Effects of Solar UV-B Radiation on Embryonic Development in Hyla cadaverina, Hyla regilla, and Taricha torosa

1998 ◽  
Vol 12 (3) ◽  
pp. 646-653 ◽  
Author(s):  
Christopher R. Anzalone ◽  
Lee B. Kats ◽  
Malcolm S. Gordon
2008 ◽  
Vol 12 (3) ◽  
pp. 646-653 ◽  
Author(s):  
Christopher R. Anzalone ◽  
Lee B. Kats ◽  
Malcolm S. Gordon

1969 ◽  
Vol 43 (2) ◽  
pp. 220-228 ◽  
Author(s):  
Harriet M. McCurdy

The DOPA-reaction was used to identify tyrosinase in the nucleus and cytoplasm of the neural crest melanoblast of Taricha torosa, the California newt. In this urodele there is a nuclear DOPA-positive response during the normal embryonic development from the late blastula stage to the nucleus of the early melanocyte. During the gastrula stages, all nuclei of this newt are DOPA-positive. This positive nuclear response fades away after the formation of the neural crest, save in the melanoblasts. The only cells that give a positive DOPA marking in the cytoplasm are the melanoblasts. This cytoplasmic reaction appears while the melanoblast nucleus still gives a DOPA-positive reaction. Tyrosinase activity, as marked by unlabeled DOPA, has ceased in the fully mature melanocyte. The red nuclei, seen in some of the animals in the maturing melanocyte and adjacent tissues, may be in the hallachrome stage of melanin formation. There is a diffuse distribution of DOPA reactivity in the resting nucleus, and an adherence of the DOPA-marking in the region of the dividing chromosomes in the mitosis of DOPA-positive nuclei of the melanoblast. These observations suggest that tyrosinase may be among the chromosomally bound enzymes of the chromatin space.


1997 ◽  
Vol 75 (7) ◽  
pp. 1081-1088 ◽  
Author(s):  
Kristiina Ovaska ◽  
Theodore M. Davis ◽  
Iñigo Novales Flamarique

The aquatic stages of amphibians may be sensitive to increased levels of solar ultraviolet B radiation (UV-B, 280–320 nm) that have been observed at higher latitudes over the past several decades, but the effects on most species are unknown. We exposed eggs and larvae of Hyla regilla and Rana aurora to three experimental treatments: (1) solar UV < 450 nm blocked (control), (2) ambient solar UV, and (3) solar UV-B enhanced 15 and 30% above ambient levels at midday to simulate conditions predicted for the next decades at midlatitudes. The rearing containers were covered with acrylic filters to provide the desired radiation regimes. Hatching success of H. regilla did not differ among the treatments and was 87.7, 71.8, and 87.1% in April 1995 and 94.0, 85.1, and 97.4% in May 1995 for the control, ambient, and enhanced UV-B treatments, respectively. In contrast, hatching success of R. aurora in the enhanced UV-B treatment (56.0%) was lower than in the ambient UV (89.8%) and control (81.0%) treatments. Larval survival over the first 2 months of development was reduced to 18.4% for H. regilla and 2.6% for R. aurora in the enhanced UV-B treatment compared with the ambient UV and control treatments. We conclude that ambient UV levels at the study site did not affect the embryonic or early larval survival of either of the species tested under the experimental conditions, but both species are potentially vulnerable to increases in solar UV-B.


2001 ◽  
Vol 7 (S2) ◽  
pp. 1012-1013
Author(s):  
Uyen Tram ◽  
William Sullivan

Embryonic development is a dynamic event and is best studied in live animals in real time. Much of our knowledge of the early events of embryogenesis, however, comes from immunofluourescent analysis of fixed embryos. While these studies provide an enormous amount of information about the organization of different structures during development, they can give only a static glimpse of a very dynamic event. More recently real-time fluorescent studies of living embryos have become much more routine and have given new insights to how different structures and organelles (chromosomes, centrosomes, cytoskeleton, etc.) are coordinately regulated. This is in large part due to the development of commercially available fluorescent probes, GFP technology, and newly developed sensitive fluorescent microscopes. For example, live confocal fluorescent analysis proved essential in determining the primary defect in mutations that disrupt early nuclear divisions in Drosophila melanogaster. For organisms in which GPF transgenics is not available, fluorescent probes that label DNA, microtubules, and actin are available for microinjection.


2014 ◽  
Vol 47 (06) ◽  
Author(s):  
N Bergemann ◽  
K Boyle ◽  
WE Paulus

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