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FIG. 8 in Vertebrate paleobiodiversity of the Early Cretaceous (Berriasian) Angeac-Charente Lagerstätte (southwestern France): implications for continental faunal turnover at the J/K boundary

FIG. 8. — Actinopterygian remains from the Berriasian of Angeac-Charente: A, isolated tooth of Amiiformes indet. (ANG M-39); B, C, isolated tooth of Amiiformes indet. (ANG M-110); D, dentulous vomerine element of Amiiformes indet. (ANG M-56); E-G, isolated tooth of Ionoscopiformes indet. (ANG M-111); H, jaw frag- ment of Actinopterygii indet. (ANG M-38) in lingual view; I, vertebra of Actinopterygii indet. (ANG M-069). Scale bar: A-C, E-H, 500 µm; D, 250 µm; I, 2 mm.

FIG. 21 in Vertebrate paleobiodiversity of the Early Cretaceous (Berriasian) Angeac-Charente Lagerstätte (southwestern France): implications for continental faunal turnover at the J/K boundary

FIG. 21. — Ornithischian teeth from Angeac-Charente: A, B, Heterodontosaurid premaxillary tooth of Echinodon sp. (ANG15-R671) in lingual (A) and labial (B) views; C, D, Heterodontosaurid premaxillary tooth of Echinodon sp. (ANG14-3368) in lingual (C) and labial (D) views; E, F, hypsilophodontid premaxillary tooth (ANG M-119) in lingual (E) and labial (F) views; G, H, hypsilophodontid dentary tooth (ANG15-R927) in labial (G) and lingual (H) views; I-L, hypsilophodontid maxillary tooth (ANG 10-153) in lingual (I), distal (J), labial (K) and mesial (L) views. Scale bars: A-D, I-L, 5 mm; E-H, 3 mm.

FIG. 25 in Vertebrate paleobiodiversity of the Early Cretaceous (Berriasian) Angeac-Charente Lagerstätte (southwestern France): implications for continental faunal turnover at the J/K boundary

FIG. 25. — Sauropod embryonic or hatchling teeth from Angeac-Charente: A, tooth of Macronaria indet. (ANGM-18) in lingual view; B, C, tooth of Turiasauria indet. (ANGM-118) in labial (B) and lingual (C) views. Scale bar: 500 µm.

FIG. 20 in Vertebrate paleobiodiversity of the Early Cretaceous (Berriasian) Angeac-Charente Lagerstätte (southwestern France): implications for continental faunal turnover at the J/K boundary

FIG. 20. — Pterosaur teeth from Angeac-Charente: A, Pterodactyloidea indet. A (ANG M-24) in labial view; B, Pterodactyloidea indet. A (ANG M-10) in lingual view; C, D, Pterodactyloidea indet. A, (ANG M-42) in lingual (C) and mesial (D) views; E, F, Pterodactyloidea indet. B, (ANG M-43) in lingual (E) and mesial (F) views; G, H, Pterodactyloidea indet. B, (ANG M-112) in lingual (G) and mesial (H) views; I, Pterodactyloidea indet. B, (ANG M-40) in lingual view; J, K, Pterosauria indet. (ANG M-41) in labial (J) and distal (K) views; L, M, Pterosauria indet. (ANG M-113) in lingual (L) and mesial (M) views. Scale bar: 500 µm.

FIG. 24 in Vertebrate paleobiodiversity of the Early Cretaceous (Berriasian) Angeac-Charente Lagerstätte (southwestern France): implications for continental faunal turnover at the J/K boundary

FIG. 24. — Sauropod teeth from Angeac-Charente: A-D, posterior left maxillary tooth of Turiasauria indet. (ANG11-837) in labial (A), mesial (B), lingual (C) and distal (D) views; E-H, left maxillary tooth of Turiasauria indet. (ANG15-R905) in labial (E), mesial (F), lingual (G) and distal (H) views; I-L, left maxillary tooth of Turiasauria indet. (ANG13-2330) in labial (I), mesial (J), lingual (K) and distal (L) views; M-P, left premaxillary tooth of Turiasauria indet. (ANG14-R289) in labial (M), mesial (N), lingual (O) and distal (P) views; Q-T, dentary tooth of Turiasauria indet. (ANG14-3495) in labial (Q), mesial (R), lingual (S) and distal (T) views; U-X, left dentary tooth of Turiasauria indet. (ANG14- R435) in labial (U), mesial (V), lingual (W) and distal (X) views; Y-AA, maxillary tooth of Macronaria indet. (ANG R-1732) in labial (Y), distal (Z) and lingual (AA) views. Scale bar: A-X, 2 cm; Y-AA, 1 cm.

FIG. 30 in Vertebrate paleobiodiversity of the Early Cretaceous (Berriasian) Angeac-Charente Lagerstätte (southwestern France): implications for continental faunal turnover at the J/K boundary

FIG. 30. — Ornithomimosaur remains from Angeac-Charente: A-C, proximal end of right tibia (ANG12-1893) in posterior (A), anterior (B) and lateral (C) views; D, distal end of right tibia (ANG10-56) in anterior view; E, proximal end of right fibula (ANG11-696) in medial view; F-H, Left astragalus and calcaneum (ANG12- 1803) in anterior (F), posterior (G) and dorsal (H) views. Scale bar: A-E, 4 cm; F-H, 2 cm.

FIG. 26 in Vertebrate paleobiodiversity of the Early Cretaceous (Berriasian) Angeac-Charente Lagerstätte (southwestern France): implications for continental faunal turnover at the J/K boundary

FIG. 26. — Sauropod caudal vertebrae from Angeac-Charente: A-C, anterior caudal vertebra of Turiasauria indet. (ANG15-R679) in left lateral (A), posterior (B) and dorsal (C) views; D-F, anterior caudal vertebra of Turiasauria indet. (ANG15-R698) in right lateral (D), posterior (E) and dorsal (F) views; G-I, anterior caudal vertebra of Turiasauria indet. (ANG15-R921) in right lateral (G), posterior (H) and dorsal (I) views; J-L, middle caudal vertebra of Turiasauria indet. (ANG15-R652) in right lateral (J), posterior (K) and dorsal (L) views. Scale bar: 10 cm.

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Data to "The first reconstruction of the head anatomy of a Cretaceous insect, †Gerontoformica gracilis (Hymenoptera, Formicidae), and the early evolution of ants"

Data to Richter et al. 2022 "The  first reconstruction of the head anatomy of a Cretaceous insect, &dagger;Gerontoformica gracilis (Hymenoptera, Formicidae), and the early evolution of ants" in Insect Systematics and Diversity. The dataset contains PDFs of ACCTRAN and DELTRAN parsimony reconstructions of character evolution,  image and data files of an anlysis of mandibular muscle fiber lengths, a ORS Dragonfly file containing the segmentation of head structures of &dagger;Gerontoformica gracilis, the focal study object of the article, and 4µCT scans of wasps used as outgroups in the study.  Details of these µCT scans can be found in the methods section of the related article. The scans are provided in 2D TIF files and represent datasets cropped to just the head and transformed to align the main head axes with the viewing planes, and resampled  with a bin 2x2x2 in ImageJ for easier data handling, as they were used in the article. The scan files also include scan parameter log files; importantly, due to binning, the given camera pixel size has to be multiplied by 2. The datasets cover Parischnogaster sp. (de Saussure, 1852) (Hymenoptera, Vespidae), Methocha sp.(Hymenoptera, Thynnidae), Ampulex sp. (Fabricius, 1781) (Hymenoptera, Ampulicidae), and Sceliphron caementarium (Drury, 1773) (Hymenoptera, Sphecidae). All taxa were stained in a 2% iodine solution in ethanol for a week prior to scanning. They were transferred to a sealed off pipette tip of appropriate size filled with ethanol and mounted on a metal sample holder. They were scanned at a SkyScan 2211 (Bruker, Billerica, USA) at the Max Planck Institute for the Science of Human History in Jena, equipped with a high resolution (4000 × 2600 pixel) X-ray sensitive CCD camera in the nanofocus mode. Scanning parameters for the extant taxa are summarized in <a>Table 2</a> of the related article.

Text-fig. 2. Map of Partizansk coal basin with early angiosperm localities. a: Severosuchan Formation, Aptian; b: Frentsevka Formation, early-middle Albian. 1 – Novoveselaya village; 2 – 3rd Kamenka River; 3 – Bolshoy Kuvshin; 4 – Andreev Inlet. in Angiosperm Diversification In The Early Cretaceous Of Primorye, Far East Of Russia

Text-fig. 2. Map of Partizansk coal basin with early angiosperm localities. a: Severosuchan Formation, Aptian; b: Frentsevka Formation, early-middle Albian. 1 – Novoveselaya village; 2 – 3rd Kamenka River; 3 – Bolshoy Kuvshin; 4 – Andreev Inlet.

Text-fig. 4. Porechye open pit coal mine. a: photography of the Lipovtsy Formation section; b: stratigraphic column, 1 – sandstone, 2 – conglomerate, 3 – coal, 4 – tuff dated by U-Th-Pb geochronology, 5 – siltstone, 6 – mudstone, 7 – palynological samples with angiosperm pollen, 8 – dispersed angiosperm cuticles. in Angiosperm Diversification In The Early Cretaceous Of Primorye, Far East Of Russia

Text-fig. 4. Porechye open pit coal mine. a: photography of the Lipovtsy Formation section; b: stratigraphic column, 1 – sandstone, 2 – conglomerate, 3 – coal, 4 – tuff dated by U-Th-Pb geochronology, 5 – siltstone, 6 – mudstone, 7 – palynological samples with angiosperm pollen, 8 – dispersed angiosperm cuticles.

Text-fig. 3. Map of Razdolnaya coal basin with early angiosperm localities. a: Lipovtsy Formation, Aptian; b: Galenki Formation, early-middle Albian. 1 – Porechye coal mine; 2 – Konstantinovka; 3 – Aleksee-Nikolskoe coal mine; 4 – Fedorovsky Rudnik; 5 – Podgorodenka coalfield; 6 – Firsov Cape. in Angiosperm Diversification In The Early Cretaceous Of Primorye, Far East Of Russia

Text-fig. 3. Map of Razdolnaya coal basin with early angiosperm localities. a: Lipovtsy Formation, Aptian; b: Galenki Formation, early-middle Albian. 1 – Porechye coal mine; 2 – Konstantinovka; 3 – Aleksee-Nikolskoe coal mine; 4 – Fedorovsky Rudnik; 5 – Podgorodenka coalfield; 6 – Firsov Cape.

Text-fig. 8. SEM (a, b) and SRXTM (c, d) images of fruit associated with Miranthus elegans and Miranthus kvacekii; Mira locality, Portugal. a: Apical view of capsular fruit with five, partly open valves revealing the enclosed reticulate seeds (arrows). b: Detail of fruit wall showing an enclosed seed (arrow). c: Transverse section (orthoslice xy1200) of fruit showing central column (cc) of placenta and numerous angular and bitegmic seeds; note that the outer integument (black arrow) is thicker than inner integument (white arrow). d: Longitudinal section (orthoslice yz1239) of fruit showing perigynous attachment of calyx, central column (cc) of the placenta and sections through seeds. Specimen, Mira 99-S156331 (a–d). Scale bars = 600 µm (a, c, d), 200 µm (b). in Early Flowers Of Primuloid Ericales From The Late Cretaceous Of Portugal And Their Ecological And Phytogeographic Implications

Text-fig. 8. SEM (a, b) and SRXTM (c, d) images of fruit associated with Miranthus elegans and Miranthus kvacekii; Mira locality, Portugal. a: Apical view of capsular fruit with five, partly open valves revealing the enclosed reticulate seeds (arrows). b: Detail of fruit wall showing an enclosed seed (arrow). c: Transverse section (orthoslice xy1200) of fruit showing central column (cc) of placenta and numerous angular and bitegmic seeds; note that the outer integument (black arrow) is thicker than inner integument (white arrow). d: Longitudinal section (orthoslice yz1239) of fruit showing perigynous attachment of calyx, central column (cc) of the placenta and sections through seeds. Specimen, Mira 99-S156331 (a–d). Scale bars = 600 µm (a, c, d), 200 µm (b).

Text-fig. 3. SRXTM images of Miranthus elegans gen. et sp. nov.; Mira locality, Portugal. a, b: Volume renderings of flower bud in two different lateral views showing long pedicel, distinct calyx (ca) with almost equiaxial epidermal cells and corolla (co) with nearly smooth surface. c–e: Transverse sections (c, orthoslice xy1500; d, orthoslice xy1760; e, orthoslice xy1850) through flower bud at levels below the anthers showing stamen filaments (yellow) opposite the corolla lobes (co) and smaller staminodes (orange) in Early Flowers Of Primuloid Ericales From The Late Cretaceous Of Portugal And Their Ecological And Phytogeographic Implications

Text-fig. 3. SRXTM images of Miranthus elegans gen. et sp. nov.; Mira locality, Portugal. a, b: Volume renderings of flower bud in two different lateral views showing long pedicel, distinct calyx (ca) with almost equiaxial epidermal cells and corolla (co) with nearly smooth surface. c–e: Transverse sections (c, orthoslice xy1500; d, orthoslice xy1760; e, orthoslice xy1850) through flower bud at levels below the anthers showing stamen filaments (yellow) opposite the corolla lobes (co) and smaller staminodes (orange)

Text-fig. 5. SRXTM images of Miranthus elegans gen. et sp. nov.; Mira locality, Portugal. a, b: Transverse sections of flower (a, orthoslice xy0665 close to the apex of placenta; b, orthoslice xy0800 in middle part of placenta) showing remains of calyx with distinct bundles (arrows), ovary wall (ow) and numerous ovules (ov) on the central mushroom-shaped globose placenta (pl) with central column (cc). c: Transverse section of flower (orthoslice xy0620) through perianth and ovary (ow) at a level above the placenta showing ovules (ov) and cellular preservation of the sepal bundles (arrows shown for one sepal); note abaxial surface of sepals with thick-walled epidermal cells, thick cuticle, and fine pointed verrucae. d: Longitudinal section of flower (orthoslice xz0500) showing perigynous position of calyx and semi-inferior ovary (ow, ovary wall) with a central placenta (pl), central column (cc) and numerous ovules (ov); note spiny verrucae on abaxial surface of calyx lobes. Specimens, Mira 100-S153145 (a, b), Mira 100-S170155 (c, d, holotype). Scale bars = 600 µm (a–d). in Early Flowers Of Primuloid Ericales From The Late Cretaceous Of Portugal And Their Ecological And Phytogeographic Implications

Text-fig. 5. SRXTM images of Miranthus elegans gen. et sp. nov.; Mira locality, Portugal. a, b: Transverse sections of flower (a, orthoslice xy0665 close to the apex of placenta; b, orthoslice xy0800 in middle part of placenta) showing remains of calyx with distinct bundles (arrows), ovary wall (ow) and numerous ovules (ov) on the central mushroom-shaped globose placenta (pl) with central column (cc). c: Transverse section of flower (orthoslice xy0620) through perianth and ovary (ow) at a level above the placenta showing ovules (ov) and cellular preservation of the sepal bundles (arrows shown for one sepal); note abaxial surface of sepals with thick-walled epidermal cells, thick cuticle, and fine pointed verrucae. d: Longitudinal section of flower (orthoslice xz0500) showing perigynous position of calyx and semi-inferior ovary (ow, ovary wall) with a central placenta (pl), central column (cc) and numerous ovules (ov); note spiny verrucae on abaxial surface of calyx lobes. Specimens, Mira 100-S153145 (a, b), Mira 100-S170155 (c, d, holotype). Scale bars = 600 µm (a–d).

Text-fig. 7. SEM (a) and SRXTM (b–e) images of Miranthus kvacekii sp. nov.; Mira locality, Portugal. a: Lateral view of flower bud showing corolla lobes extending beyond calyx; note surface of pedicel, calyx and corolla with small equiaxial epidermal cells and indumentum of densely spaced, short stiff trichomes. b, c: Longitudinal sections through floral bud in two directions perpendicular to each other (a, orthoslice yz1024; b, orthoslice xz0950) showing corolla (co), calyx (ca), stamens (st) and semi-inferior ovary with thin ovary wall (ow) and central mushroom-shaped globose placenta (pl) bearing numerous ovules (ov). d, e: Transverse sections through floral bud above placenta (d, orthoslice xy0915; e, orthoslice xy1095) showing calyx (ca), corolla (co), ovary wall (ow) and ovules (ov); yellow outlines indicate the positions of anthers (d) and filaments (e); orange outlines indicate the position of three of the possible staminodes. Specimen, Mira 100-S170157 (a–e, holotype). Scale bars = 600 µm (a–c), 300 µm (d, e). in Early Flowers Of Primuloid Ericales From The Late Cretaceous Of Portugal And Their Ecological And Phytogeographic Implications

Text-fig. 7. SEM (a) and SRXTM (b–e) images of Miranthus kvacekii sp. nov.; Mira locality, Portugal. a: Lateral view of flower bud showing corolla lobes extending beyond calyx; note surface of pedicel, calyx and corolla with small equiaxial epidermal cells and indumentum of densely spaced, short stiff trichomes. b, c: Longitudinal sections through floral bud in two directions perpendicular to each other (a, orthoslice yz1024; b, orthoslice xz0950) showing corolla (co), calyx (ca), stamens (st) and semi-inferior ovary with thin ovary wall (ow) and central mushroom-shaped globose placenta (pl) bearing numerous ovules (ov). d, e: Transverse sections through floral bud above placenta (d, orthoslice xy0915; e, orthoslice xy1095) showing calyx (ca), corolla (co), ovary wall (ow) and ovules (ov); yellow outlines indicate the positions of anthers (d) and filaments (e); orange outlines indicate the position of three of the possible staminodes. Specimen, Mira 100-S170157 (a–e, holotype). Scale bars = 600 µm (a–c), 300 µm (d, e).

Text-fig. 2. SEM images of Miranthus elegans gen. et sp. nov.; Mira locality, Portugal. a, b: Flowers in oblique lateral view showing remains of calyx and slightly semi-inferior ovary with elongated apical style (a); note larger openings in the floral tissue (asterisk) interpreted as schizogenous secretory cavities and the stomata-like secretory structures on the upper portion of the ovary (arrows) that are interpreted as nectariferous (b). c: Detail of ovary surface showing secretory stomata-like structures (arrows). d: Flower in lateral view showing fragmentary calyx and broken slightly semi-inferior ovary with secretory stomata-like structures; note the point of attachment of the central placenta (pl). e: Cluster of seeds removed from the ovary in (d) showing reticulate surface. f: Outer (abaxial) surface of calyx lobe showing the slightly pointed papillae and scattered, fine trichomes (arrows). g: Triaperturate pollen grains from the ovary surface. Specimens, Mira 100-S153146 (a, b), Mira 100-S170155 (c), Mira 100-S101266 (d, e), Mira 105-S100732 (f), Mira 100-S170125 (g). Scale bars = 600 µm (a, b, d), 300 µm (f), 100 µm (c, e), 10 µm (g). in Early Flowers Of Primuloid Ericales From The Late Cretaceous Of Portugal And Their Ecological And Phytogeographic Implications

Text-fig. 2. SEM images of Miranthus elegans gen. et sp. nov.; Mira locality, Portugal. a, b: Flowers in oblique lateral view showing remains of calyx and slightly semi-inferior ovary with elongated apical style (a); note larger openings in the floral tissue (asterisk) interpreted as schizogenous secretory cavities and the stomata-like secretory structures on the upper portion of the ovary (arrows) that are interpreted as nectariferous (b). c: Detail of ovary surface showing secretory stomata-like structures (arrows). d: Flower in lateral view showing fragmentary calyx and broken slightly semi-inferior ovary with secretory stomata-like structures; note the point of attachment of the central placenta (pl). e: Cluster of seeds removed from the ovary in (d) showing reticulate surface. f: Outer (abaxial) surface of calyx lobe showing the slightly pointed papillae and scattered, fine trichomes (arrows). g: Triaperturate pollen grains from the ovary surface. Specimens, Mira 100-S153146 (a, b), Mira 100-S170155 (c), Mira 100-S101266 (d, e), Mira 105-S100732 (f), Mira 100-S170125 (g). Scale bars = 600 µm (a, b, d), 300 µm (f), 100 µm (c, e), 10 µm (g).

Text-fig. 1. SEM images of flowers of Miranthus elegans gen. et sp. nov.; Mira locality, Portugal. a, b: Flowers in lateral view showing elongated pedicel, narrowly triangular sepals and elongated protruding style (a); note the large openings in the floral tissue and pedicel (asterisks) interpreted as schizogenous secretory cavities. c: Flower in lateral view with portion of the calyx missing exposing the ovary wall and slightly raised nectariferous ring with probable stomata-like secretory structures (arrow). d: Flower in lateral view showing long pedicel and three of the five tepals; note the elongated narrowly triangular form of the sepals. e: Flower in oblique lateral view with portion of the calyx missing exposing the ovary and elongated style. f, g: Flowers in apical view showing the bases of five sepals (f) and apex of the five-parted ovary; note larger openings in the floral tissue (asterisk) interpreted as schizogenous secretory cavities. Specimens, Mira 100-S170155 (a, holotype), Mira 100-S153145 (b, c, g), Mira 100- S101267 (d), Mira 105-S100732 (e), Mira 100-S101268 (f). Scale bars = 600 µm (a–g). in Early Flowers Of Primuloid Ericales From The Late Cretaceous Of Portugal And Their Ecological And Phytogeographic Implications

Text-fig. 1. SEM images of flowers of Miranthus elegans gen. et sp. nov.; Mira locality, Portugal. a, b: Flowers in lateral view showing elongated pedicel, narrowly triangular sepals and elongated protruding style (a); note the large openings in the floral tissue and pedicel (asterisks) interpreted as schizogenous secretory cavities. c: Flower in lateral view with portion of the calyx missing exposing the ovary wall and slightly raised nectariferous ring with probable stomata-like secretory structures (arrow). d: Flower in lateral view showing long pedicel and three of the five tepals; note the elongated narrowly triangular form of the sepals. e: Flower in oblique lateral view with portion of the calyx missing exposing the ovary and elongated style. f, g: Flowers in apical view showing the bases of five sepals (f) and apex of the five-parted ovary; note larger openings in the floral tissue (asterisk) interpreted as schizogenous secretory cavities. Specimens, Mira 100-S170155 (a, holotype), Mira 100-S153145 (b, c, g), Mira 100- S101267 (d), Mira 105-S100732 (e), Mira 100-S101268 (f). Scale bars = 600 µm (a–g).

Text-fig. 16. Reconstruction of herbaceous angiosperms from Bolshoy Kuvshin locality, Frentsevka Formation, early-middle Albian. a: undescribed species, spec. IBSS 320-137; b: Achaenocarpites capitellatus KRASSILOV et VOLYNETS. in Angiosperm Diversification In The Early Cretaceous Of Primorye, Far East Of Russia

Text-fig. 16. Reconstruction of herbaceous angiosperms from Bolshoy Kuvshin locality, Frentsevka Formation, early-middle Albian. a: undescribed species, spec. IBSS 320-137; b: Achaenocarpites capitellatus KRASSILOV et VOLYNETS.

Text-fig. 15. Reconstruction of herbaceous angiosperms from Bolshoy Kuvshin locality, Frentsevka Formation, early-middle Albian. a: Asiatifolium elegans G.SUN, SHUANG X.GUO et SHAO L.ZHENG; b: Jixia pinnatipartita SHUANG X.GUO et G.SUN. in Angiosperm Diversification In The Early Cretaceous Of Primorye, Far East Of Russia

Text-fig. 15. Reconstruction of herbaceous angiosperms from Bolshoy Kuvshin locality, Frentsevka Formation, early-middle Albian. a: Asiatifolium elegans G.SUN, SHUANG X.GUO et SHAO L.ZHENG; b: Jixia pinnatipartita SHUANG X.GUO et G.SUN.

Text-fig. 14. Bolshoy Kuvshin, Frentsevka Formation, early-middle Albian. a, e: Asiatifolium elegans G.SUN, SHUANG X.GUO et SHAO L.ZHENG, a – spec. IBSS 320-8, e – spec. IBSS 320-75; b, c: Jixia pinnatipartita SHUANG X.GUO et G.SUN, b – spec. IBSS 320-359, c – spec. IBSS 320-367; d: Achaenocarpites capitellatus KRASSILOV et VOLYNETS, spec. IBSS 320-120; f: Ternaricarpites floribundus KRASSILOV et VOLYNETS, spec. IBSS 320-10; g: undescribed species, spec. IBSS 320-137. Scale bar 1 cm in a, e–g and 5 mm in b–d. in Angiosperm Diversification In The Early Cretaceous Of Primorye, Far East Of Russia

Text-fig. 14. Bolshoy Kuvshin, Frentsevka Formation, early-middle Albian. a, e: Asiatifolium elegans G.SUN, SHUANG X.GUO et SHAO L.ZHENG, a – spec. IBSS 320-8, e – spec. IBSS 320-75; b, c: Jixia pinnatipartita SHUANG X.GUO et G.SUN, b – spec. IBSS 320-359, c – spec. IBSS 320-367; d: Achaenocarpites capitellatus KRASSILOV et VOLYNETS, spec. IBSS 320-120; f: Ternaricarpites floribundus KRASSILOV et VOLYNETS, spec. IBSS 320-10; g: undescribed species, spec. IBSS 320-137. Scale bar 1 cm in a, e–g and 5 mm in b–d.