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Figure 2 in Molecular tool for monitoring the safety of Aedes (Stegomyia) aegypti Rockefeller rearing in arthropod containment facilities
Figure 2 Single Nucleotide Polymorphisms sites distribution in Aedes aegypti haplotypes according to the ND5 molecular marker. A) Phylogenetic estimation using the UPGMA method. Aa Rock 1 to 22, A. aegypti Rockefeller sequences obtained from 22 laboratory-bred Rock strain individuals. Aa, A. aegypti sequences obtained from towns located in the southeast of Buenos Aires Province (Lezama (LEZ), Castelli (CAS), Dolores (DOL), San Clemente del Tuyú (SC), Chascomús (CHA), La Plata City (LP) and from Buenos Aires City (BA). H1 to H14, 14 haplotypes reported by Albrieu Llinás and Gardenal (2012) and Díaz-Nieto et al. (2016) Rock contig 1 to 14, Illumina-contigs (A. aegypti Rock_Contig 1 to 14). Aa LVP, sequence from mitochondrial genome of A. aegypti Liverpool strain (LVP_AGWG). LVPib, A. aegypti inbred sub-strain LVPib12 according to Table 1. B) Its distribution along South America. The map was drawn from free maps of the website of the National Geographic Institute http://www.ign.gob.ar/AreaServicios/Descargas/MapasEscolares. The areas on the map were colored using Adobe Illustrator CS6 program.
Text-fig. 2. Eospondylus primigenius (STÜRTZ) Bundenbach, Eschenbach-Bocksberg quarry, Lower Devonian, Lower Emsian (Zlichovian), Hunsrück Slate,, NM S 4764, x 3. Specimen with ventral arm coiling. The specimen is on its dorsum in slate with all five rays curled ventrally inward toward mouth area on underside of disk. Barely visible are tips of two jaws; slightly exposed are proximal parts of rays in oral view extending outward from disk. The location of abrupt ventral bending of rays is indicated by emergence from slate of five rays in aboral view that point inward toward buried disk. Based on ventral bending of rays and intimate association with crinoids Eospondylus has been interpreted as stratigraphic first occurrence of Order Euryalida, which contains epizoic gorgonocephalid and euryalid basket-stars of modern oceans. This status is rejected using new evidence from isolated vertebrae. [Photo by Alexander Glass]. in Isolated Ossicles Of The Family Eospondylidae Spencer Wright, 1966, In The Lower Devonian Of Bohemia (Czech Republic) And Correction Of The Systematic Position Of Eospondylid Brittlestars (Echinodermata: Ophiuroidea: Oegophiurida)
Text-fig. 2. Eospondylus primigenius (STÜRTZ) Bundenbach, Eschenbach-Bocksberg quarry, Lower Devonian, Lower Emsian (Zlichovian), Hunsrück Slate,, NM S 4764, x 3. Specimen with ventral arm coiling. The specimen is on its dorsum in slate with all five rays curled ventrally inward toward mouth area on underside of disk. Barely visible are tips of two jaws; slightly exposed are proximal parts of rays in oral view extending outward from disk. The location of abrupt ventral bending of rays is indicated by emergence from slate of five rays in aboral view that point inward toward buried disk. Based on ventral bending of rays and intimate association with crinoids Eospondylus has been interpreted as stratigraphic first occurrence of Order Euryalida, which contains epizoic gorgonocephalid and euryalid basket-stars of modern oceans. This status is rejected using new evidence from isolated vertebrae. [Photo by Alexander Glass].
Fig. 3 in Do container size and predator presence affect Culex (Diptera: Culicidae) oviposition preferences?
Fig. 3. Predator abundance per liter as a function of sampling day and container size. The 100 and 200-L barrels are represented by the closed triangles and closed circles, respectively. The open circles represent the 15-L buckets, and asterisks represent the 1-L cups. The bars represent standard error. Different letters indicate different means among the treatments.
Fig. 2 in Do container size and predator presence affect Culex (Diptera: Culicidae) oviposition preferences?
Fig. 2. Numbers of Culex sp. 1 (left) and C. eduardoi (right) egg rafts as a function of sampling day and container size. The 100 and 200-L barrels are represented by closed triangles and closed circles, respectively. The open circles represent the 15-L buckets, and asterisks represent the 1-L cups. The bars represent standard error. Different letters indicate different means among the treatments.
Fig. 1 in Do container size and predator presence affect Culex (Diptera: Culicidae) oviposition preferences?
Fig. 1. Numbers of eggs rafts number as a function of sampling days and container size.The 100 and 200-L barrels are represented by closed triangles and closed circles, respectively. The open circles represent the 15-L buckets, and asterisks represent the 1-L cups. The bars represent standard error. Different letters indicate different means among the treatments.
Fig. 2 in Field capture of male oriental fruit flies (Diptera: Tephritidae) in traps baited with solid dispensers containing varying amounts of methyl eugenol
Fig. 2. Captures of Bactrocera dorsalis males on Oahu, Hawaii, USA, in Jackson traps baited with fresh liquid methyl eugenol or weathered, polymeric plugs containing 3, 6, or 10 g of methyl eugenol, where accompanying dichlorvos squares were either weathered (A, Experiment 2) or replaced prior to each trapping period (B, Experiment 3). Symbols represent means ± 1 SE; n = 12 in all cases. For a given trapping interval, means marked with different letters differed significantly (P <0.05, Tukey test).
Fig. 1 in Field capture of male oriental fruit flies (Diptera: Tephritidae) in traps baited with solid dispensers containing varying amounts of methyl eugenol
Fig. 1. Captures of Bactrocera dorsalis males on the Big Island, Hawaii, USA (Experiment 1) in Jackson traps baited with fresh liquid methyl eugenol or weathered, polymeric plugs containing 3, 6, or 10 g of methyl eugenol. Symbols represent means ± 1 SE; n = 12 in all cases.
Fig. 4 in On the largest Ichthyosaurus: A new specimen of Ichthyosaurus somersetensis containing an embryo
Fig. 4. Right forefin of Ichthyosaurus somersetensis Lomax and Massare, 2017 (NLMH 106234) from the Lower Jurassic (lower Hettangian) of Doniford Bay, Watchet, Somerset, UK; in dorsal view (anterior to the right). Grey indicates plaster filler (elements are not genuine); black indicates crushed and displaced portion of humerus. Arrow points to bifurcation. Photograph (A), explanatory drawing (B).
Fig. 7 in On the largest Ichthyosaurus: A new specimen of Ichthyosaurus somersetensis containing an embryo
Fig. 7. Embryo of Ichthyosaurus somersetensis Lomax and Massare, 2017 (NLMH 106234) from the Lower Jurassic (lower Hettangian) of Doniford Bay, Watchet, Somerset, UK. A. Articulated vertebral column, isolated forefin, probable scapula (white arrow), ribs, and isolated centra. B. Close-up of the forefin. Arrows point to probable notching of the?radiale,?distal carpal, and?metacarpal.
Fig. 5 in On the largest Ichthyosaurus: A new specimen of Ichthyosaurus somersetensis containing an embryo
Fig. 5. Close-up of some mid-posterior dorsal vertebrae of Ichthyosaurus somersetensis Lomax and Massare, 2017 (NLMH 106234) from the Lower Jurassic (lower Hettangian) of Doniford Bay, Watchet, Somerset, UK; showing the unusual V-shape morphology of the neural spine apices. Note, the second, third, and fourth neural spine from the left are mostly reconstructed and the morphology is not genuine.
Fig. 6 in A new Middle Devonian cystoporate bryozoan from Germany containing a new symbiont bioclaustration
Fig. 6. Spionid polychaete symbionts in the Recent cheilostome bryozoan Celleporaria brunnea (Hincks, 1884), Point Loma, San Diego, California. A. Living associations showing two long palps emerging from a spionid tube (arrowed), shorter tentacles of the bryozoan and black opercula. B. Spionid palps extending above level of bryozoan lophophores. C. Scanning electron microscope of bleached colony (NHM 2010.11.30.1) showing numerous spionid worm bioclaustrations varying in shape and size but consistently larger than the bryozoan orifices and new buds. D. Scanning electron micrograph of dried, unbleached colony showing mud tube constructed by a spionid worm surrounded by calcareous tube formed by the bioclaustrating bryozoan (NHM 2010.11.30.1).
Fig. 3 in A new Middle Devonian cystoporate bryozoan from Germany containing a new symbiont bioclaustration
Fig. 3. Fistuliporid bryozoan Stellatoides muellertchensis gen. et sp. nov., Middle Devonian (Lower Givetian, Ahbach Formation) of the abandoned "Müllertchen Quarry" (Hillesheim Syncline, Eifel, Rhenish Massif, northwestern Rhineland-Palatinate, Germany). A. Paratype SMF 21.115, goblet-shaped colony, side view. B. Paratype SMF 21.110, fragment of goblet-shaped colony showing maculae.
Fig. 2 in A new Middle Devonian cystoporate bryozoan from Germany containing a new symbiont bioclaustration
Fig. 2. Lowermost Lower Givetian stratigraphy of the "Type Eifelian Profile" sensu Struve (1982); light grey: biostratigraphic distribution of fistuliporid bryozoan Stellatoides muellertchensis gen. et sp. nov.; dark grey: maximum distribution.
Fig. 1 in A new Middle Devonian cystoporate bryozoan from Germany containing a new symbiont bioclaustration
Fig. 1. Map showing location of the abandoned Müllertchen Quarry within the Hillesheim Syncline. Geological overview of the Rhenish Massif (A), showing the studied area (taken from Bohatý et al. 2012; modified from Korn 2008 after Walter 1995) and detailed view of the Eifel Synclines (B) with the fossil locality 1 (modified after Struve 1996c).
Fig. 5 in A new Middle Devonian cystoporate bryozoan from Germany containing a new symbiont bioclaustration
Fig. 5. Cylindrical embedment trace (bioclaustration) Chaetosalpinx tapanilai ichnosp. nov., Middle Devonian (Lower Givetian) of the Rhenish Massif, north-western Rhineland-Palatinate, Germany. A. Paratype SMF 21.115, colony surface of fistuliporid bryozoan Stellatoides muellertchensis gen. et sp. nov. showing tubes of C. tapanilai. B. Paratype SMF 21.122, tangential section of tubes of C. tapanilai. C. Holotype SMF 21.118, longitudinal section of a tube.
Fig. 4 in A new Middle Devonian cystoporate bryozoan from Germany containing a new symbiont bioclaustration
Fig. 4. Fistuliporid bryozoan Stellatoides muellertchensis gen. et sp. nov., Middle Devonian (Lower Givetian) of the Rhenish Massif, north-western Rhineland-Palatinate, Germany. A. Holotype SMF 21.108, transverse section showing autozooecial chambers and vesicular skeleton (A), tangential sec1 tions showing autozooecial apertures with lunaria and vesicles (A 2 –A 5). B. Paratype SMF 21.113, longitudinal section showing multilayered secondary overgrowths.
Figure 4. The bio-secure container facility a in The conservation breeding of two foot-flagging frog species from Borneo, Staurois parvus and Staurois guttatus
Figure 4. The bio-secure container facility a modern Noah´s Ark, which houses Staurois guttatus and S. parvus at the Vienna Zoo Schönbrunn. Image by D. Preininger.
Data described in the article "Nitrogen-Containing Flavonoids─Preparation and Biological Activity"
<p>The dataset includes supplementary data, i.e. the results of optimization of Ullmann reaction, cellular antioxidant and anti-inflammatory activity, cytotoxicity, antibacterial activity, and molecular docking, <sup>1</sup>H, <sup>13</sup>C{<sup>1</sup>H} NMR data, HPLC, and HRMS analyses of the study titled "Nitrogen-Containing Flavonoids─Preparation and Biological Activity" available here: <a href="https://doi.org/10.1021/acsomega.4c04627">https://doi.org/10.1021/acsomega.4c04627</a></p>
Figure 8 in From Eradication to Containment: Invasion of French Polynesia by Bactrocera dorsalis (Hendel) (Diptera: Tephritidae) and Releases of Two Natural Enemies: A 17-Year Case Study
Figure 8. Dates of detection of B. dorsalis and introduction of F. arisanus on the various islands of French Polynesia.
Chemical composition and mixing state of elemental carbarn-containing particles from solid fuel combustion
<p>The above data set contains the mass spectrum information of EC-containing particles obtained from the single particle aerosol mass spectrometer (SPAMS) and some related processing methods. Specifically, it includes: (1)Average positive and negative mass spectra of 5 solid fuels, (2)Average mass spectra for each particle cluster from 5 solid fuels, (3)Cluster composition of EC-containing particles, (4)cluster composition of EC-containing particles, (5)Particle size distribution of EC-containing and (6)Mixing state characteristics of EC-containing particles.</p>
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.