The anatomy and ultrastructure of the antennal circulatory organs in the cockchafer beetle Melolontha melolontha L. (Coleoptera,Scarabaeidae)

Summary The antennal circulatory organs of Melolontha are described for the first time. They consist of small sac-like ampullae located near the base of each antenna and connected to a long non-muscular antennal blood vessel. Small branches of this vessel extend into each lamella of the antennal club and open out distally. The membranous wall of the ampulla provides no contractile structures. An outer adjacent compressor muscle is responsible for the pumping movements of the ampulla and antagonist to it is an obviously elastic connective tissue band. The position of this elastic band causes the uncontracted muscle to be pulled away from the ampulla. As a consequence blood can enter the dilated ampulla through a valvular ostium. The functional type of the antennal circulatory organs in Melolontha is compared to that found in other insects and their histologic structure is interpreted in relation to mechanical and hemodynamical aspects. Furthermore the possible function of the antennal hearts in connection with the spreading of its lamellate antennal club is discussed.Dedicated to Prof. Dr. M. Gersch's 70th birthday.Supported by project 3,106 of the Fonds zur Förderung der wissenschaftlichen Forschung in Österreich     

Cephalic anatomy of Sphaeriusidae and a morphology‐based phylogeny of the suborder Myxophaga (Coleoptera)

Myxophaga are a small group of beetles, but phylogenetically crucial as one of the four coleopteran suborders. The monogeneric Sphaeriusidae, one of four myxophagan families, comprise about 20 species, most of them living in moist substrate at river edges. The morphology of the minute hemispherical adult is very insufficiently known. Consequently, we document external and internal head structures using scanning electron microscopy, microtome sections and three‐dimensional reconstructions. The results are discussed with respect to effects of miniaturization and also functional aspects, especially microphagous feeding habits. The head of Sphaerius is less affected by size reduction compared with other beetles of the same size class (e.g. larger Ptiliidae, Corylophidae). Features related to very small size are the absence of externally visible ridges and a partial shift of the brain into the prothorax. The cephalic musculature is apparently not affected. The feeding apparatus is similar to what is found in microphagous species of Polyphaga, especially in Scirtoidea and Staphyliniformia. However, in contrast to polyphagans with similar feeding habits, the hypopharyngeal longitudinal ridge (or process) of Sphaerius is strongly reduced and a fimbriate galea is lacking. The observed features are also evaluated in a cladistic analysis of larval and adult characters. The results are distinctly in conflict with branching patterns suggested by analyses of molecular data, but in agreement with previous morphological studies. In contrast to a pattern obtained in a recent molecular study – (Hydroscaphidae + (Torridincolidae + (Sphaeriusidae + Lepiceridae))) – our analyses yielded Lepiceridae as sister to the remaining Myxophaga (branch support 9), and Sphaerius as sister taxon of Hydroscaphidae (branch support 5). The monophyletic origin of the latter two taxa is supported by unusual synapomorphies of adults and larvae. Sphaerius is characterized by numerous autapomorphies of the head: a labro‐mandibular locking device, a bipartite M. frontoepipharyngalis (M9) with subcomponents oriented in the opposite direction, a deep antennal furrow, an intercalary antennomere with a structure resembling a sucking disc, a strongly elongated flagellomere 1, a compact three‐segmented antennal club, strong bundles of M. tentorioscapalis (M4) originating on the posterior head capsule, a concave anterior side of maxillary palpomere 2, and an elongated second pair of tormae posteriorly connected with a process of the hypopharyngeal suspensorium.     

Gross and fine structure of the antennal circulatory organ in cockroaches (Blattodea,Insecta)

The antennal circulatory organ of Periplaneta americana and Blaberus craniifer was investigated by light and electron microscopy. This organ consists of two pulsatile ampullae located near the antennal base which are interconnected by a large transverse muscle and associated blood vessels which run into the antennae. Diastole is caused simultaneously in both ampullae by the transverse muscle. Systole is produced passively by the elasticity of the wall of the ampullae and minute accessory tendons. Both elastic structures contain fine unbanded extracellular filaments. The antennal vessels possess two distinct regions: a proximal convoluted region lying within the hemocoel of the head and a narrower distal region running through the antenna and opening near the antennal apex. The length of the proximal portion increases markedly during ontogeny in correlation with the growing antenna. Its wall consists of a high-prismatic epithelium ensheathed by a thick layer of collagen fibrils. The structure of the wall cells is comparable to that found in some salt transporting epithelia: it shows a polar organization with basal infoldings, a large number of mitochondria, and typical arrangement of the junctions or mitochondrial-scalariform junctional complexes. The possible physiological function of this epithelium in ionic or osmoregulation of the hemolymph entering the antenna is discussed. The wall of the distal vessel region consists of a flat single-layered epithelium and seems to be specialized only for delivery of hemolymph to antennae. The structure and function of the antennal heart in cockroaches is compared to that found in other insects.     

Expression of <Emphasis Type="Italic">defective proventriculus</Emphasis> during head capsule development is conserved in <Emphasis Type="Italic">Drosophila</Emphasis> and stalk-eyed flies (<Emphasis Type="Italic">Diopsidae</Emphasis>)

Hypercephaly, in the form of lateral extensions of the head capsule, is observed in several families of Diptera. A particularly exaggerated form is found in Diopsid stalk-eyed flies, in which both eyes and antennae are laterally displaced at the end of stalks. The processes of early development and specification of the head capsule in stalk-eyed flies are similar to those in Drosophila melanogaster. In Drosophila the homeobox gene ocelliless (oc) shows a mediolateral gradient of expression across the region of the eye-antennal imaginal disc that gives rise to the head capsule and specifies the development of different head structures. The genes and developmental mechanisms that subsequently define head shape in Drosophila and produce hypercephaly in stalk-eyed flies remain unclear. To address this, we performed an enhancer trap screen for Drosophila genes expressed in the same region as oc and identified the homeobox gene defective proventriculus (dve). In the eye-antennal imaginal disc, dve is coexpressed with oc in the region that gives rise to the head capsule and is active along the medial edge of the antennal disc and in the first antennal segment. Analyses of dve expression in mutant eye-antennal discs are consistent with it acting downstream of oc in the development of the head capsule. We confirm that orthologues of dve are present in a diverse panel of five stalk-eyed fly species and analyse patterns of dve sequence variation within the clade. Our results indicate that dve expression and sequence are both highly conserved in stalk-eyed flies.M. Carr and I. Hurley contributed equally to this work.     

On the head morphology of Grylloblattodea (Insecta) and the systematic position of the order,with a new nomenclature for the head muscles of Dicondylia

External and internal head structures of adults of Galloisiana yuasai (Grylloblattodea) are described. The results are compared with conditions found in representatives of other lower neopteran lineages, notably in Austrophasma and Karoophasma (both Mantophasmatodea). Sutures and ridges of the head capsule are discussed. A new nomenclature for head muscles is presented for the entire Dicondylia (= Zygentoma + Pterygota). Galloisiana (like its sister taxon Grylloblatta) is mostly characterized by plesiomorphic features, such as the largely unspecialized orthopteroid mouthparts, the multisegmented filiform antennae, the presence of trabeculae tentorii, the absence of muscles associated with the antennal ampullae, the presence of musculus stipitalis transversalis (0mx11) and the presence of musculus tentoriofrontalis anterior (0te2). Autapomorphies of Grylloblattodea are: (i) compound eyes composed of only 60 ommatidia or less; (ii) a lacinia with a proximal tooth; (iii) a rounded submentum; (iv) loss of musculus craniohypopharyngealis (0hy3); and (v) loss of musculus labroepipharyngealis (0lb5). The phylogenetic evaluation of 104 characters of the head yields a branching pattern with Grylloblattodea as a sister group of Mantophasmatodea in clade Xenonomia. Putative synapomorphies of both taxa are: (i) a distinct angle (more than 60°) between the submentum and the mentum; (ii) posteriorly oriented labial palpi; (iii) a flat and lobe‐like hypopharynx with a suspensorium far ventrad of the anatomical mouth opening; (iv) loss of musculus tentorioparaglossalis (0la6); and (v) a connection between the antennal ampulla and the supraoesophageal ganglion containing nuclei. Xenonomia is placed in a clade with the two dictyopteran terminals. Another monophyletic group is Embioptera + Phasmatodea. Most branches of the single tree obtained in our analysis are weakly supported. The results clearly show that more data and a much broader taxon sampling are required to clarify the phylogenetic interrelationships of the lower neopteran orders. However, our results narrow down the spectrum of possible solutions, and represent a starting point for future phylogenetic analyses, with an extensive concatenated dataset.     

The adult head structures of Tipulomorpha (Diptera,Insecta) and their phylogenetic implications

Schneeberg, K. and Beutel, R.G. 2011. The adult head structures of Tipulomorpha (Diptera, Insecta) and their phylogenetic implications. —Acta Zoologica (Stockholm) 92 : 316–343. Head structures of adults of Tipula paludosa, Limonia sp. and Trichocera saltator were examined and described. The results are compared with conditions found in other dipterans and other antliophoran groups, notably Nannochoristidae. Several potential synapomorphies of a dipteran–nannomecopteran–siphonapteran clade are present in Tipuloidea and Trichocera, the labro‐epipharyngeal food channel, the loss of the galea and the postpharyngeal pumping apparatus. The sensorial field of the maxillary palpomere 3, a potential dipteran–nannomecopteran synapomorphy, is also present but modified. The presence of M. clypeolabralis, labellae and mandibular stylets are groundplan apomorphies of Diptera, with secondary loss of the mandibles in Tipuloidea, Trichoceridae and many other groups. Tipuloidea is supported by the origin of M. tentorioscapalis anterior on the head capsule, the reduction of M. frontobuccalis anterior and the loss of the ocelli. The reduced tentorium, the origin of two further antennal muscles on the head capsule, the maxillary sensorial field with sensilla in individual pits, the lacking dorsal prelabial concavity and the unpaired salivary channel entering the head are apomorphies of Tipulidae. Closer affinities of Tipulidae and Cylindrotomidae are suggested by pseudotracheae of the advanced type, which have evolved independently in this lineage. The results do neither support a basal placement of Tipuloidea nor close affinities with Brachycera.     

A new species of Zorotypus (Insecta,Zoraptera, Zorotypidae) and the earliest known suspicious mating behavior of Zorapterans from the mid‐cretaceous amber of northern Myanmar

A new species of the insect order Zoraptera, Zorotypus pusillus, sp. n., is described and illustrated based on two ill‐preserved specimens in mid‐Cretaceous amber from the Hukawng Valley in northern Myanmar. Compared with known extinct zorapterans, the new species possesses eight‐segmented antennae and can be readily distinguished from all other extinct and recent members of the order in the presence of a shallow groove connecting two antennal sockets and by unique spination of the metafemur and metatibia. The earliest known suspicious mating behavior of Zoraptera, the intromittent organ of the fossil zorapterans, the egg, and the earliest known basal plate of the male genitalia are briefly discussed. The genitalia of new species are used as an intromittent organ in the majority of mating patterns among living zorapterans. The mating patterns (a copula is performed by males and females) of the most extant species have been present since at least the mid‐Cretaceous. A shared similar aedeagal structure in the new species and in the most extant species suggests an analogous mating behavior.     

Oldest webspinners from the Middle Jurassic of Inner Mongolia,China (Insecta: Embiodea)

The oldest webspinners, Sinembia rossi gen. et sp. nov. and Juraembia ningchengensis gen. et sp. nov. , are described in the new family Sinembiidae fam. nov. from the Middle Jurassic of Inner Mongolia, China. They differ from the Cretaceous and more recent Embiodea in several plesiomorphic characters, namely they have a long ovipositor, three‐segmented cerci, eyes situated on the posterolateral angles of the head, and the prothoracic prescutum is absent: these characters suggest habits that strongly differ from those of the recent taxa. The loss of the ovipositor and the reduction in the number of cerci can no longer be considered as synapomorphies of the ((Embiodea + Zoraptera) + Plecoptera) and (Embiodea + Zoraptera) clades, respectively.     

On the evolution of adult head structures and the phylogeny of Hydraenidae (Coleoptera, Staphyliniformia)

External and internal head structures of adults of Orchymontiinae, Prosthetopinae, Hydraeninae and Ochthebiinae were studied and those of Ochthebius semisericeus and Limnebius truncatellus are described in detail. The results are evaluated with respect to their relevance for a reconstruction of hydraenid phylogeny and also compared with structural features found in adults of other staphyliniform families. The monophyly of Hydraenidae is supported by the presence of a plate‐like, trilobed premento‐hypopharyngeal extension, an unusual origin of m. tentoriohypopharyngalis, dorsal tentorial arms firmly fused with the head capsule, modified basal antennomeres, and palpigers connected by a transverse sclerotized bar. Orchymontiinae are monophyletic and the basal sister group of the remaining Hydraenidae. The presence of a ventral transverse genal bulge and of a pubescent antennal club with more than two antennomeres (reversal in some prosthetopines: e.g. Mesoceration abstrictum) are possible apomorphies of Hydraenidae excluding Orchymontiinae. Prosthetopinae are probably monophyletic and the sister group of Ochthebiinae + Hydraeninae. The latter clade is characterized by a distinct cupula formed by antennomere VI, a loose five‐segmented pubescent antennal club, and a modified antennal musculature. The presence of an unusual tentorio‐pharyngeal dilator is a shared derived feature of Ochthebiinae and the genus Davidraena. The monophyly of Ochthebiinae was confirmed and Ochtheosus is the sister group of the remaining ochthebiine genera, which are characterized by a perforated wall‐like structure formed by the posterior tentorial arms. The absence of this tentorial modification and the fimbriate galea are plesiomorphies retained in Ochtheosus. Calobius differs strongly from other subgenera of Ochthebius and a generic status may be appropriate. The monophyly of Hydraeninae is not supported. Hydraena was confirmed as a clade and Laeliaena and Limnebius are sister groups. The latter genus is characterized by several autapomorphies. The basal position of Orchymontiinae and Prosthetopinae suggests a Gondwanan origin of Hydraenidae and a primary preference for life in running water. Important evolutionary changes of head structures are complex transformations of the antennae and related structures. Yet, the use of the antennae as accessory breathing organs is not a groundplan feature of the family. The results of this study strengthen the case of staphylinoid affinities of Hydraenidae.     

The larval head morphology of Xyela sp. (Xyelidae, Hymenoptera) and its phylogenetic implications

Larval head structures of Xyela sp. are described in detail. The characters are compared to conditions found in larvae of other groups of Hymenoptera and Endopterygota. Like other symphytan larvae the immature stages of Xyelidae are mainly characterized by presumably plesiomorphic features of the head. The head sutures are well developed and all parts of the tentorium are present. The labrum is free and a complete set of labral muscles is present. The maxillae are in a retracted position. In contrast to other hymenopteran larvae Xyela possesses a clypeofrontal suture, a comparatively long antenna and three well‐developed antennal muscles. Apomorphic features of Xyela are the absence of muscles associated with the salivarium and the complete absence of Musculus craniocardinalis. A clade comprising Orussidae and Apocrita is supported by the unsegmented maxillary and labial palps and the absence of the lacinia. Six potential autapomorphies for the Hymenoptera were revealed: (1) the caudal tentorial apodeme, (2) the bifurcated tendon of Musculus craniomandibularus internus, (3) the lateral lobe of the cardo, (4) the origin of M. tentoriohypopharyngalis from the posterior head capsule, (5) the exceptionally strong prepharyngo‐pharyngeal longitudinal muscle and (6) the longitudinal muscle of the silk press. The maxillolabial complex, the vestigial M. craniocardinalis and a distinctly developed labio‐hypopharyngeal lobe bearing the opening of the salivary duct are potential synapomorphies of Hymenoptera and Mecopterida. The globular, orthognathous head capsule, the modified compound eyes, the occipital furrow and the X‐shaped tentorium are features with unclear polarity shared by Hymenoptera and Mecoptera.     

Antennal circulatory organs in Onychophora,Myriapoda and Hexapoda: Functional morphology and evolutionary implications

Summary A comparative investigation of the antennal circulatory organs in representatives of the Onychophora, all subtaxa of the Myriapoda and numerous taxa of the Hexapoda (comprising a total of 54 species) revealed an unexpected diversity in structure and function.In the Onychophora, antennal vessels exist which are connected to the enlarged anterior end of the aorta dorsal to the brain.In the Chilopoda, Diplopoda and Symphyla, antennal vessels exist which originate from the dorsal vessel caudal to the brain. They extend under the optic lobes, lateral to the circumoesophageal connectives, into the antennae.In the Hexapoda, the investigations include representatives of all higher taxa, apart from the Paraneoptera and the Holometabola. Generally, antennal vessels exist. In the Diplura, they originate from the anterior end of the aorta in front of the brain. In all other insects the antennal vessels are separate from the dorsal vessel. Their proximal ends form ampullary enlargements which are attached to the frontal cuticle near the antenna bases. They communicate via valved ostia with the haemolymph sinus in front of the brain. In the Archaeognatha, Zygentoma, Odonata, certain Plecoptera and the Notoptera, no muscles are connected to these organs. In all other groups the ampullae are pulsatile as a result of associated muscles (antennal hearts). These muscles diverge widely in their attachments and act either as compressors (Dermaptera) or dilators of the ampullae (Embioptera, Blattopteroidea, Orthopteroidea, and some Plecoptera).In the Collembola and Ephemeroptera, special antennal circulatory organs are lacking. In some forms the anatomical arrangement of the inner organs, in conjunction with short diaphragms at the antenna bases, apparently leads to a channelling of haemolymph flow. This condition may be explained by the very short antennae of these insects and is considered as a convergent and apomorphic state in these taxa.The antennal vessels are supposed to be homologous within the Tracheata and to represent the lateral arteries of the antenna segment. An origin from the dorsal vessel is considered an ancestral state, which was lost in the stem lineage of the Ectognatha. Specific space constraints within the cephalic capsule are discussed as the possible reason for this loss. The evolution of pulsatile antennal circulatory organs in the Neoptera is the result of the association of muscles with the proximal ampullary ends of the antennal vessels. The attachments and innervation of these muscles indicate a derivation from precerebral pharyngeal dilators.Abbreviations Amp ampulla - Ant antenna - ant anterior - AN antennal nerve - Ao aorta - AV antennal vessel - Br brain - BrSi brain sinus - CC corpora cardiaca - CoeC circumoesophageal connectives - CM compressor muscle of ampulla - CT connective tissue - Dia diagphragm - do dorsal - DM dilator muscle of ampulla - DM1 ampullo-ampullary dilator muscle - DM2 ampullo-pharyngeal dilator muscle - DM3 ampullo-frontal dilator muscle - DM Acc accessory dilator muscle of ampulla - DV dorsal vessel - EB elastic band - FbDM fronto-buccal pharynx dilator muscle - FG frontal ganglion - FSa frontal sac - FSe frontal septum - FSi frontal sinus - Lb labium - LV lateral vessel of aorta - MA mouth-angle - Nr nervus recurrens - Oc ocellus - Oe oesophagus - OeSi oesophageal sinus - Ost ostium - Ph pharynx - Pl labial palpus - RM retractor muscle of mouth-angle - RMl lateral retractor of mouth-angle - RMm medial retractor of mouth-angle - SceSi supracerebral sinus - SD salivary duct - T tentorium     

Notes on Neotropical Zoraptera, with descriptions of two new species

Characters used un specific identification of Zoraptera are briefly discussed. A list of Neotropical species is given, and the difficulties of associating sexes of some species outlined. Two new species are described and figured (Zorotypus weidneri sp.n., ♂, ♀, Brazil; Z.hamiltoni sp.n., ♂, ♀, Colombia) and additional records and information given on Z.shannoni Gurney (♂, Brazil) and Z.huxleyi Bolivar y Pieltain & Coronado G (♂, ♀, recorded from Brazil for the first time).     

Head capsule, chephalic central nervous system and head circulatory system of an aberrant orthopteran, Prosarthria teretrirostris (Caelifera, Hexapoda)

The head capsule, the circulatory system and the central nervous system of the head of Prosarthria teretrirostris (Proscopiidae) is described in detail, with special consideration of modifications resulting from the aberrant head shape. The transformations of the head are completely different from those found in phasmatodeans, which are also characterised by twig mimesis. The circulatory system is distinctly modified. A hitherto undescribed additional structure in the posterior head region very likely functions as a pulsatile organ. The cephalic central nervous system is strongly elongated, with changes in the position of the suboesophageal ganglion, the corpora cardiaca and the course of the nervus mandibularis. Three-dimensional reconstructions of these two organ systems in combination with the pharynx were made using Alias Maya 6.0 software. Comparisons with other representatives of Caelifera suggest a clade comprising Proscopiidae and Morabinae. The presence of a transverse muscle connecting the antennal ampullae in Prosarthria shows that this structure likely belongs to the groundplan of Orthoptera, even though it is missing in different representatives of this group. The transverse ampullary muscle is a potential synapomorphy of Orthoptera, Phasmatodea and Dictyoptera.     

Functional morphology and evolutionary aspects of unusual antennal circulatory organs in Labidura riparia Pallas (Labiduridae), Forficula auricularia L. and Chelidurella acanthopygia géné (Forficulidae) (Insecta : Dermaptera)

The antennal circulatory organs in the earwigs Labidura riparia Pallas (Labiduridae), Forficula auricularia L. and Chelidurella acanthopygia Géné (Forficulidae) (Dermaptera) represent a functional type that has not been found in other insects. An independent organ exists for each antenna, consisting of a pulsatile ampulla connected to an antennal blood vessel. The ampulla is attached to the frontal cuticle medial to the antenna base and forms a thin-walled sac with a valved ostium on its ventral side. The ampulla wall epithelium is not muscular, but consists of elastic connective tissue. The pumping movements are affected by a precerebral frontopharyngeal muscle, which causes systolic compression of the ampulla upon contraction. The elasticity of both the ampulla and a band of connective tissue, which suspends it in the head capsule, passively effect diastole. The antennal vessel is quite voluminous in the head capsule, but narrows remarkably upon entrance into the antenna. It extends with a constant diameter to the apex, where it opens with a terminal pore. At the base of the vessel, near the ampulla, is a very delicate valve flap which prevents hemolymph backflow during diastole. A comparison of the antennal heart types in insects revealed fundamental differences in the attachments and functions of the associated muscles. In the Dermaptera, the involvement of a precerebral frontopharyngeal muscle suggests an ancestral condition.     

TWO TYPES OF AUXILIARY CELL AMPULLAE IN GRATELOUPIA (HALYMENIACEAE,RHODOPHYTA), INCLUDING G. TAIWANENSIS SP. NOV. AND G. ORIENTALIS SP. NOV. FROM TAIWAN BASED ON rbcL GENE SEQUENCE ANALYSIS AND CYSTOCARP DEVELOPMENT1

Few species in the genus Grateloupia have been investigated in detail with respect to the development of the auxiliary cell ampullae before or after diploidization. In this study, we document the vegetative and reproductive structures of two new species of Grateloupia, G. taiwanensis S.‐M. Lin et H.‐Y. Liang sp. nov. and G. orientalis S.‐M. Lin et H.‐Y. Liang sp. nov., plus a third species, G. ramosissima Okamura, from Taiwan. Two distinct patterns are reported for the development of the auxiliary cell ampullae: (1) ampullae consisting of three orders of unbranched filaments that branch after diploidization of the auxiliary cell and form a pericarp together with the surrounding secondary medullary filaments (G. taiwanensis type), and (2) ampullae composed of only two orders of unbranched filaments in which only a few cells are incorporated into a basal fusion cell after diploization of the auxiliary cell and the pericarp consists almost entirely of secondary medullary filaments (G. orientalis type). G. orientalis is positioned in a large clade based on rbcL gene sequence analysis that includes the type species of Grateloupia C. Agardh 1822 , G. filicina. G. taiwanensis clusters with a clade that includes the generitype of Phyllymenia J. Agardh 1848 , Ph. belangeri from South Africa; that of Prionitis J. Agardh 1851 , Pr. lanceolata from Pacific North America; and that of Pachymeniopsis Y. Yamada ex Kawab. 1954, Pa. lanceolata from Japan. A reexamination of the type species of the genera Grateloupia, Phyllymenia, Prionitis, and Pachymeniopsis is required to clarify the generic and interspecific relationships among the species presently placed in Grateloupia.     

Functional morphology of the muscles in Philodina sp. (Rotifera: Bdelloidea)

Whole-mounts of Philodina sp., a bdelloid rotifer, were stained with fluorescent-labeled phalloidin to visualize the musculature. Several different muscle types were identified including incomplete circular bands, coronal retractors and foot retractors. Based on the position of the larger muscle bands in the body wall, their function during creeping locomotion and tun formation was inferred. Bdelloid creeping begins with the contraction of incomplete circular muscle bands against the hydrostatic pseudocoel, resulting in an anterior elongation of the body. One or more sets of ventral longitudinal muscles then contract bringing the rostrum into contact with the substrate, where it presumably attaches via adhesive glands. Different sets of ventral longitudinal muscles, foot and trunk retractors, function to pull the body forward. These same longitudinal muscle sets are also used in `tun' formation, in which the head and foot are withdrawn into the body. Three sets of longitudinal muscles supply the head region (anterior head segments) and function in withdrawal of the corona and rostrum. Two additional pairs of longitudinal muscles function to retract the anterior trunk segments immediately behind the head, and approximately five sets of longitudinal retractors are involved in the withdrawal of the foot and posterior toes. To achieve a greater understanding of rotifer behavior, it is important to elucidate the structural complexity of body wall muscles in rotifers. The utility of fluorescently-labeled phalloidin for the visualization of these muscles is discussed and placed in the context of rotifer functional morphology.     

Antennal motor system of the cockroach, <Emphasis Type="Italic">Periplaneta americana</Emphasis>

The organization of the antennal muscles, nerves, and motor neurons has been investigated in the cockroach, Periplaneta americana. Antennal movements have been observed by video analysis, muscle actions have been determined by dissection and direct mechanical testing, and the motor neurons innervating each muscle have been defined with a recently developed selective backfill method. A model of the antennomotor system of Periplaneta has thus been established and compared with that of crickets. Five muscles located within the head capsule insert on the most proximal antennal segment, the scape. By their action, they allow the scape to move in essentially any direction within the dorsoventral and anteroposterior planes. An additional pair of muscles, one dorsal and one ventral, are found within the scape. They insert on the pedicel and move the pedicel in the dorsal-ventral plane. These seven muscles are controlled by at least 17 motor neurons with somata located in the deutocerebrum. By their action, these motor neurons enable cockroaches to move the long flagellum of each antenna through a wide range of positions in the frontal space, medio-laterally, and also allow depression toward the substrate and elevation well above the level of the head. The antennal motor neurons have been classified into five morphological types based on soma and axon location. Each morphological type has been correlated with a particular pattern of muscle innervation and control. The neurites of all motor neurons are located along the medial aspect of the dorsal lobe of the deutocerebrum. This research was supported by grant nos. IBN 96-04629 and 04-22883 from the National Science Foundation.