ALBERT

Notes: New data on the brain of Latimeria indicate that previous estimates of the brain weight were too high by a factor of two. Our data suggest a brain weight of 1.1-1.5 grams for a specimen with a body weight of 30 kilograms. Quantitative data on major divisions of the brain are presented for the first time, and the relative size of the major brain divisions is similar to that of sturgeons and generalized sharks (such as hexanchids and squalids). Examination of brain component weight (s): body weight plots in a sample of non-teleost actinopterygian fishes indicates that all major divisions of the brain, except the telencephalon, are larger than in Latimeria. Brain component sizes in Latimeria are more similar to those extrapolated for amphibian brains than to those for actinopterygians. However, the cerebellum of Latimeria is considerably larger than that of amphibians.

Notes: The Champy-Maillet osmium tetroxide-zinc iodide technique and a new method using azur B-sodium thioglycolate were used to study the general nervous tissue structure in planarians. A subepidermal and a submuscular nerve plexus, partially reported by earlier authors, are described, and a gastrodermal plexus is reported for the first time in triclads. The possible functions for each one of these plexuses are discussed. By the Champy-Maillet method, the innervation within the parenchyma appears as an array of numerous single nerve fibers that course between the parenchyma cells making apparent synaptic contacts. The pharynx has outer and inner nerve nets similar in structure to the submuscular nerve plexus. Both nerve nets are connected to each other by radial nerves.The central nervous system has a sponge-like structure with many lacunae filled with cell bodies, dorso-ventral muscle fibers, parenchymal cell processes and excretory ducts. The existence of this sponge-like nervous tissue structure is discussed in relation to the still incomplete centralization of the nervous tissue in these organisms, to the lack of a true vascular system and to the acoelomate level of organization. A comparison with the nervous tissue structure of more advanced groups like polyclads and nemertines is suggested.

Notes: Secretion in the salivary glands of Gromphadorhina portentosa involves three cell types: parietal cells, secretory cells, and duct cells. The organization and role of the parietal and secretory cells are here considered. Parietal cells have numerous mitochondria, indicating an active metabolic role and the subsequent production of ATP. Plasma membrane invaginations and intracellular ductules containing microvilli appear to function in the absorption of solutes from the hemolymph and finely-tapered ductules. Secretory cells contain abundant rough endoplasmic reticulum, the three forms (stacked, vesicular, and diffuse) of which appear to develop sequentially during maturation. Secretory vesicle formation is asynchronous between adjacent secretory cells, and apparently the large vesicles often coalesce. The secretory vesicles also show differing degrees of electron density, indicating distinct biochemical composition.

Notes: Studies were undertaken of the microcirculation and histology of the gill of Protopterus aethiopicus as a prerequisite for elucidating the function of the gills in a bimodal respiratory system. The lamellae of the gill-bearing arches (I, IV, V, VI) resembles the arborescent external gill of the larval amphibian rather than the gill of the teleost or selachian.The arterio-arterial system (a-a) of the gill consists of an afferent artery, a series of large capillaries, and an efferent artery on each of the primary, secondary and tertiary lamellae. There are no pillar cells and the loose capillaries are covered with a multilayered epithelium. While living in water, the minimum distance for gas exchange is of the order of 5 μ. An afferent-efferent arterial shunt at the base of each primary lamella may be involved in control of lamellar blood flow and the resistance of the gill vasculature.The arterio-venous system originates primarily from the efferent side of the arterio-arterial system and drains into large branchial veins. Numerous contractile cisternae, interposed between intercellular channels and veins, presumably function as micropumps that collect fluid from intercellular epithelial spaces and inject it into the venous circulation.During aestivation, the epithelial layer of the gill lamellae becomes thinner. The entire gill vasculature, including the capillaries and afferent-efferent shunts on arches IV-VI, are very dilated which presumably promotes blood flow through these gill arches to the lungs.

Notes: The movements of the shoulder girdle of eight adult cats during overground stepping were studied, using standard slow motion cinematographic techniques. The patterns of activity of shoulder muscles were examined, using simultaneous intramuscular electromyography. Walking, trotting and galloping steps were analyzed from digitized single motion picture frame images. Angular movements of the shoulder girdle consist of biphasic flexion and extension of the shoulder joint and a monophasic flexion-extension alternation of the scapula on the thorax during each step cycle. In addition, the center of the scapula moves craniad during the swing phase and caudad during the stance phase with respect to a fixed reference point on the animal. Similar vertical movements of the center of the scapula also occur in each step cycle. Results of EMG studies of the 17 muscles capable of acting on the shoulder girdle indicate that three overall patterns of activity are found: (1) a pattern typical of extensor muscles, active during all the extension epochs; (2) a pattern typical of flexor muscles, active during the flexion epoch; and (3) a biphasic pattern of activity, active twice in each step. These data are used, along with a re-examination of previous models of the mechanics of the shoulder girdle of carnivores to examine the function and mechanics of shoulder motion. It is concluded that the rotary and translatory movements of the shoulder girdle during stepping combine to enhance step length.

Notes: The most striking morphological feature of the ovarian epithelium of Cymatogaster is the presence of intercellular dilations during much of the year. These dilations increase markedly in volume during the several months prior to ovulation and fertilization, and decrease in volume during the months of embryogenesis and gestation. The epithelium then returns to its initial, relatively undifferentiated state. The extracellular material within the dilations likely is synthesized in the cells adjacent to or within the dilations. Apparently most of this material is released into the ovarian lumen when the apicolateral margins of adjacent epithelial cells pull apart; possibly it serves as nutrient for developing embryos.In addition to supporting embryogenesis, the ovarian epithelium also apparently is involved in sperm storage. Sperm are maintained within pockets in the ovarian epithelium for the several months between insemination and fertilization. The cells lining the sperm pocket do not develop the intercellular dilations characteristic of most of the ovarian epithelium, and sperm remain associated only with the sperm pocket cells.

Notes: The antennae of Folsomia candida and Hypogastrura copiosa are provided with tactile hairs on all four segments and, in addition, with chemoreceptors on segments three and four. The cuticle of the thin-walled chemo-receptors of Folsomia, as in most other insects, is penetrated by many small pores uniformly distributed over the surface. In contrast, the cuticle of the thin-walled chemoreceptors of Hypogastrura is unusual in that a band of cuticle without perforations spirals around, or partly around, the hair. The cuticle between the spirals is very thin, and has extremely small openings in it. The tip of the antenna of Folsomia is thin, permeable to dyes in aqueous solution and apparently glandular. The antennal tip of Hypogastrura is definitely glandular.

Notes: After hemisection of the spinal cord and medulla oblongata, a projection has been traced to the inner half of the tectal white of the tiger salamander, using Fink-Heimer degeneration staining. By microelectrode recording it was found that the tectal projection forms a topographic somatosensory map of the contralateral half of the body. This map is in register with the overlying retino-tectal visual projection. Using the Falck-Hillarp technique, it was found that the somatosensory tectal input is associated with yellow-fluorescing 5-hydroxytryptamine fibers.

Notes: A comparative morphological study concerning typology and topography of chemoreceptors on the prothoracic legs of Calliphora vicina, Phormia terranovae and Musca domestica has been carried out. The typological criteria of Grabowski and Dethier ('54) and Hansen and Heumann ('71) were used. A single criterion, the shape of the tip, was used to define the different types of chemoreceptors.A-hairs have a rhombic pore at the side of the tip; B-hairs have an oval pore at the tip apex and D-hairs have a rectangular pore under an undulated, cap-like structure at the hair tip. A-, B-and D-hairs were found in the tarsomeres of Phormia; in Musca and Calliphora only B- and D-hairs were found. An opening and closing mechanism may operate on the pores of the tips of the chemoreceptors. Chemoreceptors were counted and a topographical map was completed, using SEM-techniques. Topographical maps are of value in electrophysiological and behavioural research, where only a limited optical magnification is possible.

Notes: The structures of the lantern tracheoles of three genera of flashing fireflies are compared. All three genera have stiff, reinforced tracheoles which resist folding or collapsing under conditions which flatten more typical tracheoles. This common specialization supports the hypothesis that the tracheoles play a major role in flash control in these fireflies, especially as the morphological basis of the stiffening is different in the three genera. Study of the tracheoles of other tissues reveals that there is great variety in structure and flexibility of these vessels from tissue to tissue and organism to organism, suggesting that tracheolar specialization may be a general phenomenon, with the fine structure of these air tubes being tailored to the particular demands and conditions of the tissues in which they are found.

Notes: Tibiotarsal segments of 12-day chick embryos homozygous for the crooked neck dwarf gene (cn/cn) were examined histologically following routine methods of preparation. The myogenic mass fails to divide into separate muscle bundles during the early stages of differentiation. Myoblasts and myotubes are observed, although the proportion favors the mononucleate cell population. Multinucleate myotubes are often wavy in appearance and many contain eosinophilic cytoplasmic inclusions. The entire tissue mass of mutants appears more compacted than in control limbs. Poor organization of muscle appears related to the lack of a suitable connective tissue system. Epimysia, perimysia, and subcutaneous connective tissue fail to develop properly. Tendons are poorly developed or absent. Comparisons between mutant and control embryos show no differences in peripheral innervation. Nerve fascicles penetrate deeply into the developing muscle of both species. The distribution of vascular elements is seemingly normal also. Skeletal muscle of cn/cn embryos is capable of differentiating to the myotube stage, after which it undergoes cellular degeneration without achieving a functional state. Comparisons of this mutant with alleged chemical phenocopies show important differences.

Notes: The histology and carbohydrate histochemistry of eight teleostean stomachs are compared. Three gross anatomical types of stomachs are described and their shapes appear to correlate somewhat with feeding habits. Each type can be divided histologically into a corpus and pylorus. Gastric glands, containing only one cell type, occur in the copora of all species, but are present in the pylori of esocids only. As a single cell can produce both enzymes and hydrochloric acid such cells may be comparable to those of amphibians but not mammals. Lamina propria and submucosa are indistinctly separated in corpora but better defined in pylori by an intervening muscularis mucosa. The arrangement of the muscularis into inner circular and outer longitudinal layers is the opposite of that seen in the esophagus. Gastric mucous cells show species variations in localization of epithelial mucosubstances, which in broad terms are recognized as sulfomucins, sialomucins and neutral mucosubstances. A piscivorous diet does not appear to demand any particular type of carbohydrate. Within the Centrarchidae, gastric pit cells vary in carbohydrate content from only neutral mucosubstance to only weakly acidic sulfomucin; two species contain both types. A positive PAS reaction on the surface of gastric epithelial cells is suggestive of a striated border and thus possibly absorptive function. The absence of stomachs in some teleosts and the evolutionary and dietary significances are discussed.

Notes: The American cockroach has a total of 368 muscles inserting on the post-coxal segments of its legs. By using a narrow morphological definition for delimiting individual muscles, it is shown (i) that the protrochanteral musculatures (23 muscles/leg) differ from the essentially identical meso- and metatrochanteral musculatures (24 and 26 muscles/leg) in number and disposition of extensors and in having a completely different flexor composition, and (ii) that the musculatures of the more distal segments of the legs are completely serially homologous, there being 2 muscles for moving each femur, 23 for each tibia, 7 for each first tarsomere, and 5 for each of the paired pretarsal claws. In all six legs, the trochanteral and tibial musculatures each contain single slender muscles that may be acting proprioceptively to measure the angular displacements between, respectively, the coxas and trochanters, and the femurs and tibias. Neurological and phylogenetic considerations are used to demonstrate why a narrow morphological definition should be employed, and why the widely used functional definition of Snodgrass ('35) is not only fallacious on evolutionary grounds, but also leads to making erroneous conclusions regarding the manner in which insect musculature is controlled by the insect central nervous system. Finally, it is hypothesized that the physiological limitations imposed by having an open circulatory system and the problems inherent in the neural control of large muscles may have been major evolutionary factors in forcing insects to use many slender muscles to control their body movements.

Notes: Among piscivorous cichlids consistent differences have been recorded between ambush and pursuit hunters with respect to electromyographic, kinematic, pressure and behavioral profiles during prey capture by high speed inertial suction. Piscivorous cichlids possess a repertoire of at least two patterns of prey capture, each of which is characterized by an extreme regularity of the kinematic, pressure, electromyographic and behavioral profiles. The nature and locomotory behavior of the prey, visually analyzed by the predator during the prestrike stalk, determine which of the two preprogrammed patterns is recruited. Agile and elusive prey invariably will elicit a preprogrammed motor output (stereotyped motor pattern) that produces the greatest suction velocities in both ambush and pursuit hunters. The greater the kinematic and suction velocities, the greater the overlap of the firing sequences of antagonistic muscle complexes. The opercular and branchiostegal apparati function as an exceedingly effective anti-backwash device, damping potential fluid oscillations within the oropharynx. Mastication occurs by triphasic movements and actions of muscles of the upper and lower pharyngeal jaws in both ambush and pursuit hunters. The lower pharyngeal jaw is acted upon by a force couple of which the fourth levator externus on one hand and the pharyngocleithralis externus and pharyngohyoideus on the other hand are the antagonistic components. Furthermore, the lower pharyngeal jaw is suspended by a muscular sling, the tension of which can be modified continuously. It is postulated that the switch from insectivorous to piscivorous feeding regimes (and perhaps vice versa) is accomplished by very minor structural and functional modifications, because the modulatory multiplicity and total range of repertories of the feeding machinery of the two trophic groups overlap significantly. Piscivorous cichlids may not have arisen by orthoselection in gradually-changing lineages, but represent the differential success of subsets from a random pool of speciation events. Adaptive features identified as characteristic for piscivory could have evolved in multiple and independent lineages at a punctuational mode and tempo.

Notes: Eggs of Chelydra serpentina were shifted during incubation between the female producing temperatures of 20°C or 30°C and the male producing temperature of 26°C. In the 20°C and 26°C combination, the stages during which incubation temperature determined sex were stage 14 through stage 16 (stages of normal series, Yntema, '68). In the 30°C and 26°C combination, the temperature sensitive stages for sex determination were stage 14 through stage 19. Incubation at 26°C throughout this period was needed to produce all males. Incubation at 30°C during either the first or second half of the period produced nearly all females; shorter periods of incubation at 30°C were more effective in producing females during the second half of the sensitive period. In the 20°C and 26°C combination, incubation at 20°C or 26°C for parts of the sensitive period produced both males and females. In three of the 57 clutches of eggs used in the experiments, incidence of females was atypically high.

Notes: The purpose of this investigation was to relate the morphology of connective tissues in the mandibular symphysis to the behavioral and experimental evidence for mobility and mechanical stress at the symphysis. The anatomy of the symphysis was examined histologically in 6 mammalian orders encompassing 22 species. Behavioral and experimental evidence of stress during the power stroke of the chewing cycle correspond with stresses at the symphysis implied by the location and orientation of symphyseal connective tissues. These stresses are: (1) dorsoventral shear of the symphysis due to the transfer of force from balancing to chewing sides, (2) bending of the symphysis causing tension along the inferior and compression along superior borders due to torsion on the dentaries from the jaw closing muscles, and (3) antero-posterior shear of the symphysis due to an anteriorly directed stress on the chewing side. Interspecific comparisons suggest that leaf eaters can resist greater dorsoventral shear than fruit or insect eaters, but no correlations exist between diet and bending or antero-posterior shear. This suggests that chewing leaves requires larger biting forces.

Notes: The unusual lymphogranulopoietic bone marrow of the large lungless salamander Plethodon glutinosus was examined by light and electron microscopy. Developing neutrophils, eosinophils, and fat cells were found in large numbers, while lymphocytes of various sizes, plasma cells, plasmablasts, macrophages, pigment cells, and fibroblasts were present in more moderate numbers. Basophils were observed only rarely. Macrophages were found in extravascular locations and did not appear to be associated directly with the walls of the blood vessels supplying the marrow. Both neutrophils and eosinophils seemed to arise from small precursor cells whose ultrastructural features bore a resemblance in some ways to those of mammalian myeloblasts described by Bainton and Farquhar ('66). Developing neutrophils and eosinophils seemed to produce only single populations of specific cytoplasmic granules, rather than both primary (azurophilic) and secondary (specific) inclusions, as are produced typically by mammalian granulocytes. Both eosinophilic and neutrophilic granules were formed in association with Golgi complexes; and eosinophilic granules were much larger, more densely stained, and more regularly rounded in shape than the inclusions of developing neutrophils. Peroxidase activity was associated with the specific granules of neutrophils but seemed to be lacking in the granules of eosinophils. The specific granules of eosinophils were especially unusual because they contained irregularly shaped, lightly stained cores which occasionally displayed a distinctly crystalline substructural organization. The specific granules of basophils also possessed a prominent crystalline organization. The overall appearance of the marrow of Plethodon suggests that it functions not only as a valuable source of neutrophils, eosinophils, and cells of the lymphoid series, but also as a part of the phagocytic system of the animals and as an important repository for fat.

Notes: The central nervous system of the sessile barnacle, Semibalanus cariosus (Pallas), has been studied with the particular aim of determining the locations of neuron somata in relation to peripheral nerves. This was accomplished by tracing peripheral nerves using dissection and methylene blue staining techniques, histological methods, and by permitting cobaltous chloride to diffuse via axons into ganglia (“backfilling”).The neuron maps resulting from the study reveal some well-defined sub-systems, a considerable degree of functional clumping of neuron somata, and some unexpected projections of neurons in the CNS. Neurophysiological studies based on these findings are in progress.

Notes: The effect of germanium on the secretion of siliceous spicules by the freshwater sponge Spongilla lacustris was investigated by exposing germinating and hatching gemmules to varying concentrations of germanium (Ge) in the presence of silicon (Si). Results were analyzed quantitatively and qualitatively and demonstrate that a [Ge]/[Si] (= molar ratio) of 1.0 completely inhibits silicon deposition. Intermediate ratios (0.5, 0.1, 0.01) which are permissive to spicule appearance result in fewer, shorter, and thinner spicules, in proportionately fewer microscleres, and in short bulbous megascleres. The size of the bulb increases with increasing [Ge]/[Si], while the length of the bulbous megascleres decreases with increasing [Ge]/[Si]. Microscleres do not demonstrate these graded responses suggesting that they are secreted in an all or none manner. Swellings produced in pond water and bulbs produced in germanium appear to decrease in size with time indicating a spreading of the accumulated silica. The effect of germanium on spicule secretion can be partially explained by its ability to uncouple the growth in length of the axial filament from the growth of the surrounding silicalemma. Under these conditions excess silicalemma is produced in which silica accumulates as bulbs in short spicules. Continuous exposure to Ge is necessary to produce this altered morphology. It is conjectured that the bulbs may be retained due to an inhibition of spreading. which in turn may be caused by the incorporation of germanium into the silica.

Notes: Four differentiated Malpighian tubules (primary tubules) extend from the junction of the midgut and hindgut in newly hatched Periplaneta americana. Secondary tubules begin to develop near the base of the primary tubules before hatching and successive nymphal molts. The newly initiated tubules undergo cell division and extensive elongation through the middle of the following intermolt period. During this time, the cells of the distal, middle, and lower middle tubule regions are surrounded by a cellular sheath, have few cytoplasmic processes extending along their basal surfaces, have a small or nonexistent lumen, and contain extremely dilated cisternae of endoplasmic reticulum. The cellular sheath differentiates into the muscle which coils around the mature tubule. Tubules which begin development toward the end of one intermolt period begin to undergo cytodifferentiation toward the end of the next intermolt period. By the middle of an additional intermolt period, the basal infoldings and microvilli of cells in the distal, middle, and lower middle regions have the conformations typical for those regions in differentiated tubules; granular concretions and stellate cells are present within the middle region of the tubule.

Notes: The infracerebral gland of Nereis is made up of three types of cells. C1 cells are hypertrophied pericapsular elements, whereas C2 and C3 cells have the morphological and cytological features of neurosecretory neurons. C2 and C3 cells give rise to centripetal “proximal processes” which extend into the brain through the midventral pocket formed by delamination of the brain capsule. Their “distal processes” terminate within the gland or its immediate vicinity. “Centrifugal fibers” arise from nerve cells located within the brain and appear to synapse upon the proximal processes of C2 cells in the region of the midventral pocket and in the ventral region of the brain. The cytology of C2 and C3 cells suggests that they are the source of distinct peptide hormones.

Notes: Exercise affects the growth of the dorsal longitudinal flight muscles in the tsetse fly. Examination of electron micrographs of flight muscles taken from flies subjected to enforced exercise, “ormal” exercise and no exercise reveals that both mitochondrial and myofibrillar fractions of the muscles are stimulated to grow at a faster rate by enforced exercise but that the mitochondria respond more rapidly.

Notes: Ultrastructure and shell formation in the testaceous ameba, Lesquereusia spiralis, were investigated with both scanning and transmission electron microscopy and X-ray microanalysis. The nucleus, surrounded by a fibrous lamina, contains multiple nucleoli. The cytoplasm, containing a well developed granular endoplasmic reticulum, also contains remnants of starch granules in stages of digestion. Spherical aggregates of ribosome-like particles may be seen. Golgi complexes seem to produce both a nonordered fibrous material and an electron dense vesicle. Only the latter appears to bleb off from the Golgi complex. X-ray microanalysis demonstration of silicon in Golgi vesicles and in some dense vesicles suggests that the fibrous component of the cisternae may take up and concentrate silica to form the electron-dense component of the vesicles. Membrane-bound siliceous crystals are often seen adjacent to the Golgi, suggesting either a Golgi origin or platelet formation in vesicles after release from the Golgi complex. Both electron-dense bodies and siliceous platelets are released from the cell by a process similar to apocrine secretion and may be seen outside the cell in route to the shell during shell morphogenesis. Shell development involves fusion of electron-dense bodies to form a matrix, positioning of siliceous platelets in this matrix parallel to the shell surface, and development of a system of matrix chambers. A particulate glycoconjugate is released to the shell surface upon rupture of the matrix chamber.

Notes: Stereological analysis of the ultrastructural composition of the pulmonary alveolo-capillary region of mice living at sea level compared with that of the same species (Phyllotis darwini) genetically adapted to life at 4,660 m reveals a trend at high altitude towards a greater volume percentage of tissue components. On a weight-specific basis, non-circulating tissue occupies a significantly greater volume in high-altitude mice, but air space and capillary contents are not correspondingly greater. Since the arithmetic mean thickness of the tissue layers and of the air-blood barrier are the same in the two altitudinal groups, the average alveolus must have a smaller volume in the high-altitude mice.Epithelial, endothelial, and erythrocyte surface areas per gram body weight are significantly greater in the high-altitude mice.Nuclear counts indicate that the larger lungs of mice adapted to high altitude are due to larger Pneumocyte I and II and endothelial cells rather than to an increase in the number of these cells. Hematocrits measured within the pulmonary capillaries in the two altitudinal groups were equal.An heretofore unrecognized feature of possible adaptive value is the surface/volume ratio of erythrocytes, which is similar for erythrocytes in alveolar space of mice at low and high altitudes but within lung capillaries is 14.7% greater at high altitude.

Notes: The neck region of the mature spermatozoon of Discus rotundatus is described. No evidence for a centriole or centriolar derivative is obtained. Nine striated coarse fibres and the two central fibres of the axoneme extend into the base of the implantation fossa. The axonemal doublet system is disrupted in the neck region. There are two fibrous accessory structures located between the central doublet and the striated coarse fibres.

Notes: Explants of 4.5-day-old chick embryonic neuroretinas with mesenchyme were exposed to Methotrexate (MTX) in medium 199 with embryo extract. Proliferative responses of the cultured neuroretinas were followed radioautographically by administration of 3H-thymidine to the cultures. The DNA synthetic, mitotic and pyknotic responses of the ventricular cells of the neuroretina were followed over a 16-hour period. The responses observed suggested that MTX caused a synchronization of the ventricular cells in the pre-mitotic phases with no direct inhibition of mitosis. Furthermore, prolonged exposure to MTX resulted in the accumulation of labeled pyknotic cells, indicating a decline in the regenerative capacity of the proliferative ventricular cells.

Notes: Successive tracheal cuticles of the dorsal longitudinal trunks are studied with the electron microscope. Minor differences seen at the light microscope level are seen as major qualitative and quantitative ones at the ultrastructural level. The larval and pupal cuticles are secreted by similar epithelial cells; these possess large polytene chromosomes. Cell division and possibly cell replacement occur prior to adult cuticle secretion. The findings are discussed in terms of cell specificity, intra- and inter-cellular pattern formation. This simple epithelium, the individual cells of which are capable of producing different cuticles, is interesting since the system is also shown to be responsive to hormone application.

Notes: Eggs of the common snapping turtle, Chelydra serpentina, were incubated at constant temperatures ranging from 20°C to 30°C, At hatching, the oviducts were absent or incomplete in males; the testes were differentiated. In females at hatching, the oviduct was intact hut in some cases the gonad retained bisexual characteristics. Three months after hatching, the ovary was differentiated and contained follicles. Eggs incubated at 20°C and at 30°C developed into females in 100% of the cases. At 26°C, 99% of the individuals were males; at 24°C, 100% were males. More males than females developed at incubation temperatures of 22°C and 28°C.

Notes: New blastozooids of Polyzoa vesiculiphora, the polysytelid ascidian are produced by pallial budding of three types depending on the method of “isolated bud” formation; stolonic, planktonic and intermediate types. Differences among each type of bud are attributed to behavior of test-vessels composing a part of the bud. Isolated buds produced by each type are essentially equal in terms of their internal structures and their subsequent fate, and develop independently of their parent zooids. New test-vessels originate directly from the epidermis of a “prefunctional zooid,” while the test-vessels derived from the parent zooid finally disintegrate. The new test-vessels extended with branching under the ventral side of a “functional zooid,” ascend to the lateral side of it and participate in bud formation. Budding regions exist in three dimensions on the lateral wall of the mantle of the functional zooid, especially the right posterior part. During the life cycle of one functional zooid, the stolonic type buds appear at early and/or aged stages. Appearances of the stolonic type buds in early stages tend to repress those of the planktonic types. The number of planktonic type buds formed on a functional zooid at the same time is many more than that of the stolonic type. Such budding features are discussed from the viewpoint of behavior of the test-vessel system.

Notes: Fine structural changes in mitochondrial morphology pertaining to size, number and growth were examined in flight muscles of normal and experimentally dewinged male Drosphila melanogaster ranging up to 26 days of age. In the normal winged flies, the number of mitochondria decreases during the first week of adult life whereas the size of individual mitochondrial profile increases significantly. Changes in mitochondrial size and number are due to the fusion of mitochondria. Fused mitochondria are extremely large in size and irregular in shape. In 26-day old normal flies, the number of mitochondria increases while the mitochondrial size is reduced indicating mitochondrial division. In comparison to the normal flies, dewinged flies exhibit a similar degree of mitochondrial fusion and growth during the first week of life. However, the extent of mitochondrial fission in 26-day old dewinged flies is greater than in the normal flies of this age. Structural mechanisms of mitochondrial fusion and fission are described. The objective of this study was to examine the relative effects of age and flight activity on the mitochondria.

Notes: The morphology of the abdominal defensive glands and associated structures of 115 species of tenebrionid beetles was studied on KOH cleared material. The glands and reservoirs of all Tenebrionidae are homologous and evolved as a pair of sacs from the intersegmental membrane between sternites VII and VIII. On the basis of reservoir morphology and secretory cell tubule termination, seven provisional gland types were established. Several of the types include species from several tribes, and several tribes contain several gland types, indicating possible incongruencies between the taxonomy and phylogeny of the family. Morphological trends in the evolution of the glands include: increase of reservoir capacity, constriction of the proximal portion of the sacs into distinct exit ducts, release of secretion by exuding or spraying rather than everting, and concentration of the secretory cell tubule terminations into restricted fields, collecting ducts or ampullae. The morphology of the glands of 58 species is illustrated and the results are discussed in light of the current taxonomy of the Tenebrionidae.

Notes: Fine structure of the ion transporting epithelium of the neck organ in the brine shrimp (Artemia salina) nauplius is described. The neck organ is a dome-like gland situated atop the cephalothorax of the larva and is composed of 50 to 60 cuboidal epithelial cells. These cells possess many of the characteristics of salt-secretory cells from other tissues. They contain many mitochondria and exhibit a high degree of plasma membrane elaboration. This membrane amplification takes two forms; the apical plasmalemma is infolded into irregular loops, while the basal and lateral membranes penetrate the cytoplasm in the form of branching sinusoids. The labyrinth of tubular reticulum thus formed fills most of the cell volume. Mitochondria in the labyrinth are often in intimate contact with these tubular membranes and regular arrays of parallel mitochondria with constricted intervening sinusoids are often observed. Other organelles including Golgi complexes, multivesicular bodies, and rough endoplasmic reticulum are also numerous, particularly in the narrow rim of cytoplasm which lies between the apical infolds and the labyrinth. Yolk platelets and glycogen fields are conspicuous in the basal perinuclear regions of the cells.

Notes: Correlative studies of luminescent responses, light and electron microscopy of Porichthys photophores during development were conducted. The photophores differentiate as an outgrowth of the basal cell layer of the epidermis, from which they delaminate into the dermis. Reflector cells are formed from dermal fibroblasts. Early photophore cells differentiate into three distinct cell types: photocytes, supportive and lens cells. Elaborate profiles of endoplasmic reticulum, Golgi bodies and vesicles suggest intense secretory activity in the early photocytes, while supportive and lens cells differentiate by two different transformations of the microfilament arrangement of primordial photophore cells.Luminescent capabilities of Porichthys photophores arise in two successive phases: (1) an aneural phase during which photophores become fluorescent, photocytes are in process of maturation and respond only to chemical stimulation and (2) a neural phase in which photophores luminesce upon electrical and pharmacological stimulation and are densely innervated with terminals showing relatively narrow neurophotocyte gaps. The presence of neural elements intimately associated with the early photophore anlagen suggests the involvement of the peripheral nervous system in the formation of photophores.

Notes: The degree of minced rat muscle regeneration in the absence of nerve fibers was compared with that of normal regenerates between one and 270 days postoperatively. Up to around 30 days, the number of muscle fibers and their morphology were comparable in both normal innervated and denervated regenerates; both showed clear cross striations and peripherally located nuclei. Histochemically, SDH and myofibrillar ATPase (pH = 9.4) reactions were positive, but there were no typical signs of fiber types in either case of regeneration. The only consistent difference in the early period was the smaller fiber cross sectional areas in denervated regenerates than in innervated ones. Starting about 40 days, the muscle fibers in innervated regenerates became differented into different fiber types (fast-twitch-oxidative-glycolytic, FOG., fast-twitch-glycolytic, FG., slow-twitch-oxidative, SO.) but there were no such activities in denervated regenerates, although their SDH and myofibrillar ATPase reactions remained positive for a long time. Degenerating muscle fibers could no longer be identified in innervated regenerates. In the denervated regenerates, however, muscle fibers underwent atrophic or degenerative changes and were replaced by connective tissue. The complete disappearance of muscle fibers varied with individual regenerates. In some cases, it occurred about 90 days and in others, traces of muscle fibers could still be seen as late as 150 days postoperatively. Thus, nerves seem to be important primarily in the late phase of regeneration; namely, differentiation of fiber types and maintenance of the structural integrity of muscle fibers.

Notes: The pulmonary veins of albino Wistar rats were studied by means of light and electron microscopy. The media of larger veins consists of cardiac muscle fibers which extend until the vessels attain about 100 μ in diameter. This coat consists of external longitudinal fibers and internal circular fibers. The vasa vasorum are well developed and the capillaries show pseudofenestrations. The numerous adrenergic and cholinergic nerve endings do not form typical motor end-plates as seen in skeletal muscles. The ultrastructure of these media muscle fibers is similar to that of rat hearts. The smooth muscle layer of larger pulmonary veins is not continuous as it is in smaller veins where it forms cushions. Comparisons of albino rats and other rodents reveal striking differences.Action potential shape and propagation velocity (0.5-1.2 m/s) along the myocardial coat of the pulmonary vein were similar to those observed in the left atrium and so was their sensitivity to locally applied acetylcholine. The physiological direction of propagation in rat pulmonary veins is toward the lung. This finding lends support to the hypothesis of a rhythmic, valve-like action of the striated musculature of the pulmonary venous wall during the systole and a possible role in the capacitance of the pulmonary circulation.

Notes: Latero-frontal, para-latero-frontal, and frontal ciliary tracts on the gill filaments of Crassostrea virginica (Gmelin) were studied with light microscopy and scanning electron microscopy. Latero-frontal cirri are complex structures composed of varying numbers of paired cilia. The multiple pairs of cilia which constitute a single cirrus are closely appressed for a portion of their length; they then branch laterally from the central axis in a plume-like fashion. Latero-frontal cirri of adjacent gill filaments create a filtration sieve which should be capable of retaining particles smaller than 1 μm in diameter. Para-latero-frontal cilia are short, closely spaced cilia arranged as a staggered row along the frontal side of each tract of latero-frontal cirri. Latero-frontal cirri and para-latero-frontal cilia occur on ordinary, principal, and transitional gill filaments. Frontal ciliary tracts of ordinary filaments are divided into a central, ventrally directed coarse tract, flanked on either side by a dorsally directed fine ciliary tract. The coarse tract is covered by cirri which are comprised of five to eight cilia, while the fine frontal tracts are made up of individually functioning cilia. The frontal ciliary tracts of principal and transitional filaments bear only dorsally directed fine cilia. The unique direction of effective beat of the coarse frontal cirri of ordinary filaments, in combination with the action of fine frontal cilia and the strategic location of mucus producing cells, is used to describe a possible mechanism for the sorting of filtered particles.

Notes: The skeletal structure of the stomachs of several decapod Crustacea is described in detail. The general organization of the ossicles is similar for all species and the homologies of the elements can be recognized despite large variations from group to group. The Reptantia are characterized by a complex ossicle organization while the Natantia, on the other hand, are characterized by a simple organization. The various types of ossicle organization found in the decapod stomach can be arranged in a series ranging from simple to complex. The Brachyura have the most complex ossicle system and the Penaeidea the most simplified. This graded series of complexity closely follows the evolution of the Decapoda.

Notes: Records of electrical activity in the tracheal muscles of domestic chickens were obtained for a variety of ad libitum vocalizations. Primary attention was given to an analysis of events during the most complex call, crowing.Three pairs of muscles, Mm. tracheohyoideus, tracheolateralis, and sternotrachealis, can affect the configuration of a chicken's syrinx. The firing patterns of the three muscle pairs are related to their different abilities to affect the tension of the syringeal membranes. The influence of M. tracheohyoideus is most indirect and imprecise, and its role the least clearly defined. It appears to adjust the position of the trachea so that the syrinx is isolated from unpredictable and/or undesirable consequences of nuchal position and tracheal elasticity, and also helps draw the glottis caudad, thereby deepening the pharyngeal chamber. The other two muscles interact to control the tension of the vocal membranes. M. sternotrachealis relaxes the membranes by drawing the drum of the trachea caudad, or, via the syringeal ligament, by rotating the pessulus cranioventrad, or both. M. tracheolateralis tenses the membranes and/or prevents caudal movement of the origin of M. sternotrachealis, a necessity if the syringeal ligament is to rotate the pessulus.Vocalization depends on both syringeal configuration and appropriate air flow. Hence, tracheal muscles, syrinx, air sacs, and ventilatory muscles cooperate to form a vocal system. Cooperation elicits a surprising degree of redundancy. At least one call, a high pitched wail, may be produced by two very different techniques.

Notes: Dissection of the cervical and basicranial regions in three species of snakes indicates that compared to Crotalus viridis and Lichanura roseofusca, Masticophis flagellum possesses relatively high numbers of compound axial muscle insertions on the atlas-axis and vertebrae numbers 3-5. It is suggested that the condition in Masticophis facilitates its vertical-neck-horizontal-head foraging posture and has allowed axial muscles inserting on the dorsocaudal braincase in this snake to generate vertical and lateral head movements more effectively.

Notes: The osteology of the pectoral limb of small captorhinids is described and figured in detail. A cartilaginous sternum was present. The glenoid was not a simple sliding or rocking joint, as was previously supposed, but considerable rotation was also an integral part of the humeral movement. The structure of the elbow joint is such that when the lower arm was extended, its distal end swung forward and extended the anterior reach of the hand. When the lower arm was flexed, the posterior reach of the hand was extended. Articulated specimens allow a recontruction of the manus. There was no well developed wrist joint, but rather the manus, as a whole, was a flexible structure. A pisiform was present. Sesamoid bones were developed in the tendons of the palmaris communis profundus muscle.Study of forelimb musculature of living reptiles based on dissections and the literature indicates that its evolution has been very conservative. The forelimb musculature of small captorhinids probably was very similar to that of all living reptiles except turtles.

Notes: Cochleae (125) from 26 species of the rodent family Heteromyidae (genera Dipodomys. Microdipodops, Perognathus, and Liomys) were compared. In Perognathus and Liomys the scala tympani in the apical portion is extremely narrow with a correspondingly minute helicotrema. In Liomys there is no bone separating scala tympani from spiral ganglion in the upper second and entire third turn. In all species studied the zona pectinata of the basilar membrane is enlarged, with a hyaline mass between upper and lower basilar membrane fibers. This zona pectinata hypertrophy is least at the base of the cochlea and greatest in the upper second turn, decreasing again toward the apex. Basilar membrane width increases rapidly in the first turn and then changes only slightly.Except for Liomys, all the heteromyids studied have hypertrophied Hensen's cells with long apical processes supporting and forming an elevated reticular lamina. These Hensen's cells reach their maximum size in the upper second and lower third turns; throughout they rest on inner Claudius' cells rather than the basilar membrane. Relative to naso-occipital length the cochlear specializations are greatest in Microdipodops and least in Liomys just as is the case for middle ear modifications.The morphological data are consistent with the concept that standing wave phenomena may be important in heteromyid cochlear biomechanics. Single unit data of other workers are also consistent with this interpretation. Like middle ear morphology, inner ear morphology appears adapted to low-frequency sensitivity-especially in Dipodomys and Microdipodops.

Notes: The developmental rates of male and female embryos of Xyleborus ferrugineus were compared by charting for each sex the mean age for each of ten discrete morphological stages of embryogenesis from pole cell exclusion to eclosion. Male and female embryos developed synchronously from stage 1 (which begins with pole cell exclusion) through stage 4 (which ends with the completion of germ band extension and metamerization). After stage 4 and throughout the remainder of embryogenesis, the mean ages per morphological stage of male embryos were significantly greater than those for female embryos. The expected physiological consequences of a haploid genome in the male embryo as compared to a diploid condition in the female embryo are discussed as the possible basis for the persistent lag observed in male developmental rate after stage 4.

Notes: The morphology of the chaetae of the maldanid polychaetes Clymenella torquata (Leidy) and Euclymene oerstedi (Claparède) (= Caesicirrus neglectus Arwidsson, '11) are described and related to movements observed in the laboratory. Graphs are constructed of the number and length of the neuropodial chaetae of each chaetiger throughout the body of Clymenella and of species of the genera Euclymene, Macroclymene and Axiothella, and show a characteristic and relatively constant pattern for each species. This work suggests that in making taxonomic decisions, more attention should be paid to the overall pattern of the neuropodial chaetae and less to the confusing distinction between aciculae and rostral uncini.

Notes: Four kinds of neurosecretory cells A, B, U and C are distinguished in the central nervous system of Dendrobaena atheca Cernosvitov. A cells, which show different morphological characteristics under different physiological states and during their cyclic changes, are the most active neurosecretory cells. They form the outer layer of the cortical cell zone in the cerebral ganglion. B cells are large and medium sized and are distributed in all parts of the central nervous system. U cells are found only in the sub-pharyngeal ganglion while C cells are distributed in the sub-pharyngeal as well as in the ventral nerve cord ganglion. The number and secretory activity of C cells decrease in caudal direction. Further, Gomori-positive cells are also observed in the ganglia of the vegetative nervous system.A rudimentary neurohaemal organ, the storage zone, has been observed in the cerebral ganglion and there appears to be another neurohaemal area in the ventral nerve cord ganglion. The storage zone is formed by the terminal ends of the axons of A cells. The chrome alum haematoxylin phloxin (CHP) and aldehyde fuchsin (AF) positive substances in the form of granules are found in this area. The cerebral ganglion is richly supplied by blood capillaries. The distal end of the axons of B cells are swollen like a bulb while in some cases the axons are united to form an axonal tract. Extra-cellular material is abundant in different parts of the nervous system. In all cell types, the perinuclear zone is the first to show activity in the secretory cycle. It appears that the nucleus may be involved in the elaboration of the neurosecretory material in the cells.

Notes: The blood circulation of the Stannius corpuscles, like that of the kidneys to which the corpuscles are attached, represents a portal system. The corpuscles receive blood from the dorsal caudal vein and from a vein coming from the hypaxial musculature. They are drained by veins which enter the caudal parts of the kidneys and therefore endocrine substances released by the corpuscles pass through the kidneys before they enter the general body circulation. The corpuscles are penetrated by sympathetic nerves coming from a small subvertebral ganglion. It is likely that these nerves innervate the muscular coat around the blood vessels. The muscular coat surrounding the renal blood vessels, the collecting tubules and part of the ureters, is innervated by nerves from the same ganglion. The secretory activity of the gland cells appears to be controlled by blood borne factors, because neither synaptic contacts with these cells, nor gap junctions among the cells, have been found in thin sections and freeze-etch replicas of the corpuscles.The corpuscles contain two cell types, both presumed to have endocrine function. Histochemical and ultrastructural data indicate that the gland cells produce glycoproteins. It is likely that the contents of the secretory granules are released by exocytosis. One cell type is structurally similar to the cells described in many other teleosts and thought to be engaged in the synthesis of a hypocalcemic hormone. The ultrastructure of the second cell type resembles cells described only in other migratory species: salmonids and eels. It may be involved in the control of monovalent ions.

Notes: The glandular layer constitutes the greatest bulk of the human soft palate and is composed of individual compound tubulo-acinar salivary glands. Connective tissue partitions of the submucosa divide the glandular layer into lobules of irregular shapes and sizes. The glands are interwoven and bound firmly together by a connective tissue stroma rich in elastic fibers. The secretory units consist of elongated, branched, and sometimes convoluted tubules lined by a single layer of pyramidal mucous cells.Mucous secretion by acini is supplemented to some degree by mucous acinar cells, which were found as epithelial components of all ducts except the main excretory ducts, suggesting a diffuse distribution of progenitor cells. Some mucous acini communicate with highly convoluted intercalated ducts which occupy partially isolated positions within inter- and intralobular connective tissue septa. These ducts follow the connective tissue septa and eventually join the main duct system. The significance of this system of intercalated ducts is not known. A supplemental functional role is hypothesized.

Notes: Normal gill structure and thyroxine induced resorptive changes were studied in Ambystoma mexicanum. The gill is normally composed of a mesenchymal core covered with a multilayered epithelium. The general architecture is simpler than that of the teleost and elasmobranch, but the vascular arrangement is analogous. There are three basic cell types in the epithelium: a characteristic epithelial cell containing tonofibrils and mucus, a ciliated cell with an ultrastructure similar to that of the chloride cell, and the mucin-filled Leydig cell. The basal lamella and mesenchymal tissue appear typical of amphibians.Cytologic changes during thyroxine induced gill resorption varied with cell type. Some epithelial cells demonstrated a cytoplasmic response with swelling of mitochondria and rough endoplasmic reticulum and late, lytic nuclear changes, while others remained viable and went on to cornify. Ciliated cells showed early changes in nuclear chromatin pattern followed by rapid, progressive dilatation of endoplasmic reticulum. Leydig cells sustained variable changes leading to collapse of the perinuclear mucus, and cells of this type were absent in mature epidermis. Early basement membrane changes included widening and reduplication of the adepidermal membrane followed by morphologic fraying of collagen plies. There is no cytologic evidence to suggest that autolysis plays a major role in gill tissue dissolution.Resorption involved the maintenance of structural integrity in the face of diminishing physical dimensions. The epithelium became cornified, the basement lamellae dissolved, and the mesenchymal tissue was resorbed through action of macrophages in an orderly distal to proximal direction.

Notes: Sea cucumbers, Stichopus moebii, have a unique specialization of their blood vascular system: The vascular follicle network is composed of numerous small chambers (follicles) interconnected by minute vessels. The fine structure of the follicle system was studied in detail. The follicles are composed of several layers: an external ciliated epithelium, neuromuscular layer and basement membrane, connective tissue, and a fenestrated endothelial lining. The follicle lumen is filled with coelomocytes and necrotic cells surrounding particles of iron. The follicle may function in coelomocyte production and destruction.

Notes: Timed-sequence studies have shown that reticulate scales on the ventral footpads of birds do not undergo “epidermal placode” formation during their morphogenesis, but arise as symmetrical evaluations similar to the scales of snakes and lizards. Unlike the scutellate scales on the dorsal surface of the foot, in which the formation of an “epidermal placode” and its subsequent morphogenesis result in distinct outer and inner epidermal surfaces, the reticulate scales elaborate only one type of epidermal surface.

Notes: The arrangement and distribution of oxytalan fibers in Australian marsupials has not previously been reported. Periodontal tissues of wombat, wallaby, possum, and marsupial mouse were examined to ascertain oxytalan fibre organization. Despite adaptation of the marsupial masticatory apparatus to different diets the oxytalan fibre organization in the periodontal ligament shows a basic pattern which corresponds with that reported in other animals. The oxytalan system forms a continuous meshwork of fine, branching fibres which completely invests each tooth root and connects adjacent teeth. Thick ribbon-like apico-occlusally orientated oxytalan fibres, thought to form by the coalescence of thinner fibres, are restricted to the periodontal ligament. The oxytalan fibres are embedded in cementum and attached to blood vessels in the periodontal ligament. Oxytalan fibres do not insert into alveolar bone. Histological evidence indicates functional remodelling of the oxytalan fibre system in continuously erupting teeth.

Notes: In Patella vulgata the 32-cell stage represents a pause in the mitotic activity prior to the differentiation of the mesentoblast mother cell 3D. At the onset of this stage, the embryo is radially symmetrical. Nevertheless, the plane of bilateral symmetry is indicated as it passes through the macromeres forming the vegetal cross-furrow. From the early beginning of the 32-cell stage, all four macromeres intrude far into the interior and touch the centrally radiating cells of the first quartet of micromeres. The two cross-furrow forming macromeres (3B and 3D) intrude the farthest and come into contact with the greatest number of micromeres. Finally, the contacts are extended significantly and maintained with only one of these macromeres. From that moment, this cell can be called the macromere 3D and the dorsoventral axis is determined. The evolution of the internal cell contacts between the micromeres of the first quartet and the macromeres indicates an essential role of the former in the determination of one of the latter as the mesentoblast mother cell, and thus in the determination of dorsoventral polarity.

Notes: The structure of the testis of Poecilia latipinna is described with particular reference to Sertoli cell-germ cell relationships during development and maturation of the germinal cyst. The cyst develops when primary spermatocytes become surrounded by a single layer of Sertoli cells at the testis periphery. As spermatogenesis and then spermiogenesis proceed, the cyst moves centrally in the testis toward the ducts comprising the vasa efferentia. In addition to being a structural part of the germinal cyst, the Sertoli cells phagocytize residual bodies cast off by developing spermatids and form an association with mature sperm, which resembles that observed in mammals, before the sperm are released into the vasa efferentia as a spermatozeugmata.The results of this investigation are discussed in view of what is known concerning testis structure in other teleosts and similarities between cell functions in teleosts and mammals. It is concluded that teleost Sertoli cells, teleost lobule boundary cells and mammalian Sertoli cells are homologous.

Notes: The dendritic patterns of cells in the optic tectum of the tegu lizard, Tupinambis nigropunctatus, were analyzed with the Ramon-Moliner modification of the Golgi-Cox technique. Cell types were compared with those described by other authors in the tectum of other reptiles; particular comparisons of our results were made with the description of cell types in the chameleon (Ramón, 1896), as the latter is the most complete analysis in the literature. The periventricular gray layers 3 and 5 consist primarily of two cell types  -  piriform or pyramidal shaped cells and horizontal cells. Cells in the medial portion of the tectum, in an area coextensive with the bilateral spinal projection zone, possess dendrites that extend across the midline. The latter cells have either fusiform or pyramidal shaped somas. The central white zone, layer 6, contains fibers, large fusiform or pyramidal shaped cells, fusiform cells, and small horizontal cells. The central gray zone, layer 7, is composed predominantly of fusiform cells which have dendrites extending to the superficial optic layers, large polygonal cells, and horizontal cells. The superficial gray and white layers, layers 8-13, contain polygonal, fusiform, stellate, and horizontal elements. Layer 14 is composed solely of afferent optic tract fibers.Several differences in the occurrence and distribution of cell types between the tegu and the other reptiles studied are noted. Additionally, the laminar distribution of retinal, tectotectal, telencephalic, and spinal projections in the tegutectum can be related to the distribution of cell types, and those cells which may be postsynaptic to specific inputs can be identified. The highly differentiated laminar structure of the reptilian optic tectum, both in regard to cell type and to afferent and efferent connections, may serve as a model for studying some functional properties of lamination common to cortical structures.

Notes: The antennae and their sense organs in nymphs and adult roaches of Gromphadorhina brunneri, were investigated and described. The number of segments and sensillae of the nymphal antennae depend on the developmental stage. Sexual dimorphism is pronounced. Males have longer antennae than females as well as an abundance of especially long sensory hairs (long wavy hairs), which are probably responsible for the perception of female sex pheromones. They also have more thin-walled sensory hairs, for instance, sensilla trichodea. On a morphological basis the sensillae of Gromphadorhina brunneri, were named and classified. Long wavy hairs and large sensory hairs appear to be present also in a related species, G. portentosa, but are lacking in others. Their distribution on the antennae varies greatly from that in G. portentosa but their structure varies only slightly. These two types of sense organs are considered to be specialized forms of sensilla chaetica. They are contact chemoreceptors, as are two other types of sensilla chaetica. Furthermore, thin-walled chemoreceptors are present, such as sensilla trichodea, sensilla basiconica, sensilla coeloconica and a typical mechanoreceptor, the sensillum campaniformium.

Notes: This paper describes the different regions of the Malpighian tubules and the associated structures (ampulla, midgut, ileum) in the cockroach, Periplaneta americana. There are about 150 tubules in each insect. Each tubule consists of at least three parts. The short distal region is thinner than the other parts and is highly contractile. The middle region comprises most of the tubule length and is composed of primary and stellate cells. Primary cells contain numerous refractile mineral concretions, while stellate cells have smaller nuclei, fewer organelles, simpler brush border, and numerous multivesicular bodies. Symbiont protozoa are sometimes present within the lumen of the middle region near where it opens into the proximal region of the tubule. The latter is a short region that drains the tubular fluid into one of the six ampullae. These are contractile diverticula of the intestine located at the midgut-hindgut junction. The ampulla is highly contractile, and consists of a layer of epithelial cells surrounding a cavity that opens into the gut via a narrow slit lined by cells of unusual morphology. The proximal region of the tubule and the ampulla resemble the midgut in that they have similar microvilli, basal infolds, and distribution of mitochondria. This suggests an endodermal origin and reabsorptive function for the proximal region of the tubule and for the ampulla. A number of inclusions found within the tubule cells are described, including peroxisomes and modified mitochondria. Current theories of fluid transport are evaluated with regard to physiological and morphological characteristics of Malpighian tubules. The possible role of long narrow channels such as those between microvilli and within basal folds is considered, as is the mechanism by which these structures are formed and maintained. Also discussed is the role of peroxisomes and symbionts in the excretory process.

Notes: The fine structure of the intersegmental glands of the sixth abdominal sternum in 1-week old females of Nomia melanderi is presented. The plasma membrane of the secretory cell is unfolded in many places and is covered by a basement membrane. The microvillous surface is invaginated to form a rather long sinuous cavity. The endoplasm is almost entirely filled by secretory granules. Many secretory granules are located close to the inner surface of the invaginated plasma membrane. The invagination contains a porous ductule, apparently of cuticulin origin, that is connected directly with the inner layer of the transport duct of the duct-forming cell. This type of arrangement allows the direct flow of the secretory substance to the outside in a continuous way. The cylindrical duct-forming cell, besides having typical cell organelles, contains a cuticular transport duct. This duct is composed of a thin cuticulin layer surrounded by a rather thick epicuticular one. The results suggest that the secretory cell has two secretory cycles. The first occurs while the gland is differentiating (at the pupal stage) and is involved in secretion of the cuticulin that forms the porous ductule. The second cycle, which starts by the beginning of nesting, is involved in the secretion of a substance that is carried to the outside via the transport duct of the duct-forming cell.

Notes: Volumetric and histological changes of the central nervous system were studied during post embryonic development of a spider, Argiope aurantia.The neural mass of Argiope grows allometrically with respect to volume of the cephalothorax and body weight. In the first instar 46% of the cephalothoracic volume constitutes the neural mass and this is reduced to 4% in the female (9th stage) and 12% in the male (7th stage) spider.Growth curves for the cephalic ganglion, measured at all stages, represent a straight line. The neural mass of females is two and a half times larger than that of the males. The ganglion increased 24 fold in female and 10 fold in male spiders. Addition of neural mass occurs in all stages.The brain volume is greater than that of the subesophageal ganglion in the first two instars. In subsequent stadia, the subesophageal ganglion grows faster, and in females it is finally three times and in males two times larger than the brain.Growth of cortex and neuropile depict exponential curves. Comparison of growth patterns of these shows an inverse relationship during development. While the volume of the cortex is higher in the first two or three stages, the volume of the neuropile is higher in the remaining stadia. The causes for this growth pattern are discussed.Counts of cell numbers show that there is a constant population of neurons throughout the post-embryonic development. The number of nerve cells in females is higher than in males, 11% in the subesophageal ganglion and 58% in the brain.The growth of the cortex is partly accomplished by an increase in cell volume. In male and female spiders the increase in Type-B cells is 20 and 50 fold, while that of large motor neurons is 200 and 600 fold respectively. The motor neurons of 20 μ and above number 63 in male and 916 in female adult spiders.The growth of neuropile occurs through an increase of dendritic arborization and axonal branching. The largest axons measure 1 μ in the first and 16 μ in adult stages. An increase of incoming sensory fibers is also noticed during development.Invasion of neural lamella into cortex and neuropile increases during development. Neural lamella which are 1-2 μ in the first stage grow to 40-100 μ thickness in adult female spiders, near the origin of the main nerves. One type of astral cells, counted in neuropile, increases 10 fold.The appearance of a central body and the beginning of web construction coincide during the second instar. The relationship between these two is discussed.

Notes: A process of nucleolar reorganization apparently identical to that encountered in intestinal epithelial cells (Adamstone and Taylor, '72) develops in kidney cells of aging rats. The polymorphic nucleoli of young tubule cells soon change to amphinucleoli and, while terminal nucleolar reorganization is delayed in cells of collecting tubules, in the nephrons nucleoli soon begin to undergo terminal reorganization becoming bipartite structures with separate plasmosomes and karyosomes. This suggests disruption of the DNA-dependent RNA protein transcription system and failure to maintain the flow of messenger RNA into the cytoplasm. Old cells are not discarded immediately from the kidney tubules and they retain much rough endoplasmic reticulum, numerous ribosomes and polysomes and large plasmosomes. Thus a high RNA concentration is known to develop in old kidney tissue while protein synthesis is also known to be low (Kanungo et al., '70; Buetow and Ghandi, '73). Nucleolar counts show gradual increase in bipartite nucleoli at the expense of amphinucleoli and in the senescent kidney bipartite nucleoli predominate. It is suggested that nucleolar reorganization, with final separation of plasmosomes and karyosomes, includes the process of nucleolar segregation and is triggered by some innate nucleolar mechanism in response to encoded genetic information stored in the nucleolus during nucleogenesis. At this time both DNA and RNA are incorporated into the developing nucleolus. It is also to be noted that two shifts in nucleolar dominance occur with advancing age. These may be fundamental to the process of aging and to the onset of senescence. Furthermore, the changes in dominant nucleolar types are the direct result of the process of nucleolar reorganization.

Notes: There are two discrete lobes comprising the armadillo subman-dibular gland. These two lobes can be defined grossly, histochemically and morphologically with the light and electron microscope. The minor lobe stains more intensely with PAS and AB. When viewed in the electron microscope, the secretory granules of the acinar cells within this lobe appear mucous-like. The granules of the demilune cells are slightly different in appearance. The secretory granules of the acinar cells in the major lobe contain many dense foci embedded in a fibrillar matrix, a substructure not described previously. The demilune cells of this lobe contain secretory granules with a mucous-like structure which is consistent throughout the entire lobe. As in the minor lobe, these demilune cells stain very intensely with PAS and AB.

Notes: End-plate distributions have been determined for three frog muscles of different morphology in order to relate end-plate topography to spatial muscle structure and nerve branching. Koelle's cholinesterase technique was applied, both on whole muscles and frozen sections. The end-plates of the short parallel-fibered cutaneus pectoris muscle appeared to be located in short bands along the nerve branches. The nerve tree is restricted to a zonal area across the middle part of the muscle. Depending on the way the nerve branches, the end-plate bands form innervation patterns, varying from one single continuous band to multiple distributed bands. In the latter case one frequently observes that different end-plate bands do not run across the same longitudinal muscle fiber area, although the respective nerve branches run parallel across this area. The long parallel-fibered sartorius muscle has a wider nerve tree and exhibits the same phenomenon for close parallel nerve branches, but end-plate bands along parallel nerve branches far apart cover the same muscle fiber area. The end-plate distribution in the bipennate, short-fibered gastrocnemius is zonal throughout the muscle except in certain compartments containing tonic fibers. The end-plate zone centers around the inner aponeurosis about half-way between the muscle tendon junctions of the fibers and is visible only at the muscle surface where muscle fibers run over their entire length at that surface. The results are of general use in the electrophysiology of neuromuscular transmission because they illustrate how in certain twitch muscles neuromuscular morphology may help to localize end-plates.

Notes: When a larva of Haplothrips verbasci is ready to feed, it grasps the surface of the leaf with its pretarsi, sinks down between its front legs, lifts its head, and places the tip of its mouthcone against the surface. It then shortens its mouthcone and punches a hole in the epidermis by rapidly and repeatedly protracting and retracting its left mandibular stylet. The thrips then inserts its two maxillary stylets as a unit into the wound with a series of rapid thrusts and withdrawals, salivating continuously while doing so. When a food source in the epidermis or mesophyll is found, probing and salivation stop and cibarial pumping begins. Cytoplasm is sucked into the opening at the tip of the protracted stylets, up the food canal between them and into the cibarium.Probing and feeding can occur without mandibular intervention but uptake of liquid seems to require use of the mutually coadapted maxillary stylets, even when these are fully retracted.Prior to molting, the larva protracts its maxillary stylets maximally and, in the pharate state, seems incapable of feeding or drinking.Structures used in feeding are fully described and are shown to resemble those of Hemiptera except for the presence of maxillary and labial palpi and the absence of the loral lobes, right mandible and of a salivary canal between the protracted maxillary stylets. Seven single and 18 paired muscles function in the feeding act, nine less than in adults of the same species.Differences in the feeding mechanism of terebrantian and tubuliferous thrips are discussed and evidence is presented to suggest that the simplified and more highly specialized mouthparts of the latter insects are adaptations for feeding in confining spaces.

Notes: In contemporary entomology the morphological characters of insects are not always treated according to their phylogenetic rank. Fossil evidence often gives clues for different interpretations. All primitive Paleozoic pterygote nymphs are now known to have had articulated, freely movable wings reinforced by tubular veins. This suggests that the wings of early Pterygota were engaged in flapping movements, that the immobilized, fixed, veinless wing pads of Recent nymphs have resulted from a later adaptation affecting only juveniles, and that the paranotal theory of wing origin is not valid. The wings of Paleozoic nymphs were curved backwards in Paleoptera and were flexed backwards at will in Neoptera, in both to reduce resistance during forward movement. Therefore, the fixed oblique-backwards position of wing pads in all modern nymphs is secondary and is not homologous in Paleoptera and Neoptera. Primitive Paleozoic nymphs had articulated and movable prothoracic wings which became in some modern insects transformed into prothoracic lobes and shields. The nine pairs of abdominal gillplates of Paleozoic mayfly nymphs have a venation pattern, position, and development comparable to that in thoracic wings, to which they are serially homologous. Vestigial equivalents of wings and legs were present in the abdomen of all primitive Paleoptera and primitive Neoptera. The ontogenetic development of Paleozoic nymphs was confluent, with many nymphal and subimaginal instars, and the metamorphic instar was missing. The metamorphic instar originated by the merging together of several instars of old nymphs; it occurred in most orders only after the Paleozoic, separately and in parallel in all modern major lineages (at least twice in Paleoptera, in Ephemeroptera and Odonata; separately in hemipteroid, blattoid, orthopteroid, and plecopteroid lineages of exopterygote Neoptera; and once only in Endopterygota). Endopterygota evolved from ametabolous, not from hemimetabolous, exopterygote Neoptera.The full primitive wing venation consists of six symmetrical pairs of veins; in each pair, the first branch is always convex and the second always concave; therefore costa, subcosta, radius, media, cubitus, and anal are all primitively composed of two separate branches. Each pair arises from a single veinal base formed from a sclerotized blood sinus. In the most primitive wings the circulatory system was as follows: the costa did not encircle the wing, the axillary cord was missing, and the blood pulsed in and out of each of the six primary, convex-concave vein pair systems through the six basal blood sinuses. This type of circulation is found as an archaic feature in modern mayflies. Wing corrugation first appeared in preflight wings, and hence is considered primitive for early (paleopterous) Pterygota. Somewhat leveled corrugation of the central wing veins is primitive for Neoptera. Leveled corrugation in some modern Ephemeroptera, as well as accentuated corrugation in higher Neoptera, are both derived characters. The wing tracheation of Recent Ephemeroptera is not fully homologous to that of other insects and represents a more primitive, segmental stage of tracheal system.Morphology of an ancient articular region in Palaeodictyoptera shows that the primitive pterygote wing hinge in its simplest form was straight and composed of two separate but adjoining morphological units: the tergal, formed by the tegula and axillaries; and the alar, formed by six sclerotized blood sinuses, the basivenales. The tergal sclerites were derived from the tergum as follows: the lateral part of the tergum became incised into five lobes; the prealare, suralare, median lobe, postmedian lobe and posterior notal wing process. From the tips of these lobes, five slanted tergal sclerites separated along the deep paranotal sulcus: the tegula, first axillary, second axillary, median sclerite, and third axillary. Primitively, all pteralia were arranged in two parallel series on both sides of the hinge. In Paleoptera, the series stayed more or less straight; in Neoptera, the series became V-shaped. Pteralia in Paleoptera and Neoptera have been homologized on the basis of the fossil record.A differential diagnosis between Paleoptera and Neoptera is given. Fossil evidence indicates that the major steps in evolution, which led to the origin first of Pterygota, then of Neoptera and Endopterygota, were triggered by the origin and the diversification of flight apparatus. It is believed here that all above mentioned major events in pterygote evolution occurred first in the immature stages.

Notes: Studies of the response of adult mammalian and amphibian ventricle to injury have indicated the formation of a connective tissue scar in the place of the wounded or amputated muscle. It has been demonstrated that amphibian myocytes adjacent to a wound surface, unlike mammalian myocytes, have a proliferative capacity. In the present study, a minced cardiac muscle graft was placed into the adult newt ventricle in order to increase the number of myocytes near a wound surface. With such an increased number of reactive myocytes, it was thought a new wall consisting primarily of muscle might be formed. One-sixteenth to one-eighth of the ventricular apex was removed, minced and returned to the amputation surface of the ventricle. General histological and autoradiographic studies were conducted on two sham-operated animals and on five experimental animals which were killed at 5, 10, 20, 30, 50 and 70 days after surgery. Major events of the repair and reorganization of minced cardiac muscle included blood clot formation followed by necrosis of the blood clot and much of the muscle graft. By ten days, an apparent coalescence of muscle fragments and continuity of ventricular and graft lumina were observed, although the graft area never formed an integrated unit with the wounded ventricular wall. The peak of mitotic activity (3.19%) and thymidine labeling (28.1%) of graft cells, including many cells which resembled cardiac myocytes, was observed at 20 days. At 30 days, the graft was observed as a continuous wall composed primarily of muscle fibers. Several 30-, 50- and 70-day grafts had rhythmic contractions. These results suggest that amphibian cardiac muscle has histogenetic and proliferative capacities not attributable to mammalian cardiac muscle.

Notes: Thirty-six harbor porpoises, Phocaena phocaena, were caught off the coast of Southern New Brunswick and Nova Scotia as part of a study of the biology and ecology of these animals. The formalin-preserved heart was examined first in situ, then measured and studied in detail. If the weight of the thick layer of blubber is discounted, the heart is heavy relative to the total body weight as may be expected in an animal capable of fast swimming, great agility and frequent emergence from the water to breathe. The shape of the heart, the relative size of atria and atrial appendages, the morphology of the ventricular septum, the thickness of the walls of the sinus and conus of the right ventricle and the anatomy of the pulmonary veins were found to be constant for this animal and unlike that of non-cetaceans. It is suggested that the absence of respiratory movements during diving may lead to these modifications of cardiac structure in an animal that is particularly well adapted to a totally aquatic existence.

Notes: An ultrastructural comparison of mouse oocytes isolated at various stages of growth and meiotic competence has been carried out. Progressive changes in the nucleoli, ribosomes, mitochondria, endoplasmic reticulum, Golgi complex, and other organelles and inclusions of the oocyte have been examined as a function of oocyte size by transmission electron microscopy. The observations presented support the idea that growth of the mammalian oocyte involves not just tremendous enlargement of the cell, but extensive alterations in its overall metabolism as reflected in the ultrastructure of the oocyte at various stages of growth.

Notes: The mammalian ovary has been studied by optical microscopy and by scanning and transmission electron microscopy with the purpose of presenting an integrated view of the differentiating mammalian follicle. During follicular development, changes in the granulosa cells are particularly noteworthy and include dramatic modifications in cell shape coincident with antrum formation. The cytoplasmic processes of those granulosa cells immediately surrounding the oocyte, as well as the more peripheral granulosa cells comprising a second and third layer, traverse the zona pellucida, infrequently interdigitate with the microvilli of the egg, and make both desmosomal and gap junction contacts with the oocyte. The zona pellucida is thus distinguished by numerous fenestrations of varying diameters. The membrana limitans (basal lamina) is a bipartite structure composed of (a) a homogeneous stratum upon which the peripheral layer of granulosa cells rests, and (b) an outer region of collagen-like fibers. The specific advantages and limitations of the different methodologies utilized to study folliculo-genesis are discussed.

Notes: Rabbits are unique among mammals in that their ears can regenerate tissues from the margins of full thickness holes which grow in and completely fill the opening in about two months. The circular blastema that forms around the edges of the hole differentiates a new sheet of cartilage as it regenerates in a centripetal direction. Similar holes in other mammals fail to regenerate and form scar tissue instead of a blastema. Histological studies of the healing around the edges of rabbit ear holes reveal that during the second week, when the epidermis is completing its migration across the wound from the opposite sides of the ear, conspicuous tongues of epidermal cells grow down into the underlying tissues at the edges of the wound. These epidermal downgrowths are situated between the original intact dermis of the skin and the more central tissues which give rise to the blastema. Such downgrowths are of a transient nature, and are no longer found once the blastema rounds up toward the end of the second week. Since they are not found in the healing of similar wounds in rabbit ears prevented from regenerating by prior removal of their cartilaginous sheets, nor in the naturally nonregenerating ears of sheep and dogs, it is considered that these downgrowths of healing epidermis may play a role in the unusual regenerative response of ear tissues in the rabbit.

Notes: The abdominal escutcheon, and certain aspects of pre-anal organ morphology, have been studied in Sphaerodactylus spp. and Gekko vittatus respectively. These epidermal modifications are male characteristics. The sphaerodactyline escutcheon becomes larger by the peripheral addition of specialized scales with increasing size of the individuals: this relationship is much more clearcut in S. cinereus than in the notatus species group (sensu Shreves, '68), and the possible reasons for this are discussed. The number of pre-anal organs varies between populations of G. vittatus, but within populations remains constant throughout life. Individual organs increase steadily in size throughout life. These data are discussed with reference to current interpretations of gekkonid gland evolution, and of factors controlling epidermal cell proliferation and differentiation.

Notes: In vivo and in vitro experiments on the endocrine relationships of epidermal glands in the tokay Gekko gecko, and the common house gecko Hemidactylus bowringii are reported. The results show that certain aspects of ß-gland differentiation involve a synergistic action between androgens and those hormones responsible for controlling the normal shedding cycle, while other aspects are solely under androgenic control. Pre-anal organ activity appears to be solely under androgenic control.

Notes: The gross and microscopic anatomy of epidermal glands has been studied in laboratory maintained tokays (Gekko gecko), and house geckos (Hemidactylus bowringii) captured from the wild throughout the year. Annual testicular activity in the house gecko has also been studied. While no significant differences in glandular development at various times have been observed in G. gecko, there are clear-cut annual cycle in H. bowringii. The evolution of epidermal glands in gekkonid lizards is reviewed; the cellular dynamics of β-glands are compared with those of unspecialized epidermis; the possibility that gekkonine epidermal glands respond to quantitative variation in circulating testosterone titers is discussed.

Notes: Cell suspensions obtained by the dissociation of unincubated chick embryo blastoderms were allowed to reaggregate on a gyratory shaker for 24-48 hours. The reaggregates which form during this period consist of an inner phase of tightly packed cohesive cells surrounded by an external phase of loosely packed cells. This sorted out arrangement achieves its definitive form between 24 and 48 hours of rotation culture. It was determined that the external phase consists of primitive ectoderm and that the internal phase consists of primitive endoderm. Both 24- and 48-hour reaggregates were examined in the electron microscope and observations were directed to areas of close membrane apposition between cells. In 48-hour reaggregates, primitive ectoderm cells were joined by predominantly unspecialized junctions while primitive endoderm cells were joined by many specialized junctions (desmosomes). The formation of desmosomes in reaggregates of dissociated unincubated chick embryo cells was correlated with the sorting out process.

Notes: The gross external morphology of the salivary glands of Gromphadorhina portentosa is described from light, scanning, and transmission electron microscopic observations. Various techniques, such as cryofracturing and epoxy-fracturing followed by plastic removal, were employed. Internally, the transportation system is characterized by a cuticle-lined lumen bordered by duct cells. The duct collects secretory products, some of which are reabsorbed by duct cells. Products are transported to intercalary ducts and eventually to the hypopharynx and/or salivary reservoirs. Transmission electron micrographs demonstrate distinctive morphological differences between duct cells bordering ductules and those which line expanded regions of the duct. Duct cells which surround ductules have a microvillous-lined apical border in which the cuticular coat of the lumen may be only partially developed. Duct cells in other regions may retain microvilli, or the apical plasma membrane may invaginate and vesiculate. In some cells the apical region has neither microvilli nor invaginations, but possesses two morphologically different forms of microtubules. Some duct cells are characterized by the presence of lamellar bodies in the nuclear region and/or collagenous material above the basal lamina in the area where the acinar duct becomes confluent with the intercalary duct. The plasma membranes between adjacent duct cells within acini become convoluted, forming loops filled with cytoplasm. These loops, along with contact and septate desmosomes formed between membranes, may serve dual functions: adherent mechanisms between cells and/or transportation of materials between cells.

Notes: Fertilization in Notophthalmus viridescens is internal and involves passage of the sperm through five layers of egg jelly (J5-J1, from outermost to innermost), each of which is secreted by a discrete region of the oviduct. Polyspermy is normal. Passage of the sperm through the jelly and into the egg was studied by a technique of artificial insemination similar to natural insemination, in that undiluted fluid from the vas deferens was applied directly to eggs with various layers of jelly present, followed by flooding with water three to five minutes later. In general, successful fertilization increased as the number of jelly layers increased; jellyless coelomic eggs were not fertilizable. Sperm passage through the jelly and into the egg usually occurs within one to three minutes. Upon hydration of the jelly, barriers to sperm penetration develop in layers J5 and J3. Changes in the egg jelly thus seem to be involved in the restriction of polyspermy to a low level.

Notes: In Tilapia mossambica organized lymphoid tissues are present in the thymus, head-kidney and spleen, whereas they are lacking in pericardial tissue, liver, mesonephros, intestine and rectum. No lymphoid tissue was observed in the chondrocranium and cartilaginous viscerocranium of young adults.The thymus in Tilapia is encapsulated by thin strands of collagen fibers and consists of outer, middle and inner zones. While middle and inner zones are comparable to the thymic cortex and medulla of higher vertebrates, the homology of the outer zone is not clear. At the anterior end of the thymus, a loose aggregation of lymphocytes without a definite boundary has been observed.The head-kidney is characterized by the presence of lymphoid follicles, a subcapsular sinus, a hilus-like area and lymphatic vessels. The spleen is grossly divisible into white pulp and red pulp; the white pulp contains only a reticular area without definite lymphoid centers and the latter contains predominantly erythrocytes. Morphological changes in the lymphoid organs associated with immune response have been discussed.

Notes: The complex and conspicuous basket-like structure attached to the third segment of each maxillary palp of Melittomma sericeum males is densely covered with tactile hairs on its outer or convex surface and with thinwalled chemoreceptors on its inner or concave surface. In a living male the structure is highly mobile and is extended laterally and ventrally. It evidently serves to detect odors produced by the female.

Notes: This study of the postnatal development (from 1 to 60 days) of smooth muscle elements in the rat testicular capsule has demonstrated that while such elements are identifiable by light microscopy at 30 days, myocytes are present at birth as seen by electron microscopy. The differentiation of smooth muscle from birth to 30 days has been described, by which time it is of adult morphology and content. Perhaps significantly, it is at 30 days that the testis achieves a scrotal position, although sexual maturity does not occur until about 60 days. Presumably, at 30 days the testicular capsule of the rat is capable of the spontaneous contractions which are known to occur in the adult and which are assumed to aid the transport of non-motile spermatozoa from the testis to the epididymis.The presence of occasional striated muscle fibers in the rat testicular capsule as reported previously has not been confirmed by this investigation, although their possible origin is discussed.

Notes: A chromatolysis study, 14 to 21 days following denervation, showed the spinal cord representation of the nerve to the posterior latissimus dorsi muscle to be in the ventrolateral cell column between cervical ganglia 14 and 15. To characterize cervical neurons not undergoing chromatolysis, histochemical studies were done on the cords of additional nondenervated animals. Staining reactions for beta-hydroxybutyrate dehydrogenase, succinic dehydrogenase and cholinesterase did not reveal any quantitative differences between motor neurons in cervical segments 14 and 15 of normal and dystrophic birds. Motor neurons are positive for beta-hydroxybutyrate dehydrogenase and succinic dehydrogenase, but the surrounding neuropil is positive for the latter only. No pseudochlinesterase activity is found in the ventral horn cells, but true cholinesterase is present in most of the neurons. With the periodic acid-Schiff reaction the dystrophic cords exhibit many neurons with large amounts of glycogen in them. Normal cords examined show either no glycogen positive cells or an occasional ventral horn cell with much glycogen in it. Normal muscles contain less succinic dehydrogenase and beta-hydroxybutyrate dehydrogenase positive fibers than dystrophic muscle. More periodic acid-Schiff positive fibers are present in normal muscles than in dystrophic muscle. The motor endplates in normal muscle contain only true cholinesterase. Both true and pseudocholinesterase activity is present in the motor endplates of dystrophic muscle.

Notes: High speed cinematography was used to record the feeding activities of terrestrial Ambystoma tigrinum melanostictum. A description of these activities based on films of more than 50 feeding sequences is presented, and the mechanical units involved are defined, described, and functionally analyzed. Evolutionary implications of the feeding system are discussed.In a typical feeding sequence, A. t. melanostictum stations and maintains its lower jaw 3-5 mm from the prey. The mouth is then opened to form a gape of ∼60° by raising the anterior end of the flexed skull and by elevating and advancing the trunk while the mental symphysis of the lower jaw remains stationary. As the mouth opens the bulging tongue is recontoured so that the posterior glandular region becomes the tip of the fully protruded tongue, which may extend 3 to 7 mm beyond the symphysis. Dorsally the protruded tongue has a deep central depression and pronounced anterolateral rims. The anterior rim collapses on contact, thereby engulfing the prey in a sticky trough that retains it during tongue withdrawal. The cervical region is then flexed and the skull snaps downward. If the prey resists the tongue and is captured by marginal teeth, A. t. melanostictum relies on repeated tongue protraction and retraction, in some cases accompanied by inertial feeding. Swallowing involves gular expansion and contraction, and is accompanied by eye depression. When the mouth is opened during ingestive activities, the lower jaw remains in place.Apparently, A. t. melanostictum uses the dorsal trunk, the cucullaris major and the robust heads of the depressor mandibulae muscles to open the mouth. During skull elevation the lower jaw is partially immobilized by the geniohyoideus, and rectus cervicis superficialis muscles. The subarcualis rectus I muscles are prime movers in tongue projection. Hebosteoypsiloideus muscles assist in tongue protrusion by slackening the rectus cervicis profundus muscles that would otherwise restrict anterior displacement of the otoglossal cartilage and copula. Tongue contouring is performed by the complex genioglossus musculature. Sublingual and anterolingual sinuses facilitate protrusion and contouring by providing space and lubrication. Rectus cervicis muscles (profundus and superficialis) are responsible for tongue withdrawal. Closure of the mouth is accomplished by the four levator mandibulae muscles, and again the lower jaw is immobilized, mostly by ventral longitudinal muscles.Skull-trunk elevation during prey capture and ingestion was also observed and filmed in several other species of Ambystoma, in Dicamptodon ensatus, and in two salamandrid species. Apparently raising and straightening the craniovertebral axis, while the mental symphysis retains contact with the substratum, is a common feature of urodele feeding systems, and does not require peculiar morphological adaptations.

Notes: The functional anatomy of the head of Flabelliderma commensalis is described and compared to other flabelligerid polychaetes. Prostomial parts include the dorsal lip, the palps, two pairs of nuchal organs, four eyes and the prostomial lobe and ridge. The eyes are inverse pigment cup types with the medial portions of the sensory cells expanded to form a clear lens-like body. Peristomial parts include the median and ventral lips, the branchial membrane and the branchiae. The derivation of the nephridiopore is unknown. The spiraled branchiae of Coppingeria and the gill books of Diplocirrus are newly described variations in branchial structure. The head is retractable in some species and the anterior setigers are modified to form a protective setal cage. Two methods are employed for feeding: one for host fecal pellets and the other for detrital materials. Chemoreception, respiration, feeding and cleaning rely on a complex pattern of ciliary currents.

Notes: After dissecting a variety of vertebrate hearts and extensively reviewing the literature, I have drawn some conclusions concerning the phylogeny of the tetrapod heart that differ from commonly expressed viewpoints in the literature. It is probable that the absence of an interventricular septum in amphibians is a primitive feature (rather than representing a loss). The complete interventricular septum of crocodilians and birds probably evolved primarily from the major horizontal septum of the typical (noncrocodilian) reptilian heart, with a smaller part representing a new development. The interventricular septum of mammals probably also evolved primarily from the reptilian horizontal septum. There is no reason to assume that the mammalian heart and aortic arches evolved directly from a pre-reptilian stage, as is often assumed. The evidence upon which these conclusions are based is given.

Notes: The morphology of the hyoid, laryngeal and pharyngeal regions of the following rodent genera was studied: Cryptomys, Bathyergus, Georychus, Heliophobius, Heterocephalus, Ctenomys, Petromus, Thryonomys, Geomys, Cannomys, and Tachyoryctes. A number of morphological conditions unique to bathyergids, and associated with the use of the head and lower incisors in burrowing are described. The conditions include the formation of functional complexes of MM. sterno-geniohyoideus and omo-mylohyoideus, the presence of a unique deep oblique part of M. transversus mandibulae and a strong separate slip of M. platysma myoides pars mentalis. The hyoid skeleton is modified to allow the muscle complexes to act independently of the basihyal bone, and to allow the unusually protrusible tongue to be withdrawn. The nerves of the jugular foramen do not form a true pharyngeal plexus, and their configuration is influenced by the absence of a well developed internal carotid artery in hystricognaths. The morphology of the regions studied indicates a natural grouping of bathyergids, but one in which Heterocephalus is somewhat separate from the remaining bathyergid genera. The grouping of bathyergids and New and Old World hystricognath rodents into a suborder Hystricognatha is supported.

Notes: A survey of 69 of the 74 currently recognized chelonian genera revealed that 21 genera in three families (Emydidae, Platysternidae and Testudinidae) possess paired integumentary glands or gland vestiges in the anterior throat skin. These glands are here termed mental glands; they are holocrine and may be classified morphologically as follows: Class I mental glands are large, complex, multilobed, have specialized ducts, and are found only in the genus Gopherus: Class II mental glands are small, simple sacklike invaginations containing secretory cells or keratinizing cells. The structure of Class II glands varies from distinctive and saccular to shallow keratinized invaginations having no glandular tissue; they are found only in the families Platysternidae and Emydidae.Mental glands occur in 17 of the 22 genera in the subfamily Batagurinae (sensu McDowell, 64); only 2 of 9 genera in the subfamily Emydinae have these glands. The taxonomic occurrence of mental glands suggests that they are primitive structures. The loss of mental glands in most emydines is interpreted as a subfamilial trend toward integumentary simplification.

Notes: This investigation was undertaken to examine the observations of Becker ('72) pertaining to the electrical facilitation of partial limb regenerative responses by means of Ag-Pt wire couples applied to the limb stumps of young, forelimb-amputated white rats. Additionally, in order to examine the possible role of mechanical effects of such device implantations, we have employed uncoupled devices delivering no current or potential difference. In the present experiments, in response to coupled device implantation, cartilage and bone were actively formed in the vicinity of the Pt electrode tip. These tissues contributed to the lengthwise extension of the limb and to the partial restoration of the distal humeral extremity. In limbs bearing the uncoupled electrical devices, qualitatively similar responses were noted, but osteogenesis was diminished in extent compared to that seen in limbs bearing the active or coupled devices. It is therefore necessary to consider the role of mechanical factors in the elicitation of the observed regenerative responses. Myogenesis was enhanced in electrically stimulated limbs, but not in those rats bearing uncoupled devices.

Notes: The most complete account of the hind leg muscles of the kiwi was published a century ago by Sir Richard Owen, in his seventy-fifth year. This extensively-cited work has several omissions and errors, and while certain of these were corrected by subsequent authors, sufficient uncertainty remains to warrant a reinvestigation. In the present study a detailed description of the hind leg musculature is given, based upon dissections of two frozen specimens. An indication of the possible function of each muscle is given by assessing its size, action, and fiber-arrangement, together with tentative data on the relative abundance of twitch and tonus fibers.The correlation between surface features of bones and muscle attachments is investigated with a view to interpreting palaeontological material. Although the limb and pelvic bones are marked by numerous features which suggest muscle attachments, relatively few can be positively identified with specific muscles. Only 23% of the muscle origins and insertions can be identified, and, with three possible exceptions, no indication of relative size is given by the scars. The possibility of being able to reconstruct the musculature of the kiwi from its skeletal anatomy, much less that of its extinct relatives, is remote.

Notes: Branchial food traps are regions of specialized secretory tissue in the tadpole pharynx, where suspended food particles are trapped in mucus.Light and scanning electron microscopy were used to study branchial food traps from larvae of ten anuran families (36 species). Most anuran larvae from “advanced” (suborder Neobatrachia) families (e.g., Hylidae, Ranidae, Bufonidae) have distinct secretory pits at the posterior margins of the branchial food traps and secretory ridges elsewhere on these surfaces. The apices of columnar PAS-positive, secretory cells are exposed on the floors of the secretory pits or in rows at the tops of the secretory ridges (secretory zone).Tadpoles from most “archaic” (suborder Archaeobatrachia) families (Ascaphidae, Discoglossidae and Pelobatidae) either lack secretory pits, or have them poorly defined. They also lack secretory ridges but have columnar, mucus-secreting cells whose apices are exposed in a seemingly random fashion in the branchial food traps. Rhinophrynus (Archaeobatrachia: Rhinophrynidae) has secretory ridges, but the apices of secretory cells are not arranged in rows at the tops of the ridges; instead they erupt singly or in small clusters on the epithelial surface, in a pattern similar to that in Ascaphus, the discoglossids and the pelobatids. It is proposed that the generalized condition for the branchial food trap mucosa is one where the apices of secretory cells are exposed haphazardly on a flat epithelium and the derived condition is one where the surface is organized into ridges. The morphology of the branchial food traps in Rhinophrynus suggests that, phylogenetically, ridges preceded the coalescing of secretory cell apices into distinct rows.Pipidae and Microhylidae have unique patterns in the gross and microanatomy of their branchial food traps specific to their families.Branchial food trap morphology relates to diets of tadpoles as well as to taxonomy. Obligate macrophagous (e.g., carnivorous) tadpoles, irrespective of family, tend to have reduced branchial food traps, regularly lack secretory ridges and, in extreme cases, lack columnar mucus-secreting cells. Obligate microphagous forms (midwater suspension feeding of Xenopus, microhylids and Agalychnis), have straight parallel secretory ridges with narrow secretory zones and shallow troughs between the ridges.Secretory ridges may help to form mucus strands in which food particles are trapped, but they are not essential for planktonic entrapment. The hydrodynamic implications of the various topographic patterns remain unclear.

Notes: Tactile hairs, small chemoreceptor pegs, thick-walled chemoreceptors, thin-walled chemoreceptors of several types, coeloconic sense organs and campaniform sense organs are present on the flagellum of a stonefly, Allocapnia recta (Claassen).

Notes: Glycogen metabolism has been studied during the development of the early chick embryo, at the cytochemical and ultrastructural levels. Two waves of glycogen synthesis and breakdown have been found. In the first, free clusters of glycogen particles are synthesized at late oogenesis. These clusters are found later in invaginations of the membrane of vesicles containing a floc-cular material (FLOV). The glycogen clusters are degraded there during ovulation and the first hours in the oviduct. The second wave of glycogen synthesis begins before cleavage, reaching a maximum at mid-uterine age. This second wave occurs in another type of vesicle (GLYV), which eventually disintegrates releasing free clusters of glycogen granules. This glycogen is degraded in membranous structures containing a floccular material, as in the first wave of degradation. The degradation ends at the late uterine stages, and at the same time numerous ribosomes are formed. This period corresponds to area pellucida formation, which probably depends on the energy liberated during the second wave of glycogen degradation.

Notes: The hindgut of the semi-terrestrial tardigrade, Milnesium tardigradum was examined with light and electron microscopy. The hindgut consists of a cloaca and an anterior hindgut. It is delineated anteriorly by the pylorus into which four Malpighian tubules empty and posteriorly, by a broad cloacal slit. A single oviduct enters the hindgut at the junction between the cloaca and the anterior hindgut. Two pairs of muscles insert on the cloaca and anterior hindgut respectively. Electron microscopic observations demonstrate that the anterior hindgut is a specialized transporting epithelium. The luminal surface is covered by a thin layer of cuticle which penetrates into channel-like invaginations. Numerous mitochondria are concentrated apically. The basal and lateral surfaces are also folded. The cells are joined apically by deep tight junctions and a simple basal lamina lines the entire hindgut. The cloaca which receives the contents of the gut and Malpighian tubules as well as gametes of the reproductive tract is a transitional organ that exhibits several characteristics of the hypodermis and anterior hindgut. The cuticle of the cloaca changes sequentially from the complex structure of the integument to a simple layer of the anterior hindgut. The function of the hindgut is discussed with emphasis on the possible response of the anterior hindgut to a hypoosmotic habitat, evaporative water loss during the induction of anhydrobiosis and low oxygen tension.