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Fig. 43 in Molecular and morphological recognition of species boundaries in the neglected ant genus Brachymyrmex (Hymenoptera: Formicidae): toward a taxonomic revision
Fig. 43 Brachymyrmex nebulosus: a–c head, dorsal, and lateral view of a worker (from www.antweb.org; photographer: Ryan Perry)
Fig. 16 in Molecular and morphological recognition of species boundaries in the neglected ant genus Brachymyrmex (Hymenoptera: Formicidae): toward a taxonomic revision
Fig. 16 Brachymyrmex bruchi: a, c, e head, dorsal, and lateral view of the lectotype worker; b, d, f B. giardi var. nitida: head, dorsal, and letral view of a syntype worker
Fig. 36 in Molecular and morphological recognition of species boundaries in the neglected ant genus Brachymyrmex (Hymenoptera: Formicidae): toward a taxonomic revision
Fig. 36 Brachymyrmex heeri: a, c, e B. giardi var. cordobensis: head, dorsal, and lateral view of a syntype worker; b, d, f head, dorsal, and lateral view of a syntype of the putative worker- queen intercaste
Fig. 50 in Molecular and morphological recognition of species boundaries in the neglected ant genus Brachymyrmex (Hymenoptera: Formicidae): toward a taxonomic revision
Fig. 50 Brachymyrmex santschii: a, c, e head, dorsal, and lateral view of a worker (from www. antweb.org; photographer: Will Ericson); b, d, f head, dorsal, and lateral view of a putative worker- queen intercaste
Fig. 35 in Molecular and morphological recognition of species boundaries in the neglected ant genus Brachymyrmex (Hymenoptera: Formicidae): toward a taxonomic revision
Fig. 35 Brachymyrmex heeri: a, c, e head, dorsal, and lateral view of the lectotype worker; b, d, f Brachymyrmex var. goeldii n. syn.: head, dorsal, and lateral view of a syntype worker
Fig. 5 in Molecular and morphological recognition of species boundaries in the neglected ant genus Brachymyrmex (Hymenoptera: Formicidae): toward a taxonomic revision
Fig. 5 Morphological characteristics of the head of Brachymyrex. (a1) clypeus with five hairs of which a single long apical hair is positioned near the anterior margin, two in mediolateral position and two near the toruli (black arrow); (a2) clypeus with a row of long, thick hairs near the anterior margin (black arrow), toruli touching but not surpassing the posterior clypeal margin in oblique anterodorsal view (gray arrow); (a3) toruli surpassing the posterior clypeal margin in oblique anterodorsal view (gray arrow); (b1) eyes below the cephalic midline; (b2) eyes on cephalic midline; (c1) eyes with three or four ommatidia along the maximal diameter of the eye; (c2) eyes with more than four ommatidia along
Fig. 3 in Molecular and morphological recognition of species boundaries in the neglected ant genus Brachymyrmex (Hymenoptera: Formicidae): toward a taxonomic revision
Fig. 3 Habitus of a selection of males of Brachymyrmex: head and lateral view of a, b B. coactus, c, d B. myops, e, f B. longicornis var. immunis (junior synonym of B. admotus), and g, h B. australis var. curta (junior synonym of B. australis)
Fig. 4 in Molecular and morphological recognition of species boundaries in the neglected ant genus Brachymyrmex (Hymenoptera: Formicidae): toward a taxonomic revision
Fig. 4 The native distribution range of Brachymyrmex as reconstructed from the unique georeferenced localities of the here studied material (black circles) and the Brachymyrmex records available in the Global
Fig. 2 in Molecular and morphological recognition of species boundaries in the neglected ant genus Brachymyrmex (Hymenoptera: Formicidae): toward a taxonomic revision
Fig. 2 Habitus of a selection of queens of Brachymyrmex: head and lateral view of a, b B. admotus, c, d B. antennatus, e, f B. aphidicola, and g, h B. giardi
FIGURE 5 in Recognition of a new species of Hedysarum (Fabaceae, Hedysareae) from China based on morphological and molecular evidence
FIGURE 5. Morphology comparison of leaflets, flowers and legumes of Hedysarum cuonanum, H. longigynophorum and H. xizangense. A, H. longigynophorum (from Chang et al. 2013206, WUK, except for the loment which is from Xu et al. Xu130346, WUK); B, H. cuonanum (from Holotype); C, H. xizangense (from Chen et al. 13-0886, WUK). For specimen details, see Appendix. le, leaflets; b, bracteoles; c, calyx; s, standard; w, wings; k, keels; a, androecium; o, ovary; lo, loment.
FIGURE 2 in Recognition of a new species of Hedysarum (Fabaceae, Hedysareae) from China based on morphological and molecular evidence
FIGURE 2. Bayesian tree based on combined plastid psbA-trnH, trnC-petN, petN-psbM sequences. The Bayesian posterior probabilities are below the branches, and the maximum parsimony (left) and maximum likelihood (right) bootstrap supports are above the branches.
FIGURE 1 in Recognition of a new species of Hedysarum (Fabaceae, Hedysareae) from China based on morphological and molecular evidence
FIGURE 1. Bayesian tree based on combined nuclear ETS and ITS sequences. The Bayesian posterior probabilities are below the branches, and the maximum parsimony (left) and maximum likelihood (right) bootstrap supports are above the branches. A dash indicates a branch that is not found in the maximum likelihood tree.
Fig. 3 in A morphological and molecular study supports the recognition of Rhipilia psammophila sp. nov. and Rhipilia baculifera comb. nov. (Halimedaceae, Chlorophyta) from southern Australia
Fig. 3. Rhipilia psammophila. (a) Specimen in situ at Two Peoples Bay, Western Australia, growing among seagrasses. (b) Clustered specimens growing in sandy substrata. (c) The pressed holotype specimen (PERTH 09389660). (d) Siphons bearing perpendicular lateral branches with terminal tenacula (indicated by arrows). (e) Tenacula adhering to adjacent filament (indicated by arrow). (f) Fertile filaments with numerous lateral gametangia. (g) Closer view of lateral gametangia. Scale bars: 1 cm (c); 60 µm (d, e); 600 µm (f); 300 µm (g). Vouchers: (a, b, d, e) J.M.Huisman 2.1.22.1 (PERTH [holotype]); (f, g) A.Dekker, C.Nutt, K.Murray & H.Botha s.n. (PERTH 08188459). Photos: J. M. Huisman.
Fig. 1 in A morphological and molecular study supports the recognition of Rhipilia psammophila sp. nov. and Rhipilia baculifera comb. nov. (Halimedaceae, Chlorophyta) from southern Australia
Fig. 1. Phylogeny of the Halimedineae suborder of Bryopsidales, showing the placement of Rhipilia baculifera (indicated with a triangle) and Rhipilia psammophila (indicated with a star) in the genus Rhipilia of the tribe Rhipileae. The phylogeny is based on concatenated rbcL and tufA sequences, with bootstrap support indicated at branches (when>70). The scale is in estimated substitutions per site. Outgroups were pruned from the original tree for this visualisation. The concatenated alignment was 94.8% complete, with 7 of 127 sequences missing for rbcL and 6 of 127 sequences missing for tufA. Lineage 1 and 2 annotations refer to the naming of these lineages by Cremen et al. (2019).
Fig. 4 in A morphological and molecular study supports the recognition of Rhipilia psammophila sp. nov. and Rhipilia baculifera comb. nov. (Halimedaceae, Chlorophyta) from southern Australia
Fig. 4. Rhipilia baculifera. (a) Specimen in situ at type locality at Point Lonsdale, Victoria, growing among the seagrass Amphibolis antarctica. (b) Freshly collected specimens, with a limited basal aggregation of siphons. (c) Pressed specimen dredged from deep water, south of Rottnest Island, with a substantial stipe. (d) Closer view of aggregated siphons at base of specimens in Fig. 4b. (e) Free siphons that are dichotomously divided with occasional shallow constrictions. A reproductive tuft is developing at the apex of the right-hand siphon. (f) View of densely branched reproductive tuft, with moniliform lower siphons. Scale bars: 2 cm (b, c); 1 mm (d–f). Voucher: (a, b) H.Verbruggen HV03984 (MELU); (c) C.Sim s.n. (PERTH 08822182); (d–f) living material, vouchers not retained. Photos: H. Verbruggen (a, b, d–f); J. M. Huisman (c).
Fig. 2 in A morphological and molecular study supports the recognition of Rhipilia psammophila sp. nov. and Rhipilia baculifera comb. nov. (Halimedaceae, Chlorophyta) from southern Australia
Fig. 2. Densely sampled gene trees of (a) rbcL and (b) tufA for the genus Rhipilia, including the new species R. psammophila (indicated with a star) and the newly transferred R. baculifera (indicated with a triangle).
FIGURE 1 in Morphological and molecular evidence for the recognition of Caloglossa fonticola sp. nov. (Delesseriaceae, Rhodophyta) from an underground spring in Guangxi, China
FIGURE 1. Map of China showing the location of the study area, Baimo Cave in Bama County, Guangxi, China, where samples of Caloglossa fonticola sp. nov. were collected.
FIGURE 4 in Morphological and molecular evidence for the recognition of Caloglossa fonticola sp. nov. (Delesseriaceae, Rhodophyta) from an underground spring in Guangxi, China
FIGURE 4. Caloglossa (Ceramiales, Rhodophyta) maximum likelihood tree based on the rbcL DNA sequences data. Bootstrap supports for maximum likelihood, and Bayesian inference (ML/BI) are shown on branches. '*' denotes the branch differed in the BI topology (data not shown).
FIGURE 3 in Morphological and molecular evidence for the recognition of Caloglossa fonticola sp. nov. (Delesseriaceae, Rhodophyta) from an underground spring in Guangxi, China
FIGURE 3. Drawing of Caloglossa fonticola sp. nov. thallus at the node follows Kamiya et al. (1999, 2003). Transverse pericentral cells are omitted. Axial cells are brown, wing cells are purple, and rhizoids are cyan. AB, abaxial side; AD, adjacent side to the lateral branch; AX, adaxial side; FLA, first axial cell of the lateral axis; FMA, first axial cell of the main axis; LA, lateral axis; LPC, lateral pericentral cell; MA, main axis; NA, nodal axial cell; OP, opposite side to the lateral branch; WC, wing cell; Rhizoids form from groups of second and third-order cells arising from the first three axial cells of the main and lateral axes (type B in Kamiya et al. 2003). Scale bar = 200 µm.
Data from: Molecular phylogeny and morphological analysis of Tetraglochin (Rosaceae: Rosoideae: Sanguisorbeae) and recognition of the new species T. andina
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