Modification of Experimental Protocols for a Space Shuttle Flight and Applications for the Analysis of Cytoskeletal Structures During Fertilization, Cell Division , and Development in Sea Urchin Embryos

To explore the role of microgravity on cytoskeletal organization and skeletal calcium deposition during fertilization, cell division, and early development, the sea urchin was chosen as a model developmental system. Methods were developed to employ light, immunofluorescence, and electron microscopy on cultures being prepared for flight on the Space Shuttle. For analysis of microfilaments, microtubules, centrosomes, and calcium-requiring events, our standard laboratory protocols had to be modified substantially for experimentation on the Space Shuttle. All manipulations were carried out in a closed culture chamber containing 35 ml artificial sea water as a culture fluid. Unfertilized eggs stored for 24 hours in these chambers were fertilized with sperm diluted in sea water and fixed with concentrated fixatives for final fixation in formaldehyde, taxol, EGTA, and MgCl2(exp -6)H2O for 1 cell to 16 cell stages to preserve cytoskeletal structures for simultaneous analysis with light, immunofluorescence, and electron microscopy, and 1.5 percent glutaraldehyde and 0.4 percent formaldehyde for blastula and plueus stages. The fixed samples wre maintained in chambers without degradation for up to two weeks after which the specimens were processed and analyzed with routine methods. Since complex manipulations are not possible in the closed chambers, the fertilization coat was removed from fixation using 0.5 percent freshly prepared sodium thioglycolate solution at pH 10.0 which provided reliable immunofluorescence staining for microtubules. Sperm/egg fusion, mitosis, cytokinesis, and calcium deposition during spicule formatin in early embryogenesis were found to be without artificial alterations when compared to cells fixed fresh and processed with conventional methods

Estimating group size and population density of Eurasian badgers Meles meles by quantifying latrine use

1. Conservation issues and a potential role in disease transmission generate the continued need to census Eurasian badgers Meles metes, but direct counts and sett counts present difficulties. The feasibility of estimating social group size and population density of badgers by quantifying their use of latrines was evaluated. 2. The number of latrines, or preferably the number of separate dung pits, which were known from bait-marking to be used by members of a social group, was positively correlated with adult group size estimated from mark-recapture studies at Woodchester Park and North Nibley (south-west England). In the latter study area both latrine-use measures were also significantly associated with total group size (i.e. including cubs and adults). 3. In spring 1997 and 1998, we quantified latrine use along strip transects, following linear features across four and five areas, respectively, in England, where badger density in summer was known from mark-recapture/resight studies. 4. Seven latrine-use measures were evaluated with regard to their potential to predict badger density. Each measure separately explained between 62% and 91% of the variation in population density in a given year. The simplest measures (latrines km(-1) and pits km(-1)) were most stable between years. 5. For these two simple latrine-use measures, a linear model without an intercept term explained the highest proportion of variation in population density. A stepwise procedure to produce the best model selected only one (latrines km(-1)) of the two measures as an explanatory variable., indicating that pits km(-1) is colinear with the former variable. 6. A badger census technique based on simple measurements of latrine use has great promise but needs to be validated across a wider range of badger populations, habitats, years, seasons and weather condition