95 research outputs found
Cladoceran birth and death rates estimates
I. Birth and death rates of natural cladoceran populations cannot be measured directly. Estimates of these population parameters must be calculated using methods that make assumptions about the form of population growth. These methods generally assume that the population has a stable age distribution.
2. To assess the effect of variable age distributions, we tested six egg ratio methods for estimating birth and death rates with data from thirty-seven laboratory populations of Daphnia pulicaria. The populations were grown under constant conditions, but the initial age distributions and egg ratios of the populations varied. Actual death rates were virtually zero, so the difference between the estimated and actual death rates measured the error in both birth and death rate estimates.
3. The results demonstrate that unstable population structures may produce large errors in the birth and death rates estimated by any of these methods. Among the methods tested, Taylor and Slatkin's formula and Paloheimo's formula were most reliable for the experimental data.
4. Further analyses of three of the methods were made using computer simulations of growth of age-structured populations with initially unstable age distributions. These analyses show that the time interval between sampling strongly influences the reliability of birth and death rate estimates. At a sampling interval of 2.5 days (equal to the duration of the egg stage), Paloheimo's formula was most accurate. At longer intervals (7.5–10 days), Taylor and Slatkin's formula which includes information on population structure was most accurate
Specific Heat Study of the Magnetic Superconductor HoNi2B2C
The complex magnetic transitions and superconductivity of HoNi2B2C were
studied via the dependence of the heat capacity on temperature and in-plane
field angle. We provide an extended, comprehensive magnetic phase diagram for B
// [100] and B // [110] based on the thermodynamic measurements. Three magnetic
transitions and the superconducting transition were clearly observed. The 5.2 K
transition (T_{N}) shows a hysteresis with temperature, indicating the first
order nature of the transition at B=0 T. The 6 K transition (T_{M}), namely the
onset of the long-range ordering, displays a dramatic in-plane anisotropy:
T_{M} increases with increasing magnetic field for B // [100] while it
decreases with increasing field for B // [110]. The anomalous anisotropy in
T_{M} indicates that the transition is related to the a-axis spiral structure.
The 5.5 K transition (T^{*}) shows similar behavior to the 5.2 K transition,
i.e., a small in-plane anisotropy and scaling with Ising model. This last
transition is ascribed to the change from a^{*} dominant phase to c^{*}
dominant phase.Comment: 9 pages, 11 figure
Genetic relationship between Escherichia coli strains isolated from dairy mastitis and from the stable fly Stomoxys calcitrans
The major histocompatibility complex a la carte: are there analogies to plant disease resistance genes on the menu?
- …