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Figure 10 from: Jochum A, Slapnik R, Klussmann-Kolb A, Páll-Gergely B, Kampschulte M, Martels G, Vrabec M, Nesselhauf C, Weigand AM (2015) Groping through the black box of variability: An integrative taxonomic and nomenclatural re-evaluation of Zospeum isselianum Pollonera, 1887 and allied species using new imaging technology (Nano-CT, SEM), conchological, histological and molecular data (Ellobioidea, Carychiidae). Subterranean Biology 16: 123-165. https://doi.org/10.3897/subtbiol.16.5758
Figure 10 - NanoCT−SEM Plate 4. A–F Zospeum kupitzense (RS3291), Ložekarjeva zijalka G. Zospeum alpestre (SMNH 2216), Kamniška jama H, I−L Zospeum isselianum Ihanščica cave J−K Zospeum amoenum (RS59), Potočka zijalka.
Figure 1 from: Jochum A, Slapnik R, Klussmann-Kolb A, Páll-Gergely B, Kampschulte M, Martels G, Vrabec M, Nesselhauf C, Weigand AM (2015) Groping through the black box of variability: An integrative taxonomic and nomenclatural re-evaluation of Zospeum isselianum Pollonera, 1887 and allied species using new imaging technology (Nano-CT, SEM), conchological, histological and molecular data (Ellobioidea, Carychiidae). Subterranean Biology 16: 123-165. https://doi.org/10.3897/subtbiol.16.5758
Figure 1 - Zospeum isselianum potential distribution collated from the literature and museum collections (I. Sajko, CSR SASA).
Figure 15 from: Jochum A, Slapnik R, Klussmann-Kolb A, Páll-Gergely B, Kampschulte M, Martels G, Vrabec M, Nesselhauf C, Weigand AM (2015) Groping through the black box of variability: An integrative taxonomic and nomenclatural re-evaluation of Zospeum isselianum Pollonera, 1887 and allied species using new imaging technology (Nano-CT, SEM), conchological, histological and molecular data (Ellobioidea, Carychiidae). Subterranean Biology 16: 123-165. https://doi.org/10.3897/subtbiol.16.5758
Figure 15 - Light micrograph showing histological appearance of the radular complex of Zospeum sp. (Konečka zijalka) (CSR SASA 21675). A Odontoblasts (odb) grouped in lower posterior section of radular sheath, radular teeth (rt), odontophore (od), and collostyle (col) B Section through an acinus of the ovotestis showing some stages of development of sustentacular cells (Sertoli cells) (sc) with spermatogonia (spg), spermatids (sp) and oogonia (og).
Figure 3 from: Jochum A, Slapnik R, Klussmann-Kolb A, Páll-Gergely B, Kampschulte M, Martels G, Vrabec M, Nesselhauf C, Weigand AM (2015) Groping through the black box of variability: An integrative taxonomic and nomenclatural re-evaluation of Zospeum isselianum Pollonera, 1887 and allied species using new imaging technology (Nano-CT, SEM), conchological, histological and molecular data (Ellobioidea, Carychiidae). Subterranean Biology 16: 123-165. https://doi.org/10.3897/subtbiol.16.5758
Figure 3 - Geographical position and river drainage systems of the Julian Alps and the Kamnik Savinja Alps range. Sampling sites: 1 Turjeva jama 2 Ložekarjeva jama 3 Konečka zijalka 4 Potočka zijalka 5 Jama na Zgornjih Brsnikih 6 Tomažičeva zijalka 7 Kamniška jama 8 Ihanščica cave. Digital terrain model from Jarvis et al., 2008. River network data courtesy of Public Information of Slovenia, the Surveying and Mapping Authority of the Republic of Slovenia, DPK1000V (2008).
Figure 9 from: Jochum A, Slapnik R, Klussmann-Kolb A, Páll-Gergely B, Kampschulte M, Martels G, Vrabec M, Nesselhauf C, Weigand AM (2015) Groping through the black box of variability: An integrative taxonomic and nomenclatural re-evaluation of Zospeum isselianum Pollonera, 1887 and allied species using new imaging technology (Nano-CT, SEM), conchological, histological and molecular data (Ellobioidea, Carychiidae). Subterranean Biology 16: 123-165. https://doi.org/10.3897/subtbiol.16.5758
Figure 9 - SEM Microstructures Plate 3. A−F Zospeum isselianum (CSR SASA 37013 conspecific), Turjeva jama G−H Zospeum sp. (CSR SASA 21675), Konečka zijalka I−L Zospeum kupitzense (SMNH 3291), Ložekarjeva jama M−O Zospeum amoenum (RS103), Ihanščica cave.
Figure 1 from: Martine CT, Cantley JT, Frawley ES, Butler AR, Jordon-Thaden IE (2016) New functionally dioecious bush tomato from northwestern Australia, Solanum ossicruentum, may utilize "trample burr" dispersal. PhytoKeys 63: 19-29. https://doi.org/10.3897/phytokeys.63.7743
Figure 1 - Solanum ossicruentum sp. nov. A Typical habitat, Mirima National Park, WA B Leaf morphology C Female individual, Mirima NP D Close-up of functionally female (morphologically hermaphrodite) flower E Abaxial side of functionally female flower showing elongated calyx lobes F Male individual, Mirima NP G Male flower, abaxial view H Developing fruit within calyx I Immature fruits showing blood-red staining at 2 minutes (lower) and 5 minutes (above) after cutting J Mature bony fruits removed from calyces and (lower right) as collected from ground beneath plant. Yellow scale bars as follows: 3 cm (B, C, F); 1 cm (D); 2 cm (E, G, H, J); 0.75 cm (I). Photos A, C, F, and J by C.T. Martine; all others by J.T. Cantley.
Figure 3 from: Martine CT, Cantley JT, Frawley ES, Butler AR, Jordon-Thaden IE (2016) New functionally dioecious bush tomato from northwestern Australia, Solanum ossicruentum, may utilize "trample burr" dispersal. PhytoKeys 63: 19-29. https://doi.org/10.3897/phytokeys.63.7743
Figure 3 - Map showing distribution of Solanum ossicruentum sp. nov. accessions held at the Northern Territory Herbarium, Palmerston (DNA) and examined for this description. Map base layer generated from ArcGIS.
Figure 2 from: Martine CT, Cantley JT, Frawley ES, Butler AR, Jordon-Thaden IE (2016) New functionally dioecious bush tomato from northwestern Australia, Solanum ossicruentum, may utilize "trample burr" dispersal. PhytoKeys 63: 19-29. https://doi.org/10.3897/phytokeys.63.7743
Figure 2 - SEM images of Solanum ossicruentum sp. nov. pollen grains. A Functional pollen produced by male flowers, and B Inaperturate pollen produced by morphologically hermaphrodite, yet functionally female, flowers. Images by A. Butler.
Figure 2 from: Martine CT, Frawley ES, Cantley JT, Jordon-Thaden IE (2016) Solanum watneyi, a new bush tomato species from the Northern Territory, Australia named for Mark Watney of the book and film "The Martian". PhytoKeys 61: 1-13. https://doi.org/10.3897/phytokeys.61.6995
Figure 2 - Illustration of Solanum watneyi. Mature branch with flowers and a developing fruit. Based on plant grown at Bucknell University from seeds of Martine and Martine 4065. Drawing by Rachel F. Martine.
Figure 1 from: Martine CT, Frawley ES, Cantley JT, Jordon-Thaden IE (2016) Solanum watneyi, a new bush tomato species from the Northern Territory, Australia named for Mark Watney of the book and film "The Martian". PhytoKeys 61: 1-13. https://doi.org/10.3897/phytokeys.61.6995
Figure 1 - Distribution map of Solanum watneyi and Solanum eburneum based on accessions held by DNA, BUPL and CONN. Specimens of Solanum eburneum mapped are cited in Appendix 1.
Figure 3 from: Martine CT, Frawley ES, Cantley JT, Jordon-Thaden IE (2016) Solanum watneyi, a new bush tomato species from the Northern Territory, Australia named for Mark Watney of the book and film "The Martian". PhytoKeys 61: 1-13. https://doi.org/10.3897/phytokeys.61.6995
Figure 3 - Comparisons of Solanum eburneum and Solanum watneyi. A–C Solanum eburneum in habitat (gray cracked clay), in flower, and mature fruits D–F same for Solanum watneyi (habit showing reddish sandy loam) G corolla comparisons of staminate (upper) and hermaphrodite (lower) flowers for Solanum eburneum (left) and Solanum watneyi (right) H leaf shape across varying leaf ages for Solanum watneyi (top) and Solanum eburneum (bottom) in cultivation; I) field growth habit of Solanum eburneum (left) and Solanum watneyi (right) showing the more sprawling and prostrate nature of Solanum watneyi. Photos A, C, D, E, F, I by CTM; B, G by JC; H by EF.
Supplementary material 1 from: Wood CT, Nihei SS, Araujo PB (2018) Woodlice and their parasitoid flies: revision of Isopoda (Crustacea, Oniscidea) – Rhinophoridae (Insecta, Diptera) interaction and first record of a parasitized Neotropical woodlouse species. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 401-414. https://doi.org/10.3897/zookeys.801.26052
Compilation of Isopoda-Rhinophoridae records (Dataset) :
Supplementary material 2 from: Wood CT, Nihei SS, Araujo PB (2018) Woodlice and their parasitoid flies: revision of Isopoda (Crustacea, Oniscidea) – Rhinophoridae (Insecta, Diptera) interaction and first record of a parasitized Neotropical woodlouse species. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 401-414. https://doi.org/10.3897/zookeys.801.26052
Rhinophoridae larva from a Neotropical woodlouse species :
Figure 5 from: Wood CT, Nihei SS, Araujo PB (2018) Woodlice and their parasitoid flies: revision of Isopoda (Crustacea, Oniscidea) – Rhinophoridae (Insecta, Diptera) interaction and first record of a parasitized Neotropical woodlouse species. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 401-414. https://doi.org/10.3897/zookeys.801.26052
Figure 5 Rhinophoridae larva obtained from the Neotropical isopod Balloniscusglaber. Morphotype 2, 3rd instar A dorsal view B detail from anterior part showing the cephaloskeleton and anterior spiracles C detail of the posterior spiracle.
Figure 4 from: Wood CT, Nihei SS, Araujo PB (2018) Woodlice and their parasitoid flies: revision of Isopoda (Crustacea, Oniscidea) – Rhinophoridae (Insecta, Diptera) interaction and first record of a parasitized Neotropical woodlouse species. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 401-414. https://doi.org/10.3897/zookeys.801.26052
Figure 4 Rhinophoridae larva obtained from the Neotropical isopod Balloniscusglaber. Morphotype 1, 3rd instar A detail view of the cephaloskeleton on dorsal view B detail view of the anterior spiracle C alive larva with transparent integument D fixed larva, dorsal view.
Figure 3 from: Wood CT, Nihei SS, Araujo PB (2018) Woodlice and their parasitoid flies: revision of Isopoda (Crustacea, Oniscidea) – Rhinophoridae (Insecta, Diptera) interaction and first record of a parasitized Neotropical woodlouse species. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 401-414. https://doi.org/10.3897/zookeys.801.26052
Figure 3 Balloniscusglaber infected with 3rd instar Rhinophoridae larva A alive B.glaber clinging to the substrate B secretion discharged from uropod glands C–D dorsal (C) and ventral (D) views of Balloniscusglaber with a third instar Rhinophoridae larva inside E–F partially dissected Balloniscusglaber infected with Rhinophoridae larva showing the empty gut on dorsal view (E) and the calcium plates on ventral view (F).
Figure 2 from: Wood CT, Nihei SS, Araujo PB (2018) Woodlice and their parasitoid flies: revision of Isopoda (Crustacea, Oniscidea) – Rhinophoridae (Insecta, Diptera) interaction and first record of a parasitized Neotropical woodlouse species. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 401-414. https://doi.org/10.3897/zookeys.801.26052
Figure 2 Distribution map of native and introduced Rhinophoridae species in the Neotropical region (area in gray) including the new larvae record. Apomorphytoinbio records from Pape (2010) and Cerretti et al. (2014); Bezzimyia spp. records from Pape and Arnaud (2001); Shannoniella spp. records from Nihei et al. (2016); Trypetidomima spp. records from Nihei and Andrade (2014); Melanophoraroralis records from Parker (1953), Guimarães (1977), González (1998), Cerretti and Pape (2009) and Mulieri et al. (2010); Steveniadeceptoria records from Mulieri et al. (2010). Base map modified from: commons.wikimedia.org/
Figure 1 from: Wood CT, Nihei SS, Araujo PB (2018) Woodlice and their parasitoid flies: revision of Isopoda (Crustacea, Oniscidea) – Rhinophoridae (Insecta, Diptera) interaction and first record of a parasitized Neotropical woodlouse species. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 401-414. https://doi.org/10.3897/zookeys.801.26052
Figure 1 Schematic representation of the infection cycle of a Rhinophoridae fly in a woodlouse host. 3 is modified from Thompson (1934).
Confocal and micro-CT data of Delteredolaemus hei, holotype, NIGP200000
<p>This dataset contains the raw confocal laser scanning microscopy (CLSM) slices and X-ray microtomography (micro-CT) slices for the holotype of <em>Delteredolaemus hei</em> (NIGP200000) from mid-Cretaceous Burmese amber. This dataset is associated with the publication "Earliest teredid beetle from mid-Cretaceous amber of northern Myanmar (Coleoptera: Coccinelloidea: Teredidae): new genus and species" (DOI:10.1590/S1984-4689.v39.e22042).</p> <p>Confocal images were obtained with a Zeiss LSM710 confocal laser scanning microscope, using the 488 nm (Argon) laser excitation line. The original CZI files are provided, which could be opened by the ZEISS ZEN software.</p> <p>Micro-CT data were obtained with a Zeiss Xradia 520 Versa 3D X-ray microscope. Scanning parameters were as follows: isotropic voxel size, 2.2514 μm; power, 3 W; acceleration voltage, 40 kV; exposure time, 2 s; projections, 2701. The TIFF stack is provided.</p>
Data accompanying article "A Bayesian Approach to CT Reconstruction with Uncertain Geometry"
<p>This record contains three datasets for reproducing the results of the paper</p> <p>"A Bayesian Approach to CT Reconstruction with Uncertain Geometry" </p> <p>by </p> <p>Frederik H. Pedersen, Jakob S. Jørgensen and Martin S. Andersen</p> <p>currently available as a preprint at</p> <p>https://arxiv.org/abs/2203.01045</p> <p>The datafiles are provided as mat-files saved from MATLAB. Using these files, and the accompanying codes at github the results and figures of the paper can be reproduced. Each of the files correspond to one of the three cases presented in the paper.</p>
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