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403 results for “morphological characteristics”
FIGURE 5 in Morphological characteristics and phylogenetic analyses revealed two new species of Agaricus subg. Minoriopsis from Mexico
FIGURE 5. Microscopic characteristics of Agaricus xalapensis. a–e. (J2367, holotype). a. Basidia; b. Spores; c. Cheilocystidia; d. Hyphae of the lower surface of the annulus; e. Pileipellis hyphae. Scale bars = 5 μm.
FIGURE 4 in Morphological characteristics and phylogenetic analyses revealed two new species of Agaricus subg. Minoriopsis from Mexico
FIGURE 4. Macroscopic characteristics of Agaricus xalapensis. a–b. Basidiomata in situ; c. Annulus detail; d. Context discoloration when exposed; e. stipe surface with tinny erected-fibrillose scales; f–g. Basidiomata in situ. a–e. (J2367, holotype); f–g. (J2953). Scale bars = 10 mm.
FIGURE 1 in Morphological characteristics and phylogenetic analyses revealed two new species of Agaricus subg. Minoriopsis from Mexico
FIGURE 1. Maximum likelihood phylogram of Agaricus subg. Minoriopsis resulting from analysis of ITS sequence data. The bootstrap support values greater than 50% and Bayesian posterior probabilities greater than 0.8 are indicated above branches (BS/PP). New species are in bold. T = Type specimen.
FIGURE 2 in Morphological characteristics and phylogenetic analyses revealed two new species of Agaricus subg. Minoriopsis from Mexico
FIGURE 2. Macroscopic characteristics of Agaricus calolepidotus. a, c. Basidiomata in situ (LD201929, holotype); b. Annulus and stipe detail (LD201949); d. Context discoloration when exposed (LD201942). Scale bars = 10 mm.
FIGURE 3 in Luteoporia tenuissima sp. nov. (Polyporales, Basidiomycota), evidenced by morphological characteristics and phylogenetic analysis
FIGURE 3. Microscopic structures of Luteoporia tenuissima (Holotype). a Basidiospores. b Basidia. c Basidioles. d Hyphae from trama. e Hyphae at dissepiment edge. Drawings by: Kai-Yue Luo.
FIGURE 2. A in Luteoporia tenuissima sp. nov. (Polyporales, Basidiomycota), evidenced by morphological characteristics and phylogenetic analysis
FIGURE 2. A basidioma of Luteoporia tenuissima in situ (Holotype, Dai 25825). Scale bar = 1.0 cm. Photo by: Yu-Cheng Dai.
FIGURES 30–34 in Morphology of Neoheegeria dalmatica Schmutz, 1909 (Thysanoptera, Phlaeothripidae) larvae-their diagnostic characteristics
FIGURES 30–34. Characteristics of second larval instars: Haplothrips verbasci: (30) pronotum; (31) setae of tergites VII–XI; (32) setae of sternite IX; Neoheegeria verbasci: (33) pronotum; (34) setae of sternite IX.
FIGURES 20–29 in Morphology of Neoheegeria dalmatica Schmutz, 1909 (Thysanoptera, Phlaeothripidae) larvae-their diagnostic characteristics
FIGURES 20–29. Neoheegeria dalmatica characteristics of second instar larva and pupae: (20) sculpture and setae of sternites VI–VII; (21) tergal seta with knobbed apex; (22) sternal seta with acute apex; (23) lateral part of segment VIII with knobbed setae and spiracle; (24) abdominal segments VIII–XI; (25) ventral side of abdominal segments IX–XI and distal setae; (26) forked seta V2 on sternite IX; (27) pupa I—head and pronotum; (28) pupa II—head ventral side; (29) pupa II—abdominal projection.
FIGURES 10–19 in Morphology of Neoheegeria dalmatica Schmutz, 1909 (Thysanoptera, Phlaeothripidae) larvae-their diagnostic characteristics
FIGURES 10–19. Neoheegeria dalmatica characteristics of second instar larva: (10) total body; (11) head—dorsal side; (12) head—ventral side; (13) mouth cone with maxillary palpi; (14) pronotum; (15) mesonotum; (16) spiracle on mesonotum; (17) metanotum; (18) sculpture and setae of tergite II; (19) sculpture and setae of tergites VI–VII.
FIGURES 1–9 in Morphology of Neoheegeria dalmatica Schmutz, 1909 (Thysanoptera, Phlaeothripidae) larvae-their diagnostic characteristics
FIGURES 1–9. Neoheegeria dalmatica characteristics of first instar larva: (1) total body; (2) antenna; (3) sculpture and seta of sternite II; (4) pronotum (5) sculpture, spiracle and seta on tergite II; (6) sculpture of sternites V–VII; (7) sculpture of sternites VIII–X; (8) lateral part of segment VIII; (9) colour, sculpture and setae V1 on sternites VIII–X.
FIGURE 27 in Nitzschia austriaca Hustedt: a characteristic diatom of Hungarian inland saline waters including a morphological comparison with the type material
FIGURE 27. Box plots showing variation in chemical variables, (a) conductivity (mS cm-1), (b) pH, (c) TSS (mg L-1) and (d) TP (mg L-1) values of ponds, in which N. austriaca is present (1) or absent (0).
FIGURES 20–24 in Nitzschia austriaca Hustedt: a characteristic diatom of Hungarian inland saline waters including a morphological comparison with the type material
FIGURES 20–24. SEM micrographs of N. austriaca from the type material (sample E9708 from Austria). Arrow indicates the central nodule on Fig. 24.
FIGURE 25 in Nitzschia austriaca Hustedt: a characteristic diatom of Hungarian inland saline waters including a morphological comparison with the type material
FIGURE 25. The Hungarian occurrences of N. austriaca. Dot: Hungarian surveillance monitoring and our former data, star: data from present study.
FIGURES 14–19 in Nitzschia austriaca Hustedt: a characteristic diatom of Hungarian inland saline waters including a morphological comparison with the type material
FIGURES 14–19. SEM micrographs of N. austriaca from the Apaj population (Hungary). White arrows indicate the central raphe endings on Fig. 15 and the central nodule on Fig. 18.
FIGURE 1 in Nitzschia austriaca Hustedt: a characteristic diatom of Hungarian inland saline waters including a morphological comparison with the type material
FIGURE 1. Ordination diagram of NMDS (a) with the 95% confidence interval (point: population of Apaj, plus: population of type material) and the Shepard plot (b). R2=0.95.
FIGURE 4 in A new species of Postia (Basidiomycota) based on morphological and molecular characteristics
FIGURE 4. Basidiospores of Postia cylindrica and P. leucomallella. a: Postia cylindrica. b: Postia leucomallella.
FIGURE 3 in A new species of Postia (Basidiomycota) based on morphological and molecular characteristics
FIGURE 3. Microscopic structures of Postia cylindrica. a: Basidiospores. b: Basidia and basidioles. c: Hyphae from trama. d: Hyphae from subiculum. e: Gloeoplerous hyphal ends of cuticular layer.
FIGURE 1 in A new species of Postia (Basidiomycota) based on morphological and molecular characteristics
FIGURE 1. Strict consensus tree illustrating the phylogeny of Postia cylindrica and other species generated by Bayesian analysis and most parsimonious based on ITS sequences included in the study. Numbers at branches indicate Bayesian posterior probabilities values and parsimony bootstrap values higher than 50%.—Indicates lack of support or support less than 50% for an articular clade.
FIGURE 3 in Tuberculina photiniae sp. nov. (Helicobasidiales, Basidiomycota) supported by morphological characteristics and phylogenetic data
FIGURE 3. Macro-morphological characteristics of Tuberculina photiniae (the holotype). (A, B) Mycoparasite on the aecia of Aecidium wenshanese. (C, D) Aecidia of the rust on leaves and young shoots of plant. Bars: A, B = 10 mm; C, D = 5 mm.
FIGURE 1 in Tuberculina photiniae sp. nov. (Helicobasidiales, Basidiomycota) supported by morphological characteristics and phylogenetic data
FIGURE 1. Maximum Parsimony strict consensus tree illustrating the phylogeny of Tuberculina photiniae and related species based on ITS sequences. Branches are labelled with maximum likelihood bootstraps higher than 70%, parsimony bootstrap proportions higher than 50% and Bayesian posterior probabilities greater than 0.95. Clade names follow Lutz et al. (2004b).
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
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