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FIGURE 9 in Two new species of Pisolithus (Sclerodermataceae) from Australasia, and an assessment of the confused nomenclature of P. tinctorius
FIGURE 9. Pisolithus tympanobaculus sp. nov. a–b sporocarp (PDD75026); c–d SEMs of spores (PDD75026); e spores (PDD75026).
FIGURE 8 in Two new species of Pisolithus (Sclerodermataceae) from Australasia, and an assessment of the confused nomenclature of P. tinctorius
FIGURE 8. Pisolithus thermaeus sp. nov. a sporocarp (PDD74168); b sporocarp (PDD100265); c SEM of spores (PDD77425); d–e spores (PDD74526).
FIGURE 2. Bayesian 50 in Two new species of Pisolithus (Sclerodermataceae) from Australasia, and an assessment of the confused nomenclature of P. tinctorius
FIGURE 2. Bayesian 50% majority-rule consensus tree of the ITS nrDNA of Pisolithus, with boletoid outgroup. Bayesian posterior probabilities (PP) values are indicated above or below branches. Novel sequences bold. Phylogenetic lineages A–C indicated as per Phosri et al. (2012), and species numbering continuing on from Martin et al. (2002).
FIGURE 3. Bayesian 50 in Two new species of Pisolithus (Sclerodermataceae) from Australasia, and an assessment of the confused nomenclature of P. tinctorius
FIGURE 3. Bayesian 50% majority-rule consensus tree of the ITS nrDNA of the Australasian taxa Pisolithus, with some European clades as outgroup. Bayesian posterior probabilities (PP) values are indicated above or below branches. Novel sequences bold. Species clade numbering indicated as per Martin et al. (2002) and Phosri et al. (2012).
FIGURE 6. Pisolithus marmoratus. a in Two new species of Pisolithus (Sclerodermataceae) from Australasia, and an assessment of the confused nomenclature of P. tinctorius
FIGURE 6. Pisolithus marmoratus. a sporocarp (PDD93554); b SEM of spores (PDD77426); c–d spores (PDD77289).
FIGURE 5. Pisolithus croceorrhizus. a in Two new species of Pisolithus (Sclerodermataceae) from Australasia, and an assessment of the confused nomenclature of P. tinctorius
FIGURE 5. Pisolithus croceorrhizus. a sporocarps (PDD77286); b (PDD74169); c–d spores (PDD77431); e SEM of spores (PDD77437).
FIGURE 4. Pisolithus albus. a in Two new species of Pisolithus (Sclerodermataceae) from Australasia, and an assessment of the confused nomenclature of P. tinctorius
FIGURE 4. Pisolithus albus. a sporocarp (PDD77432); b–c SEMs of spores (PDD77430); d–e spores (PDD77430).
FIGURE 1 in Two new species of Pisolithus (Sclerodermataceae) from Australasia, and an assessment of the confused nomenclature of P. tinctorius
FIGURE 1. Typical habitat. New Zealand: a. thermal area with vents in middle distance and surrounding pine plantations visible (T. Lebel); b. fruitbodies of Pisolithus albus along path edge in thermal area (T. Lebel); c. sampling for Pisolithus, steam vents visible in background (T. Lebel); d. Pisolithus thermaeus fruitbodies at edge of steam vent (T. Lebel). Australia: e. typical disturbed ground in gravel track (S. McMullan-Fisher); f. fruitbodies along edge of walking path (S. McMullan-Fisher).
FIGURES 62–65 in Resolving the confusion between two fossil freshwater diatoms from Otago, New Zealand: Encyonema jordanii and Encyonema jordaniforme (Cymbellaceae, Bacillariophyta)
FIGURES 62–65. Scanning electron micrographs from sample AT82 (Encyonema jordani, Otago, New Zealand, Weissflog Collection, Jordan, 4/1882) present in the Hustedt Collection in Bremerhaven (Germany). 62. External view of an entire valve. 63. External view of the valve apex showing the terminal raphe fissure. 64. Internal view of an entire valve showing the helictoglossa and the deflected proximal raphe endings. 65. Internal view of the central area showing the intermissio and the square-shaped areolae. Scale bar represent 10 μm in figs 62, 64 and 1 μm for figs 63, 65.
FIGURES 25–61. E. jordanii. 25–43 in Resolving the confusion between two fossil freshwater diatoms from Otago, New Zealand: Encyonema jordanii and Encyonema jordaniforme (Cymbellaceae, Bacillariophyta)
FIGURES 25–61. E. jordanii. 25–43. Light micrographs from sample AT82 (Encyonema jordani, Otago, New Zealand, Weissflog Collection, Jordan, 4/1882) present in the Hustedt Collection in Bremerhaven (Germany). 44–61. Light micrographs from sample Slide VIII-2-B1 (Van Heurck Collection, Botanic Garden Meise, Belgium). Scale bar represents 10 μm.
FIGURES 85–89 in Resolving the confusion between two fossil freshwater diatoms from Otago, New Zealand: Encyonema jordanii and Encyonema jordaniforme (Cymbellaceae, Bacillariophyta)
FIGURES 85–89. Scanning electron micrographs of E. jordaniforme from Foulden Maar. 85. External view of an entire valve. 86. External view of the central area showing small rounded areolae and almost straight proximal raphe endings. 87. External view of a valve apex showing the terminal raphe fissure. 88. Internal view of an entire valve. 89. Internal view of the central area showing the deflected proximal raphe endings with a broad intermissio. Scale bar represent 10 μm for figs 85, 88 and 1 μm for figs 86, 87, 89.
FIGURES 1–24. 1–2. P. T in Resolving the confusion between two fossil freshwater diatoms from Otago, New Zealand: Encyonema jordanii and Encyonema jordaniforme (Cymbellaceae, Bacillariophyta)
FIGURES 1–24. 1–2. P. T. Cleve's original figures of Encyonema jordanii. 3–10. E. jordanii from Hustedt in A.Schmidt Atlas plate 379. 11–16. E. jordanii sensu Foged 1979, Krammer's type for E. jordaniforme. 17. Foged's sample phial 508 photographed by Nina Lindholm. 18–24. Raeside's figures of Cymbella jordanii. Scale bars represent 10 μm.
FIGURES 66–84 in Resolving the confusion between two fossil freshwater diatoms from Otago, New Zealand: Encyonema jordanii and Encyonema jordaniforme (Cymbellaceae, Bacillariophyta)
FIGURES 66–84. Light micrographs of E. jordaniforme from Foulden Maar (sample 7 U. K.). Scale bar represents 10 μm.
FIGURE 1. Dracula agnosia. A. Habit. B in Dracula agnosia (Orchidaceae: Pleurothallidinae), a long confused undescribed species
FIGURE 1. Dracula agnosia. A. Habit. B. Column and lip attached to ovary. C. Upper surface of lip, lower surface of lip. D. Outer surface of petal, profile of petal, inner surface of petal. E. Dorsal sepal, lateral sepal, both with a portion of the tail removed. Drawn from the holotype Doucette 4001.
FIGURE 3 in Dracula agnosia (Orchidaceae: Pleurothallidinae), a long confused undescribed species
FIGURE 3. Comparison of species similar to Dracula agnosia. A–C. D. maduroi. D. D. agnosia Davis s.n., E. D. agnosia, Doucette 4003, F. D. agnosia, Doucette 4001. G–I. D. olmosii.
FIGURE 6 in The relationship and different C Kranz anatomy of Bassia eriantha and Bassia eriophora, two often confused Irano-Turanian and Saharo-Sindian species
FIGURE 6. The scanning electron microscopy images of C4 structures in Bassia eriophora. A) Overall view of BS cells; chloroplasts are arranged close to the vascular bundles, BS cells contain few numbers of mitochondria; B) close view of granal poor BSC chloroplasts; C) close view of granal rich chloroplasts of M cells. VB: Vascular Bundles, Chl: Chloroplast, Mt: Mitochondria.
FIGURE 5 in The relationship and different C Kranz anatomy of Bassia eriantha and Bassia eriophora, two often confused Irano-Turanian and Saharo-Sindian species
FIGURE 5. Perianth shape and floral anatomy in Bassia eriantha (A–C) and. B. eriophora (D–G). Dissected tepal (A), anatomy of hyaline tepal and upper dentate segments (B) and cross section of lower tubular portion of connate tepal (C) of B. eraintha. Dissected tepal (D), anatomy of upper green part of perianths showing kochioid-like type of C4 anatomy (E), close up of crystaliferous cells in which the arrows show the lignified "U-shape" side of the cell wall (F) and lower hyaline part lacking photosynthetic structures (G) in B. eriophora.
FIGURE 2. A & B in The relationship and different C Kranz anatomy of Bassia eriantha and Bassia eriophora, two often confused Irano-Turanian and Saharo-Sindian species
FIGURE 2. A & B) Venation in floral leaves of Bassia eriantha (A) and B. eriophora (B), arrow shows freely ending veinlets; C & D) hand section of the fresh leaves collected from natural habitat shows atriplicoid type for B. eriantha, Akhani et al. 22225 (C) and kochioid type for B. eriophora, Akhani et al. 22048 (D); E & F) fruits in B. eriantha Akhani et al. 22225 (E) and B. eriophora Akhani et al. 20885 (F) after removal of hairs.
FIGURE 1 in The relationship and different C Kranz anatomy of Bassia eriantha and Bassia eriophora, two often confused Irano-Turanian and Saharo-Sindian species
FIGURE 1. Bassia eriantha (A–C) and B. eriophora (D–F) in natural condition and in cultivation. A) Habit in nature (50 km E of Esfahan towards Naein, Esfahan Province, Iran), B) seedling and C) vegetative plant of B. eriantha; D) Habit in nature (east of Mahshahr towards Hendijan, Khuzestan Province, Iran), E) seedling and F) vegetative plant of B. eriophora. Note that B and E, and C and F are the same age cultivated under laboratory conditions. Scale bar=1 cm (photos A, D by H. Akhani, others by R. Khoshravesh).
FIGURE 9 in The relationship and different C Kranz anatomy of Bassia eriantha and Bassia eriophora, two often confused Irano-Turanian and Saharo-Sindian species
FIGURE 9. Frequency of the species Bassia eriantha and B. eriophora in relation to annual mean temperature (A) and mean temperature of warmest quarte (B).
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