ALBERT

Notes: Pyroantimonate precipitate indicates that the epithelium of the proximal tubule is the only segment of the tubular nephron of the fresh water lamprey where large accumlations of cations are distributed. Unusually large amounts of reaction product are located within the lateral intercellular spaces and within vesicles closely associated with the plasma membrane at the lateral and basal surfaces. This technique suggests the continuity of these vesicles with the plasma membrane and alludes to the possibility of an endomembranous system of vesicles and the intercellular spaces as vehicles for ion transport. Lateral intercellular spaces of proximal tubules of lower vertebrates may play a different role in kidney function that their counterparts in higher vertebrates.Osmium-zinc iodide has a specificity for certain cells within the proximal, intermediate, and distal segments, but no structural differences are noted when these cells are compared to unstained cells. Smooth endoplasmic reticulum remains unstained in the distal segment but the stain has a strong affinity for elements of the Golgi apparatus, lysosomes, and the nuclear envelope of all cell types. This technique does not suggest a structural or functional similarity between cells of the distal segment and the chloride cells of the gills of teleosts.

Notes: Anatomical analysis of the forebrain and midbrain of Anelytropsis, Dibamus and feyliniids reveals structural similarities with those of skinks and snakes. Skinks and feyliniids are probably derived from a common ancestral stock. This is suggested by mutual reduction of several telencephalic nuclei, by similar trends in the development of the dorsal thalamus, and by similarities in the lamination of their optic tecta. Anelytropsis, Dibamus, feyliniids and snakes show interdigitation of the periventricular gray zones of the optic tectum and enlargement of lamina 7 of the posterior colliculus. Of these three taxa, Dibamus is most similar to burrowing snakes and many of its brain characters are intermediate between skinks and burrowing snakes. These similarities may suggest common ancestry between Dibamus and snakes rather than parallelism.

Notes: It is possible to monitor the electrical activity of the motor neurons of Drosophila by recording the electrical activity of the muscle fibers. We have found that it is possible to specify the location of the subcuticular terminations and to describe the orientation within the thorax for the individual muscle fibers, because of the large size of the fibers and because the surface anatomy of Drosophila is known in detail. A map has been made to indicate the location of the muscle fibers with respect to superficial landmarks. The importance of the stereotaxic map for physiological studies is discussed.

Notes: The functional anatomy of pulmonary ventilation in Thamnophis elegans was studied by electromyography. Flow of air into and out of the lungs follows a triphasic pattern and occurs while the glottis is held open by a dilator muscle. Non-ventilatory rest periods characterized by a closed glottis and lack of ventilatory movements occur between breaths. Exhalation is caused by contraction of a pair of dorsolateral sheets of muscle that extends from the ventral surface of the vertebral column to the medial surfaces of the ribs and a pair of ventro-lateral sheets that extends from the medial surfaces of the ribs to the mid-ventral skin. Inspiration is powered by contraction of a series of rib levators and retractors. The last phase of the ventilatory cycle is a passive expiration that may be caused by elastic recoil of the walls of the filled lungs and relaxation of muscles used during inspiration. The site of respiratory pumping is shifted craniad after large prey items have been completely ingested. The significance of this shift and its anatomical basis are considered.

Notes: As seen in transverse section, doublet elements of the axial unit of spermatozoa of Haematolocchus medioplexus, a frog lung-fluke, possess walls made up of protofibrillar subunits 50-60 Å in diameter. The partition between A and B members of a doublet element often show extra protofibrils which may partially occlude the “lumen” of the A tubule. Each A tubule possesses outer and inner lateral arms which repeat at longitudinal intervals of about 215 Å and which appear to be structurally dissimilar; the outer arm is expanded at its free end and the inner arm often connects to the B tubule of the adjacent doublet element. Regularly-spaced radial links connect the central sheath of an inner core complex to the A tubules of the peripheral doublet elements. Tests for magnesium-activated ATPase activity provide evidence that the enzyme is associated with the surfaces of doublet elements and the surface of the central sheath. Finally, study of an axial unit which developed in an abnormal manner suggests that normal differentiation of an axial unit may depend on the elaboration of a core complex and radial links.

Notes: This is the first demonstration of an apparent acrosome reaction by the use of negative staining (phosphotungstic acid) and electron microscopy. It is also the first report of such a reaction in spermatozoa of an oligochaete annelid (Lumbricus terrestris). The morphology of the negatively stained unreacted acrosomal complexes is entirely comparable to that seen in sectioned material. After reaction, a short straight filament is extruded and the compartmentalization seen in unreacted spermatozoa is no longer visible. In the flagellar axoneme there are short cross-bridges linking the two central singlet microtubules at 150-170 Å intervals. Two fibrous elements are also present, forming, with the singlets, a tetragon. All four of these structures apparently change their elastic properties after incubation in distilled water for two hours, so that instead of following the doublet microtubules in gentle coils, the central complex components fall as a unit in jagged configurations.

Notes: Serial sections of embryonic rat eyes were stained with hematoxylin and eosin, quantified (by counting pycnotic and viable nuclei), reproduced by camera lucida on wax plates, and moulded into reconstructions in order to study the normal progression of cellular death during morphogenesis. At least nine distinct necrotic loci (A through I) can be distinguished. Immediately following contact between the retina and surface ectoderm (day 11) degenerating cells were observed in (A) the ventral extent of the optic vesicle, beginning in the mid-retinal primordium and continuing ventrally in the optic stalk, (B) in the rostral optic stalk base, and (C) in the surface ectoderm encircling the early lens placode. No degeneration was observed in the dorsal half of the presumptive retina, in the entire pigment epithelium, or in the lens placode proper. During day 11.5 the lens placode thickens and forms a degenerating locus (D) in its ventral portion opposite the underlying pycnotic zone in the retina (A). During day 12 the ventral pycnotic zone (A) divides into two subunits (A1 and A2). Invagination of the lens displaces its marginal and ventral components (C and D) so that they come to occupy the lens pore area and presumptive corneal epithelium. Simultaneous invagination of the retinal rudiment juxtaposes the pigment epithelium which concurrently forms a necrotic area (E) adjacent ventrally to that in the retina (A1). Degeneration appears in the caudal optic stalk (I). The density of viable cells decreases adjacent to pycnotic areas in the retina and pigment epithelium and increases within these death centers. During day 13 the optic fissure forms within the subunits of the ventral pycnotic zone (A1 and A2). Degenerations are seen in the dorsal optic stalk (F) and in the walls of the optic fissure (G and H). Throughout these stages necrosis appears only in those portions of the eye rudiment where invagination is either retarded or completely absent.In part, these observations suggest that cell death serves (1) to retard or inhibit invagination within death centers, (2) to integrate the series of invaginations which mould the dorsal optic cup and optic fissure, (3) to assist formation of the pigment epithelium monolayer, and (4) to orient the lens vesicle within the eye cup. The spatio-temporal relationship between necrotic loci suggests that pycnotic cells in the retina may influence their production in the lens and pigment epithelium. Preliminary observations on the mouse, pig, and human substantiate those on the rat.

Notes: The ultrastructural features of cardiac muscle cells and their innervation were examined in the tarantula spider Eurypelma marxi Simon. The cells are transversely striated and have an A band length of about three microns. H zones are indistinct and M lines are absent. Thick and thin myofilament diameters are approximately 200 and 70 Å respectively. Eight to 12 thin filaments usually surround each thick one. Accumulations of thick and thin myofilaments occur perpendicular to the bulk of the myofilaments in some cells. The Z line is discontinuous and thick filaments may pass through the spaces in the Z line. Extensive systems of sarcoplasmic reticulum and transverse tubules are present; these form numerous dyadic junctions in both A and I band regions. Sarcolemmal invaginations form Z line tubules; lateral extensions of the plasma membrane portion of these invaginations form dyads. Nerve branches of the cardiac ganglion make multiple neuromuscular synapses with at least some of the cardiac muscle cells. Both large granular and small agranular vesicles are present in the presynaptic terminals. Intercalated discs similar to those present in other arthropod hearts occur between the ends of adjacent cardiac muscle cells.

Notes: A cinematographic analysis of the unrestrained walking, trotting, galloping, jumping and landing movements of 11 adult cats was undertaken to provide previously unavailable information concerning the demands imposed on the nervous system for the control of low and high speed movements and the demands imposed by such natural movements on muscle performance and proprioceptive response.With due regard for the swing (F and E1) and stance (E2 and E3) phases of the step cycle of an individual limb, single frame analysis of the film permitted measurement of instantaneous angles of the lower spine, hip, knee, ankle and metatarsophalangeal joints. Appropriate lever arm measurements were also made on 50 freshly dispatched cats and 25 cadavers such that the Law of Cosines could be used to calculate instantaneous lengths of select hind limb muscles that would apply to the natural movements of adult cats of small (1.5-2.5 Kg), intermediate (2.6-3.5 Kg) and large (3.6-4.5 Kg) size. Muscle displacements were analyzed relative to maximum and minimus in situ lengths and the lengths associated with quiet standing. Use was also made of a previous electromyographic analysis of hind limb muscles during unrestrained locomotion (Engberg and Lundberg, '69).The sequential relations between the four phases of the step cycle are maintained as forward speed increases from walking ( 〈 2 mph) to high speed galloping ( 〉 16 mph). There are significant differences in the time consumed by each phase, however, with a greater reduction in the E3 phase, little reduction in the E2 and E1 phases and virtually no reduction in the F phase. When each phase is expressed as a relative percentage of the duration of the total step cycle, the greatest reduction is again in E3 with little change in the E2 phase. In contrast F and E1 phases increase in the percent of time they occur in each cycle, with the greatest increase in the F phase. For all speeds, analysis of the phase relations between movements of various sections of the hind limb revealed a remarkable unity of knee and ankle joint movement. The hip joint is largely out of phase with the knee and ankle during E1 and E2, all three joints being in phase in F and E3. The digits are essentially out of phase with the other joints except in the stance phase of the gallop.Rates and extents of muscle displacement during natural movements are greater than might be anticipated when expressed in absolute mm's and mm/sec but not when considered in relation to maximum and minimum in situ length and the length associated with quiet standing (Ls). During stepping a progressive increase in forward speed results in: (a) a greater usage of muscles at lengths between Ls and maximum in situ length; (b) for knee and ankle extensors, pronounced increase in the lengthening contraction associated with the E2 (yield) phase of step; and, (c) for both flexor and extensor muscles, an increased active phase of lengthening or near isometric contraction immediately prior to periods of active shortening. In contrast to these changes in active muscle status, the change from walking to galloping has little effect on the extent and rate of passive muscle displacements, particularly the F phase stretch of extensors.For the soleus muscle, calculations were made of the relation between changes in overall muscle length during natural movements and the length of the average muscle fiber and the tendon of insertion. These measurements revealed that the increases in fiber length when passive and decreases in length during active shortening are less than would be anticipated from the extensive liteature on extirpated fibers. In contrast, the increase in fiber length when active is greater than would be expected from the admittedly sparse literature on this subject.The results of this study are discussed largely in relation to two points of neurophysiological interest: the physiological range of muscle stretch as it pertains to the responsiveness of muscle spindles and tendon organs; and those mechanical aspects of lengthening contractions that give insight into the neural control of stepping. For exciting both spindles and tendon organs passive muscle stretch and shortening contractions are shown to be relatively ineffective and lengthening and isometric contractions particularly effective movements. It is suggested that, just as recent literature has emphasized the co-activation of efferent alpha and gamma motoneurons as a muscle becomes active, so too is there a synchronous activation of afferents, particularly the Ia and group II endings of muscle spindles and Ib endings of tendon organs. Finally the thesis is advanced that, while it has been convenient to separate E2 from E3 in the description of the stance phase of the step cycle, extensor muscles are actually undergoing a single mechanical event: an active stretch-shorten cycle for knee and ankle extensors and an active isometric-shorten cycle for hip extensors. This hypothesis has significant implications for the neural control program that regulates the stepping sequence in that it emphasizes the extent to which appropriate changes must be preprogrammed in the mechanical properties of muscles for the smooth execution of stepping.

Notes: Cytological and cytochemical methods were used to identify and characterzie six distinct regions of the crayfish kidney: coelomosac, labyrinth I and II, and nephridial canal I, II, and III. Cells of the coelomosac possess cytoplasm which is strongly PAS-positive, but poor in RNA and protein. Their nuclei possess unusual projections which extend to the basal plasmalemma. Labyrinth I contains columnar cells rich in glycogen. Labyrinth II is characterized by a distended lumen and by shorter cells with high cytoplasmic RNA, many possessing a large intracellular vacuole. A PAS-positive brush border is unique to the two portions of the labyrinth. Cells in the nephridial canal show strong reactions for RNA and Mg++-dependent ATPase. In nephridial canal I and II, cells are flattened to cuboidal with the lumen being more distended in nephridial canal I than anywhere else in the tubule. In nephridial canal III, the cells are large and columnar, and the cytoplasmic RNA concentration is greatest apically. Nuclei in all regions of the tubule epithelium, except coelomosac, are large and react strongly for protein. Coelomosac nuclei and those in blood cells are condensed and contain little protein. The cytoplasm of blood cells displays a significant amount of RNA, and traces of polysaccharide material.These observations demonstrate the presence of highly specialized morphological and histochemical alterations along the length of the kidney tubule and indicate sequential modification of urine in the lumen. Evident morphological and cytochemical likenesses between analogous regions of the mammlian nephron and the crayfish kidney tubule suggest that basic physiological similarities may also exist.

Notes: In the tiger salamnder the distribution of optic fibers, as revealed by the Fink-Heimer method, is compared with the localization of acetylcholinesterase, as revealed by histochemical methods. AChE activity coincides with optic nerve axons in the optic fiber layer of the retina, in the optic nerve, in the optic tracts and in every optic projection. Reginons of optic fiber terminals show heavier activity than optic fibers of passage. Comparison with other vertebrates is also made.

Notes: The spleen of the adult gerbil (M. unguiculatus) is characterized by the absence of venous sinuses and ellipsoid sheaths. The follicle (white pulp) is separated from the surrounding red pulp by a distinct marginal zone. The cell types in the marginal zone are common to both the follicle and red pulp. Separating the marginal zone from the follicle is a vascular channel of capillary dimension, the marginal sinus. A number of terminal segments of the arterial vessels within the follicle were observed to form a direct connection with the marginal sinus. Ultrastructurally, discontinuities were evident within the walls of the marginal sinus that would permit passage of both cellular and plasma components from the marginal sinus to either marginal zone or the follicle.

Notes: The innervation of each of the muscles involved in mediating head movement in the desert locust Schistocerca gregaria is described in detail. The number of motor neurones to each muscle and the neutral pathway and ganglion of origin of each are deduced from both histological and electrophysiological evidence. Only two of the muscles are, on histological evidence, innervated by as few as four different neurones, while several receive more than ten, and one at least 13. Individual muscles are shown physiologically to receive, in a few cases, as many as six different motor neurones. At least six muscles are innervated by motor neurones originating in more than one ganglion. One group of four muscles consisting in total of less than 100 muscle fibres receives more than 20 different motor neurones from three different ganglia through three or four different nerve roots. In these muscles, many single muscle fibres receive innervation from at least two different ganglia. It is concluded that the segmental nature of an insect muscle can not be deduced solely from a knowledge of the ganglion of origin of the motor innervation to that muscle. The innervation patterns that exist today must reflect past evolutionary development, but changes in the peripheral distribution of motor neurones, or migration of motor neurone cell bodies from one ganglion to another, or the development of additional motor neurones, or several of these factors together, must have formed a part of that development.

Notes: 1. Forty-eight species of oribatids in 37 families representing most of the superfamilies were collected from various environments (littoral, salt marsh, litter, sod, and freshwater) and sectioned.2. The coxal gland is composed of a sacculus and a labyrinth in all stages of all oribatid species. Muscles, originating on the body wall, insert at several points on the thin-walled sacculus which opens into the labyrinth. The labyrinth has an internal, chitinous supporting skeleton. The type A labyrinth has 3-180° bends, producing four parallel regions, and occurs in all inferior oribatids. The type B labyrinth has 1-180° bend, producing two parallel regions, and occurs in all superior oribatids. The coxal gland duct and the lateral gland duct join, penetrate the body wall, and empty into the posterior end of the podocephalic canal. All oribatids have lateral accessory glands, but only inferior oribatids have rostral and medial glands. Three ductless coxendral bodies are always present.3. The labyrinth length in oribatids is correlated with body size and the environment of the species. Oribatids from sod, leaflitter, or moss show a simple correlation of labyrinth length (X) to total body length (Y) where Y = 4.64X. Freshwater species have a labyrinth length greater than that of comparably sized terrestrial species and salt water (littoral) species have a labyrinth length less than that of comparably sized terrestrial species. There is a greater reduction in labyrinth length in species restricted to salt marshes than in species not restricted to salt marshes.4. The probable function of oribatid coxal glands is osmoregulation. Hemolymph filtration would occur across the sacculus by positive hemolymph pressure and contraction of the sacculus muscles. Resorption of ions would occur in the labyrinth, which is noncollapsible due to the internal skeleton. The hypothesis is that in freshwater species the rate of filtration is high and resorption of ions would have to be very efficient, therefore they have an elongated labyrinth; but in salt water species water loss must be minimized and preservation of ions would be a disadvantage, therefore they have a shortened labyrinth. Excre ion may also be a function of the coxal glands. The lateral gland may possibly function as an endocrine gland involved with production of a molting hormone. The rostral glands in inferior oribatids may have a salivary function.5. The coxal glands of Peripatus, some millipedes, apterygote insects, decapod crustaceans, and all arachnid orders are homologous. The Tetrastigmata, Notostigmata, Cryptostigmata, and soft ticks have typical arachnid coxal glands. The coxal glands of higher Prostigmata may be modified into salivary, silk, or venom glands. The coxal glands in Mesostigmata, Astigmata, and hard ticks are lacking or highly modified.

Notes: The blood system of the flabelligerid polychaete, Flabelliderma commensalis has been explored by dissection, light and electron microscopy and absorption spectrophotometry. The main longitudinal vessels are the dorsal, ventral, perineural, sub-oesophageal, supra-oesophageal and heart. Each segment has a segmental vessel which communicates with the dorsal vessel in thoracic setigers and the gut sinus in abdominal setigers. Branches of the segmental vessels in setigers 2-9 supply the gonads. A blood sinus envelopes most of the gut. Circulation is maintained by the pumping of the heart which immediately supplies blood to the supra-oesophageal ganglion, the branchiae and the palps. These are paralleled by a system of collecting vessels. The sinus of the supra-oesophageal ganglion receives a number of different axonal endings, some of which may be neurosecretory. The retroperitoneal vessels in their most developed form are composed of an intima, longitudinal and circular muscles and a peritoneum. The heart vessel contains a cardiac body whose cells appear to contain vacuoles of blood pigment. The blood pigment exhibits the absorption characteristics of a chlorocruorin with maxima at 438, 558 and 606 nm.

Notes: Attachment of muscle of the integument was studied in two species of Balanidae, Balanus balanoides and B. improvisus with electron microscopy. Specilalized epithelial cells (tendon cells) intervene between the muscle and overlying cuticle. An extensive desmosome-like junction exists between these two tissues. The tendon cell contains huge amounts of microtubules aligned parallel to the long axis of the inserting muscle. Tension exerted by contracting muscles is conveyed to the chitinous exoskeleton via the specially organized tendon cells and the extensive myo-tendinal cell junctions.

Notes: Among ants, Cataglyphis bicolor shows the best performance in optical orientation. Its eye is of the apposition type with a fused rhabdom. Morphological studies on the general struture of the eye as well as the effect of light have been carried out with transmission and scanning electron microscopy.An ommatidium is composed of a dioptric apparatus, consisting of a cornea, corneal process and a crystalline cone, the sensory retinula, which is made up of eight retinula cells in the distal half and of an additional ninth one in the proximal half. The ommatidia are separated from each other by two primary pigment cells, which surround the crystalline cone and an average of 12 secondary pigment cells, which reach from cornea to the basement membrane.The eye of Cataglyphis bicolor possesses a light intensity dependent adaptation mechanism, which causes a radial and distal movement of the pigment granules within the retinula cells and a dilatation of cisternae of the ER along the rhabdom.Until now, no overall order in arrangement of retinula cells or direction of microvilli has been found from ommatidium to ommatidium. Such an order, however, must exist, either on the retina or the lamina level, since we have proven the ant's capacity for polarized light analysis.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Notes: The morphology of the rectal pads of two cockroaches, Blattella germanica and Blaberus giganteus is described and contrasted with that of Periplaneta americana, studied previously. The columnar absorptive cells of the three species are similar in structure. However, Blattella and Blaberus rectal pads have a second type of cell, termed the secondary cell, that is not present in Periplaneta. The secondary cells are embedded in the pad epithelium and have crypts of cavities opening into the subepithelial sinus. In addition, a multilayered sheath is present between the pad cells and the sinus. The sheath acts as a barrier, perhaps of low permeability, between the subepithelial sinus and the pads. It is interrupted only at the borders of the secondary cells. A mechanism for fluid absorption is presented and the possible role of secondary cells is discussed. It is proposed that the secondary cells reabsorb solute from the sinus and that this solute can then be recycled through the pad cells. Structures resembling neurosecretory terminals within the cavities of the secondary cells may be involved in regulation of recycling. The arrangement of the rectal pads in these insects has structural and perhaps functional similarities with other transporting systems, particularly the cryptonephric system.

Notes: Light and electron microscope studies indicate that the old ependyma just proximal to the plane of amputation in early lizard tail regenerates shows a sequence of morphological changes which suggests that it as well as the new ependyma growing into the regenerate may play an active role in the initiation and maintenance of early tail regeneration.The old ependyma close to the plane of amputation undergoes hypertrophy and/or hyperplasia causing a partial closure of the central canal and pseudostratification. Its nuclei shift from an original apical position to a basal one. The ependymal processes become more prominent and extend to the pia, a condition not found more rostrally. There is also a significant increase in the amount of Golgi substance and a moderate increase in the rough endoplasmic reticulum. These observations lead to the thought that these cellular changes may be an expression of enhanced secretion and other activities in the old and new ependyma just proximal or distal to the plane of amputation.

Notes: Statistical analyses of chromatophore densities and morphological states in wild type, burnsi, and kandiyohi: adult Rana pipiens integument yielded the conclusion that disruptive pigmentary pattern is permanently defined by regional chromatophore densities. Spatial chromatophore patterning is enhanced and rendered more visible by the morphological and physiological differences among chromatophores within the various pattern regions. Specifically, (1) chromatophores were differentialy distributed among pattern regions, (2) greater complexity of gross disruptive patterning had greater underlying melanophores densities, (3) there were significant density differences among non-sib individual animals, among fertilization, and among shipment batches, but not among full-sibs, and (4)kandiyohi individuals had more while burnsi individuals had fewer total melanophores than wild type. A stellate morphology was significantly correlated with high melanophore density, although the relationship of melanophore density to melanophore morphology differed among pattern regions and among genotypes. The functional interrelationships of density and morphology, and their role in disruptive patterning and coloration, are discussed.

Notes: The male rotifer copulatory organ is composed of a urethral canal extending from the tip of the copulatory organ internally to a layer of microvilli. The microvilli project from two different cell types, referred to as the internal and peripheral microvillar cells according to their location. At this microvillar junction a second canal, the vas deferens, continues posteriorly and enters the sperm duct region of the testis. The channel of the vas deferens is formed from the inner wall of three separate cells; the cap, intermediate and basal cells. Peripheral to these cells and parallel to them for their entire length, cross sections of seven prostate gland cells can be observed. Anteriorly, these gland cells are connected to the basal end of the microvillar layer via a short neck region, through which glandular secretion occurs only during copulation. The mechanism of secretion appears to be a form of exocytosis whereby the secretory granule membrane fuses with the cell plasmalemma so that rupturing at the point of fusion will release the granule content into the neck region.The prostate gland cells contain an abundance of autophagic vacuoles while most of the other cells of the copulatory organ contain primary lysosomes and cytolosomes. These organelles may be associated with the aging process in rotifers, or, as in the case of the prostate gland-autophagic vacuoles, with a fast organelle turnover during secretion.

Notes: Spermatogonia of the nine-banded armadillo, Dasypus novemcinctus mexicanus, were studied morphologically using light and electron microscopy and examined histochemically using light microscopy. Immature flat type spermatogonia have ovoid or irregular nuclei with loosely condensed chromatin. Free ribosomes are abundant while profiles of rough endoplasmic reticulum are scarce. Smooth endoplasmic reticulum is a prominent feature occasionally taking an unusual cylindrical form. Mature spermatogonia exhibit rounder nuclei with greater degrees of chromatin clumping. Smooth endoplasmic reticulum is no longer prominent whereas profiles of rough endoplasmic reticulum are quite common. Occasional lysosomal configurations are found in mature spermatogonia.The majority of spermatogonial cells exhibit weak to moderate reactivity when stained with the periodic acid-Schiff (PAS) reaction. Certain cells in each tubular cross section stain vividly with this reaction and the PAS positivity is removable with salivary amylase. Because of nuclear characteristics, position of the cell immediately upon the basal lamina, intensity of the PAS reaction and the relative paucity of the vividly staining cells, it is suggested that they are members of the immature spermatogonial cell line, perhaps acting as stem cells. None of the several other histochemical procedures employed was capable of selectively demonstrating these cells.

Notes: The duodenal glands of four marsupial species, the kangaroo, native cat, marsupial mouse, and bandicoot, form a narrow lobular collar immediately distal to the gastrointestinal junction. In two species, the koala and wombat, the duodenal glands are diffuse and scattered along the intestinal tract distal to the gastrointestinal junction for considerable distances. The glands of all species examined empty independently into the intestinal lumen. Histochemical studies indicate that the latter two species, the koala and wombat, elaborate an acid mucin whereas the former species produce a neutral mucosubstance. Ultrastructural examination shows that generally the duodenal glands are comprised of large pyramidal cells that show a definite polarity, with basally-placed nuclei and apically-situated secretory granules. Species differences, with regard both to the morphology and nature of the secretory granules and to the proportions of cell organelles, exist. The diversity of diet between species is discussed.

Notes: Cytodifferentiation of the myoepithelial cells (MEC) of the rat submandibular gland (SMG) was observed by studying the prenatal and postnatal development of the gland in vivo and in vitro by light and electron microscopy. The anlage of the SMG first appeared on the fourteenth day of gestation and, from its earliest inception, was surrounded by an intact basal lamina. Presumptive myoepithelial cells were first seen at 18 days of gestation coinciding with the onset of secretion in the rudiment. These cells were flattened, peripherally located and subjacent to the epithelial basal lamina. Initial deposition of cytofilaments in the MEC's was observed during the first three days following birth and fully matured cells were seen as early as one week after birth. Presumptive and immature MEC's were observed undergoing mitosis, but once cytofilament deposition had begun in the cells they did not divide. Myoepithelium developed in relation to embryonic secretory structures and were only observed surounding acini and intercalated ducts in the adult gland. New myoepithelial cells were formed as long as new acinar-intercalated duct units were formed. Myoepithelial cells did not produce secretory type granules at any time during their development or in their mature state.Development of the MEC's in vitro paralleled that in vivo and supported the above observations.

Notes: Larval compound (jointed) setae of the polychaete Nereis vexillosa Grube were examined by scanning and transmission electron microscopy and by polarization microscopy. Long-bladed spinigers and short-bladed falcigers are described. The proximal shaft of each of these types of setae flares distally into a serrated collar and encloses the proximal end of a toothed blade. The collar projects on one side as a boss. The blade and the cortex of the shaft have longitudinal channels. A large excentric cavity in the shaft (the medullary channel) contains a loose meshwork of trabeculae. In the distal part of the shaft these trabeculae are aggregated into diaphragms. The seta is invested with an electron dense layer of enamel. Juvenile setae contain both chitin and protein. With respect to the long axis of the seta, the blade and the cortex of the shaft are positively birefringent and the medullary diaphragms are negatively birefringent. KOH extraction renders the setae negative to a test for protein and reverses the sign of birefringence of the cortical material of the shaft.

Notes: The marine priapulid Priapulus caudatus has a voluminous body cavity filled with a blood-like fluid containing erythrocytes and leucocytes (amoebocytes). The hematocrit of animals weighing 0.5-14 gm was 2-10%. The erythrocytes contain a hemerythrin blood pigment. The structure of the coelomocytes was studied by light and electron microscopy. The erythrocytes are nucleated and contain marginal bands, vacuoles and occasionally crystals. The cytoplasm has few organelles. The leucocytes are amoeboid motile cells, the cytoplasm of which contains numerous organelles. The most conspicuous of these are oval particles, probably representing developmental stages of lysosomes. Most of these organelles contain tubules stretching from one pole to another. In the hind part of the animal, certain tissues, primarily the posterior warts contain large numbers of coelomocytes. The histological picture is complicated, showing some resemblance to the lymphoepithelial tissues of vertebrates.

Notes: The dissected tooth bearing bones of 20 specimens of Amia calva (Pisces:Holostei) ranging from the third to tenth season have been examined radiographically and in alizarin red S stained and cleared specimens. Although forms of alternate (1:1) tooth series replacement (sensu Edmund, '60) were frequently observed, even in the youngest, immature specimens, many examples of irregular replacement were recorded. In several bones, the maxillae in particular, series with every third (2:1) or fourth (3:1) tooth replacing were seen and possible patterns of 2:2, were recorded. It is concluded that these data are not consistent with the Zahnreihen concept but support a morphogenic field concept of tooth development.

Notes: The first description of vertebral development in a plethodontid salamander is presented. Eurycea bislineata has larvae that hatch at a rather early stage of development. Somites and the notochord appear early. Somitic differentiation is slight, and no distinct sclerotome can be found. As a result, there is no clear primary segmentation of the skeletogenous tissue. No evidence of a sclerocoele can be found. The amount of sclerotomal cells surrounding the notochord is very low, relative to other tetrapods. Yet discrete perichordal rings of cells do form, in nearly midsegmental positions, and these give rise to the intervertebral cartilages. Osteogenesis of the centra is initiated prior to hatching and is coincidental with ossification of the neural arch. There is no sign of a neurocentral suture. The centrum forms as a thin shell of bone directly from sclerotomal cells. The notochord is a prominent feature of the vertebral column throughout life, retaining its integrity until late in life when some disintegration occurs locally. The notochord is filled with cartilage midvertebrally in late larval stages, and some additional cartilage forms later in life. The intervertebral cartilage enlarges greatly in late larval life. An opisthocoelous joint forms in this cartilage, apparently as a result of differential changes in the cells of the perichordal ring rather than by an invasion of cells from an external source. The intervertebral cartilage is a dominant structural and highly important functional feature of the adult vertebra. In metamorphosed individuals it may become extensively mineralized, and it consists of many different structural kinds of cartilage.The cranio-vertebral joint seems to form in a single segment, contrary to the condition reported by some early investigators. It is complex, and consists of articulations between the odontoid process of the atlas and the occipital arch, as well as between the occipital condyles and atlantal cotyles. The notochord plays a dominant role in the early development of the odontoid, but then changes radically and is absent in the adult process.The anterior trunk region seems to be much more conservative than posterior parts of the column. The patterns of nerve routes and nature of development of the ribs and rib bearers differs greatly from conditions elsewhere in the column. The rib patterns are similar to presumed ancestral conditions. Rib development on the sacral and caudosacral vertebrae is in some ways more similar to that of the anterior vertebrae than of the central trunk vertebrae.Quantitative aspects of variation in the vertebrae of adult salamanders are presented. There is more regional variation and less site variation than would be expected from literature reports.Evolutionary aspects of the origin of the cranio-vertebral joint, transverse process and ribs, patterns of segmentation, and centrum development are considered in the light of the new information on Eurycea. There is no evidence that more than one vertebra is involved developmentally or evolutionarily in the cranio-vertebral joint. The most generalized condition of rib bearers in living salamanders is one in which the dorsal and ventral bearers are in cartilaginous continuity during development. There are many variations on this theme in living species. It is inappropriate to speak of a resegmentation of the sclerotome in Eurycca, even though the adult vertebra is a transsegmental structure, because there is no primary segmentation of the scanty sclerotome. The important feature found in vertebral development in all tetrapods is the perichordal tube and its subsequent differentiation. Questinos concerning precise homologies of the salamander vertebral centrum with those of other vertebrates cannot be answered by data from development sequences with currently used criteria of homology. On the other hand, it appears that all centra, regardless of subdivision, are homologous in all tetrapods.

Notes: The Oberhautchen of scales from the dorsal, parietal, and ventral regions of Sceloporus occidentalis (Iguanidae), Gerrhonotus multicarinatus (Anguinidae), and Anniella pulchra (Anniellidae) were examined with a scanning electron microscope. At low magnification, all scales of S. occidentalis exhibit well-defined outlines of cells belonging to the Oberhautchen layer and the previously overlying clear layer. The dorsal and parietal cells of this species exhibit a minutely dentate Oberhautchen that forms tooth-like spinules 0.2 to 0.5 μ long and arranged in irregular rows. Minute pits 0.1 to 0.3 μ in diameter characterize the Oberhautchen of a ventral scale.Cell outlines are not evident on the scales of G. multicarinatus. The Oberhautchen of dorsal and parietal scales of this species is prominently laminated. Laminae are less prominent on scales of the lateral fold, and no intrinsic surface structure is evident on a ventral scale. In contrast, the fossorial anguinomorph Anniella pulchra exhibits Oberhautchen surfaces with practically no intrinsic microornamentation. However, what appear to be outlines of Oberhautchen cells are visible on the dorsal and ventral scales.These observations suggest that modifications of Oberhautchen microornamentation may have evolved to reduce friction with the substrate or other scales. The lack of pronounced microornamentation of the Oberhautchen on some body scales may indicate that a complex interdigitation between clear layer and Oberhautchen cells is not essential to the sloughing process.

Notes: Stolonic growth has been compared among several genera of calyptoblastic (Campanularia flexuosa, C. calceolifera, Gonothyraea and Sertularia) and gymnoblastic (Pennaria, Bougainvillia, Eudendrium and Cordylophora) hydroids with respect to such features as the (1) complexity and uniformity of the tip movements, (2) constancy of growth cycle duration, (3) variability in growth among cycles, (4) growth rate, and (5) variability of retractions among cycles.The “growth cycle,” previously described in C. flexuosa, is the basis for elongation in all species observed. Its pattern is indistinguishable between the Campanularia species; however, at the generic level the tip movements show peculiarities which delineate each genus from all others. In addition, the movements in all calyptoblasts are uniform from cycle to cycle and comparatively simple, whereas those of the gymnoblasts are complicated by the variable appearance of one or more secondary forward thrusts between crests.A dichotomy is seen between the calyptoblasts and most gymnoblasts in other respects as well. Cycle time is very predictable and cycle-to-cycle variability in growth is relatively narrow in all calyptoblasts. However, in most gymnoblasts both features are much more loosely regulated: only Pennaria shows some degree of control to its timing mechanism, and only in Bougainvillia and Eudendrium does the uniformity of growth per cycle reach the calyptoblast level.On the premise that calyptoblasts are evolutionarily the more advanced group, simplicity and regularity of growth movements are concluded to be the evolved, and complexity and variability the primitive, conditions. On this basis the evolutionary relations among the four gymnoblasts, as deduced from their stolonic growth behavior alone, are consistent in many but not all respects with those interpreted from morphological considerations.

Notes: In order to clarify the morphology of the circulatory system of amphioxus the blood vessels were investigated using modern techniques of light and electron microscopy.The pattern of circulation in amphioxus is forward ventrally and backwards dorsally. In addition, circulating corpuscles, usually associated with the blood of higher chordates, are absent.The circulatory system of amphioxus consists of well defined contractile vessels and vascular spaces or sinuses within a connective tissue matrix. The contractile vessels have a discontinuous endothelial lining resting on a basal lamina and are enclosed by a simple layer of contractile myoepithelial cells. Discontinuous endothelial linings occur throughout the vascular tree, including major and minor afferent and efferent vessels and blood sinuses. This is in contrast to higher animals where the endothelium forms a more or less continuous lining along the inner surface of the boundary layer.It is suggested that the endothelial cells of amphioxus, like the endothelial cells in capillaries of higher chordates, most likely play a role in the physiology of the circulatory system by removing residues of filtration from the basal lamina, thereby facilitating an exchange of materials to and from the surrounding tissues.

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

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

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

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

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

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

Notes: Blood follicles of the earthworm Amynthas are hemoglobin-containing, sac-like dilatations of blood vessels which connect to the general circulation. Grape-like clusters of follicles are found posterior to the pharynx, among tufts of micronephridia, and single follicles are located among cells of the pharyngeal gland. In Lumbricus, follicles take the form of simple swellings and irregular-shaped diverticula of nephridial capillaries.The fundamental structure of the wall of follicles and of vessels in both genera is the same and consists of two layers: an extracellular vascular lamina and an outer (coelomic) covering of smooth muscle-like myoperithelial cells. Hemocytes may be free and circulating or they may facultatively attach to the vascular lamina as littoral cells, constituting an incomplete endothelium-like surface. Hemocytes that appear to be in the process of attaching or detaching are rounded, while adherent cells are flattened and elongate. Free and littoral hemocytes actively endocytose packets of circulating extracellular hemoglobin.Hemocytes within follicles possess radiating cell processes which also endocytose hemoglobin. Although these cells were presumed to secrete hemoglobin, staining with 3,3′-diaminobenzidine confirms the presence of hemoglobin only within pinosomes and not within protein-synthesizing or packaging organelles. The presence of hemosiderin-like bodies suggests that follicular hemocytes catabolize hemoglobin.Blood follicles apparently provide a means of significantly increasing cell-surface area for hemoglobin processing, without substantially increasing the volume and pumping load of the circulatory system.

Notes: The nucleoli of rat liver cells duplicate in great detail the lifelong series of reorganizational changes encountered in kidney and intestinal epithelial cells. The ultrastructural components of the large, loosely organized polymorphous nucleoli, which are dominant in the rapidly multiplying stem cells of embryos, are readily accessible for chemical activities. Smaller, more compact amphinucleoli are dominant in more mature cells, which were characterized by Smetana ('70) as “idling” cells, showing slowly continuing ribosome formation and RNP synthesis. In older cells bipartite nucleoli become dominant and are reorganized in increasing numbers from the younger amphinucleoli. These, however, are not replaced in equal numbers from the shrinking pool of polymorphs of young cells which have greatly reduced mitotic potential. Paralleling the shifts in dominant nucleolar types, the high level of protein synthesis declines in older cells not only in the quantity of proteins synthesized but also in kinds of enzymes produced. These fail to meet the structural and functional requirements of aging cells leading ultimately to the onset of age-related degenerative changes. Again it is noted that separation of the karyosomal DNA from the plasmosomal RNA-protein complex of the nucleolus may lead to possible breakdown of the DNA-dependent RNA-protein transcription system ultimately bringing protein synthesis to a very low level in the senescent animal.

Notes: The heart of Crocodylus porosus is described, and deemed to be typical of living crocodilians after examination of the hearts of Alligator mississippiensis, Caiman crocodilus ssp., Crocodylus johnstoni and Crocodylus n. novaeguineae. Some inconsistencies between the anatomy and supposed patterns of blood flow are discussed. The crocodilian heart is compared with, and seen as an advancement of, the heart of non-crocodilian reptiles. The varanid ventricle is re-examined, as it appeared to contain many crocodilian features, along with the ophidian characteristics described previously. The broad similarities within the three groups are interpreted as adaptations towards a high pressure systemic circulation. Consequently varanids and snakes show the same left and right ventricles, as do crocodilians and birds. The evolution of the complete interventricular septum of crocodilians and birds appears to have involved three major trends: firstly, the development of a high pressure left ventricle and the fusion of most of the combined atrio-ventricular valve to the ostium of the right systemic artery; secondly, a line in which right to left shunting became gradually redundant and the vertical septum was completed to the aortico-pulmonary septum (giving rise to the avian ventricle); and thirdly, a line in which right to left shunting became increasingly important, and the vertical septum completed to the interaortic septum (giving rise to the crocodilian ventricle). Perhaps the crocodilian ancestry included a crocodile that was far more aquatic than any extant species.

Notes: In considering primate and hominoid phylogeny, the fundamental position assigned to opossums is explained partially by the characteristic morphology of their hands and feet. One of the main functional features of the human hand is the ability to make a stabilized arch of the finger. Because the extensor assembly plays a key role in establishing an arched finger, the extensor systems of the digits of both the hands and feet were studied in two species of opossum, Philander opossum and Didelphis marsupialis.In the foot, two extensor tendons join in each toe to form one tendinous plate, which inserts onto the base of the second phalanx. Lumbricals join this plate along the tibial side, and interosseus insertions are found, although a true interosseus wing is lacking. At the proximal interphalangeal level, a terminal tendon takes its origin from this tendinous plate. This terminal tendon is oval in cross-section and contains elastic structures. Oblique bands arise from this terminal tendon and run proximally along the proximal interphalangeal joint inserting onto the base of the first phalanx. There are elastic structures in the flexor tendon on the dorsal side near its site of insertion.In the hand, the main extensor tendons are arranged differently and the interossei contribute substantially to the extensor assembly. Otherwise, the extensor assembly of the hands and feet are quite similar. The function of the so-called paratendinous intravaginal flexors is discussed as are evolutionary aspects of the extensor assembly.

Notes: New schemata of the liver are presented to discuss the combination of the three kinds of liver lobules known until today in a chalk-talk-manner. Terminology is also discussed. Further investigations are needed involving the construction and the vascular pattern of compound lobules of the three individial lobules of the liver in different species.

Notes: The blood supply of muscle spindles was studied in serial cross sections in macaque, cat, rabbit, guinea pig, mouse and pigeon muscles which had been incubated in a medium containing 3,3′ diaminobenzidine. Lumina of blood vessels were recognized by the reaction product that was localized within erythrocytes. The outer capsule was well vascularized, but few or no capillaries were seen in the periaxial space. The inner spindle capsule, which closely invests the axial bundle, was rarely contacted by periaxial capillaries at the equator and juxtequator. Capillaries occurred more frequently adjacent to intrafusal fibers at the polar region and beyond the end of the outer capsule. Shorter diffusion distances and, usually, higher capillary densities were found at the polar region than at the spindle midsection. This suggests that transcapillary exchange at the polar segment is nearer to conditions prevalent in extrafusal muscle than elsewhere in the spindle, provided the inner and outer capsules are not less permeable at the poles than at the midsection. Differences in blood supply among mammalian species appear to be related to receptor size.

Notes: The role of dying cells in the optic stalk in relation to retinal fiber migration was investigated in the chick embryo. Cell death was analysed at various stages of development by counting pycnotic nuclei and also by the Gomori acid phosphatase reaction, while nerve fibers were visualised by the Bodian method. A wave of cell death, beginning in the neural retina at stage 18 and advancing with time through the stalk towards the diencephalon, occurred simultaneously or slightly prior to differentiation and migration of ganglion cell axons. Cell death stopped and gliogenesis occurred in the stalk after penetration by retinal fibers. Cell death occurred in the stalk even when fiber penetration was prevented by optic cup ablation. In this case, necrosis ensued until almost complete degeneration of the stalk, usually within three days after the operation, and gliogenesis did not occur. As the stalk degenerated, its cells became heavily pigmented. These observations suggest that the onset of cell death in the optic stalk is determined prior to and independently of retinal fiber penetration. On the other hand, cessation of cell death and subsequent gliogenesis occur only in the presence of ingrowing optic fibers.

Notes: Somatic portions of gonads in two phanerozonian sea-stars, Ctenodiscus crispatus and Hippasteria phrygiana, were similar in all aspects of gross structure and histology seen previously in both forcipulate and spinulosan asteroids. For the first time, detailed ultrastructural observations have been made of cells and tissues that reveal several features believed to be of universal occurrence in the gonads of asteroids. These include flagellated-collar cells in the visceral peritoneum and other coelomically derived epithelia, muscular-flagellated-collar cells in the visceral peritoneum and genital coelomic (perihaemal) sinus, the digestion of collagen fibers by cells in the connective tissue layer, and the intimate relationship of the genital haemal sinus and the entire germinal epithelium.Structural and functional compartmentalization are discussed in relation to major activities of the gonad throughout the annual reproductive cycle. The distinctive ultrastructure and current generation of flagellated-collar cells found in the visceral peritoneum are analyzed relative to their role in nutrient transport to gonadal tissues. The single flagellum of each flagellated-collar cell beats in coordination with those on neighboring cells to produce extremely rapid, oriented currents of coelomic fluid. The form of beating in an individual flagellum is planar, and the resulting synchronized activity of many adjacent flagella is non-metachronal; both of these characteristic aspects of current production have, thus far, been encountered together only in the Echinodermata. Flagellated-collar cells are efficient in generating currents which mix contents of the coelomic fluid, and they can presumably supply themselves with nutrients. It is concluded that nutrients so obtained are generally not passed through the wall of the gonad to the germinal epithelium and, as a result, have little to do with nutrition of somatic and germinal cells of the germinal epithelium. Alternatively, well-developed genital portions of the haemal system of the sea-star are advanced as the major channels supplying nutrients to germinal epithelia during gametogenesis.

Notes: The light and electron microscopic structure of the pineal complex of the domestic goose was studied. The complex is tubulofollicular but there is no direct connection between the constituent system of ducts and the third ventricle of the brain. Within the pineal, blood vessels accompanied by sympathetic nerve bundles are confined to the connective tissue. Other nerve fibers and occasional nerve cell bodies, however, do occur among the pineal cells.Three basic pineal cell types were distinguished: (1) elongate epithelial cells which are arranged around follicles and ducts and resemble degenerate photo-receptor cells; (2) intramural supportive cells which are interspersed with elongate epithelial and intramural supportive cells; and (3) small supportive cells which lie between the bases of the elongate epithelial and intramural supportive cells. The follicular structure, vascularization, presence of secretory granules, and the nature of the elongate epithelial cells indicate that the pineal complex is primarily endocrine though a possible photoreceptive function cannot be ignored. Vesicles, 100-300 and 40-100 nm wide, were found within nerves and intramural supportive cells. The larger vesicles, present in pineals collected in the night, probably contain peptidic hormones. The smaller vesicles present in both day and night samples probably contain aminergic hormones.

Notes: Cell surface coats are important in adhesion and other cellular activities. The lamprey egg possesses a surface coat that has been divided into two morphologically and functionally distinct regions. The amorphous apical tuft forms a cap over the animal pole, while the elaborately-textured adhesive coat covers the ventral two-thirds of the egg. This latter area is composed of saccules that form rosettes over the egg surface and is derived from the remains of specialized follicular cells which break down during ovulation. The adhesive qualities of these coats may be inhibited or abolished by various proteins and sulphydryl-blocking agents, thereby implicating, as a possible source of this adhesion, classes of acid and sulphated glycoproteins and glycosaminoglycans which occur on the egg surface.

Notes: Two-toed sloths have evolved a wrist complex that includes the following traits: (1) diminution and distal migration of the pisiform, with a loss of contact with the ulna; (2) reduction of the distal end of the ulna to a styloid process; and (3) extremely reduced contact between the ulna and triquetrum. These traits were proposed by Lewis ('65, '74) to be indicative of brachiating habits and to be a unique adaptation of the Hominoidea. Cartmill and Milton ('77) recently found a similar complex in the wrists of the lorisines. Very similar adaptations of the wrist among the Hominoidea, lorisines, and two-toed sloths clearly refute contentions of Lewis and strengthen the hypothesis of Cartmill and Milton that the traits common to those animals are due to similar slow, cautious, but acrobatic locomotion.

Notes: Although a number of recent studies describe the facilitation of limb regeneration by electrical and other forms of stimulation, little is known of innate regenerative capacity in the mammalian limb. The present report describes spontaneous regenerative responses following subtotal forelimb amputation in the young white rat. In one group of animals the forelimb was amputated through the lower humerus and the skin sutured closed. In a second group, adjacent muscle tissue still attached to bone at its origin(s) was interposed between the cut surface of the humerus and the skin. Among animals of the first group (skin closure only) bone growth and limb regenerative responses were generally not observed. Animals of the second group displayed significant elaborations of cartilage and bone at the limb terminus. The appearance and subsequent modification of these tissues suggest that some capacity for limb regeneration exists innately in the young rat and can be more readily evoked than has been recognized heretofore. It is concluded that extant and forthcoming reports of electrically stimulated skeletal tissue growth, repair and regeneration among eutherial mammals should be examined to determine whether reported responses to stimulation represent advances beyond what might be expected from innate replacement processes alone.

Notes: The minimum number of secretion products used by the spiders Araneus trifolium and Argiope trifasciata to construct their orb webs has been established by selective enzyme digestion and histochemical staining, as well as differential isotope localization in these webs. Three fiber types are present in the webs: (a) a major fiber found throughout the web, (b) a minor fiber found only in radial threads, and (c) the core fibers of the sticky spiral thread. Three nonfibrous secretions are found on these fibers. These include a water soluble viscid coating of the sticky spiral and two adhesives which fasten the threads of the web together; one found only at junctions of sticky spiral and radial threads and the other at all other thread connections. The possible glandular sources of these secretions are discussed.

Notes: The tesserate pattern of endoskeletal calcification has been investigated in jaws, gill arches, vertebral arches and fins of the sharks Carcharhinus menisorrah, Triaenodon obesus and Negaprion brevirostris by techniques of light and electron microscopy. Individual tesserae develop peripherally at the boundary between cartilage and perichondrium. An inner zone, the body, is composed of calcified cartilage containing viable chondrocytes separated by basophilic contour lines which have been called Liesegang waves or rings. The outer zone of tesserae, the cap, is composed of calcified tissue which appears to be produced by perichondrial fibroblasts more directly, i.e., without first differentiating as chondroblasts. Furthermore, the cap zone is penetrated by acidophilic Sharpey fibers of collagen. It is suggested that scleroblasts of the cap zone could be classified as osteoblasts. If so, the cap could be considered a thin veneer of bone atop the calcified cartilage of the body of a tessera. By scanning electron microscopy it was observed that outer and inner surfaces of tesserae differ in appearance. Calcospherites and hydroxyapatite crystals similar to those commonly seen on the surface of bone are present on the outer surface of the tessera adjacent to the perichondrium. On the inner surface adjoining hyaline cartilage, however, calcospherites of variable size are the predominant surface feature. Transmission electron microscopy shows calcification in close association with coarse collagen fibrils on the outer side of a tessera, but such fibrils are absent from the cartilaginous matrix along the under side of tesserae. Calcified cartilage as a tissue type in the endoskeleton of sharks is a primitive vertebrate characteristic. Calcification in the tesserate pattern occurring in modern Chondrichthyes may be derived from an ancestral pattern of a continuous bed of calcified cartilage underlying a layer of perichondral bone, as theorized by Ørvig (1951); or the tesserate pattern in these fish may itself be primitive.

Notes: A detailed account is given of the structure of the gills of Clarias batrachus, Heteropneustes (= Saccobranchus) fossilis, Channa punctata, Monopterus (= Amphipnous) cuchia and Boleophthalmus boddaerti, based upon light and electron microscopy. In all five species the basic organization into primary and secondary lamellae is apparent but the latter are very much more modified in Monopterus.Three main layers separate the water and blood on the surface of the secondary lamellae. The outer epithelium is usually two layered but may be multilayered close to the origin of the secondary lamellae from the gill filament. The basement membrane is relatively thin and a middle dense layer containing collagen fibrils separates two clear layers. The pillar cells, so characteristic of secondary lamellae, are present in all except Monopterus and flanges from these cells surround the blood channels with the exception of the marginal channels. The latter are lined by endothelial cells which line all the blood channels of Monopterus.The overall thickness of the three layers comprising the water/blood barrier ranges from 1.5 to 13 microns. A number of modifications to this basic organization can be related to the degree of dependence of the different species on air-breathing.Boleophthalmus is the only species commonly found in brackish water and its secondary lamellae have well developed lymphoid spaces between two layers of the epithelium. Special densely-stained regions of the pillar cell flanges were also present in this fish and may have a supporting function.

Notes: Serial coronal sections of the teeth and their surrounding tissues in the agamid lizard, Uromastix aegyptius, were examined with the light microscope in order to determine how these structures change as the teeth wear. Because new teeth are added only at the posterior end of the tooth row and older teeth are not replaced, the series of sections included the youngest as well as the oldest teeth. Two types of changes occur as the teeth become older: bone under the teeth changes from cancellous to compact, and the pulp chamber of the tooth is obliterated. Although the labial surface of the dentary lacks a periosteal covering and some of the bone lacks any covering at all, it remains functional throughout the life of the animal.

Notes: The nervous system of the planula larva of Anthopleura elegantissima consists of an apical organ, one type of endodermal receptor cell, two types of ectodermal receptor cells, central neurons and nerve plexus. Both interneural and neuromuscular synapses are found in the nerve plexus.The apical organ is a collection of about 100 long, columnar cells each bearing a long cilium and a collar of about 10 microvilli. The cilia of the apical organ are twisted together to form an apical tuft. The ciliary rootlets of the apical organ cells are extremely long, reaching to the basal processes of the cells adjacent to the mesoglea.All three types of sensory cells are tall and slender in profile and are identified by the presence of one or more of the following features: microtubules, small vesicles, membrane-bound granules and synapses. The interneurons are bipolar cells with somas restricted to the aboral end, adjacent to the apical organ. All synapses observed are polarized or asymmetrical.A diagram including all the elements of the nervous system is presented and the possible functions of the nervous system are discussed in relation to larval behavior.

Notes: Comparison of germ cells in male and female embryos of the arrhenotokous thrips, Haplothrips verbasci, yields the following observations: A mean of 11 cleavage energids enter the posterior pole plasm of the egg after the sixth cleavage division and apparently become pole cells when they take up polar granules in their cytoplasm. The cells proliferate asynchronously prior to and during anatrepsis to yield a mean of 36 germ cells in male embryos and 31 in females. Visible sexual differentiation of germ cells begins during germ band elongation and is completed shortly after the appearance of appendages. Female germ cells are larger than those of the males and may contain two nucleoli. The germ cells separate into two groups just before katatrepsis and mesodermal cells collect about these to form the primary epithelial sheaths of the gonads and the primordia of the gonoducts shortly after revolution is completed. Each gonad contains a mean of 13 germ cells in male embryos and 7 in females - a number that persists until mitosis resumes after hatching. During ketatrepsis, a mean of 11 germ cells in male embryos and 2.6 in females fail to be enclosed within the gonads, become dispersed in the yolk and perhaps transform into vitellophages.Germ cell development in H. verbasci embryos resembles similar events taking place in psocid embryos, providing additional evidence for a close phylogenetic relationship between Thysanoptera and Psocoptera.

Notes: A sensory papilla is described in the eyestalk of the crayfish Astacus leptodactylus during the last embryonic stages and during larval stages by light microscopy. This region was also investigated with the scanning electron microscopy, which showed sensory hairs in the postmolt adult; they disappear during intermolt and premolt. Simultaneous cyclic changes in hair papillae are observed in the hypodermis. The possibility of a chemoreceptive function is discussed.

Notes: Formation of nuclear envelopes during the last cleavage mitosis and the formation of the cell membranes during the cellularization of the blastoderm have been studied ultrastructurally in the blowfly egg. Dense bodies arising from yolk granules by budding could contain membrane material destined to be incorporated into the new membranes of the blastoderm. The presence of transitional structures indicates that these bodies can be converted into dark multivesicular bodies. Large amounts of endoplasmic reticulum are found around the mitotic nuclei. Clusters or branched chains of vesicles associated with this are interpreted as evidence for the formation of endoplasmic reticulum by the breakdown of dark multivesicular bodies. Nuclear envelopes of mitotic daughter nuclei probably originate from endoplasmic reticulum. The egg contains both intranuclear and extranuclear annulate lamellae.The main events of cytokinesis are furrow initiation and cell membrane growth during the slow first phase, but probably only cytokinetic movement during the rapid second phase. On the assumption that cell membrane growth occurs by incorporation of complete membrane pieces, the addition of coated vesicles and/or light multivesicular bodies is definitely most probable. Some intermediate profiles indicate that light and dark multivesicular bodies are related. The membrane needed for second phase cytokinesis could well be provided by the unfolding of surface microvilli and protuberances of the furrow canal.

Notes: The development of the polarity and bilateral asymmetry of the future adult zooid has been traced to their earliest morphological expression in the palleal bud of Botryllus. The account is based upon continued observation of living buds. The polarized antero-posterior and dorso-ventral axes are first expressed by the skewing of a symmetrical, hemispherical bud towards the anterior end of the parental bud. Identification of these axes is reinforced by the development of a loop-like blood circulation, the primary circulation, in the horizontal plane during the enlargement of the skewed hemisphere to form a stalked vesicle. Bilateral asymmetry is first expressed by the asymmetrical expansion of the vesicle stage. The right posterior corner of the vesicle expands further posteriorly and becomes more acute than the left posterior corner. This larger expansion persists throughout the development of the right atrial cavity, which finally expands across the mid-line to partially surround the gut. The bilateral asymmetry, expressed in the expanded vesicle, is reinforced by the development in sequence of a rounded gut rudiment and a pericardial rudiment in positions that would be expected from the asymmetry of the expanded vesicle. The first appearance of the gut rudiment occurs earlier than had been recognized previously. Conflicting accounts of the time and mode of formation of the pericardial rudiment have been clarified. The results of this study are discussed in the context of determination of bud territory, polarity and bilateral asymmetry.

Notes: Four glands of the house sparrow, chicken and turkey were examined histologically and for their content of amylase. These were the external and intermediate mandibular glands, the maxillary gland and glandula anguli oris of the sparrow and the anterior and posterior mandibular, maxillary and anguli oris glands of the chicken and turkey. Amylase was determined by a starch substrate slide method and by biochemical assay. General morphology and mucopolysaccharide staining are described.All four glands of the sparrow demonstrated significant amylolytic activity by the assay. In the external mandibular and anguli oris glands this activity could be traced to mucous and seromucous cells of origin by means of the starch substrate slide procedure. None of the glands of the chicken or turkey displayed significant amylolytic activity.

Notes: The distribution of monoamine (catecholamine and 5-hydroxytryptamine)-containing nerve cell bodies in the brain stem and hypothalmus of the frog (Rana temporaria) was investigated with the help of the histofluorescence technique of Falck and Hillarp ('62). At the level of the hypothalmus of this amphibian brain, catecholamine-containing nerve cell bodies are found mainly within three areas of the periventricular gray substance, namely the peroptic recess organ, the paraventricular organ and the lateral recess region. On the other hand, most of the 5-hydroxytryptamine (serotonin)-containing nerve cell bodies of the brain stem of Rana temporaria appear to be concentrated within the midbrain tegmentum. This huge mesencephalic nerve cell collection can be subdivided into medial and lateral groups. More caudally, at the level of the isthmic tegmentum, another group of 5-hydroxytryptamine-containing perikarya located close to the midline, within the so-called raphae region, is clearly outlined. The latter group of neurons extends caudally as far as the level of the medulla oblongata. In addition, a small group of catecholamine-containing nerve cell bodies is also found in the ventromedial portion of the rostral midbrain tegmentum, whereas a few other catecholamine type neurons are scattered throughout the lower brain stem of the frog and more especially near the ependymal wall of the fourth ventricle. As a whole, the 5-hydroxytryptamine-containing neuronal systems of the brain stem of Rana temporaria are much more elaborated than the catecholamine neuronal systems of the same structure.

Notes: The guinea pig soleus muscle is a convenient model for the study of slow-twitch intermediate (STI) fiber ultrastructure because it is composed entirely of fibers of this class. Such fibers were compared with fast-twitch red (FTR) and fast-twitch white (FTW) fibers from the vastus lateralis muscle.FTW fibers are characterized by small, sparse mitochondria, a narrow Z line and, an extensive sarcoplasmic reticulum arranged primarily in longitudinal profiles at the A band and with numerous expansions at the I band. Abundant mitochondria with a dense matrix and subsarcolemmal and perinuclear aggregations are typical of FTR fibers. These fibers contain a plexus of sarcoplasmic reticulum at the A band and a less extensive network at the I band. The Z lines are wider (890 ± 74 Å) than those of FTW fibers (582 ± 62 Å). STI intermediate fibers are distinguished from other types by wide Z lines (1205 ± 58 Å), a faint M band, and a less extensive sarcoplasmic reticulum. Compared to FTR fibers, STI fiber mitochondria are usually smaller with less notable subsarcolemmal accumulations.FTW fibers have a more limited capillary supply, rarely contain lipid inclusions, and thus may be restricted to phasic activity. Extensive capillarity, mitochondrial and lipid context, and fast contraction times indicate possible phasic and tonic roles for FTR fibers. STI fibers, characterized by numerous lipid inclusions, extensive capillarity, relatively numerous mitochondria, but slow contraction-relaxation cycles, are morphologically suited for tonic muscle activity.

Notes: The haemocytes of Calpodes ethlius are described with the light and electron microscopes. Five fine structurally distinct types are distinguishable. However only three of these, the granular haemocytes, sphaerule cells and oenocytoids can be positively identified using a series of histochemical stains on smears and on thick sections of araldite-embedded material. The classification is based entirely on the structural features even though several suggestions concerning their function can be made from their fine structure. Intermediates having features of more than one cell type suggest developmental relationships.

Notes: Four hemocyte types have been identified in the late last larval instar of Galleria mellonella. Plasmatocytoids are round to spindle shaped cells, 10-20 μ long and 5-10 μ wide. The cytoplasm contains no distinguishing inclusions. Golgi complexes, rough endoplasmic reticulum and free ribosomes are abundant. Granular hemocytes are oval shaped cells, 10-20 μ long and 5-10 μ wide. The granules, their most characteristic feature, have a diameter of 0.2 μ, a microtubular sub-structure, and are made up of acidic mucosubstances. Lipid droplets may be present in these cells at some stage of development. These cells appear to be phagocytic. Spherule cells are oval shaped, 15-20 μ long and 5-10 μ wide. The spherules, approximately 2 μ in diameter, have a highly ordered substructure and are made up of acidic mucosubstances. Oenocytoids are the largest cells, 20 by 40 μ. The cytoplasm contains mostly free ribosomes and microtubules.

Notes: The epineurium of the esophageal complex of the gastropod pulmonate Triodopsis divesta was examined by electron microscopy. The epineurium consists of two main regions: an inner dense fibrous region adjacent to the avascular neural tissue of the ganglion and an outer cellular region comprised of a variety of cell types embedded in a connective tissue matrix. The dense fibrous region contains smooth muscle cells and associated nerve processes and is invested on the neural side by thin processes of glial cells. The outer highly cellular region contains smooth muscle cells, nerve processes, wandering cells (amebocytes), globular cells, and myoepithelial cells comprising the walls of the vascular system. In addition, a cell type not previously identified in other gastropod epineuria is present. These cells resemble neurosecretory cells. The morphology and structural interrelationships of these various constituents are presented and the possible functions of individual cell types and the epineurium in general are discussed in relation to information available on other molluscs.

Notes: The muscles of the head, neck and thorax of the adult cabbage looper Trichoplusia ni are described for the first time. They are compared to those of Choristoneura fumiferana, Manduca sexta, Smerinthus geminatus, Antheraea polyphemus, Sphinx convolvuli, Crymodes devastator, and Danaus plexippus.

Notes: A precise sequence of four morphological stages of head regeneration in the planarian Dugesia tigrina has been determined by light and electron microscopy. Each stage is identified by a particular morphogenetic process: I, wound healing; II, blastema development; III, growth; IV, differentiation. A wound epidermis consisting of a thin, sheet-like layer of cells, rapidly forms from undamaged epidermal cells at the wound margin. The early blastema is comprised of neoblasts which mature into regeneration cells. The maturational changes include the appearance of a nucleolus, nuclear pores, and perinuclear dense aggregates of granulofibrillar material in these cells. These elements are not evident in the neoblasts of the younger blastema. No mitotic cells are encountered in the blastema or wound epidermis. Cytoplasmic expansion of the regeneration cells is correlated with the formation of numerous microtubules radiating from a juxtanuclear centrosphere. During differentiation of muscle cells, distended, granule-studded cisternae, having moderately fibrillar contents, are regularly disposed adjacent to small patches of myofilaments. Presumptive epidermal cells are recognized by prominent “islands” of finely fibrillar cytoplasm. These cytoplasmic zones persist for a time during definitive differentiation when Golgi bodies, vacuoles, mucous droplets, and rhabdites become evident. The newly formed epidermal cells become inserted among the cells of the wound epidermis. Thus, cells of both the blastema and of the wound epidermis contribute to the reconstituted epidermis.