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FIGURE 3 in Re-examination of the type specimens of Lecithoceridae (Lepidoptera), deposited in the Royal Museum for Central Africa (RMCA), Belgium, with descriptions of ten new species from DR Congo belonging to Thubdora Park and Torodora Meyrick

FIGURE 3. Thubdora ealaensis sp. nov.: A, adult, holotype; B, labial palpus, lateral view; C. male genitalia, holotype, gen. slide no. CIS-7243/Park; D, ditto, aedeagus; E, abdominal segments VII–VIII, with hair-like pencils.

FIGURE 7 in Re-examination of the type specimens of Lecithoceridae (Lepidoptera), deposited in the Royal Museum for Central Africa (RMCA), Belgium, with descriptions of ten new species from DR Congo belonging to Thubdora Park and Torodora Meyrick

FIGURE 7. Thubdora neobarbata sp. nov.: A, adult, holotype; B, close-up of head, dorsal view; C. male genitalia, holotype gen. slide no. CIS-7157/Park; D, ditto, aedeagus; E, abdominal segments IV–VIII, with hair-like pencils.

FIGURE 2 in Re-examination of the type specimens of Lecithoceridae (Lepidoptera), deposited in the Royal Museum for Central Africa (RMCA), Belgium, with descriptions of ten new species from DR Congo belonging to Thubdora Park and Torodora Meyrick

FIGURE 2. Thubdora barbata (Meyrick): A, adult, holotype; B, ditto, lateral view; C, labels; D, male genitalia, holotype, gen. slide no. CIS-7136/Park; E, ditto, aedeagus; F, abdomen, with a pair of long hair-like pencils. Scale bar for the genitalia and aedeagus: 1.0 mm (same in the following figures).

FIGURE 14 in Re-examination of the type specimens of Lecithoceridae (Lepidoptera), deposited in the Royal Museum for Central Africa (RMCA), Belgium, with descriptions of ten new species from DR Congo belonging to Thubdora Park and Torodora Meyrick

FIGURE 14. Lecithocera dicentropa Meyrick: A, adult, holotype; B, labels; C, determined label; D, male genitalia, holotype, gen. slide no. CIS-7139/Park; E, ditto, aedeagus; F, abdominal segment VIII.

Figure 6 in An unprecedented new genus and family of Tetractinellida (Porifera, Demospongiae) from New Zealand's Colville Ridge, with a new type of mitochondrial group I intron

Figure 6. Megascleres and microscleres of Stupenda singularis gen. et sp. nov., holotype NIWA 86177, Colville Ridge, Kermadec Volcanic Arc, 387–422 m: A, oxea, one end showing strong attenuation, scale bar = 1000 μm; B, orthotriaene I megascleres with clubbed clads, scale bar = 1000 μm; C, orthotriaene I megascleres with clubbed bulbous clads, scanning electron microscopy (left), light microscopy (LM) (right), scale bar = 200 μm; D, orthotriaene I megasclere with reduced irregular clads, scale bar = 200 μm; E, orthotriaene I megascleres with diaene modifications, scale bar = 200 μm; F, orthotriaene I megasclere with monaene modification, LM, scale bar = 200 μm; G, orthotriaene II megasclere with normal clads, scale bar = 200 μm; H, orthotriaene II megasclere with irregular reduced clads, entirely smooth, scale bar = 200 μm; I, sigmaspires, scale bar = 5 μm.

Figure 2. Tetractinellida 18S in An unprecedented new genus and family of Tetractinellida (Porifera, Demospongiae) from New Zealand's Colville Ridge, with a new type of mitochondrial group I intron

Figure 2. Tetractinellida 18S rDNA maximum likelihood (ML) tree reconstructed with RAxML under the generalized time-reversible Gamma (GTRGAMMA) model: 89 sequences. At each key node, ML bootstrap supports (100 bootstrap replicates) and Bayesian posterior probabilities are given (only bootstrap supports above 50 are shown). GenBank accession numbers are given after each taxon name; when sequences have been merged, two accession numbers are given. 'K94' indicates that this is a short 18S sequence (V4–V5 region) from Kelly-Borges & Pomponi (1994) (accession numbers KT356876–KT356885).

Figure 3. Tetractinellida cytochrome c oxidase subunit I in An unprecedented new genus and family of Tetractinellida (Porifera, Demospongiae) from New Zealand's Colville Ridge, with a new type of mitochondrial group I intron

Figure 3. Tetractinellida cytochrome c oxidase subunit I (COI) maximum likelihood (ML) trees reconstructed with RAxML under the generalized time-reversible Gamma – GTRGAMMA – model: 140 sequences At each key node, ML bootstrap supports (100 bootstrap replicates) and Bayesian posterior probabilities are given. There are two bootstrap supports: nucleotide analyses/amino-acid analyses (only bootstrap supports above 50 are shown). GenBank accession numbers are given after each taxon name. Presence of mitochondrial introns are given in the COI tree (the number given to each intron indicates its position with respect to the Amphimedon queenslandica complete COI as reference).

Figure 5 in An unprecedented new genus and family of Tetractinellida (Porifera, Demospongiae) from New Zealand's Colville Ridge, with a new type of mitochondrial group I intron

Figure 5. Morphology and skeletal architecture of Stupenda singularis gen. et sp. nov., holotype NIWA 86177, Colville Ridge, Kermadec Volcanic Arc, 387–422 m: A, preserved specimen, scale bar = 10 mm; B, preserved specimen showing thick cortex and strictly radiating skeleton, emanating from a centrum, scale bar = 10 mm; C, D, histological thick section showing strictly radiating megascleres in cortex, scale bars = 200 μm.

Figure 4 in An unprecedented new genus and family of Tetractinellida (Porifera, Demospongiae) from New Zealand's Colville Ridge, with a new type of mitochondrial group I intron

Figure 4. Mitochondrial intron of Stupenda singularis gen. et sp. nov. COI, cytochrome c oxidase subunit I gene; COB, cytochrome b gene; nt, nucleotide; ORF, open reading frame.

Figure 1 in An unprecedented new genus and family of Tetractinellida (Porifera, Demospongiae) from New Zealand's Colville Ridge, with a new type of mitochondrial group I intron

Figure 1. Study area showing the collection locality for Stupenda singularis gen. et sp. nov. (●), Colville Ridge volcano, Colville Ridge, New Zealand Exclusive Economic Zone.

Data for MAPS: Pathologist-level Cell Type Annotation from Tissue Images through Machine Learning

Extracted datasets and processed images used to generate figures in manuscript "MAPS: Pathologist-level Cell Type Annotation from Tissue Images through Machine Learning".

opennotspecifiedDec 2007View details →

Fig. 1. Permomerope australis Tillyard, 1926, specimen AMF 130800 in Permomerope natalensis sp. n. from the Lopingian of South Africa, and a redescription of the type species of Permomerope (Trichoptera: Protomeropidae)

Fig. 1. Permomerope australis Tillyard, 1926, specimen AMF 130800, details of the wing venation and enlarged view of the basal half of the specimen. Scale bar = 1 mm.

FIGURE 4. Type specimens studied for this work. A in A new species of Uroxys Westwood, 1842 (Coleoptera: Scarabaeidae: Scarabaeinae) from central Brazil, and taxonomical remarks on Uroxys epipleuralis (Boucomont, 1928)

FIGURE 4. Type specimens studied for this work. A, Choeridium epipleurale Boucomont, 1928 (currently, Uroxys epipleuralis), lectotype; B, U. thoracalis Balthasar, 1940, holotype; C, U. dureti Martínez, 1947, holotype. A and B courtesy of Fernando Z. Vaz-de-Mello; C courtesy of Mario Cupello.

Replication package for: "P-Hacking, Data Type and Data-Sharing Policy".

See Readme file. Journal article abstract: "This paper examines the relationship between p-hacking, publication bias, and data-sharing policies. We collect 38,876 test statistics from 1,106 articles published in leading economic journals between 2002--2020. We find that while data-sharing policies increase the provision of data, they do not decrease the extent of p-hacking and publication bias. Similarly, articles that use hard-to-access administrative data or third-party surveys, as compared to those that use easier-to-access (e.g., author-collected) data are not different in their p-hacking and publication extent. Voluntary provision of data by authors on their homepages offers no evidence of reduced p-hacking."

Data and code used in the article "Driving Factors of TOC Concentrations in Four Different Types of Estuaries"

Data and code used in the article "Driving Factors of TOC Concentrations in Four Different Types of Estuaries", specifically included water quality, meteorological, and nutrient data from 4 in situ observations for the years 2002-2008, and example code for implementing BRT using R. Data (Figures 2, 3, 4, 10) can be uploaded for review purposes. Figures 5, 6, 7, 8, and 9 represent the output results of the machine learning model. These data can help the reader to better understand and replicate our research.

Data for "Coherent control of a few-channel hole type gatemon qubit"

The files contain the raw and processed data used for the publication "Coherent control of a few-channel hole type gatemon qubit" in ASCII format. See readme.txt for details.

FIGURE 52 in Scanning electron microscopy study of Lars Silén's cheilostome bryozoan type specimens in the historical collections of natural history museums in Sweden

FIGURE 52. Sphaerulobryozoon ovum (Smitt, 1873) n. comb. North Atlantic Ocean, off Tennessee Reef, Florida, United States. A–G. Paralectotypes SMNH-Type-1799b-e. H, I. Lectotype (designated here) SMNH-Type-1799a. A, C, F–H. Lateral views of the four paralectotypes and the lectotype. B. Close-up of two zooids showing the terminal, cormidial orifice and interzooidal avicularia along the zooidal margins. D, E. Close-up of orifices and avicularia. I. Ovicellate zooid. Scale bars: A, C, F, H = 500 µm; B, D = 200 µm; E = 100 µm; G = 1 mm; I = 300 µm.

FIGURE 49 in Scanning electron microscopy study of Lars Silén's cheilostome bryozoan type specimens in the historical collections of natural history museums in Sweden

FIGURE 49. Anoteropora latirostris Silén, 1947a. Indian Ocean, Bab-el-Mandeb, Aden Island. A, B. Paralectotype SMNH- Type-8746b. C, D. Paralectotype SMNH-Type-8746c. E, F. Paralectotype SMNH-Type-8746d. A, C. General view of two young, subcircular colonies with ancestrulae. B, D. Close-up of the ancestrula and periancestrular zooids. E. View of the dorsal side of a colony fragment. F. Close-up of the dorsal side showing the large, distal pore chamber window and part of the ovicells at the colony growing edge. Scale bars: A, C, E = 1 mm; B, D = 500 µm; F = 400 µm.

FIGURE 47 in Scanning electron microscopy study of Lars Silén's cheilostome bryozoan type specimens in the historical collections of natural history museums in Sweden

FIGURE 47. Flabellopora lingua Silén, 1947a. Holotype UPSZTY 2221, Japan. A. General view of the colony fragment subsampled from the holotype. B–D. Autozooids and avicularia of different sizes at colony edge. E. Close-up of an autozooid surrounded by avicularia. Scale bars: A = 200 µm; B, D, E = 100 µm; C = 50 µm.

FIGURE 51. Fedora edwardsi Jullien, 1882. North Atlantic Ocean, Josephine Bank. A–D. SMNH-128030. A, C in Scanning electron microscopy study of Lars Silén's cheilostome bryozoan type specimens in the historical collections of natural history museums in Sweden

FIGURE 51. Fedora edwardsi Jullien, 1882. North Atlantic Ocean, Josephine Bank. A–D. SMNH-128030. A, C. Lateral views of two colonies. B. Group of zooids with operculum, some also with an adventitious avicularium. D. Close-up of two zooids showing the orifice. E–G. SMNH-128029. E, G. Proximal view of two colonies with emanation point of zooidal rows. F. Closeup of the proximal end with?ancestrula. H, I. SMNH-127677. H. Proximal view of a colony with?ancestrula. I. Group of autozooids with adventitious avicularia. Scale bars: A, C = 1 mm; B, E = 400 µm; D, F = 200 µm; G, I = 300 µm; H = 500 µm.