Organization of ampullary electric receptors in Gymnotidae (Pisces)

1968 ◽  
Vol 169 (1017) ◽  
pp. 345-378 ◽  
Keyword(s):  
Fine Structure ◽  
Evolutionary Relationships ◽  
Type I ◽  
Type Ii ◽  
Sense Organs ◽  
Large Numbers ◽  
Mode Of Operation ◽  
Points Of View ◽  
Eigenmannia Virescens ◽  
Electron Microscopes

Investigation of 14 species of gymnotid has established that large numbers of ampullary lateralis sense organs are present in each case. These organs have been examined with the light and electron microscopes. Two distinct types occur, and these are referred to as type I and type II; the latter is more common. The fine structure of the receptors in one species ( Eigenmannia virescens ) is described in detail, and is discussed from two points of view: (i) the function and mode of operation of the organs, and (ii) the evolutionary relationships to different receptors of the vertebrate acoustic-lateralis system.

Temporal Bone Studies of the Human Peripheral Vestibular System

2000 ◽  
Vol 109 (5_suppl) ◽  
pp. 3-13 ◽  
Author(s):  
Saumil N. Merchant ◽  
Kojiro Tsuji ◽  
Conrad Wall ◽  
Luis Velázquez-Villaseñor ◽  
Robert J. Glynn ◽  
...  
Keyword(s):  
Hair Cell ◽  
Hair Cells ◽  
Type I ◽  
Type Ii ◽  
Sense Organs ◽  
Age Related ◽  
The Mean ◽  
Cell Densities ◽  
Temporal Bones ◽  
Total Type

Quantitative studies of the vestibular system with serially sectioned human temporal bones have been limited because of difficulty in distinguishing hair cells from supporting cells and type I from type II hair cells. In addition, there is only a limited amount of normative data available regarding vestibular hair cell counts in humans. In this study, archival temporal bone sections were examined by Nomarski (differential interference contrast) microscopy, which permitted visualization of the cuticular plate and stereociliary bundle so as to allow unambiguous identification of hair cells. The density of type I, type II, and total numbers of vestibular hair cells in each of the 5 sense organs was determined in a set of 67 normal temporal bones that ranged from birth through 100 years of age. The mean total densities at birth were 76 to 79 cells per 0.01 mm2 in the cristae, 68 cells per 0.01 mm2 in the utricle, and 61 cells per 0.01 mm2 in the saccule. The ratio of type I to type II hair cells at birth was 2.4:1 in the cristae and 1.3:1 in the maculae. There was a highly significant age-related decline in all sense organs for total, type I, and type II hair cell densities that was best fit by a linear regression model. The cristae lost type I cells with advancing age at a significantly greater rate than the maculae, whereas age-related losses for type II cells occurred at the same rate for all 5 sense organs. Hair cell densities in the cristae were significantly higher at the periphery than at the center. There were no significant sex or interaural differences for any of the counts. Mathematical models were developed to calculate the mean and 95% prediction intervals for the total, type I, and type II hair cell densities in each sense organ on the basis of age. There was overall good agreement between the hair cell densities determined in this study and those reported by others using surface preparation techniques. Our data and related models will serve as a normative database that will be useful for comparison to counts made from subjects with known vestibular disorders.

The fine structure of the developing macrogamete of Eimeria maxima

Parasitology ◽  
1979 ◽  
Vol 79 (2) ◽  
pp. 259-265 ◽  
Author(s):  
R. M. Pittilo ◽  
S. J. Ball
Keyword(s):  
Endoplasmic Reticulum ◽  
Fine Structure ◽  
Parasitophorous Vacuole ◽  
The Other ◽  
Granular Endoplasmic Reticulum ◽  
Type I ◽  
Type Ii ◽  
Eimeria Maxima ◽  
Lipid Inclusions

SUMMARYThe fine structure of the developing macrogamete of Eimeria maxima was studied from chicks killed at intervals from 138 to 147 h after inoculation. The macrogamete developed within a parasitophorous vacuole. Lying within this vacuole and extending for some distance around the periphery of the macrogamete were intravacuolar tubules, grouped in certain areas, and in some cases they were seen to make direct connexions with the cytoplasm of the parasite. During development, electron-pale vesicles were pinched off externally from the surface of the macrogamete. There appeared to be 2 forms of wall-forming bodies of the Type I during development, one form being less osmiophilic than the other. Other organelles present, such as wall-forming bodies of Type II, granular endoplasmic reticulum, mitochondria, canaliculi, lipid inclusions and intravacuolar folds, were similar in structure to those of other Eimeria species.

The Fine Structure of Cockroach Campaniform Sensilla

1969 ◽  
Vol 27 ◽  
pp. 250-251
Author(s):  
D. T. Moran ◽  
K. M. Chapman ◽  
R. A. Ellis
Keyword(s):  
Fine Structure ◽  
Nerve Impulse ◽  
Mechanical Stimulus ◽  
Campaniform Sensilla ◽  
Sense Organs ◽  
Electron Microscopes

Insects are equipped with mechanoreceptors, sense organs that transduce a mechanical stimulus into a nerve impulse. Among the mechanoreceptors associated with the cuticle of the cockroach are the proprioceptive campaniform sensilla. To provide correlation of structure with the function of these mechanoreceptors, the proprioceptive campaniform sensilla on the tibia of the cockroach, Blaberus cranifer, have been investigated with the light and electron microscopes.

scholarly journals Controlling the type I and type II errors in mapping quantitative trait loci.

Genetics ◽  
1994 ◽  
Vol 138 (3) ◽  
pp. 871-881 ◽  
Author(s):  
R C Jansen
Keyword(s):  
Quantitative Trait Loci ◽  
Quantitative Trait ◽  
Type I Error ◽  
Interval Mapping ◽  
Mapping Method ◽  
Type I ◽  
Type Ii ◽  
Large Numbers ◽  
Trait Loci ◽  
Type Ii Errors

Abstract Although the interval mapping method is widely used for mapping quantitative trait loci (QTLs), it is not very well suited for mapping multiple QTLs. Here, we present the results of a computer simulation to study the application of exact and approximate models for multiple QTLs. In particular, we focus on an automatic two-stage procedure in which in the first stage "important" markers are selected in multiple regression on markers. In the second stage a QTL is moved along the chromosomes by using the preselected markers as cofactors, except for the markers flanking the interval under study. A refined procedure for cases with large numbers of marker cofactors is described. Our approach will be called MQM mapping, where MQM is an acronym for "multiple-QTL models" as well as for "marker-QTL-marker." Our simulation work demonstrates the great advantage of MQM mapping compared to interval mapping in reducing the chance of a type I error (i.e., a QTL is indicated at a location where actually no QTL is present) and in reducing the chance of a type II error (i.e., a QTL is not detected).

scholarly journals Type-I and Type-II Confinement in Quantum Dots: Excitonic Fine Structure

2016 ◽  
Vol 129 (1a) ◽  
pp. A-66-A-69 ◽  
Author(s):  
V. Křápek ◽  
P. Klenovský ◽  
T. Šikola
Keyword(s):  
Quantum Dots ◽  
Fine Structure ◽  
Type I ◽  
Type Ii

An Orange-Reddish Pigmentation in Roquefort Cheese

1986 ◽  
Vol 49 (6) ◽  
pp. 412-416 ◽  
Author(s):  
GRACIELA FONT de VALDEZ ◽  
GRACIELA SAVOY de GIORI ◽  
AIDA PESCE de RUIZ HOLGADO ◽  
GUILLERMO OLIVER
Keyword(s):  
Sodium Chloride ◽  
No Production ◽  
Type I ◽  
Type Ii ◽  
Color Intensity ◽  
Orange Pigment ◽  
Ripening Process ◽  
Brevibacterium Linens ◽  
Ripening Period ◽  
Large Numbers

The presence of an anomalous orange-reddish coloration in Roquefort cheese during its ripening period was studied. No pigmented colonies were isolated from milk, curd, or cheeses after pressing, but their presence in relatively large numbers was observed after salting (7 d) up to the end of the ripening process (90 d). About 37% of the strains isolated (32 in all) were orange-pigment producers in light as well as in the dark (type I), whereas about 25% produced an orange coloration only in the light (type II). No production of pigment was observed at pH 6.0 or below in the absence of sodium chloride, and the highest color intensity was registered at pH 7.0 in the presence of sodium chloride. Morphological and physiologic studies of the orange-pigmented strains revealed that most of them were closely related to Brevibacterium linens.

Heat-Etching with a Bullivant Type II Simple Freeze-Cleave Device

1970 ◽  
Vol 28 ◽  
pp. 106-107 ◽  
Author(s):  
Ronald S. Weinstein ◽  
N. Scott McNutt
Keyword(s):  
New Zealand ◽  
General Hospital ◽  
Massachusetts General Hospital ◽  
Type I ◽  
Type Ii ◽  
Collaborative Effort ◽  
Temperature And Pressure ◽  
The University

The Type I simple cold block device was described by Bullivant and Ames in 1966 and represented the product of the first successful effort to simplify the equipment required to do sophisticated freeze-cleave techniques. Bullivant, Weinstein and Someda described the Type II device which is a modification of the Type I device and was developed as a collaborative effort at the Massachusetts General Hospital and the University of Auckland, New Zealand. The modifications reduced specimen contamination and provided controlled specimen warming for heat-etching of fracture faces. We have now tested the Mass. General Hospital version of the Type II device (called the “Type II-MGH device”) on a wide variety of biological specimens and have established temperature and pressure curves for routine heat-etching with the device.

Two- or three-way observations of the identical cell elements within the same sections by LM, TEM and/or SEM

1978 ◽  
Vol 36 (2) ◽  
pp. 82-83 ◽  
Author(s):  
Nakazo Watari ◽  
Yasuaki Hotta ◽  
Yoshio Mabuchi
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Fine Structure ◽  
Light Microscopy ◽  
Thin Sections ◽  
Transmission Electron ◽  
Identical Cell ◽  
Electron Microscopes ◽  
Scanning Electron

It is very useful if we can observe the identical cell elements within the same sections by light microscopy (LM), transmission electron microscopy (TEM) and/or scanning electron microscopy (SEM) sequentially, because, the cell fine structure can not be indicated by LM, while the color is; on the other hand, the cell fine structure can be very easily observed by EM, although its color properties may not. However, there is one problem in that LM requires thick sections of over 1 μm, while EM needs very thin sections of under 100 nm. Recently, we have developed a new method to observe the same cell elements within the same plastic sections using both light and transmission (conventional or high-voltage) electron microscopes.In this paper, we have developed two new observation methods for the identical cell elements within the same sections, both plastic-embedded and paraffin-embedded, using light microscopy, transmission electron microscopy and/or scanning electron microscopy (Fig. 1).

Labelling of non-A, non-B hepatitis infected chimpanzee hepatocytes with nuclease-gold conjugates

1984 ◽  
Vol 42 ◽  
pp. 250-251
Author(s):  
G. D. Gagne ◽  
M. F. Miller ◽  
D. A. Peterson
Keyword(s):  
Endoplasmic Reticulum ◽  
Experimental Infection ◽  
Uranyl Acetate ◽  
Type I ◽  
Cellular Injury ◽  
Type Ii ◽  
Tubular Structures ◽  
Type Iii ◽  
Type Iv ◽  
Infected Chimpanzee

Experimental infection of chimpanzees with non-A, non-B hepatitis (NANB) or with delta agent hepatitis results in the appearance of characteristic cytoplasmic alterations in the hepatocytes. These alterations include spongelike inclusions (Type I), attached convoluted membranes (Type II), tubular structures (Type III), and microtubular aggregates (Type IV) (Fig. 1). Type I, II and III structures are, by association, believed to be derived from endoplasmic reticulum and may be morphogenetically related. Type IV structures are generally observed free in the cytoplasm but sometimes in the vicinity of type III structures. It is not known whether these structures are somehow involved in the replication and/or assembly of the putative NANB virus or whether they are simply nonspecific responses to cellular injury. When treated with uranyl acetate, type I, II and III structures stain intensely as if they might contain nucleic acids. If these structures do correspond to intermediates in the replication of a virus, one might expect them to contain DNA or RNA and the present study was undertaken to explore this possibility.

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