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FIGURE 3 in Recircumscription of the genera Goniozus and Sierola (Hymenoptera: Bethylidae) based on morphological and molecular evidence
FIGURE 3. One of the most-parsimonious trees showing branch lengths, with all terminals labelled. Labels include genus or morphogroup (e.g. Sierola open cell, Goniozus s.s., "Parasierola"), species if known, country of origin, BOLD process ID, and GenBank number if applicable.
FIGURE 1. Fore wing venation. A in Recircumscription of the genera Goniozus and Sierola (Hymenoptera: Bethylidae) based on morphological and molecular evidence
FIGURE 1. Fore wing venation. A) Goniozus sensu stricto: G. williamsi (reversed image of left wing). B) "Parasierola": G. emigratus. C) Typical Sierola: S. oahuensis. D) Australian Sierola with cell 2R1 open: undescribed, BOLD process ID AUSMA313-14.
FIGURE 4 in Recircumscription of the genera Goniozus and Sierola (Hymenoptera: Bethylidae) based on morphological and molecular evidence
FIGURE 4. Consensus parsimony tree from PAUP*. Bootstrap values>50 are below branches. Within Sierola, light orange indicates taxa with cell 2R1 open; the group marked "non-Australian Sierola" includes one New Guinea, one New Zealand, and four Australian taxa. Within Goniozus, dark blue branches are "Parasierola" and light pink are Goniozus s.s. The lower group of Goniozus noted as having palpal formula 4:2 probably includes the entire surrounding clade of Goniozus s.s., but only one definite species name could be associated here.
FIGURE 2 in Recircumscription of the genera Goniozus and Sierola (Hymenoptera: Bethylidae) based on morphological and molecular evidence
FIGURE 2. Comparison of insertions and deletions in bethyline genera. Codons are numbered at the top by position 3' from primer LepF1 and colored by amino acid translation. Country and region abbreviations: Aus = Australia, Ban = Bangladesh, Can = Canada, CR = Costa Rica, Egy = Egypt, Haw = Hawaii, Ind = India, Mad = Madagascar, Mal = Malaysia, NZ = New Zealand, SAf = South Africa.
FIGURE 13 in Taxonomizing a truly morphologically cryptic complex of dwarf geckos from Madagascar: molecular evidence for new species-level lineages within the Lygodactylus tolampyae complex
FIGURE 13. Habitat of species of the Lygodactylus tolampyae complex. A. Dry deciduous forest at Ampijoroa (Ankarafantsika) where L. morii sp. nov. occurs in high densities. B. View of remains of dry deciduous Ampondrabe forest (habitat of L. morii sp. nov. and L. herilalai sp. nov.) with large areas of forest destroyed by fire in the foreground. C, D. Transitional forest on Sahamalaza Peninsula, habitat of L. schwitzeri sp. nov. E. Forest in the Tsingy de Bemaraha, habitat of L. tolampyae. All photos by the authors except A by P. Galán.
FIGURE 11 in Taxonomizing a truly morphologically cryptic complex of dwarf geckos from Madagascar: molecular evidence for new species-level lineages within the Lygodactylus tolampyae complex
FIGURE 11. Ventral views of the heads of the holotypes of the three new species of Lygodactylus described herein, and one representative specimen of L. tolampyae. The images on the right show the mental region magnified and strongly sharpened to improve visibility of sutures between scales. For the holotype of L. morii sp. nov., the typical arrangement of scales in the mental region in this species complex is labelled: M, mental scales (semi-divided by incomplete sutures), PM, post-mentals (typically three), IL1, first infralabial (which maintains a broad contact with the mental). Scale bars (referring to the images on the left) represent 1 mm.
FIGURE 12 in Taxonomizing a truly morphologically cryptic complex of dwarf geckos from Madagascar: molecular evidence for new species-level lineages within the Lygodactylus tolampyae complex
FIGURE 12. Lateral views of the heads of the holotypes of the three new species of Lygodactylus described herein, and one representative specimen of L. tolampyae. The scale bar represents 1 mm.
FIGURE 10 in Taxonomizing a truly morphologically cryptic complex of dwarf geckos from Madagascar: molecular evidence for new species-level lineages within the Lygodactylus tolampyae complex
FIGURE 10. Preserved holotypes of the three new species of the Lygodactylus tolampyae complex described herein, photographed in May 2023.
FIGURE 4 in Taxonomizing a truly morphologically cryptic complex of dwarf geckos from Madagascar: molecular evidence for new species-level lineages within the Lygodactylus tolampyae complex
FIGURE 4. Individuals of Lygodactylus tolampyae from Tsingy de Bemaraha National Park, all photographed in 2006. The upper three individuals are not unambiguously assignable to voucher specimens but correspond to samples included in the mitochondrial tree (Fig. 1) and grouped in lineage A+B; the lowermost picture shows the female ZSM 6/2006 (FGZC 676).
FIGURE 9 in Taxonomizing a truly morphologically cryptic complex of dwarf geckos from Madagascar: molecular evidence for new species-level lineages within the Lygodactylus tolampyae complex
FIGURE 9. Female holotype of Lygodactylus schwitzeri sp. nov., ZSM 419/2000 (FGMV 2000.155), from Berara Forest, Sahamalaza, in life, photographed in February 2000.
FIGURE 5 in Taxonomizing a truly morphologically cryptic complex of dwarf geckos from Madagascar: molecular evidence for new species-level lineages within the Lygodactylus tolampyae complex
FIGURE 5. Male holotype of Lygodactylus morii sp. nov., ZSM 501/2001 (FGMV 2001.300) from Ampijoroa, Ankarafantsika National Park, in life, photographed in February 2001.
FIGURE 2 in Taxonomizing a truly morphologically cryptic complex of dwarf geckos from Madagascar: molecular evidence for new species-level lineages within the Lygodactylus tolampyae complex
FIGURE 2. Map of Madagascar with genetically confirmed sampling localities of the Lygodactylus tolampyae complex. Colours correspond to those used for mitochondrial lineages. The black square marks the town Morondava from which no samples were analyzed; it is likely that the type locality of L. tolampyae is located in the wider Morondava area.
FIGURE 6 in Taxonomizing a truly morphologically cryptic complex of dwarf geckos from Madagascar: molecular evidence for new species-level lineages within the Lygodactylus tolampyae complex
FIGURE 6. Individuals of Lygodactylus morii sp. nov. from near Ampijoroa (Ankarafantsika National Park) in life, photographed in November 2022. A. specimen with sample number MVTIS 33402/33488 (not collected). B. paratype ZSM 159/2022 (ZCMV 15703).
FIGURE 8 in Taxonomizing a truly morphologically cryptic complex of dwarf geckos from Madagascar: molecular evidence for new species-level lineages within the Lygodactylus tolampyae complex
FIGURE 8. Female holotype of Lygodactylus herilalai sp. nov., ZSM 161/2022 (ZCMV 15707) from Ampondrabe, Ankarafantsika National Park, in life, photographed November 2022.
FIGURE 1 in Taxonomizing a truly morphologically cryptic complex of dwarf geckos from Madagascar: molecular evidence for new species-level lineages within the Lygodactylus tolampyae complex
FIGURE 1. Maximum Likelihood tree calculated from DNA sequences of the mitochondrial 16S rRNA gene (alignment length: 517 bp) for 70 samples of the L. tolampyae complex. A sample of L. bivittis was used as outgroup. Numbers are bootstrap support values in percent (500 replicates). Clades are defined on the basis of an analysis with ASAP.
FIGURE 7 in Taxonomizing a truly morphologically cryptic complex of dwarf geckos from Madagascar: molecular evidence for new species-level lineages within the Lygodactylus tolampyae complex
FIGURE 7. Four individuals of Lygodactylus morii sp. nov. photographed in November 2022 at different sites near Ampijoroa (Ankarafantsika National Park) in life, resting at night on terminal twigs of trees as is typical for the L. tolampyae complex. Individuals not individually assignable to sample or voucher specimen numbers, but corresponding to sequences included in Fig. 1.
FIGURE 2 in Morphology and molecular evidence reveal hidden diversity among snapping shrimp of the Alpheus obesomanus group (Decapoda: Alpheidae) with the description of a new species from Brazil
FIGURE 2. Alpheus coralvivo sp. nov., Parque Municipal Marinho do Recife de Fora, Porto Seguro, Bahia, Brazil: A, B, D–J, female holotype (MZUSP 36753); C, male paratype (MOUFPE 18749). (A) major chela, mesial view; (B) same, lateral view (C) male major chela, lateral view; (D) detail of major chela, ventral view; (E) minor chela, lateral view; (F) minor chela, detail of tip of fingers, ventral view; (G) second pereiopod, lateral view; (H) third pereiopod, lateral view; (I) same, detail of dactylus and propodus; (J) fourth pereiopod, lateral view; (K) same, detail of dactylus and propodus; (L) fifth pereiopod, lateral view. Scale bars = 1 mm.
FIGURE 5 in Morphology and molecular evidence reveal hidden diversity among snapping shrimp of the Alpheus obesomanus group (Decapoda: Alpheidae) with the description of a new species from Brazil
FIGURE 5. Currently known distribution of the shrimp species Alpheus coralvivo sp. nov., A. saxidomus (Holthuis, 1980), and A. simus Guérin-Méneville, 1856 based on the material examined and literature records. Created by L.A. Nascimento.
FIGURE 1 in Morphology and molecular evidence reveal hidden diversity among snapping shrimp of the Alpheus obesomanus group (Decapoda: Alpheidae) with the description of a new species from Brazil
FIGURE 1. Alpheus coralvivo sp. nov., Parque Municipal Marinho do Recife de Fora, Porto Seguro, Bahia, Brazil: A, C–F, female holotype (MZUSP 36753); B, male paratype (MOUFPE 18749); G–L, female paratype (MZUSP 36754, dissected); (A) frontal region and cephalic appendages, dorsal view; (B) same, male dorsal view; (C) frontal region and cephalic appendages, lateral view; (D) posterior region of carapace and pleon, lateral view, appendages omitted; (E) telson and uropods, dorsal view; (F) telson, detail of distal margin; (G) mandible, lateral view; (H) first maxilla, mesial view; (I) second maxilla, mesial view; (J) first maxilliped, mesial view; (K) second maxilliped, lateral view; (L) third maxilliped, lateral view. Scale bars = 1 mm.
FIGURE 4 in Morphology and molecular evidence reveal hidden diversity among snapping shrimp of the Alpheus obesomanus group (Decapoda: Alpheidae) with the description of a new species from Brazil
FIGURE 4. Phylogenetic tree of species of the obesomanus group including Alpheus coralvivo sp. nov., obtained using Bayesian Inference analysis and cytochrome oxidase subunit I. Numbers indicate the support values for posterior probabilities; values <0.80 are not showed. Abbreviations: Atl, Atlantic Ocean; BA, Bahia; Pac, Pacific Ocean; SP, São Paulo.
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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.