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Text-fig. 3. a: Panoramic reconstruction of the portion of the Govone outcrop from intervals GLA10 to GLA20 in condition of low river level. b: Transported leaf assemblage in the bottom part of bed GLA20. c: Detail of the outcrop of the leaf-bearing bed GLA20 and the underlying wood-rich layer GLA19. in Remains Of A Subtropical Humid Forest In A Messinian Evaporitebearing Succession At Govone, Northwestern Italy - Preliminary Results
Text-fig. 3. a: Panoramic reconstruction of the portion of the Govone outcrop from intervals GLA10 to GLA20 in condition of low river level. b: Transported leaf assemblage in the bottom part of bed GLA20. c: Detail of the outcrop of the leaf-bearing bed GLA20 and the underlying wood-rich layer GLA19.
Text-fig. 8. a–e: Quercus aff. cerris. a: Cup, Oriolo MSF 984. b: Cup, Oriolo MSF 982. c: Leaf, Oriolo MSF 689. d: Leaf, Oriolo MSF 659. e: Oriolo MSF 657. f: Quercus aff. pubescens Oriolo MSF 688. g: Quercus sect. Quercus acorn, Oriolo MSF 658. h–j: Quercus iberica. h: Oriolo MSF 694. i: Oriolo MSF 639. j: Oriolo MSF 698. Scale bars 10 mm (a, b, g), 50 mm (c–f, h–j). in The Late Early Pleistocene Flora Of Oriolo, Faenza (Italy): Assembly Of The Modern Forest Biome
Text-fig. 8. a–e: Quercus aff. cerris. a: Cup, Oriolo MSF 984. b: Cup, Oriolo MSF 982. c: Leaf, Oriolo MSF 689. d: Leaf, Oriolo MSF 659. e: Oriolo MSF 657. f: Quercus aff. pubescens Oriolo MSF 688. g: Quercus sect. Quercus acorn, Oriolo MSF 658. h–j: Quercus iberica. h: Oriolo MSF 694. i: Oriolo MSF 639. j: Oriolo MSF 698. Scale bars 10 mm (a, b, g), 50 mm (c–f, h–j).
Text-fig. 14. a, b: Acer aff. campestre. a: Oriolo MSF 664. b: Oriolo MSF 666. c, d: Acer aff. monspessulanum. c: Oriolo MSF 641. d: Oriolo MSF 662. e: Acer aff. opulus subsp. obtusatum Oriolo MSF 669. f, g: Acer aff. cappadocicum subsp. lobelii. f: Oriolo MSF 675. g: Oriolo MSF 631. h, i: Cornus sp. Oriolo MSF 655, two views of a strongly folded leaf impression. Scale bars 50 mm (a, e–g), 10 mm (b–d, h, i). in The Late Early Pleistocene Flora Of Oriolo, Faenza (Italy): Assembly Of The Modern Forest Biome
Text-fig. 14. a, b: Acer aff. campestre. a: Oriolo MSF 664. b: Oriolo MSF 666. c, d: Acer aff. monspessulanum. c: Oriolo MSF 641. d: Oriolo MSF 662. e: Acer aff. opulus subsp. obtusatum Oriolo MSF 669. f, g: Acer aff. cappadocicum subsp. lobelii. f: Oriolo MSF 675. g: Oriolo MSF 631. h, i: Cornus sp. Oriolo MSF 655, two views of a strongly folded leaf impression. Scale bars 50 mm (a, e–g), 10 mm (b–d, h, i).
Text-fig. A2. a: Ulmus carpinifolia GLED., 1773 syn. of Ulmus minor MILL., 1768, (herbarium E00824885). b: Ulmus carpinifolia GLED., 1773 syn. of Ulmus minor MILL., 1768, (herbarium E00824885). c: Ulmus carpinifolia GLED., 1773 syn. of Ulmus minor MILL., 1768, (herbarium E00824885 detail of (a)). d, e: Ulmus elliptica K.KOCH, 1849 (herbarium E00034393). f, g: Ulmus lancifolia ROXB., 1814, nom. inval. (herbarium NMNH03413489). h: Ulmus lancifolia ROXB., 1814, nom. inval. (herbarium NMNH03413488). Asterisks indicate different types of asymmetric leaf base. Scale bars 50 mm (a, d, e, f), 10 mm (b, c, g, h). in The Late Early Pleistocene Flora Of Oriolo, Faenza (Italy): Assembly Of The Modern Forest Biome
Text-fig. A2. a: Ulmus carpinifolia GLED., 1773 syn. of Ulmus minor MILL., 1768, (herbarium E00824885). b: Ulmus carpinifolia GLED., 1773 syn. of Ulmus minor MILL., 1768, (herbarium E00824885). c: Ulmus carpinifolia GLED., 1773 syn. of Ulmus minor MILL., 1768, (herbarium E00824885 detail of (a)). d, e: Ulmus elliptica K.KOCH, 1849 (herbarium E00034393). f, g: Ulmus lancifolia ROXB., 1814, nom. inval. (herbarium NMNH03413489). h: Ulmus lancifolia ROXB., 1814, nom. inval. (herbarium NMNH03413488). Asterisks indicate different types of asymmetric leaf base. Scale bars 50 mm (a, d, e, f), 10 mm (b, c, g, h).
Text-fig. A3. a: Leaf morphotype 1 Tebano MSF SG 049. b: Leaf morphotype 2 Oriolo MSF 631. c: Leaf morphotype 3 Oriolo MSF n.n. d, f: Leaf morphotype 4. d: Oriolo MSF 891. e: Oriolo MSF 856. f: Oriolo MSF 858. g: Leaf morphotype 5 Oriolo MSF 783. h: Leaf morphotype 6 Oriolo MSF 952. i: Leaf morphotype 7 Oriolo MSF 862. j, l: Leaf morphotype 8. j: Oriolo MSF 912. k: Oriolo MSF 662. l: Oriolo MSF 662-1. m: Leaf morphotype 9 Oriolo MSF 715. n: Leaf morphotype 10 Oriolo MSF 716. o: Leaf morphotype 11, overview and detail of margin Oriolo MSF 880. p–z: Various rosaceous leaves/ leaflets. p: Oriolo MSF 943. q: Oriolo MSF 890. r: Oriolo MSF 950. s: Oriolo MSF 958. t: Oriolo MSF 966 aff. Sorbus. u: Oriolo MSF 956. v: Oriolo MSF 961. w: Oriolo MSF 962. x: Oriolo MSF 874. y: Oriolo MSF 883. z: Oriolo MSF 960. in The Late Early Pleistocene Flora Of Oriolo, Faenza (Italy): Assembly Of The Modern Forest Biome
Text-fig. A3. a: Leaf morphotype 1 Tebano MSF SG 049. b: Leaf morphotype 2 Oriolo MSF 631. c: Leaf morphotype 3 Oriolo MSF n.n. d, f: Leaf morphotype 4. d: Oriolo MSF 891. e: Oriolo MSF 856. f: Oriolo MSF 858. g: Leaf morphotype 5 Oriolo MSF 783. h: Leaf morphotype 6 Oriolo MSF 952. i: Leaf morphotype 7 Oriolo MSF 862. j, l: Leaf morphotype 8. j: Oriolo MSF 912. k: Oriolo MSF 662. l: Oriolo MSF 662-1. m: Leaf morphotype 9 Oriolo MSF 715. n: Leaf morphotype 10 Oriolo MSF 716. o: Leaf morphotype 11, overview and detail of margin Oriolo MSF 880. p–z: Various rosaceous leaves/ leaflets. p: Oriolo MSF 943. q: Oriolo MSF 890. r: Oriolo MSF 950. s: Oriolo MSF 958. t: Oriolo MSF 966 aff. Sorbus. u: Oriolo MSF 956. v: Oriolo MSF 961. w: Oriolo MSF 962. x: Oriolo MSF 874. y: Oriolo MSF 883. z: Oriolo MSF 960.
Text-fig. 11. a: Sapindopsis sp., 3rd Kamenka, Frentsevka Formation, early-middle Albian, spec. IBSS 40-1; b, c: Trochodendroides sp., Konstantinovka, Galenki Formation, early-middle Albian, spec. IBBS 11/145, b – upper part of leaf, c – crenate margin; d: Dicotylophyllum sp. 2, Konstantinovka, Galenki Formation, early-middle Albian, spec. IBBS 11/133; e: Sapindopsis cf. angusta (HEER) SEWARD et V.M.CONWAY, Andreev Inlet, Frentsevka Formation, early-middle Albian, spec. IBSS 28/104; f: Sapindopsis variabilis FONTAINE, Bikin River, Alchan Formation, early-middle Albian, spec. IBSS 4561/124-1; g: Laurophyllum sp., Konstantinovka, Galenki Formation, early-middle Albian, spec. IBBS 11/131. Scale bar 1 cm in a, b, d, f, g and 5 mm in c, e. in Angiosperm Diversification In The Early Cretaceous Of Primorye, Far East Of Russia
Text-fig. 11. a: Sapindopsis sp., 3rd Kamenka, Frentsevka Formation, early-middle Albian, spec. IBSS 40-1; b, c: Trochodendroides sp., Konstantinovka, Galenki Formation, early-middle Albian, spec. IBBS 11/145, b – upper part of leaf, c – crenate margin; d: Dicotylophyllum sp. 2, Konstantinovka, Galenki Formation, early-middle Albian, spec. IBBS 11/133; e: Sapindopsis cf. angusta (HEER) SEWARD et V.M.CONWAY, Andreev Inlet, Frentsevka Formation, early-middle Albian, spec. IBSS 28/104; f: Sapindopsis variabilis FONTAINE, Bikin River, Alchan Formation, early-middle Albian, spec. IBSS 4561/124-1; g: Laurophyllum sp., Konstantinovka, Galenki Formation, early-middle Albian, spec. IBBS 11/131. Scale bar 1 cm in a, b, d, f, g and 5 mm in c, e.
Text-fig. 17. Angiosperm leaf morphotypes in late Aptian and early-middle Albian of Primorye. a, k: Dicotylophyllum sp. 1, 2; b: Araliaephyllum vittenburgii GOLOVN. et VOLYNETS; c: Araliaephyllum ussuriense (KRASSILOV) GOLOVN.; d: Trochodendroides sp., e: undescribed species, spec. IBSS 320-137; f: Asiatifolium elegans G.SUN, SHUANG X.GUO et SHAO L.ZHENG; g: Sapindopsis cf. angusta (HEER) SEWARD et V.M.CONWAY; h: Sapindopsis sp.; i: Achaenocarpites capitellatus KRASSILOV et VOLYNETS; j: Jixia pinnatipartita SHUANG X.GUO et G.SUN; l: Pandanites ahnertii (KRYSHT.) GOLOVN.; m: Araliaephyllum luciferum (KRYSHT.) GOLOVN. in Angiosperm Diversification In The Early Cretaceous Of Primorye, Far East Of Russia
Text-fig. 17. Angiosperm leaf morphotypes in late Aptian and early-middle Albian of Primorye. a, k: Dicotylophyllum sp. 1, 2; b: Araliaephyllum vittenburgii GOLOVN. et VOLYNETS; c: Araliaephyllum ussuriense (KRASSILOV) GOLOVN.; d: Trochodendroides sp., e: undescribed species, spec. IBSS 320-137; f: Asiatifolium elegans G.SUN, SHUANG X.GUO et SHAO L.ZHENG; g: Sapindopsis cf. angusta (HEER) SEWARD et V.M.CONWAY; h: Sapindopsis sp.; i: Achaenocarpites capitellatus KRASSILOV et VOLYNETS; j: Jixia pinnatipartita SHUANG X.GUO et G.SUN; l: Pandanites ahnertii (KRYSHT.) GOLOVN.; m: Araliaephyllum luciferum (KRYSHT.) GOLOVN.
Text-fig. 9. a–d: Nyssidium orientale SAMYLINA, Partizansk, Starosuchan Formation, Barremian, a – spec. BIN 506/3749, general view of four fruits, b1 – spec. BIN 506/3749-1, holotype, b2 – spec. BIN 506/3749-2, c – spec. BIN 506/3749-6, d – spec. BIN 506/3749-5; e–f: Cercidiphyllum sujfunense KRASSILOV, Konstantinovka, Galenki Formation, early-middle Albian, e – spec. IBSS 11-135, fruit, f – spec. IBSS 11-134, leaf, holotype. Scale bar 5 mm in a, e, f and 2 mm in b–d. in Angiosperm Diversification In The Early Cretaceous Of Primorye, Far East Of Russia
Text-fig. 9. a–d: Nyssidium orientale SAMYLINA, Partizansk, Starosuchan Formation, Barremian, a – spec. BIN 506/3749, general view of four fruits, b1 – spec. BIN 506/3749-1, holotype, b2 – spec. BIN 506/3749-2, c – spec. BIN 506/3749-6, d – spec. BIN 506/3749-5; e–f: Cercidiphyllum sujfunense KRASSILOV, Konstantinovka, Galenki Formation, early-middle Albian, e – spec. IBSS 11-135, fruit, f – spec. IBSS 11-134, leaf, holotype. Scale bar 5 mm in a, e, f and 2 mm in b–d.
Text-fig. 10. a–d: Araliaephyllum luciferum (KRYSHT.) GOLOVN., Partizansk, Severosuchan Formation, Aptian, a – spec. TSNIGRM 3013/1, lectotype, b – spec TSNIGRM 3013/2, c – spec. TSNIGRM 3013/4, d – spec. TSNIGRM 3013/3; e, j: Pandanites ahnertii (KRYSHT.) GOLOVN., Konstantinovka, Lipovtsy Formation, Aptian, TSNIGRM 3013/5, e – fragment of leaf margin, j – general view, j1 – lectotype, j2 – leaf, figured in (e); f: Araliaephyllum ussuriense (KRASSILOV) GOLOVN., Andreev Inlet, Frentsevka Formation, early-middle Albian, spec. IBBS 28/103; g: Araliaephyllum vittenburgii GOLOVN. et VOLYNETS, Podgorodenka coalfield, Galenki Formation, early-middle Albian, spec. IBBS 41/1, g1 – spec. IBBS 41/1a, holotype, g2 – spec. IBBS 41/1b; h: Dicotylophyllum sp. 1, Podgorodenka coalfield, Lipovtsy Formation, Aptian, spec. IBBS 28L-4; i: Sapindopsis sp., 3rd Kamenka, Frentsevka Formation, early-middle Albian, spec. IBSS 325/8. Scale bar 5 mm in a–h and 1 cm in i, j. in Angiosperm Diversification In The Early Cretaceous Of Primorye, Far East Of Russia
Text-fig. 10. a–d: Araliaephyllum luciferum (KRYSHT.) GOLOVN., Partizansk, Severosuchan Formation, Aptian, a – spec. TSNIGRM 3013/1, lectotype, b – spec TSNIGRM 3013/2, c – spec. TSNIGRM 3013/4, d – spec. TSNIGRM 3013/3; e, j: Pandanites ahnertii (KRYSHT.) GOLOVN., Konstantinovka, Lipovtsy Formation, Aptian, TSNIGRM 3013/5, e – fragment of leaf margin, j – general view, j1 – lectotype, j2 – leaf, figured in (e); f: Araliaephyllum ussuriense (KRASSILOV) GOLOVN., Andreev Inlet, Frentsevka Formation, early-middle Albian, spec. IBBS 28/103; g: Araliaephyllum vittenburgii GOLOVN. et VOLYNETS, Podgorodenka coalfield, Galenki Formation, early-middle Albian, spec. IBBS 41/1, g1 – spec. IBBS 41/1a, holotype, g2 – spec. IBBS 41/1b; h: Dicotylophyllum sp. 1, Podgorodenka coalfield, Lipovtsy Formation, Aptian, spec. IBBS 28L-4; i: Sapindopsis sp., 3rd Kamenka, Frentsevka Formation, early-middle Albian, spec. IBSS 325/8. Scale bar 5 mm in a–h and 1 cm in i, j.
Fine-root biomass production, sedge root, sedge leaf, and moss shoot decomposition, soil water-table level, and temperature data from two sedge fens in Finland
<p>Dataset including fine-root biomass production, mass loss of sedge (<em>Carex rostrata</em>) roots and leaves, and moss (<em>Sphagnum</em> <em>fallax</em>) shoots, along with environmental data (soil water-table level, air temperature, soil temperature at 5 cm, and soil temperature at 15 cm) from two sedge fens located in southern Finland (Lakkasuo, Orivesi, 61°48' N 24°19'E) and northern Finland (Lompolojänkkä, Kittilä, 68°N 24°12'E). Data are from a climate change experiment, where warming was induced with open top chambers (OTCs) and drying with shallow ditching. Data are from years 2011-2013.</p>
Data for: Associations between leaf developmental stability, canalization and phenotypic plasticity in an architectural perspective
<p class="MsoNormal"><span>Associations between developmental stability, canalization and phenotypic plasticity have been predicted, but rarely supported by direct evidence. Architectural analysis may provide a more powerful approach to finding correlations among these mechanisms in plants. T</span><span>o investigate the relationships among the three mechanisms in architectural perspective, w</span><span>e </span><span>subjected plants of </span><em><span>Abutilon theophrasti</span></em><span> to three densities, measured and calculated </span><span>fluctuating asymmetry (FA), coefficients of variation (CV)</span><span> and </span><span>plasticity (PI) of three leaf traits, to analyze the </span><span>correlations among these variables.</span><span> As density increased, mean leaf size, petiole length and angle of most layers and mean leaf FA of some layers decreased (at both stages), CV of petiole angle increased (at day 50), and PI of petiole length and angle across all layers decreased (at day 70); leaf FA and CV of traits generally increased with higher layers at all densities. At both stages, there were more positive correlations between FA and CV at lower vs. high densities; at day 50, little correlation of plasticity with FA or CV was found; at day 70, more positive correlations between FA and PI occurred for response to high vs. low density than for response to medium vs. low density, and more positive correlations between CV and PI occurred at lower vs. high densities. Results suggested that developmental instability, decreased canalization and plasticity can be cooperative and the relationships between decreased canalization and plasticity are more likely to be positive if decreased canalization is due to vibrant growth rather than stressful effects. The relationships of plasticity with developmental instability differed from its relationship with decreased canalization in the way of variation. Decreased canalization should be more beneficial for possible plasticity in the future, while canalization may result from already-expressed plasticity.</span></p>
Figs 161–166 in New leaf- and litter-dwelling species of the genus Pholcus from Southeast Asia (Araneae, Pholcidae)
Figs 161–166. Epigyna, ventral views, and cleared female genitalia, ventral and dorsal views. 161–163. Pholcus domingo Huber sp. nov. (ZFMK, Ar 15721). 164–166. P. matutum Huber sp. nov. (ZFMK, Ar 15731).
Figs 145–147 in New leaf- and litter-dwelling species of the genus Pholcus from Southeast Asia (Araneae, Pholcidae)
Figs 145–147. Pholcus domingo Huber sp. nov., tips of left procursi, retrolateral views. 145. Dimapatoy (ZFMK, Ar 15728). 146. Santo Domingo (type locality) (ZFMK, Ar 15720). 147. Mt. Mupo (ZFMK, Ar 15727). Scale bar = 0.3 mm.
Figs 140–144 in New leaf- and litter-dwelling species of the genus Pholcus from Southeast Asia (Araneae, Pholcidae)
Figs 140–144. Pholcus domingo Huber sp. nov. (ZFMK, Ar 15720–21). 140–141. Left male palp, prolateral and retrolateral views. 142. Male chelicerae, frontal view. 143–144. Cleared female genitalia, ventral and dorsal views. Scale bars: 140–141 = 0.5 mm; 142–144 = 0.3 mm.
Figs 93–100. Live specimens. 93–96 in New leaf- and litter-dwelling species of the genus Pholcus from Southeast Asia (Araneae, Pholcidae)
Figs 93–100. Live specimens. 93–96. Pholcus tambunan Huber sp. nov., Crocker Range, ♂, penultimate ♂, and ♀ with egg-sac. 97–100. P. bario Huber sp. nov., Bario, ♂ and ♀ with egg-sac.
Figs 114–119 in New leaf- and litter-dwelling species of the genus Pholcus from Southeast Asia (Araneae, Pholcidae)
Figs 114–119. Pholcus tambunan Huber sp. nov., SEM micrographs (ZFMK, Ar 15711, 15715). 114. Male left palpal tarsal organ. 115. Tip of left embolus. 116. Male gonopore. 117. Base of trichobothrium on male palpal tibia. 118. Female ALS. 119. Epigynum, ventral view. Scale bars: 114, 118 = 20 µm; 115 = 50 µm; 116 = 40 µm; 117 = 8 µm; 119 = 200 µm.
Figs 59–66. Live specimens. 59–62 in New leaf- and litter-dwelling species of the genus Pholcus from Southeast Asia (Araneae, Pholcidae)
Figs 59–66. Live specimens. 59–62. Pholcus bukittimah Huber sp. nov., Dairy Farm, ♂, penultimate ♂, and ♀ with partly parasitized egg-sac. 63–66. P. barisan Huber sp. nov., Bukit Barisan, ♂ and ♀♀ with variably expanded abdomens.
Figs 54–58. Pholcus ledang Huber, 2011 in New leaf- and litter-dwelling species of the genus Pholcus from Southeast Asia (Araneae, Pholcidae)
Figs 54–58. Pholcus ledang Huber, 2011, SEM micrographs (ZFMK, Ar 15704–05). 54. Left procursus, retrolateral view. 55. Right procursus, distal view. 56. Cuticular processes on whitish retrolateral area of left procursus. 57. Male gonopore. 58. Epigynum, ventral view. Scale bars: 54, 58 = 200 µm; 55 = 100 µm; 56 = 10 µm; 57 = 30 µm.
Figs 32–38. Live specimens. 32–35. Pholcus gombak Huber, 2011 in New leaf- and litter-dwelling species of the genus Pholcus from Southeast Asia (Araneae, Pholcidae)
Figs 32–38. Live specimens. 32–35. Pholcus gombak Huber, 2011, Kemensah (32) and Gunung Liang (33–35), ♂, ♀ with parasitized egg-sac seven days before eclosion of wasps (33), one day before eclosion (34), and at eclosion (35). 36–38. P. ledang Huber, 2011, Gunung Ledang, ♂ and ♀ with egg-sac.
Figs 15–19 in New leaf- and litter-dwelling species of the genus Pholcus from Southeast Asia (Araneae, Pholcidae)
Figs 15–19. Pholcus uludong Huber sp. nov. (ZFMK, Ar 15695–96). 15–16. Left male palp, prolateral and retrolateral views; arrow points at uncus-like process of proximal bulbal sclerite. 17. Male chelicerae, frontal view. 18–19. Cleared female genitalia, ventral and dorsal views. Scale bars: 15–16, 18–19 = 0.5 mm; 17 = 0.3 mm.
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