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Fig. 8–11 in Taxonomic Status Of Neoechinorhynchus Agilis (Acanthocephala, Neoechinorhynchidae), With A Description Of Two New Species Of The Genus From The Atlantic And Pacific Mullets (Teleostei, Mugilidae)

Fig. 8–11. Line drawings of the syntype specimens of Neoechinorhynchus (Neoechinorhynchus) agilis. 8 — Female proboscis. 9 — Female reproductive system. 10 — Hooks with root system. 11 — Female reproductive system.

Fig. 12–18 in Taxonomic Status Of Neoechinorhynchus Agilis (Acanthocephala, Neoechinorhynchidae), With A Description Of Two New Species Of The Genus From The Atlantic And Pacific Mullets (Teleostei, Mugilidae)

Fig. 12–18. Line drawings of the Neoechinorhynchus (Hebesoma) personatus sp. n. 12 — Female, total view. 13 — Female reproductive system. 14 — Eggs from the body cavity. 15 — Female proboscis in section, hooks with root system. 16 — Female proboscis. 17 — Male reproductive system, bursa everted. 18 — Male, entire view.

Fig. 19–24 in Taxonomic Status Of Neoechinorhynchus Agilis (Acanthocephala, Neoechinorhynchidae), With A Description Of Two New Species Of The Genus From The Atlantic And Pacific Mullets (Teleostei, Mugilidae)

Fig. 19–24. Line drawings of the Neoechinorhynchus (Hebesoma) yamagutii sp. n. 19 — Female proboscis. 20 — Female, total view. 21 — Male proboscis in section, hooks with root system. 22 — Female reproductive system. 23 — Eggs from the body cavity. 24 — Male, entire view.

Fig. 1–7 in Taxonomic Status Of Neoechinorhynchus Agilis (Acanthocephala, Neoechinorhynchidae), With A Description Of Two New Species Of The Genus From The Atlantic And Pacific Mullets (Teleostei, Mugilidae)

Fig. 1–7. Line drawings of the Neoechinorhynchus (Neoechinorhynchus) agilis. 1 — Female, entire ventral view. 2 — Female reproductive system, papilla everted minimally. 3 — Male, entire view. 4 — Female reproductive system, papilla everted maximally. 5 — Posterior end of female in section, papilla everted maximally, cement cap is present. 6 — Eggs from the body cavity. 7— Female proboscis in section, hooks with root system.

opencc-by-4.0Nov 2015View details →

Fig. 1 in Finding Of Two Species From The Tribe Synhimantea (Nematoda, Acuariidae) In The Kyiv Zoological Park

Fig. 1. De. sagitattus and Di. nasuta: 1 — anterior end of De. sagitattus; 2 — anterior end of Di. nasuta; 3 — anterior end of the larva Di. nasuta; 4 — posterior end of the larva Di. nasuta; pl — pseudolabia, bc — buccal capsule, cp — cervical papilla, nr — nerve ring, c — cordons, em — muscular esophagus, eg — glandural esophagus; a — anal pore. Scale bar 100 µm.

opencc-by-4.0Apr 2022View details →

COCO BBOB-constrained Benchmark Results of Two Evolution Strategy Variants

The three zip-files of this data set provide the performance data of the algorithms presented in the paper "Benchmarking 𝜖MAg-ES and BP-𝜖MAg-ES on the bbob-constrained Testbed" submitted to the GECCO 2022 Workshop "<a href="https://gecco-2022.sigevo.org/Workshops#BBOB 2022">BBOB 2022 — Black Box Optimization Benchmarking 2022</a>". <ul> <li>coco2.6.2_bbob-constrained_epsMAg.zip <-- results of the 𝜖MAg-ES on COCO version 2.6.2</li> <li>coco2.6.2_bbob-constrained_BPepsMAg.zip <-- results of the BP-𝜖MAg-ES on COCO version 2.6.2</li> <li>coco2.6.2_bbob-constrained_fmincon.zip <-- results of FMINCON (Matlab 2021b) on COCO version 2.6.2</li> </ul>

opencc-by-4.0Apr 2022View details →

Supplementary files for Transcriptomic alterations in roots of two contrasting Coffea arabica cultivars after hexanoic acid priming

Supplementar files for Transcriptomic alterations in roots of two contrasting Coffea arabica cultivars after hexanoic acid priming. Supplementary Table 1. Differentially expressed genes (DEGs) identified in Obatã and Catuaí cultivars Supplementary Table 2. Gene ontology (GO) enrichment analysis of differentially expressed genes (DEGs) identified in Obatã and Catuaí cultivars Supplementary Table 3. MapMan pathway analysis of differentially genes expressed (DEGs) identified in Obatã and Catuaí cultivars Supplementary Table 4. FPKM values for Catuaí cultivar genes and Roots DEGs Supplementary Table 5. FPKM values for Obatã cultivar genes and Roots DEGs

openother-openApr 2022View details →

Code and data for: Manipulating actions: a selective two-option device for cognitive experiments in wild animals

Code and data for recreating survival analyses in 'Manipulating actions: a selective two-option device for cognitive experiments in wild animals'

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Genetic architecture of adaptive radiation across two trophic levels

Evolution of trophic diversity is a hallmark of adaptive radiation. Yet, transitions between carnivory and herbivory are rare in young adaptive radiations. Haplochromine cichlid fish of the African Great Lakes are exceptional in this regard. Lake Victoria was colonized by an insectivorous generalist and in less than 20,000 years, several clades of specialized herbivores evolved. Carnivorous versus herbivorous lifestyles in cichlids require many different adaptations in functional morphology, physiology, and behaviour. Ecological transitions in either direction thus require many traits to change in a concerted fashion, which could be facilitated if genomic regions underlying these traits were physically linked or pleiotropic. However, linkage/pleiotropy could also constrain evolvability. To investigate components of the genetic architecture of a suite of traits that distinguish invertivores from algae scrapers, we performed Quantitative Trait Locus (QTL) mapping using a second-generation hybrid cross. While we found indications of linkage/pleiotropy within trait complexes, QTLs for distinct traits were distributed across several unlinked genomic regions. Thus, a mixture of independently segregating variation and some pleiotropy may underpin the rapid trophic transitions. We argue that the emergence and maintenance of associations between the different genomic regions underpinning co-adapted traits that evolved and persist against some gene flow required reproductive isolation.

opencc-zeroApr 2022View details →

Fig. 30 in Revision of the intertidal and semiterrestrial crab genera Chiromantes Gistel, 1848, and Pseudosesarma Serène & Soh, 1970 (Crustacea: Brachyura: Sesarmidae), using morphology and molecular phylogenetics, with the establishment of nine new genera and two new species

Fig. 30. Male anterior thoracic sternum and pleon of Pseudosesarma. A, P edwardsii, lectotype male (17.5 × 16.1 mm) (RMNH-D17a), Mergui Archipelago; B, P. edwardsii, male (13.4 × 11.9 mm) (ZRC 1965.8.2.81), Pulau Pawai, Singapore; C, P. crassimanum, male (15.9 × 14.5 mm) (RMNH-D23313), Singapore; D, P. glabrum, holotype male (13.8 × 12.0 mm) (CUSAT 2016-1), Kerala, India; E, P. anteactum, holotype male (16.7 × 14.7 mm) (ZRC 2016.0602), Sri Lanka; F, P. anteactum, paratype male (21.2 × 19.7 mm) (ZRC 2016.0603), Sri Lanka; G, P. brehieri, holotype male (17.4 × 15.7 mm) (ZRC 2016.0593), Myanmar; H, P. boulengeri, lectotype male (26.9 × 23.5 mm) (NHM 1919.11.14.1), Basra, Iraq.

Fig. 27 in Revision of the intertidal and semiterrestrial crab genera Chiromantes Gistel, 1848, and Pseudosesarma Serène & Soh, 1970 (Crustacea: Brachyura: Sesarmidae), using morphology and molecular phylogenetics, with the establishment of nine new genera and two new species

Fig. 27. Outer view of chela of Pseudosesarma. A, P. edwardsii, lectotype male (17.5 × 16.1 mm) (RMNH-D17a), Mergui Archipelago; B, P. edwardsii, male (13.4 × 11.9 mm) (ZRC 1965.8.2.81), Pulau Pawai, Singapore; C, P. edwardsii, male (19.4 × 17.3 mm) (ZRC 1971.9.24.8), Singapore; D, P. crassimanum, male (15.9 × 14.5 mm) (RMNH-D23313), Singapore; E, P. anteactum, holotype male (16.7 × 14.7 mm) (ZRC 2016.0602), Sri Lanka; F, P. glabrum, holotype male (13.8 × 12.0 mm) (CUSAT 2016-1), Kerala, India; G, P. brehieri, holotype male (17.4 × 15.7 mm) (ZRC 2016.0593), Myanmar; H, P. boulengeri, lectotype male (26.9 × 23.5 mm) (NHM 1919.11.14.1), Basra, Iraq.

Fig. 37. A–G in Revision of the intertidal and semiterrestrial crab genera Chiromantes Gistel, 1848, and Pseudosesarma Serène & Soh, 1970 (Crustacea: Brachyura: Sesarmidae), using morphology and molecular phylogenetics, with the establishment of nine new genera and two new species

Fig. 37. A–G, Pseudosesarma brehieri, paratype female (14.9 × 13.4 mm) (ZRC 2016.0594), Myanmar; F, G, P. brehieri, male (15.0 × 13.6 mm) (ZRC 2013.0209), West Bengal, India; H, I, P. brehieri, male (14.5 × 13.0 mm) (ZRC 2013.0209), West Bengal, India; J–O, P. boulengeri, lectotype male (26.9 × 23.5 mm) (NHM 1919.11.14.1), Basra, Iraq. A, K, male pleon; B, F, L, left G1 (ventral view, denuded); D, G, M, left G1 (dorsal view, denuded); E, left G2; H, O, left distal part of G1 (dorsal view, denuded); I, N, left distal part of G1 (ventral view, denuded); J, anterior thoracic sternites 1–4. Scales: A = 4.0 mm; B–E, N, O = 1.0 mm; F–I = 0.5 mm; J, K = 5.0 mm; L, M = 2.0 mm. A–E, after Ng (2018: fig. 7E–I).

Fig. 25 in Revision of the intertidal and semiterrestrial crab genera Chiromantes Gistel, 1848, and Pseudosesarma Serène & Soh, 1970 (Crustacea: Brachyura: Sesarmidae), using morphology and molecular phylogenetics, with the establishment of nine new genera and two new species

Fig. 25. Frontal view of cephalothorax of Pseudosesarma. A, P. edwardsii, lectotype male (17.5 × 16.1 mm) (RMNH-D17a), Mergui Archipelago; B, P. edwardsii, male (13.4 × 11.9 mm) (ZRC 1965.8.2.81), Pulau Pawai, Singapore; C, P. crassimanum, male (15.9 × 14.5 mm) (RMNH-D23313), Singapore; D, P. anteactum, holotype male (16.7 × 14.7 mm) (ZRC 2016.0602), Sri Lanka; E, P. glabrum, holotype male (13.8 × 12.0 mm) (CUSAT 2016-1), Kerala, India; F, P. brehieri, holotype male (17.4 × 15.7 mm) (ZRC 2016.0593), Myanmar; G, P. boulengeri, lectotype male (26.9 × 23.5 mm) (NHM 1919.11.14.1), Basra, Iraq; H, Contusarma bocourti, male (25.3 × 23.3 mm) (ZRC 2000.0952), Bangkok, Thailand; I, Contusarma cheirogonum, neotype male (24.5 × 21.5 mm) (ZRC 1995.225), Bako National Park, Sarawak; J, Miersarma granosimanum, lectotype male (16.9 × 14.8 mm) (NHM 1880.6), Borneo.

Fig. 22. Overall habitus, Pseudosesarma species. A, P in Revision of the intertidal and semiterrestrial crab genera Chiromantes Gistel, 1848, and Pseudosesarma Serène & Soh, 1970 (Crustacea: Brachyura: Sesarmidae), using morphology and molecular phylogenetics, with the establishment of nine new genera and two new species

Fig. 22. Overall habitus, Pseudosesarma species. A, P. edwardsii, lectotype male (17.5 × 16.1 mm) (RMNH-D17a), Mergui Archipelago; B, P. edwardsii, male (13.4 × 11.9 mm) (ZRC 1965.8.2.81), Pulau Pawai, Singapore; C, P. edwardsii, male (12.9 × 11.8 mm) (ZRC 1971.9.24.9), Singapore; D, P. crassimanum, male (15.9 × 14.5 mm) (RMNH-D23313), Singapore; E, P. anteactum, holotype male (16.7 × 14.7 mm) (ZRC 2016.0602), Sri Lanka; F, P. glabrum, holotype male (13.8 × 12.0 mm) (CUSAT 2016-1), Kerala, India; G, P. brehieri, holotype male (17.4 × 15.7 mm) (ZRC 2016.0593), Myanmar; H, P. boulengeri, lectotype male (26.9 × 23.5 mm) (NHM 1919.11.14.1), Basra, Iraq.

Fig. 36. A–G in Revision of the intertidal and semiterrestrial crab genera Chiromantes Gistel, 1848, and Pseudosesarma Serène & Soh, 1970 (Crustacea: Brachyura: Sesarmidae), using morphology and molecular phylogenetics, with the establishment of nine new genera and two new species

Fig. 36. A–G, Pseudosesarma anteactum, holotype male (16.7 × 14.7 mm) (ZRC 2016.0602), Sri Lanka; H–L, P. glabrum, holotype male (13.8 × 12.0 mm) (CUSAT 2016-1), Kerala, India. A, I, left G1 (ventral view); B, J, left G1 (dorsal view); C, D, distal part of left G1 (ventral view, slightly different angles); E, K, ventro-mesial view of distal part of left G1; F, distal part of left G1 (dorsal view); G, L, left G2; H, pleon. Scales: A, B, G = 1.0 mm; C–F, I–L = 0.5 mm; H = 2.0 mm. A–G, after Ng & Schubart (2017: fig. 17); H–L, after Ng et al. (2017a: fig. 4).

Fig. 12 in Unveiling an enigma from the Cerrado: taxonomic revision of two sympatric species of Apostolepis Cope, 1862 (Dipsadidae: Xenodontinae: Elapomorphini) from central Brazil

Fig. 12. Apostolepis dimidiata (Jan, 1862), putative sister-species of Apostolepis albicollaris Lema, 2002, adult specimen from Estação Ecológica Santa Bárbara, São Paulo, Brazil. Photograph credit: Giordano Rossi.

Fig. 11 in Unveiling an enigma from the Cerrado: taxonomic revision of two sympatric species of Apostolepis Cope, 1862 (Dipsadidae: Xenodontinae: Elapomorphini) from central Brazil

Fig. 11. Lateral (A, E), medial (B, F), dorsal (C, G), and ventral (D, H) views of the lower jaw based on μCT imagery. A–D. Apostolepis albicollaris Lema, 2002, holotype (MCP 8355). E–H. A. cerradoensis Lema, 2003, holotype (MCP 15219). Different skull elements are digitally colored to improve visualization. Abbreviations: AN = angular; CP = compound bone; D = dentary; DPD = dorsal process of dentary; PCR = prearticular crest of compound bone; RP = retroarticular process of compound bone; SAC = surangular crest of compound bone; SP = splenial; VDP = ventral process of dentary.

Fig. 10 in Unveiling an enigma from the Cerrado: taxonomic revision of two sympatric species of Apostolepis Cope, 1862 (Dipsadidae: Xenodontinae: Elapomorphini) from central Brazil

Fig. 10. Anterior (A, C) and posterior (B, D) views of the skull and lower jaw based on μCT imagery. A–B. Apostolepis albicollaris Lema, 2002, holotype (MCP 8355). C–D. A. cerradoensis Lema, 2003, holotype (MCP 15219). Different skull elements are digitally colored to improve visualization. Abbreviations: AN = angular; BO = basioccipital; BS = basisphenoid; CP = compound bone; D = dentary; EXO = exoccipital; F = frontal; MX = maxilla; NA = nasal; P = parietal; PAL = palatine; PFR = prefrontal; PMX = premaxilla; PRO = prootic; PT = pterygoid; Q = quadrate; SMX = septomaxilla; SO = supraoccipital; SP = splenial; ST = supratemporal.

Fig. 9 in Unveiling an enigma from the Cerrado: taxonomic revision of two sympatric species of Apostolepis Cope, 1862 (Dipsadidae: Xenodontinae: Elapomorphini) from central Brazil

Fig. 9. Dorsal (A, D), lateral (B, E), and ventral (C, F) views of the skull based on μCT imagery. A–C. Apostolepis albicollaris Lema, 2002, holotype (MCP 8355). D–F. A. cerradoensis Lema, 2003, holotype (MCP 15219). Different skull elements are digitally colored and the mandible is removed for better visualization. Abbreviations: BO = basioccipital; BS = basisphenoid; ECP = ectopterygoid; EXO = exoccipital; F = frontal; MX = maxilla; NA = nasal; P = parietal; PAL = palatine; PFR = prefrontal; PMX = premaxilla; PRO = prootic; PT = pterygoid; Q = quadrate; SMX = septomaxilla; SO = supraoccipital; ST = supratemporal; V = vomer.

Fig. 8 in Unveiling an enigma from the Cerrado: taxonomic revision of two sympatric species of Apostolepis Cope, 1862 (Dipsadidae: Xenodontinae: Elapomorphini) from central Brazil

Fig. 8. Consensus topology of Apostolepis Cope, 1862 BI and ML phylogenetic relationships, support given in Bootstrap (top,> 80) for maximum likelihood inference and Consensus Support (bottom,> 80) for Bayesian inference. Scale bar = molecular distance. Inset photograph: Apostolepis albicollaris Lema, 2002 by Luís Felipe Carvalho de Lima.