We discovered a highly virulent variant of subtype-B HIV-1 in the Netherlands. One hundred nine individuals with this variant had a 0.54 to 0.74 log 10 increase (i.e., a ~3.5-fold to 5.5-fold increase) in viral load compared with, and exhibited CD4 cell decline twice as fast as, 6604 individuals with other subtype-B strains. Without treatment, advanced HIV—CD4 cell counts below 350 cells per cubic millimeter, with long-term clinical consequences—is expected to be reached, on average, 9 months after diagnosis for individuals in their thirties with this variant. Age, sex, suspected mode of transmission, and place of birth for the aforementioned 109 individuals were typical for HIV-positive people in the Netherlands, which suggests that the increased virulence is attributable to the viral strain. Genetic sequence analysis suggests that this variant arose in the 1990s from de novo mutation, not recombination, with increased transmissibility and an unfamiliar molecular mechanism of virulence.

Life-history and pace-of-life syndrome theory predict that populations are comprised of individuals exhibiting different reproductive schedules and associated behavioural and physiological traits, optimized to prevailing social and environmental factors. Changing weather and social conditions provide in situ cues altering this life-history optimality; nevertheless, few studies have considered how tactical, sex-specific plasticity over an individual's lifespan varies in wild populations and influences population resilience. We examined the drivers of individual life-history schedules using 31 years of trapping data and 28 years of pedigree for the European badger (Meles meles L.), a long-lived, iteroparous, polygynandrous mammal that exhibits heterochrony in the timing of endocrinological puberty in male cubs. Our top model for the effects of environmental (social and weather) conditions during a badger's first year on pace-of-life explained <10% of variance in the ratio of fertility to age at first reproduction (F/α) and lifetime reproductive success. Conversely, sex ratio (SR)and sex-specific density explained 52.8% (males) and 91.0% (females) of variance in adult F/α ratios relative to the long-term population median F/α. Weather primarily affected the sexes at different life-history stages, with energy constraints limiting the onset of male reproduction but playing a large role in female strategic energy allocation, particularly in relation to ongoing mean temperature increases. Furthermore, the effects of social factors on age of first reproduction and year-to-year reproductive success covaried differently with sex, likely due to sex-specific responses to potential mate availability. For females, low same-sex densities favoured early primiparity; for males, instead, up to 10% of yearlings successfully mated at high same-sex densities.We observed substantial SR dynamism relating to differential mortality of life-history strategists within the population, and propose that shifting ratios of 'fast' and 'slow' life-history strategists contribute substantially to population dynamics and resilience to changing conditions. K E Y W O R D Sdemographic variability, HIREC, individual strategies, life history, pace-of-life syndrome, population resilience

It is time to acknowledge and overcome conservation's deep-seated systemic racism, which has historically marginalized Black, Indigenous and people of colour (BIPOC) communities and continues to do so. We describe how the mutually reinforcing ‘twin spheres’ of conservation science and conservation practice perpetuate this systemic racism. We trace how institutional structures in conservation science (e.g. degree programmes, support and advancement opportunities, course syllabuses) can systematically produce conservation graduates with partial and problematic conceptions of conservation's history and contemporary purposes. Many of these graduates go on to work in conservation practice, reproducing conservation's colonial history by contributing to programmes based on outmoded conservation models that disproportionately harm rural BIPOC communities and further restrict access and inclusion for BIPOC conservationists. We provide practical, actionable proposals for breaking vicious cycles of racism in the system of conservation we have with virtuous cycles of inclusion, equality, equity and participation in the system of conservation we want.

No abstract

The reproductive cycle of male and female badgers in the south‐west of England was studied by post‐mortem examination of 1875 badgers collected in 1973–80. The sample was obtained by several methods and showed that animals obtained as road casualties were not representative of the total population samples. Active spermatogenesis was present throughout the year, and in some males aged 8–9 months. A few females first ovulated as yearlings but most primiparous females were adults. Births were in general confined to the early part of the year, but ovulations and matings also occurred at other times. Almost all (97%) adult females possessed corpora lutea. Unimplanted blastocysts were found in females for 11 months of the year (over 80% of adult females in July‐November). Implanted embryos were found in only 32% of adults in January and February: the number of blastocysts per female and the number of implanted embryos per female were not significantly different, indicating that sows implanted all blastocysts or none. Foetal mortality was 36% and post‐natal losses were estimated at 42% from the proportion of lactating females.

Animals living at high population densities are expected to experience greater exposure to disease, leading to greater parasite burdens. However, social animals can accrue immunological and hygienic benefits from group living, and individuals can often minimise exposure using avoidance behaviours, so the costs and benefits of sociality for disease are often uncertain. Here, we show in wild European badgers that population density was negatively correlated with infection with three arthropod ectoparasites and one gastrointestinal protozoan, despite highly contrasting spatial distributions among parasites. Combined survival, spatial, and social network analyses suggested that parasite avoidance was the likely cause of this negative density-dependence. These findings demonstrate that animals can organise their societies in space to minimise infection, providing evidence for a “landscape of disgust”.

Early-life environmental conditions can provide a source of individual variation in life-history strategies and senescence patterns. Conditions experienced in early life can be quantified by measuring telomere length, which can act as a biomarker of survival probability. Here, we investigate whether seasonal changes, weather conditions, and group size are associated with early-life and/or early-adulthood telomere length in a wild population of European badgers (Meles meles). We found substantial intraannual changes in telomere length during the first three years of life (both between and within individuals), with shorter telomere lengths from spring to winter and longer telomere lengths over the 2 winter torpor period. In terms of weather conditions, linked to food availability and foraging success, cubs born in warmer, wetter springs with low rainfall variability had longer early-life (<1 year old) telomere lengths. Additionally, cubs born in groups with more cubs did not have significantly shorter early-life telomeres, providing no evidence of resource constraint from cub competition. We also found that our previously documented positive association between early-life telomere length and cub survival probability remained when social and weather variables were included. Finally, after sexual maturity, in early adulthood (i.e. 12-36 months) we found no significant association between same-sex adult group size and telomere length (i.e. no effect of intra-sexual competition). Overall we show that controlling for seasonal effects is important in telomere length analyses, and that badger telomere length functions as a biomarker that reflects the physiological consequences of early-life adversity and subsequent effects on cub survival probability.

Animals living at high population densities commonly experience greater exposure to disease, leading to increased parasite burdens. However, social animals can benefit immunologically and hygienically from cooperation, and individuals may alter their socio-spatial behaviour in response to infection, both of which could counteract density-related increases in exposure. Consequently, the costs and benefits of sociality for disease are often uncertain. Here, we use a long-term study of a wild European badger population ( Meles meles ) to investigate how within-population variation in host density determines infection with multiple parasites. Four out of five parasite taxa exhibited consistent spatial hotspots of infection, which peaked among badgers living in areas of low local population density. Combined movement, survival, spatial and social network analyses revealed that parasite avoidance was the likely cause of this negative density dependence, with possible roles for localized mortality, encounter-dilution effects, and micronutrient-enhanced immunity. These findings demonstrate that animals can organize their societies in space to minimize parasite infection, with important implications for badger behavioural ecology and for the control of badger-associated diseases.