Temporal variability in the way local habitat affects duck population growth

Climate change is expected to lead to greater temporal climatic variability across broad spatial extents. A potential consequence is that shifts in climatic conditions might alter how local habitat affects the population growth of animals dependent on those habitats for at least part of their life cycle. We tested whether such a phenomenon occurred when the North American Prairie Pothole Region transitioned through periods of wet and dry conditions by modeling the population growth of seven duck species over 52 years (1961–2012). We found that the influence of local habitat quality—indexed by wetland availability—on duck population growth varied in magnitude and direction on an annual basis. While the effect of wetlands was relatively small in most years, there were some years in which wetlands strongly affected duck population growth in both positive and negative directions (e.g., negative in 2002 and positive in 2008). Contrary to our expectation, inter-annual variability in the effect of wetlands on duck population growth did not depend on regional precipitation. We also found that for two species—American Wigeon (Anas americana) and Green-winged Teal (A. carolinensis)—duck population growth in the presence of wetlands rarely differed from what would be expected solely under density dependence. Our study is the first to demonstrate that the effect of local habitat on population growth varies over time even if the cause of that variation remains unexplained. Consequently, any study that attempts to identify a species’ critical habitat using time series abundance data must consider that local relationships are non-stationary. More complicated measures of climate change may reveal how local drivers of population growth depend on broader temporal climatic patterns.     

Assessing reproductive potential and gestation in nurse sharks (Ginglymostoma cirratum) using ultrasonography and endoscopy: An example of bridging the gap between field research and captive studies

Over a period of 3 years, five reproductively active female nurse sharks (Ginglymostoma cirratum) from a wild, actively mating population of nurse sharks were captured, confined, and periodically examined through the course of gestation to determine the gestation period and characterize paternity. In the final year of the study, candidate animals were first evaluated in the field by ultrasonography, and the selected animals were then transported from the study site to holding facilities at SeaWorld Adventure Parks in Orlando, Florida. Periodic monitoring of the animals was conducted by ultrasonography, endoscopy, and routine blood analysis. Gestation was determined to be a minimum of 131 days, multiple paternity was shown for two individual litters, and ultrasonography and endoscopy were shown to be useful adjuncts for assessing pregnancy and monitoring gestation in this species. Poor survival of offspring, and small litter size may be a consequence of handling and transporting the animals, and the use of invasive procedures such as endoscopy. Zoo Biol 22:179–187, 2003. © 2003 Wiley‐Liss, Inc.     

Visualization of Mitochondrial DNA Replication in Individual Cells by EdU Signal Amplification

Mitochondria are key regulators of cellular energy and mitochondrial biogenesis is an essential component of regulating mitochondria numbers in healthy cells^1-3. One approach for monitoring mitochondrial biogenesis is to measure the rate of mitochondrial DNA (mtDNA) replication⁴. We developed a sensitive technique to label newly synthesized mtDNA in individual cells in order to study mtDNA biogenesis. The technique combines the incorporation of 5-ethynyl-2''-deoxyuridine (EdU)^5-7 with a tyramide signal amplification (TSA)⁸ protocol to visualize mtDNA replication within subcellular compartments of neurons. EdU is superior to other thymidine analogs, such as 5-bromo-2-deoxyuridine (BrdU), because the initial click reaction to label EdU^5-7 does not require the harsh acid treatments or enzyme digests that are required for exposing the BrdU epitope. The milder labeling of EdU allows for direct comparison of its incorporation with other cellular markers^9-10. The ability to visualize and quantify mtDNA biogenesis provides an essential tool for investigating the mechanisms used to regulate mitochondrial biogenesis and would provide insight into the pathogenesis associated with drug toxicity, aging, cancer and neurodegenerative diseases. Our technique is applicable to sensory neurons as well as other cell types. The use of this technique to measure mtDNA biogenesis has significant implications in furthering the understanding of both normal cellular physiology as well as impaired disease states.