Reproduction in the European hare in southern Sweden

Reproduction in the European hare Lepus europaeus Pallas populations was studied in three study areas in South Sweden during 1974–1976; two on the mainland and the third on the Island of Ven in Öresund. The monthly birth rates was calculated on the basis of the age of juvenile hares shot in autumn. The first births always occurred in February, indicating that the onset of the breeding season was governed by day length rather than by climate. Later, the reproduction rate was determined by temperature, snow cover, and precipitation. Low temperatures in spring delayed the reproduction; high temperatures in autumn favoured a prolongation of the breeding season. Low precipitation in May-July caused a decline in reproduction in July in a sandy pasture area, mainly because water amount was low in the green forage. Annual fertility, estimated on the basis of placental scars, varied between 6.8 and 8.9 young per female. There was a significant negative correlation between fertility and population density. The largest variations were recorded in one-year-old females, and on average the values were significantly higher in three-year-old females. 68% of all females examined had three litters annually; four litters were found in only 13% of all females. The mean litter size for the whole period was about 2.9 in all areas. The size of the first litter was significantly higher in females producing one or two litters than in females with three or four litters. The postnatal losses were on average 30–35% lower in the island population than in the mainland populations (73–84%), probably due to lack of predators, sparse road traffic, and inhibited juvenile dispersal.     

Influence of multiple predators decreases body condition and fecundity of European hares

1. We assessed the hypothesized negative correlation between the influence of multiple predators and body condition and fecundity of the European hare, from 13 areas in the Netherlands.
2. Year‐round abundance of predators was estimated by hunters. We quantified predator influence as the sum of their field metabolic rates, as this sum reflects the daily food requirements of multiple individuals. We determined the ratio between body mass and hindfoot length of hares as an index of body condition and the weight of their adrenal gland as a measure of chronic exposure to stress, and we counted the number of placental scars to estimate fecundity of hares.
3. As hypothesized, we found that the sum of field metabolic rate of predators was negatively correlated with body condition and the number of placental scars, whereas it was positively related to the weight of the adrenal glands. In contrast to the sum of the field metabolic rate, the total number of predators did not or weakly affect the investigated risk responses.
4. The sum of the field metabolic rate can be a useful proxy for the influence of multiple predators and takes into account predator abundance, type, body weight, and food requirements of multiple predators.
5. With our findings, our paper contributes to a better understanding of the risk effects of multiple predators on prey fitness. Additionally, we identify a potential contributor to the decline of European hare populations.

     

Evidence of autumn reproduction in female European hares (Lepus europaeus) from southern Europe

Information on reproductive biology of the European hare (Lepus europaeus) in different environmental and landscape conditions comprises part of fundamental knowledge regarding species’ adaptive responses as well as many aspects of its biology. Most of the studies conducted on European hare reproduction are confined to midlatitude and northern populations, whereas no data exist on the indigenous southern populations. Here, we present information on reproductive characteristics of European hares inhabiting Mediterranean ecosystems on the island of Crete, Greece for two successive hunting seasons. Although the annual reproductive cycle of the species is well known, with an autumn sexual inactivity, the duration of this period is subjected to fluctuations in different years and for different areas. According to our data, hare populations of Crete present an autumn–early winter reproductive activity with high proportions of pregnant females observed in all the months of the study. Furthermore, the estimated mean litter size (1.54 SE ± 0.07) while signed to the lowest values ever observed for European hares is similar to values obtained in continuous breeding species of the same genus, Lepus granatensis, Lepus corsicanus, Lepus (capensis) mediterraneus, and Lepus capensis also inhabiting warm climates. In conclusion, our results suggest that Cretan European hare populations exhibit a reproductively active period during autumn–early winter where proportions of pregnant females and litter size give a strong indication of a continuous reproduction throughout the year.     

Growth and body composition of mice selected for high body weight

To elucidate the influence of high body weight selection on body compositional relationships, the accumulation of lipid, protein, and ash was investigated in two lines of mice selected for high 42-day body weight (H lines) and an unselected foundation population (FP). The two H lines differed in population size and were designated as the high-large (HL) and high-small (HS) lines. Logistic body growth curves revealed that HL mice exhibited an accelerated growth rate and reached a higher mature body weight than FP or HS mice. Over the range of body weights examined, HL mice had more lipid, less protein, and less ash than FP or HS mice of the same sex and body weight. However, HL lipid accumulation (relative to body weight increase) was not accelerated in comparison to that of FP mice. This study suggests that the existing model of selection-mediated compositional changes requires expansion to account for the ability of high-growth selection to direct an acceleration of body growth without a correlated enhancement of the relative rate of fat accumulation.     

Factors related to the occurrence of hybrids between brown hares Lepus europaeus and mountain hares L. timidus in Sweden

Hybridization occurs among many species, and may have implications for conservation as well as for evolution. Interspecific gene flow between brown hares Lepus europaeus and mountain hares L. timidus has been documented in Sweden and in continental Europe, and has probably to some extent occurred throughout history in sympatric areas. What local factors or ecological relationships that correlate with or trigger hybridization between these species has however been unclear. We studied spatial distribution of hybrids between brown hares and mountain hares in Sweden in relation to characteristics of the sampled localities (hunting grounds). In a sample of 70 brown hares collected from 39 populations in south‐central Sweden during 2003–2005, 11 (16%) showed introgressed mtDNA from mountain hares. Among the brown hares from their northern range, i.e. in general the most recent establishments, the corresponding figure was 75% (9/12). The frequency of samples with hybrid ancestry increased significantly with latitude, altitude and hilliness, and were higher (p<0.1) in recently established populations and/or where the proportion of arable land was low. Several site‐specific parameters were correlated, e.g. latitude as expected to hilliness, and no parameter explained the occurrence of hybrids exclusively. Instead, the appearance of mountain hare mtDNA among brown hares was associated with a conglomerate of parameters reflecting landscapes atypical for the brown hare, e.g. forest dominated and steep areas where the species quite recently was established. We suggest that these abiotic factors mirror the main aspect influencing hybridization frequency, namely the density or relative frequency of the two species. In atypical brown hare landscapes with recent establishment, mountain hares are probably relatively more common. When one species dominate in numbers, or when both species display low densities, increased frequency of hybridization is expected due to low availability of conspecific partners, a phenomenon referred to as Hubbs’ principle.     

Differences in body mass, health status and genetic variation between insular and mainland brown hares (Lepus europaeus) in Sweden

Introduced populations can be affected by random processes such as genetic drift, deterministic processes given by the local environmental conditions and anthropogenic factors such as hunting and management. Geographically constrained populations are particularly exposed to these processes, and altogether, these factors may result in rapid differentiation from the ancestral populations. The introduced European brown hare (Lepus europaeus) population on the island Ven is isolated from the Swedish and Danish mainland. Undocumented observations suggest that the hares on the island have been increasingly diseased in recent years and also decreased in body size. To test the substance of these observations, as well as the potential for inbreeding depression in this geographically constrained population, a total of 321 hares from Ven and three reference populations on the Swedish mainland were analysed with respect to body mass, general health status and genetic variation. The results confirm that the hares on Ven have lower body mass than hares on the mainland, but there are no indications of health deficits. We argue that the difference in body mass primarily is an island effect of stress and/or nutritional shortage, possibly induced by high population density, anthropogenic selection regimes and absence of mammalian meso-predators. Further, the genetic data indicate that the insular population is substructured, and subadults from these two subpopulations differ in body mass. This apparent substructuring could be due to chance effects, but may also be related to assortative mating or presence of sustained populations with different ancestry.     

European brown hare syndrome virus in free-ranging European brown hares from Argentina

From 1998 to 2000, serum samples of 80 shot European brown hares (Lepus europaeus) from Argentina were examined for antibodies against European brown hare syndrome virus (EBHSV) and 80 spleen samples were tested for EBHSV-antigen by enzyme linked immunosorbent assay (ELISA). Nine hares were positive for EBHSV-antigen. Antibodies against EBHSV were detected in only one individual. Based on negative staining electron microscopy of spleen homogenates, we observed calicivirus in one of five EBHSV-antigen positive hares. However, EBHS has not been reported to cause abnormal mortality in these hares. This is the first report of antibodies to EBHSV, EBHSV-antigen, and electron microscopy findings in free-ranging European brown hares from South America.     

European brown hare syndrome in free-ranging European brown and mountain hares from Switzerland.

From 1997 to 2000, complete necropsy and histopathologic investigations were performed on 157 free-ranging European brown hares (Lepus europaeus) found dead throughout Switzerland. Organ samples of all these individuals (157 livers and 107 spleens available) were tested for European brown hare syndrome virus (EBHSV)-antigen by enzyme-linked immunosorbent assay (ELISA) test kit. Furthermore, 60 additional blood samples were tested for antibodies against EBHSV by ELISA. In addition, liver samples of 87 free-ranging mountain hares (Lepus timidus) hunted in 1996 were tested for EBHSV-antigen. In two European brown hares from southern Switzerland lesions suggestive of changes induced by EBHSV were present, and high titers of EBHSV-antigen were detected in both liver and spleen samples of these animals. Based on negative staining electron microscopy investigations of liver and spleen homogenates, we observed calicivirus in one antigen-positive hare. Low EBHSV-antigen titers were found in three additional European brown hares from central and western Switzerland, but EBHS-lesions were absent. Antibodies against EBHSV were not detected in any of the sera of European brown hares, and EBHSV-antigen was not found in the samples of mountain hares. This is the first report of EBHS in European brown hares from Switzerland.     

Continentality affects body condition and size but not yearly reproductive output in female European hares (Lepus europaeus)

Life history in reproductive pattern in hares are affected by ambient temperature. We hypothesized that European hares dwelling in areas of higher energy demands would have larger body sizes, larger fat depots and a delayed first reproduction. To test this assumption we compared yearly reproductive output as well as age, body size, body weight and body condition of female European hares from Belgium (temperate oceanic climate) and Lower Austria (temperate continental climate). Our results reveal that there was no effect of study site on annual reproductive output in female European hares. However, adult female hares from Belgium were significantly smaller and had significantly lower body condition in late autumn compared to the Lower Austrian sample, although Belgian individuals were actually older than Lower Austrians. These findings suggest that females in Belgium are more under an r-selection regime whereas Lower Austrian females might be more under K-selection within the r-K-continuum.     

Sexing European rabbits (Oryctolagus cuniculus), European brown hares (Lepus europaeus) and mountain hares (Lepus timidus) with ZFX and ZFY loci

We describe a new method for the sex determination of tissue originating from Oryctolagus cuniculus (European rabbit), Lepus europaeus (European brown hare) and Lepus timidus (mountain hare) based on PCR-RFLP analysis of point mutations that differentiate the ZFX and ZFY gene sequences. Among several applications, this PCR-RFLP method could be used to investigate gender ratio and evaluate the population dynamics of these species using samples collected when sex cannot be identified.     

Effects of live-trapping and toe-clipping on body weight of European and African rodent species

Summary Changes in body weights of four species of small rodents were monitored to evaluate the method of toe-clipping for individual identification. If carefully applied the method was found to be without any biologically meaningful effects on the animals. Secondly, body weight changes in prolonged live-trapping studies were evaluated in five species of small rodents. It was found that the animals generally do not recover from the stress of trapping within 24 h. Absolute weight losses were small on a daily basis but mounted up when animals were trapped day after day.