had not occurred.     

Morphology of the prosomal endoskeleton of Scorpiones (Arachnida) and a new hypothesis for the evolution of cuticular cephalic endoskeletons in arthropods

Skeletomuscular anatomy of the scorpion prosoma is examined in an attempt to explain the evolution of two endoskeletal features, a muscular diaphragm dividing the prosoma and opisthosoma and cuticular epistomal entapophyses with a uniquely complex arrangement of muscles, tendons and ligaments. Both structures appear to be derived from modifications of the mesodermal intersegmental endoskeleton that is primitive for all major arthropod groups. The scorpion diaphragm is a compound structure comprising axial muscles and pericardial ligaments of segments VI to VIII and extrinsic muscles of leg 4 brought into contact by longitudinal reduction of segment VII and integrated into a continuous subvertical sheet. This finding reconciles a long-standing conflict between one interpretation of opisthosomal segmentation based on scorpion embryology and another derived from comparative skeletomuscular anatomy. A new evolutionary-developmental mechanism is proposed to account for the complex morphology of the epistomal entapophyses. Each entapophysis receives 14 muscles and tendons that in other taxa would attach to the anterior connective endoskeleton in the same relative positions. This observation suggests that the embryological precursor to the connective endoskeleton can initiate and guide ectodermal invagination and thereby serve as a spatial template for the development of cuticular apodemes. This mesoderm-template model of ectodermal invagination is potentially applicable to all arthropods and may explain structural diversity and convergence in cephalic apodemes throughout the group. The model is used to interpret the cephalic endoskeletons of two non-chelicerate arthropods, Archaeognatha (Hexapoda) and Symphyla (Myriapoda), to demonstrate the generality of the model.     

Coxal organs in geophilomorpha (Chilopoda). Organization and fine structure of the transporting epithelium

Summary The coxal organs of different Geophilomorpha were studied by scanning and by transmission electron microscopy.1) The coxae of the last trunk-segment contain pores in different arrangements and numbers. They are the openings of the coxal organs.2) The coxal organs are formed by four different cell types: the main epithelium consists of radially arranged transporting cells, surrounded by junctional cells, gland cells, and the cells of the pore channel.3) The cells of the transporting epithelium show an enlargement of the apical and basal surface. Deep and narrow extracellular channels of the apical infoldings are closely associated by mitochondria (plasmalemma-mitochondrial complexes). The epithelium is covered by a prominent cuticle with a spacious subcuticle.4) A distinct mucous layer covers the cuticle of the transporting epithelia, and is secreted by the gland cells.5) A small cellular sheath separates the epithelium of the coxal organ against the haemolymph.6) The possible function of the coxal organs in ion and fluid transport is discussed.     

Functional morphology and evolution of specialized mouthparts of Cephenniini (Insecta,Coleoptera, Staphylinidae,Scydmaeninae)

We present the results of a morphological study of the labium and labial (premental) discs in Cephenniini, ant-like stone beetles feeding on oribatid mites. The discs are composed of a cuticular plate connected by a circumferential ring with the hypopharyngeal suspensorium. The discs have likely developed from the premental cuticle and from internal sclerotizations of the labium. The shape of the external plate can be changed from flat to concave and vice versa by contractions and relaxations of the labial muscles. Contractions result in a flat or only slightly concave shape whereas during relaxation the discs become strongly concave and adhere tightly to the captured mite. Once this is achieved, detaining of the prey is energy-free. Based on known hypotheses concerning the evolution of Oribatida and Staphylinidae, we exclude the possibility of a co-evolution of “proto-Cephenniini” with yet unarmored “proto-Oribatida”, and suggest three alternative scenarios: i) the predators co-evolved with a particular early lineage of Oribatida that has acquired the hard armor relatively recently; ii) ancestors of Cephenniini gradually shifted from feeding on other types of prey towards fully armored Oribatida; or iii) the labial discs have originally developed for functions not related to feeding.     

Anatomy of the extrinsic gut musculature of Gammarus minus (Crustacea: Amphipoda)

Inserting on the buccal and esophageal foregut of Gammarus minus are numerous pairs of serially arranged dorsal dilator muscles, a single pair of lateral muscles, and two pairs of posterior muscles. Muscles of the cardiac stomach include three dorsal sets, a single pair associated with the pterocardiac ossicles, and two pairs inserting on the ventral aspect. A single pair of muscles inserts on the lateral aspect of the pyloric stomach. The extrinsic muscles of the foregut originate from exoskeletal apodemes of the cephalothoracic cuticle, sockets of the mandible, and a maxillary bridge that lies just ventral to the cardiac stomach. The extrinsic musculature of the hindgut is restricted to the rectal region and consists of paired dorsal and ventral series in an X-configuration. A single unpaired muscle inserts on the ventral midline. Extrinsic muscles of the hindgut originate from the integument of the last pleonic segment. The general arrangement of extrinsic gut muscles in G. minus is similar but not identical to that of other amphipods studied. However, the pattern is quite different from that of other malacostracans.     

Neural mechanisms governing distribution of cardiac output in an isopod crustacean,Bathynomus doederleini: reflexes controlling the cardioarterial valves

In Bathynomus doederleini all of the cardioarterial valves located at the origin of the lateral arteries are dilated by impulses of lateral cardiac nerves. Tactile stimuli applied to sensillar setae depress impulse activities of the 1st and 5th lateral cardiac nerves. The 1st lateral cardiac nerve controls the valve of the lateral artery which runs to the walking-legs and viscera. The 5th lateral cardiac nerve controls the valve of the lateral artery which runs to the swimmeret muscles. The response indicates that tactile receptor reflexes bring about decreased haemolymph flow to the organs. Augmented swimmeret movements were always accompanied by an increased firing rate in the 5th lateral cardiac nerve. Artificial full protraction of swimmerets simultaneously induced excitation of the 5th lateral cardiac nerve and inhibition of the 1st lateral cardiac nerve. The excitation corresponds to an increase in haemolymph flow to the swimmerets, and the inhibition a decrease in haemolymph flow to walking-legs and viscera. Three kinds of mechanoproprioceptors which were activated by swimmeret movements were found. Two of the mechanoproprioceptors are located at the base of the basipodite. The other mechanoproprioceptor supplies processes to a nerve to the retractor muscles. Activation of three kinds of mechanoproprioceptors, induced by artificial swimmeret protraction, triggered lateral cardiac nerve reflex responses.Abbreviations LA lateral artery - LCN lateral cardiac nerve - RMN nerve to retractor muscles - StR stretch receptor     

Regulation of air and blood flow through the booklungs of the desert scorpion, Paruroctonus mesaensis

Injections of dye, latex and India ink were used to reveal the path of hemolymph circulation through the scorpion booklungs. Fine, branched arteries carry blood directly to muscle and other organs. The blood returns through venous channels to the ventral mesosoma where it passes laterally through the booklungs and into the pneumocardial veins just beneath the pleural cuticle. Blood flows dorsally through these veins to the pericardial sinus and heart. The scorpion has four pairs of booklungs located in the anterior segments of the ventral mesosoma. Each booklung has a spiracle which opens into an atrium enclosed by cuticular membrane. Air passes from the atrium into the booklung lamellae. Agitation of the animal or application of CO(2) causes retraction of the anterior and posterior atrial membrane. This expands the atrial chamber and allows gas exchange in the booklung lamellae. The posterior atrial membrane has a specialized region which forms a springy valve. This normally closes the spiracle unless pulled open by contraction of the attached poststigmaticus muscle. The pectens and receptors within the atrium may mediate the responses to CO(2). Slender hypocardial ligaments containing muscle fibers extend from the heart (dorsal mesosoma) to the booklungs in the ventral mesosoma. Heart movements thus cause dorso-ventral movement of the booklungs. The significance of these movements is as yet unclear. They may increase ventilation, help force blood to the heart and/or agitate the blood and booklung lamellae and thereby aid gas exchange. Passage of blood through the booklungs is regulated by dorsal and ventral muscles attached to the atrium at the lateral edge of the booklung. Contraction of the ventral atrial muscle closes the excurrent channel for passage of blood from the booklung into the pneumocardial vein. Electrical stimulation of the segmentai nerves from the subesophageal and first three abdominal ganglia causes spiracle opening and contraction of muscles attached to the atrial membrane. A previous study showed that these same segmental nerves also modulate heart activity. They thus provide a major pathway for regulation of the respiratory and circulatory systems.     

Distribution of cuticular protein mRNAs in silk moth integument and imaginal discs

The distributions of mRNAs for two cuticular proteins of Hyalophora cecropia were examined with RT-PCR and in situ hybridization. For major regions of larval and pupal cuticle, there was a strong correspondence between the type of cuticle and the predominant cuticular protein message found. Epidermal cells underlying soft cuticle had mRNA for HCCP12, with a RR-1 consensus attributed to soft cuticle, while the epidermal cells associated with hard cuticle had predominantly mRNA for HCCP66, a protein with the RR-2 consensus attributed to hard cuticle. Both messages were found in all areas of the pupal fore- and hind-wings, with modest area-specific difference in concentration being much less than differences in the relative abundance of these cuticular proteins.

mRNA for HCCP12 was present in imaginal discs of feeding larvae of H cecropia. Data from Bombyx mori available at SilkBase (http://www.ab.a.u-tokyo.ac.jp/silkbase/) revealed that imaginal discs from feeding larvae had abundant mRNA for RR-1 cuticular proteins, representing six distinct gene products. Only discs from spinning larvae had mRNAs that coded for RR-2 proteins arising from 10 distinct genes. Thus, lepidopteran wing imaginal discs can no longer be regarded as inactive in larval cuticle production.     

The eye muscles and their innervation in the gobiid fishTridentiger trigonocephalus

The morphology and innervation of the six oculomotor muscles in the gobiid fishTridentiger trigonocephalus are described. Every rectus muscle is composed of two types of muscle fibres. Muscles attach onto the cartilaginous or fibrous sclerotica. Oblique muscles attach onto the ethmoidal plate; recti muscles attach onto the parasphenoid or a thick fibrous membrane. There is no myodome. The common oculomotor nerve is composed of four bundles, the trochlear and the externus of two. The two kinds of fibres of the lateral rectus and the two distinct bundles of the nerve VI suggest a possible homology between this muscle in fishes and the lateral rectus+retractor bulbi in mammals.     

Immunocytochemical mapping of FMRFamide-like peptides in the argasid tick Ornithodoros parkeri and the ixodid tick Dermacentor variabilis

FMRFamide-like immunoreactivity was studied in the argasid tick Ornithodoros parkeri and the ixodid tick Dermacentor variabilis using immunocytochemistry based on the peroxidase-antigeroxidase method. FMRFamide-like immunoreactive cells are widely distributed in various regions of the tick synganglion including protocerebral, cheliceral, stomodeal, palpal, pedal I–IV, and opisthosomal regions in both species. However, there is one layer of immunoreactive cells located on the dorsal surface of the postoesophageal part of the synganglion that is found only in D. variabilis. Besides the immunoreactivity within the cell body and its axons, the neuropile and the neural lamella (the extracellular sheath of the synganglion) are rich in immunoreactive materials. Some coxal muscles are innervated by the FMRFamide-like immunoreactive processes of the nerve from the pedal ganglion.     

Cyanoglucoside storing cuticle of Zygaena Larvae (Insecta,Lepidoptera)

Summary As a deterrent against predators, larvae of Zygaena trifolii release droplets of fluid containing cyanoglucosides from segmentally arranged cuticular cavities. Histological examinations show that during the moulting period, the old cuticle, including the cavities and the secretion within them, is degraded, with the exception of a thin mesocuticular layer forming the exuviae. When the endocuticular layer of the new cuticle is deposited, the cuticle detaches from the underlying epidermis in specific areas, which leads to the formation of the cuticular cavities. During a moult-intermoult sequence the concentration of cyanoglucosides in both the haemolymph and the defensive secretion shows specific changes. These changes seem to be related to the formation and degradation of the cavities. We suggest that during the moult the cyanoglucosides are transported through the epidermis into the haemolymph to prevent them from being wasted with the exuviae and, after ecdysis, are retranslocated into the newly formed cavities.     

The genitalia and accessory glands of the pseudoscorpion Cheiridium museorum (Cheiridiidae)

The genitalia of the male Cheiridium museorum Leach consists of a cup-shaped ejaculatory canal atrium which opens into a simple saccate genital atrium. Associated with the genital atrium are a number of thickened regions of the cuticle: the dorsal apodeme, lateral apodemes and lateral rods. These both support the genital atrium and provide regions for muscle attachment. Two pairs of accessory glands, anterior and posterior dorsal glands, are present.
The genital atrium of the female is divided into a median and two lateral diverticula. Lateral apodemes are present, as are two sets of accessory glands, lateral and median glands.
The possible function of the genitalia of the male is considered.