Epidermal Sensory Organs of Moles, Shrew Moles, and Desmans: A Study of the Family Talpidae with Comments on the Function and Evolution of Eimer’s Organ

2000 ◽  
Vol 56 (3) ◽  
pp. 146-174 ◽  
Author(s):  
Kenneth C. Catania
Keyword(s):  
Sensory Organs ◽  
The Family ◽  
Eimer's Organ

scholarly journals A New and Primitive Retrobursal Planarian from Australian Fresh Waters (Platyhelminthes, Turbellaria, Tricladida)

1977 ◽  
Vol 47 (2) ◽  
pp. 149-155 ◽  
Author(s):  
Ian R. Ball
Keyword(s):  
Southern Hemisphere ◽  
Present Species ◽  
Sensory Organs ◽  
Freshwater Planarian ◽  
Fresh Waters ◽  
Evolutionary Line ◽  
The Family ◽  
Female Genital

A primitive freshwater planarian, Eviella hynesae gen. et sp. nov. is described from Australia. It is characterized by its lack of eyes and pigment, possession of caudally branched oviducts, and fully fused testes. Although a primary bursa is absent, its function being taken over by the modified female genital canal, the female copulatory system is posterior to the male system. Despite this maricolan feature, and other similarities with primitive southern hemisphere freshwater planarians that have been classified in the Maricola, the present species is placed in the family Dugesiidae of the Paludicola. Evidence from its sensory organs suggests that it belongs on the main evolutionary line from which the majority of Australasian freshwater planarians have been derived.

Scale Microstructures of Pygopodid Lizards (Gekkota: Pygopodidae): Phylogenetic Stability and Ecological Plasticity

2021 ◽  
Vol 28 (5) ◽  
pp. 291-308
Author(s):  
Tatjana Nikolayevna Dujsebayeva ◽  
Natalia Ananjeva ◽  
Aaron M. Bauer
Keyword(s):  
Cell Surface ◽  
Time Scale ◽  
Morphological Structure ◽  
Cellular Level ◽  
The Body ◽  
Sensory Organs ◽  
Ecological Plasticity ◽  
The Family ◽  
Stable Characteristic ◽  
Derivatives Of

The skin, as the interface of the body with the outside world, is directly exposed to the impacts of the environment. We have examined the microstructure of scale surfaces and the numerical distribution and morphology of skin sensory organs (SSO) in Australian limbless lizards of the family Pygopodidae. We have shown that the hairy sensory organs, as complex morphological structures, are a stable characteristic of the scale integument of pygopodids. This feature reflects their relationship to geckos and is shared homoplastically with some iguanian families (Dactyloidae, Leiosauridae, Opluridae, Chamaeleonidae). At the same time, scale micro-ornamentation as an elementary morphological structure is more plastic and, although the basic spinulate pattern is dominant, other variants occur on the scales of the serpentine body of pygopodids. We accept the spinules of MiO and the hairs of SSO as homologous structures at the cellular level since they are both derivatives of the Oberhäutchen cell surface. We propose to characterize the hair-bearing SSO of gekkotan and iguanian lizards as Oberhäutchen hairy sensory organs (ObHSO). Domination of SP MiO and presence of ObHSO in the integument of Gekkota and several families of Iguania, and sporadic occurrence of SP MiO in autarchoglossan taxa provide justification for regarding these characters as plesiomorphic. We characterize the high abundance (iterative state) of SSO in the scales of the head of pygopodids as representing the phenomenon of «overiteration», in which the phylogenetically established condition is enhanced by functional demands on the organism.

Ecomorphological trends in the Artedidraconidae (Pisces: Perciformes: Notothenioidei) of the Weddell Sea

2003 ◽  
Vol 15 (2) ◽  
pp. 211-218 ◽  
Author(s):  
ANTONI LOMBARTE ◽  
IGNACIO OLASO ◽  
ANNA BOZZANO
Keyword(s):  
Adaptive Radiation ◽  
Weddell Sea ◽  
Close Connection ◽  
Ecological Data ◽  
Sensory Organs ◽  
Ecological Divergence ◽  
Bathymetric Distribution ◽  
Morphometric Features ◽  
The Family

An ecomorphological study was performed on ten species of the family Artedidraconidae, the most benthic of the suborder Notothenioidei. These species are sympatric on the shelf of the Weddell Sea. The results show that the four genera comprising the family (Artedidraco, Dolloidraco, Histiodraco and Pogonophryne) can be differentiated by just a few morphometric features of their sensory organs and mouth. The genera were also clearly defined by the composition of their diet (benthic and epibenthic), the size of their prey, and their bathymetric distribution. Comparison of the morphological and ecological data shows a very close connection between sensory organs development, the mouth and bathymetric distribution. The morphological and ecological divergence observed can be explained as the result of the rapid adaptive radiation of the artedidraconids. The results confirm that characteristics of the sensory organs and alimentary structures are very suitable for the ecomorphological study of fishes.

Triassic sponges (Sphinctozoa) from Hells Canyon, Oregon

1988 ◽  
Vol 62 (03) ◽  
pp. 419-423 ◽  
Author(s):  
Baba Senowbari-Daryan ◽  
George D. Stanley
Keyword(s):  
Endemic Species ◽  
Upper Triassic ◽  
Island Arc ◽  
Tropical Island ◽  
The Family ◽  
Wallowa Terrane ◽  
Unique Condition ◽  
Hells Canyon

Two Upper Triassic sphinctozoan sponges of the family Sebargasiidae were recovered from silicified residues collected in Hells Canyon, Oregon. These sponges areAmblysiphonellacf.A. steinmanni(Haas), known from the Tethys region, andColospongia whalenin. sp., an endemic species. The latter sponge was placed in the superfamily Porata by Seilacher (1962). The presence of well-preserved cribrate plates in this sponge, in addition to pores of the chamber walls, is a unique condition never before reported in any porate sphinctozoans. Aporate counterparts known primarily from the Triassic Alps have similar cribrate plates but lack the pores in the chamber walls. The sponges from Hells Canyon are associated with abundant bivalves and corals of marked Tethyan affinities and come from a displaced terrane known as the Wallowa Terrane. It was a tropical island arc, suspected to have paleogeographic relationships with Wrangellia; however, these sponges have not yet been found in any other Cordilleran terrane.

Electron Microscopy of Mycoplasma Pneumoniae

1971 ◽  
Vol 29 ◽  
pp. 258-259 ◽  
Author(s):  
E. S. Boatman ◽  
G. E. Kenny
Keyword(s):  
Electron Microscopy ◽  
Light Microscopy ◽  
Growth Phase ◽  
Hela Cells ◽  
Sulfonic Acid ◽  
Gamma Globulin ◽  
Horse Serum ◽  
Morphological Aspects ◽  
The Family

Information concerning the morphology and replication of organism of the family Mycoplasmataceae remains, despite over 70 years of study, highly controversial. Due to their small size observations by light microscopy have not been rewarding. Furthermore, not only are these organisms extremely pleomorphic but their morphology also changes according to growth phase. This study deals with the morphological aspects of M. pneumoniae strain 3546 in relation to growth, interaction with HeLa cells and possible mechanisms of replication.The organisms were grown aerobically at 37°C in a soy peptone yeast dialysate medium supplemented with 12% gamma-globulin free horse serum. The medium was buffered at pH 7.3 with TES [N-tris (hyroxymethyl) methyl-2-aminoethane sulfonic acid] at 10mM concentration. The inoculum, an actively growing culture, was filtered through a 0.5 μm polycarbonate “nuclepore” filter to prevent transfer of all but the smallest aggregates. Growth was assessed at specific periods by colony counts and 800 ml samples of organisms were fixed in situ with 2.5% glutaraldehyde for 3 hrs. at 4°C. Washed cells for sectioning were post-fixed in 0.8% OSO4 in veronal-acetate buffer pH 6.1 for 1 hr. at 21°C. HeLa cells were infected with a filtered inoculum of M. pneumoniae and incubated for 9 days in Leighton tubes with coverslips. The cells were then removed and processed for electron microscopy.

Exposure of protein VP7 on the surface of bluetongue virus

1990 ◽  
Vol 48 (3) ◽  
pp. 600-601
Author(s):  
A.D. Hyatt
Keyword(s):  
Bluetongue Virus ◽  
Structural Proteins ◽  
Major Constituent ◽  
Outer Coat ◽  
Virus Particles ◽  
Antibody Recognition ◽  
The Core ◽  
The Family ◽  
Electron Microscopical ◽  
Physical Accessibility

Bluetongue virus (BTV) is the type species os the genus orbivirus in the family Reoviridae. The virus has a fibrillar outer coat containing two major structural proteins VP2 and VP5 which surround an icosahedral core. The core contains two major proteins VP3 and VP7 and three minor proteins VP1, VP4 and VP6. Recent evidence has indicated that the core comprises a neucleoprotein center which is surrounded by two protein layers; VP7, a major constituent of capsomeres comprises the outer and VP3 the inner layer of the core . Antibodies to VP7 are currently used in enzyme-linked immunosorbant assays and immuno-electron microscopical (JEM) tests for the detection of BTV. The tests involve the antibody recognition of VP7 on virus particles. In an attempt to understand how complete viruses can interact with antibodies to VP7 various antibody types and methodologies were utilized to determine the physical accessibility of the core to the external environment.

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