Impact of environmental factors on survival of larval and juvenile Cape anchovy Engraulis encrasicolus (G.) in the southern Benguela upwelling region, determined from hatchdate distributions: implications for recruitment

2005 ◽  
Vol 56 (5) ◽  
pp. 561 ◽  
Author(s):  
M. R. Wilhelm ◽  
S. J. Painting ◽  
J. G. Field ◽  
M. Kerstan ◽  
M. D. Durholtz
Keyword(s):  
Electron Microscopy ◽  
Success Rate ◽  
Critical Period ◽  
Mortality Rates ◽  
Sea Surface ◽  
Planktonic Food ◽  
First Feeding ◽  
Benguela Upwelling ◽  
Scanning Electron ◽  
Age Estimates

March larval and May juvenile Cape anchovy of the unusually strong 1999/2000 year-class were collected off South Africa. Age estimates were obtained from daily increment counts on otoliths using light microscopy for March larvae (14–70 mm standard length, SL, n = 193, 92% success rate), and scanning electron microscopy for May juveniles (52–110 mm SL, n = 80, 22% success rate). Differences between March and May hatchdate distributions were related to the prevailing temperatures. March larval hatchdate distributions showed slight modes in October/November 1999 and January/February 2000, each a month later than May juvenile hatchdate distributions (September/October and November/December). Thus, mortality rates of larvae hatched after mid-December seem to have been higher. Large areas of warm water (19–26°C sea surface temperature) on the Agulhas Bank, mid-November 1999 to March 2000, indicated conditions conducive to spawning and reduced offshore advection of spawning products. A period of strong upwelling, March to May 2000, is likely to have increased availability of planktonic food for older larvae; also causing offshore dispersal of younger larvae and food patches required by these, possibly leading to starvation mortality of younger larvae during strong upwelling. The critical period thus seemed to be later than at first-feeding.

Mortality of First-Feeding Postlarval Walleye (Stizostedion vitreum) in Culture Ponds

1993 ◽  
Vol 50 (9) ◽  
pp. 1835-1843 ◽  
Author(s):  
Thomas A. Johnston ◽  
J. A. Mathias
Keyword(s):  
Critical Period ◽  
Mortality Rates ◽  
Predation Pressure ◽  
Stizostedion Vitreum ◽  
Exogenous Feeding ◽  
Natural Lakes ◽  
First Feeding ◽  
Zooplankton Density ◽  
Food Concentrations ◽  
Order Of Magnitude

We examined mortality rates of postlarval walleye (Stizostedion vitreum) at the onset of exogenous feeding in extensive culture ponds. Food concentrations (≥49 zooplankters∙L−1) were apparently sufficient to support successful first feeding, and no critical period of starvation mortality was evident at this stage of life. The highest observed mortality rates were associated with interspecific or intraspecific predation pressure. At low predation pressure, mean survival from stocking to the 12-mm stage was 87% in 1988 and 90% in 1989, and instantaneous mortality rates were an order of magnitude lower than those reported for postlarval walleye in natural lakes. Mortality rates calculated over the early postlarval period (stocking to 12 mm; 9–11 d) were similar to those calculated over the entire culture period (88–107 d) when predation pressure was low. At low predation pressure and 49–159 zooplankters∙L−1, there was no significant relationship between postlarval mortality rates and zooplankton density. The condition of first-feeding postlarvae captured from the pond with the lowest mean zooplankton density (49∙L−1) was significantly higher than that of postlarvae deprived of food for 48 h. Starvation is probably not a major cause of postlarval morality when zooplankton densities are ≥50∙L−1.

Validation of the ageing of 0+ carp (Cyprinus carpio L.)

2003 ◽  
Vol 54 (8) ◽  
pp. 1005 ◽  
Author(s):  
Benjamin B. Smith ◽  
Keith F. Walker
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
South Australia ◽  
Day Range ◽  
Otolith Increments ◽  
Carp Cyprinus Carpio ◽  
Otolith Increment ◽  
Increment Formation ◽  
Scanning Electron ◽  
Age Estimates

Forty carp larvae were reared from eggs spawned in the Torrens River, Adelaide, South Australia, and their otoliths were examined at the time of hatching or at 6, 10, 15 or 20 days after hatching (post-hatch). Using light- and scanning electron microscopy (SEM), otolith increments were counted and compared with known post-hatch ages. Typically, the counts were one day (range 0–2 days) more than the known post-hatch age, but increment formation was daily to at least age 20 days. Thus, age estimates derived from otolith increment counts of wild-caught 0+ carp should be reduced by one day. Comparison with SEM data showed that light microscopy alone offers sufficient resolution for ageing 0+ carp.

Pathogenesis of Human Hair Defects

1974 ◽  
Vol 32 ◽  
pp. 12-13
Author(s):  
P.S. Porter ◽  
T. Aoyagi ◽  
R. Matta
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Human Hair ◽  
Standard Techniques ◽  
Scanning Electron

Using standard techniques of scanning electron microscopy (SEM), over 1000 human hair defects have been studied. In several of the defects, the pathogenesis of the abnormality has been clarified using these techniques. It is the purpose of this paper to present several distinct morphologic abnormalities of hair and to discuss their pathogenesis as elucidated through techniques of scanning electron microscopy.

The Critical Point Drying Method Applied to Scanning Electron Microscopy of L-929 Cells

1970 ◽  
Vol 28 ◽  
pp. 278-279
Author(s):  
Charles TurnbiLL ◽  
Delbert E. Philpott
Keyword(s):  
Electron Microscopy ◽  
Carbon Dioxide ◽  
Surface Tension ◽  
Critical Point ◽  
Freeze Drying ◽  
Attractive Alternative ◽  
Crystal Formation ◽  
Critical Point Drying ◽  
Time Required ◽  
Scanning Electron

The advent of the scanning electron microscope (SCEM) has renewed interest in preparing specimens by avoiding the forces of surface tension. The present method of freeze drying by Boyde and Barger (1969) and Small and Marszalek (1969) does prevent surface tension but ice crystal formation and time required for pumping out the specimen to dryness has discouraged us. We believe an attractive alternative to freeze drying is the critical point method originated by Anderson (1951; for electron microscopy. He avoided surface tension effects during drying by first exchanging the specimen water with alcohol, amy L acetate and then with carbon dioxide. He then selected a specific temperature (36.5°C) and pressure (72 Atm.) at which carbon dioxide would pass from the liquid to the gaseous phase without the effect of surface tension This combination of temperature and, pressure is known as the "critical point" of the Liquid.

Ultrastructural Analysis of the Salivary Glands of Gromphadorhina Portentosa (Schaum)

1977 ◽  
Vol 35 ◽  
pp. 638-639
Author(s):  
P.J. Dailey
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Salivary Glands ◽  
Secretory Vesicles ◽  
The Past ◽  
Transmission Electron ◽  
Means Of Transmission ◽  
Gromphadorhina Portentosa ◽  
Scanning Electron ◽  
Topographical Relief

The structure of insect salivary glands has been extensively investigated during the past decade; however, none have attempted scanning electron microscopy (SEM) in ultrastructural examinations of these secretory organs. This study correlates fine structure by means of SEM cryofractography with that of thin-sectioned epoxy embedded material observed by means of transmission electron microscopy (TEM).Salivary glands of Gromphadorhina portentosa were excised and immediately submerged in cold (4°C) paraformaldehyde-glutaraldehyde fixative1 for 2 hr, washed and post-fixed in 1 per cent 0s04 in phosphosphate buffer (4°C for 2 hr). After ethanolic dehydration half of the samples were embedded in Epon 812 for TEM and half cryofractured and subsequently critical point dried for SEM. Dried specimens were mounted on aluminum stubs and coated with approximately 150 Å of gold in a cold sputtering apparatus.Figure 1 shows a cryofractured plane through a salivary acinus revealing topographical relief of secretory vesicles.

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).

Sem Studies of Co-Cr-Mo Surgical Implant Alloy Corrosion Behavior

1982 ◽  
Vol 40 ◽  
pp. 520-521
Author(s):  
Ann Chidester Van Orden ◽  
John L. Chidester ◽  
Anna C. Fraker ◽  
Pei Sung
Keyword(s):  
Electron Microscopy ◽  
Corrosion Behavior ◽  
Anodic Polarization ◽  
Saline Solution ◽  
Saturated Calomel Electrode ◽  
Physiological Saline ◽  
X Ray ◽  
Physiological Saline Solution ◽  
Scanning Electron

The influence of small variations in the composition on the corrosion behavior of Co-Cr-Mo alloys has been studied using scanning electron microscopy (SEM), energy dispersive x-ray analysis (EDX), and electrochemical measurements. SEM and EDX data were correlated with data from in vitro corrosion measurements involving repassivation and also potentiostatic anodic polarization measurements. Specimens studied included the four alloys shown in Table 1. Corrosion tests were conducted in Hanks' physiological saline solution which has a pH of 7.4 and was held at a temperature of 37°C. Specimens were mechanically polished to a surface finish with 0.05 µm A1203, then exposed to the solution and anodically polarized at a rate of 0.006 v/min. All voltages were measured vs. the saturated calomel electrode (s.c.e.).. Specimens had breakdown potentials near 0.47V vs. s.c.e.

Spontaneous Cataract in Nude Athymic Mice

1977 ◽  
Vol 35 ◽  
pp. 512-513
Author(s):  
Ronald H. Bradley ◽  
R. S. Berk ◽  
L. D. Hazlett
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Nude Mouse ◽  
Cellular Immunity ◽  
Phosphate Buffer ◽  
Osmium Tetroxide ◽  
Athymic Mice ◽  
Transmission Microscopy ◽  
Mouse Lens ◽  
Scanning Electron

The nude mouse is a hairless mutant (homozygous for the mutation nude, nu/nu), which is born lacking a thymus and possesses a severe defect in cellular immunity. Spontaneous unilateral cataractous lesions were noted (during ocular examination using a stereomicroscope at 40X) in 14 of a series of 60 animals (20%). This transmission and scanning microscopic study characterizes the morphology of this cataract and contrasts these data with normal nude mouse lens.All animals were sacrificed by an ether overdose. Eyes were enucleated and immersed in a mixed fixative (1% osmium tetroxide and 6% glutaraldehyde in Sorenson's phosphate buffer pH 7.4 at 0-4°C) for 3 hours, dehydrated in graded ethanols and embedded in Epon-Araldite for transmission microscopy. Specimens for scanning electron microscopy were fixed similarly, dehydrated in graded ethanols, then to graded changes of Freon 113 and ethanol to 100% Freon 113 and critically point dried in a Bomar critical point dryer using Freon 13 as the transition fluid.

Scanning and Transmission Microscopy of Nematocyst Batteries in Epitheliomuscular Cells of Hydra

1971 ◽  
Vol 29 ◽  
pp. 410-411 ◽  
Author(s):  
Jane A. Westfall ◽  
S. Yamataka ◽  
Paul D. Enos
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Osmium Tetroxide ◽  
External Surface ◽  
Three Dimensional ◽  
Surface Structures ◽  
Transmission Microscopy ◽  
Transmission Electron ◽  
Freeze Dried ◽  
Scanning Electron

Scanning electron microscopy (SEM) provides three dimensional details of external surface structures and supplements ultrastructural information provided by transmission electron microscopy (TEM). Animals composed of watery jellylike tissues such as hydras and other coelenterates have not been considered suitable for SEM studies because of the difficulty in preserving such organisms in a normal state. This study demonstrates 1) the successful use of SEM on such tissue, and 2) the unique arrangement of batteries of nematocysts within large epitheliomuscular cells on tentacles of Hydra littoralis.Whole specimens of Hydra were prepared for SEM (Figs. 1 and 2) by the fix, freeze-dry, coat technique of Small and Màrszalek. The specimens were fixed in osmium tetroxide and mercuric chloride, freeze-dried in vacuo on a prechilled 1 Kg brass block, and coated with gold-palladium. Tissues for TEM (Figs. 3 and 4) were fixed in glutaraldehyde followed by osmium tetroxide. Scanning micrographs were taken on a Cambridge Stereoscan Mark II A microscope at 10 KV and transmission micrographs were taken on an RCA EMU 3G microscope (Fig. 3) or on a Hitachi HU 11B microscope (Fig. 4).

Application of Scanning Electron Microscopy to Medical Research

1969 ◽  
Vol 27 ◽  
pp. 12-13
Author(s):  
J. D. Hutchison
Keyword(s):  
Electron Microscopy ◽  
Electron Microscope ◽  
Medical Research ◽  
Prosthetic Heart Valve ◽  
School Of Medicine ◽  
Transmission Electron ◽  
Definition Of ◽  
Mechanism Of Failure ◽  
The Brain ◽  
Scanning Electron

When the transmission electron microscope was commercially introduced a few years ago, it was heralded as one of the most significant aids to medical research of the century. It continues to occupy that niche; however, the scanning electron microscope is gaining rapidly in relative importance as it fills the gap between conventional optical microscopy and transmission electron microscopy.IBM Boulder is conducting three major programs in cooperation with the Colorado School of Medicine. These are the study of the mechanism of failure of the prosthetic heart valve, the study of the ultrastructure of lung tissue, and the definition of the function of the cilia of the ventricular ependyma of the brain.

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