Porcine reproductive and respiratory syndrome virus (PRRSV) remains among the most costly diseases in North America (Holtkamp
Aim: The evolution of key innovations promotes adaptive radiations by opening access to novel ecological opportunity. The acquisition of viviparity (live-bearing reproduction) has emerged as one such innovation explaining reptile proliferations into extreme climates. By evolving viviparity, females provide embryos with internally stable environments to complete development. The classical hypothesis suggests that natural selection for viviparity arises from low temperatures in cold-climates, which promote prolonged egg retention in the mother’s body. An alternative hypothesis proposes that declines in atmospheric oxygen at high elevations create natural selection for embryo retention to provide them with optimal oxygen levels during development. However, although experimental studies support the negative effects of low oxygen on egg development, this ‘hypoxia’ hypothesis has never been tested quantitatively. Here, we compete the hypoxia hypothesis against the ‘cold-climate’ hypothesis, using a highly-diverse lizard genus.\ud Location: South America\ud Major taxa: Liolaemus lizards.\ud Methods: We employ a multivariate dataset covering 121-species varying extensively in geographic and climatic distribution (including extreme thermal and oxygen gradients), and parity mode. Based on a new molecular phylogeny for the genus, we use phylogenetic logistic regressions to generate a range of models ranking environmental factors as a function of their effects on parity mode transitions.\ud Results: Elevation and oxygen declines correlate nearly perfectly, and both were identified as the dominant predictors of oviparity-to-viviparity transitions, while the role for temperature (dominated by the coldest winter temperatures and daily fluctuations) is significant but secondary. Overall, we show that oxygen-deprivation and low temperatures both play a role in the evolution of viviparity.\ud Main conclusions: Our findings support the role for selection from declines in oxygen concentrations as the primary driver behind viviparity. However, selection arising from cold temperatures and from reduced fluctuations in daily temperatures contribute to the evolution of these transitions by creating multivariate selection on parity mode
Body size shapes ecological interactions across and within species, ultimately influencing the evolution of large‐scale biodiversity patterns. Therefore, macroecological studies of body size provide a link between spatial variation in selection regimes and the evolution of animal assemblages through space. Multiple hypotheses have been formulated to explain the evolution of spatial gradients of animal body size, predominantly driven by thermal (Bergmann's rule), humidity (‘water conservation hypothesis’) and resource constraints (‘resource rule’, ‘seasonality rule’) on physiological homeostasis. However, while integrative tests of all four hypotheses combined are needed, the focus of such empirical efforts needs to move beyond the traditional endotherm–ectotherm dichotomy, to instead interrogate the role that variation in lifestyles within major lineages (e.g. classes) play in creating neglected scenarios of selection via analyses of largely overlooked environment–body size interactions. Here, we test all four rules above using a global database spanning 99% of modern species of an entire Order of legless, predominantly underground‐dwelling amphibians (Gymnophiona, or caecilians). We found a consistent effect of increasing precipitation (and resource abundance) on body size reductions (supporting the water conservation hypothesis), while Bergmann's, the seasonality and resource rules are rejected. We argue that subterranean lifestyles minimize the effects of aboveground selection agents, making humidity a dominant selection pressure – aridity promotes larger body sizes that reduce risk of evaporative dehydration, while smaller sizes occur in wetter environments where dehydration constraints are relaxed. We discuss the links between these principles with the physiological constraints that may have influenced the tropically‐restricted global radiation of caecilians.
SummaryPorcine reproductive and respiratory syndrome virus (PRRSV) remains widespread in the North American pig population. Despite improvements in virus characterization, it is unclear whether PRRSV infections are a product of viral circulation within a farm, within production systems (local) or across production systems (external). Here we examined the dissemination dynamics of PRRSV and the processes facilitating its spread within and among pig farms in three production systems. Overall, PRRSV genetic diversity declined since 2018, while phylodynamic results support frequent transmission across-production systems. We found that PRRSV dissemination occurred mostly through transmission between farms of different production companies, which were predominant for several months, especially from November until May when PRRSV tends to peak in the studied region. Within production systems, dissemination occurred mainly through regular pig flow (from sow to nursery and then to finisher farms); nevertheless, an important flux of PRRSV dissemination from finisher to sow and nursery farms highlighted the importance of downstream farms as sources of the virus. Farms at areas with pig density from 500 to 1000 pig/km2 and farms located at a range within 0.5 km and 0.7 km from major roads were more likely to infect by PRRSV, whereas farms at elevation between 41 and 61 meters and denser vegetation acted as dissemination barriers. Although remains a challenge, there is a need to disentangle the route of PRRSV transmission, results evidenced that dissemination among commercially unrelated pig production systems was intense, reinforcing the importance of farm proximity on PRRSV spread. Thus, consideration of farm location and their geographic characteristics may help to forecast dissemination. The understanding of PRRSV transmission routes has the potential to inform targeted strategies for its prevention and control. Further studies are needed to quantify the relative contribution of PRRSV transmission routes.
Chemical communication plays a central role in social, sexual and ecological interactions among animals. However, the macroevolutionary diversification of traits responsible for chemical signaling remains fundamentally unknown. Most research investigating evolutionary diversification of glands responsible for the production of chemical signals has focused on arthropods, while its study among vertebrates remains neglected. Using a global-scale dataset covering > 80% (7,904 species) of the living diversity of lizards and snakes (squamates), we investigate rates, trajectories and phylogenetic patterns of diversification of their follicular glands for chemical communication. We observed these glands in 13.66% of species, that their expression has varying phylogenetic signal among lineages, and that the crown squamate ancestor lacked follicular glands, which therefore originated and diversified subsequently during their evolutionary history. Additionally, our findings challenge the longstanding view that within squamates the Iguania are visually oriented while Scleroglossa are chemically-oriented, given that Iguania doubles Scleroglossa in the frequency of glands. Our phylogenetic analyses identified stabilizing selection as the best model describing follicular gland diversification, and revealed high rates of disparity. We provide the first global-scale analysis investigating the diversification of one of the main forms of communication among reptiles, presenting a macroevolutionary angle to questions traditionally explored at microevolutionary scale.
Aim Body size explains most of the variation in fitness within animal populations and is therefore under constant selection from ecological and reproductive pressures, which often promote its evolution in sex‐specific directions, leading to sexual size dimorphism (SSD). Several hypotheses have been proposed to explain the vast diversity of SSD across species. These hypotheses emphasize: (a) the mate competition benefits to larger male size (sexual selection); (b) the benefits of larger female size for fecundity (fecundity selection); (c) the simultaneous benefits of niche divergence for males and females to reduce intersexual competition for ecological resources (natural selection); and (d) the underlying impact of geographical variation in climatic pressures expected to shape large‐scale patterns of SSD in synergy with the above selection pressures (e.g., intensification of fecundity selection as breeding seasons shorten). Based on a new, global‐scale amphibian dataset, we address the shortage of large‐scale, integrative tests of these four hypotheses. Location Global. Time period Extant. Major taxa studied Class Amphibia. Methods Using a > 3,500 species dataset spanning body size, ecological, life‐history, geographical and climatic data, we performed phylogenetic linear models to address the sexual, fecundity, ecological and climatic hypotheses of SSD. Results Evolution of SSD is discordant between anurans and salamanders. Anuran SSD is shaped by climate (male‐biased SSD increases with temperature seasonality) and by nesting site. In salamanders, SSD converges across species that occupy the same types of microhabitats (“ecodimorphs”), whereas reproductive or climatic pressures have no effects on their SSD. These contrasts are associated with latitudinal gradients of SSD in anurans, but not in salamanders. Main conclusions Amphibian SSD is driven by ecological and climatic pressures, whereas no roles for sexual or fecundity selection were detected. We show that macroevolutionary processes determined by different forms of selection lead to latitudinal patterns of trait diversity, and the lack of them.
Nairobi Sheep Disease virus (NSDv) is a zoonotic and tick-borne disease that can cause over 90% mortality in small ruminants. NSDv has historically circulated in East Africa and has recently emerged in the Asian continent. Despite efforts to control the disease, some regions, mostly in warmer climates, persistently report disease outbreaks. Consequently, it is necessary to understand how environmental tolerances and factors that influence transmission may shed light on its possible emergence in other regions. In this study, we quantified the available literature of NSDv from which occurrence data was extracted. In total, 308 locations from Uganda, Kenya, Tanzania, Somalia, India, Sri Lanka and China were coupled with landscape conditions to reconstruct the ecological conditions for NSDv circulation and identify areas of potential disease transmission risk. Our results identified areas suitable for NSDv in Ethiopia, Malawi, Zimbabwe, Southeastern China, Taiwan, and Vietnam. Unsuitable areas included Democratic Republic of Congo, Zambia, and Southern Somalia. In summary, soil moisture, livestock density, and precipitation predispose certain areas to NSDv circulation. It is critical to investigate the epidemiology of NSDv in order to promote better allocation of resources to control its spread in regions that are more at risk. This will help reduce disease impact worldwide as climate change will favor emergence of such vector-borne diseases in areas with dense small ruminant populations.
Important part of the multivariate selection shaping social and interspecific interactions among and within animal species emerges from communication. Therefore, understanding the diversification of signals for animal communication is a central endeavor in evolutionary biology. Over the last decade, the rapid development of phylogenetic approaches has promoted a stream of studies investigating evolution of communication signals. However, comparative research has primarily focused on visual and acoustic signals, while the evolution of chemical signals remains largely unstudied. An increasing interest in understanding the evolution of chemical communication has been inspired by the realization that chemical signals underlie some of the major interaction channels in a wide range of organisms. In lizards, in particular, chemosignals play paramount roles in female choice and male–male competition, and during community assembly and speciation. Here, using phylogenetic macro‐evolutionary modeling, we show for the very first time that multiple compounds of scents for communication in lizards have diversified following highly different evolutionary speeds and trajectories. Our results suggest that cholesterol, α‐tocopherol, and cholesta‐5,7‐dien‐3‐ol have been subject to stabilizing selection (Ornstein–Uhlenbeck model), whereas the remaining compounds are better described by Brownian motion modes of evolution. Additionally, the diversification of the individual compounds has accumulated substantial relative disparity over time. Thus, our study reveals that the chemical components of lizard chemosignals have proliferated across different species following compound‐specific directions.
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