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Figure 2 from: Bossert S (2019) Monotypic no more – a new species of the unusual genus Schwarzia (Hymenoptera, Apidae, Biastini). Journal of Hymenoptera Research 69: 23-37. https://doi.org/10.3897/jhr.69.32966
Figure 2 Comparison of selected diagnostic characteristics of males of Schwarziaelizabethae Bossert, sp. n. (left column: A, C, E, G) vs. S.emmae Eardley, 2009 (right column: B, D, F, H) A–B discs of T1 and T2 C–D head characteristics in lateral view. Arrows point to finely pitted protrusions on frontal area of S.emmae and to the intended inner margin of the compound eye E–F antennae G–H tegulae.
Figures 8-11 from: Engel MS, Alqarni AS, Shebl MA, Thomas JC (2019) New genera of meliturguline bees from Saudi Arabia and Persia, with notes on related genera and a key to the Arabian fauna (Hymenoptera: Andrenidae). Journal of Hymenoptera Research 69: 1-21. https://doi.org/10.3897/jhr.69.32561
Figures 8-11 Female heads and mouthparts in profile and details of glossal apexes. 8 Head profile of Belliturgulanajdica Engel, gen. et sp. n., from Saudi Arabia 9 glossal apex of B.najdica10 head profile of Flavomeliturgula (Flavomeliturgula) lacrymosa (Popov) from Iran 11 glossal apex of F. (F.) lacrymosa.
Figure 1 from: Bossert S (2019) Monotypic no more – a new species of the unusual genus Schwarzia (Hymenoptera, Apidae, Biastini). Journal of Hymenoptera Research 69: 23-37. https://doi.org/10.3897/jhr.69.32966
Figure 1 Schwarziaelizabethae Bossert, sp. n., holotype, male A habitus, dorsal view B head, frontal view C habitus, lateral view D head, dorsal view E tergum 7 with pygidial plate and genital capsule F label information as deposited with the holotype. Scale bars: 0.5 mm.
Figures 5-7 from: Engel MS, Alqarni AS, Shebl MA, Thomas JC (2019) New genera of meliturguline bees from Saudi Arabia and Persia, with notes on related genera and a key to the Arabian fauna (Hymenoptera: Andrenidae). Journal of Hymenoptera Research 69: 1-21. https://doi.org/10.3897/jhr.69.32561
Figures 5-7 Female faces of representative Meliturgulina. 5Belliturgulanajdica Engel, gen. et sp. n., from Saudi Arabia (note arched outer subantennal sulci) 6Khuzimelissadeserta (Warncke), comb. n., from Pakistan 7Flavomeliturgula (Flavomeliturgula) lacrymosa (Popov) from Iran (note straight outer subantennal sulci).
Figures 24-26 from: Engel MS, Alqarni AS, Shebl MA, Thomas JC (2019) New genera of meliturguline bees from Saudi Arabia and Persia, with notes on related genera and a key to the Arabian fauna (Hymenoptera: Andrenidae). Journal of Hymenoptera Research 69: 1-21. https://doi.org/10.3897/jhr.69.32561
Figures 24-26 Female pygidial plates. 24Belliturgulanajdica Engel, gen. et sp. n. 25Khuzimelissadeserta (Warncke), comb. n. 26Flavomeliturgula (Flavomeliturgula) lacrymosa (Popov).
Figures 3- 4 from: Engel MS, Alqarni AS, Shebl MA, Thomas JC (2019) New genera of meliturguline bees from Saudi Arabia and Persia, with notes on related genera and a key to the Arabian fauna (Hymenoptera: Andrenidae). Journal of Hymenoptera Research 69: 1-21. https://doi.org/10.3897/jhr.69.32561
Figures 3- 4 Female of Belliturgulanajdica Engel, gen. et sp. n., from central Saudi Arabia. 3 Lateral habitus 4 dorsal habitus.
Figures 22- 23 from: Engel MS, Alqarni AS, Shebl MA, Thomas JC (2019) New genera of meliturguline bees from Saudi Arabia and Persia, with notes on related genera and a key to the Arabian fauna (Hymenoptera: Andrenidae). Journal of Hymenoptera Research 69: 1-21. https://doi.org/10.3897/jhr.69.32561
Figures 22- 23 Female of Flavomeliturgula (Flavomeliturgula) lacrymosa (Popov) from Iran. 22 Dorsal habitus 23 lateral habitus.
Figures 19-21 from: Engel MS, Alqarni AS, Shebl MA, Thomas JC (2019) New genera of meliturguline bees from Saudi Arabia and Persia, with notes on related genera and a key to the Arabian fauna (Hymenoptera: Andrenidae). Journal of Hymenoptera Research 69: 1-21. https://doi.org/10.3897/jhr.69.32561
Figures 19-21 Female of Khuzimelissadeserta (Warncke), comb. n., from Pakistan. 19 Head and mouthparts in profile 20 dorsal-frontal view of mouthparts 21 extended labiomaxillary complex in profile.
Figures 1- 2 from: Engel MS, Alqarni AS, Shebl MA, Thomas JC (2019) New genera of meliturguline bees from Saudi Arabia and Persia, with notes on related genera and a key to the Arabian fauna (Hymenoptera: Andrenidae). Journal of Hymenoptera Research 69: 1-21. https://doi.org/10.3897/jhr.69.32561
Figures 1- 2 Female of Belliturgulanajdica Engel, gen. et sp. n., at flowers of Carthamus L. (Asteraceae) in central Saudi Arabia.
Figures 16-18 from: Engel MS, Alqarni AS, Shebl MA, Thomas JC (2019) New genera of meliturguline bees from Saudi Arabia and Persia, with notes on related genera and a key to the Arabian fauna (Hymenoptera: Andrenidae). Journal of Hymenoptera Research 69: 1-21. https://doi.org/10.3897/jhr.69.32561
Figures 16-18 Female of Khuzimelissadeserta (Warncke), comb. n., from Pakistan. 16 Dorsal habitus 17 lateral habitus 18 detail of mesosoma and anterior metasomal dorsum.
Figures 12-15 from: Engel MS, Alqarni AS, Shebl MA, Thomas JC (2019) New genera of meliturguline bees from Saudi Arabia and Persia, with notes on related genera and a key to the Arabian fauna (Hymenoptera: Andrenidae). Journal of Hymenoptera Research 69: 1-21. https://doi.org/10.3897/jhr.69.32561
Figures 12-15 Labial palpi of representative species (to same scale) and labiomaxillary complex of Khuzimelissadeserta (Warncke), comb. n. (not to same scale), all in ventral view. 12 Labial palpus of Belliturgulanajdica Engel, gen. et sp. n. 13 labial palpus of K.deserta14 labial palpus of Flavomeliturgula (Flavomeliturgula) lacrymosa (Popov) 15 photograph of labiomaxillary complex of K.deserta.
Supplementary material 1 from: Tan MK, Lee H, Tan HTW (2019) The floriphilic katydid, Phaneroptera brevis, is a frequent flower visitor of non-native, flowering forbs. Journal of Orthoptera Research 28(1): 21-26. https://doi.org/10.3897/jor.28.33063
: Explanation note: Supplementary Information on Statistical Analysis.
Supplementary material 2 from: Ney G, Schul J (2019) Epigenetic and genetic variation between two behaviorally isolated species of Neoconocephalus (Orthoptera: Tettigonioidea). Journal of Orthoptera Research 28(1): 11-19. https://doi.org/10.3897/jor.28.28888
: Explanation note: Matrix of MS-AFLP called fragments for all individuals.
Figure 5 from: Ney G, Schul J (2019) Epigenetic and genetic variation between two behaviorally isolated species of Neoconocephalus (Orthoptera: Tettigonioidea). Journal of Orthoptera Research 28(1): 11-19. https://doi.org/10.3897/jor.28.28888
Figure 5 Scatterplot of between-individual Euclidean genetic and epigenetic distance showing significant positive correlation between genetic and epigenetic differentiation. The correlation was tested using a Mantel test and 10,000 permutations of the design matrix to determine significance.
Figure 1 from: Ney G, Schul J (2019) Epigenetic and genetic variation between two behaviorally isolated species of Neoconocephalus (Orthoptera: Tettigonioidea). Journal of Orthoptera Research 28(1): 11-19. https://doi.org/10.3897/jor.28.28888
Figure 1 Species assignment based on call pulse period ratio and center frequency. Labeled boxes indicate the calls classified as N.robustus and N.bivocatus. Individuals that fall outside of species classifications were removed from further epigenetic and genetic analyses (as described in Ney and Schul 2017).
Figure 4 from: Ney G, Schul J (2019) Epigenetic and genetic variation between two behaviorally isolated species of Neoconocephalus (Orthoptera: Tettigonioidea). Journal of Orthoptera Research 28(1): 11-19. https://doi.org/10.3897/jor.28.28888
Figure 4 Consensus shared ancestry population structure for epigenetic and genetic loci. A. and C. Bar plots using MS-AFLP loci to estimate genetic (A) and epigenetic (C) structure among N.robustus and N.bivocatus using the software package STRUCTURE. B. and D. Delta K graphs for K = 1–10 genetic clusters showing moderate support for K = 2 genetic clusters (B) and low support for K = 4 epigenetic clusters (D).
Figure 3 from: Tan MK, Lee H, Tan HTW (2019) The floriphilic katydid, Phaneroptera brevis, is a frequent flower visitor of non-native, flowering forbs. Journal of Orthoptera Research 28(1): 21-26. https://doi.org/10.3897/jor.28.33063
Figure 3 High flower abundance was associated with high abundance of P.brevis (estimate = 0.07, p-value = 0.011, 95% CI [0.02, 0.13], R2GLMM(m) = 0.06, R2GLMM(c) = 0.22, n = 107). Generalized linear mixed-effects models with Poisson errors were fitted with the replicate number as the random effect.
Figure 2 from: Tan MK, Lee H, Tan HTW (2019) The floriphilic katydid, Phaneroptera brevis, is a frequent flower visitor of non-native, flowering forbs. Journal of Orthoptera Research 28(1): 21-26. https://doi.org/10.3897/jor.28.33063
Figure 2 Comparison of the least-square means of the frequency of visitors on flowers between P.brevis and other flower visitors. A generalized linear mixed-effects model with Poisson errors was fitted with different flower visitor as the fixed effect and the replicate number as the random effect. The significance between P.brevis and each flower visitor group is denoted as follows: **P<0.01; ***P<0.001.
Figure 1 from: Tan MK, Lee H, Tan HTW (2019) The floriphilic katydid, Phaneroptera brevis, is a frequent flower visitor of non-native, flowering forbs. Journal of Orthoptera Research 28(1): 21-26. https://doi.org/10.3897/jor.28.33063
Figure 1 A. Immature and B. Adult male individuals of Phaneropterabrevis visiting a capitulum of Sphagneticolatrilobata (A) and an inflorescence of Sesbaniasesban (B) at the study site in Singapore in the day (A) and at night (B). The arrows in the inset (a–i) indicate pollen grains attached to the body of the individual.
Figure 3 from: Ney G, Schul J (2019) Epigenetic and genetic variation between two behaviorally isolated species of Neoconocephalus (Orthoptera: Tettigonioidea). Journal of Orthoptera Research 28(1): 11-19. https://doi.org/10.3897/jor.28.28888
Figure 3 PCoA of N.robustus and N.bivocatus utilizing genetic (A) and epigenetic (B) data. Plotted are the two most informative principal components calculated for the genetic and epigenetic loci datasets, as derived from the MS-AFLP fragment analysis. A. Genetic Euclidean distance with individuals grouped by species assignment. B. Epigenetic Euclidean distance with individuals grouped by species assignment. Group labels show the centroid of the points for each group. The long axis of the ellipse represents the direction of maximum dispersion and the short axis the direction of minimum dispersion.
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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.