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Fig. 25. I–IV in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants

Fig. 25. I–IV instar caterpillars of Melitaea shahvarica sp. nov. (a = view from above; b = lateral view). A. First instar caterpillar after hatching. B. First instar caterpillar before molting. C. Second instar caterpillar. D. Third instar caterpillar. E. Fourth instar caterpillar.

Fig. 26. V–VI in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants

Fig. 26. V–VI instar caterpillars of Melitaea shahvarica sp. nov. (a = view from above; b = lateral view). A. Fifth instar caterpillar. B. Sixth instar caterpillar. C. Sixth instar caterpillar, head capsule, front view. D. Sixth instar caterpillar, head capsule, lateral view.

Fig. 20 in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants

Fig. 20. Eggs of Melitaea timandra binaludica subsp. nov., Iran, Kuh-e-Binalud Mts. A–C. Lateral view. D–F. View from above. G–I. Micropile area.

Fig. 19. Male genitalia and harpe. A–C in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants

Fig. 19. Male genitalia and harpe. A–C. Melitaea timandra timandra Coutsis & van Oorschot, 2014. D–I. M. timandra binaludica subsp. nov. A–C. Turkmenistan, Sary-Yazy, alt. 300 m. D–F. Iran, Rezavi Khorassan Prov., Kuh-e-Binalud Mts, Dorrud v. vicinity, alt. 2430 m. G. Afghanistan, Bamian Prov., Band-e-Amir, alt. 3200 m. H. Afghanistan, Bamian Prov., Band-e-Amir, Dzhudoi-Kvak Gorge, alt. 3200 m. I. Afghanistan, Band-e-Amir, Hazarajat.

opencc-by-4.0Jun 2022View details →

Systematic review reveals sexually antagonistic knockouts in model organisms data and code

R Code and data for manuscript titled "Systematic review reveals sexually antagonistic knockouts in model organisms". Drosophila data is from Ruzicka, F., Hill, M.S., Pennell, T.M., Flis, I., Ingleby, F.C., Mott, R., Fowler, K., Morrow, E.H., Reuter, M., 2019. Genome-wide sexually antagonistic variants reveal long-standing constraints on sexual dimorphism in fruit flies. PLoS Biol. 17, e3000244. https://journals.plos.org/plosbiology/article?id=10.1371/journal.pbio.3000244 Human data is from Harper, J.A., Janicke, T., Morrow, E.H., 2021. Systematic review reveals multiple sexually antagonistic polymorphisms affecting human disease and complex traits. Evolution 75, 3087–3097. https://doi.org/10.1111/evo.14394 https://onlinelibrary.wiley.com/doi/full/10.1111/evo.14394

Publication rate of systematic reviews in the Lens.org database

Figure 2. The number of articles (document count) in the Lens.org database between 1990 and 2021 by publication year referring to the terms ‘systematic review*’, ‘systematically review*’ or ‘systematic literature review*’ in their titles, abstracts, keywords or indexed fields of study (see <a href="https://www.doi.org/10.5281/zenodo.6942304">https://www.doi.org/10.5281/zenodo.6942304</a> for raw data and exact search query).

opencc-by-4.0Aug 2022View details →

FIGURE 1 in Comparisons of two cryptic Ampedus species (Coleoptera: Elateridae) by using classical systematics, ecological niche modeling, and DNA barcoding

FIGURE 1. Habitus photos and aedeagi drawings of examined species. A-B. Ampedus platiai, C-D. A. samedovi, E-F. A. pomonae (Aedeagi of A. platiai and A. samedovi are redrawn from Kabalak 2010 and aedeagus of A. pomonae is redrawn from Platia 1994.). BML: Basal struts of median lobe, BP: Basal piece, ML: Median Lobe, PDT: Paramere distal tooth, PR: Paramere.

opencc-by-4.0Aug 2022View details →

Systematic Literature Review about Text Classification

This work represents a Systematic Literature Review about Text Classification with search keys and query results. Also the classification criteria of the examples for the SLR.

Figs 50–53 in Morphology of the larvae and biology of the adults of Psilorrhynchus bifasciatus do not confirm previous hypotheses about systematics and feeding habits (Coleoptera: Cantharidae)

Figs 50–53. Habitus of fixed and live Psilorrhynchus specimens. 50–51 – museum specimens of P. bifasciatus (Blanchard) (50) and P. abdominalis (Perty) (51) as presented in the genus revision (Bංൿൿං 2017a) showing a pale-yellow elytral background colouration. 52–53 – live specimens of P. abdominalis from Rio de Janeiro state, showing an intense reddish elytral colouration. Figs 50 and 51 adapted from Bංൿൿං (2017a); 52 by Diogo Luiz (available at inaturalist.org/observations/31961589); 53 by Eric Freitas de Abreu (available at inaturalist.org/observations/56266908).

Figs 39–49 in Morphology of the larvae and biology of the adults of Psilorrhynchus bifasciatus do not confirm previous hypotheses about systematics and feeding habits (Coleoptera: Cantharidae)

Figs 39–49. Morphology of Psilorrhynchus bifasciatus (Blanchard, 1844), second and first instar larvae. 39 – head, second instar; 40 – nasale, second instar; 41–49 – first instar; 41 – head; 42 – nasale; 43–44 – antenna (ventral, dorsal views); 45 – maxillo-labial complex; 46 – foreleg; 47–48 – pretarsus (lateral, ventral views); 49 – apex of abdomen (dorsal view). Scale bars = 0.05 mm, except 39, 41, 46, 49 = 0.1 mm.

Figs 36–38 in Morphology of the larvae and biology of the adults of Psilorrhynchus bifasciatus do not confirm previous hypotheses about systematics and feeding habits (Coleoptera: Cantharidae)

Figs 36–38. Morphology of Psilorrhynchus bifasciatus (Blanchard, 1844), second instar larva (dorsal, ventral, lateral views). Scale bar = 0.5 mm.

Figs 19–35 in Morphology of the larvae and biology of the adults of Psilorrhynchus bifasciatus do not confirm previous hypotheses about systematics and feeding habits (Coleoptera: Cantharidae)

Figs 19–35. Morphology of Psilorrhynchus bifasciatus (Blanchard, 1844), third instar larva. 19 – head, dorsal view; 20 – nasale; 21–22 – antenna (dorsal and ventral views); 23–24 – third antennomere (ventral and dorsal views); 25–26 – mandibula (dorsal and ventral views); 27 – maxillo-labial complex; 28 – hypopharynx; 29 – maxillary palp (dorsal view); 30 – third maxillary papomere (ventral view); 31–32 – second labial palpomere (ventral and dorsal views); 33 – mesothoracic spiracle; 34 – foreleg; 35 – pretarsus. Scale bars = 0.1 mm, except 29 = 0.05 mm, 33 = 0.5 mm, and 34 = 0.5 mm.

Figs 14–18 in Morphology of the larvae and biology of the adults of Psilorrhynchus bifasciatus do not confirm previous hypotheses about systematics and feeding habits (Coleoptera: Cantharidae)

Figs 14–18. Morphology of Psilorrhynchus bifasciatus (Blanchard, 1844), third instar larva. 14 – head and pronotum in dorsal view; 15 – head, ventral view; 16 – head in lateral view; 17–18 – abdominal segments VIII–X in dorsal (17) and ventral views (18). Scale bars = 0.5 mm.

Figs 6–9 in Morphology of the larvae and biology of the adults of Psilorrhynchus bifasciatus do not confirm previous hypotheses about systematics and feeding habits (Coleoptera: Cantharidae)

Figs 6–9. Eggs and larvae of Psilorrhynchus bifasciatus (Blanchard, 1844), 6–7 – eggs pile laid on the soil; 8–9 – first instar larvae hatching.

Figs 1–5 in Morphology of the larvae and biology of the adults of Psilorrhynchus bifasciatus do not confirm previous hypotheses about systematics and feeding habits (Coleoptera: Cantharidae)

Figs 1–5. Live adults of Psilorrhynchus bifasciatus (Blanchard, 1844). 1–2 – habitus of female; 3–5 – specimens in copula and foraging on Matayba guianensis Aubl. (Sapindaceae) in Selvíria, MS, Brazil.

Figs 10–13 in Morphology of the larvae and biology of the adults of Psilorrhynchus bifasciatus do not confirm previous hypotheses about systematics and feeding habits (Coleoptera: Cantharidae)

Figs 10–13. Psilorrhynchus bifasciatus (Blanchard, 1844), third instar larva in dorsal (10), lateral (11), ventral (12) and dorso-lateral views (13). Specimen stained in iodine. Scale bar = 1.0 mm.

Figure 1 in Description, biology and conservation of a new species of Australian tree frog (Amphibia: Anura: Hylidae: Litoria) and an assessment of the remaining populations of Litoria genimaculata Horst, 1883: systematic and conservation implications of an unusual speciation event

Figure 1. Distribution of Litoria myola sp. nov. (formerly termed iS) and the northern (N) and southern (S) lineages of Litoria genimaculata in the Wet Tropics, northeast Queensland. CT, Carbine Tableland; BMC, Black Mountain Corridor; LR, Lamb Range; BK, Bellenden Ker Range; AT, Atherton Tableland; MT, Malbon Thompson Range; GR, Graham Range.

Figure 2 in Description, biology and conservation of a new species of Australian tree frog (Amphibia: Anura: Hylidae: Litoria) and an assessment of the remaining populations of Litoria genimaculata Horst, 1883: systematic and conservation implications of an unusual speciation event

Figure 2. Litoria myola, sp. nov., males (A, a pale individual; B, a heavily marked individual), Kuranda, north-east Queensland.

Figure 3 in Description, biology and conservation of a new species of Australian tree frog (Amphibia: Anura: Hylidae: Litoria) and an assessment of the remaining populations of Litoria genimaculata Horst, 1883: systematic and conservation implications of an unusual speciation event

Figure 3. Spectrogram of the courtship call of Litoria myola sp. nov. (recorded at an air temperature of 25 °C). The spectrogram displays a single courtship call consisting of six notes ('tocs'). The degree of shading displays call intensity.

Figure 7 in Description, biology and conservation of a new species of Australian tree frog (Amphibia: Anura: Hylidae: Litoria) and an assessment of the remaining populations of Litoria genimaculata Horst, 1883: systematic and conservation implications of an unusual speciation event

Figure 7. Rainforest stream habitat, with rocky (A) and sandy (B) substrate, Kuranda, north-east Queensland. Litoria myola sp. nov. and Litoria genimaculata are present at both sites.