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  • Springer  (43,712)
  • MDPI Publishing
  • 1980-1984  (43,712)
  • 1955-1959
  • 1981  (43,712)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Zoomorphology 97 (1981), S. 31-52 
    ISSN: 1432-234X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The coronar growth of a cidaroid and an aulodont echinoid are investigated by means of tetracycline labelling. The results are compared with earlier investigations on a stirodont and on a camarodont echinoid in order to evaluate the general features of coronar growth. In all echinoids new coronar plates are added at the apical end of the corona throughout the life cycle. The plates are shifted towards the peristome and they grow peripherically. In cidaroids ambulacral (A-) plates are detached from the firm corona. They are transformed into scales covering the peristomial field. The interambulacral (IA-) plates, however, are partially reabsorbed at the peristomial margin. In this manner the oldest solitary interambulacral plates are lost. The subsequent plates are arranged in pairs. The cidaroids thus show interradial growth even at their peristomial margin. This is unique to echinoids. In non-cidaroids there is a perignathic girdle made up of paired ambulacral auricles with interambulacral ridges in between. In some species the ridge is a solitary element. Therefore interradial growth cannot occur in the peristomial margin. In other species the ridge consists of several elements, but it also grows as a whole. Slight resorption of calcite occurs in places at the peristomial margin. In other places, however, calcite is added onto the peristomial edge. In non-cidaroids, therefore, the widening of the peristome is achieved solely by means of lateral growth in the plates bordering the peristome. The shift of the coronar plates from apicad to orad in noncidaroids is a relative shift only. In all echinoids the coronar plates are arranged in meridional columns. All plates grow up to the peristome. Their growth rates are relatively uniform towards the adambulacral sutures (which run between A- and IA-columns). Their growth rates towards the perradius and the interradius respectively are high in younger plates which are positioned above the ambitus, and decrease rapidly in plates located below the ambitus. Near the peristome the interradiad and perradiad growth rates are always considerably lower than adradiad growth rates. Perradial and interradial growth serve to adjust the plates in size and shape to their respective position in the corona.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Zoomorphology 97 (1981), S. 101-119 
    ISSN: 1432-234X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Description / Table of Contents: Zusammenfassung Die Ultrastruktur der Schalendrüsen von Microdalyellia fairchildi (Graff) wird dargestellt. Die Drüsen bestehen aus zwei Zelltypen, Drüsenzellen I und II genannt. Die erste Zellart bildet zwei Büschel langstieliger Zellen am proximalen Oovitellodukt. Auffällige Merkmale dieser Zellen sind: das umfangreich entwickelte rauhe E.R., das aus stark erweiterten Zisternen besteht und in zahlreiche blasen- oder sackartige Teilräume aufgegliedert ist, die granuläres Material enthalten; ferner der schlauchförmige Sekretionsfortsatz, der mit gedrängt liegenden Sekretionsvakuolen angefüllt ist und den Eindruck eines vielkammerigen Sekretspeichers macht, sowie Autolysosomen. Sekretsubstanz ist in den Vesikeln nicht dargestellt. Der kanalförmige Endteil des Fortsatzes besitzt peripher liegende Mikrotubuli und bildet im mündungsnahen Bereich eine septierte Kontaktzone mit den Epithelzellen des Oovitellodukts, in den er ventrolateral ausmündet. Die Drüsenzellen II liegen — ebenfalls in zwei Gruppen geordnet — weiter distal. Sie sind wesentlich kleiner, haben ein englumiges rauhes E.R. und membranumschlossene Sekretgrana mit dichtgranulärem Material. Vereinzelt wurden Autolysosomen beobachtet. Die Fortsätze der Zellen bilden einen rohrartigen Endabschnitt, der in der Feinstruktur dem der ersten Zellart entspricht. Sie münden ventrolateral in den Oovitellodukt. Die erste Drüsenzellart von Microdalyellia besitzt eine Reihe von Übereinstimmungen mit bestimmten Zellen der Mehlisschen Drüse parasitischer Plathelminthen, den sog. S2-Zellen der Trematoden. Diese Zelltypen sind wahrscheinlich homolog. Andererseits ergeben sich aus der Ultrastruktur der Drüsenzellen II und der einer weiteren Zellform der Mehlisschen Drüse, den S1-Zellen, keine sicheren Anzeichen für eine gemeinsame phylogenetische Herkunft.
    Notes: Summary The ultrastructure of the shell gland of Microdalyellia fairchildi (Graff) is described. The gland is composed of two types of secretion cells termed gland cell I and II. The first type consists of two bundles of large flasklike cells placed in opposite positions at the proximal ovovitelloduct. Distinguishing features of these cells are the amply developed rough E.R. with distended cisternae, forming several circular or elongate vesicles, which contain a granular substance, the long cell process with densely packed secretion vacuoles constituting a honeycomblike structure, and autolysosomes. No condensed material is seen in the vacuoles. The process terminates with a narrow channellike part lined by peripheral microtubules and forming septate desmosomal junctions with the epithelial cells of the ovovitelloduct, into which the cells open ventrolaterally. The second cell type is likewise arranged in two lateral clusters at a more distal part of the genital duct. The cells are essentially smaller and the rough E.R. has the usual appearance with flattened cisternae. The secretion bodies are surrounded by a membrane and contain a central core of dense granular material. Some autolysosomes are also present. The fine structure of the endpiece of the process passing through the ventrolateral epithelium of the ovovitelloduct is similar to that of the gland cell I. There are special similarities between the first cell type of Microdalyellia and certain Mehlis gland cells of parasitic flatworms termed S2 cells in Trematoda, indicating that these are homologous. On the other hand there are no such hints concerning the gland cell II and another cell type of the Mehlis gland called the S1 cell.
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  • 3
    Electronic Resource
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    Springer
    Zoomorphology 97 (1981), S. 225-245 
    ISSN: 1432-234X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The development of abdominal segments in Spirorbis moerchi (Polychaeta: Annelida) was studied by light and electron microscopy. Abdominal segments develop in strict succession from anterior to posterior. Segmentation is initiated in the mesoderm and is followed by segmentation of the ectoderm. The mesoderm of the abdominal segments arises entirely from pygidial residual mesoderm; inward migration of cells from the pygidial ectoderm to give rise to mesoderm does not occur. The primordial germ cells remain distinct from the residual mesoderm of the pygidial growth region. After several abdominal segments have developed, the primordial germ cells “migrate” posteriorly from the achaetous region, invade the abdominal segments, and give rise to the retroperitoneal gonads. Abdominal segment formation is discussed in terms of heteronomy, primordial germ cell origin, gonad formation, and development of the circulatory system.
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  • 4
    Electronic Resource
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    Springer
    Zoomorphology 98 (1981), S. 1-16 
    ISSN: 1432-234X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The cerebral and epidermal ocelli of the Müller's larva and the cerebral and tentacular eyes of the adult turbellarian Pseudoceros canadensis were studied by electron microscopy. The right cerebral ocellus of the larva consists of one cup-shaped pigmented cell and three sensory cells that bear microvilli. The left cerebral eye of the larva has the above named cells plus a sensory cell with many cilia. Evolutionary significance is attributed to the presence of both ciliary and microvillar photoreceptors in an eye of a flatworm. The one epidermal ocellus of the larva is composed of two cells: a cup-shaped pigmented one bearing flattened cilia, the presumed photoreceptors, and a cell above the cup that adds a few nonciliary lamellae to the stack of ciliary ones from the pigmented cell. The adult eyes contain only microvillar receptors; cilia were not observed.
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  • 5
    Electronic Resource
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    Springer
    Zoomorphology 98 (1981), S. 47-67 
    ISSN: 1432-234X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Description / Table of Contents: Zusammenfassung 1. Die Zellen des Ventralepithels bilden keine Mikrovilli, sondern ein schwammartiges Maschenwerk gefensterter Leisten und Falten, welches bei der Haftung des Tieres an der Unterlage und/oder bei der extrasomatischen Vorverdauung der Nahrung eine Rolle spielen dürfte. 2. Während der Zellteilungen treten typische Centriole an den Spindelpolen auf. 3. Die wachsenden Eizellen phagocytieren Fortsätze der Faserzellen, die als Trophocyten fungieren. 4. Unter den gleichen Bedingungen, die zur Eibildung führen, können sogen. S-Zellen auftreten. Einige ultrastrukturelle Befunde sprechen dafür, daß es sich um Spermien handelt.
    Notes: Summary 1. The cells of the ventral epithelium form no microvilli but a spongy meshwork of fenestrated ledges and folds which may play a rôle in the adhesion of the animal to the substratum and/or in the extrasomatic predigestion of the food. 2. During cell division typical centrioles occur at the spindle poles. 3. The growing egg cells phagocytize projections of the fiber cells which function as trophocytes. 4. Under the same conditions leading to egg formation so-called S-cells may occur. Some ultrastructural data suggest that they are sperm cells.
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  • 6
    ISSN: 1432-234X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The mesogastropod Pyrazus ebeninus, produces true spermatozoa (here termed euspermatozoa) and multi-flagellate, mobile cells (here termed paraspermatozoa). The mature paraspermatozoon consists of an elongateconical ‘head’ (6.5–8.5 μm in length), constructed of an electron-dense mosaic sheath surrounding a similarly dense, rod-shaped nuclear core (which runs almost the full length of the head). An acrosome-like structure forms the apex of the head. Five to eight axonemes are fixed to the posterior extremity of the nuclear core, each by means of an attachment complex (dense attachment rod, centriolar cap and centriole). A short (3–4 μm) ‘midpiece’ zone follows the head and consists of the multiple axonemes interspersed with very elongate mitochondria. A tuft of short (20 μm) tails (termed minor tails) emerges from the midpiece in addition to one very long tail (termed the major tail) ensheathed in dense granules which resemble glycogen granules. A single membrane surrounds head, midpiece and tails whilst the nuclear core retains the original double nuclear membrane. Developmentally, the multiple axonemes arise from one of a pair of wheel-shaped arrangements of centrioles and attach to posterior indentations in the nucleus prior to its transformation into the nuclear core. Dense vesicles, derived apparently from the endoplasmic reticulum, accumulate along and around the developing nuclear core and (in the presence of microtubules) condense into the mosaic head sheath. Cytoplasmic mitochondria elongate and collect at the posterior axis of the cell, where, together with the axonemes, they form the midpiece. Features not previously reported in other ultrastructural studies of paraspermatozoa include the acrosome-like structure of the head, the structure of the midpiece zone, the glycogen sheath of the major tail, the dense annular structure at the junction of the midpiece and major tail and the presence of microtubules in the final phase of head and midpiece maturation. Some features of the euspermatozoon are also described and the comparative ultrastructure of mature and developing paraspermatozoa and their possible functions in the Gastropoda, are reviewed.
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  • 7
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    Springer
    Zoomorphology 98 (1981), S. 227-231 
    ISSN: 1432-234X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary A previously undescribed receptor in the coxo-trochantinal region of the metathoracic leg of the cockroach Periplaneta americana was found to have central cell bodies. This cockroach stretch receptor is the second sensory receptor in insects reported to possess somata in the CNS and its remarkable similarity to a locust proprioceptor suggests it to be homologous.
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  • 8
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    Springer
    Zoomorphology 98 (1981), S. 241-260 
    ISSN: 1432-234X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The structural organization of the ocelli of several diplopod species has been studied by means of electron microscopy. The results provide evidence that diplopodan ocelli are derived from typical mandibulate ommatidia, which consequently had been present in diplopod ancestors. The recent representatives of the two sister groups, Pselaphognatha and Chilognatha are characterized by two essentially different types of eye morphology: The eyes of the Pselaphognatha comprise a bilayered rhabdom (built up by 3+4 retinular cells), a few corneagenous cells, a corneal lens, and two vitreous bodies. The latter probably represent relics of a former crystalline cone. On the contrary, the ocelli of the Chilognatha consist of a multilayered rhabdom (built up by a large number of retinular cells), numerous corneagenous cells, and a corneal lens. The dioptric apparatus lacks a crystalline cone. Further structural elements, the distribution of which varies, are the covering cells and processes of hypodermal cells which contain screening pigments. Whereas the eye of the Pselaphognatha can be traced back to a single ommatidium, the ocellus of the Chilognatha can only be interpreted as a merging product of several associated ommatidia or as the result of multiplication and rearrangement of former ommatidial elements. This concept is substantiated by analogous phenomena which occur within other arthropod groups and thus serve as models for the phylogeny of the diplopodan eyes. The comparison of the morphology and the ecology of palaeozoic and recent diplopods demonstrates that the disintegration of former facetted eyes and the modification of ommatidia were induced by the adaptation to cryptic modes of life.
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  • 9
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    Springer
    Wood science and technology 15 (1981), S. 1-29 
    ISSN: 1432-5225
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Summary That the behavior of wood in service results from its “structure” is generally accepted by wood scientists. No doubt this acceptance is due to the broad interpretation of such a term. Structure can refer to the organization of elements on a macro scale, such as in a laminated beam, as well as to the arrangement of cellulose molecules in the crystalline region of an elementary fibril. This presentation focuses on a structural domain that appears increasingly to be a critical one in wood behavior-ultrastructure. The spectrum of terminology that has been used in profusion during the “electron microscopic era” must first be defined so that confusion is minimized. Then a historical evolution of the field of wood ultrastructure can be presented to provide perspective. Structures that have been shown to affect or indeed to control certain processes can be identified. The role of a “non-structure”, the elusive transient capillary, can be illustrated. Microfibrillar organization and cell wall archictecture fall into the realm of ultrastructure as well. The past decade of research in wood science has been productive to a significant extent because of scanning electron microscopy and its accessory tools and techniques. The exploration of wood penetration by wood preservatives, pulping liquors and coatings using this approach has yielded much new evidence. One can speculate about the anticipated contributions of computer-driven SEM, stereology, STEM, and even higher resolution microscopy in the near future.
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  • 10
    Electronic Resource
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    Springer
    Wood science and technology 15 (1981), S. 171-177 
    ISSN: 1432-5225
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Summary Problems associated with handling non-steady liquid flow data are discussed. It is shown that the Darcian flow model is fundamentally imprecise when applied to non-steady state flow in wood due to: 1) the observed decrease in permeability with increased specimen length 2) the wide range of diameters encountered in wood pores. Because of this wide range of pore sizes, liquid penetrates some flow paths more rapidly than others. This may give rise to the occurrence of surface forces resisting penetration, with both “wetting” and “non-wetting” liquids. It seems unlikely that these various factors can be accurately quantified. Hence the precise prediction of liquid penetration rate from steady state permeability data may be illusory.
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