Despite claims of an insect decline worldwide, our understanding of extinction risk in insects is incomplete. Using bionomic data of all odonate (603 dragonflies and damselflies) North American species, we assessed (i) regional extinction risk and whether this is related to local extirpation; (ii) whether these two patterns are similar altitudinally and latitudinally; and (iii) the areas of conservation concern. We used geographic range size as a predictor of regional extinction risk and body size, thermal limits and habitat association as predictors of local extirpation. We found that (i) greater regional extinction risk is related to narrow thermal limits, lotic habitat use and large body size (this in damselflies but not dragonflies); (ii) southern species are more climate tolerant but with more limited geographic range size than northern species; and (iii) two priority areas for odonate conservation are the cold temperate to sub-boreal northeastern USA and the transversal neo-volcanic system. Our approach can be used to estimate insect extinction risk as it compensates for the lack of abundance data.

1. Analysis of geographic patterns of extinction must be accompanied by knowledge of biodiversity patterns. Such analysis is not yet available in insects given three shortfalls. First, knowledge of insect species' distribution is poor. Second, insect inventories have taxonomic, geographical, temporal and habitat biases. Third, the accelerated loss of insect species likely surpasses the rate at which the authors are discovering new species.2. The authors have examined the state of the art of knowledge of the geographical distribution of insect extinction risk and diversity, as well as their relation with human footprint.3. Insect records are highly scattered. Geographically, inventories are incomplete worldwide, except for some areas in Europe. Although the description of new insect species has increased in the last 40 years, this is biased towards lepidopterans and coleopterans. Comparably, IUCN-listed species has also increased in the last 40 years, yet with biases towards odonates and lepidopterans. Likewise, aquatic species have been more intensively sampled and considered by the IUCN than terrestrial species. Of high priority are some pristine areas but with few insect records, whereas the east coast of the United States, Europe and Japan raise concerns given that the human footprint exceeded the species richness of insects registered.

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Mexico is one of the most biodiverse countries in the world, with an important proportion of endemism mainly because of the convergence of the Nearctic and Neotropical biogeographic regions, which generate great diversity and species turnover at different spatial scales. However, most of our knowledge of the Mexican ant biota is limited to a few well‐studied taxa, and we lack a comprehensive synthesis of ant biodiversity information. For instance, most of the knowledge available in the literature on Mexican ant fauna refers only to species lists by states, or is focused on only a few regions of the country, which prevents the study of several basic and applied aspects of ants, from diversity and distribution to conservation. Our aims in this data paper are therefore (1) to compile all the information available regarding ants across the Mexican territory, and (2) to identify major patterns in the gathered data set and geographic gaps in order to direct future sampling efforts. All records were obtained from raw data, including both unpublished and published information. After exhaustive filtering and updating information and synonyms, we compiled a total of 21,731 records for 887 ant species distributed throughout Mexico from 1894 to 2018. These records were concentrated mainly in the states of Chiapas (n = 6,902, 32.76%) and Veracruz de Ignacio de la Llave (n = 4,329, 19.92%), which together comprise half the records. The subfamily with the highest number of records was Myrmicinae (n = 10,458 records, 48.12%), followed by Formicinae (n = 3,284, 15.11%) and Ponerinae (n = 1,914, 8.8%). Most ant records were collected in the Neotropical region of the country (n = 12,646, 58.19%), followed by the Mexican transition zone (n = 5,237, 24.09%) and the Nearctic region (n = 3,848, 17.72%). Native species comprised 95.46% of the records (n = 20,745). To the best of our knowledge, this is the most complete data set available to date in the literature for the country. We hope that this compilation will encourage researchers to explore different aspects of the population and community research of ants at different spatial scales, and to aid in the establishment of conservation policies and actions. There are no copyright restrictions. Please cite this data paper when using its data for publications or teaching events.

Insects are reportedly experiencing widespread declines, but we generally have sparse data on their abundance. Correcting this shortfall will take more effort than professional entomologists alone can manage. Volunteer nature enthusiasts can greatly help to monitor the abundance of dragonflies and damselflies (Odonata), iconic freshwater sentinels and one of the few nonpollinator insect groups appreciated by the public and amenable to citizen science. Although counting individual odonates is common in some locations, current data will not enable a global perspective on odonate abundance patterns and trends. Borrowing insight from butterfly monitoring efforts, we outline basic plans for a global volunteer network to count odonates, including organizational structure, advertising and recruiting, and data collection, submission, and synthesis. We hope our proposal serves as a catalyst for richer coordinated efforts to understand population trends of odonates and other insects in the Anthropocene.

Sexual selection theory indicates that ornament expression in males is in close relation to their condition. This “honesty” relationship serves as the basis for female choice: Females would mate with healthy males over sick males after assessing male ornament signal expression and derive benefits for their progeny. Here, we investigated female mate choice for infected and non‐infected males, male survival after infection (to corroborate the negative effect of infection), and fitness consequences of female preferences using Tenebrio molitor beetles. Male infection was produced having two types of challenges as follows: males infected with entomopathogenic fungi and males infected with nylon implants. Similar to previous studies, we corroborated that females preferred fungus‐infected males over positive control, negative control, and nylon‐challenged males. Survival was the lowest for fungus‐treated males followed by nylon‐treated and control males. Females mated with fungus‐treated males laid fewer and smaller eggs, and the laid eggs had less lipid content with a reduced eclosion success compared to females mated with non‐challenged males. Our interpretation is that fungus‐treated males invested their energetic resources to increase their attractiveness at the risk of survival, in a terminal investment fashion. Females, however, would have corrected their choice by investing less in their offspring.

The taxonomic diversity (TD) of tropical flora and fauna tends to increase during secondary succession. This increase may be accompanied by changes in functional diversity (FD), although the relationship between TD and FD is not well understood. To explore this relationship, we examined the correlations between the TD and FD of ants and forest age in secondary forests at the α‐ and β‐diversity levels using single‐ and multi‐trait‐based approaches. Our objectives were to understand ant diversity patterns and to evaluate the role of secondary forests in the conservation of biodiversity and in the resilience of tropical forests. Ant assemblages were sampled across a chronosequence in the Lacandon region, Mexico. All species were characterized according to 12 functional ecomorphological traits relevant to their feeding behavior. We found that TD and FD were related to forest age at the alpha level, but not at the beta level. α‐functional richness and divergence increased linearly with species richness and diversity, respectively. Also, the relationship between taxonomic and functional turnover was linear and positive. Our results indicated that functional traits were complementary across the chronosequence. The increase in FD was mainly driven by the addition of rare species with relevant traits. The older secondary forests did not recover all of the functions of old growth forest but did show a tendency to recovery. Because older successional stages support more TD and FD, we suggest developing agriculture and forestry management practices that facilitate rapid post‐agricultural succession and thereby better preserve the functionality of tropical forests.

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