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Figure 10 in Descriptions of seven new species of Brueelia Kéler 1936 (Phthiraptera: Ischnocera: Philopteridae) from North American sparrows (Aves: Passeriformes: Passerellidae), and review of host use by Brueelia vulgata
Figure 10. Brueelia canyonica sp. nov. ex Melozone fusca (Swainson 1827). (a) male head, dorsal and ventral views; (b) male genitalia, dorsal view (c) male mesosome, ventral view; (d) male paramere, dorsal view; (e) female subgenital plate and vulval margin, ventral view.
Figure 11 in Descriptions of seven new species of Brueelia Kéler 1936 (Phthiraptera: Ischnocera: Philopteridae) from North American sparrows (Aves: Passeriformes: Passerellidae), and review of host use by Brueelia vulgata
Figure 11. Brueelia chlorurae sp. nov. ex Pipilo chlorurus (Audubon 1839). (a) male habitus, dorsal and ventral views; (b) female habitus, dorsal and ventral views.
Figure 9 in Descriptions of seven new species of Brueelia Kéler 1936 (Phthiraptera: Ischnocera: Philopteridae) from North American sparrows (Aves: Passeriformes: Passerellidae), and review of host use by Brueelia vulgata
Figure 9. Brueelia canyonica sp. nov. ex Melozone fusca (Swainson 1827). (a) male habitus, dorsal and ventral views; (b) female habitus, dorsal and ventral views.
Figure 2 in Descriptions of seven new species of Brueelia Kéler 1936 (Phthiraptera: Ischnocera: Philopteridae) from North American sparrows (Aves: Passeriformes: Passerellidae), and review of host use by Brueelia vulgata
Figure 2. Brueelia vulgata (Kellogg 1896) ex Junco hyemalis hyemalis (Linnaeus 1758). (a) male head, dorsal and ventral views; (b) male genitalia, dorsal view (c) male mesosome, ventral view; (d) male paramere, dorsal view; (e) female subgenital plate and vulval margin, ventral view.
Figure 8 in Descriptions of seven new species of Brueelia Kéler 1936 (Phthiraptera: Ischnocera: Philopteridae) from North American sparrows (Aves: Passeriformes: Passerellidae), and review of host use by Brueelia vulgata
Figure 8. Brueelia californica sp. nov. ex Melozone crissalis (Vigors 1839). (a) male head, dorsal and ventral views; (b) male genitalia, dorsal view (c) male mesosome, ventral view; (d) male paramere, dorsal view; (e) female subgenital plate and vulval margin, ventral view.
Figure 6 in Descriptions of seven new species of Brueelia Kéler 1936 (Phthiraptera: Ischnocera: Philopteridae) from North American sparrows (Aves: Passeriformes: Passerellidae), and review of host use by Brueelia vulgata
Figure 6. Brueelia hesperides sp. nov. ex Pooecetes gramineus confinis Baird 1858. (a) male head, dorsal and ventral views; (b) male genitalia, dorsal view (c) male mesosome, ventral view; (d) male paramere, dorsal view; (e) female subgenital plate and vulval margin, ventral view.
Figure 3 in Descriptions of seven new species of Brueelia Kéler 1936 (Phthiraptera: Ischnocera: Philopteridae) from North American sparrows (Aves: Passeriformes: Passerellidae), and review of host use by Brueelia vulgata
Figure 3. Brueelia angustifrons (Carriker 1902) ex Chondestes grammacus strigatus Swainson 1827. (a) male habitus, dorsal and ventral views; (b) female habitus, dorsal and ventral views.
Figure 1 in Descriptions of seven new species of Brueelia Kéler 1936 (Phthiraptera: Ischnocera: Philopteridae) from North American sparrows (Aves: Passeriformes: Passerellidae), and review of host use by Brueelia vulgata
Figure 1. Brueelia vulgata (Kellogg 1896) ex Junco hyemalis hyemalis (Linnaeus 1758). (a) male habitus, dorsal and ventral views; (b) female habitus, dorsal and ventral views.
Figure 4 in Descriptions of seven new species of Brueelia Kéler 1936 (Phthiraptera: Ischnocera: Philopteridae) from North American sparrows (Aves: Passeriformes: Passerellidae), and review of host use by Brueelia vulgata
Figure 4. Brueelia angustifrons (Carriker 1902) ex Chondestes grammacus strigatus Swainson 1827. (a) male head, dorsal and ventral views; (b) male genitalia, dorsal view (c) male mesosome, ventral view; (d) male paramere, dorsal view; (e) female subgenital plate and vulval margin, ventral view.
Figure 7 in Descriptions of seven new species of Brueelia Kéler 1936 (Phthiraptera: Ischnocera: Philopteridae) from North American sparrows (Aves: Passeriformes: Passerellidae), and review of host use by Brueelia vulgata
Figure 7. Brueelia californica sp. nov. ex Melozone crissalis (Vigors 1839). (A) male habitus, dorsal and ventral views; (b) female habitus, dorsal and ventral views.
Figure 5 in Descriptions of seven new species of Brueelia Kéler 1936 (Phthiraptera: Ischnocera: Philopteridae) from North American sparrows (Aves: Passeriformes: Passerellidae), and review of host use by Brueelia vulgata
Figure 5. Brueelia hesperides sp. nov. ex Pooecetes gramineus confinis Baird 1858. (a) male habitus, dorsal and ventral views; (b) female habitus, dorsal and ventral views.
Data from: Experimental assemblage of novel plant-herbivore interactions: ecological host shifts after 40 million years of isolation
Geographic isolation is the first step in insect herbivore diet specialization. Such specialization is postulated to increase insect fitness, but may simultaneously reduce insect ability to colonize novel hosts. During the Paleocene-Eocene, plants from the order Zingiberales became isolated either in the Paleotropics or in the Neotropics. During the Cretaceous, rolled-leaf beetles diversified in the Neotropics concurrently with neotropical Zingiberales. Using a community of Costa Rican rolled-leaf beetles and their Zingiberales host plants as study system, we explored if previous geographic isolation precludes insects to expand their diets to exotic hosts. We recorded interactions between rolled-leaf beetles and native Zingiberales by combining DNA barcodes and field records for 7450 beetles feeding on 3202 host plants. To determine phylogenetic patterns of diet expansions, we set 20 field plots including five exotic Zingiberales, recording beetles feeding on these exotic hosts. In the laboratory, using both native and exotic host plants, we reared a subset of insect species that had expanded their diets to the exotic plants. The original plant-herbivore community comprised 24 beetle species feeding on 35 native hosts, representing 103 plant-herbivore interactions. After exotic host plant introduction, 20% of the beetle species expanded their diets to exotic Zingiberales. Insects only established on exotic hosts that belong to the same plant family as their native hosts. Laboratory experiments show that beetles are able to complete development on these novel hosts. In conclusion, rolled-leaf beetles are pre-adapted to expand their diets to novel host plants even after millions of years of geographic isolation.
Data from: Temperature effects on long-term population dynamics in a parasitoid-host system
Long-term environmental changes will likely alter the strengths of interactions between species and consequently their population dynamics, leading to changes in the stability of ecological systems. While an increasing number of empirical studies have shown that environmental changes can alter the strengths of species interactions, these studies are typically short (<1–2 generations) and therefore give only partial information about longer term population dynamics. To focus on longer term dynamics, we investigated population cycles of pea aphids and their most common parasitoid, Aphidius ervi, in Wisconsin, USA. Data collected over three years in alfalfa fields showed an apparent host–parasitoid population cycle. Furthermore, higher pea aphid population growth rates and increased parasitism were correlated with higher naturally occurring temperatures. While these effects were observed with seasonal fluctuations in temperature, they beg the question of how long-term changes in mean annual temperature might change aphid–parasitoid population cycles, a question which we further pursued with laboratory experiments. To quantify temperature-dependent demographic parameters, we used short-term (<1 generation) experiments conducted at 20°C and 27°C. The higher temperature increased aphid and parasitoid development rates, adult aphid life span and fecundity, and parasitoid attack rates. We then conducted multi-generation population-level laboratory experiments to reveal the effects of temperature (20°C vs. 27°C) on population dynamics. We fit the resulting time series data using a nonlinear age-structured state-space model to estimate population-level processes that could not be estimated in short-term laboratory experiments. Using the model, we parsed out the demographic rates that had the largest impacts on aphid–parasitoid population cycles. This analysis showed that there were frequent contrasts in the effects of temperature operating through different demographic rates. For example, the temperature-dependent increase in aphid development rate decreased cycle amplitude, while the increase in parasitoid attack rate increased cycle amplitude. There were also striking interactions among demographic rates. For example, the temperature-dependent increase in aphid development rate could either increase or decrease the cycle period depending on the values of other demographic rates. Although these complexities make predictions difficult, overall they suggest that increasing long-term mean temperature will decrease the period, increase the amplitude, and tend to destabilize pea aphid–A. ervi dynamics.
Data from: Metapopulation structure of a seed-predator weevil and its host plants in arms race coevolution
Although the importance of gene flow in the geographic structuring of host–parasite interactions has been well discussed, little is known about how dispersal drives the spatial dynamics of other types of coevolutionary interactions in nature. We evaluated the roles of gene flow in the geographically structured processes of a predator–prey arms race involving a seed-predatory weevil with a long mouthpart and its host camellia plant with a thick fruit coat. Molecular genetic analyses showed that both weevil and camellia populations were structured at a spatial scale of several kilometers. Importantly, the spatial pattern of the migration of weevils, but not that of camellias, imposed significant effects on the geographic configuration of the levels of coevolutionary escalation. This result suggests that even if migration is limited in one species (camellia), local coevolution with the other species that migrates between neighboring localities (weevil) can reduce the inter-population difference in the local adaptive optima of the former species. Thus, gene flow of a species potentially homogenizes local biological environments provided by the species and thereby promotes the evolutionary convergence of its coevolving counterparts. Consequently, by focusing on coevolutionary interactions in natural communities, "indirect" effects of gene flow on the adaptive divergence of organisms could be identified.
Data from: Molecular analysis of parasitoid linkages (MAPL): gut contents of adult parasitoid wasps reveal larval host
Metamorphosing insects often have complex and poorly known life-histories. In particular, what they feed on during their larval stages remains unknown for the vast majority of species and its documentation only results from difficult and time-intensive field observations, rearing or dissections. Through the application of a DNA analysis of gut contents in adult parasitoid wasps, we were able to selectively sequence a diagnostic DNA marker that permitted the identification of the host used by these wasps during their larval stages. By reproducing these results in species with different life-histories, we excluded other potential sources of host DNA, confirming that after ingestion by the parasitoid larva the host DNA can persist through metamorphosis in the abdominal contents of the adult wasp. Our discovery considerably extends the applicability of molecular analysis of gut contents by enabling documentation of the food used by insects during their larval stages and thus increasing the accuracy and precision of food web-studies. The 24% success rate of our approach is surprisingly high considering the challenging context for host DNA preservation, and we discuss the factors possibly affecting this rate. We propose Molecular Analysis of Parasitoid Linkages (MAPL) as a new method to document host-parasitoid associations at a faster pace and with unrivalled precision. Because of the key regulatory role of parasitoid wasps in ecosystems, which makes them the most commonly used biological control agents, MAPL will have immediate applications in both basic and applied biological sciences.
Data from: Sympatric diversification vs. immigration: deciphering host-plant specialization in a polyphagous insect, the stolbur phytoplasma vector Hyalesthes obsoletus (Cixiidae)
The epidemiology of vector transmitted plant diseases is highly influenced by dispersal and the host-plant range of the vector. Widening the vector's host range may increase transmission potential, whereas specialization may induce specific disease cycles. The process leading to a vector's host shift and its epidemiological outcome is therefore embedded in the frameworks of sympatric evolution vs. immigration of preadapted populations. In this study, we analyse whether a host shift of the stolbur phytoplasma vector, Hyalesthes obsoletus from field bindweed to stinging nettle in its northern distribution range evolved sympatrically or by immigration. The exploitation of stinging nettle has led to outbreaks of the grapevine disease bois noir caused by a stinging nettle-specific phytoplasma strain. Microsatellite data from populations from northern and ancestral ranges provide strong evidence for sympatric host-race evolution in the northern range: Host-plant associated populations were significantly differentiated among syntopic sites (0.054 < FHT < 0.098) and constant over 5 years. While gene flow was asymmetric from the old into the predicted new host race, which had significantly reduced genetic diversity, the genetic identity between syntopic host-race populations in the northern range was higher than between these populations and syntopic populations in ancestral ranges, where there was no evidence for genetic host races. Although immigration was detected in the northern field bindweed population, it cannot explain host-race diversification but suggests the introduction of a stinging nettle-specific phytoplasma strain by plant-unspecific vectors. The evolution of host races in the northern range has led to specific vector-based bois noir disease cycles.
Data from: Getting there and around: host range oscillations during colonisation of the Canary Islands by the parasitic nematode Spauligodon
Episodes of expansion and isolation in geographic range over space and time, during which parasites have the opportunity to expand their host range, are linked to the development of host-parasite mosaic assemblages and parasite diversification. In this study we investigated whether island colonisation events lead to host range oscillations in a taxon of host-specific parasitic nematodes of the genus Spauligodon in the Canary Islands. We further investigated if range oscillations also resulted in shifts in host breadth (i.e. specialization), as expected for parasites on islands. Parasite phylogeny and divergence time estimates were inferred from molecular data with Bayesian methods. Host divergence times were set as calibration priors after a priori evaluation with a global-fit method of which individual host-parasite associations likely represent cospeciation links. Parasite colonisation history was reconstructed, followed by an estimation of oscillation events and specificity level. The results indicate the presence of four Spauligodon clades in the Canary Islands, which originated from at least three different colonisation events. We found evidence of host range oscillations to truly novel hosts, which in one case led to higher diversification. Contemporary host-parasite associations show strong host specificity, suggesting that changes in host breadth were limited to the shift period. Lineages with more frequent and wider taxonomic host range oscillations prior to the initial colonisation event showed wider range oscillations during colonisation and diversification within the archipelago. Our results suggest that a lineage's evolutionary past may be the best indicator of a parasite's potential for future range expansions.
Data from: Global patterns in helminth host specificity: phylogenetic and functional diversity of regional host species pools matter
Host specificity has a major influence on a parasite's ability to shift between human and animal host species. Yet there is a dearth of quantitative approaches to explore variation in host specificity across biogeographical scales, particularly in response to the varying community compositions of potential hosts. We built a global dataset of intermediate host associations for nine of the world's most widespread helminth parasites (all of which infect humans). Using hierarchical models, we asked if realised parasite host specificity varied in response to regional variation in the phylogenetic and functional diversities of potential host species. Parasites were recorded in 4-10 zoogeographical regions, with some showing considerable geographical variation in observed versus expected host specificity. Parasites generally exhibited the lowest phylogenetic host specificity in regions with the greatest variation in prospective host phylogenetic diversity, namely the Neotropical, Saharo-Arabian and Australian regions. Globally, we uncovered notable variation in parasite host shifting potential. Observed host assemblages for Hydatigera taeniaeformis and Hymenolepis diminuta were less phylogenetically diverse than expected, suggesting limited potential to spillover into unrelated hosts. Host assemblages for Echinococcus granulosus, Mesocestoides lineatus and Trichinella spiralis were less functionally diverse than expected, suggesting limited potential to shift across host ecological niches. By contrast, Hydatigera taeniaeformis infected a higher functional diversity of hosts than expected, indicating strong potential to shift across hosts with different ecological niches. We show that the realised phylogenetic and functional diversities of infected hosts are determined by biogeographical gradients in prospective host species pools. These findings emphasise the need to account for underlying species diversity when assessing parasite host specificity. Our framework to identify variation in realised host specificity is broadly applicable to other host-parasite systems and will provide key insights into parasite invasion potential at regional and global scales.
Data from: Specialized avian Haemosporida trade reduced host breadth for increased prevalence
Parasite specialization on one or a few host species leads to a reduction in the total number of available host individuals, which may decrease transmission. However, specialists are thought to be able to compensate by increased prevalence in the host population and increased success in each individual host. Here, we use variation in host breadth among a community of avian Haemosporida to investigate consequences of generalist and specialist strategies on prevalence across hosts. We show that specialist parasites are more prevalent than generalist parasites in host populations that are shared between them. Moreover, the total number of infections of generalist and specialist parasites within the study area did not vary significantly with host breadth. This suggests that specialists can infect a similar number of host individuals as generalists, thus compensating for a reduction in host availability by achieving higher prevalence in a single host species. Specialist parasites also tended to infect older hosts, whereas infections by generalists were biased towards younger hosts. We suggest that this reflects different abilities of generalists and specialists to persist in hosts following infection. Higher abundance and increased persistence in hosts suggest that specialists are more effective parasites than generalists, supporting the existence of a trade-off between host breadth and average host use among these parasites.
Data from: Cryptic diversity, high host specificity and reproductive synchronization in army ant-associated Vatesus beetles
Army ants and their arthropod symbionts represent one of the most species-rich animal associations on Earth, and constitute a fascinating example of diverse host-symbiont interaction networks. However, despite decades of research, our knowledge of army ant symbionts remains fragmentary due to taxonomic ambiguity and the inability to study army ants in the lab. Here we present an integrative approach that allows us to reliably determine species boundaries, assess biodiversity, match different developmental stages and sexes, and to study the life cycles of army ant symbionts. This approach is based on a combination of community sampling, DNA barcoding, morphology and physiology. As a test case, we applied this approach to the staphylinid beetle genus Vatesus and its different Eciton army ant host species at La Selva Biological Station, Costa Rica. DNA barcoding led to the discovery of cryptic biodiversity and, in combination with extensive community sampling, revealed strict host partitioning with no overlap in host range. Using DNA barcoding, we were also able to match the larval stages of all focal Vatesus species. In combination with studies of female reproductive physiology, this allowed us to reconstruct almost the complete life cycles of the different beetle species. We show that Vatesus beetles are highly adapted to the symbiosis with army ants, in that their reproduction and larval development are synchronized with the stereotypical reproductive and behavioral cycles of their host colonies. Our approach can now be used to study army ant-symbiont communities more broadly, and to obtain novel insights into co-evolutionary and ecological dynamics in species-rich host-symbiont systems.
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.