Subcellular distribution of neurophysin in rats subjected to haemorrhage,salt-loading and lactation and in rats with hereditary diabetes insipidus (brattleboro strain)

Summary The subcellular distribution of radioactive neurophysin and the release of neurophysin from isolated neurosecretory granules (NSG) from the posterior pituitary gland were studied at various time intervals after injection of (³⁵S) cysteine into the supraoptic nucleus under various functional conditions. In consistency with previous findings (Norström, 1972), increased amounts of radioactive neurophysin were recovered extra-granularly at longer time intervals after isotope injection. Increased quantities of free labelled neurophysin were found in lactating rats and homozygous diabetes insipidus (DI) rats 7 and 1 day after injection, respectively. Salt-loading for 4 days did not affect the subcellular distribution of radioactive neurophysin 1 day after injection of (³⁵S) cysteine. 8.5 days after isotope injection acute haemorrhage was followed by augmented amounts of radioactive neurophysin among the soluble proteins, but at 1 day no difference was observed between bled animals and controls. The spontaneous release of neurophysin form NSG was higher in stimulated animals and increased with time after isotope injection in controls as well as in experimental animals. The absolute increase in release of neurophysin in response to ATP was higher in stimulated rats whereas NSG from DI rats did respond poorly to ATP.The present work was supported by grants from Svenska Livförsäkringsbolags nämnd för medicinsk forskning, Wilhelm och Martina Lundgrens fond, Albert Wallins fond and the University of Göteborg. I am indebted to Miss Gull Grönstedt for careful secretarial work.     

Isolation and characterization of neurosecretory granules of the rat posterior pituitary gland

Summary Neurosecretory granules (NSG) of rat posterior pituitary glands were prepared by differential centrifugation techniques mainly according to the procedure as described by Barer, Heller and Lederis (1963). As revealed by electron microscopy, the recovery of neurophysin and the contents of enzymes, purified NSG were obtained in a pellet at 30 000 g/60 min (0.44 M sucrose). Eighteen h after injection of (³⁵S) cysteine into the supraoptic nucleus 60% of the recovered radioactivity in the neural lobe was found in the NSG, whereas 20% was found in the final supernatant (100 000 g/120 min). Sixteen days after injection the NSG and the final supernatant fraction contained fairly equal amount of (³⁵S) cysteine (approximately 40%). It is suggested that after a period of intragranular maturation neurophysin is extruded into an extragranular pool of neurosecretory material.With the use of conventional polyacrylamide-gel electrophoresis it was shown that the predominating proportion of radioactivity in the NSG after a hypothalamic injection of (³⁵S) cysteine was located within the neurophysin fraction A and in fraction B. Fraction B is suggested to be partly bound to the NSG membranes. When the NSG soluble and NSG insoluble proteins, obtained after lysis of NSG, were separated on polyacrylamide gels in the presence of sodium dodecylsulphate, the highly radioactive soluble protein was shown to consist of two components with average molecular weights of 12 300 and 14 600. Most of the proteins in the lysate were found in the NSG membranes, though less radioactive. A component with a mol.wt. of 37 000 was enriched in the membrane fraction. At longer times after isotope injection the high mol.wt. proteins, particularly those of the NSG membranes, contained increased amounts of radioactivity.Abbreviations NSG neurosecretory granule - NSM neurosecretory material - SON supraoptic nucleus The present investigation was supported by grants from Svenska Livförsäkringsbolags nämnd för medicinsk forskning from Svenska Sällskapet för Medicinsk forskning, from the Medical Faculty, University of Göteborg, and from the Swedish Medical Research Council (B 72-12X-2543-04A).We are indebted to Mrs. Marie-Louise Eskilsson, Mrs. Wally Holmberg and Mrs. Ulla Svedin for technical assistance, and to Miss Gull Grönstedt for careful secreterial work.     

Release in vitro of neurohypophysial proteins from neural lobe tissue slices and from isolated neurosecretory granules of the rat

Summary The release of neurophysin from neural lobe tissue slices and isolated neurosecretory granules of the rat was studied at various time intervals after injection of (³⁵S) cysteine into the supraoptic nucleus. For hours after isotope injection the release of radioactive neurophysin from neural lobe tissue was increased by depolarizing concentration of potassium in the presence of calcium ions. Fourteen and 30 days after isotope injection the release of radioactive neurophysin was relatively decreased in a medium of high potassium concentration which might be explained by the heterogeneity of the pool of neurophysin within the neural lobe. Four h after isotope injection the spontaneous release of neurophysin from neural lobe tissue was higher in dehydrated rats than in controls, and the neural lobes of these animals did not respond with an increased release of radioactive neurophysin when exposed to high potassium concentration.Eighteen h after isotope injection the predominating proportion of neurophysin-bound radioactivity was found in the neurosecretory granule fraction, whereas 14 days after injection a fairly equal amount of radioactivity was found in this fraction and in the soluble protein fraction. This indicates that with time an increasing amount of radioactive neurophysin passes from an intragranular to an extragranular pool.The spontaneous release of radioactive neurophysin from isolated neurosecretory granules was higher, and the increase of release upon exposure to an ATP-regenerating system was higher 14 days after isotope injection than 18 h after injection. This may imply that the neurosecretory material undergoes an intragranular maturation process to become more easily releasable. The release of radioactive neurophysin was inhibited in the presence of AMP and EDTA, which demonstrates the dependence of the release process of an ATPase and, probably, of calcium ions.Neurosecretory granules from dehydrated rats possessed a higher spontaneous release than those of control rats 18 h after injection, which may indicate an enhanced intragranular maturation process of the neurosecretory material due to osmotic stimulation.Abbreviations NSG neurosecretory granule - NSM neurosecretory material The present work was supported by grants from Carl-Bertel Nathhorsts vetenskapliga stiftelse, from Svenska Livförsäkrings bolags nämnd för medicinsk forskning, from Överläkare Albert Wallins fond and from the Medical Faculty of the University of Göteborg. I am most indebted to Miss Gull Grönstedt for careful secreterial work.     

Immunocytochemistry and ultrastructure of the neuropil located ventral to the rat supraoptic nucleus

Summary The neuropil located ventral to the SON was investigated by the use of immunoperoxidase staining for neurophysins, oxytocin and vasopressin, and electron miroscopy. The study was performed in six groups of rats: 1) control; 2) infusion of isotonic saline into the CSF; 3) infusion of hypertonic saline into the CSF; 4) drinking hypertonic saline for 4 days; 5) same as group 4 but injection of colchicine into the CSF on second day of dehydration; 6) salt loading for 3 months. In the control rats the ventral neuropil contained a few immunoreactive processes, the general morphology of which was completely different from that of the neurosecretory axons emerging from the SON at its dorsal aspect. In rats of groups 3 to 6 the ventral processes (VP) became loaded with neurosecretory granules, whereas the perikarya and axons were depleted. Based on their general morphology and reactivity pattern it is suggested that the VP are dendrites. Most of these dendrites were embedded in a glial cushion formed by the processes of a particular type of marginal glia. Some of these dendrites enveloped an arteriole penetrating the optic tract. All VP were rich in synaptic contacts. The possibility that the VP of neurosecretory cells may be functionally related to the subarachnoid CSF and the arteriolar blood flow is discussed.Supported by Grant RS-82-18 from Direccíon de Investigaciones, Universidad Austral de Chile     

The effect of chlorpromazine and tetracaine on the rapid axonal transport of neurosecretory material in the hypothalamo-neurohypophysial system of the rat

Summary The effects of chlorpromazine (cpz) and tetracaine (tc) on the rapid axonal transport of neurosecretory material (NSM) in the hypothalamo-neurohypophysial system was investigated. Following subarachnoidal injection of these drugs, the incorporation of (³⁵S) cysteine into proteins of the supraoptic nucleus was slightly depressed. The protein-bound radioactivity in the posterior pituitary was markedly lowered in experimental rats which indicates a partial blockage of the rapid axonal transport of NSM along the hypothalamoneurohypophysial tract. Both cpz and tc induced an increase in the number of mitochondria and profiles of granular endoplasmic reticulum. The axons in the infundibulum and neurohypophysis were enlarged by dammed organelles, indicating a blockage of axonal transport. There was an increased number of microvesicles, often arranged in a crystalloid pattern, in the terminals. The number and distribution of neurotubuli and neurofilaments were not changed. A possible stimulatory effect of cpz on the release of NSM from the neural lobe is assumed Possible mechanisms for the action of mitotic inhibitors, transquilizers and local anesthetics are discussed.The present work was supported by grants from Svenska Livforsäkringsbolags Fond, H. Hiertas stiftelse, Magnus Bergwalls stiftelse, The Swedish Medical Research Council No. B73-12X-2543-05B, Statens naturvetenskapliga forskningsråd No. 2535-8 and from the Medical Faculty, University of Göteborg. We are indebted to Mrs. Margareta Andersson, Mrs. Wally Holmberg, Mrs. Elisabeth Norström and Mrs. Ulla Svedin for excellent technical assistance, and to Miss Gull Grönstedt for careful secretarial work.     

Intra- and extraganglionic nerve endings formed by neurosecretory cells of the cerebral ganglion of the earthworm (Lumbricus terrestris L.)

Summary In the cerebral (= supraesophageal, suprapharyngeal) ganglion of the earthworm, a number of neurosecretory Gomori-positive perikarya are bipolar; others are unipolar, or multipolar. Some of the neurosecretory cell processes project centrally into a fibrous zone; peripheral processes enter small nerves which leave the dorsocaudal aspect of the ganglion.In the central fibrous zone, the neurosecretory fibers form varicose Gomoripositive terminals. Here, also zinc-iodine-osmium (ZIO)-positive fibers and monoamine fluorescent fibers are found. With the electron microscope, nerve terminals containing synaptic vesicles and either large neurosecretory peptidergic granular vesicles (diameter more than 1500 Å), or smaller granular vesicles (diameter about 1300 Å, or 900 Å) are observed. These axon endings mainly form axo-dendritic synapses. Peptidergic profiles are both pre- and postsynaptic. Some of the extraganglionic peptidergic fibers appear to terminate around vessels, but most of them form terminals on the visceral muscle cells which surround the ganglion.We think that the central neurosecretory processes communicate with the fibers of the synaptic zone of the ganglion. The peripheral neurosecretory peptidergic fibers are supposed to form a primitive neurohemal area and/or to function as vasomotor nerves. The fibers innervating the visceral muscle cells may represent vegetative nerves.     

Vasopressin-immunoreactive cells in the dorsomedial hypothalamic region,medial amygdaloid nucleus and locus coeruleus of the rat

Summary Recently, the existence of a vasopressin-immunoreactive cell group was described in the bed nucleus of the stria terminalis (van Leeuwen and Caffé 1983). In the present investigation additional nuclei containing vasopressin-immunoreactive cells were found, after colchicine pretreatment, in the dorsomedial hypothalamus, medial amygdaloid nucleus and the locus coeruleus.Vasopressin-immunoreactive cells in the dorsomedial hypothalamus and medial amygdaloid nucleus are small (8–14 m and 10–14 m, respectively), while those in the locus coeruleus are medium-sized (20–25 m). Incubation with anti-bovine neurophysin II and anti-rat neurophysin revealed staining of the same cell group in the above-mentioned areas. None of these cell groups show stained cells after incubation with anti-oxytocin and anti-bovine neurophysin I. When sections of the homozygous Brattleboro rat, which shows a deficiency in vasopressin synthesis, are incubated with anti-vasopressin, anti-bovine neurophysin II, or anti-rat neurophysin, no immunoreactivity can be observed in these brain regions.The above-mentioned cell groups may contribute to the vasopressinergic innervation of brain sites that have been reported to persist after lesioning of the suprachiasmatic, paraventricular and bed nuclei of the stria terminalis.     

Detection and partial characterization of two antigenically distinct β-amylases in developing kernels of wheat

A -amylase (EC 3.2.1.2) was identified in the outer pericarp (P) of developing seeds of wheat (Triticum aestivum L.) and compared with the well known -amylase which is synthesized during seed development in the starchy endosperm (E). The enzyme P already exists in the tissues before anthesis and vanishes at the time when E starts to accumulate. The isoelectric-focusing patterns of P and E are very similar. The relative molecular weight (M_r) of P is slightly higher than that of E (66 and 64.5 kDa, respectively). Both P and E exhibit common epitopes in addition to epitopes specific for each of them. The two enzymes were identified in small amounts in the green tissues of the developing seeds (inner pericarp and testa). No antigenic difference was detected between P and the -amylases of roots and leaves.Abbreviations P pericarp -amylase - E endosperm -amylase - IS1 anti--amylase immune serum - IS2 anti- and anti- amylase immune serum - IS3 anti- amylase immune serum - IEF isoelectric focusing - IgG immunoglobulin G The authors thank Dr. P. Ziegler (Universität Bayreuth, FRG) for stimulating discussion and for useful suggestions during the writing of the text. The authors thank Miss C. Mayer for her skillful technical assistance.     

Studies on the neurosecretory system of Iphita limbata Stal.

Summary The present paper gives an account of some experiments upon the insect Iphita limbata Stal. (Hemiptera: Pyrrhocoridae). The experiments were carried out in order to find out whether in the adult animal there is a relationship between the activity of the neurosecretory cells and the water balance. Under varying conditions one group of the neurosecretory cells of the pars intercerebralis of the brain, the so called A-cells, show histological differences. It has been seen that under conditions stimulating hydration there is a marked retention of the stainable colloids in the cytoplasm of A cells. This retention probably indicates a relationship between the secretions of A cells and the water balance of the insect.The author is indebted to Mr. N. R. Prabhoo and Miss Maya Menon of this Department for a critical discussion of the paper.     

Inhibition of axonal transport in vitro in frog sciatic nerves by chlorpromazine and lidocaine

Summary The effects of chlorpromazine hydrochloride (CPZ HCl) and prochlorperazin-metansulfonate (PCPZ) on the fast axonal transport of labelled proteins were examined in vitro in a peripheral frog nerve.A 0.1 mM concentration of CPZ HCl and PCPZ reduced the amount of transported proteins by more than 50 per cent. An almost complete block was obtained with a 0.5 mM concentration of these two drugs. The lower concentration hardly affected the protein synthesis. The transport inhibiting effect of 0.1 mM of the drugs was reversible but not that of the higher concentration.The number of microtubuli was strongly decreased and the number of filaments increased at the transport inhibiting concentrations. The ultrastructural changes induced by 0.1 mM of the phenothiazine tranquilizer were largely reversible. The local anesthetics lidocaine (18.3 mM) and tetracaine (3.3 mM) both caused similar changes, i.e. a reduction in the number of microtubuli. No ultrastructural effects were observed after treatment with 1 mM ouabain. These three drugs are known to block the axonal flow in the present system at the above mentioned concentrations.The biochemical and ultrastructural results are discussed in relation to those induced by other drugs affecting axonal transport.The present work was supported by grants from Statens Naturvetenskapliga Forskningsråd (No. 2535-8), C.-B. Nathorsts Vetenskapliga och Allmännyttiga Stiftelser, the Swedish Medical Research Council (B73-12X-2543-05B), H. Hierta's Stiftelse and W. och M. Lundgrens Stiftelse. Thanks are due to Mrs B. Egnér, Mrs E. Fjällstedt, Mrs. E. Norström and Mrs U. Svedin for expert technical assistance.     

Genetics of Ia-like alloantigens in chickens and linkage withB major histocompatibility complex

Two sets of backcross matings were performed to test for linkage between genes coding for the Ia-like antigens (Ia) and the B erythrocyte antigens (Ea-B) of the chicken. Evidence is presented which indicates that the la antigens are determined by a single codominant locus and that theEa-B and Ia loci are on the same chromosome. Failure to detect a single recombinant between theEa-B and Ia loci out of 208 progeny suggests close linkage of the two genes with a map distance of up to about 2 centimorgans. The Ia genes are thus included in theB major histocompatibility complex of the chicken.     

Regional specialization of the sperm membrane in the tick Amblyomma hebraeum koch (Acari: Ixodidae)

Summary The spermatozoon of Amblyomma hebraeum is about 200 m long and comprises: (1) a thick, club-shaped anterior part, about 20 m long bearing at its apex a tactile hemisphere, and (2) an elongated tail-like part, about 180 m long. The surface of the tactile hemisphere is covered by numerous bulbous expansions, attached to it by short stalks. The base of the hemisphere is surrounded by a fringe of thin motile processes; the remaining surface of the spermatozoon is covered with long cellular processes which run more or less parallel to one another.The membrane-associated particles found on the membrane beneath the cellular processes are regularly arranged as groups of parallel strands. The external surface of the so-called peripheral granules, as revealed by freeze-etching, is smooth with a very small number of particles. Internally the particles exhibit a regular hexagonal pattern which has not been observed, so far, on any other membrane of these sperm cells.The regional specialization of the spermatozoon surface membrane in relation to sperm motility is discussed. The results obtained indicate that processes of three types: (1) bulbous expansions, (2) motile processes, and (3) cellular processes are regional specializations, all engaged in aspects of sperm motility.The technical assistance of Mr. R. Haemmerle of Balzers Research Laboratories, Mrs. F. Seif and Miss C. Pugin, is gratefully acknowledged     

Die Eisosphäriten (Basalkalotten) der Schwanen-Eischale

Zusammenfassung Einleitend werden die Gründe dafür dargelegt, die altgewohnte Schichteneinteilung der Kalkschale des Vogeleies in Mammillen- und Schwammlage aufzugeben. Unter Beachtung der Strukturverhältnisse und der Bildung der Schale — durch Zusammenwachsen zunächst völlig getrennter Calcitsphärokristalle — läßt sich an jedem dieser Bausteine unterscheiden: der in die Membran einwachsende Eisosphärit und der nach außen sich entwickelnde Exosphärit, und weiter am letzten basal der Kegel und distal die Säule. Demgemäß ist von Kegel- und Säulenlage zu sprechen. Die Bezeichnung Mammillen sollte nur bei der Innenansicht der ihrer Membran beraubten Kalkschale benutzt werden.Die Struktur der Eisosphäriten (= Kalotten) wird beim Schwan (Cygnus olor) des Näheren untersucht, sowohl aufgrund des Totalpräparates an der freigelegten Innenseite der Kalkschale, als an Querschliffen. Von den letzten wurden einzelne durch Auskochen in Glycerinkalilauge der die Kalotten durchziehenden Schalenhautfasern beraubt. Während an gewöhnlichen Schliffen in der Kalotte nur luftumhüllte Schalenhautfasern hervortreten, lassen sich an luft- und an faserfreien Kalotten die Fasern bzw. ihr Ort an der Änderung der Polarisationsfarbe des Calcits verfolgen.Nicht selten wurden Kalotten beobachtet, deren Bildungszentrum nicht, wie gewöhnlich, unmittelbar auf der Schalenmembran, sondern in einigem Abstand darüber liegt; alsdann entwickelt die sphäritische Anlage auch gegen die Membran hin zunächst die gleiche Struktur wie im Exosphäriten; erst mit dem Einwachsen in die Schalenmembran nimmt der Kalk eisosphäritischen Charakter an.Die Mammillen beim Schwan sind vielfach polysphäritisch; d.h. eine Mammille umfaßt mehrere Calcosphäriten. Dieses, auch bei manchen anderen Vögeln zu beobachtende Verhalten läßt es zweckmäßig erscheinen, anstatt der Zahl der Mammillen auf der Flächeneinheit der Schaleninnenfläche die der Kegel auf dem Flachschliff zu bestimmen, d.h. die Anzahl der sphäritischen Schalenbausteine.An Flachschliffen, bei denen der äußere Teil der Schale abgetragen ist, läßt sich der Eisosphärit durch den Rest des Exosphäriten hindurch beobachten. In dessen Zentrum zeigt sich der (auch an Querschliffen nachweisbare) Primärsphärit: er ist kugelig (Durchmesser 10–15 ) und von seiner Umgebung scharf abgesetzt; die radialen Calcitkeile des Kegels lassen sich zugeschärft bis an sein Zentrum verfolgen, das ein Körnchen oder mehrere beherbergt.

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Summary To begin with, the reasons are given for abandoning the traditional habit of dividing the stratification of the avian egg shell into mamillary and spongy layer. Taking into consideration structure and development of the shell (coalescence of calcitespherocrystals, originally completely separated) the following parts can be distinguished in each spheritic element: the l"eisospherite, growing from the formation centre into the membrane, and the exospherite, growing outwards. The exospherite consists of a basal cone and a distal column. Hence the term layer of cones and layer of columns ought to be used. The term mamilla should be reserved only for the inner aspect of the shell, depleted of its membrane.The structure of the eisopherites (basal caps) is studied in the egg shell of the swan (Cygnus olor) in total preparations of the inner shell surface after removing the membrane and in transverse or tangential ground sections. Some of the transverse ground sections by boiling them in glycerol-potassium hydroxide have been depleted of the membrane fibres permeating the basal caps. In ordinary ground sections only membrane fibres surrounded by air are prominent in the cap, whereas in caps devoid of air or of fibres the sites of fibres can be traced through the variation of the polarization colour of the calcite.Not infrequently caps are observed whose centre is situated at greater distance as normally above the shell membrane. In this cases the primary spherite first of all until the membrane forms exospheritic structure. Only with the growing into the shell membrane will the calcite acquire eisospheritic character.In swans the mamillae are mostly polyspheritic; i.e. each mamilla comprises several calcospherites. This phenomenon is also observed in many other avian species. It seems therefore expedient to determine not the number of mamillae per surface unit of the shell inside, but the number of cones in a tangential ground section i.e. the number of spheritic structure units per shell unit.In tangential ground sections, which are devoid of the columnar layer, the eisospherite can be observed through the rest of the exospherite. In its centre appears the primary spherite (which is also visible in transverse ground sections). It is spherical (its diameter being 10–15 m) and clearly demarcated from its surroundings. The radial calcite wedges of the cone can be followed up to the centre of the primary spherite, which contains one or more granules.

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Herrn Dr. Henri Dumur in Wetzlar zum 80. Geburtstage.     

Vergleichende fluoreszenzmikroskopische und elektronenmikroskopische Untersuchungen am zentralen Nervensystem von Planorbarius corneus L. (Basommatophora)

Zusammenfassung Durch Vergleich fluoreszenz- und elektronenmikroskopischer Untersuchungen am zentralen Nervensystem von Planorbarius corneus L. wird nachgewiesen, daß in den Schlundringganglien Neurosekretzellen vorkommen (Nachweis mit Pseudoisocyaninchlorid), die mit Nervenzellen nicht identisch sind, die durch ihren hohen Gehalt an biogenen Aminen auffallen (Nachweis durch die Methode von Falck und Owman, 1965). Es können daher im Schlundring von Planorbarius corneus peptiderge und aminerge Neurosekretzellen unterschieden werden. Die PSC-positiven Neurosekretzellen enthalten elektronendichte Elementargrana und die aminergen Neurone dense-core Vesikel. Der Nachweis biogener Amine in einigen Nervenzellen von Planorbarius corneus spicht für deren chemische Identität mit Transmittersubstanzen, ihre hohe Konzentration aber für eine Abgabe in die Körperflüssigkeit.

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Comparative fluorescence- and electron microscopic studies of the central nervous system of Planorbarius corneus L. (Basommatophora)

Summary The neurosecretory system of the snail Planorbarius corneus has been investigated by fluorescence and electron microscopy. With the fluorochrome Pseudoisocyanin the established neurosecretory system in the cerebral ganglia and single neurosecretory cells in the other ganglia show an intensive yellow fluorescence. Electron micrographs reveal the presence of electron dense granules (elementary granules) in the pericarya and the axons of neurones which have the same localisation in the ganglia as the pseudoisocyanin-positive cells. The fluorescence technique for biogenic amines produces yellow and green fluorescence within neurons and in the neuropil and nerves. The fluorescence obtained in determinable areas and neurones correlates well with the electron microscopic location of dense-core vesicles within the pericarya and axons of cells in even the same areas. It is discussed, that in this animal both types of cells are so-called neurosecretory cells, because the high content of elementary granules in the peptidergic neurosecretory cells and of dense-core vesicles in the aminergic neurosecretory cells is an indication for secretion of these products in neurohaemal areas (circulatory channels).

     

Localization of neurophysin in the neurosecretory elements of the hypothalamus and neurohypophysis of the normal and osmotically stimulated guinea-pig as demonstrated by immunofluorescence histochemical techniques

Summary Antisera to porcine neurophysin-II and ovine neurophysin-III were used to localize neurophysin-like material in the hypothalamus and neurohypophysis of guinea-pigs with an immunofluorescence technique. Although the guinea-pig appears to have only one major neurophysin it was found to be localized in both of the bilateral magnocellular nuclei. Neurophysin-like material was also present in extreme rostral portions of the hypothalamus, in cells lying between the third ventricle and the supraoptic nucleus and in a cluster of cells dorsomedial to the fornix. Immunofluorescence was observed in neurosecretory fibres that followed pathways previously characterized with classical histological stains for neurosecretory material.The immunofluorescence in the hypothalamic elements of a normal guinea-pig was not greatly different from that in fluorescent structures present in an animal that had been severely dehydrated. In contrast, there was a marked depletion of neurophysin from the posterior pituitary gland of the dehydrated guinea-pig. The lack of graded fluorescence in the hypothalamus of the dehydrated animal is discussed.This work was financed by a grant from the New Zealand Medical Research Council and the Auckland Medical Research Foundation.     

The ultrastructure of the herring bodies in rats subjected to different experimental conditions

Summary A study of the morphology of Herring bodies of the posterior pituitary lobe of rats treated with colchicine and/or exposed to low temperatures has been performed. After treatment with colchicine (20 g in distilled water injected intracisternally) a predominance of Herring bodies with a large number of small synaptic-like vesicles surrounded by neurosecretory granules is found. Exposures to low temperature (4–6° C) result in an increase in the neurosecretory material and the Herring bodies show many neurosecretory granules of different densities. After treatment with colchicine and subsequent exposure to low temperatures, the Herring bodies are characterized by having a great number of autophagic bodies which become more numerous as the length of the exposure is increased; later autophagic vacuoles and lamellar bodies become evident.     

The nervous system of Microstomum lineare (Turbellaria,Macrostomida)

Summary The ultrastructure of release sites of neurochemical messenger substances in the microturbellarian Microstomum lineare was examined. Aminergic neurites form conventional synapses and synapse-like structures (SLS). Variants of true synapses include: single synapses with symmetric pre- and postsynaptic densities, shared synapses, i.e., contacts between 1 pre- and 2 postsynaptic fibres, en passant synapses between parallel axonal membranes, and synapses without thickenings having only clustered vesicles in the presynaptic terminal. SLS on a nerve cell soma or facing an intercellular stromal channel near muscles are described. Peptidergic neurites containing large granular vesicles (LGV) form synaptoids and signs of putative neurosecretory release. Synaptoids between neurites and between neurite and muscle have lucent vacuoles (about 100nm) and dense material at the contact site. In en passage synaptoids dense-core vesicles are embedded in electron-dense material at the contact site. Putative signs of release of neurosecretory material other than typical exocytosis have been observed.     

Die Büschelsphäriten (Corymben) auf der Eischale von Lappentauchern

Zusammenfassung Die Prismen der Äußeren Säulenlage der Eischale von Podiceps cristatus neigen — ähnlich wie bei den Pinguinen — an ihrem Oberrand zu sphäritischer Differenzierung, zur Ausbildung von Conuli, (Schmidt, 1968). Diese verlängern sich aber in die organische Deckschicht hinein als zarte, dicht stehende Büschel, die bis an die freie Oberfläche der Schale reichen können, meist aber kürzer bleiben. Diese Corymben sind von zahlreichen, oft ansehnlichen Globularinklusionen durchsetzt und spalten sich nach außen hin radiär auf. Sie liefern sowohl am Quer- wie am Flachschliff zwischen gekreuzten Polars negative Sphäritenkreuze. Daneben finden sich, in weiterem Abstand voneinander, größere scheibenartige Sphäriten mit ausgezacktem Rand und mucronaten, d.h. gestreckten, radial orientierten, nach außen hin zugeschärften Globularinklusionen. — Podiceps minor besitzt ebenfalls Corymben, jedoch sind sie bescheidener entwickelt.

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Tufted spherites (Corymbi) on the egg-shell of podicipediformes

Summary The prisms of the Outer columnar layer in egg-shells of Podiceps cristatus tend to show, as in penguins, spheritical differentiation at the surface, namely, the formation of conuli (Schmidt, 1968). But, in Podiceps cristatus the conuli grow out into the organic tegmentum of the shell, thus producing corymbi, that is, lightly packed, delicate tufts some of which reach the outermost surface of the shell. These corymbi which contain larger globular inclusions split radially into fine branches. Radial and tangential thin sections, produced by grinding, show, between crossed nicols, a negative cross in each corymbus. Larger negative spherites, disclike and with indented margins, contain mucronate inclusions sharpened distally and orientated radially. Podiceps minor also shows corymbi, but these are less well developed.

     

Entwicklungsgeschichtliche Untersuchungen an zentrischen Diatomeen IV

Zusammenfassung 1. Die Entwicklung vonStephanopyxis turris sowie die zu ihrer Untersuchung geeigneten Methoden werden beschrieben und diskutiert.2. Der vollständige Lebenszyklus einer zentrischen Diatomee nach Beobachtungen im Leben und mit den Grundzügen der zugehörigen Karyologie in Mitose, Meiosis, Befruchtung und Auxosporenbildung sowie Entstehung und Keimung der Dauersporen wird erstmalig dargestellt (Abb. 18).3. Neuartige Beobachtungen betreffen Kollaps, Blitztod und Lichtresistenz, die Dritte Linie, die Darstellung von Kern und Spindel in Mitose und Meiosis sowie die mit Kernkonkurrenz abschließenden acytokinetischen Karyokinesen in Oogon und Auxospore im Leben, die Keimung der Dauersporen, den lichtmikroskopischen Nachweis der Kieselschuppen in der Auxosporenmembran.4. Die Entwicklungsvorgänge werden vergleichend diskutiert und dabei die Termini depauperierende Teilung und heterovalvate Zytokinese in Vorschlag gebracht.5. Weitere Überlegungen gelten dem cyclischen Turgeszenzwechsel der Diatomeenzelle.6. Die Methode der Vegetativen Zellvergrößerung erlaubt es,Stephanopyxis-Klone beliebiger Breite aber unveränderten Genotypus für das Experiment bereitzustellen.

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Ontogenetic investigations on centric diatoms IVThe planktonic diatomStephanopyxis turris — its treatment and life history

This paper presents a detailed account of the life cycle, development and cellular mechanics of the centric diatomS. turris. Special attention is paid to culture methods, nutritional requirements and the mechanism of vegetative cell enlargement. Instructions are outlined for experimental manipulations of developmental features. Various aspects of development are treated in details, e. g. cellular structures, cell division and morphogenesis, development and germination of resting spores, differentiation of gametangia (spermatogonangia, spermatogonia and oogonia), meiosis in the gametocytes, fertilization and auxospore differentiation (including the formation of the rejuvenated first cell and the accompanying metagamic mitoses).S. turris has one-egged oogonia. Its spermatogonangia develop their spermatogonia according to theBiddulphia granulata-type and their spermiums according to theMelosira-type (Fig. 18). Two new termini, i. e. heterovalvate cytokinesis and depauperizing mitosis are introduced (p. 232, p. 238). Among the more important results are observations on karyokinesis in vivo, meiosis and karyogamy, and on the peculiar process of destruction of supernumerary nuclei following each karyokinesis in the oocyte, and later in the young auxospore. Relations between osmotic cell rhythms, karyokinetic cycle and morphogenesis are discussed at the end of the paper.

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Herrn Professor Dr.Adolf Bückmann zum 65. Geburtstag in Verehrung gewidmet.

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Diese Studie enthält Teile der Dissertation vonG. Drebes.     

Electron microscopic study on the larval and adult corpus allatum of Oncopeltus fasciatus dallas (insecta,heteroptera)

Summary 1. The ultrastructure of the corpora allata of last larval instars and adults of Oncopeltus was studied. The unpaired gland undergoes submicroscopic alterations and shows signs of degradation in old animals. The organ is partly covered and penetrated by corpus cardiacum tissue. Axons with different types of neurosecretory granules form synaptoid contacts with the corpus allatum cells.2. Dark and light gland cells can be differentiated on account of the degree of electron density. The former predominate during the last larval stage and in the young imago, the latter in mature males and females. It is highly probable that the light cells are the active (i.e. hormone producing) ones and the dark cells the inactive ones.3. The active cells are characterized by rough endoplasmatic reticulum (often in whorls), small amounts of smooth endoplasmatic reticulum and many multivesicular bodies. Abundant free ribosomes, a not particularly well developed Golgi apparatus, dense bodies, and cytolysomes are present in active and inactive cells.4. The nuclei contain one to four prominent and variously shaped nucleoli, which show differences between adult males and females with respect to their location in the nucleus.5. The corpus allatum cells of Oncopeltus are obviously engaged in extensive protein synthesis. Tangible structural indications for the manufacture of juvenile hormone were not observed. Possible sites of hormone release are discussed.This study was made possible by a fellowship and grants from the Deutsche Forschungsgemeinschaft and was supported by research grants, administered by Prof. Scharrer, from the U.S.P.H. Service (NB-05219; NB-00840 and NS-07512). Present address of author: Institut für Allgemeine Zoologie der Johannes Gutenberg-Universität, D-6500 Mainz, Saarstraße 21, Bundesrepublik Deutschland.I am indebted to Prof. Scharrer for guidance and criticism. I also wish to express my appreciation to Mrs. S. Wurzelmann and Mr. S. Brown for their excellent technical assistance.