Intra-specific variation and taxa- sampling affects the home range — body mass relationship

The relationship between home range size and body mass is a frequently studied allometric relationship. However, the results of various studies differ greatly, leading to much debate about the nature of the relationship. We argue that this confusion is not surprising, due to intra-specific variation in home range size caused by ecological variability rather than by body mass. By random resampling of different studies from within 16 Carnivora species, we show that the scaling exponent ranged from 0.30–1.54 depending on the particular studies included for each species. Of these exponents, 10% did not contain 0.75 within their confidence limits, and 5.5% did not contain 1.00. Furthermore, by randomly sub-sampling 16 species from a total sample of 58 species, we found that the scaling exponent varied between 0.18 and 2.76. Of these exponents, 42.2% did not contain 0.75 within their confidence limits, whereas 16.8% did not contain 1.00. Therefore, we strongly recommend that greater consideration be paid to intra-specific ecological variability and taxa selection when dealing with both allometry and cross-species life history studies.     

Inferring temperature adaptation from thermal performance curves of somatic growth rate: The importance of growth measurements and mortality

When comparing somatic growth thermal performance curves (TPCs), higher somatic growth across experimental temperatures is often observed for populations originating from colder environments. Such countergradient variation has been suggested to represent adaptation to seasonality, or shorter favourable seasons in colder climates. Alternatively, populations from cold climates may outgrow those from warmer climates at low temperature, and vice versa at high temperature, representing adaptation to temperature. Using modelling, we show that distinguishing between these two types of adaptation based on TPCs requires knowledge about (i) the relationship between somatic growth rate and population growth rate, which in turn depends on the scale of somatic growth (absolute or proportional), and (ii) the relationship between somatic growth rate and mortality rate in the wild. We illustrate this by quantifying somatic growth rate TPCs for three populations of Daphnia magna where population growth scales linearly with proportional somatic growth. For absolute somatic growth, the northern population outperformed the two more southern populations across temperatures, and more so at higher temperatures, consistent with adaptation to seasonality. In contrast, for the proportional somatic growth TPCs, and hence population growth rate, TPCs tended to converge towards the highest temperatures. Thus, if the northern population pays an ecological mortality cost of rapid growth in the wild, this may create crossing population growth TPCs consistent with adaptation to temperature. Future studies within this field should be more explicit in how they extrapolate from somatic growth in the lab to fitness in the wild.     

Spatial distribution and settlement strategies in willow ptarmigan

In heterogeneous landscapes individuals select among several habitat patches. The fitness rewards of these choices are assumed to play an important role in the distribution of individuals across landscapes. Individuals can either use environmental cues to directly assess the quality of breeding sites, or rely on social cues to guide the settlement decision. We estimated the density of adult birds and per capita reproductive success of willow ptarmigan over 5–15 years in 42 survey areas, nested within 5 spatially separated populations in south-central Norway. Our aims were to (1) examine spatial and temporal patterns of variation in densities of adult birds (i.e., the breeding densities) and reproductive success (juveniles/pair) measured in autumn and (2) evaluate which habitat distribution model best described the distribution of willow ptarmigan across heterogeneous mountain landscapes. Variation in density of adult birds was primarily attributable to variation between survey areas which could arise from spatial heterogeneity in adult survival or as a consequence of spacing behavior of juveniles during the settlement stage. In contrast, reproductive success was more variable between years and did not vary consistently between survey areas once year effects were accounted for. The lack of any relationship between the density of adult birds and reproductive success supported the predictions of an ideal free distribution (IFD), implying that within years, the mean reproductive success was approximately equal across survey areas. However, analysis based on Taylor's power law (i.e., the relationship between logarithms of spatial variance and mean density of adult birds) suggested that aggregation was stronger than expected under IFD. This implies that the relative change in density of adult birds was larger in areas with high mean densities than in areas with low densities. The exact mechanisms causing this statistical pattern are unclear, but based on the breeding biology of willow ptarmigan we suggest that yearlings are attracted to areas of high densities during the settlement period in spring. Our study was conducted during a period of low overall density and we suggest that this pattern might be particular to such situations. This implies that the presence of conspecifics might represent a cue signaling high adult survival and thus high habitat quality.     

Why are population growth rate estimates of past and present hunter–gatherers so different?

Hunter–gatherer population growth rate estimates extracted from archaeological proxies and ethnographic data show remarkable differences, as archaeological estimates are orders of magnitude smaller than ethnographic and historical estimates. This could imply that prehistoric hunter–gatherers were demographically different from recent hunter–gatherers. However, we show that the resolution of archaeological human population proxies is not sufficiently high to detect actual population dynamics and growth rates that can be observed in the historical and ethnographic data. We argue that archaeological and ethnographic population growth rates measure different things; therefore, they are not directly comparable. While ethnographic growth rate estimates of hunter–gatherer populations are directly linked to underlying demographic parameters, archaeological estimates track changes in the long-term mean population size, which reflects changes in the environmental productivity that provide the ultimate constraint for forager population growth. We further argue that because of this constraining effect, hunter–gatherer populations cannot exhibit long-term growth independently of increasing environmental productivity.This article is part of the theme issue ‘Cross-disciplinary approaches to prehistoric demography’.     

Patterns of variation in reproductive parameters in Eurasian lynx (<Emphasis Type="Italic">Lynx lynx</Emphasis>)

Detailed knowledge of the variation in demographic rates is central for our ability to understand the evolution of life history strategies and population dynamics, and to plan for the conservation of endangered species. We studied variation in reproductive output of 61 radio-collared Eurasian lynx females in four Scandinavian study sites spanning a total of 223 lynx-years. Specifically, we examined how the breeding proportion and litter size varied among study areas and age classes (2-year-old vs. >2-year-old females). In general, the breeding proportion varied between age classes and study sites, whereas we did not detect such variation in litter size. The lack of differences in litter sizes among age classes is at odds with most findings in large mammals, and we argue that this is because the level of prenatal investment is relatively low in felids compared to their substantial levels of postnatal care.     

Aerodynamic evaluation of the empty nose syndrome by means of computational fluid dynamics

The potential outcome of a surgical enlargement of internal nasal channels may be a complication of nasal breathing termed the Empty Nose Syndrome (ENS). ENS pathophysiology is not entirely understood because the expansion of air pathways would in theory ease inhalation. The present contribution is aimed at defining the biophysical markers responsible for ENS. Our study, conducted in silico, compares nasal aerodynamics in pre- and post-operative geometries acquired by means of computer tomography from the same individual. In this article, we elucidate and analyse the deviation of airflow patterns and nasal microclimate from the healthy benchmarks. The analysis reveals 53% reduction in flow resistance, radical re-distribution of nasal airflow, as well as dryer and colder nasal microclimate for the post-operative case.     

Patterns of hunting mortality in Norwegian moose (Alces alces) populations

We used a simple life table approach to examine the age-specific patterns of harvest mortality in eight Norwegian moose populations during the last 15 years and tried to determine if the observed patterns were caused by hunter selectivity. The general opinion among local managers is that hunters prefer to shoot female moose not in company with calves to keep a high number of reproductive females in the population (and because of the emotional stress involved in leaving the calf/calves without a mother), and relatively large males because of the higher return with respect to meat and trophy. In support of the former view, we found the harvest mortality of adult females to be higher among pre-prime (1–3 years old) than prime-aged age classes (4–7 years old). This is probably because prime-aged females are more fecund and, therefore, more likely to be in company with one or two calves during the hunting season. As the season progressed, however, the selection pressure on barren females decreased, probably due to more productive females becoming ‘legal’ prey as their calf/calves were harvested. In males, we did not find any evidence of strong age-specific hunter selectivity, despite strong age-dependent variation in body mass and antler size. We suggest that this was due to the current strongly female-biased sex ratio in most Norwegian moose populations, which leaves the hunters with few opportunities to be selective within a relatively short and intensive hunting season. The management implications of these findings and to what extent the results are likely to affect the future evolution of life histories in Norwegian moose populations are discussed.Electronic Supplementary Material Supplementary material is available for this article at and accessible for authorised users.