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Text-fig. 8. Lanfrancia subglobosa E.REID et M.CHANDLER. a–c, e–g: Holotype V. 23014. a: reflected light. b, c: Surface renderings from micro-CT data. a, b: Lateral views with dorsal surface of locule facing forward and locule casts protruding in upper part. c: Apical view. d: Fruit showing two locule casts the dorsal surfaces of which face to the left and the right, V. 30417(1). e–g: Successive digital transverse sections showing four u to v to c-shaped locules from micro-CT data. h: Physical transverse section of specimen in (d). i–k: Physical transverse section, V. 30419 from Herne Bay, blue lines in K indicating limits of fibre layer lining the locule. l: Detail from (h), showing sclerenchyma composing the septa and central axis. m: Transverse section, enlargement from (i), showing anatomy of tissues adjacent to the dorsal infold. Blue lines indicate limits of the fibre layer lining the locule. n: Part of (m) recut, tangential section transecting the dorsal infold (central), both limbs of the locule cast, and peripheral parts of the pericarp on either side. o: Detail from (n), showing anatomy of the infold. Scale bars 5 mm in (a–h) (a–g share the same bar), 3 mm in (i), 1 mm in (j–m), 0.5 mm in (n), 0.2 mm in (o). in Mastixioid Fruits (Cornales) From The Early Eocene London Clay Flora: Morphology, Anatomy And Nomenclatural Revision
Text-fig. 8. Lanfrancia subglobosa E.REID et M.CHANDLER. a–c, e–g: Holotype V. 23014. a: reflected light. b, c: Surface renderings from micro-CT data. a, b: Lateral views with dorsal surface of locule facing forward and locule casts protruding in upper part. c: Apical view. d: Fruit showing two locule casts the dorsal surfaces of which face to the left and the right, V. 30417(1). e–g: Successive digital transverse sections showing four u to v to c-shaped locules from micro-CT data. h: Physical transverse section of specimen in (d). i–k: Physical transverse section, V. 30419 from Herne Bay, blue lines in K indicating limits of fibre layer lining the locule. l: Detail from (h), showing sclerenchyma composing the septa and central axis. m: Transverse section, enlargement from (i), showing anatomy of tissues adjacent to the dorsal infold. Blue lines indicate limits of the fibre layer lining the locule. n: Part of (m) recut, tangential section transecting the dorsal infold (central), both limbs of the locule cast, and peripheral parts of the pericarp on either side. o: Detail from (n), showing anatomy of the infold. Scale bars 5 mm in (a–h) (a–g share the same bar), 3 mm in (i), 1 mm in (j–m), 0.5 mm in (n), 0.2 mm in (o).
Figure 6 in Blue and red light photoemitters as approach to inhibit Staphylococcus aureus and Pseudomonas aeruginosa growth
Figure 6. Percentage of growth inhibition induced by blue light on bacteria inoculated on saline solution or nutrient rich BHI broth. *Statistically significant difference using Mann-Whitney U test (p <0.05) between blue light exposed S. aureus in saline solution and BHI broth.
Figure 5 in Blue and red light photoemitters as approach to inhibit Staphylococcus aureus and Pseudomonas aeruginosa growth
Figure 5. Effect of blue and red light on S. aureus e P. aeruginosa diluted in BHI nutrient rich medium applied for a period of 3 hours. *Statistically significant difference using Mann-Whitney U test (p <0.05) between blue light exposed and control groups.
Figure 3 in Blue and red light photoemitters as approach to inhibit Staphylococcus aureus and Pseudomonas aeruginosa growth
Figure 3. Determination of the influence of glass or polystyrene plate on the antimicrobial effect of red or blue light in S. aureus and P. aeruginosa cultures. *Statistically significant difference using Mann-Whitney U test (p <0.05) between blue light exposed group and control groups.
Figure 4 in Blue and red light photoemitters as approach to inhibit Staphylococcus aureus and Pseudomonas aeruginosa growth
Figure 4. Effect of blue and red light on S. aureus e P. aeruginosa diluted in saline solution (0.9% NaCl) applied for a period of 3 hours. *Statistically significant difference using Mann-Whitney U test (p <0.05) between blue light exposed group and control groups.
Figure 2 in Blue and red light photoemitters as approach to inhibit Staphylococcus aureus and Pseudomonas aeruginosa growth
Figure 2. Diameter of S.aureus and P. aeruginosa surviving colonies after exposure to blue and red light for 6 hours and incubated for 24 hours (A) and 48 hours (B). *Statistically significant difference using Mann-Whitney U test (p <0.05) for independent samples.
◂Fig. 5 Gametogenesis in male and female Veneriserva pygoclava. A–D Semi-thin histological sections of female Veneriserva pygoclava, stained with toluidine blue. A Cross-section of a female Veneriserva. B Close-up of large mature oocytes without discernible nurse cells. C Developing oocytes attached to mesenteries (mes), and oogonia proliferating from the ventral side of the dorsal blood vessel (bv). D Details of vitellogenic oocytes and nurse cells. Arrowheads indicate brownstained yolk platelets and yolk bodies. E Live sperm cells captured in a light micrograph. F–G Cross-sections of male Veneriserva. Note the absence of a gut in the cross-sections. Abbreviations—ac acicula, acr acrosome, bv blood vessel, coe coelomic cavity, mes mesentery, nc nurse cell, nn nurse cell nucleus, nu sperm cell nucleus, Oo oocyte, on oocyte nucleus, sp spermatogonia, vnc ventral nerve cord in Hardly Venus's servant-morphological adaptations of Veneriserva to an endoparasitic lifestyle and its phylogenetic position within Dorvilleidae (Annelida)
◂Fig. 5 Gametogenesis in male and female Veneriserva pygoclava. A–D Semi-thin histological sections of female Veneriserva pygoclava, stained with toluidine blue. A Cross-section of a female Veneriserva. B Close-up of large mature oocytes without discernible nurse cells. C Developing oocytes attached to mesenteries (mes), and oogonia proliferating from the ventral side of the dorsal blood vessel (bv). D Details of vitellogenic oocytes and nurse cells. Arrowheads indicate brownstained yolk platelets and yolk bodies. E Live sperm cells captured in a light micrograph. F–G Cross-sections of male Veneriserva. Note the absence of a gut in the cross-sections. Abbreviations—ac acicula, acr acrosome, bv blood vessel, coe coelomic cavity, mes mesentery, nc nurse cell, nn nurse cell nucleus, nu sperm cell nucleus, Oo oocyte, on oocyte nucleus, sp spermatogonia, vnc ventral nerve cord
◂Fig. 6 Gynoecial development, fruit and seedling of C. crenata %yellow frames), C. cf. grandicalyx %blue frames) and C. sinensis %pink frames; A–F light microscopy, G–K stereo microscopy of endocarp, mesocarp removed; L–O field images; TS in horizontal orientation). A, B TS of anthetic flower %note two to three abortive ovules and strongly stained, peripheral tissue). C, D TS of anthetic flower %note two to three abortive ovules and lignifying portions of prospective mesocarp). E Young fruit %note developing endocarp and flashily pink portions of the mesocarp). F TS of postanthetic flower %note three abortive ovules and lignifying portions of prospective mesocarp). G TS of endocarp, with three developed embryos removed %note scanty endosperm). H Endocarp. J TS of endocarp. K Endocarp. L Immature fruits. M Mature fruits. N Seedlings %note short hypocotyl and long petioles of cotyledons). O Seedlings %note long hypocotyl and short petioles of cotyledons; image taken from cultivated plant, accession number 2012–0005, in the Botanical Garden Munich) %LS, longisection; TS, transverse section; ao, abortive ovule; cot, cotyledon; db, dorsal bundle; c, calyx; ec, endocarp; ens, endosperm; ex, exocarp; fr, fruit; h, hypocotyl; int, integument; lb, lateral bundle; mc, mesocarp; o, ovule; pet, petiolus; sty, style; ut, peripheral tissue; vs, ventral slit) in Observations on flower and fruit anatomy in dioecious species of Cordia (Cordiaceae, Boraginales) with evolutionary interpretations
◂Fig. 6 Gynoecial development, fruit and seedling of C. crenata %yellow frames), C. cf. grandicalyx %blue frames) and C. sinensis %pink frames; A–F light microscopy, G–K stereo microscopy of endocarp, mesocarp removed; L–O field images; TS in horizontal orientation). A, B TS of anthetic flower %note two to three abortive ovules and strongly stained, peripheral tissue). C, D TS of anthetic flower %note two to three abortive ovules and lignifying portions of prospective mesocarp). E Young fruit %note developing endocarp and flashily pink portions of the mesocarp). F TS of postanthetic flower %note three abortive ovules and lignifying portions of prospective mesocarp). G TS of endocarp, with three developed embryos removed %note scanty endosperm). H Endocarp. J TS of endocarp. K Endocarp. L Immature fruits. M Mature fruits. N Seedlings %note short hypocotyl and long petioles of cotyledons). O Seedlings %note long hypocotyl and short petioles of cotyledons; image taken from cultivated plant, accession number 2012–0005, in the Botanical Garden Munich) %LS, longisection; TS, transverse section; ao, abortive ovule; cot, cotyledon; db, dorsal bundle; c, calyx; ec, endocarp; ens, endosperm; ex, exocarp; fr, fruit; h, hypocotyl; int, integument; lb, lateral bundle; mc, mesocarp; o, ovule; pet, petiolus; sty, style; ut, peripheral tissue; vs, ventral slit)
◂Fig. 4 Gynoecium of C. crenata %yellow frames), C. cf. grandicalyx %blue frames) and C. sinensis %pink frames; A–R light microscopy; TS in horizontal orientation). A Secantial section. B, C TS %note cellular organisation). D Secantial section. E, F TS %note cellular organisation). G Secantial section of young gynoecium showing cellular organisation. H–J TS %note lacking cellular organisation, localisation in K–M). K–M LS at different levels from outside to inside of the same specimen %note strongly stained peripheral tissue; asterisks indicate tissue illustrated in H–J). N TS %note dehiscence lines of the prospective endocarp). O, P TS showing transmission tissue and dorsal bundles at top of style. Q vascularisation at base of gynoecium %note strongly stained peripheral tissue). R Vascularisation at base of flower %LS, longisection; TS, transverse section; db, dorsal bundle; dl, dehiscent line; ep, epidermis; lb, lateral bundle; tt, transmission tissue; ut, peripheral tissue; vb, ventral bundle; vs, ventral slit) in Observations on flower and fruit anatomy in dioecious species of Cordia (Cordiaceae, Boraginales) with evolutionary interpretations
◂Fig. 4 Gynoecium of C. crenata %yellow frames), C. cf. grandicalyx %blue frames) and C. sinensis %pink frames; A–R light microscopy; TS in horizontal orientation). A Secantial section. B, C TS %note cellular organisation). D Secantial section. E, F TS %note cellular organisation). G Secantial section of young gynoecium showing cellular organisation. H–J TS %note lacking cellular organisation, localisation in K–M). K–M LS at different levels from outside to inside of the same specimen %note strongly stained peripheral tissue; asterisks indicate tissue illustrated in H–J). N TS %note dehiscence lines of the prospective endocarp). O, P TS showing transmission tissue and dorsal bundles at top of style. Q vascularisation at base of gynoecium %note strongly stained peripheral tissue). R Vascularisation at base of flower %LS, longisection; TS, transverse section; db, dorsal bundle; dl, dehiscent line; ep, epidermis; lb, lateral bundle; tt, transmission tissue; ut, peripheral tissue; vb, ventral bundle; vs, ventral slit)
◂Fig. 3 Gynoecium of C. crenata %yellow frames), C. cf. grandicalyx %blue frames) and C. sinensis %pink frames; A, B stack shot images; C–K light microscopy; G polarised light; TS in horizontal orientation). A, B Anthetic female flower, calyx and corolla partly removed. B LS of gynoecium. C LS of functionally female flower %note strongly stained peripheral tissue of corolla, anther and gynoecium). D LS of gynoecium. E, F TS of functionally female flower %note strongly stained, peripheral tissue). G TS of functionally female flower %note crystal deposition). H LS of ovule %note stalked embryo sac). J TS of functionally male flower with non-functional ovules. K LS of functionally male flower %style lacking, original position indicated by an asterisk) %LS, longisection; TS, transverse section; a,anther; bs, basal septum; c, calyx; car, carpel; co, corolla; db, dorsal bundles; es, embryo sac; fs, false septum; lb, lateral bundles; o, ovule; stg, stigma; sty, style; t, trichomes; tt, transmission tissue; ut, peripheral, strongly stained tissue; vb, ventral bundles; vs, ventral slit) in Observations on flower and fruit anatomy in dioecious species of Cordia (Cordiaceae, Boraginales) with evolutionary interpretations
◂Fig. 3 Gynoecium of C. crenata %yellow frames), C. cf. grandicalyx %blue frames) and C. sinensis %pink frames; A, B stack shot images; C–K light microscopy; G polarised light; TS in horizontal orientation). A, B Anthetic female flower, calyx and corolla partly removed. B LS of gynoecium. C LS of functionally female flower %note strongly stained peripheral tissue of corolla, anther and gynoecium). D LS of gynoecium. E, F TS of functionally female flower %note strongly stained, peripheral tissue). G TS of functionally female flower %note crystal deposition). H LS of ovule %note stalked embryo sac). J TS of functionally male flower with non-functional ovules. K LS of functionally male flower %style lacking, original position indicated by an asterisk) %LS, longisection; TS, transverse section; a,anther; bs, basal septum; c, calyx; car, carpel; co, corolla; db, dorsal bundles; es, embryo sac; fs, false septum; lb, lateral bundles; o, ovule; stg, stigma; sty, style; t, trichomes; tt, transmission tissue; ut, peripheral, strongly stained tissue; vb, ventral bundles; vs, ventral slit)
◂Fig. 1 Morphology of thecate and coccoid cells, with labelled thecal plates. a–c, i, m Light microscopy, d–h, k–l scanning electron microscopy. a Ventral view of strain GeoM*788; b dorsal view of strain GeoM*793; c apical view of strain GeoK*044; d ventral view of strain GeoK*037; e dorsal view of strain GeoM*788; f apical view of strain GeoK*024, with the dehiscence of epithecal opening indicated by a blue line; g antapical view of strain GeoK*044; h leftlateral view of strain GeoM*866; i motile cell of strain GeoK*037; k–m coccoid cells showing variability in shape and size of strains k GeoM*866, l GeoM*793 and m GeoK*024. Abbreviations: n′: apical plate, n′′: precingular plate, n′′′: postcingular plate, n′′′′: antapical plate, na: anterior intercalary plate, nC: cingular plate, Sa: anterior sulcal plate, Sd: right sulcal plate, Sp: posterior sulcal plate. Ss: left sulcal plate. Scale bar: 10 µm. UA: 15 kV in Morphological and molecular variability of Peridinium volzii Lemmerm. (Peridiniaceae, Dinophyceae) and its relevance for infraspecific taxonomy
◂Fig. 1 Morphology of thecate and coccoid cells, with labelled thecal plates. a–c, i, m Light microscopy, d–h, k–l scanning electron microscopy. a Ventral view of strain GeoM*788; b dorsal view of strain GeoM*793; c apical view of strain GeoK*044; d ventral view of strain GeoK*037; e dorsal view of strain GeoM*788; f apical view of strain GeoK*024, with the dehiscence of epithecal opening indicated by a blue line; g antapical view of strain GeoK*044; h leftlateral view of strain GeoM*866; i motile cell of strain GeoK*037; k–m coccoid cells showing variability in shape and size of strains k GeoM*866, l GeoM*793 and m GeoK*024. Abbreviations: n′: apical plate, n′′: precingular plate, n′′′: postcingular plate, n′′′′: antapical plate, na: anterior intercalary plate, nC: cingular plate, Sa: anterior sulcal plate, Sd: right sulcal plate, Sp: posterior sulcal plate. Ss: left sulcal plate. Scale bar: 10 µm. UA: 15 kV
◂Fig. 7 Iberozospeum vasconicum. Light blue clade; (a) NMBE 557198, Cueva de la Fuente de Estragueña, 16.6.2011, sh: 1.26 mm; (b) NMBE 557138, Castro, Laredo, La Baja, 12.4.2017, sh: 1.11 mm; (c) NMBE 557232, Triano, Galdames, Mina Princesa (superior), 3.7.2016, sh: 1.51 mm; (d) NMBE 557211, Triano, Güenes, Grazal, 2.10.2016, sh: 1.49 mm; (e) NMBE 557174, Triano, Galdames, Escachabel-2 (Urallaga), 1.4.2013, sh: 1.44 mm; (f) NMBE 557200, Triano, Galdames, Bitzkaia, Cueva de la San Juan, 10.6.2012, sh: 1.23 mm; (g) NMBE 557189, Durang, Atxondo, Azkillar (= Galtaikoba), 16.3.2014, sh: 1.19 mm; (h) NMBE 557182, Durang, Zeberio, Cueva Hatxondo, 30.12.2012, sh: 1.28 mm; (i) NMBE 557221, Aralar, Arbizu, Cueva Irutxin, 20.6.2015, sh: 1.54 mm; (j) NMBE 557242, Ason, Matienzo, Cueva Cubija (= Marcos), 19.7.2016, sh: 1.34 mm; (k) NMBE 557178, Salvada, Berberana, Las Paules, 21.6.2011, sh: 1.3 mm; (l) NMBE 557180, Salvada, Izarra, Torca Lejazar, 28.12.2013, sh: 1.29 mm; (m) NMBE 557244, Salvada, Berberana, Las Paules, 9.11.2013, sh: 1.28 mm; (n) NMBE 557158, Aizkorri, Eskoriatza, Saiturri-2, 22.2.2017, sh: 1.47 mm; (o) NMBE 557187, Aralar, Ataun, Cueva Akaitz Txiki, 14.1.2014, sh: 1.47 mm; (p) NMBE 557188, Aralar, Ataun, Cueva Akaitz Txiki, 14.1.2014, sh: 1.32 mm. NMBE 557162, Aizkorri, Parzoneria, Perusaroi-1, 15.5.2017 (subadult shell, not shown on plate). No pictures of NMBE 540551.1, 540552.1, 540552.3, 540553.1 (shells destroyed). — All phot.× 40 in Molecular investigation and description of Iberozospeum n. gen., including the description of one new species (Eupulmonata, Ellobioidea, Carychiidae)
◂Fig. 7 Iberozospeum vasconicum. Light blue clade; (a) NMBE 557198, Cueva de la Fuente de Estragueña, 16.6.2011, sh: 1.26 mm; (b) NMBE 557138, Castro, Laredo, La Baja, 12.4.2017, sh: 1.11 mm; (c) NMBE 557232, Triano, Galdames, Mina Princesa (superior), 3.7.2016, sh: 1.51 mm; (d) NMBE 557211, Triano, Güenes, Grazal, 2.10.2016, sh: 1.49 mm; (e) NMBE 557174, Triano, Galdames, Escachabel-2 (Urallaga), 1.4.2013, sh: 1.44 mm; (f) NMBE 557200, Triano, Galdames, Bitzkaia, Cueva de la San Juan, 10.6.2012, sh: 1.23 mm; (g) NMBE 557189, Durang, Atxondo, Azkillar (= Galtaikoba), 16.3.2014, sh: 1.19 mm; (h) NMBE 557182, Durang, Zeberio, Cueva Hatxondo, 30.12.2012, sh: 1.28 mm; (i) NMBE 557221, Aralar, Arbizu, Cueva Irutxin, 20.6.2015, sh: 1.54 mm; (j) NMBE 557242, Ason, Matienzo, Cueva Cubija (= Marcos), 19.7.2016, sh: 1.34 mm; (k) NMBE 557178, Salvada, Berberana, Las Paules, 21.6.2011, sh: 1.3 mm; (l) NMBE 557180, Salvada, Izarra, Torca Lejazar, 28.12.2013, sh: 1.29 mm; (m) NMBE 557244, Salvada, Berberana, Las Paules, 9.11.2013, sh: 1.28 mm; (n) NMBE 557158, Aizkorri, Eskoriatza, Saiturri-2, 22.2.2017, sh: 1.47 mm; (o) NMBE 557187, Aralar, Ataun, Cueva Akaitz Txiki, 14.1.2014, sh: 1.47 mm; (p) NMBE 557188, Aralar, Ataun, Cueva Akaitz Txiki, 14.1.2014, sh: 1.32 mm. NMBE 557162, Aizkorri, Parzoneria, Perusaroi-1, 15.5.2017 (subadult shell, not shown on plate). No pictures of NMBE 540551.1, 540552.1, 540552.3, 540553.1 (shells destroyed). — All phot.× 40
Text-fig. 3. Palaeogeographic distribution of Schloenbachia lymensis (red dots) in the Upper Cenomanian Calycoceras guerangeri through the Metoicoceras geslinianum Zones. Light blue – shallow epicontinental sea, dark blue – deep marine settings, yellow – land. * asterisk – occurrence in the BCB (modified after Wilmsen 2012). in Taxonomy And Stratigraphic Distribution Of The Ammonite Schloenbachia Neumayr, 1875 From The Bohemian Cretaceous Basin
Text-fig. 3. Palaeogeographic distribution of Schloenbachia lymensis (red dots) in the Upper Cenomanian Calycoceras guerangeri through the Metoicoceras geslinianum Zones. Light blue – shallow epicontinental sea, dark blue – deep marine settings, yellow – land. * asterisk – occurrence in the BCB (modified after Wilmsen 2012).
Data of the paper "Combining Blue Light and Yellow Curcumin to Obtain a "Green" Tool for Berry Preservation against Bacterial Contamination: A Preliminary Investigation" by I Stura et al.
<p>This file contains the data of three experiments on berries' preservation by a coating of curcumin+beta-cyclodestrin.</p> <p>Microbiological data of the three experiments are summarized (number of colonies). The measures are given for each berry's type at T0, after 24 and 48 hours. We considered both smoothed berries and only washing water as starting samples.</p>
Blue light attracts nocturnally migrating birds
<p>Light pollution is increasing and artificial light sources have great impacts on animals. For migrating birds, collisions caused by artificial light pollution are a significant source of mortality. Laboratory studies have demonstrated that birds have different visual sensitivities to different colors of light, but few field experiments have compared birds' responses to light of different wavelengths. We used three monochromatic lights (red, green, and blue) and polychromatic yellow light to study the impact of wavelength on phototaxis at two gathering sites of nocturnally migrating birds in Southwest China. For both sites, short-wavelength blue light caused the strongest phototactic response. In contrast, birds were rarely attracted to long-wavelength red light. The attractive effect of blue light was greatest during nights with fog and headwinds. As rapid urbanization and industrialization cause an increase in artificial light, we suggest that switching to longer wavelength lights is a convenient and economically effective way to reduce bird collisions.</p>
First-principles simulations of exciton transfer between N-heterocyclic carbene iridium (III) complexes in blue organic light-emitting diodes
<p>N-heterocyclic carbene (NHC) iridium (III) complexes are promising for the use as blue emitters in organic light-emitting diodes. Exciton transfer between such organometallic complexes is investigated using time-dependent density functional theory calculations. Casida's equation is solved to study absorption and emission of the neutral and charged complexes using the ORCA package. The Sternheimer equation implemented in the Octopus code is extended to take into account spin-orbit coupling and is applied to investigate triplet excitations. Real-time propagation as implemented in the Octopus code is used to simulate exciton dynamics in an emitter dimer and to extract the exciton coupling via explicit integration of transition densities.</p>
Highly-efficient blue InGaN nanoscale light-emitting diodes
<p>Atomic structure files used for DFT calculation for manuscript "Highly-efficient blue InGaN nanoscale light-emitting diodes"<strong> </strong></p>
Data on the Blackthorn fruit peel: phenolic compounds and antimicrobial synergy with blue light against Listeria monocytogenes
<p>The dataset contains results obtained during a project funded by the National Science Centre, Poland [Grant number 2022/45/B/NZ9/00299 (OPUS-23)].</p>
Machine Learning Integrated High Quantum Yield Blue Light Carbon Dots for Real-time and On-site Detection of Cr(VI) in Groundwater and Drinking Water
<p>RGB和Kmeans提取后含有Cr(VI)水样的图像数据</p>
Raw data of the publication titled "First-row d6 metal complex enables photon upconversion and initiates blue light-dependent polymerization with red light"
<p>Raw data of the publication in Angew. Chem. Int. Ed. titled "First-row d<sup>6</sup> metal complex enables photon upconversion and initiates blue light-dependent polymerization with red light "</p>
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