ALBERT

Notes: 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.

Notes: An investigation of the structure of the iridescent scales of the green hairstreak, Callophrys rubi, reveals an internal lattice which is probably cubic close-packed in form. We present a model which explains the formation of the lattice in terms of packing of spheres and surface tension forces and generalize these results to internal structures in other Lepidopteran scales.

Notes: There are 36 to 42 taste bristles on each half of the labellum of Drosophila melanogaster; most of them are two-pronged with a pouch between them. Some end bluntly with a pore at the tip.Each taste-bristle has two lumina: one is circular, the other crescent-like in cross section. In most bristles four dendrites of chemoreceptor neurons run along the circular lumen. In five to seven taste-bristles only two chemoreceptor neurons are found. A mechanoreceptor neuron sends a dendrite to the base of each taste-bristle.The dendrites are surrounded by four concentrically-arranged sheath cells. The inner cell secretes the cuticular sheath; cells II and III are presumably two trichogens, one secreting the bristle material around the circular lumen, the other around the crescent-like lumen. Cell IV, especially rich in bundles of microtubules, secretes the cuticle of the socket, and corresponds to the tormogen. The neurons have the typical structure found in insect sensilla. In many sensilla one neuron is less electron-dense than the others and may be the water-sensor.On the medial side of the labellum between the pseudotracheae are rows of taste pegs covered by folds. In each peg one chemoreceptor and one mechanoreceptor are found.The number of axons in each labial nerve agrees with the total number of dendrites in all taste organs of each lobe.

Notes: Stichopus moebii, a sea cucumber, has a closed circulatory system which is unique in its degree of development for the phylum Echinodermata. The gross anatomy, histology and fine structure of the system were studied. Blood vessels consist of a coelomic surface of ciliated epithelium, a layer of muscle and nerve cells, followed by connective tissue and luminal lining of endothelium. Basically the blood vascular system consists of two major vessels running parallel to the gut: the dorsal vessel pumps colorless blood via the vessels within the walls of the intestine into the ventral vessel. There are two specialized areas of the circulation: (1) At the upper small intestine 120 to 150 muscular single-chambered hearts pump blood from the dorsal vessel into a series of intestinal plates. (2) At the lower region of the small intestine the vasculature is associated with the left respiratory tree. Blood passing from the dorsal pulmonary vessel can take two routes to the gut, it either passes through myriads of minute respiratory shunt vessels entangled with the respiratory tree or it passes through a unique follicle network consisting of tiny channels periodically dilated into chambers filled with iron deposits, necrotic cells and developing coelomocytes.

Notes: Anatomical components of afferent innervation in the rim of the octopus sucker are described. In the sensory epithelium under the smooth cuticle two associated ciliated receptor cell-types (presumably chemosensitive) occur in clusters. A third ciliated receptor cell-type under the toothed cuticle may be a mechanoreceptor. A non-ciliated receptor cell-type of unknown function, under the toothed cuticle, is characterized by a microvillus-lined apical canal containing dense granular material. The axons of the latter two receptors go directly into large nerve tracts which nm through the infundibular muscle and on to the ganglion of the sucker. The axons of the first cell-types terminate on interneurons either in the base of the epithelium or below the epithelium. All the interneurons of the basal region of the epithelium migrate centripetally and develop into encapsulated interneurons. Within the epithelium, fine fibers provide collateral contact among cluster receptors. Collateral interaction among basal and encapsulated interneurons occur in the infundibular plexus. The microanatomy of the rim of the sucker suggests that chemosensory cues are funneled into the interneurons where they are concentrated into integrated signals, while other sensory input is probably sent directly to the ganglia of the sucker and/or arm.

Notes: The pyloric region of Eosentomon and Acerentomon (Insecta, Protura) is described. In both species the posterior cells of the midgut carry short microvilli. Beneath the epithelial cells there is a muscular pyloric sphincter for closing the intestinal lumen. Behind the sphincter is a wide pyloric chamber lined by cells with very long microvilli which point anteriorly toward the midgut. These cells regulate the passage of the intestinal contents into the hindgut. Secretions from the Malpighian papillae are emitted into the gut at this level. In Eosentomon three regions (R1, R2 and R3) are visible in the Malpighian papillae, whereas in Acerentomon region R1 is lacking. The R1 region contains secretory cells with elaborate glycoprotein-containing granules. The R2 region is composed of cells somewhat resembling the secretory cells of Malpighian tubules of insects. Presumably R1 and R2 cells emit secretions into the central cavity of each papilla. Cells of R3 form a duct for the secretion. It is suggested that the R2 region represents a basic excretory region, common to Protura, whereas the R1 region, in Eosentomon, may be a specialized area performing supplementary excretory functions.

Notes: This manuscript describes in precise detail the ultrastructural alterations produced as a result of laser microirradiation of nucleoli and nucleoplasm of tissue culture cells. Because of the general difficulty of single cell recovery, flat embedding, and serial sectioning, very few studies have ever been conducted on microbeam irradiated cells; yet the use of the microbeam technique has become widespread in functional studies of the nucleus. The results presented here demonstrate two classes of lesion material: small spherical electron dense bodies 0.05-0.02 μm in diameter and a larger, more irregular electron dense material up to 1 μm in length. The occurrence of these different types of lesion materials is described in control irradiated nucleoli and nucleoplasm, irradiated nucleoli and nucleoplasm in quinacrine treated cells, irradiated nucleoli and nucleoplasm in actinomycin D treated cells, and irradiated nucleoli and nucleoplasm in combined actinomycin D and quinacrine treated cells. In all the cells in which actinomycin D was employed, nucleoli were selectively irradiated in either their granular or fibrillar zones. The results of the ultrastructural studies are discussed in light of earlier functional studies.

Notes: The general form and adaptation of the digastric muscle in carnivores are reviewed and discussed. The digastric muscle differs from the general plan in certain aquatic carnivores and felids. In the pertinent aquatic species the muscle is enlarged. The observations suggest that the enlargement is an adaptation for rapidly opening the jaws against the resistance of water. In felids, the insertion of the muscle is much farther forward than in most other carnivores. The observations suggest that the development of short jaws in felids necessitated a compensatory anterior relocation of the digastric insertion in order to preserve the ability to achieve a large gape.

Notes: Homolid crabs (Hypsophrys) from water deeper than 700 m in the Straits of Florida and Arabian Sea have smooth darkened oval spots contrasting with the surrounding roughened integument on inner and outer surfaces of each pincer at the base of the fixed finger. Cuticle is thinner over these spots than over surrounaing tissues. Beneath each spot is an organ composed of two markedly contrasting layers of tissue: (1) an outer, densely staining layer of tightly packed tubules, relatively straight and perpendicular to the overlying surface proximally but progressively convoluted and narrowed distally, finally ending blindly in association with the overlying thinned cuticle; (2) an inner layer of relatively large, eosinophilic, irregular cells with dark nuclei also trending at a right angle to the integument and bulging into the hemal sinus of the hand but separated from it by an epidermal lining. Droplets secreted from the inner layer apparently move into and along the tubules. Similar organs are known in no other crabs. The function is unknown but the structure suggests that they may be photophores.

Notes: The swimbladder system of the plainfin midshipman consists of a gas-filled bladder and two intrinsic sonic muscles which are attached to the bladder at opposite sides. An experimental and analytical study was conducted to define the physical characteristics of this dynamic system, and to relate these characteristics to radiated acoustical pressure pulses. Results indicate that the system has two degrees of freedom, being comprised of two inertial, stiffness and damping components; the first and second mode components of a 23.1-centimeter midshipman are 0.002 and 0.019 kg (inertial) 2130 and 106,000 newtons per meter (stiffness) and 0.25 and 0.10 (damping) respectively. This system is excited by the sonic muscle forcing function which equals \documentclass{article}\pagestyle{empty}\begin{document}$ 0.00236{\rm}\sin \frac{{2\pi {\rm t}}}{{0.0045{\rm}\sec}}{\rm newtons}. $\end{document}Two system frequency response peaks were observed; the first was 110 hertz, at the flat section next to the sonic muscle, and was very near the repetition frequency of the sonic muscle pulses; the second was 350 hertz, at the hemispherical section, which was the frequency of the acoustical pressure pulse. These phenomena describe a dynamical system closely “tuned” to its forcing function, and a system which is highly responsive to acoustical pressure pulses radiated by neighboring midshipmen. The acoustical pressure pulse coincides in wave form with the hemispherical bladder wall acceleration.

Notes: The ultrastructure of a well studied insect chemosensory unit is presented in this report. Two separate lumina are present in this chemosensory unit, the trichogen and sensillar lumina. The fluid within the trichogen lumen exclusively bathes the dendritic terminals, and may be involved with the reception and/or modulation of environmental stimuli. Cytoplasmic extensions of the trichogen cell which line the trichogen lumen may be involved in the production of the cuticular sheath. The sensillar lumen is bordered by the tormogen and a sleeve cell, and is continuous with the unoccupied channel of the setal shaft. Functions for the various cellular components of the blowfly chemoreceptor sensillum are offered.

Notes: This study indicates that eggs containing calcium carbonate crystals occur in at least 36 of the 65 known families of the land snails (class Gastropoda: order Stylommatophora). Eggs from 22 of these families were available for examination. The x-ray diffraction data, available for the first time for 21 of these families, shows that these egg shells are all made of calcite only, or of a combination of calcite with smaller amounts of aragonite. All of the snail (body) shells examined were made of aragonite only. This is the first ultrastructural investigation of these egg shells, and it indicates that the eggs exhibit enough structural diversity to allow identification of parental animals to genus, and often to species level solely on the basis of egg shell ultrastructure.All of the calcified eggs may be divided into two groups: (1) partly calcified, with discrete crystals of CaCo3 dispersed in the jelly layer, and (2) heavily calcified, with a hard, brittle egg shell made of fused crystals of CaCO3 much like an avian egg. Both types of calcified eggs occur in oviparous as well as in ovoviviparous snails. Because of the wide distribution of calcified eggs in the Stylommatophora, and because of the occurrence of heavily calcified eggs in ancient families such as Partulidae, Endodontidae, and Zonitidae, the calcified egg is viewed as a primitive land snail trait associated with terrestrial adaptation. The function of the calcified egg shell, in addition to mechanical support of egg contents, is to supply the developing embryo with enough calcium to form the embryonic shell by the time of hatching.

Notes: (1) In an animal where the corpus allatum complex is inhibited by glucose feeding, the ovariole develops to a certain size without yolk deposition in the oocytes. Histologically this can be registered as: (a) Lipid spheres are found in the young oocytes in the vicinity of the Balbiani body (as in young normal oocytes). However, this lipid decreases in amount and “new” lipid (from the fat body via haemolymph) is not deposited in the later oocytes. (b) No carbohydrate/protein yolk is formed. (c) Glycogen is not synthesized in the oocytes. (d) The follicle cells aggregate glycogen instead of lipid. (e) No qualitative differences have been observed regarding the contributions from the tropharium (the so-called Type 1 vacuole, ribosomes, mitochondria, annulated lamellae: Schreiner, '77).(2) Implantation of a corpus allatum complex results in deposition of lipid, carbohydrate/protein and glycogen yolk. However, the restoration period differs histologically from the normal development as: (a) Glycogen appears in the oocyte earlier than normal, i.e., at Stage 4, while normally at Stage 6′. (b) Glycogen appears in the nutritive tube adjacent to the interfollicular plug cells. (c) Both the inner and outer layer of the ovariole sheath contain glycogen, the outer layer contains lipid spheres as well.

Notes: The odontophore and connective tissue-filled portion of the radular sac (called the “collostyle”) of the slug, Limax maximus, were examined by light and electron microscopy. While both of these structures grossly resemble vertebrate cartilage, neither is composed of a type of tissue with the microscopic appearance and histochemical properties of cartilage. The roughly U-shaped odontophore possesses a thin capsule composed of connective tissue. The parenchyma of the odontophore consists of modified muscle cells which are organized into irregular groups by incomplete trabeculae composed of conventional muscle cells. The odontophoral cells are variable in size; they contain glycogen-filled “cores” as well as bundles of peripherally located filaments resembling myofilaments; and they are innervated like muscle cells. The nuclei of the cells are located eccentrically in the glycogen-filled portions of the cells and typically contain prominent nucleoli. The nuclei are surrounded by multiple small Golgi complexes and pleomorphic dense bodies resembling lysosomes. The extracellular matrix of the odontophore is very sparse and contains glycogen and fibrillar material but no histochemically demonstrable acidic mucosubstances. The collostyle consists of a gelatinous type of tissue somewhat like vertebrate mucoid connective tissue. The abundant extracellular matrix contains cross banded filaments, a flocculent material disposed in wavy indefinite strands, and small electron-dense particles. The matrix contains histochemically demonstrable neutral and weakly acidic mucosubstances. The cell population of the collostyle includes solitary muscle cells and fibrocytes containing large quantities of glycogen.

Notes: This ultrastructural study on the localization of Ca+2 in developing skeletal muscle indicates that the formation of calcium-accumulating components begins during embryonic development. Both oxalate and pyroantimonate techniques are used to localize Ca+2 in distinct cellular components of chick pectoral and sartorius muscles. Two major sites for Ca+2 accumulation are present in ultrathin sections of embryonic and post-embryonic muscles: the terminal cisternae of the sarcoplasmic reticulum and specific lines in the I-bands. Calcium oxalate-accumulating vesicles are present in the smallest recognizable myotubes at the twelfth day of incubation, but calcium-accumulating components are not seen at myofibrillar I-band sites until the fourteenth to seventeenth days of incubation. The fact that myofibrils first form and later in development accumulate a Ca+2-binding component suggests that this Ca+2-binding component is not necessary for the formation of myofibrils, but is added to myofibrils before hatching to serve a probable regulatory role in contraction.

Notes: This report is an ultrastructural analysis of the organization of the isolated oral apparatus of Tetrahymena pyriformis, strain WH-6, syngen 1. Attention has been focused on the organization of microtubules and filaments in oral apparatus membranelles. Oral apparatus membranellar basal bodies were characterized with respect to structural differentiations at the distal and proximal ends. The distal region of membranellar basal bodies contains the basal plate, accessory microtubules and filaments. The proximal end contains a dense material from which emanate accessory microtubules and filaments. There are at least two possibly three different arrangements of accessory structures at the proximal end of membranellar basal bodies. All membranellar basal bodies appear to have a dense material at the proximal end from which filaments emanate. Some of these basal bodies have accessory microtubules and filaments emanating from this dense material. A possible third arrangement is represented by basal bodies which have lateral projections, from the proximal end, of accessory microtubules and filaments which constitute cross or peripheral connectives. There are at least three examples of direct associations between oral apparatus microtubules and filaments: (1) filaments which form links between basal body triplet microtubules, (2) filaments which link the material of the basal plate to internal basal body microtubules, (3) filaments which link together microtubule bundles from membranellar connectives. KCI extraction of the isolated oral apparatus resulted in the selective solubilization of oral apparatus basal bodies, remnants of ciliary axonemes and fused basal plates. Based on their response to KCl extraction two distinct sets of morphologically similar microtubules can be identified: (a) microtubules which constitute the internal structure of basal bodies and ciliary axonemes, (b) microtubules which constitute the fiber connectives between basal bodies.

Notes: Ultrastructural analysis of initial development of actinotrichia, the skeleton anlage of the pelvic fin buds, was performed on the rainbow trout, Salmo gairdneri. It shows that the first actinotrichial rudiments appear in the subepidermal space of the pseudoapical cap. No mesenchymal cell bodies or their filopods are present. Hyaloplasmic protrusions of the basal epidermal cells are seen in the subepidermal space, limited by a dermoepidermal boundary reduced to a discontinuous thin adepidermal lamina without a collagenous layer. These morphological data suggest that the epidermal pseudoapical cap probably initiates the development of actinotrichia. Later, mesenchymal cells invade the subepidermal space and are probably involved in the further growth of actinotrichia.

Notes: Synaptic organization of the nucleus rotundus was studied with the electron microscope in three teleost species belonging to the same order. In spite of the different histological organization (non-laminated, incompletely laminated, and laminated), the same kinds of axon terminals (S and F) are observed in all species. A fibrous layer which is clearly formed only in the laminated nucleus is composed of F1 terminals and dendrites from a layer of small cells. The same kind of synapses formed between F1 terminals and dendrites of small cells are also found among glomeruli in the non-laminated and incompletely laminated nuclei. The main constituents of glomeruli are S and F2 terminals and dendrites of large cells in the non-laminated and incompletely laminated nuclei, and are S terminals and star-like structures which correspond to the tips of the dendrites of large cells in the laminated nucleus. The star-like structure contains numerous mitochondria and clusters of small polymorphic vesicles. Some of the vesicles aggregate at thickened cell membranes of the structure as in presynaptic dendrites.

Notes: Freshwater sponges, Corvomeyenia carolinensis Harrison, were placed into tap water to induce degenerative reduction body formation. Reduction bodies were examined using light and electron microscopy in order to define their histochemical and ultrastructural characteristics. The reduction body of freshwater sponges is an extremely simple developmental system consisting primarily of an archeocyte reserve delimited by a simple squamous pinacoderm. The freshwater sponge reduction body displays many similarities to overwintering phases of marine sponges. The system presents an unusually straightforward vehicle for investigations of degeneration and regeneration as processes in developmental biology and may represent a reasonable vehicle in which to examine the process of the genesis of lysosomes.

Notes: The aquiferous systems of three common, coastal, marine Demospongiae, Halichondria panicea (Pallas), Haliclona permollis (Bowerbank) and Microciona Prolifera (Ellis and Solander), are analyzed by measurements of cross-sectional areas of conducting elements. The patterns in demosponges of extremely different organizational morphologies are found to be quantitatively similar. The porocyte nature of the ostia is established for all three species. Choanocyte chamber densities range from 1 to 1.8 × 107 chambers ml-1 with 57 to 95 choanocytes per chamber (means). Cross-sectional area of the intervillar space of the choanocyte collars is calculated to be 12 to 56 times the lateral surface area of the specimen. Velocities of water movement through specific elements of the aquiferous system are calculated from cross-sectional area data and measured oscular flow of Haliclona permollis. The calculated Reynolds numbers lie below the critical value and fluid flow is thus considered laminar throughout the aquiferous systems of these sponges.

Notes: The intrinsic organization of medial cortex in snakes, primarily of the genera Natrix and Boa, was studied using Golgi and electron microscopic techniques. The area has three distinct layers, each containing a characteristic population of neurons. Stellate cells comprise a relatively small population of neurons with their somata and dendrites restricted to layer 1, the most superficial layer. Their axons course horizontally in layer 1. Candelabra cells form the largest population of neurons in medial cortex. Their somata lie densely packed in layer 2 and are joined by specialized junctions. Ascending dendrites extend from the somata into layer 1. They consist of spine-free proximal segments and spine bearing distal segments. Descending dendrites extend from the somata into the upper half of layer 3. The proximal segments bear few spines but branch into several tapered, distal segments which have a moderate covering of spines. One or two axons originate from the descending dendrites and descend through layer 3. The axons bear collaterals in the deep half of layer 3 and eventually bifurcate in the alveus. The medial branches run into the septum; the lateral branches course through other cortical areas. The axons bear frequent varicosities within medial cortex. Periventricular cells lie in the deep half of layer 3, either singly or in clusters. Their ascending dendrites extend radially into layer 1 where they branch into distal segments which resemble those of the candelabra cells. Their descending dendrites arborize horizontally in the alveus and bear a moderate covering of spines. Ependymal cells line the ventricular surface and send radial processes through the area's depth bearing lamellate processes.

Notes: The sex-linked mutation fs(1)42 was induced by ethyl methane sulfonate. It has no effect on either the external morphology or longevity of adult hemizygotes or homozygotes. Heterozygotes and hemizygotes are fertile, but homozygotes are sterile. Egg chamber development proceeds through stage 8, and thereafter chambers degenerate. Dying follicle cells are seen in chambers at all positions in the ovarioles. Profollicle cells also die within germaria, and clusters of sister cystocytes take longer than normal to receive their coverings of follicle cells. Egg chambers in the vitellarium contain only about 60% the normal number of follicle cells, these generally have greater lateral dimensions, and their nuclei and nucleoli are also larger than normal. The follicular envelope of mutant chambers often contains gaps through which cystocytes send cytoplasmic projections. Abnormalities seen in development of the fs(1)42 oocyte are likely to be due to its envelope of defective follicle cells.

Notes: Reproductive organs of four botryllid ascidians, Botryllus primigenus, Botryllus schlosseri, Botrylloides violaceus and Botrylloides leachi, were studied histologically. In every species, the egg follicle consisting of an egg and its inner and outer follicles, is attached to the follicle stalk, the vesicle being composed of a flat epithelium, which in its turn is connected to the atrial epithelium or to the brood pouch specialized from it. In B. schlosseri, the egg is ovulated into the atrial cavity and remains there held by the brood cup, of which the inner epithelium is derived from the follicle stalk and the outer one from the atrial epithelium. In B. primigenus, the brood pouch develops as a diverticulum of the atrial cavity, around the entrance of which a fold differentiates from the atrial epithelium and closes the pouch during embryogenesis. In both species of Botrylloides, the brood pouch is formed by the outgrowth of the thickened atrial epithelium into the blood space, the entrance of which is closed during embryogenesis. The discarded outer follicle completely disintegrates soon after ovulation in B. schlosseri, but part of it remains throughout embryogenesis in the blood space in B. primigenus or projecting into the interior of the brood pouch in Botrylloides. In B. primigenus, the testis, when it accompanies the egg follicle, is placed at the bottom of the brood pouch and the sperm is shed through the pouch prior to ovulation. In B. schlosseri and the Botrylloides species, the testis is located independently from the egg follicle and the sperm matures after ovulation.

Notes: The cells of the follicular epithelium of the ovarioles of the mosquito, Aedes aegypti (L.), and of the stable fly, Stomoxys calcitrans (L.), have been found to be interconnected by cytoplasmic bridges. Cytoplasmic bridges have been reported between sibling gamete cells of both male and female insects, but these bridges have not been previously reported to exist between somatic cells of insects.

Notes: An unusual organelle in the oocytes of the marine mud snail Ilyanassa obsoleta is described and called a polymerosome, because of its several components. Polymerosomes appear at the beginning of vitellogenesis and persist, in part, through postvitellogenesis. The persistent part is similar to an organelle that has been described by other workers in the vegetal region and the polar lobe of the Ilyanassa egg.

Notes: An analysis of mechanical and architectural aspects of three hamstring muscles in the cat, semitendinosus (ST), semimembranosus anterior (SMa), and semimembranosus posterior (SMp), is presented based on whole muscle tetanic tension profiles. Length-active tension curves for each muscle were obtained by electrical stimulation of the whole muscle with a train of stimuli at 100 pulses per second (pps) for 600 milliseconds.Information from motion picture analysis (Goslow et al., '73) and electromyographic (EMG) activity (Engberg and Lundberg, '69) as seen during the step cycle is combined with analysis of joint torques to present a picture of the differential functions of the three muscles. The length-active tension characteristics of ST and SMa are such that they develop high amounts of tension throughout their physiological excursions. Maximal tension is produced over a much more limited range by SMp. A division of labor for the three muscles is proposed: the one-joint SMa is shown to be a primary hip extensor whose action facilitates smooth oscillation of the leg. Torque and electrical activity during the step cycle indicate the two-joint ST is a primary knee flexor. The more limited range of maximum torque and variable EMG pattern of the other two-joint muscle, SMp, relate to the fact that it has primary activity during high speed gaits when it may act to initiate spine flexion and assist in hip extension.Excursion and activity data have led to the conclusion that biarticular muscles (ST and SMp) may benefit from the combined action of two joints to maintain near maximal tension and torque during active phases of the step cycle. Thus, biarticular muscles may have evolved as much for the mechanical and physiological benefits they derive as for two-joint action itself.

Notes: Oogenesis has been investigated utilizing both light and electron microscopical techniques in the squid, Loligo pealei. This complex process has been divided into five stages according to the structure of the follicle. Because of the highly coordinated differentiation of the follicle cells (and follicular syncytium) and the oocyte, their development is described in concert. Specific attention is given to the contribution of the follicular syncytium to vitellogenesis and the formation of the extracellular egg envelope or chorion. Our observations indicate heterosynthetic yolk production and the synthesis of the secondary envelope by the follicular syncytium.

Notes: A recently presented model of tongue projection dynamics is used to generate a series of predictions concerning morphologies to be expected under selection for increased distance of projection, increased speed of projection, and increased directional versatility. A general understanding of biomechanical events and the model are used as points of departure for making specific predictions concerning details of structure in skeletal, muscular and connective tissue components of the tongue and associated structures. Comparative methods are used to examine these predictions in the genera of plethodontid salamanders. These salamanders are known to project their tongues to different degrees, and this knowledge is used to test the hypotheses concerning morphological specialization. Three distinct groups of plethodontid salamanders have evolved specializations for long distance projection, and these genera differ from one another in important ways in respect to specific character complexes. For example, the tropical genera and Hydromantes use CBII as the major force transmission element in the skeleton, while Eurycea and its allies use CBI in this role. Hydromantes differs from both in having a uniquely proportioned and structured hyobranchial skeleton and associated musculature. Less extreme specializations for tongue projection are found in different combinations in three other groups. Finally, two distinct groups of generalized species having only limited tongue projection capabilities are recognized, each having a unique complex of inter-related features. Each of these eight groups is recognized and characterized as a functional mode, and hypotheses concerning the biomechanical meaning of the character complexes of each are formulated.

Notes: The mechanical properties of the whole muscle and fast-twitch muscle units of the cat hindlimb pretibial flexors have been explored and related to normal locomotion. Tibialis anterior (TA) is parallel-fibered and functionally crosses a single joint, the ankle, whereas extensor digitorum longus (EDL) is pinnate and spans the ankle, knee, metatarsophalangeal and interphalangeal joints. The active tetanic tension of TA remains near its peak value over a range of muscle lengths associated with normal ankle movement. In contrast, the length-tension curve of EDL is sharply peaked. However, normal corollary action of the knee, ankle and metatarsophalangeal joints during stepping minimizes EDL's excursion and maintains it at or near a length optimal for peak tension development. EDL is capable of producing synchronous but sterotyped digit and ankle movements while TA provides for independent ankle flexion at all relevant joint angles.The mechanical properties of 84 TA and 98 EDL fast-twitch muscle units were studied by measuring twitch contraction time (≤45 msec), peak tetanic tension, response to repetitive stimulation, and contractile fatigue resistance during electrical stimulation of single alpha axons, functionally isolated from ventral root filaments. These mechanical properties were essentially similar for both muscles with the exception of mean peak tetanic tension which was 30% lower for TA units (14 gm-wt) than for EDL units (20 gm-wt). A high proportion of units in both muscles demonstrated fatigue resistance which is reflective of the repetitive, phasic demand upon these muscles during locomotion.

Notes: A survey is made of some ultrastructural features of the developing cornea of Macaca mulatta. The observations are confined to the anterior central area, starting with the lens vesicle stage and progressing through midgestation, when the morphologic characteristics of the cornea are fully established. Subepithelial filaments and some partially aggregated collagen fibrils are present in the earliest embryo and are of a size and appearance similar to those in the future vitreous cavity. Epithelial secretory activity points to, but does not prove direct contribution to the deposition of the acellular matrix components beneath it. No trace of a structured, orthogonal collagenous stroma can be visualized. The primitive endothelium forms prior to the fibroblast invasion of the distended filamentous matrix. Bowman's layer has undoubted epithelial contributions. Its aggregated collagen fibrils have approximately the same diameter as those of the anterior stroma. Intraepithelial appearance of single nerve fibers and fascicles takes place during the first trimester of gestation, as soon as the two continuous epithelial layers are formed. Terminal areas approach closely to the basal cell's nucleus, without touching it. The plasmalemma of the invaginating nerve fiber is surrounded by that of the epithelial cell in a mesaxon-like manner, with occasional gap junctions uniting adjoining neural and epithelial cell membranes. The fetal neurites contain microtubules, some clear vesicles and dense vacuoles resembling those of mature monamine and non-monamine neurons. Mitochondria are small and compact, their presence indicating a high rate of metabolic activity in the immature terminal area.

Notes: The structural features of sinus hair follicles in Sorex unguiculatus were studied by macroscopic dissection, serial section light microscopy and electron microscopy. The shrew has about 540 sinus hairs regularly arranged on the snout. The maxillary nerves innervating them are extremely thick, while the optic nerves are very thin. Thus the follicle must be one of the most important sense organs in this animal. In the follicle the ring sinus is well-developed and the trabeculae of the cavernous sinus are reduced in number and thickness. The ring bulge is not a unified structure but a pair of bodies which consist of head, stalk and attachment plaque. It is characterized by the presence of numberous thick collagen fibrils (400 nm) and appears to be mechanically rigid. Lanceolate nerve terminals, free endings, Merkel cells with nerve terminals and unmyelinated fibers are observed, but encapsulated endings are lacking in and around the follicles. Straight lanceolate terminals on the posterior side of the follicle are thick and three-sided in cross section, while those on the anterior side are thin and two-sided. Free endings are located on the anterior side of the follicle. These and other findings are discussed on the basis of the assumption that the Sorex sinus hair follicle is more specialized as a vibrating system than in other mammals.

Notes: Neurosecretory cells are arranged in 16 NSC centers in the different regions of the brain of O. tholozani. The component cells belong to 13 different types, of which five types are paraldehyde fuchsin positive and the remaining types are negative. Three of these cell types are here described for the first time. Some of these NSC show an affinity to certain localities inside the brain. Cells comprising a neurohaemal organ were found near the exit of the esophagus.

Notes: Yolk platelets in differentiating embryonic amphibian cells degrade by a membranous “unraveling” or “delamination” process. Acid phosphatase activity was demonstrated at the peripheries of those platelets which were in the process of degrading and thus this lytic enzyme appears to be involved in the breakdown process. We believe that this relationship provides a means by which early cells obtain the nutrients necessary for early differentiation.

Notes: The coelomocytes of Lumbricus terrestris have been classified and described, based on Wright's stained preparations and on living cells. The five major categories consist of basophils, acidophils, neutrophils, granulocytes and chloragogen cells. Both the acidophil and chloragogen cell groups contain two subgroups. Granulocytes also exhibit heterogeneity with respect to staining properties of granules. Some possess acidophilic granules, some basophilic granules, and others contain both types. Granules of acidophils have been observed to be occasionally excreted from the cells. All cell types, with the exception of chloragogen cells, produce pseudopodia and are capable of phagocytosis, a vital component of the earthworm's immune response.

Notes: Newly metamorphosed Kenyan reed frogs, Hyperolius viridiflavus ferniquei, are able to regenerate amputated digits. The terminal digital pad is also completely reformed. Differentiation of the regenerating digital pad was studied by scanning electron microscopy. External differentiation of the digital pad began late in the second postamputational week with the appearance of small patches of specialized epidermal cells on the ventral surface of the regenerating digit. The differentiation of the pad spread out radially until late in the fourth week, when its overall shape approximated that of the normal digital pad. The appearance of patches of digital pad epidermis on the ends of spike regenerates arising from the forearm was also confirmed.

Notes: The objectives of this research were to investigate the morphology of the thoracic skeleton and muscles of the mosquito, Culiseta inornata (Williston). The results are presented in 25 text figures and descriptions of each skeletal part and muscle. Undescribed exoskeletal structures are the postmediotergite, intersegmental cleft on the caudal margin of the metapleuron, and the parascutellar process. This process is considered a homologue of the fourth axillary. The acrotergite 2 and subalifer were identified. The prescutum has been called the paratergite by previous authors. The morphological basis for self amputation of legs is described. Undescribed parts of the endoskeleton are: lateral arm of sternal apophysis 1 and its socket on the mesal surface of coxa 1, furcopleural apodeme on sternal apophysis 1, precoxal and postcoxal apodemes arising from the ventral pleural arm, upper and lower laterotergite apodemes on the postnotum, and the pleural and intersegmental apodemes for attachment of halter muscles. Seventy-two muscles are illustrated with their attachments and the origin, insertion, and action of each is described. Ten of the muscles are newly described for the mosquito. There are no muscles inserted on the subalare, second axillary, or third axillary.

Notes: The results of reversing the polarity of the middle gastric region in Hydra viridis with multiple-gastric region grafts (3grp animals) are contrasted to previously reported results on comparably elongated animals (3g animals) whose middle gastric regions retain their original polarity. The middle gastric regions of 3grp animals are also bisected (the animals are hemisected) at various times after grafting. Compound heads and compound feet form at the proximal and distal graft borders, respectively, in nearly all 3grp animals. The regeneration of structures at points is a built-in property, not influenced by reversing the polarity of pieces during grafting. Regeneration is accelerated when comparable wound surfaces are brought together by grafting with reversed polarity. Graft rejection is influenced by the total length of an animal and distances from terminal structures, but not the polarity of pieces. Budding is also influenced by total length and distance, but is dependent on polarity and diminished by head regeneration. When fresh wound surfaces are made on the middle piece of 3grp animals, an initial refractory period, during which head and foot (but not budding region) regeneration is inhibited in about half the animals, is followed by an indefinite period in which head and foot regeneration is permitted (and budding region regeneration prevented). Hemisection does not interfere with the regeneration of compound structures already in progress. These results are interpreted in terms of theories of competence, negative dominance, threshold (positional value), inhibition (positional signal), and induction (positive or constructive dominance, stimulation or enhancement).

Notes: Neurosecretory A cells in the pars intercerebralis of O. fasciatus were identified at the ultrastructural level. Fine structural study of the A cells of female insects during the period of production of the first batch of eggs revealed that these cells undergo qualitative and quantitative changes during the first eight days of adult life. The A cells appear to be inactive in the newly emerged females. There is a significant depletion of neurosecretory granules (NSG) in the perikarya in the 2-day-old females followed by an increase and decrease in the 4- and 6-day-old females, respectively. The A cells in the 8-day-old females showed an accumulation of NSG. The mitochondrial population increases after adult emergence reaching a peak in the 4-day-old females, and then declines gradually in the subsequent age groups. The effect of sublethal dose of gamma radiation on the ultrastructure of the A cells was also investigated. Radiation damage is evident as early as four hours after irradiation with 10 kR. There is considerable swelling of the lysosomes and the membrane system in the A cells of irradiated insects. Synthetic activity of the A cells, based on the distribution of the endoplasmic reticulum, Golgi complex and mitochondria, as well as release of the NSG are apparently inhibited after irradiation. Radiation-induced damage becomes more conspicuous as post-irradiation interval increases. It is surmised that the damage to the A cells might have contributed at least in part, to the failure of yolk deposition in the irradiated insects.

Notes: The junction between human primary dentine and regular and irregular secondary dentine was examined with a number of different light and electron microscopic techniques. In decalcified material, a narrow band along the innermost surface of the primary dentine stained intensely. The walls of the tubules within the band stained intensely, whereas the tubular walls within the bulk of the primary dentine were not stained. Generally, the walls of the tubules in both types of secondary dentine were also preferentially stained. Although not readily apparent in ground sections, observations of thin sections revealed a dramatic reduction in the number of tubules in regular secondary dentine. Generally, the radiodensity of the intertubular matrix was the same in primary and secondary dentine and the intensely stained band was not seen radiographically. The pulpal ends of the tubules in primary dentine were often occluded with a material having the same radiodensity as peritubular matrix. Both patent and occluded tubules were seen in irregular secondary dentine. Scanning electron microscopy of acid-etched specimens of secondary dentine revealed that some tubules had irregular walls of highly mineralized matrix which was less acid-soluble than the peritubular matrix of primary dentine.

Notes: Simultaneous cine and electromyographic records of freely feeding, unanesthetized golden hamsters show that their motion and muscular activity during mastication differ from those of albino rats (Weijs, '75). Rats show only propalinal motion while hamsters show lateral translation as well. The masticatory muscles of hamsters and rats are generally similar, but their molar dentitions differ. The interlocking molar cusps of hamsters restrict propalinal protrusion and retrusion when the molars are in occlusion; however, hamsters readily unlock occlusion by a twisting movement in the horizontal plane. Rats may perform propalinal movements even with the teeth in occlusion.In mastication the hamstery's jaw moves laterally as well as vertically and anteroposteriorly. Chewing orbits typically reverse after one to three orbits. Reversal begins at the start of the upstroke and involves a lateral shift in the opposite direction with the mouth closed.Electromyograms show that symmetric and asymmetric activities of closing protrusive and closing retrusive muscles produce a unilateral force couple on both sides. (This couple accompanies a midline closing stroke.) When the mouth is closed, unilateral activity of closing retrusors and closing protrusors also induces lateral translation. A bilateral force couple pits the retrusors of one side against the protrusors on the opposite side. Simultaneous with lateral excursion to the opposite side of midline and the action of these closing muscles, the anterior digastric and lateral pterygoid muscles of one side fire asymmetrically.The mandible moves downward coincidently with bilateral activity of the digastrics and lateral pterygoids. As the jaw opens further, activity differences of the lateral pterygoids accompany a shift of the mandible toward midline. At the end of the downstroke, all masticatory muscles studied are silent. The jaw returns to midline when the adductors fire asymmetrically at the start of closing.Trituration appears to coincide with an initial simple protrusion, which is subsequently accompanied by lateral translation. Different food types are reduced by distint chewing patterns with the differences clearest when the teeth are near occlusion. During gnawing the lateral pterygoids and digastrics fire longer, and the closing muscles fire less strongly. Chewing patterns in golden hamsters appear more generalized than those of rats; the differences may be directly associated with the ability of hamsters to store food in their cheek pouches.

Notes: Projection microradiography was used to determine the density and orientation of the force transmitting structures, i.e., trabeculae and bone lying between approximately parallel vascular canals, within the bones of cat skulls. The organisation in the skulls was confirmed statistically for a total of ten cats. The results of the observations showed that within specific areas of the skull a high degree of structural orientation and an increased density of osseous structures was present. The distribution of these characters corresponded in contiguous bones such that a continuum of structural organisation was established between the alveolar region and the site of attachment of the temporalis and masseter muscles and the glenoid region.The patterns of force transmission during jaw closure were determined when a resistance was placed initially between the canines and then the carnassials. An analysis was first carried out on dry skulls using colophonium resin to determine the direction of the force distribution. The nature and the approximate magnitude of the forces were ascertained by replacing the resin with strain gauges. The basic similarities in the strain patterns recorded from the dry skulls and those from the ten anaesthetised cats in which strain gauges had been intra-vitally implanted, substantiated the recordings made on the dry skulls. Combination of the results from the three sets of experiments defined the patterns of force distribution in the cat skull during the closure of the mandible against a resistance. The results showed that: (1) the combined action of the temporalis and masseter muscles tended to reduce the overall strain in the skull bones, and that the deformations produced by the action of the masseter were greater than that exerted by the temporalis muscles; (2) during biting, whether the resistance was placed between the canines or carnassials, compressive forces predominated in the facial bones; (3) small movements observed between facial bones indicated the presence of a flexible component within the skull, thus allowing large forces to be exerted during biting without overstressing the facial bones; (4) the glenoid fossa is part of a force bearing joint; (5) forces generated during biting were resisted within the skull by forces of an opposite nature generated within the system, the incompressible nature of bone and by the effect of the soft tissues; (6) the nature and the magnitude of the strain altered when a resistance was placed at the canines and then at the carnassials; however, the pattern of force distribution within the skull remained the same; (7) there was a direct correspondence between the detailed structural organisation of the bones and the patterns of force distribution. This conclusion would appear to apply in general to mammalian skulls. The study also emphasises the importance, neglected hitherto, of carrying out a variety of experiments to determine the patterns of force distribution in bones.The Trajectorial Theory of bone organisation is discussed and, on the basis of the results obtained, a modified theory is proposed. This states that: the structural continuum is common to the compact and cancellous bone and comprises bony bars which are aligned in the optimum direction for the transmission of force to a region in the bone or bones where it is effectively resisted.

Notes: The tarsi of all three pairs of legs of both sexes of Aedes aegypti (L.) bear spine sensilla, five types of hair sensilla, which are designated A, B, C1, C2 and C3, and campaniform sensilla. Type A and B hairs, spines, and cam-paniform sensilla are innervated by one neuron with a tubular body, a characteristic of cuticular mechanoreceptors. In particular the hairs and spines are tactile receptors and the campaniform sensilla are proprioceptors. The C1, C2, and C3 hair sensilla have the morphological features of contact chemoreceptors. Type C1 and C3 hairs are innervated by five and four neurons, respectively, which extend to the tip of the hair. Type C2 is innervated by five neurons, one of which terminates at the base of the hair in a tubular body while the remaining four extend to the tip of the hair. The role of the type C hairs in oviposition behavior, nectar feeding, and recognition of conspecific females is discussed. Presumed efferent neurosecretory fibers occur near the spine and hair sensilla.

Notes: Serial histological sections of kangaroo rats of postnatal ages 0-, 3-, 7-, 10-, and 14-days were prepared and studied. At birth the middle ear is mostly filled with mesenchyme and small in size, having only a small hypotympanum and a very small epitympanic recess. During the first postnatal two weeks, much of the hypertrophy found in the adult middle ear develops. Because an entotympanic element is never formed, the previously called entotympanic chamber is here renamed the hypotympanum. The epitympanic recess greatly expands to form what has been called the dorsal (or anterior) mastoid sinus. Since this chamber has no relation to the mastoid, it is here renamed the epitympanum. Posteriorly, the previously called posterior mastoid sinus develops from the growth of the hypotympanum into and beyond the region of the posterior and horizontal semicircular canals. In development and adult position it is comparable to the primate antrum and so is here renamed the antrum.At birth the organ of Corti is very immature but its major cell types can be identified. During the first two weeks of development the following events occur: (1) the vas spirale disappears, (2) the inner spiral sulcus cells atrophy, (3) the hair cells and supporting cells mature, (4) the cells of Hensen differentiate with their apical processes elevating the reticular lamina, (5) the innermost cell of Claudius migrates under and supports the Hensen's cells, and (6) the hyaline mass of the zona pectinata of the basilar membrane loses its connective tissue cells and expands in size. The developmental events support the previous description and identification of Hensen's and Claudius' cells.

Notes: The micro-anatomy of the corpuscles of Stannius of the toadfish, Opsanus tau, an aglomerular marine teleost, has been studied by light and electron microscopy. The corpuscles are composed of extensively anastomosed cords of epithelial cells which maintain intimate contact with blood capillaries. Most of the epithelial cells contain acidophilic granules which also show a positive reaction with the periodic acid-Schiff technique and aldehyde fuchsin. On the basis of fine structural criteria, three cell types can be recognized. The granular cells contain abundant quantities of granular endoplasmic reticulum, ribosomes, Golgi apparatus with prosecretory granules, coated vesicles, polymorphic mitochondria with lamellar cristae, filaments, microtubules, a cilium, a variety of lysosome-like dense bodies, glycogen particles, lipid droplets, secretory granules and intranuclear lipid-like inclusions. One variety of agranular cell (type I) is characterized by the total absence of secretory granules, but it contains large amounts of granular endoplasmic reticulum and ribosomes, conspicuous profiles of Golgi apparatus, coated vesicles and sometimes an abundance of glycogen. Another variety of agranular cell (type II) has poorly developed cytoplasmic organelles. The perivascular space between the capillary and parenchyma contains connective tissue cells and abundant nerve fibers. The different types of epithelial cells observed in the corpuscles of Stannius of this fish may represent functional stages of the secretory cycle in a single cell type.

Notes: The nervous system of the maldanid polychaetes Clymenella torquata (Leidy) and Euclymene oerstedi (Claparede) (= Caesicirrus neglectus [Arwidsson, '11-'12]) retains its primitive association with the epidermis. It shows only slight metamerism in the presence of larger collections of neurones opposite the parapodia and of larger nerves at the segmental boundaries. Multicellular giant fibers are present in the ventral nerve cord; giant neurones which show a characteristic pattern of distribution in each species are also present. The cerebral ganglia supply nerves to the prostomial wall, nuchal grooves and the wall of the buccal cavity, and a pair of large nerves from the circumpharyngeal connectives also appear to join the buccal system. The organs of special sense are the elongated prostomial nuchal grooves, and prostomial ocelli in Euclymene but not in Clymenella. Statocysts are absent.Four pairs of nephromixia are present. They lie in the aseptate anterior trunk, in chaetigers 5-9 of Clymenella, and 6-10 of Euclymene. The nephridiopores lie at the ventral ends of the neuropodia of chaetigers 6-9 and 7-10, respectively. Each nephromixium consists of coelomostome, tubule and contractile bladder. The wall of the tubule and bladder consists of both excretory and ciliated cells. Most of the cytoplasm of the latter forms a bounding layer at the outer surface. The cytoplasm of the excretory cells contains lipid material and appears to synthesize lipofuscin. The tips of the excretory cells swell, fill with granules, and break off in the form of vesicles which are periodically expelled in clouds from the nephridiopores. Glycogen is present, especially in the ciliated cells of the tubule and coelomostome.Granules of a lipoid nature accumulate in (or between) cells of the nephridia, epidermis, and some regions of the gut, and may be excretory. Lipid granules also appear to be synthesized by coelomocytes which eventually end up in masses in the ventrolateral coelomic cavities of the tail.The nephridia act as gonoducts, but show no seasonal variation in either size or histological structure.

Notes: The ascophoran Pentapora foliacea was studied from epoxy sections of skeletal and soft (hard-soft) tissues. The basal wall is double, indicating the colony grew as two independent layers, back to back. The structure of the vertical walls and interzooidal communication organs indicates that zooids were budded in the usual way as in most encrusting cheilostomes. Secondary layers of the frontal wall are of acicular aragonite. The ovicell develops as a flattened cuticular bladder in early ontogeny; the aragonitic layer of the frontal wall later engulfs it. A median vesicle, an evagination of the vestibular wall, is present but the eggs may be supplied with sufficient yolk to nurture the embryo. The overall ovicell structure is similar to that of hyperstomial ovicells in other cheilostomes.

Notes: This investigation describes the pre-natal morphogenesis of the type I pneumocyte subsequent to its differentiation from pulmonary epithelium. Cells lining subpleural alveolar septa were photographed from serial sections with the electron microscope, and a three-dimensional representation of each cell was obtained by transferring the contours of the cell membranes from montages to transparent plastic sheets which were then spaced to scale and stacked. The results of this study indicate that: The nascent blood-air barrier of a 50-day reconstructed cell was twice as thick as the average definitive barrier; definitive barrier thickness was observed in some areas in a 63-day reconstructed cell; the amorphous component of elastic tissue which appears peripherally in septal connective tissue during pre-natal morphogenesis may be directly juxtaposed to the basal lamina of the alveolar epithelium; the orientation of the cell junction between a pneumocyte and its neighboring cells, as observed in sections of alveolar septa, changes as the contour of the pneumocyte changes from simple abutment to overlapping patterns.

Notes: The fine structure of the mid-gut musculature of the desert locust, Schistocerca gregaria is described and compared with that of the visceral muscles of other species. The gross morphology and fine structure of the nervous system which supplies the mid-gut muscle fibres is described.

Notes: The integument of Paranthessius anemoniae has been studied with light and electron microscopy. A cuticle with clearly defined epicuticular, exocuticular and endocuticular regions overlies a cellular hypodermal layer. The distribution of carbohydrate, lipid and protein components of the cuticle were demonstrated histochemically. Parabolic striations in oblique sections of cuticle suggest that its molecular architecture fits a “twisted sheet” theory proposed for other species.Arthrodial membranes at body and limb joints have a homogeneous structure, lacking exocuticle and endocuticle. Subcuticular glands appear to secrete substances thought to be responsible for the immunity which Paranthessius seems to have to the nematocysts of its host. Small hairs, situated in cuticular cups which occur over the dorsal body surface are considered to function as rheoreceptors.

Notes: The larval epithelium of the sea urchin, Lytechinus pictus, consists of squamous cells and bands of columnar epithelial cells bearing cilia. During metamorphosis this tissue undergoes a series of rapid, complex changes. Through the scanning and transmission electron microscope, we describe and analyse these changes. The changes can be divided into three steps. (1) The larval arms bend away from the left side of the larva, exposing the urchin rudiment. Cells which are identical to smooth muscle cells are in a position to bring about this bending. (2) The squamous epithelial cells assume a cuboidal shape. This change in shape results in the collapse of the larval epithelium onto the presumptive aboral surface. These cells possess a subapical band of microfilaments. The cellular shape change but not the bending of the arms is reversibly inhibited by Cytochalasin B. These observations suggest a mechanism for this change. (3) The former lining of the vestibule of the urchin rudiment comes to lie over the collapsed larval tissue and forms the adult epithelium. At this point, after only one hour, the larva has assumed the external shape of an adult sea urchin.

Notes: The mucous gland of the red-spotted newt, Notophthalamus viridescens viridescens, Rafinesque was examined by histochemical and ultrastructural techniques and its cytological responses to various hormonal conditions were studied. Its secretory epithelial cells produce and release in merocrine fashion a neutral, unsulphated mucosubstance. The secretory epithelium is bounded peripherally by a thin, but apparent non-functional, myo-epithelium. The duct of this mucous gland consists of a single keratinized tubular cell that extends from the neck region of the gland to the surface of the epidermis.Mucous secretion is absent or greatly reduced on the skins of newts maintained under laboratory conditions for a few weeks but reappears after injection of ovine prolactin. Mucous glands in laboratory conditioned animals show a 4-fold increase in volume brought about by the engorgement of their epithelial cells with secretory granules. Ovine prolactin reduces the volume of the glands to unconditioned levels with a corresponding reduction in granular content, suggesting that prolactin functions in the release of the granules. This view is reinforced by the findings that autotransplantation of the pituitary gland prevents the conditioning effect and that glandular volume increases in auto-transplanted animals given ergocornine. Granular accumulation begins also in hypophysectomized newts but ceases after a week, indicating the need for some hypophyseal factor in the synthesis as well as the release of the granules. Ovine prolactin restores mucous glands of hypophysectomized newts to the unconditioned state. Contrary to earlier findings, ovine prolactin induces a reduction in the volume of the mucous gland in thyroidectomized newts.

Notes: The process of coelomic pouch formation in Pisaster ochraceus was studied with light microscopy, transmission and scanning electron microscopy and time-lapse cinemicrography as well as with the drug cytochalasin B. As in most asteroids, the paired coelomic pouches of Pisaster ochraceus are formed from outpocketing of the archenteron.Arrays of 50 Å microfilaments are found in the presumptive coelomic pouch cells at the apex of the archenteron as well as in the filopodia of the mesenchyme cells. Both cell types undergo active movements throughout the entire process. Treatment of embryos with cytochalasin B (CCB) during coelomic pouch formation results in the loss of cell movements and the regression of the coelomic pouches; this is accompanied by the loss of microfilament arrays in both cell types. Cell movements and microfilament arrays reappear on removal of CCB and coelomic pouch formation resumes.Our evidence suggests that the microfilaments in the presumptive coelomic pouch cells provide the main force for the outpocketing movement. The major role of the microfilament arrays in the filopodia of the mesenchyme cells associated with the coelomic pouches is to determine the definitive shape and location of the pouches.

Notes: Morphological changes of the ovary of the Chinese cobra, Naja naja, throughout the annual reproductive cycle are described. A single clutch of between 6 and 22 eggs is produced in late June. From July to the following April the ovary remains quiescent and contains small previtellogenic, hydration stage follicles. The growth of an ovarian follicle from a primary oocyte to maturation and ovulation is estimated to take three years. The histology of the germinal epithelium and the follicular granulosa shows seasonal changes correlated with the growth of the oocyte. During the quiescent period, the germinal epithelium lacks mitotic activity, but during April, when yolk deposition and rapid growth of the preovulatory follicles take place, the germinal epithelium shows intense mitotic activity. The growth of the smallest hydration stage follicles, and the occurrence of cytoplasmic bridges between the pyriform cells of the granulosa and the developing oocyte, also appear to increase during this period. The possible function of the pyriform cell is discussed and the literature on the origin and fate of these cells in the squamate ovary is reviewed. Postovulatory follicles (corpora lutea) and two types of atresia are described and compared with what is known of these structures in other reptiles.

Notes: An experiment was undertaken to determine which sensory structures of the mouse embryo inner ear developed from what portion of the mouse otocyst. Otocysts of gestation days 10, 11, 12 and 13 were divided by surgical dissection into six anatomical groups: dorsal, ventral, anterior, posterior, medial and lateral halves. They were organ cultured separately. After a period of ten days, the explanted tissues were harvested and processed histologically for microscopic analysis. The surgical control specimens fixed at the time of explanation were composed of undifferentiated ectodermal cells for tissues of gestation days 10, 11, and 12. Otocysts of gestation day ten showed no gross morphological differentiation. Otocysts of gestation days 11 and 12 showed, during the course of their subsequent growth, that the three semicircular ducts and their associated cristae developed from the dorsal and lateral halves. Only the anterior and posterior canals and cristae originated from the medial portion. The posterior half gave rise to the posterior crista and the anterior half provided for the development of the anterior and lateral cristae. The cochlear duct and its sensory epithelium developed in all the anatomical groups except the dorsal half. The utricle developed in the dorsal section of the middle third of the otocyst, while the utricular macula developed in the anterior half of the same section of the otocyst. The saccule and its macula differentiated from the ventral section of the middle third of the anterior half.

Notes: A consideration of head development in two species of Esox, lucius and americanus (ssp. vermiculatus) representing the two subgenera Esox and Kenozoa respectively, focused on the significance of the variations of the latero-sensory canal system, its associated bones, and other skeletal elements. In living forms only aspects of “regression” or specialization can be studied. Canals tend to be reduced to pit lines first at their termini but can be broken in their course. Pit lines range from nearly canals to surface structures, or even fail to develop. The number of neuromasts varies. Canal bones develop from two centers: neuromast related and deeper membranous centers which may have no relationship to neuromasts. Tooth-bearing and non-canal-related dermal bones have only membranous (original) centers. The number of neuromasts associated with a bone usually does not affect its development or form. In the case of the circumorbital bones, the extrascapulars, and the nasal, a one to one relationship has developed by regression - towards the development of the latero-sensory component only. The idea that reductions in bone number are commonly traceable to fusion is rejected although examples of fusion are known. Most bones that disappear are simply lost (no blastema or other evidence of their presence seen in development). The relationship between dermal bone and chondral bone is examined and there is evidence of the former giving rise to the latter. The ontogenic order of appearances shows a feeding (functional) correlation.

Notes: The nucleus rotundus of 21 species of teleosts was studied by a modified Bodian and the Golgi method to clarify the histological organization, with special reference to the cell lamination and the glomerular formation.The common components of the nucleus in all species are as follows: a thick fiber bundle which comes from the commissura horizontalis and enters the nucleus from the dorsal surface, many small cells, large cells, glomeruli, and a surrounding fibrous capsule. The nuclei of all species studied are classified into three types mainly on the distribution of the small cells, and to a lesser degree on the location of the large cells and the glomeruli.The first type of nucleus has small cells. large cells and glomeruli throughout its extent. In the second type of nucleus, many small cells form a peripheral cell layer, while the large cells and glomeruli are found all over the nucleus.The third type of nucleus is clearly laminated. It is composed of four layers arranged concentrically around a central fiber net in the following order: a glomerular layer, a fibrous layer, a small-cell layer, and a peripheral fibrous capsule. In some species, the large cells are located in the fibrous capsule, and all glomeruli contain a star-like structure, which corresponds to the tips of the large cell dendrites.

Notes: The pineal-paraphyseal complex of sea turtles is an impressively large structure which projects dorsally and anteriorly above the prosencephalon. The complex was examined by light microscopy in several age classes of green sea turtles (Chelonia mydas) and from juvenile loggerhead turtles (Caretta caretta). The paraphysis is extensively fused to the distal portion of the pineal body, suggesting an interrelated function for these two tissues. No duct or canal was observed connecting the pineal lumen to the third ventricle. Two pineal cell types are described which appear to correspond to the neuroglial supportive cells and the secretory rudimentary photoreceptor cells of other amniotic vertebrates. A possible luminal secretion in the form of apical protrusions is produced by the latter cell type. No typical photoreceptive outer segments were observed.

Notes: The fine structure of the wax gland of Anomoneura nymph and its metamorphic change were investigated. In the nymph, this organ encircles the anus, and consists of two kinds of cells, derived from epidermal cells: (1) very tall, slim wax cells, which produce and secrete the wax, and (2) flat interstitial cells found among the wax cells. The whole gland is covered by a wax-secreting cuticle with a delicate surface sculpture. Each wax cell has a long, wide duct which opens at the cuticle and penetrates the entire cell. Its cytoplasm is rich in mitochondria and smooth endoplasmic reticulum while that of interstitial cells contains rough endoplasmic reticulum. During each nymphal molt, the cluster of primordial wax gland cells  -  derived from the epidermis  -  proliferates rapidly and forms the gland of the next instar. The gland of the preceding instar meanwhile degenerates. Interstitial cells play an important role in cuticle formation and shedding at each molt. These cells alone produce and deposit the new cuticle of the next instar; the wax cells, specialized for wax production, cannot produce cuticle. The apical portion of the wax cell is cut off from the main cell body by growth of the surrounding interstitial cells. Thereafter, the wax cells degenerate, resulting in the rapid disappearance of the previous instar's wax gland. Adults lack this gland entirely.

Notes: The dorsal ventricular ridge (DVR) is a subcortical, telencephalic structure in reptiles and birds that protrudes into the lateral ventricle. The structure of DVR has been studied in the red-eared turtle (Pseudemys scripta elegans) in Nissl and Golgi preparations. The DVR in Pseudemys is divided into the anterior dorsal ventricular ridge (ADVR) and the basal dorsal ventricular ridge (BDVR) by the dorsal branch of the middle ventricular sulcus. The structure of ADVR has been examined in detail.The ADVR is divided into four regions with distinct boundaries termed dorsal area, medial area, ventral area and central area. Dorsal area, medial area and ventral area border on the lateral ventricle; central area lies deep to the other areas. Three classes of neurons are found in Golgi preparations of ADVR. Juxtaependymal cells have somata near the perikarya of ependymal cells; their dendrites are found primarily in a periventricular fiber zone. Aspiny neurons were observed only in the dorsal half of ADVR and appear to be restricted to deep regions of the ridge. These multipolar neurons are rarely encountered in Golgi preparations, and the observed distribution may not represent their actual distribution in ADVR. The majority of the cells observed in ADVR are spiny neurons with dendritic fields that range from stellate to double-pyramidal. Cells in this class may be subdivided on the basis of axonal morphology into at least two groups, but further studies are needed to determine the range of axonal morphology exhibited by these neurons.An analysis of the distribution of these cell types in Golgi material shows that dorsal area, medial area and ventral area are organized in four zones concentric with the ventricular surface. Central area apparently lacks a concentric pattern of organization. Zone 1 is a periventricular fiber band that contains juxtaependymal neurons and ascending dendrites of zone 2 spiny neurons, and it may serve as a structural substrate for segregated input onto these cell populations. Zone 2 contains clusters of spiny neurons with apposed somata, which vary in size and distribution between areas. Dendrites of zone 4 neurons are also found in the deep half of zone 2. Zone 3 is a cell-poor region which lies at the center of a region of overlapping dendritic fields of zone 2 and zone 4 neurons. Zone 4 contains predominantly spiny neurons (aspiny neurons are found only in the dorsal half of ADVR) which are either isolated or in small clusters with apposed somata. Dendrites of zone 2 cells extend superficially into zone 4, so that the deep portions of zone 4 may be a substrate for segregated input to zone 4 neurons. These zones are differentially elaborated in each area. Central area, by contrast, consists of scattered spiny and aspiny neurons among fibers connecting ADVR and the lateral forebrain bundle.A comparison of these findings with the ADVR of snakes (Ulinski, '78a,b) shows both similarities and differences in DVR organization in the two taxa. Although snakes lack areal divisions, ADVR is organized in four concentric zones (zones A-D). Zones A and B resemble zones 1 and 2 in turtles, consisting of a superficial fiber zone and a subjacent cell cluster zone. The clusters are smaller in snakes than in turtles. However, snakes lack a cell-poor band deep to zone B, and dendrites of cells in zone C enter zone A. Thus, there are differences in both areal and zonal dimensions of ADVR organization in turtles and snakes.

Notes: Ultrathin sections of the nasal barbel of the channel catfish, Ictalurus punctatus, were studied in the electron microscope and the fine structure was compared to that of barbels of other teleosts and to the mandibular (dentary) barbels of I. punctatus. While the overall histology of the nasal barbel is similar to that of barbels described previously, this study revealed far greater cellular complexity and variability than was previously reported. A layer of stratified epidermal cells rests upon a connective tissue dermis containing a cartilage rod, a large number of nerve fibers and numerous blood vessels, fibroblasts and pigment cells. Taste buds are present in the epidermal layer. This layer was found to contain probably 16 kinds of cell types, several of which may represent transitional stages, in addition to taste bud cells. Observations were made pertaining to innervation and cell types in the taste buds. A new terminology for designating the barbels of I. punctatus is suggested.

Notes: Fully mature adult Eisenia foetida sensory buds are abundant on the prostomium and the first segment. In subsequent segments they are restricted to the anterior half where they form a single row aligned with the setae and encircling the worm. In the more posterior regions of the worm the buds are widely separated and fewer. The surface of each bud is a raised circular or oval area from which 15 to 100 so-called sensory hairs arise, being cylindrical and apparently flexible. The number of these projections decreases toward the posterior end of the worm.In worms newly emerged from egg cocoons, the general pattern of distribution and external form of sensory buds resembles that of adults, but the buds are much fewer and smaller than in adults. Although these worms emerge with their definitive adult number of segments, new buds and additional sensory projections are formed during post hatching development.

Notes: The distribution and morphology of phagocytic (Type II) supraependymal cells residing within the third ventricle of the guinea pig were investigated by scanning electron microscopy. Type II supraependymal cells were restricted to nonciliated regions of the ventricle. They were most numerous on the choroid plexus, abundant within the infundibular recess and were present on the ventricular floor in the region of the median eminence. Morphologically, they were characterized by a soma from which pseudopodia-like processes extended to the subjacent ependyma. Type II cells varied in configuration according to their location. Those residing on the choroid plexus typically had irregular somas and possessed processes that generally terminated in finger-like extensions. In contrast, cells on the ventricular floor and within the infundibular recess were stellate and possessed processes that terminated in fan-like cytoplasmic expansions. There were no differences noted in the frequency, distribution or morphology of Type II supraependymal cells in male and female animals. Furthermore, cell frequency did not appear to vary in relation to the estrous cycle. The data suggest that the pleomorphism exhibited by Type II supraependymal cells may reflect adaptations to diverse environmental conditions present within different regions of the third ventricle.

Notes: Study of the fine structure of the macronucleus in Euplotes eurystomus, a ciliate protozoon, during various stages of the cell division cycle has yielded new information about intranuclear helices. They are frequently observed at the periphery of chromatin bodies or next to the nuclear envelope, and they appear to be a constituent of nucleoli. The fibril that forms a helix is about 11-15 nm thick, and torus profiles of helices cut in cross section are about 35 nm in diameter. In substructure the helix is composed of a thin strand 3-5 nm thick which is coiled to form the 11-15 nm fibril; so the helix is a super-coiled structure. The intranuclear helices are present in the macronucleus throughout the cell cycle. They do not show obvious changes of relative abundance nor changes of relative localization in the nucleus, with one exception: they were never observed in the diffuse zone of replication bands. Evidence is presented indicating that nuclear helices migrate to the cytoplasm through nuclear pores. Although the chemical composition of the Euplotes intranuclear helices is unknown, information in the literature on similar helices in Amoeba indicates that they contain RNA and not DNA. The observations on Euplotes helices are consistent with a concept of “packaged” RNA for transport to the cytoplasm.

Notes: Eggs of the turtle Trionyx spiniferus are rigid, calcareous spheres averaging 2.5 cm in diameter. The eggshell is morphologically very similar to avian eggshells. The outer crystalline layer is composed of roughly columnar aggregates, or shell units, of calcium carbonate in the aragonite form. Each shell unit tapers to a somewhat conical tip at its base. Interior to the crystalline layer are two tertiary egg membranes: the outer shell membrane and the inner shell membrane. The outer shell membrane is firmly attached to the inner surface of the shell, and the two membranes are in contact except at the air cell, where the inner shell membrane separates from the outer shell membrane. Both membranes are multi-layered, with the inner shell membrane exhibiting a more fibrous structure than the outer shell membrane. Numerous pores are found in the eggshell, and these generally occur at the intersection of four or more shell units.

Notes: The afferent and efferent components of the facial nerve were traced within the brain stem of Rana catesbeiana, using three different neuroanatomical techniques. Primary afferent fibers could be traced to the spinal tract of trigeminal nerve and to fasciculus solitarius as far caudally as the first or second spinal segment, using silver degeneration methods. Cobalt filling of the entire nerve showed the same distribution of afferent fibers, as well as the filling of the cells within the mesencephalic nucleus of trigeminal, indicating the origin of a proprioceptive component of the facial nerve. Cobalt iontophoresis and horseradish peroxidase experiments showed that the motor nucleus of the facial nerve was located just ventral to the fourth ventricle, and caudal to the motor nucleus of trigeminal. The distribution of afferent fibers to fasciculus solitarius and the spinal tract of trigeminal is similar in some respects to the distribution of afferent fibers from the trigeminal and vagal nerves in the bullfrog. The afferent fibers from the three cranial nerves are found as far caudally in the brain stem as the second spinal segment.

Notes: The morphology of tooth crowns is variable inter-specifically among caecilians. Cusp number and shape, crown dimensions, and crown curvature characterize various species and have both functional and phylogenetic implications. Ichthyophis, Uraeotyphlus, Hypogeophis, and Geotrypetes have bicuspid teeth; Dermophis, Gymnopis, Caecilia, and Typhlonectes monocuspid. Crown morphology as revealed by scanning electron microscopy is associated with prey grasping and, in one case, possible specialization of prey type.

Notes: The structure of contact chemoreceptors in the cibariopharyngeal pump of the moth Trichoplusia ni (Lepidoptera: Noctuidae) is described. Two types of receptors designated A and B are located on the floor of the pump. Two groups of 9-12 A receptors are located in the anterior part of the pump, and two groups of two B receptors are in the posterior part of the pump. Five sensory dendrites extend to the tip of each A receptor and four to each B receptors. Available evidence indicates that these receptors are contact chemoreceptors and do not serve as mechanoreceptors. The receptors are compared to those of other insects.

Notes: Classical light microscopic studies on pigmentation of Fundulus heteroclitus (killifish) indicated that there are three groups of light reflecting cells; one group on the surface of scales reflects white light, while two other deeper groups (the melaniridophores and the stratum argenteum) are iridescent. The results presented here show that: (1) The scale leucophores reflect white light by a Tyndall light-scattering mechanism, by virtue of the presence of randomly oriented organelles of “novel” morphology. (2) The iridophores of the melaniridophores contain stacks of irregularly-spaced, large reflecting platelets which function as an imperfect multiple thin layer interference system. (3) The stratum argenteum consists of a continuous layer(s) of iridophores with reflecting platelets which are so regularly packed as to approach an ideal multiple thin layer interference system. (4) In all three types of light reflecting cells, the dimensions and packing (orientation) of the reflecting organelles satisfactorily account for the chromogenic properties of the cells, including colors as viewed under transmitted, reflected, or polarized light. (5) The spacial relationships between these light reflecting cells and adjoining melanophores are different for each type of light reflecting cell. Furthermore, we propose to replace the term reflecting platelet with refractosome.

Notes: The chloride cells in the interlamellar areas of the gills of young adult, anadromous sea lampreys, Petromyzon marinus L., captured in fresh water undergo structural modification during the adaptation of these animals to sea water. In fresh water the chloride cells are partially overlapped by mucus-secreting superficial cells and contain an extensive reticulum of cytoplasmic tubules, which are confluent with both lateral and basal plasma membranes, numerous mitochondria, a Golgi complex of moderate size, and numerous apical vesicles. Adaptation to sea water results in a retraction of the superficial cells, exposing the entire apical surface of the chloride cells, and a proliferation of both cytoplasmic tubules and mitochondria. Extensive enlargement of the Golgi complex in the chloride cells of these animals suggests the involvement of this organelle in the proliferation of cytoplasmic tubules. The extracellular tracer, ruthenium red, enters the tubules from the lateral or basal intercellular spaces in both freshwater- and seawater-adapted animals but never enters either tubules or vesicles from the apical surfaces, indicating that these are not confluent. The presence of dividing basal cells and newly-forming chloride cells, combined with evidence of degeneration of chloride cells, suggests that there is a turnover of this cell type. Both superficial and basal cells are phagocytic and involved in heterophagy of degenerating chloride cells. This phenomenon occurs in both fresh water and sea water indicating that the chloride cells may be functional in both environments.

Notes: This study consists of a detailed cytoarchitectonic and Golgi analysis of a major tectofugal thalamic nucleus in the red-eared turtle, Pseudemys scripta elegans. Neurons in nucleus rotundus have a unimodal soma size distribution and a common dendritic branching pattern. They have long dendrites which undergo sparse, dichotomous branchings and contribute to dendritic fields that cover a third to half the dimensions of the nucleus. Spicules, 1-2 μ long, and complex appendages, 5-20 μ long, are found with low density on many dendrites in Golgi-Kopsch material. A few cells have beaded dendritic processes. Three cytoarchitectural regions can be differentiated in nucleus rotundus: a shell, a cell-poor region and a core. The shell is a monolayer of somata forming the peripheral boundary of most of the nucleus. The cell-poor region forms a thin zone concentric with and internal to the shell. Shell cells send some of their dendrites concentrically within this zone and others radially into the core region. Core neurons are dispersed within the neuropil of the nucleus and usually have spherical dendritic fields. However, peripheral core neurons have asymmetrical fields, so their dendrites do not extend beyond the shell. Caudomedial and central subregions of the core can be defined on the basis of neuronal density and cytology. Somata in the caudomedial area of the core are densely packed and have slightly darker staining cytoplasm than those in the central subregion. However, their dendrites are similar to those of the central core neurons. There is extensive dendritic overlap between the two subregions.

Notes: As a part of a continuing study of unusual molluscan tissues, the “chondroid” tissue (Hyman, '67) associated with the anterior and posterior aortae of the slug (Limax maximus) was examined by light and electron microscopy. Unlike the odontophoral tissue of this species (Curtis and Cowden, '77), the “chondroid” tissue comprising the adventitial layer of the aorta consists of large, glycogen-filled cells with characteristic arrays of pores in their plasma membranes resembling those of the “globular” cells (Rogers, '69; Fernandez, '71); “fibrocytes” (Nicaise et al., '66; Baleydier et al., '69; Nicaise, '73); “Blasenzellen” or “Leydig” cells (Wondrak, '69; Stang-Voss, '70; Buchholz et al., '71; Stang-Voss and Staubesand, '71; Wolburg-Buchholz, '72); or “pore” cells (Sminia, '72; Beltz, '77) of other mollusks. The anterior and posterior aortae are very similar in organization, except that the anterior aorta is larger in diameter; its wall is thinner; and it lacks calcification. Both the anterior and posterior aortae possess a loosely organized (incomplete) endothelial layer surrounded by two layers of innervated smooth muscle. The smooth muscle cells possess fibrous surface specializations resembling hemidesmosomes as well as large numbers of tubular or rounded vesicles in association with their plasma membranes. Blood cells (amoebocytes) containing large glycogen deposits and distinctive membrane-enclosed cytoplasmic inclusions can be found occasionally in the walls of the vessels.

Notes: Reticulate scales develop as radial symmetrical anlagen, in contrast to scuttate scales which appear initially as “epidermal placodes.” Unlike scuttate scales whose outer and inner epidermal surfaces elaborate β-and α-type keratins, respectively, reticulate scales elaborate only one type of epidermal surface which has been reported to give an α-type, X-ray diffraction pattern. We find that, histologically and ultrastructurally, this surface differs from either epidermal surface of scuttate scales. The keratinizing cells become filled with long interweaving bundles of α-filaments which aggregate into rather homogeneous α-fibrils. Keratohyalin granules, which have been shown to be associated with other keratinizing regions in the bird, do not form during the keratinization of reticulate scale epidermis.

Notes: The ultrastructure of the parathyroid glands of adult Japanese lizards (Takydromus tachydromoides) in the spring and summer season was examined. The parenchyma of the gland consists of chief cells arranged in cords or solid masses. Many chief cells contain numerous free ribosomes and mitochondria, well-developed Golgi complexes, a few lysosome-like bodies, some multivesicular bodies and relatively numerous lipid droplets. The endoplasmic reticulum is mainly smooth-surfaced. Cisternae of the rough endoplasmic reticulum are distributed randomly in the cytoplasm. Small coated vesicles of 700-800 Å in diameter are found occasionally in the cytoplasm, especially in the Golgi region. The chief cells contain occasional secretory granules of 150-300 nm in diameter that are distributed randomly in the cytoplasm and lie close to the plasma membrane. Electron dense material similar to the contents of the secretory granules is observed in the enlarged intercellular space. These findings suggest that the secretory granules may be discharged into the intercellular space by an eruptocrine type of secretion. Coated vesicles (invaginations) connected to the plasma membrane and smooth vesicles arranged in a row near the plasma membrane are observed. It is suggested that such coated vesicles may take up extracellular proteins. The accumulation of microfilaments is sometimes recognized. Morphological evidence of synthetic and secretory activities in the chief cells suggests active parathyroid function in the Japanese lizard during the spring and summer season.

Notes: The accessory muscle of the walking leg of the horseshoe crab, Tachypleus gigas, was examined electron microscopically. The muscle fibers vary in size but are small in diameter, when compared with other arthropod skeletal muscles. They are striated with A, I, Z and poorly defined H bands. The sarcomere length ranges from 3-10 μm with most sarcomeres in the range of about 6 μm. The myofilaments are arranged in lamellae in larger fibers and less well organized in the smaller ones. Each thick filament is surrounded by 9-12 thin filaments which overlap. The SR is sparse but well organized to form a fenestrated collar around the fibrils. Individual SR tubules are also seen among the myofibrils. Long transverse tubules extend inward from the sarcolemma to form dyads or triads with the SR at the A-I junction. Both dyads and triads coexist in a single muscle fiber, a feature believed to have evolutionary significance. The neuromuscular relationship is unique. In the region of synaptic contact, the sarcolemma is usually elevated to form a large club-shaped structure containing no myofilaments and few other organelles. The axons or axon terminals and glial elements penetrate deep into the club-shaped sarcoplasm and form synapses with the fiber. As many as 13 terminals have been observed within a single section. Synaptic vesicles of two types are found in the axon terminals.

Notes: The combined techniques of light microscopy, scanning (SEM) and transmission (TEM) electron microscopy were used for the first time to study the structure of unicameral lungs of a Tegu lizard (Tupinambis nigropunctatus). The lungs are prolate spheroid bags with blood supplied by superficial branches of a dorsal pulmonary artery and returned by diffuse, more deeply located veins. The primary bronchus enters the medial aspect near the apex of the lung. The lung wall is composed of trabeculae: (1) arranged in a faviform pattern, (2) forming individual faveoli (gas exchange chambers) which appear deepest in the cranial one-half of the lung, (3) all of which have a smooth muscle core overlain by either a ciliated or nonciliated epithelium. A ciliated epithelium lines the luminal surfaces of the large primary trabeculae and parts of smaller secondary trabeculae; it is composed of cone-shaped cells with ciliated-microvillous surfaces, and of columnar serous secreting cells. Nonciliated epithelium covers the luminal surface of portions of some secondary trabeculae, abluminal surfaces of primary and secondary trabeculae and all surfaces of the small tertiary trabeculae forming the faveoli. The nonciliated epithelium overlies an extensive superficial capillary network. The blood-gas barrier (0.7-1.0 μm thick) is composed of a thin cytoplasmic flange of Type I pneumonocytes, a thick homogeneous basal lamina and an attenuated endothelial cytoplasm. Numerous surfactant-producing Type II pneumonocytes are closely associated with the Type I pneumonocytes. The nonrespiratory ciliated epithelium may function in humidification of air and clearing of the lungs.

Notes: The pineal complexes of the two closely related deep-sea fishes Cyclothone signata and C. acclinidens were compared both qualitatively and quantitatively. Photoreceptor and supportive cells were identified in both species. The deeper-dwelling species, C. acclinidens, had a significantly greater number of photoreceptor-cell outer segment saccules and a higher ratio of receptor cells to nerve fibers in the pineal stalk. It was suggested that these indicate increased photosensitivity of the pineal. Supportive cells were sometimes seen to contain arrays of undulating tubules. The functional significance of these tubules is not understood. A prominent dorsal sac is closely associated with the pineal end-vesicle. Both structures appear to have a common vascular supply suggesting that they are functionally related. Dorsal sac cells contained abundant mitochondria, glycogen, and large filament-like inclusions.

Notes: Diploid tadpoles of the discoglossid frog, Bombina orientalis, possess a distinctive rectangular network of epidermal melanophores. The ontogeny of this network was examined and utilized as a model for the comparison of tissue integrity and cellular interactions in diploid and haploid embryos.During the process of network formation in diploids, a variety of melano-phore-melanophore interactions was observed. These included temporary contacts between neighboring melanophore processes, deviations of processes toward neighboring melanophores, and lateral extensions between closely situated, parallel processes originating from different cell bodies. None of these intercellular interactions were seen in haploid embryos. Haploid melanophores displayed fewer cytoplasmic extensions, appeared to be randomly oriented, and failed to establish the ordered network seen in diploid embryos. It was also discovered that, in comparison with diploid tissues, relative densities of melanophores and epithelial cells were not uniformly regulated in haploid embryos.These findings are interpreted as indicating that haploid embryos possess fundamental cell and tissue defects, and that the “haploid syndrome” is likely based on more than one or a few defective physiological functions.

Notes: A β-keratin pattern, consisting of 30 Å filaments embedded in an amorphous matrix, is formed by fusion of membrane-bound packets with the 70 Å filaments of immature cells. This pattern occurs in the Oberhäutchen and the β-layer. When completely mature, these two components show no cell boundaries. It is suggested that this feature is associated with the process that leads to the separation of outer and inner epidermal generation. Filaments of 100-150 Å embedded in an amorphous matrix form the α-keratin pattern, which occurs in the α-layer only. The lacunar tissue is regarded as consisting of cells resembling immature α-cells, whereas mesos and clear layer show a keratin-like material consisting of 100-150 Å filaments without matrix. This is regarded as a modification of α-keratin. The cells of all components synthesizing α-keratin (α, mesos and clear layer) have the following features in common: (1) the plasma membrane is modified in that its inner leaflet is obscured by the deposition of a marginal layer, and (2) the cells have 0.06-0.1 μm mucous granules containing mucopolysaccharides, which release their content into the intercellular space.Protective and barrier functions of the epidermis are provided by the following features: (1) Oberhäutchen and β-layer merge during final maturation to a homogenous stratum of β-keratin without intercellular spaces. Their function seems to be mechanical protection. (2) The marginal layer of α-keratin containing cells, which decreases in thickness from without inwards, is highly resistant to physical and chemical influences. (3) Mesos granules contain phos-pholipid-lamellae, which are partly discharged into the intercellular space and partly remain within the mesos cells. These lipid lamellae are believed to contribute to the establishment of the permeability barrier. (4) The content of mucous granules may play a role in immunological processes. (5) Tight junctions seal off the intercellular space between the uppermost living cells of the epidermis and contribute to the permeability barrier.

Notes: When cervical segments 14 to 15 of the chicken spinal cord are cut transversely and studied by routine histological and histochemical methods, an onion-shaped region, filled with thread-like fibers, if seen to surround the ependymal cells of the central canal and to be bounded laterally by the neural elements of the spinal gray matter. This area is negative for succinic dehydrogenase, beta-hydroxybutyrate dehydrogenase and cholinesterase activity, but very strongly periodic acid-Schiff positive. Diastase controls show the positive material to be glycogen. Parasagittal sections through this cervical region and into the upper thoracic cord, show the glycogen-rich region to extend longitudinally throughout the region. Because of its location and histochemical characterization, which, He similar to that of the ventral portion of the glycogen body, the term brachial glycogen budy is proposed for this structure.

Notes: Anterior dorsal ventricular ridge (ADVR) is a major subcortical; telencephalic nucleus in snakes, Its structure was studied in Nissl, Golgi, and electron microscopic lrerarations in several species of snakes. Neurons in ADVR form a homogeneous population. They have large nuclei, scattered cisternae of rough endoplasmic reticulum in their cytoplasm, and bear dendrites from all portions of their somata. The dendrites have a moderate covering of pedunculated spines. Clusters of two to five cells with touching somata can be seen in Nissl, Golgi, and electron microscopic preparations. The area of apposition may contain a series of specialized junctions which resemble gap junctions. Three populations of axons can be identified in rapid Golgi preparations of snake ADVR. Type 1 axons course from the lateral forebrain bundle and bear small varicosities about 1 μ long. Type 2 axons arise from ADVR neurons and bear large varicosities about 5 μ. long. The origin of the very thin type 3 axons is not known; they bear small varicosities about 1 μ. long. The majority of axon terminals in ADVR are small (1 μ. to 2 μ long), contain round synaptic vesicles, and form asymmetric active zones. This type of axon terminates on dendritic spines and shafts and on somata. A small percentage of terminals are large, 5 μ in length, contain round synaptic vesicles, and form asymmetric active zones. This type of axon terminates only on dendritic spines. A small percentage of terminals are small, contain pleomorphic synaptic vesicles, and form symmetric active zones. This type of axon terminates on dendritic shafts and on somata.

Notes: Tooth development and replacement in fetal and adult viviparous caecilians (Amphibia: Gymnophiona) are described and analyzed according to current theories of tooth succession. The fetal dentition differs from that of the adult in morphology, position, and function. Teeth are used by fetuses to scrape the oviducal epithelium, thus stimulating the secretion of a nutrient substance. Fetal dentitions vary in morphology and position in different species. The ontogeny of teeth of several species is described and the patterns of addition of loci and of replacement are analyzed, Loci are added both posteriorly along the jaw and between existing loci as the jaw grows prior to ossification; subsequently addition is restricted to the posterior part of the jaw. Tooth replacement is alternate. The several rows and patches of teeth are the result of retention of replacement series on the dentigerous elements. Tooth development and replacement in a series of juveniles and adults of different sizes in a single species are also considered. Post-fetal patterns of development and replacement are similar to those seen in larvae and adults of oviparous species. Variation in numbers of teeth and proportions of teeth at particular stages occurs ontogenetically and among individuals of the same size, though proportions occur in a similar pattern throughout the series. The general pattern of tooth replacement in fetuses and adults can be explained by either Edmund's Zahnreihen theory or by Osborn's Tooth Family theory, but replacement in fetal tooth patches and the fetal-adult dentitional transition are explained by neither.

Notes: In Brallchiobdella pentodonta Whitman meiosis begins in follicles containing 16 spermatogonia. In each follicle the spermatogonia are connected by cytoplasmic bridges to a central anuclear cytoplasmic mass or cytophorus. They develop synchronously. Synaptonemal complexes are present in the primary spermatocytes. Spermatids contain a large globoid paranuclear body consisting of an acrosomal granule and coiled tubules which evidently receive the contents of the acrosomal granule and are considered the acrosome carrier. The spermatids separate from the cytophorus only when differentiation is completed.The ripe spermatozoon is relatively long. It has anteriorly the coiled tubules, followed by the nucleus, the mitochondrial sphere and the distal centriole from which the flagellum originates, A coiled ribbon-like structure encloses the flagellum along its entire length while a manchette of microtubules surrounds all the other structures of the sperm.

Notes: The muscles and bones of the pectoral fin of Serrasalmus nattereri, the piranha, resemble those of generalized, lower teleosts with specializations related to a body shape adapted for high-speed carnivory; the pectoral fins being highly mobile with strong ligaments to the rays. The presence of two occipital nerves appears primitive, while the emergence of the subclavian artery within the branchial cavity, as in Gasteropelecus sternicla, appears specialized. The muscles and bones of the latter fish, a fresh-water flying fish, are specialized for self-propelled, aerial flight in the fusion of the right and left girdles greatly expanded for insertions of complex appendicular (flight) muscles, and in the consolidation of the rays and radials into one functional unit moving vertically in flight though contraction of vertical, massive ventral flight muscles. The bony pectoral anatomy of Electrophorus electricus, the electric eel, is specialized in having a mobile joint between the primary girdle and the cleithrum, the former being suspended vertically from the cleithrum by ligaments. The proximal radials and rays are very numerous and vertically aligned. The cleithrum is shaped to accommodate the extensive sternohyoid and pharyngocleithral muscles. The sheet-like appendicular muscles extend beyond the special joint and control its movement. The deeper muscles do not cross this joint. The arterial system is specialized in lacking a deep brachial artery.

Notes: The cibarial food pumps of aquatic Heteroptera contain specialized epipharyngeal triturating devices. In the Naucoridae, striated bands and transverse plates triturate particles against the underlying hypopharynx. Anterior to them lie a pair of oblique folds which play an accessory role. The gross morphology of these devices is very similar in representatives of five genera of typical Naucoridae (Ambrysus, Pelocoris, Limnocoris, Cataractocoris, Cryphocricos) and differs from that of the atypical genus Aphelocheirus.The scanning electron microscope reveals additional differences between Aphelocheirus and the typical genera as well as variations, among the latter, which are not visible with the stereoscopic microscope. The oblique folds of the typical Naucoridae are well developed and contain processes for trapping particles; in three genera the region posterior to the folds is also modified. In Aphelocheirus only the latter region appears to trap particles, and the oblique folds are smooth and weakly developed. The striated bands of all genera bear ventral ridges arranged into transverse zones with precise patterns. The fourzoned bands of Aphelocheirus have a very different pattern than the two-zoned bands of the other genera. Among the latter, Cryphocricos has a simpler pattern of ridges than the other typical Naucoridae. The ventral surfaces of the transverse plates are highly modified in Aphelocheirus and less so in the other genera; those of Cryphocricos differ from those of the other Naucoridae.The fine structure of the cibarial epipharynx supports the views of some systematists that (1) Aphelocheirus should be placed in the monogeneric Family Aphelocheiridae rather than in the Naucoridae, (2) Cryphocricos represents a different subfamily than the other four typical Naucoridae, and (3) Cataractocoris belongs in the same subfamily as Ambrysus rather than with Cfyphocricos.

Notes: Appearance of collagen fibrils in the cuticle was seen by electron microscopy to be preceded by fonnation of a finely filamentous matrix material. At first, the fine filaments of the matrix are unorganized. However, signs of orthogonal ordering soon appear in the most superficial portion of the cuticle, and subsequently appear more basally and closer to the underlying epidermis. Meanwhile, fibrils of different staining properties and identifiable as collagen begin to be deposited in the superficial portion of the cuticle, the same region which first showed organized fine filaments. Then, like the fine filaments before them, the collagen fibrils polymerize more basally. Collagen appears to polymerize on the preformed skeleton of fine filaments as though the fine filaments caused the collagen to assemble. Neither the polymerization nor ordering of collagen fibrils seems to require direct cellular intervention but occur first in that portion of the cuticle which is furthest away from the underlying epidermis. The fine filaments may be self ordering, extracellular macromolecules which in turn determine the polymerization of collagen fibrils.

Notes: Oogenesis of the fresh-water triclad Dugesia dorotocephala has been studied by electron microscopical methods, with particular regard to the genesis and composition of the so-called “Balbiani body.” Its origin is clearly recognizable in young oocytes where the few mitochondria present seem to gather at the level of the perinuclear ooplasm. Here they surround dense masses of finely granular, fibrillar material probably coming from the nucleus. During the previtelloge ic period, mitochondria rapidly increase in number while the dense masses progressively dissolve.In the vitellogenic oocytes the Balbiani body shows its final configuration: it appears as a large area (up to 15-20 pm in diameter) consisting of innumerable densely packed mitochondria, some smooth vesicles and free ribosomes. This aggregate of cytoplasmic organelles remains unmodified in the mature oocytes.The function of the “Balbiani body” of D. dorotocephala is as yet unclear; it can only be asserted that it is not correlated with yolk production in which the endoplasmic reticulum and the Golgi complex are involved.

Notes: Whole ovaries from 16-day fetal mice were cultured for 6 to 20 days and then transplanted to the kidneys of ovariectomized adult mice where they remained for one to four weeks. After three weeks in the host's kidneys, many follicles developed within the transplants and became vesiculated. Many of the oocytes within these follicles had formed the first metaphase spindle of meiosis and several had completed the first polar body. Host mice bearing transplants that contained vesiculated follicles showed uterine stimulation and keratinization of their vaginae. However, ovaries that had been in culture for more than ten days before transplantation showed a limited response to the gonadotropins and never matured sufficiently to stimulate the host's reproductive tract. No ovulations occurred in any of the transplants.