Find research datasets worth reusing

FIGURE 2. Call measurements: 1) number of frequency peaks; 2) maximum frequency; 3) rising or falling call; 4) start frequency; 5) amplitude of the largest modulation; 6) duration up to the largest modulation; 7) minimum frequency; 8) end frequency; 9) call duration. in --Molecular--and--acoustic--evidence--support--the--species--status--of--Anthus rubescens rubescens and--Anthus [rubescens] japonicus--(Passeriformes:--Motacillidae)

FIGURE 2. Call measurements: 1) number of frequency peaks; 2) maximum frequency; 3) rising or falling call; 4) start frequency; 5) amplitude of the largest modulation; 6) duration up to the largest modulation; 7) minimum frequency; 8) end frequency; 9) call duration.

FIGURE3. Maximum-likelihood tree inferred from 998 bp of CR using a HKY+G substitution model implemented in MEGAX (Kumar et al. 2018). Bootstrap values are indicated on the nodes. in --Molecular--and--acoustic--evidence--support--the--species--status--of--Anthus rubescens rubescens and--Anthus [rubescens] japonicus--(Passeriformes:--Motacillidae)

FIGURE3. Maximum-likelihood tree inferred from 998 bp of CR using a HKY+G substitution model implemented in MEGAX (Kumar et al. 2018). Bootstrap values are indicated on the nodes.

FIGURE1. Breeding, migrating and wintering distributions of Palearctic Anthus [rubescens] japonicus and Nearctic Anthus rubescens rubescens/alticola subspecies groups (from BirdLife International 2022; illustration @Andrew Birch). Circles indicate origins of sequenced individuals and triangles indicate origins of analysed recordings of calls. Localities outside of the usual range of the species complex (e.g., Ireland, Oman and Israel) are not figured here. in --Molecular--and--acoustic--evidence--support--the--species--status--of--Anthus rubescens rubescens and--Anthus [rubescens] japonicus--(Passeriformes:--Motacillidae)

FIGURE1. Breeding, migrating and wintering distributions of Palearctic Anthus [rubescens] japonicus and Nearctic Anthus rubescens rubescens/alticola subspecies groups (from BirdLife International 2022; illustration @Andrew Birch). Circles indicate origins of sequenced individuals and triangles indicate origins of analysed recordings of calls. Localities outside of the usual range of the species complex (e.g., Ireland, Oman and Israel) are not figured here.

FIGURE 4. Polystichum xinfeniae.—A. Habit.—B. Petioles.—C in Three new species of Polystichum (Dryopteridaceae) from Xizang, China based on morphological and molecular evidence

FIGURE 4. Polystichum xinfeniae.—A. Habit.—B. Petioles.—C. Abaxial pinnae, showing sori.—D. Upper portion of adaxial lamina.— E. Middle portion of adaxial lamina.

FIGURE 3. Polystichum wusugongii.—A. Habit.—B in Three new species of Polystichum (Dryopteridaceae) from Xizang, China based on morphological and molecular evidence

FIGURE 3. Polystichum wusugongii.—A. Habit.—B. Fiddlehead (young leaves).—C. Lower portion of plant.—D. Abaxial view of lower portion of lamina.—E. Adaxial view of portion of lamina.—F. Abaxial view of upper portion of lamina.—G. Abaxial view of portion of lamina showing sori.

FIGURE 1 in Three new species of Polystichum (Dryopteridaceae) from Xizang, China based on morphological and molecular evidence

FIGURE 1. Maximum likelihood phylogeny of Polystichum based on five plastid markers (rbcL, rps4, rps4-trnS, trnL, and trnL-F). The numbers associated with branches are maximum likelihood bootstrap support (MLBS) and Bayesian posterior probability (BIPP). The asterisk indicates MLBS = 100, BIPP = 1.00.

FIGURE 3 in Morphological and molecular evidence for a new species of Fuscoporia (Hymenochaetales, Basidiomycota) from tropics

FIGURE 3. Microscopic structures of Fuscoporia kenyana (holotype, Dai 19202). a. Basidiospores. b. Basidia and basidioles. c. Cystidioles. d. Hymenial setae. e. Generative hyphae at dissepiment edge. f. Hyphae from tube trama. g. Hyphae from context. Drawing by: Qian Chen.

FIGURE 2 in Morphological and molecular evidence for a new species of Fuscoporia (Hymenochaetales, Basidiomycota) from tropics

FIGURE 2. Phylogeny of Fuscoporia inferred from ITS+nLSU dataset. Statistical values (MP/ML) are indicated for each node. The newly sequenced specimens of Fuscoporia are in bolds.

FIGURE 4 in Morphological and molecular evidence for a new species of Fuscoporia (Hymenochaetales, Basidiomycota) from tropics

FIGURE 4. Basidiocarps of Fuscoporia kenyana. A. Holotype, Dai 19202. B. Paratype, Dai 19205. Photo by: Yu-Cheng Dai.

FIGURE 1 in Morphological and molecular evidence for a new species of Fuscoporia (Hymenochaetales, Basidiomycota) from tropics

FIGURE 1. Phylogeny of Fuscoporia inferred from nLSU sequences. Statistical values (MP/ML) are indicated for each node. Names of new species are in bold.