ALBERT

Notes: Certain variations of ciliary activity in the lamellibranch gill occur which are an intrinsic part of the gill tissue and which are due to causes other than environmental changes. Experimental and morphological evidence indicates that the central nervous system is not involved in the production of these variations.A comparative study of laterofrontal and lateral ciliated cells leads to the conclusion that the coordination impulse passes through the cytoplasm of the cell and that the velocity of the propagation wave is influenced by the number of cell walls per unit length through which it passes. It is suggested that the ciliary rootlets in the laterfrontal cells, due to their arrangement bring the impulse simultaneously to both rows of cilia within a single cell.

Notes: An investigation of the spermiogenesis of Succinea ovalis Say, a small terrestrial pulmonate, has revealed: 1) The germ cells are differentiated from indifferent germinal epithelial cells. In this form the germinal epithelium is a true epithelium, and not a syncytium. 2) Forty chromosomes are found in the spermatogonial divisions and twenty in the maturation divisions. 3) Early in spermiogenesis the proximal centriole penetrates through the spermatid nucleus and, with the oxychromatin, forms an intranuclear rod similar to that reported for certain prosobranches. The homology and significance of the rod are discussed. 4) Of the cytoplasmic structures, the mitochondria and the Golgi apparatus were followed through all stages of spermatogenesis. 5) At the maturation divisions the mitochondria are grouped into peculiar. thread-like structures. Some of the mitochondria take part in the formation of the sheath around the axial filament of the spermatozoon, while the remainder are sloughed off with the cytoplasmic remnant. 6) The Golgi apparatus consists of a number of banana-shaped rods closely grouped around the idiosome. Three to five Golgi rods are found in the spermatid stages. A portion of the Golgi apparatus and idisome (acroblast) forms the acrosome, and the Golgi remnant is discarded at the end of spermatogenesis. 7) In mature sperm both head and tail have a spiral structure. The origin and nature of the spirals are pointed out.

Notes: The blood cells of the African lungfish, Protopterus ethiopicus, are very large and resemble those of urodeles. Leucocytes are especially plentiful and rich in variety, including eosinophils, special eosinophils, [meta-eosinophils] with atypical granules, monocytes, thrombocytes, lymphocytes, and basophils.The chief hemocytopoietic organs are the spleen, intestine, and kidneys. The lungfish spleen, embedded in the wall of the stomach, represents an intermediate phylogenetic stage between the disperse intra-enteral type of the hagfish and the compact extra-enteral type of other vertebrates.Erythrocytes are formed in the spleen pulp, granulocytes in the granulocytopoietic organ of the intestine and in the capsules of kidneys, gonads, and spleen. Thrombocytes and monocytes are differentiated in the spleen and general circulation. Basophils arise in the spleen and intestine. Lymphoid cells of all types arise in the spleen. Evidence is presented bearing upon the hemocytopoietic capacity of the various types. Cells with [Russell bodies] also occur in the spleen.In lungfishes subjected to long periods of dry estivation, erythrocytopoiesis practically ceases. Granulocytes, however, appear to play an important rǒle, possibly in fat metabolism. The large variety of meta-eosinophils, a unique feature of the lungfish, appears to be associated with the habit of estivation.Recovery from estivation may show numerous amitoses of erythrocytes in the general circulation. Other cells which divide in this manner are young thrombocytes, granulocytes, monocytes, and lymphoid hemoblasts.

Notes: The acrosome in Desmognathus, Spelerpes, Plethodon, salamander, Amphiuma, etc., is attached to the nucleus in connection with an acrosome seat, which forms a shallow cup, traced back to a number of granules in the early spermatid. A postnuclear plate is present in the above-mentioned urodeles, and is derived from a small number of minute granules which assemble in the spermatid and become fixed onto the nuclear membrane. The centrosomes of the spermatid are visible intravitam. The ‘vacuome’ is formed of minute neutral-red-staining globules embedded in the idiozome. No connection appears to exist between mitochondria and Golgi bodies, as is postulated by the vacuome-chondriome hypothesis (Parat).

Notes: This paper presents a study of the normal histology of the digestive tract of an herbivorous teleost, the minnow Campostoma anomalum (Raflnesque). The tunics of the buccal cavity, pharynx, esophagus, and intestine are described; particular attention is given to the mucosa because of the specializations occurring in that coat, such as taste buds, goblet cells, callous pad, etc. Because of the very decided anatomical and histological differences existing between the anterior and posterior regions of the pharynx, due to the presence of a callous pad and pharyngeal teeth, it has been deemed advisable to consider the pharynx as divisible into an anterior and a posterior region. Thyroid tissue was found in the submucosa of the anterior pharynx. No gastric epithelium was demonstrated, the ‘intestinal bulb,’ the only enlargement of the coelomic portion of the digestive tube, being lined with epithelium presenting only minor differences from that found in the coiled tubular intestine.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Notes: 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: This study is based upon a series of ontogenetic stages from just before coelom formation to maturity.Primordial germ ceils are first seen at the outer edge of the lateral mesoderm and are traced from there to a position in the genital analagen. Counts indicate that most of them succeed in reaching the genital anlagen, where they from definitive reproductive cells in both sexes.The evidence seems to show that there is some transformation of somatic cells into germ cells in the immature female, but that this transformation is not extensive. In the male the primordial germ cells are the sole source of the definitive elements.

Notes: The detailed spawning habits and hatching period are described. The larval period is divided into the inactive, when the yolk is the source of food, and the active period, when food is captured. The rate of growth and transformation of the larvae into fry is described.The cell formation passes into a syncytial period, when there are produced many nuclei without cytoplasm.c division. Around these nuclei, the cytoplasm collects to give rise to more cells. The method by which mucous cells are produced is described and also the presence of secretion masses in both the mucous cells and the syncytium of the mucosa.

Notes: The teleost fish Brachydanio rerio is strikingly marked with longitudinal black stripes, which extend into the caudal fin and across the anal fin. Removal of the anal fin is followed by complete regeneration of the fin and of its normal color pattern. Microphotographic studies show that melanophores are at first uniformly distributed in the regenerating tissue and that later the melanophores disintegrate in the zone of the future light stripe and increase in the region of the future dark stripe. Observations on the normal development of the fin where the history of the individual melanophores has been followed show the same mode of formation of the stripes.

Notes: Study of living and sectioned material throughout the life cycle shows the germ-cell history from fertilized egg to sexual maturity. This can be divided into the following five periods with definite limits: Original appearance during cleavage, period of inactivity, period of multiplication, maturation, and fertilization. Primordial germ cells of characteristic structure can be recognized just before gastrulation, when there is one large germ cell in the mass of mesoderm on either side of the blastocoel. After one division in each of these two cells, the four daughter cells remain inactive, while the remainder of the mesoderm differentiates, until division is resumed in the developing gonad. An indefinite number of gametes is produced. All are direct descendants of the two original primordial germ cells. Transformation of somatic cells into germ cells does not occur nor do germ cells become somatic cells. Cell lineage shows the two primordial germ cells to be derived from the third division of the paired mesoderm cells which have arisen by an equal division of the fourth micromere produced by cell D of the four-cell stage. Details of meiosis have not been ascertained, because of the small size of the chromosomes, their large number, and the difficulty of fixation. Nothing forecasts which primordial germ cells will become ova and which spermatozoa.

Notes: Three types of cell inclusions are demonstrated within the general protoplasm of the binucleated Protoplina, parasites of Hyla aurea. These are considered to represent mitochondria, together with associated, synthesized vegetative granules and Golgi bodies, as evidenced by their behavior, morphology, and staining reactions.The Golgi material is shown to consist of irregularly twisted rods and granules scattered at random in the cytoplasm, but possessing a very distinctive morphology and reaction to different techniques when compared with the mitochondria. No relationship could be detected between these vegetative structures and the cilia, as has been previously described.These observations have also been extended to a similar study of the cytoplasmic organs of Nyctotherus cordiformis, and it has been possible to demonstrate Golgi bodies of a similar appearance within this organism as well as to show again the nature of the basal granules and their relationship to the cilia.The procedure of identifying the mitochondria elements with great care is recommended as a preliminary means of studying the Golgi apparatus of Protozoa, particularly where osmication techniques are used exclusively.

Notes: It is shown that in Prorhynchus applanatus there exists a type of yolk elaboration which has hitherto not been reported. Formation is within the nucleus through the growth and fusion of nucleoli, but the yolk globule becomes larger than the original nucleolus. The developing individual utilizes the food material contained in the yolk cells in the following order: (1) cytoplasm of the yolk cell, (2) yolk bodies contained in this cytoplasm, (3) intranuclear yolk, (4) nucleoplasm. It is also shown that the germ cells in this form arise from the endoderm by diapedesis, but that the yolk cells are mesenchymal in origin. The sequence of formation of male and female gametes precludes the possibility of the presence of sex hormones such as are found in higher forms.

Notes: A comparative study has been made of fifteen species and subspecies of rodents to determine the range in number and variation in morphology of their chromosomes. The number range is between 40 and 86±, with an average number for known species of 52. In the family of Cricetidae there is little variation in chromosome number and a general similarity of the chromosomes. In the Muridae the range for known species is 40 to 42, but the chromosome morphology even of subspecies may be quite different. In Sciuridae a range of 48 to 62 has been found in different species. The greatest range in number is found in the Heteromyidae, 44 and 86± chromosomes having been found in two species. It is concluded that the stem number for rodents is close to 48 and that fragmentation and fusion account for variation in numbers, and these affect the morphology of the chromosomes. The evidence also indicates that variations in morphology are due to translocations and inversions, and possibly deletions accompanied by translocations.

Notes: There are in scorpions two sharply contrasting types in respect to the mode of distribution of the chondriosomes to the sperm cells. In one of these the chondriosomes, spheroidal in form and nearly definite in number, are sorted out whole without division during the spermatocyte divisions, their number being thus reduced successively to one-half and one-fourth. This type occurs in Opisthacanthus, Hadrurus, Vejovis, Euscorpius, and Palamnaeus. In the other, as yet known only in Centrurus, all the chondriosomes fuse during the spermatocyte growth period to form a single ring-shaped body; and this, during the two ensuing mitoses, is accurately divided into two, four, and eight equal parts, of which each spermatid receives two. In both types alike the chondrioma is thus distributed very nearly equally to the sperm cells, but by widely contrasting processes; and in both types the spermatid chondriosomes are drawn out to form the sheath of the axial filament in the sperm tail. In Opisthacanthus there are indications of a definite process of dictyokinesis during the spermatocyte divisions.These facts are discussed in the light of the general history of the chondriosomes in other animals, with especial reference to more general problems of cell division. The present vagueness and uncertainty of our knowledge of cell division and differentiation are emphasized.

Notes: This study is concerned with the interrelationship existing among the polymorphie soldier castes of six representative subgenera of the genus Nasutitermes. By measurements of anatomical parts and camera-lucida drawings, an attempt has been made to compare these particular subgenera on a basis of gradual divergence of certain structures. For this purpose a series of tables was compiled in which apparently unstable structures were compared to a relatively stable figure in all available species of the selected subgenera.According to my findings, it was concluded that there is no strict correspondence between the major, intermediate, and minor castes of different subgenera of the genus Nasutitermes. Particular reference is made to the work of N. Holmgren ('12) and to that of J. S. Huxley on heterogonic growth.

Notes: The branchial nerve of Mytilus edulis, traced by means of serial sections, has been found to be limited entirely to the epithelial and connective tissues bordering the axis of the gills. Most of the numerous branches which originate from the branchial nerve extend posteriorly and lie close to the interfibrillar matrix of the connective tissue which supports the epithelium of this region. Fibers of these nerves have been traced to this epithelium.The chitinous supporting structures of the gills lie in close proximity to these nerves, yet neither nerves nor nerve fibers have been observed to penetrate them. Moreover, a careful study of the gill tissues fails to reveal the presence of structures which might be interpreted as nerves or nerve fibers.Since no innervation of the gills has been demonstrated, it seems probable that the ciliary activity of the gill epithelium is not regulated by means of fibers connected with the central nervous system.

Notes: Spironympha is discussed as valid genus. It was described by Koidzumi ('16); later it was redescribed by the same author as Microspironympha ('21). Therefore, according to the rules of nomenclature, it is Spironympha.The genus is compared with the related genera: Spirotrichonympha, Holomastigotes, and Microjoenia.Spironympha is characterized by four flagellar bands which are spirally wound around the anterior part of the body; these bands occur only in the anterior end, whereas in Spirotrichonympha they extend almost to the posterior end. The parabasals are few in number, and they are attached to the basal granules of the flagellar bands; the anterior end is clear and almost free from cytoplasmic granules; and there are twenty to thirty anterior flagella which are attached to the base of the centroblepharoplast or to the basal granules of the flagellar bands. An axostyle is present.No centrosome occurs within the nucleus, but the centroblepharoplast has this kinetic function.Spironympha ovalis is described as a new species. It is ovoid; the average size is 38 μ to 44 μ. An axostyle is present. The host is Reticulitermes hesperus Banks.

Notes: Four functional types of viviparity are recognized, and the last, pseudoplacento viviparity, is illustrated by a review of the embryogeny of a species of Polyctenidae. This insect normally has ten embryos in the reproductive tract in successive stages of development. The problem of fertilization is discussed, for there seems to be no spermatheca and spermatic clumps are present in the haemocoel. No organ of Berlese can be found. One, apparently a nymph, when sectioned revealed spermatozoa in even greater abundance than the mature females. Four to six of her offspring would seem to be paedogenetic.Females liberate ova that are yolk-free, and no chorion is secreted about them. Blastomeres are distinct, the embryonic envelopes are formed as usual, and hemipteran embryology occurs. The trophserosa functions until blastokinesis takes place, when the pleuropodial extensions evaginate and encompass the embryo which now lies in a pleuropodial cavity. The pleuropodia function as Lutrient organs, or psedoplacenta, until shortly before birth. At birth the embryo is a little more than one-third the adult body length and bears strongly developed setae.

Notes: A morphologic study of the labyrinth, especially on the perilymphatic space with its physiologic aspect, is presented in this paper. The perilymphatic space starts its development with the chondrification of the auditory capsule, and is completed by the end of the first third of metamorphosis. The author divides the whole spatium into two parts: the ductus perilymphaticus et diverticula and the pars spongiosa spati perilymphatici. The ductus perilymphaticus et diverticula may play an important rǒle in carrying out the functions of both equilibrium and audition. The pars spongiosa serves not only to fasten the membranous labyrinth to the capsular wall, but acts as a safeguard for the functions of both the membranous labyrinth and the ductus perilymphaticus et diverticula. The ductus system may have more important physiologic relations than does the membranous labyrinth in connection with the cranial cavity and spinal cord, as to the change of pressure, the transmission of vibrations, the osmosis of fluids, etc. A number of microscopic and schematic figures are shown with reference to the anatomic and morphologic relations of the membranous labyrinth, auditory capsule, and spatium perilymphaticum.

Notes: This investigation was made to demonstrate the direction of the current of a perfusing fluid (hence that of blood in nature) inside the so-called [renal-portal] vein of birds and to determine if this vein has any fine capillaries in the kidney substance. A domesticated male duck was anaesthetized with ether, and a warm saline (mixed with a little urea and urine) was passed through the aorta. The [renal-portal] vein was also perfused with the same fluid through the left internal iliac vein. At first the kidneys actively secreted semisolid urine, but gradually the strength of the latter varied from a milky to a watery fluid.Later, a warm carmine solution was perfused through the left internal iliac vein, and the path of the dye could be easily traced along the whole length of the left renal afferent (left [renal-portal] vein) and its final exit through the postcaval vein. The posterior lobe of the left kidney was partially tinged with red, probably due to diffusion, since the kidney substance should have taken a uniform red hue if there was any definite capillary system. The coccygeomesenteric vein contained no dye.These results (coupled with actual caliber measurements of the two [renal-portal] veins in duck and pigeon examined, the calibers of these veins increasing gradually posteroanteriorly) indicate that: 1) blood flows anteriorly in the [renal-portal] vein; 2) this vein does not break up into capillaries in the kidney substance, but receives larger affluent veins; 3) there is no [renal-portal] system in birds; 4) the urine secreted by birds is always semisolid.

Notes: The general morphological and histological evidence accumulated by this study suggests the following facts: 1Under out-of-door conditions, in the vicinity of Philadelphia, Pennsylvania, embryonic development begins at deposition and continues to the middle or late spring, when hatching occurs. The postembryonic development is completed during the summer. Copulation and oviposition occur in the late summer and early fall.2The embryonic development may be divided as follows: aThe prerevolution period, in which the rudiments of organs and systems are formed.bThe early-revolution period, during which the direction of the embryo in the egg is reversed.cThe late-revolation period, or time of yolk circumcrescence and completion of the dorsal wall of the embryo.dThe postrevolution period. comprising development from yolk engulfment to hatching.3The sexes are differentiated during the early- and late-revolution periods.4In the differentiation of the genital rudiments, a) the germ cells are segregated into groups; b) and indifferent mesodermal element grows in among the germ cells of such a group; c) the processes of this cell (the apical cell) form intimate connections with the processes of connective-tissue elements surrounding the germ-cell group; and, d) the covering membrane of the genital rudiment grows in between the various germ-connective-tissue cell groups, completing the rudiment of the follicle.5When the adult condition is reached the testis is functionally differentiated.

Notes: A vacuome (‘Golgi apparatus’) consisting of small globular inclusions has been demonstrated in Chlamydomonas sp. These inclusions may be seen in the living, unstained organism; they are stainable vitally with neutral red; they have been stained vitally with neutral red and then blackened with osmic vapor under direct observation, and they have been impregnated by osmic and silver methods without previous treatment with neutral red.The reaction of these inclusions to the iodin test for starch suggests that they may play some rǒle, possibly one of storage, in the cycle of starch metabolism.

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: 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: 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: Homologous chromosomes entering parasynapsis are already split. This split evidently originates in each chromosome in the resting period prior to the last spermatogonial division. In the prophase of this division the daughter chromonemata in each halfchromosome were probably incompletely separated, but the succeeding telophase effects the completion of their separation. These processes are accompanied and suceeded by an elongation, straightening, and general paralleling of the split threads and by an elongation of the cell and its nuclear space.Parasynapsis begins with intimate approximation of the daughter threads in each homologue and is continued by approximation of the homologues at the usual [bouquet] and [zygotene] periods. There results the [diplotene] thread, which therefore consists of four completely distinct strands, but which exhibits a [two-strand] appearance due to parasynapsis between daughter chromonemata being further advanced than that between homologues.The pairing process begins at the distal ends and proceeds proximally. With parasynapsis complete, the nucleus enters the [diffuse] stage On emergence, disjunction is seen to have progressed from the distal ends to near the proximal ends in each pair and the [tetrads] have taken form. In the prephase that follows each strand in a tetrad may [crimp] independently, and with the condensation and matrix (?) formation that accompany it there results the spermatocyte ‘tetrad.’

Notes: An investigation into the number of chromosomes in thirty-seven species of Aphidiae belonging to twenty-seven geaera has shown that there is but one sex chromosome in the male cells of all but one species of Aphididae. That exceptional species is Euceraphis betulae Koch.The number of chromosomes and body characters are so closely correlated that we can safely judge the evolutional scale of any aphid by its number of chromosomes.In Aphididae the least number of chromosomes seems to be the most primitive.The number of chromosomes varies with the genera. The highest number is 1811 + X = 37 chromosomes, the lowest being 211 + X = 5 (diploid in male).The increase in the number of chromosomes seems to have been brought about by transverse divisions of the primitive chromosomes.The genus Tuberolachnus with 311 + X = 4 elements (♂) represents altogether different chromosomes characters from the genus Pterochlorus with 8 elements.In the genera Periphyllus and Calaphis there are species with a small m-element which is bivalent.

Notes: In an investigation of the hatchability of eggs from hens fed on a diet deficient in vitamin E Card found that all embryos from these eggs died during development. Study of these chicks showed that a variety of conditions were responsible for death:During early development the rate of growth and differentiation was definitely slower than under normal conditions, but malformations were rare. Some embryos died during the first two days, due to disintegration of the circulatory system or its failure to become established. At the end of the fourth day there was a definite critical period which few specimens survived and by this time distinet pathological conditions had arisen in extra-embryonic structures. These involved wiping out of the vitelline circulation by establishment of a lethal ring in the blastoderm. This structure was produced by intensive cell proliferation in the mesoderm which resulted in choking out vitelline blood vessels and their subsequent degeneration. It also caused obliteration of the exocoele, with consequent failure of the allantois to expand. In addition, many embryos showed profuse haemorrage into the exocoele. The source of bleeding was most frequently in the atrium of the heart, and at the actual rupture peculiar cells occurred which were probably histiocytic mesenchyme cells.Although death was due directly to causes enumerated above, the ultimate responsibility rests upon conditions set up by them, namely: starvation, asphyxiation, and loss of the medium (blood) by which to carry on metabolic exchange.

Notes: In some insects the selection of individuals which recover in equal periods of time from immersion in water may be used to obtain material of approximately uniform physiological state; Drosophila melanogaster, Meigen, was found to have a mean of recovery for the males 0.97 ± 0.542 minute later than the females, which would indicate a lower metabolic rate for the males. The Japanese beetle, Popillia japonica Newm., was found to have a mean of recovery from immersion in water of both sexes the same in August, while in September the males were retarded by 8.1 as compared with females. This would indicate that the males have and equal me abolic rate in August with the females and a lower rate in September. Carbon dioxide, hydrogen, and nitrogen produce in the flies a condition of asphyxiation similar to immersion in water. [Vestigial] flies recover from immersion in water in a fashion similar to ‘wild’ flies.The recovery periods from immersion in water in the flies can be used to group individuals into those possessing approximately equal egg-laying capacities and to isolate spent individuals from others still capable of laying eggs. Yeast appears to be more of a stimulant to egg laying than it is to larval growth. Groups of flies which were fed yeast were found to average 71 per cent increase in egg laying over groups of flies that were not fed yeast. The O2 consumption of the groups of flies actively laying eggs, as contrasted with the groups which were not so active, was found in the former to be 32.9 per cent greater.

Notes: This paper discusses very briefly the ultraviolet microscope and the developments which have led to a successful technique for optically sectioning living cells; also the ultraviolet photomicrographs of living sperm cells of certain grasshoppers, which show clearly the spinning out of the chromonema from solid blocks of the diatene stage, the pairing of same in the leptotene stage, the development of the tetrads, the final distribution of the chromosomes in the resulting spermatids and their return to a spiral chromonema, each inclosed in its own vesicle. The details of the cytoplasm are equally well brought out.

Notes: Neutral-red staining in Daphnia, legume seeds, starfish eggs, and Palaemonetes shows reactions to temperature changes which may be correlated with the thermal reactions of enzymes.

Notes: The oldest parts of the fibrous, cartilaginous, and bony head skeleton of vertebrates descend from the amphioxid ancestors of the myxinoid fishes. The skeleton of the velum and jaw bars of the amphioxids transform into the jaw apparatus and hyoid-velar head skeleton of the myxinoids, and some parts are passed on by inheritance to the teleostome fishes (sturgeons). These anatomical characters prove descent with modification. The theory of the origin of jaws and hyoid from branchial cartilages is not supported by the facts, as both jaws and hyoid structures were developed long before branchial cartilages furnished material for head building. The Velata, the oldest of living vertebrates, include the amphioxids and marsipobranchs, and are marked off from the higher forms by the important organ, the velum, which separates the prebranchial from the branchial head. A remnant of the velum inherited by all of the higher vertebrates is the hyoid mechanism - an important anatomical landmark.

Notes: This work was designed to determine the ontogenetic variability of the morphology of mitochondria of the hepatic cell.The mitochondria of the cells of the hepatic diverticulum are minute spheres. These spheres enlarge, become associated, forming beaded filaments, which in turn become smooth filaments, the process culminating in the twenty-day fetus. There is no individual or lobular variabillty in fetuses of a given length. One-half day before birth the above process is reversed, so that separate spheres are found in the eight- to twelve-hour young. This enlargement and enspherulation are accompanied by an accumulation of large quantities of glycogen. After this age, the spheres become associated into beaded filaments again and the glycogen disappears, the cycle ending at thirty-three hours. From two to eight days of age there is great individual variability.Mitochondrial morphology characterstic of the adult is first found in the fourteen-day young, when cells contain long, smooth or beaded filaments, rods, and spheres. There is no lobular variation as to types of mitochondria, but only in numbers, the cells around the central vein containing fewer mitochondria than other cells of the lobule. Variation between individuals after birth is due to something other than age, type of food, period of digestion, and length of starvation. Fat is formed within spherical chondriosomes.

Notes: There are twenty-seven spermatogonial chromosomes in Tenoder'a sinensis, three of which are larger than the others and lag behind in anaphase. These three chromosomes have been traced through the prophases of the first spermatocyte to the metaphase, where they appear as a hexad. In the first spermatocyte division two of the constituent diads of the hexad pass to one pole, the remaining one to the other, thus giving rise to two types of second spermatocytes, one with thirteen and the other with fourteen chromosomes. There are twenty-eight chromosomes in somatic metaphases of the female; four of these chromosomes are larger than the others. The sex chromosomes of the male are represented by the formula Xa + Y + Xb, that of the female by 2Xa + 2Xb.Similar conditions are reported for Mantis religiosa and Stagmomantis carolina.

Notes: The onset of hibernation in Melanoplus differentialis eggs kept at high temperatures is accompanied by a fairly abrupt cessation of cell division. The total number of mitotic figures present in the different individuals of a series of embryos of this grasshopper, from eggs kept for eighteen to twenty days at 25°C. from the time of saying, was found to vary between 1000 and 4400. In contrast to the conditions found in eggs of this age, embryos from eggs kept twenty-seven days at 25°C., as well as those older and still in the hibernating state, contained few or no dividing cells. During the course of the work it was found that, in rare cases, hibernation failed to occur, a few or many of the eggs developed without a pause when kept at 25°C., and hatched at approximately the thirty-eighth day. The detection of variations in the rate of mitotic activity over short periods, as originally planned, was found impossible, because of the comparatively small number of embryos used.

Notes: Some pathological effects of supersonic waves produced by the piezo-electric oscillator described by Wood and Loomis ('27) are described.Death of fish and frogs was due to haemolysis of erythrocytes within the gill capillaries. Disruption of gill filaments, trauma, and extravasation in the head and gill region and in the peripheral musculature were noted.No effect on the nervous system was apparent histologically.Organisms were not killed in water under hyper- or hyponormal pressures. In these cases no cavitation of gases took place.Isolated frog sartorius muscle in Ringer's was not damaged.Bubbles of gas were easily observed within the muscle cells of the tadpoles when such cells were not more violently disturbed. Such bubbles were abundant in the more fluid muscles of four- or five-day tadpoles, less abundant in 15- to 35-mm. Lebistes, and entirely lacking in adult frog sartorius. Protoplasmic viscosity differences probably explain the gradient.The above-observed intracellular cavitation explains the muscular destruction, the haemolysis, the change in specific gravity of organisms subjected to the wave treatment, and may offer light upon the stimulatory effect of such waves on excitable tissues (compare Harvey, '28).

Notes: In this paper evidence is given in support of the author's statements (Rees, '30) that in ciliates in the genus Diplodinium a neuromotor apparatus, as described and figured by Sharp ('14), could not be differentiated. For the study of minute anatomy ciliates were cut into serial sections 3 μ thick. The body which in D. medium appeared to correspond to the motorium of D. ecaudatum was shown to be a fold of the middle layer of ectoplasm. Fibers, described and figured by Sharp as connecting the motorium to the organelles of locomotion and of food taking and to a ring about the esophagus, could not be differentiated. Other fibers which Sharp designated as opercular were shown to be part of a fibrillar complex extending throughout the middle layer and the inner boundary layer of ectoplasm. The walls of the esophagus were shown to be formed by the fused middle and inner layers of the ectoplasm. The esophageal fibers therefore belong also to the above-mentioned fibrillar complex. In D. medium a system of esophageal membranelles was differentiated, described, and figured. The ciliary systems of Paramaecium ecaudatum and of Diplodinium medium were shown to be strikingly similar. The principle of descent from a common ancestor adequately explains the above similarity, but is out of harmony with the discrepancies between Sharp's account of D. ecaudatum and this account of D. medium.

Notes: The flagella of the endodermal cells of hydra have their origin in the form of a cytoplasmic spherule which appears on the cell membrane just above the blepharoplast. This spherule moves outward, and in doing so forms a small cylinder, which, in time, flattens down into a ribbon-like flagellum, the edge of which is slightly thickened. Endodermal cells were found to bear from one to five of these flagella. Dissociated endodermal cells become amoeboid and are able to move about quite freely, taking up particles of food with pseudopods; these cells are also able to elaborate flagella. In the normal well-fed hydra the endodermal cells are found to fragment endogenously; these endogenous fragments pass to the tentacles and other outlying regions, where they are taken up by the endo-epithelio cells lining these regions. The endoderm is frequently thrown into villi of quite large size: these villi, when studied over a period of days, are found to deteriorate; the cells which composed them wander to the tentacles, buds, and basal regions by means of their flagella and amoeboid movement, where they deteriorate, the cell particles being taken up by the epithelio cells lining these areas.

Notes: The most important conclusion of this investigation is that the vacuome and the classical Golgi apparatus are independent cell components in the oocytes of Ophiocephalus and Rita. The same conclusion has been arrived at by Nath in Rana tigrina. The vacuoles, the Golgi elements, and the mitochondria can be seen intra vitam side by side.In Ophiocephalus the vacuoles give rise to albuminous yolk, as has been rightly claimed by Hibbard for Discoglossus and by Hibbard and Parat for Perca and Pygosteus. The Golgi elements give rise to the fatty yolk as in so many other forms of oogenesis described by Nath and others.In Rita the fate of the vacuoles and the Golgi elements is unknown, as the fish suddenly disappeared from the Ravi during the spawning period.

Notes: Between December 10th and January 24th, using red, green, and white electric lights at equal intensities of about 1.7 foot-candles, sixty-nine males, with females, were subjected nightly to, (a) constant six- and six-and-one-quarter-hour periods of illumination; (b) periods increasing gradually from one-quarter to six and one-quarter hours; (c) no added light (controls), in a basement room lighted by day from three large windows. Relative heat intensities reaching the birds were: for white, 1; for green, 2.5; for red, 10.Birds were killed for testis study at 5, 12, 16, 22, and 23 days.Refractory period was shorter, and modification of spermatogenic activity much greater, under a than under b types of treatment, as compared with controls. Effects were also more consistent.Descending order of testis activity induced at all stages was red, white, control, green, under both a and b.Effects on testis activity are not proportional to heat intensity of incident light, but depend on wave length, since green effect is not intermediate between those of white and red, as its heat intensity is. Green inhibited germ-cell activity even in birds already at normal midwinter minimal condition.Constant six-hour red-light treatments, of this intensity, induced flrst appearance of metamorphosing sperms in twenty-three days in midwinter.Apparatus and mode of light regulation and measurement are described.

Notes: A study of cell division in the chick embryo has revealed in striated muscle and in the early stages of all the principal tissues and organs a process, followed by the greater percentage of the dividing nuclei, which resembles amitosis, but is undoubtedly a highly modified form of mitosis. This process is designated ‘modified mitosis’. The belief that this is essentially mitotic rests upon the fact that a number of discrete bodies may be distinguished in the one or two chromatin masses of each nucleus. These masses, or ‘mulberries’, might easily be mistaken for nucleoli or karyosomes were it not that they exhibit division by elongation and constriction. These structures probably represent masses of minute and closely clumped chromosomes in somatic number dividing in a qualitative and a quantitative fashion. As additional evidence there are present between the dividing mulberries exceedingly fine fibers which possibly represent an attempt at spindle fibers. Neither centrosomes nor asters are present, but since, if present, they would have to be of the intranuclear variety (the nuclear membrane never disintegrating) their absence is immaterial. The nucleus divides not by constriction, but by the formation of a nuclear plate. This process of modified mitosis is probably a device which favors the speed of nuclear proliferation necessary to such rapidly growing tissues.

Notes: The sperm of the shiner surfperch are packaged into high density aggregations which are introduced into the female genital tract at insemination. Germ cell differentiation occurs within cysts formed by nongerminal Sertoli cells. In late spermiogenesis, spermatozoa within the cysts come to lie parallel to each other and become more densely packed. These sperm packets (spermatophores), containing approximately 600 spermatozoa, then are released into the efferent sperm ducts.The exact nature of the spermatophore binding material is not known, but a major component is proteinaceous and is synthesized in the rough endoplasmic reticulum of the efferent sperm duct epithelial cells. The mechanism by which the spermatophores pass from cysts into ducts is not clear. It appears that whereas many Sertoli cells degenerate causing the cyst wall to break down, many Sertoli cells do not degenerate, but rather assume the configuration of columnar duct cells. The spermatophores remain intact within the testicular ducts, but rapidly dissolve within the female ducts in response to increased pH.

Notes: The telemetered electromyographic activity (EMG) of select hindlimb muscles of unrestrained cats during standing, walking, trotting, and galloping have been recorded. Simultaneous cinematographic records permitted close correlation of muscle activity and locomotor behavior. In general, the pattern of extensor activity of the ankle, knee, and hip during locomotion is fairly consistent, while that of the flexors is more variable.Changes in basic EMG patterns from walk, to trot, to gallop are most evident in the two-jointed muscles associated with the knee and hip. Progressively greater variation of activity onset and cessation can be seen among extensor muscle groups from the walk, to trot, to gallop. Co-activation of the joint extensors and flexors, especially of the hip, at the end of the stance phase (E3) is slight in the walk, moderate in the trot, and considerable in the gallop. These EMG changes are necessary to meet the demands imposed upon the musculature at the faster gaits, particularly galloping, which include limb rigidity as related to loading, momentum as related to the limb's directional change from the stance phase to the swing phase, and lower spinal movements.The peroneal muscles of the ankle and the gluteal muscles of the hip show extensor activity and act as joint stabilizers during locomotion. Both biceps femoris anterior muscle and biceps femoris posterior muscle show consistent hip extensor patterns at all gaits. During quiet standing, extensor activity about the knee, ankle, and metatarsophalangeal joints is evident; but the hip extensor and flexor musculature is remarkably silent.EMG data for unrestrained cats are compared to those of dogs on a treadmill (Tokuriki, '73a,b, '74; Wentink, '76) and those recorded from decerebrate cats (mesencephalic preparation) during controlled locomotion (Gambaryan et al., '71). The EMG patterns from decerebrate cats are more consistent at the walk and gallop within functional groups of muscles at the ankle, knee, and hip than the EMG patterns observed in unrestrained cats or animals moving on a treadmill.

Notes: The relationship of the cells and tissues which comprise the developing ovarian follicle in Xenopus laevis has been studied with scanning and transmission electron microscopy. The saclike ovary is covered on its coelomic side by a squamous epithelium. The cells of this epithelium are extensively interdigitated, and each bears a short, centrally positioned cilium. The lumenal surface of the ovary is covered with a layer of nonciliated squamous cells. The areas of cell-cell contact are characterized by desmosomes in both epithelia, and between the epithelia lies a connective tissue layer-the theca-which contains collagen fibers, blood vessels, nerves, smooth muscle cells and oogonia. Beneath the theca in each follicle lies a single layer of flat stellate follicle cells. Associations between adjacent follicle cells are intermittent, leaving wide spaces or channels. Junctional contacts between neighboring follicle cells are characterized by desmosomes. From the basal surface of each follicle cell extend long, broad macrovilli which penetrate the underlying acellular vitelline envelope and contact the surface of the oocyte. Evidence is presented which suggests that follicle cells may produce and release components which participate in the formation of the vitelline envelope which consists of a 3-dimensional lattice of ropey fibers. Passageways through the vitelline envelope allow the maintenance of contact between oocyte and follicle cells and also allow ready penetration of materials both to the oocyte (e.g., vitellogenin) and from it (e.g., cortical granule material) at different stages of its development.

Notes: This study reveals age related changes in the microscopic structure of the paired frontal bone of the domestic rabbit. Undecalcified ground sections were prepared from anterior frontal bone slices removed from New Zealand White rabbits ranging from birth to 24 months of age. Included were 40 females, 4 males and 6 rabbits less than 14 days old of unknown sex. The ground sections revealed both qualitative and quantitative age changes. Qualitative changes include change in bone tissue types and developmental processes, and presence or absence of primary and secondary osteones. Quantitative changes were measured by counting primary osteones in the outer table of each frontal bone half within 1.6 mm of the metopic suture. In this region, primary osteones were absent at birth, limited in number at 14 days and generally numerous between one and three months of age. In animals older than three months, numbers of primary osteones generally decreased with increasing age. No animals older than 16 months revealed primary osteones. Possible sources of variability in the relationship between observed primary osteone number and age include ability to recognize primary osteones, methods of sampling and processing bone slices, sex related differences and diseases afflicting specimen. Significance of this study includes increased knowledge of frontal bone growth and histology.

Notes: Light microscopic autoradiography with 3H-thymidine demonstrates that the three regions of the alimentary tract in the larval (ammocoete) lamprey, Petromyzon marinus L., possess different patterns for renewing their epithelium. In the oesophagus, columnar and mucous cells originate from stem cells located at the bases of folds and migrate to the tops of the folds where they are apparently extruded. Ciliated cells, located only at the tops of the folds, seem to differentiate from migrating columnar cells. In the anterior intestine, stem cells are present throughout the epithelium so that there is limited migration of cells and their extrusion occurs randomly. In the posterior intestine, the stem cells located at the bases of the typhlosole provide a continuous population that differentiates and migrates to the top of the typhlosole and to the opposite epithelial wall where they are presumably extruded. The rates of cell renewal in all three epithelial regions of the alimentary tract are slower in animals maintained at 10 ± 1°C compared with those kept at 21 ± 1°C. Comparatively, ammocoetes have the least specialized system for cell renewal known in the alimentary tract of a vertebrate.

Notes: The renal sac of the ascidian family Molgulidae (Tunicata, phylum Chordata) has been thought to function as a kidney, yet its structure, contents and activities seem incompatible with current generalizations regarding excretory processes in marine animals. The development of the renal sac is described here as part of a general effort to reexamine the organ's role in Molgula manhattensis. Light microscopy of living animals and fixed material has shown the following: (1) The renal sac begins to sequester concretions before the heart starts beating and before feeding begins. Therefore, blood circulation by heartbeat is not necessary for production or transport of the initial concretions, whatever its effects may be on the renal sac in older individuals. Ingested food cannot provide the initial concretion material. (2) In laboratory-raised animals, concretions appear in the renal sac before “renal sac organisms” (fungus-like organisms seen in the renal sac of all field-collected adults) can be detected. Thus, at least some portion of the concretions can be produced by Molgula in the absence of renal sac organisms. (3) No openings have been detected in the renal sac at any stage of its development, nor is there any evidence that concretions are dissolved or transported out of the renal sac. (4) The development and morphology of the renal sac are consistent with the hypothesis that the organ is an epicardial derivative, except that the renal sac arises from post-pharyngeal (presumptive gut) endoderm, rather than pharyngeal endoderm.

Notes: Oocytes and nurse tissue of Bruchidius differentiate from germ cells during the extended period of pupal development (7.2 ± 0.6 days). A system of 15 pupal stages correlates ovarian development with changes in pigmentation of the eyes, maxillae, alae and tarsalia. The ovarioles grow in length at a constant rate, though their width does not change.A differentiating zone, consisting of germ cells and the basal layer of interstitial cells, arises at the base of the tropharium and separates presumptive oocytes and nurse cells. Early in pupal development the germ cells are arranged in primary syncytia with the cells connected by persisting intercellular bridges filled with fusomal material, never with larger particles, such as mitochondria. At later stages membrane disintegration changes the primary syncytium into a secondary one including all nurse cell nuclei.Nutritive cords are first noticeable when differentiation of oocytes and nurse cells starts. The cords seem to be of primary origin, i.e., they are connections between sister cells which become elongated as these cells are separated during growth. This is indicated by the persistence of intercellular bridges which are sometimes found as part of the membrane of growing nutritive cords connecting young oocytes with the nurse cell syncytium.

Notes: The formation of protein-carbohydrate yolk in the statoblast of a fresh-water bryozoan, Pectinatella gelatinosa, was studied by electron microscopy. Two types (I and II) of yolk cells were distinguished. The type I yolk cells are mononucleate and comprise a large majority of the yolk cells. The type II yolk cells are small in number; they become multinucleate by fusion of cells at an early stage of vitellogenesis. In both types of yolk cells, electron-dense granules (dense bodies) are formed in Golgi or condensing vacuoles, which are then called yolk granules. For the formation of yolk granules, the following processes are considered: 1. Yolk protein is synthesized in the rough-surfaced endoplasmic reticulum (RER) of the yolk cells. 2. The synthesized protein condenses in the cisternal space of the RER and is packaged into small oval swellings, which are then released from the RER as small vesicles (Golgi vesicles, 300-600 A in diameter). 3. The small vesicles fuse with one another to form condensing vacuoles, or with pre-existing growing yolk granules. 4. In the matrix of the condensing vacuoles or growing yolk granules, electron-dense fibers are fabricated and then arranged in a paracrystalline pattern to form the dense body. 5. After the dense body reaches its full size, excess membrane is removed and eventually the yolk granules come to mature. Toward the end of vitellogenesis of the yolk cells, the cytoplasmic organelles are ingested by autophagosomes derived from multivesicular bodies and disappear.

Notes: Testis structure in four species of goodeid teleosts is described. Testicular tubules terminate blindly at the testis periphery where spermatogonia are located. In goodeid teleosts, development of sperm takes place synchronously within cysts whose periphery is made up of a single layer of Sertoli cells. Upon completion of spermiogenesis, spermiation ensues wherein sperm are shed, as spermatozeugmata, into the testis efferent duct system. Subsequently, Sertoli cells, which comprised the cyst periphery, transform into efferent duct cells.Sertoli cells phagocytize residual bodies and are involved in the formation of spermatozeugmata. The structure of the goodeid spermatozeugmatum is quite different from that observed in the related poeciliids. It is concluded, in view of this and other considerations, that the goodeids and poeciliids have independently evolved solutions to the problems of internal fertilization and gestation.