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Olixon testaceum is a widely distributed species of brachypterous parasitoid wasp (Vespoidea: Rhopalosomatidae) occurring in Meso- and South America, but little is known of its biology. Here, the first known host of O. ? testaceum is identified as the cricket Anaxipha sp. (Grylloidea: Trigonidiidae) through DNA barcoding of six Olixon larvae and their hosts. Barcoding results also indicated substantial genetic diversity within nominal O. testaceum specimens. The number of species and statistical significance of these groups were tested using Maximum Likelihood phylogenies, distance-based cluster analyses, and coalescence models. All analyses revealed at least six distinct lineages, which suggests six or more cryptic species within O. ? testaceum. Combined with what is currently known about Rhopalosoma host use, these results indicate that rhopalosomatids may be generalist rather than specialist parasitoids, and further confirm the benefits of open global collaboration and DNA barcoding in advancing taxonomic knowledge.

Abstract Global biodiversity gradients are generally expected to reflect greater species replacement closer to the equator. However, empirical validation of global biodiversity gradients largely relies on vertebrates, plants, and other less diverse taxa. Here we assess the temporal and spatial dynamics of global arthropod biodiversity dynamics using a beta-diversity framework. Sampling includes 129 sampling sites whereby malaise traps are deployed to monitor temporal changes in arthropod communities. Overall, we encountered more than 150,000 unique barcode index numbers (BINs) (i.e. species proxies). We assess between site differences in community diversity using beta-diversity and the partitioned components of species replacement and richness difference. Global total beta-diversity (dissimilarity) increases with decreasing latitude, greater spatial distance and greater temporal distance. Species replacement and richness difference patterns vary across biogeographic regions. Our findings support long-standing, general expectations of global biodiversity patterns. However, we also show that the underlying processes driving patterns may be regionally linked.

Foliage-feeding wild caterpillars have been collected and reared year-round by 1–30 rural resident parataxonomists in the Area de Conservación Guanacaste (ACG) in northwestern Costa Rica since 1978. The aim of the work was to describe the diversity and interactions of Lepidoptera and their associations with larval food plants and parasitoids in a diverse tropical community. A total of 457,816 caterpillars developed into a moth or butterfly, and these were identified to the family and species/morphospecies, with 151,316 having been successfully barcoded and assigned a Barcode Index Number (BIN) and/or “scientific name”. The host food plant was usually identified to the species or morphospecies. In addition to adult moths and butterflies, rearings also yielded many hundreds of species of parasitic wasps and tachinid flies, many of which were also DNA-barcoded and assigned a name and/or BIN. Increasingly over recent years, these have been identified or described by expert taxonomists. Here, we provide a summary of the number of species of ichneumonoid (Ichneumonidae and Braconidae) parasitoids of the caterpillars, their hosts, the host food plants involved, the bi- and tritrophic interactions, and their relationships to the caterpillar sampling effort. The dataset includes 16,133 and 9453 independent rearings of Braconidae and Ichneumonidae, respectively, collectively representing 31 subfamilies, all with parasitoid barcodes and host and host food plant species-level identifications. Host caterpillars collectively represented 2456 species, which, in turn, were collectively eating 1352 species of food plants. Species accumulation curves over time for parasitoids, hosts, and plants show various asymptotic trends. However, no asymptotic trends were detected for numbers of unique parasitoid–host and host–plant bitrophic interactions, nor for tritrophic interactions, after 1983, because climate change then began to conspicuously reduce caterpillar densities. Parasitoid host ranges, the proportions of specialists at the host species and host genus levels, host family utilisation, and host guild sizes show some differences among taxa and are discussed in turn. Ichneumonidae are shown to preferentially parasitise caterpillars of larger-bodied hosts compared to Braconidae. Several of the host plant species from which caterpillars were collected have been introduced from outside of the Americas and their utilisation by endemic parasitoids is described. The obligately hyperparasitoid ichneumonid subfamily Mesochorinae is dealt with separately and its strong association with microgastrine braconid primary parasitoids is illustrated. We discuss the implications for studies of tropical insect community food web ecology and make suggestions for future work. The aim was to make available the data from this remarkable study and to provide an overview of what we think are some of the more interesting relationships that emerge—other scientists/readers are expected to have different questions that they will go on to explore the data to answer.

This revision is part of a continuing series of taxonomic work aimed at the description of new taxa and the redescription of known taxa of the Tachinidae of Area de Conservación Guanacaste in northwestern Costa Rica. Here we describe 33 new species in the genus Belvosia Robineau-Desvoidy, 1830 (Diptera: Tachinidae). All species described here were reared from this ongoing inventory of wild-caught caterpillars spanning a variety of families (Lepidoptera: Erebidae, Eupterotidae, Noctuidae, Notodontidae, Saturniidae, and Sphingidae). We provide a morphological description of each species with limited information on life history, molecular data, and photographic documentation. In addition to the new species, the authors provide a redescription of the genus Belvosia, as well as provide a key to the identification of the species present in the Meso- and North-American fauna.The following 33 new species of Belvosia Robineau-Desvoidy, 1830, all authored by Fleming & Woodley, are described: Belvosia adrianguadamuzi Fleming & Woodley sp. n., Belvosia anacarballoae Fleming & Woodley sp. n., Belvosia angelhernandezi Fleming & Woodley sp. n., Belvosia brigittevilchezae Fleming & Woodley sp. n., Belvosia alixtomoragai Fleming & Woodley sp. n., Belvosia carolinacanoae Fleming & Woodley sp. n., Belvosia ciriloumanai Fleming & Woodley sp. n., Belvosia diniamartinezae Fleming & Woodley sp. n., Belvosia duniagarciae Fleming & Woodley sp. n., Belvosia duvalierbricenoi Fleming & Woodley sp. n., Belvosia eldaarayae Fleming & Woodley sp. n., Belvosia eliethcantillanoae Fleming & Woodley sp. n., Belvosia freddyquesadai Fleming & Woodley sp. n., Belvosia gloriasihezarae Fleming & Woodley sp. n., Belvosia guillermopereirai Fleming & Woodley sp. n., Belvosia harryramirezi Fleming & Woodley sp. n., Belvosia hazelcambroneroae Fleming & Woodley sp. n., Belvosia jorgehernandezi Fleming & Woodley sp. n., Belvosia josecortezi Fleming & Woodley sp. n., Belvosia joseperezi Fleming & Woodley sp. n., Belvosia keinoraragoni Fleming & Woodley sp. n., Belvosia luciariosae Fleming & Woodley sp. n., Belvosia manuelpereirai Fleming & Woodley sp. n., Belvosia manuelriosi Fleming & Woodley sp. n., Belvosia minorcarmonai Fleming & Woodley sp. n., Belvosia osvaldoespinozai Fleming & Woodley sp. n., Belvosia pabloumanai Fleming & Woodley sp. n., Belvosia petronariosae Fleming & Woodley sp. n., Belvosia ricardocaleroi Fleming & Woodley sp. n., Belvosia robertoespinozai Fleming & Woodley sp. n., Belvosia rostermoragai Fleming & Woodley sp. n., Belvosia ruthfrancoae Fleming & Woodley sp. n., Belvosia sergioriosi Fleming & Woodley sp. n.Belvosia canalis Aldrich, 1928 is reared and recorded from the inventory; new information relative to host is provided and the species is rediscribed.The following are proposed by Fleming & Woodley as new synonyms of Belvosia Robineau-Desvoidy, 1830: Brachybelvosia Townsend, 1927 syn. n., Belvosiomimops Townsend, 1935 syn. n.The following three new combinations are proposed as a result of the new synonymies: Belvosia brasilensis (Townsend, 1927), comb. n.; and Belvosia barbiellinii (Townsend, 1935), comb. n.The authors also propose the following new synonymies: Belvosia brasilensis (Townsend, 1927) = Belvosia aurulenta (Bigot, 1888), syn. n.; Belvosia pollinosa Rowe, 1933 = Belvosia borealis Aldrich, 1928 syn. n.; Belvosia weyenberghiana (Wulp, 1883) = Belvosia fuliginosa (Walker, 1853) syn. n.; Belvosia brasiliensis Townsend, 1927 = Belvosia fuliginosa (Walker, 1853) syn. n.; Belvosia luteola Coquillett, 1900 = Belvosia ochriventris (Wulp, 1890) syn. n.; Belvosia socia (Walker, 1853) = Belvosia proxima (Walker, 1853) syn. n.; Belvosia chrysopyga (Bigot, 1887) = Belvosia unifasciata (Robineau-Desvoidy, 1830) syn. n.; Belvosia chrysopygata (Bigot, 1888) = Belvosia unifasciata (Robineau-Desvoidy, 1830) syn. n.

Taxonomy underpins biological research because names are needed for comparative analysis, conservation status, and public communication. Despite this, many species remain undescribed and are therefore vulnerable and unprotected, particularly in the tropics. Neotropical Staphylinidae beetles (Coleoptera) are among the insect groups most likely to contain significant unknown and/or cryptic diversity. Here we used an integrative taxonomic framework to conduct a preliminary review of one particularly diverse genus of Staphylinidae (Anotylus) in Área de Conservaciόn Guanacaste, northwestern Costa Rica. We began by DNA barcoding novel collections and using Barcode Index Numbers (BINs) as an estimate of taxonomic diversity; we found 18 provisional new species. We augmented this genetic analysis with a morphometric analysis of adult morphological characters and found that we could differentiate most provisional species by external morphology as well as by elevation of collection. All the most abundant species could be differentiated from each other by differences in body size. One BIN included slight (~1%) genetic variation that corresponded with some morphological differentiation suggesting the existence of two species within a DNA BIN. Our results support the efficacy of DNA barcoding collections of tropical insects as an effective biodiversity estimator, one that can be used as a primer for integrative taxonomic studies using BINs as species hypotheses.

Amphibians are the most threatened species-rich vertebrate group, with species extinctions and population declines occurring globally, even in protected and seemingly pristine habitats. These ‘enigmatic declines’ are generated by climate change and infectious diseases. However, the consequences of these declines are undocumented as no baseline ecological data exists for most affected areas. Like other neotropical countries, Costa Rica, including Área de Conservación Guanacaste (ACG) in north-western Costa Rica, experienced rapid amphibian population declines and apparent extinctions during the past three decades. To delineate amphibian diversity patterns within ACG, a large-scale comparison of multiple sites and habitats was conducted. Distance and time constrained visual encounter surveys characterised species richness at five sites—Murciélago (dry forest), Santa Rosa (dry forest), Maritza (mid-elevation dry-rain forest intersect), San Gerardo (rainforest) and Cacao (cloud forest). Furthermore, species-richness patterns for Cacao were compared with historic data from 1987–8, before amphibians declined in the area. Rainforests had the highest species richness, with triple the species of their dry forest counterparts. A decline of 45% (20 to 11 species) in amphibian species richness was encountered when comparing historic and contemporary data for Cacao. Conservation efforts sometimes focus on increasing the resilience of protected areas, by increasing their range of ecosystems. In this sense ACG is unique containing many tropical ecosystems compressed in a small geographic space, all protected and recognised as a UNESCO world heritage site. It thus provides an extraordinary platform to understand changes, past and present, and the resilience of tropical ecosystems and assemblages, or lack thereof, to climate change.

We describe three new species of the previously monotypic genus Creagrura Townes from Central and South America: C. alejandromasisi sp. n. and C. rogerblancoi sp. n. from Costa Rica and C. allpahuaya sp. n. from Peru, all of which emphasise the unknown parasitoid insect diversity yet to be revealed in the tropics.Host relationships of the two Costa Rican species are described in detail. In addition, it is inferred that the Creagrura wasps find and oviposit in the caterpillar when it is exposed at night, rather than when it is concealed during daylight hours.

This is a response to a preprint version of “A re-analysis of the data in Sharkey et al.’s (2021) minimalist revision reveals that BINs do not deserve names, but BOLD Systems needs a stronger commitment to open science”, https://www.biorxiv.org/content/10.1101/2021.04.28.441626v2. Meier et al. strongly criticized Sharkey et al.’s publication in which 403 new species were deliberately minimally described, based primarily on COI barcode sequence data. Here we respond to these criticisms. The following points are made: 1) Sharkey et al. did not equate BINs with species, as demonstrated in several examples in which multiple species were found to be in single BINs. 2) We reiterate that BINs were used as a preliminary sorting tool, just as preliminary morphological identification commonly sorts specimens based on color and size into unit trays; despite BINs and species concepts matching well over 90% of species, this matching does not equate to equality. 3) Consensus barcodes were used only to provide a diagnosis to conform to the rules of the International Code of Zoological Nomenclature just as consensus morphological diagnoses are. The barcode of a holotype is definitive and simply part of its cellular morphology. 4) Minimalist revisions will facilitate and accelerate future taxonomic research, not hinder it. 5) We refute the claim that the BOLD sequences of Plesiocoelus vanachterbergi are pseudogenes and demonstrate that they simply represent a frameshift mutation. 6) We reassert our observation that morphological evidence alone is insufficient to recognize species within species-rich higher taxa and that its usefulness lies in character states that are congruent with molecular data. 7) We show that in the cases in which COI barcodes code for the same amino acids in different putative species, data from morphology, host specificity, and other ecological traits reaffirm their utility as indicators of genetically distinct lineages.