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Caterpillars of the Neotropical genus Lonomia (Lepidoptera: Saturniidae) are responsible for some fatal envenomation of humans in South America inducing hemostatic disturbances in patients upon skin contact with the caterpillars’ spines. Currently, only two species have been reported to cause hemorrhagic syndromes in humans: Lonomia achelous and Lonomia obliqua. However, species identifications have remained largely unchallenged despite improved knowledge of venom diversity and growing evidence that the taxonomy used over past decades misrepresents and underestimates species diversity. Here, we revisit the taxonomy and distribution of Lonomia using the most extensive dataset assembled to date, combining DNA barcodes, morphological comparisons, and geographical information. Our integrative approach leads to the recognition of 60 species, of which seven are known or strongly suspected to cause severe envenomation in humans. From a newly compiled synthesis of epidemiological data, we also examine the consequences of our results for understanding Lonomia envenomation risks and call for further investigations of other species’ venom activities. This is required and necessary to improve alertness in areas at risk, and to define adequate treatment strategies for envenomed patients, including performing species identification and assessing the efficacy of anti-Lonomia serums against a broader diversity of species.

Invasive alien species (IAS) are a leading driver of biodiversity loss worldwide, and have negative impacts on human societies. In most countries, available data on monetary costs of IAS are scarce, while being crucial for developing efficient management. In this study, we use available data collected from the first global assessment of economic costs of IAS (InvaCost) to quantify and describe the economic cost of invasions in Mexico. This description was made across a range of taxonomic, sectoral and temporal variables, and allowed us to identify knowledge gaps within these areas. Overall, costs of invasions in Mexico were estimated at US$ 5.33 billion (i.e., 109) ($MXN 100.84 billion) during the period from 1992 to 2019. Biological invasion costs were split relatively evenly between aquatic (US$ 1.16 billion; $MXN 21.95 billion) and terrestrial (US$ 1.17 billion; $MXN 22.14 billion) invaders, but semi-aquatic taxa dominated (US$ 2.99 billion; $MXN 56.57 billion), with costs from damages to resources four times higher than those from management of IAS (US$ 4.29 billion vs. US$ 1.04 billion; $MXN 81.17 billion vs $MXN 19.68 billion). The agriculture sector incurred the highest costs (US$ 1.01 billion; $MXN 19.1 billion), followed by fisheries (US$ 517.24 million; $MXN 9.79 billion), whilst most other costs simultaneously impacted mixed or unspecified sectors. When defined, costs to Mexican natural protected areas were mostly associated with management actions in terrestrial environments, and were incurred through official authorities via monitoring, control or eradication. On natural protected islands, mainly mammals were managed (i.e. rodents, cats and goats), to a total of US$ 3.99 million, while feral cows, fishes and plants were mostly managed in protected mainland areas, amounting to US$ 1.11 million in total.Pterygoplichthyssp. andEichhornia crassipescaused the greatest reported costs in unprotected aquatic ecosystems in Mexico, andBemisia tabacito terrestrial systems. Although reported damages from invasions appeared to be fluctuating through time in Mexico, management spending has been increasing. These estimates, albeit conservative, underline the monetary pressure that invasions put on the Mexican economy, calling for urgent actions alongside comprehensive cost reporting in national states such as Mexico.

Invasive alien species are responsible for a high economic impact on many sectors worldwide. Nevertheless, there is a scarcity of studies assessing these impacts in Central and South America. Investigating costs of invasions is important to motivate and guide policy responses by increasing stakeholders’ awareness and identifying action priorities. Here, we used the InvaCost database to investigate (i) the geographical pattern of biological invasion costs across the region; (ii) the monetary expenditure across taxa and impacted sectors; and (iii) the taxa responsible for more than 50% of the costs (hyper-costly taxa) per impacted sector and type of costs. The total of reliable and observed costs reported for biological invasions in Central and South America was USD 102.5 billion between 1975 and 2020, but about 90% of the total costs were reported for only three countries (Brazil, Argentina and Colombia). Costs per species were associated with geographical regions (i.e., South America, Central America and Islands) and with the area of the countries in km2. Most of the expenses were associated with damage costs (97.8%), whereas multiple sectors (77.4%), agriculture (15%) and public and social welfare (4.2%) were the most impacted sectors. Aedes spp. was the hyper-costly taxon for the terrestrial environment (costs of USD 25 billion) and water hyacinth (Eichhornia crassipes) was the hyper-costly taxon for the aquatic environment (USD 179.9 million). Six taxa were classified as hyper-costly for at least one impacted sector and two taxa for at least one type of cost. In conclusion, invasive alien species caused billions of dollars of economic burden in Central and South America, mainly in large countries of South America. Costs caused by invasive alien species were unevenly distributed across countries, impacted sectors, types of costs and taxa (hyper-costly taxa). These results suggest that impacted sectors should drive efforts to manage the species that are draining financial sources.

International audience; Invasive ants are amongst the most destructive and widespread invaders across the globe; they can strongly alter invaded ecosystems and are responsible for the loss of native ant species. Several studies have reported that invasive ants can also lead to substantial economic costs. In this study, we search, describe and analyse 1342 reported costs of invasive ants compiled in the InvaCost database. Economic costs, reported since 1930 for 12 ant species in 27 countries, totalled US dollars 51.93 billion, from which US dollars 10.95 billion were incurred, and US$ 40.98 billion were potential costs (i.e., expected or predicted costs). More than 80% of total costs were associated with only two species, Solenopsis invicta and Wasmannia auropunctata ; and two countries, the USA and Australia. Overall, damage costs amounted to 92% of the total cost, mainly impacting the agriculture, public and social welfare sectors. Management costs were primarily post-invasion management (US dollars 1.79 billion), with much lower amounts dedicated to prevention (US dollars 235.63 million). Besides the taxonomic bias, cost information was lacking for an average of 78% of the invaded countries. Moreover, even in countries where costs were reported, such information was available for only 56% of the invaded locations. Our synthesis suggests that the global costs of invasive ants are massive but largely biased towards developed economies, with a huge proportion of underreported costs, and thus most likely grossly underestimated. We advocate for more and improved cost reporting of invasive ants through better collaborations between managers, practitioners and researchers, a crucial basis for adequately informing future budgets and improving proactive management actions of invasive ants.; El coste económico mundial de las hormigas invasoras Las hormigas invasoras están entre las especies más destructivas y más ampliamente extendidas en todo el mundo. Pueden alterar fuertemente los ecosistemas y son responsables de la pérdida de numerosas especies de hormigas nativas en los ecosistemas invadidos. Muchos estudios han mostrado que las hormigas invasoras pueden producir costes económicos importantes. En este estudio, recopilamos, describimos y analizamos 1342 entradas de costes económicos de hormigas invasoras usando la base de datos InvaCost. Los costes económicos fueron reportados desde 1930, para 12 hormigas invasoras, en 27 países, alcanzando un total de 51.93 mil millones de dólares americanos de los cuales 10.95 mil millones fueron observados (costes reales) mientras que 40.98 mil millones de dólares americanos fueron costes potenciales (es decir, costes esperados, no observados). Más del 80% de los costes totales fueron causados por dos especies: Solenopsis invicta y Wasmannia auropunctata ; y en dos países: Estados Unidos y Australia. Los costes debidos a daños alcanzaron el 92% del total, afectando principalmente a los sectores agrícola y de bienestar social. Los costes de gestión se invirtieron en su mayoría en la gestión de post-invasión (1.79 mil millones de dólares), con montos mucho menores de inversión en prevención (235.63 millones de dólares). A nivel geográfico, falta información de reportes de costes económicos para aproximadamente un 78% de los países invadidos. Además, incluso en los países donde existían costes reportados, dicha información sólo estaba disponible para el 56% de los lugares invadidos. Nuestra síntesis sugiere que los costes globales de las hormigas invasoras son enormes pero en gran medida sesgados hacia las economías desarrolladas, con una gran proporción de costes sin reportar y por lo tanto gravemente subestimados. Exhortamos entonces, a un mayor y mejor reporte de los costes económicos de las hormigas invasoras a través de una mayor colaboración entre gestores, profesionales e investigadores; lo cual es la base crucial para informar adecuadamente presupuestos futuros y mejorar las actuaciones hacia una gestión proactiva de las hormigas invasoras.

Wild silkmoths (Saturniidae) are one of the most emblematic and most studied families of moths. Yet, the absence of a robust phylogenetic framework based on a comprehensive taxonomic sampling impedes our understanding of their evolutionary history. We analyzed 1,024 ultraconserved elements (UCEs) and their flanking regions to infer the relationships among 338 species of Saturniidae representing all described subfamilies, tribes, and genera. We investigated systematic biases in genomic data and performed dating and historical biogeographic analyses to reconstruct the evolutionary history of wild silkmoths in space and time. Using Gene Genealogy Interrogation, we showed that saturation of nucleotide sequence data blurred our understanding of early divergences and first biogeographic events. Our analyses support a Neotropical origin of saturniids, shortly after the Cretaceous-Paleogene extinction event (ca 64.0 [stem] - 52.0 [crown] Ma), and two independent colonization events of the Old World during the Eocene, presumably through the Bering Land Bridge. Early divergences strongly shaped the distribution of extant subfamilies as they showed very limited mobility across biogeographical regions, except for Saturniinae, a subfamily now present on all continents but Antarctica. Overall, our results provide a framework for in-depth investigations into the spatial and temporal dynamics of all saturniid lineages and for the integration of their evolutionary history into further global studies of biodiversity and conservation. Rather unexpectedly for a taxonomically well-known family such as Saturniidae, the proper alignment of taxonomic divisions and ranks with our phylogenetic results leads us to propose substantial rearrangements of the family classification, including the description of one new subfamily and two new tribes.

The regions of the Andes and Caribbean-Mesoamerica are both hypothesized to be the cradle for many Neotropical lineages, but few studies have fully investigated the dynamics and interactions between Neotropical bioregions. The New World hawkmoth genus

International audience; Global insect decline has recently become a cause for major concern, particularly in the tropics where the vast majority of species occurs. Deforestation is suggested as being a major driver of this decline, but how anthropogenic changes in landscape structure affect tropical insect communities has rarely been addressed. We sampled Saturniidae and Sphingidae moths on 27 farms located in Brazilian Amazonia (Para state) and characterised by different deforestation histories. We used functional traits (forewing length, body mass, wing load, trophic niche breadth and resource use strategy), analysed by combining RLQ and null model analyses, to investigate the responses of their taxonomic and functional diversity to landscape change dynamics and current structure. We found that communities had a higher proportion of large and polyphagous species with low wing load in landscapes with low forest quality and relative cover and high land use turnover. This was mainly due to a significant response to deforestation by saturniids, whereas the more mobile sphingids showed no significant landscape-related pattern. We also observed an overall increase of species richness and functional dispersion in landscapes that have been deforested for a long time when compared with more recent agricultural settlements. Our results highlight the complex way in which landscape structure and historical dynamics interact to shape Neotropical moth communities and that saturniid moths respond clearly to the structure of the surrounding landscape, confirming their potential use as an indicator group for environmental monitoring programmes.

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AIM: We test hypotheses on the environmental control of elevational richness patterns of sphingid moths for their global applicability and generality. Specifically, we compare effects of area with climate‐related drivers, such as primary productivity and temperature, while also considering direct effects of precipitation. MAJOR TAXA: Sphingid moths (Lepidoptera). LOCATION: Eighty‐six mountain ranges of the Old World and the Australia/Pacific region, from Scandinavia and Siberia through the African and Australasian tropics to South Africa and Southern Australia. METHODS: We used a large compilation of point locality records for 744 species, in addition to fine‐grained range maps derived from species distribution modelling of these records, to characterize the elevational pattern of species richness in 86 custom‐delineated mountain regions. For both types of data, we compared the effects of environmental drivers on richness by comparing standardized coefficients of multivariate models for pooled data after accounting for between‐region variation in richness. RESULTS: We observed varying patterns of elevational richness across the research region, with a higher prevalence of midpeaks in arid regions. We found overwhelming support for area as a main determinant of richness, modulated by temperature and productivity, whereas we detected no effect of precipitation. MAIN CONCLUSIONS: Area, productivity and temperature are the main environmental predictors explaining a large proportion of variability in sphingid richness. This is consistent not only with other elevational studies, but also with empirical and theoretical biodiversity research in a non‐elevational context (with the caveat of some unresolved issues in elevational area effects). However, distinct differences in elevational patterns remain even within the same mountain ranges when comparing with other Lepidoptera, that is, geometrid moths, which highlights the importance of understanding higher clade differentiation in ecological responses, within insects and in other groups.

The ever-increasing number of introduced species profoundly threatens global biodiversity. While the ecological and evolutionary consequences of invasive alien species are receiving increasing attention, their economic impacts have largely remained understudied, especially in France. Here, we aimed at providing a general overview of the monetary losses (damages caused by) and expenditures (management of) associated with invasive alien species in France. This country has a long history of alien species presence, partly due to its long-standing global trade activities, highly developed tourism, and presence of overseas territories in different regions of the globe, resulting in a conservative minimum of 2,750 introduced and invasive alien species. By synthesizing for the first time the monetary losses and expenditures incurred by invasive alien species in Metropolitan France and French overseas territories, we obtained 1,583 cost records for 98 invasive alien species. We found that they caused a conservative total amount ranging between US$ 1,280 million and 11,535 million in costs over the period 1993–2018. We extrapolated costs for species invading France, for which costs were reported in other countries but not in France, which yielded an additional cost ranging from US$ 151 to 3,030 millions. Damage costs were nearly eight times higher than management expenditure. Insects, and in particular the Asian tiger mosquito Aedes albopictus and the yellow fever mosquito Ae. aegypti, totalled very high economic costs, followed by non-graminoid terrestrial flowering and aquatic plants (Ambrosia artemisiifolia, Ludwigia sp. and Lagarosiphon major). Over 90% of alien species currently recorded in France had no costs reported in the literature, resulting in high biases in taxonomic, regional and activity sector coverages. To conclude, we report alarming costs and even more alarming knowledge gaps. Our results should raise awareness of the importance of biosecurity and biosurveillance in France, and beyond, as well as the crucial need for better reporting and documentation of cost data.

Funding Information: The authors acknowledge the French National Research Agency (ANR-14-CE02-0021) and the BNP-Paribas Foundation Climate Initiative for funding the InvaCost project that allowed the construction of the InvaCost database. The present work was conducted following a workshop funded by the AXA Research Fund Chair of Invasion Biology and is part of the AlienScenario project funded by BiodivERsA and Belmont-Forum call 2018 on biodiversity scenarios. AN acknowledges funding from EXPRO grant no. 19-28807X (Czech Science Foundation) and long-term research development project RVO 67985939 (The Czech Academy of Sciences). CC was supported by Portuguese National Funds through Fundation para a Ci?ncia e a Tecnologia (CEECIND/02037/2017; UIDB/00295/2020 and UIDP/00295/2020). RNC was funded by a research fellowship from the Alexander von Humboldt Foundation. TWB acknowledges funding from the European Union?s Horizon 2020 research and innovation programme under the Marie Sk?odowska-Curie grant no. 747120. MG and CD were funded by the BiodivERsA-Belmont Forum Project ?Alien Scenarios? (BMBF/PT DLR 01LC1807C). NK was partially supported by the Russian Federationn Foundation for Basic Research (grant no.19-04-01029-A) [national literature survey] and the basic project of Sukachev Institute of Forest SB RAS (project no. 0287-2021-0011) [InvaCost database contribution]. DR thanks InEE-CNRS who supports the network GdR 3647 ?Invasions Biologiques?. Funds for AJT, EA and LBM contracts come from the AXA Research Fund Chair of Invasion Biology of University Paris Saclay. BL, DR and FC are French agents (affiliated, respectively, to the Mus?um National d?Histoire Naturelle, University of Rennes and Centre National de la Recherche Scientifique); their salaries, for which they are grateful, are typically not accounted for in assessment of costs on biological invasions. At last, the authors want to express their thanks for the translation of the abstract to other European languages, namely to Paride Balzani, Antonin Kouba, Sandra Hodic, and ROS Educational Consultancy Ltd & Garnock Media Ltd

International audience; AimFuture climate changes may affect species distribution and their genetic diversity, hampering species adaptation to a new climate or tracking the suitable conditions. Amphibians have high sensitivity to environmental degradation and changes in temperature and humidity. Thus, the expected climatic changes by the end-of-century (EOC 2100) may cause local or complete extinction of some species. Here, we address the effects of climate change on genetic and phylogeographical diversity, together with the geographical distribution of the South American treefrog Scinax squalirostris Lutz, 1925. Furthermore, we assess how protected areas will conserve its genetic variation.LocationSouth America.MethodsWe combined Ecological Niche Modelling and genetic simulations to predict the effects of climate change on the geographical distribution, genetic diversity, structure and phylogeographical diversity of Scinax squalirostris, using two scenarios of CO2 emission. We also performed a spatial analysis to investigate the effectiveness of the current Protected Areas (PAs) to preserve the species’ genetic and phylogeographical diversity.ResultsScinax squalirostris' geographical range will potentially increase in the future due to the expansion of suitable areas towards its southern distribution, despite the shrinking of suitable areas in the northern part of its current distribution. Besides the shifts in suitable areas, our findings point to a genetic homogenization across the geographical range of S. squalirostris due to the displacement and loss of genetic ancestry clusters. Although existing PAs are conserving the current genetic diversity, they conserve less phylogeographical diversity than expected by chance. Scinax squalirostris may shift its distribution into areas with lower number of PAs, compromising its future conservation.Main conclusionsClimate change will potentially increase S. squalirostris range size, however, not towards regions where most of the current established PAs are located, hence driving to homogenization and loss of genetic diversity, and leading to a gap of conservation within PAs.

The Saturniidae is one of the most emblematic families of moths, comprising nearly 3000 species distributed globally. In this study, DNA barcode analysis and comparative morphology were combined to describe three new species within the genusAutomeris, which is the most diverse genus in the family.Automeris llanerosDecaëns, Rougerie & Bonilla,sp. nov.,Automeris minerosDecaëns, Rougerie & Bonilla,sp. nov., andAutomeris belemensisDecaëns, Rougerie & Bénéluz,sp. nov.are described from the Colombian Orinoco watershed, the Colombian Eastern Cordillera, and the area of endemism of Belém in the Brazilian Amazonia, respectively. They all belong to theAutomeris bilinea(Walker, 1855) species subgroup, which comprises a number of species that are sometimes difficult to distinguish from each other using morphology alone. Here, the description of these three new species is based on significant differences from their closest relatives, either in terms of wing patterns, genitalia, DNA barcodes or a combination of these features.

Invasive species can have severe impacts on ecosystems, economies, and human health. Though the economic impacts of invasions provide important foundations for management and policy, up-to-date syntheses of these impacts are lacking. To produce the most comprehensive estimate of invasive species costs within North America (including the Greater Antilles) to date, we synthesized economic impact data from the recently published InvaCost database. Here, we report that invasions have cost the North American economy at least US$ 1.26 trillion between 1960 and 2017. Economic costs have climbed over recent decades, averaging US$ 2 billion per year in the early 1960s to over US$ 26 billion per year in the 2010s. Of the countries within North America, the United States (US) had the highest recorded costs, even after controlling for research effort within each country ($5.81 billion per cost source in the US). Of the taxa and habitats that could be classified in our database, invasive vertebrates were associated with the greatest costs, with terrestrial habitats incurring the highest monetary impacts. In particular, invasive species cumulatively (from 1960–2017) cost the agriculture and forestry sectors US$ 527.07 billion and US$ 34.93 billion, respectively. Reporting issues (e.g., data quality or taxonomic granularity) prevented us from synthesizing data from all available studies. Furthermore, very few of the known invasive species in North America had reported economic costs. Therefore, while the costs to the North American economy are massive, our US$ 1.26 trillion estimate is likely very conservative. Accordingly, expanded and more rigorous economic cost reports are necessary to provide more comprehensive invasion impact estimates, and then support data-based management decisions and actions towards species invasions.

International audience; Background: Herbivorous insects represent a major fraction of global biodiversity and the relationships they have established with their food plants range from strict specialists to broad generalists. Our knowledge of these relationships is of primary importance to basic (e.g. the study of insect ecology and evolution) and applied biology (e.g. monitoring of pest or invasive species) and yet remains very fragmentary and understudied. In Lepidoptera, caterpillars of families Saturniidae and Sphingidae are rather well known and considered to have adopted contrasting preferences in their use of food plants. The former are regarded as being rather generalist feeders, whereas the latter are more specialist. New information: To assemble and synthesise the vast amount of existing data on food plants of Lepidoptera families Saturniidae and Sphingidae, we combined three major existing databases to produce a dataset collating more than 26,000 records for 1256 species (25% of all species) in 121 (67%) and 167 (81%) genera of Saturniidae and Sphingidae, respectively. This dataset is used here to document the level of polyphagy of each of these genera using summary statistics, as well as the calculation of a polyphagy score derived from the analysis of Phylogenetic Diversity of the food plants used by the species in each genus.

The range size of species co-occurring in local assemblages is a pivotal variable in assessments of a site’s conservation value. Assemblages featuring many small-ranged species are given more priority than assemblages consisting mainly of wide-ranging species. However, the assembly of relevant information can be challenging and local range size distributions of tropical invertebrates are rarely available for conservation planning. We present such data for sphingid moths in East Africa, a highly diverse region of high conservation value. We compare geographic range size distributions based on field samples with predictions from modelled range map data. Using this system as a case study, we provide evidence for a systematic sampling bias when inferring average local range sizes from field data. Unseen species (i.e., species present but missed in local sampling) are often those with small ranges (hence, of high conservation value). Using an elevational gradient, we illustrate how this bias can lead to false, counterintuitive assessments of environmental effects on local range size distributions. Furthermore, with particular reference to sphingid moths in the study region, we show that current protected areas appear unrelated to the spatial distribution of species richness or average geographic range sizes at a local scale. We discuss the need to treat field sampled data with caution and in concert with other data sources such as probabilistic models.

Despite the huge biodiversity of the Cerrado biome, a synthesis on the distribution of genetic diversity across the biome is still wanting. We describe patterns of plant genetic variation across the Cerrado biome, highlighting areas of high diversity and priority areas for conservation. We also analyze the relative importance of environmental characteristics and human footprints on patterns of genetic variation. Raw genetic data comes primarily from central and southeastern Brazil, outside conservation units (CUs). Standardized estimated genetic richness (Gest) decreases in a north–south gradient. Populations with high genetic diversity (He) and allelic richness (AR) are widespread across the biome, but both increase with distance from the center of Cerrado. Environmental variables related to energy, temperature and precipitation are associated with Gest and AR, but not He. Gest is higher in northern Cerrado, in regions with low human development index (HDI). Conversely, southern Cerrado shows higher HDI and lower genetic richness, most likely due to both high habitat fragmentation and loss. CUs in northern Cerrado tend to have higher Gest, whereas those in southeast and central Cerrado have higher He and AR. The high genetic diversity and richness in the few populations studied in northern Cerrado, coupled with the low data availability, reveal the importance of encouraging genetic studies in this region. Moreover, very limited information about population genetic diversity is available from CUs, which may constrain the access of species conservation status and decision-make on management of populations inside CUs.

Aim To map the spatial variation of range sizes within sphingid moths, and to test hypotheses on its environmental control. In particular, we investigate effects of climate change velocity since the Pleistocene and the mid-Holocene, temperature and precipitation seasonality, topography, Pleistocene ice cover, and available land area. Location Old World and Australasia, excluding smaller islands. Methods We used fine-grained range maps (based on expert-edited distribution modelling) for all 972 sphingid moth species in the research region and calculated, at a grain size of 100 km, the median of range sizes of all species that co-occur in a pixel. Climate, topography and Pleistocene ice cover data were taken from publicly available sources. We calculated climate change velocities (CCV) for the last 21 kyr as well as 6 kyr. We compared the effects of seasonality and CCV on median range sizes with spatially explicit models while accounting for effects of elevation range, glaciation history and available land area. Results Range sizes show a clear spatial pattern, with highest median values in deserts and arctic regions and lowest values in isolated tropical regions. Range sizes were only weakly related to absolute latitude (predicted by Rapoport's effect), but there was a strong north-south pattern of range size decline. Temperature seasonality emerged as the strongest environmental correlate of median range size, in univariate as well as multivariate models, whereas effects of CCV were weak and unstable for both time periods. These results were robust to variations in the parameters in alternative analyses, among them multivariate CCV. Main conclusions Temperature seasonality is a strong correlate of spatial range size variation, while effects of longer-term temperature change, as captured by CCV, received much weaker support.

Restricted gene flow may lead to the loss of genetic diversity and higher genetic differentiation among populations, but the genetic consequences of megafauna extinction for plant populations still remain to be assessed. We performed a phylogenetic-independent meta-analysis across 102 Neotropical plants to test the hypothesis that plant species with megafaunal seed dispersal syndrome have a lower genetic diversity and a higher genetic differentiation than those without it. We classified as megafauna-dependent plant species those that potentially relied only on megafauna to seed dispersal, and as megafauna-independent those that relied on megafauna and other seed dispersers. Our data comprised 98 studies using microsatellite markers. We found no statistical difference in genetic diversity and differentiation between plants with megafauna and non-megafauna seed dispersal syndrome, although the statistical power to detect differences in genetic differentiation was low. Moreover, we found no statistical difference between megafauna-dependent and megafauna-independent plant species. We then used generalized linear mixed models and phylogenetic generalized least square models to investigate the effects of megafaunal seed dispersal syndromes and reproductive traits on variation in genetic diversity and genetic differentiation. We found no effect of megafaunal syndrome, rather, reproductive traits, such as pollination mode, mating, and breeding systems, showed significant effects. Our findings show that the genetic studies of Neotropical plants performed so far show no difference in genetic diversity and differentiation in plants with megafaunal compared to those with non-megafaunal seed dispersal syndromes. Our results also provide evidence pointing out that plant species with megafaunal seed dispersal syndromes may have used different strategies to counterbalance the extinction of their mutualistic megafauna dispersers, such as the dispersal by extant mammals that may promote long-distance seed dispersal. Our results also reinforce the importance of pollination to long-distance gene flow in Neotropical plants.

Our knowledge of global biodiversity remains incomplete and beset by knowledge shortfalls affecting both the census of species (i.e. the Linnean shortfall) and our understanding of their distributions (i.e. the Wallacean shortfall; Hortal et al. 2015). While alarming rates of species extinction have been reported in most groups of organisms, our capacity to assess extinction threats is limited by these shortfalls and it has become imperative to optimize our use of existing information for the analyses of biodiversity data. There are two major challenges when integrating biodiversity data from heterogeneous sources to ultimately analyzing them: The frequent disparity in taxon names used to refer to the same organisms; Geographical inconsistencies on specimen information. The frequent disparity in taxon names used to refer to the same organisms; Geographical inconsistencies on specimen information. The first refers to disagreements about the taxon concepts attached to names alongside the different interpretations and applications (e.g. gender agreement in taxonomic names) of the existing nomenclatural rules that ensure universality and stability of scientific names. The development of new methods for species delineation, and in particular with the growing integration of genetic data in the practice of taxonomy (e.g. DNA barcoding; Ratnasingham and Hebert 2013), has increased our ability to discriminate closely related species. This enhances the resolution level at which biodiversity is documented, described and analyzed(Goldstein and DeSalle 2011). One frequent outcome is the redefinition of species boundaries; either through merging (synonymy) or splitting of previously recognized species. In understudied groups such as insects, the resulting inflation of names, sometimes provisional, further defies the reconciliation of names used by different sources. The second challenge refers to the completeness and accuracy of geographical information. Specimen records in biodiversity databases often lack GPS coordinates. Consequently we need to accurately infer the latitude and longitude from place names. Other frequent inaccuracies include erroneous georeferencing, imprecision and/or error in the location of a record (Soberón and Peterson 2004). Integration of data on the basis of taxon names and their geographic information is a major challenge that either results in excluding a significant number of records, or in merging incompatible records, leading to erroneous outcomes. Therefore, we have developed WF.ACTIAS, a computational workflow that gathers data from several sources and provides the user with tools to make objective and reproducible decisions to assign records to a consensus species name, while detecting and correcting geographical inconsistencies. Its main objective is to automate a process that can integrate information about nomenclature, taxon concepts and geographical information to reconcile taxon names from different sources. Here, we present the WF.ACTIAS workflow in the context of the analysis of diversity in two sister families of moths – the Saturniidae and Sphingidae. Species boundaries in these insects have been thoroughly and comprehensively revisited through the integration of DNA barcodes and we are tackling the reconciliation of taxon names in ca. 282 000 records of which more than 77 000 have DNA barcodes. The outcome of this data integration is essential to study patterns of biodiversity and distributions and sets the ground to extend this process to other groups of organisms.

Made available in DSpace on 2018-12-11T17:30:57Z (GMT). No. of bitstreams: 0 Previous issue date: 2017-04-01 Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) Understanding how historical and current environmental suitability and human impacts affect the genetic diversity on a large scale is essential to species management planning. However, most studies in conservation genetics are carried out at a local or regional scale and rarely on broad spatial scales such as an entire biome. We evaluated the relative contribution of historical and current environmental suitability, current landscape features and human impacts to explain genetic diversity, allelic richness and inbreeding variation among populations, using Euterpe edulis and the Atlantic forest as the model system. We fitted linear mixed models within a multiple competing hypotheses approach with model selection based on Akaike’s Information Criteria. We showed that overall genetic diversity was lower in sites with absence of large seed dispersers and higher in sites with historically stable climate. Both seedling and adults showed to be negatively influenced by human impact factors; with adults mainly affected by the reduction of forest cover while seedlings by the loss of large seed dispersers. Thus, the current pattern of genetic diversity in E. edulis is the result of historical instability during the mid-Holocene and recent anthropogenic impacts, mainly those that affect important ecological process such as seed dispersal. Thus, an efficient plan for species conservation must account for human impacts and environmental suitability and also assess the genetic diversity of seedlings and adults in fragmented landscapes. Laboratório de Genética & Biodiversidade Universidade Federal de Goiás Departamento de Ecologia Universidade Estadual Paulista (UNESP) Laboratório de Marcadores Moleculares Centro de Biotecnologia e Genética Universidade Estadual de Santa Cruz, Rodovia Ilhéus-Itabuna, km 16 Departamento de Ecologia Universidade Estadual Paulista (UNESP) FAPESP: 2014/01029-5 CNPq: 401258/2012-2 CNPq: 445353/2014-7 FAPESP: 2013/50421-2 CAPES: 88881.030318/2013-01 CAPES: 88881.068425/2014-01

International audience; Background: Bombycoidea is an ecologically diverse and speciose superfamily of Lepidoptera. The superfamily includes many model organisms, but the taxonomy and classification of the superfamily has remained largely in disarray. Here we present a global checklist of Bombycoidea. Following Zwick (2008) and Zwick et al. (2011), ten families are recognized: Anthelidae, Apatelodidae, Bombycidae, Brahmaeidae, Carthaeidae, Endromidae, Eupterotidae, Phiditiidae, Saturniidae and Sphingidae. The former families Lemoniidae and Mirinidae are included within Brahmaeidae and Endromidae respectively. The former bombycid subfamilies Oberthueriinae and Prismostictinae are also treated as synonyms of Endromidae, and the former bombycine subfamilies Apatelodinae and Phitditiinae are treated as families.New information: This checklist represents the first effort to synthesize the current taxonomic treatment of the entire superfamily. It includes 12,159 names and references to their authors, and it accounts for the recent burst in species and subspecies descriptions within family Saturniidae (ca. 1,500 within the past 10 years) and to a lesser extent in Sphingidae (ca. 250 species over the same period). The changes to the higher classification of Saturniidae proposed by Nässig et al. (2015) are rejected as premature and unnecessary. The new tribes, subtribes and genera described by Cooper (2002) are here treated as junior synonyms. We also present a new higher classification of Sphingidae, based on Kawahara et al. (2009), Barber and Kawahara (2013) and a more recent phylogenomic study by Breinholt et al. (2017), as well as a reviewed genus and species level classification, as documented by Kitching (2018).

Despite their vast diversity and vital ecological role, insects are notoriously underrepresented in biogeography and conservation, and key broad-scale ecological hypotheses about them remain untested – largely due to generally incomplete and very coarse spatial distribution knowledge. Integrating records from publications, field work and natural history collections, we used a mixture of species distribution models and expert estimates to provide geographic distributions and emergent richness patterns for all ca 1000 sphingid moth species found outside the Americas in high spatial detail. Total sphingid moth richness, the first for a higher insect group to be documented at this scale, shows distinct maxima in the wet tropics of Africa and the Oriental with notable decay toward Australasia. Using multivariate models controlling for spatial autocorrelation, we found that primary productivity is the dominant environmental variable associated with moth richness, while temperature, contrary to our predictions, is an unexpectedly weak predictor. This is in stark contrast to the importance we identify for temperature as a niche variable of individual species. Despite divergent life histories, both main sub-groups of moths exhibit these relationships. Tribal-level deconstruction of richness and climatic niche patterns indicate idiosyncratic effects of biogeographic history for some of the less species-rich tribes, which in some cases exhibit distinct richness peaks away from the tropics. The study confirms, for a diverse insect group, overall richness associations of remarkable similarity to those documented for vertebrates and highlights the significant within-taxon structure that underpins emergent macroecological patterns. Results do not, however, meet predictions from vertebrate-derived hypotheses on how thermoregulation affects the strength of temperature–richness effects. Our study thus broadens the taxonomic focus in this data-deficient discourse. Our procedures of processing incomplete, scattered distribution data are a template for application to other taxa and regions.

Aim To investigate the contribution to range filling, range extent and climatic niche space of species of information contained in the largest databank of digitized biodiversity data: the global biodiversity information facility (GBIF). We compared such information with a compilation of independent distributional data from natural history collections and other sources. Location Europe. Methods We used data for the hawkmoths (Lepidoptera, family Sphingidae) to assess three aspects of range information: (1) observed range filling in 100 km × 100 km grid cell squares, (2) observed European range extent and (3) observed climatic niche. Range extents were calculated as products of latitudinal and longitudinal extents. Areas derived from minimum convex polygons drawn onto a 2-dimensional niche space representing the two main axes of a principal component analysis (PCA) were used to calculate climatic niche space. Additionally, record-based permutation tests for niche differences were carried out. Results We found that GBIF provided many more distribution records than independent compilation efforts, but contributed less information on range filling, range extent and climatic niches of species. Main conclusions Although GBIF contributed relevant additional information, it is not yet an effective alternative to manual compilation and databasing of distributional records from collections and literature sources, at least in lesser-known taxa such as invertebrates. We discuss possible reasons for our findings, which may help shape GBIF strategies for providing more informative data.

The high rates of future climatic changes, compared with the rates reported for past changes, may hamper species adaptation to new climates or the tracking of suitable conditions, resulting in significant loss of genetic diversity. Trees are dominant species in many biomes and because they are long-lived, they may not be able to cope with ongoing climatic changes. Here, we coupled ecological niche modelling (ENM) and genetic simulations to forecast the effects of climatic changes on the genetic diversity and the structure of genetic clusters. Genetic simulations were conditioned to climatic variables and restricted to plant dispersal and establishment. We used a Neotropical savanna tree as species model that shows a preference for hot and drier climates, but with low temperature seasonality. The ENM predicts a decreasing range size along the more severe future climatic scenario. Additionally, genetic diversity and allelic richness also decrease with range retraction and climatic genetic clusters are lost for both future scenarios, which will lead genetic variability to homogenize throughout the landscape. Besides, climatic genetic clusters will spatially reconfigure on the landscape following displacements of climatic conditions. Our findings indicate that climate change effects will challenge population adaptation to new environmental conditions because of the displacement of genetic ancestry clusters from their optimal conditions.

AIM: Many taxa, especially invertebrates, remain biogeographically highly understudied and even baseline assessments are missing, with too limited and heterogeneous sampling being key reasons. Here we set out to assess the human geographic and associated environmental factors behind inventory completeness for the hawkmoths of Africa. We aim to separate the causes of differential sampling from those affecting gradients of species richness to illustrate a potential general avenue for advancing knowledge about diversity in understudied groups. Location Sub-Saharan Africa. METHODS: Using a database of distributional records of hawkmoths, we computed rarefaction curves and estimated total species richness across 200 km × 200 km grid cells. We fitted multivariate models to identify environmental predictors of species richness and used environmental co-kriging to map region-wide diversity patterns. We estimated cell-wide inventory completeness from observed and estimated data, and related these to human geographic factors. RESULTS: Observed patterns of hawkmoths species richness are strongly determined by the number of available records in grid cells. Both show spatially structured distributions. Variables describing vegetation type, emerge as important predictors of estimated total richness, and variables capturing heat, energy availability and topographic heterogeneity all show a strong positive relationship. Patterns of interpolated richness identify three centres of diversity: Cameroon coastal mountains, and the northern and southern East African montane areas. Inventory completeness is positively influenced by population density, accessibility, protected areas and colonial history. Species richness is still under-recorded in the western Congo Basin and southern Tanzania/Mozambique. MAIN CONCLUSIONS: Sampling effort is highly biased and controlling for it in large-scale compilations of presence-only data is critical for drawing inferences from our still limited knowledge of invertebrate distributions. Our study shows that a baseline of estimate of broad-scale diversity patterns in understudied taxa can be derived from combining numerical estimators of richness, models of main environmental effects and spatial interpolation. Inventory completeness can be partly predicted from human geographic features and such models may offer fruitful guidance for prioritization of future sampling to further refine and validate estimated patterns of species richness.

Aim: Conservation studies often investigate the biodiversity of one taxonomic group with the expectation that it reflects biodiversity of other taxa as well. However, previous studies have found that biodiversity patterns are often only weakly correlated across ecologically very different taxa. Using three arthropod taxa that share the same habitat, utilize similar resources and are sampled with identical technique, we investigate the applicability of two levels of biodiversity indication: (1) prediction of biodiversity patterns, and (2) inference of environment–biodiversity relationships. The second aspect is of high relevance to applied conservation management yet mostly neglected, at least in terrestrial systems, when discussing the indicator concept. Location: Northern Switzerland Methods: We used a very large data set of pitfall trap samples from different habitats for three taxonomic groups (Carabidae, Staphylinidae and Araneae). We quantified biodiversity by different metrics of local diversity (species richness, effective number of species) and of pairwise faunal dissimilarities (Sorensen, Bray–Curtis). We investigated the congruence of (1) biodiversity patterns by cross-taxa regressions, and (2) environmental models of biodiversity by comparing fitted coefficients, and resulting extrapolations across the research region. Results: We found positive yet not very strong correlations in biodiversity patterns, while environmental models differed considerably between taxa as well as between diversity metrics. Main conclusions: Inferences of environment–biodiversity relationships can differ between taxonomic groups even if biodiversity patterns alone show significant correlation. This may be either because species indeed respond differently to environmental variation or because of misspecifications inherent in ecological modelling. Both possibilities suggest a need for caution in selecting and applying biodiversity indicators. Furthermore, the choice of diversity metric can strongly affect results, and therefore, decisions about which metric to use in any given situation need to be made carefully.

Over the last two decades, macroecology – the analysis of large-scale, multi-species ecological patterns and processes – has established itself as a major line of biological research. Analyses of statistical links between environmental variables and biotic responses have long and successfully been employed as a main approach, but new developments are due to be utilized. Scanning the horizon of macroecology, we identifi ed four challenges that will probably play a major role in the future. We support our claims by examples and bibliographic analyses. 1) Integrating the past into macroecological analyses, e.g. by using paleontological or phylogenetic information or by applying methods from historical biogeography, will sharpen our understanding of the underlying reasons for contemporary patterns. 2) Explicit consideration of the local processes that lead to the observed larger-scale patterns is necessary to understand the fi ne-grain variability found in nature, and will enable better prediction of future patterns (e.g. under environmental change conditions). 3) Macroecology is dependent on large-scale, high quality data from a broad spectrum of taxa and regions. More available data sources need to be tapped and new, small-grain large-extent data need to be collected. 4) Although macroecology already lead to mainstreaming cuttingedge statistical analysis techniques, we fi nd that more sophisticated methods are needed to account for the biases inherent to sampling at large scale. Bayesian methods may be particularly suitable to address these challenges. To continue the vigorous development of the macroecological research agenda, it is time to address these challenges and to avoid becoming too complacent with current achievements.

Agrius cingulata (Lepidoptera, Sphingidae) is widespread in the Americas, but has recently begun to spread into Africa. In parts of its native range, the species is a pest of sweet potato, which is an important crop plant in Africa. We used two types of ecological niche models, based on native distribution records and climate and vegetation structure data, to estimate which regions of Africa are potentially suitable for the species to become established. The results show that, under the simplifying assumption that the species will occupy the same ecological niche in Africa as in its native range, A. cingulata may find a suitable habitat across wide stretches of sub-Saharan Africa. We conclude that early monitoring programmes of the spread and actual status of the species in Africa may be worthwhile implementing.

We studied genetic diversity and differentiation patterns in Neotropical plants to address effects of life history traits (LHT) and ecological attributes based on an exhaustive literature survey. We used generalized linear mixed models (GLMMs) to test the effects as fixed and random factors of growth form, pollination and dispersal modes, mating and breeding systems, geographical range and habitat on patterns of genetic diversity (HS, HeS, π and h), inbreeding coefficient (FIS), allelic richness (AR) and differentiation among populations (FST) for both nuclear and chloroplast genomes. In addition, we used phylogenetic generalized least squares (pGLS) to account for phylogenetic independence on predictor variables and verify the robustness of the results from significant GLMMs. In general, GLMM revealed more significant relationships among LHTs and genetic patterns than pGLS. After accounting for phylogenetic independence (i.e., using pGLS), FST for nuclear microsatellites was significantly related to pollination mode, mating system and habitat. Plants specifically with outcrossing mating system had lower FST. Moreover, AR was significantly related to pollination mode and geographical range and HeS for nuclear dominant markers was significantly related to habitat. Our findings showed that different results might be retrieved when phylogenetic non-independence is taken into account and that LHTs and ecological attributes affect substantially the genetic pattern in Neotropical plants, hence may drive key evolutionary processes in plants.

The coexistence of numerous tree species in tropical forests is commonly explained by negative dependence of recruitment on the conspecific seed and tree density due to specialist natural enemies that attack seeds and seedlings ('Janzen-Connell' effects). Less known is whether guilds of shared seed predators can induce a negative dependence of recruitment on the density of different species of the same plant functional group. We studied 54 plots in tropical forest on Barro Colorado Island, Panama, with contrasting mature tree densities of three coexisting large seeded tree species with shared seed predators. Levels of seed predation were far better explained by incorporating seed densities of all three focal species than by conspecific seed density alone. Both positive and negative density dependencies were observed for different species combinations. Thus, indirect interactions via shared seed predators can either promote or reduce the coexistence of different plant functional groups in tropical forest.

[This corrects the article DOI: 10.1371/journal.pone.0158660.].

Many amphibian lineages show terrestrialization of their reproductive strategy and breeding is partially or completely independent of water. A number of causal factors have been proposed for the evolution of terrestrialized breeding. While predation has received repeated attention as a potential factor the influence of other factors such as habitat has never been tested using appropriate data or methods. Using a dataset that comprises 180 amphibian species from various East African habitats we tested whether species occurring in different habitats show different patterns of terrestrialization in their breeding strategy. We recovered a significant association between terrestrialized breeding strategies and forest habitats. In general forest seems to act as a facilitator providing a permissive environment for the evolution of terrestrialized breeding strategies. However while terrestrial oviposition is strongly correlated with lowland and montane forest habitat complete terrestrial development is significantly correlated with montane forest only indicating different selective pressures acting at different steps towards complete terrestrial development. © 2013 The Author(s) Published by the Royal Society.