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Fig. 1 in Population counts and potential impact of two successful invaders in a town of Northern Italy: the case of ring-necked parakeet and Alexandrine parakeet in Reggio Emilia
Fig. 1 - Male individuals of ring-necked parakeet (left) and Alexandrine parakeet (right) in Reggio Emilia. / Individui di sesso maschile di parrocchetto dal collare (sinistra) e parrocchetto di Alessandro (destra) a Reggio Emilia. (Photo: / Foto: S. Manfredini).
Fig. 2 in Population counts and potential impact of two successful invaders in a town of Northern Italy: the case of ring-necked parakeet and Alexandrine parakeet in Reggio Emilia
Fig. 2 - Population counts at night roosts showing the growing trends of both RNPs and APs in Reggio Emilia. Counts recorded during our 2019-2020 survey are shown in a blue rectangle. The 2008-2018 counts were obtained from the literature and citizen-science web platforms (Chessa, 2020). / Conteggi di parrocchetti ai dormitori notturni, con tendenze crescenti sia di parrocchetto dal collare sia di parrocchetto di Alessandro a Reggio Emilia. I conteggi del 2019-2020 sono riportate nel rettangolo blu. I conteggi 2008-2018 sono stati ottenuti da letteratura e da piattaforme web di citizen-science (Chessa, 2020).
Fig. 2 in Changing Of Wintering Site Or Recovery Provision - An Analysis Of Ringing Data Of Hungarian Lapwings, Vanellus Vanellus
Fig. 2. Recoveries of Lapwings ringed in Hungary between 1974–2005 and recovered in the Mediterranean area (dots) or in the Atlantic region (squares)
Fig. 1 in Changing Of Wintering Site Or Recovery Provision - An Analysis Of Ringing Data Of Hungarian Lapwings, Vanellus Vanellus
Fig. 1. Recoveries of Lapwings ringed in Hungary between 1909–1932 and recovered in the Mediterranean area (dots) or in the Atlantic region (squares)
Рис. 2. Морфотипы Зрелых сперматоЗоидов (СЭМ) у Mytilus trossulus (A–G), Crenomytilus grayanus (H–L) и Mytilus coruscus (M–R): a – акросома; br – basal ring; n – Ядро; m – митохондриЯ; fl – Жгутик. Масштаб линейки – 1 мкм. in Study on sperm heteromorphism in some mussels (Bivalvia: Mytilidae) from the Sea of Japan
Рис. 2. Морфотипы Зрелых сперматоЗоидов (СЭМ) у Mytilus trossulus (A–G), Crenomytilus grayanus (H–L) и Mytilus coruscus (M–R): a – акросома; br – basal ring; n – Ядро; m – митохондриЯ; fl – Жгутик. Масштаб линейки – 1 мкм.
Рис. 3. Teratocephalon hexahamus gen. n., sp. n.: A — трофико-сенсорный отΑеΛ теΛа; B — трофико-генитаΛьный отΑеΛ теΛа; C, D — переΑний конец теΛа. a — анус, am — амфиΑы, v — вуΛьва, cc — гоΛовная капсуΛа, ve — «жеΛуΑочек», pu — заΑняя матка, nr — нервное коΛьцо, rc — прямая кишка, au — переΑняя матка, r — ренетта, ep — экскреторная пора, o — яичник, e — яйцо Fig. 3. Teratocephalon hexahamus gen. n., sp. n.: A — trophic-sensory part of the body; B — trophic-reproductive part of the body; C, D — anterior end of the body. a — anus; am — amphids; v — vulva; cc — cephalic capsule; ve — "ventricle"; pu — posterior uterus; nr — nerve ring; pu — anterior uterus; r — renetta; rc — rectum; ep — excretory pore; o — ovary; e — egg in Recent data on soil nematodes of the families Teratocephalidae and Metateratocephalidae from Primorsky Region, Russia
Рис. 3. Teratocephalon hexahamus gen. n., sp. n.: A — трофико-сенсорный отΑеΛ теΛа; B — трофико-генитаΛьный отΑеΛ теΛа; C, D — переΑний конец теΛа. a — анус, am — амфиΑы, v — вуΛьва, cc — гоΛовная капсуΛа, ve — «жеΛуΑочек», pu — заΑняя матка, nr — нервное коΛьцо, rc — прямая кишка, au — переΑняя матка, r — ренетта, ep — экскреторная пора, o — яичник, e — яйцо Fig. 3. Teratocephalon hexahamus gen. n., sp. n.: A — trophic-sensory part of the body; B — trophic-reproductive part of the body; C, D — anterior end of the body. a — anus; am — amphids; v — vulva; cc — cephalic capsule; ve — "ventricle"; pu — posterior uterus; nr — nerve ring; pu — anterior uterus; r — renetta; rc — rectum; ep — excretory pore; o — ovary; e — egg
Fig. 5 in Towards incorporating insect isotope analysis using cavity ring-down spectroscopy into area-wide insect pest management programs
Fig. 5. Cumulative standard deviation of the mean carbon isotope signature of individual moths, field-caught LBAM (circles), mass-reared pink bollworm (squares) and mass-reared LBAM (triangles), analysed using the CM-CRDS module.
Fig. 3 in Towards incorporating insect isotope analysis using cavity ring-down spectroscopy into area-wide insect pest management programs
Fig. 3. Carbon isotope signature of common cutworm leg samples from different moths reared on the artificial laboratory diet or caught in the wild (circles, n = 5, Bars +/- 3 SD). The spermatophore data point (triangle) is the carbon isotope signature of spermatophores dissected from laboratory-reared females mated with field-caught males (n = 5, Bars +/- 3 SD). All samples measured using CM-CRDS.
Fig. 1 in Towards incorporating insect isotope analysis using cavity ring-down spectroscopy into area-wide insect pest management programs
Fig. 1. Carbon isotope ratios of 16 different common dietary components measured using either elemental analysis isotope ratio mass spectrometry (EAIRMS) or combustion module cavity ring down spectrometry (CM-CDRS).
Fig. 2 in Towards incorporating insect isotope analysis using cavity ring-down spectroscopy into area-wide insect pest management programs
Fig. 2. Carbon isotope ratios of 3 populations of the common cutworm measured using either elemental analysis isotope ratio mass spectrometry (EA-IRMS) or combustion module cavity ring down spectrometry (CM-CDRS): Field-caught moths: squares; synthetic diet-reared moths: circles and laboratory-reared on castor diet moths: triangles.
BRAIN Journal-A Synoptic of Software Implementation for Shift Registers Based on 16th Degree Primitive Polynomials-Figure 7. Ring Implementation for the Polynomial X6+X^12+X^3+X+1
<p>VlăduŃiu and Crişan (1989) show three types of schemes for a 4th degree polynomial. Similar to it, there were developed the three different implementations for the Primitive Polynomial X^16+X^12+X^3+X+1. It can be specified that these schemes are according to the well-known Galois Form, Fibonacci representation and some other Forms that are rarely used, called Ring Implementation. All of these Implementations have the same function, because they describe a linear feedback shift register. In the experimental work there has been analyzed the behavior of 14 Primitive Polynomial degrees, 16 randomly selected. For each of these polynomials there has been developed the simulation of the specific functioning with a program. Because the goal of this experimental work was to compare the different obtained results, a few rows of input data of a different length have been selected. </p>
Molecular Architecture of the Major Membrane Ring Component of the Nuclear Pore Complex
<p>This repository contains the modeling files and the analysis related to the article <a href="https://www.ncbi.nlm.nih.gov/pubmed/28162953">"Molecular Architecture of the Major Membrane Ring Component of the Nuclear Pore Complex"</a> by Upla et al. in Structure 2017.</p> <p><strong>For more information</strong> about how to reproduce this modeling, see the <a href="https://salilab.org/pom152/">Sali lab website</a> or the README file.</p>
Text-fig. 1. Amblypterus latus AGASSIZ, 1833. Pen and ink drawing (A) and photo (B) of the skull in lateral view. Mb. F. 3809b, scale bar represents 10 mm. Cl – cleithrum; Dent – dentalosplenial; Dhy – dermohyal; Dpt – dermopterotic; Dsph –dermosphenotic; Extl – extrascapular lateral; Fr –frontal; Gu – gular; Infs – infraorbital superior; Ju – jugal; La – lacrimal; Mx – maxilla; Na – nasal; Op – operculum; Pa – parietal; Pmx – premaxillar; Pop – preoperculum; Pp – postparietal; Pt – posttemporal; Rbr – branchiostegal rays; Sbo – suborbital; Scl – supracleithrum; Soant – supraorbital anterior; Sop – suboperculum; Spi – spiracular; sr – sclerotical ring. in New Data On The Osteology Of The Actinopterygian Fish Amblypterus And The Relationship Between Amblypterus And Paramblypterus
Text-fig. 1. Amblypterus latus AGASSIZ, 1833. Pen and ink drawing (A) and photo (B) of the skull in lateral view. Mb. F. 3809b, scale bar represents 10 mm. Cl – cleithrum; Dent – dentalosplenial; Dhy – dermohyal; Dpt – dermopterotic; Dsph –dermosphenotic; Extl – extrascapular lateral; Fr –frontal; Gu – gular; Infs – infraorbital superior; Ju – jugal; La – lacrimal; Mx – maxilla; Na – nasal; Op – operculum; Pa – parietal; Pmx – premaxillar; Pop – preoperculum; Pp – postparietal; Pt – posttemporal; Rbr – branchiostegal rays; Sbo – suborbital; Scl – supracleithrum; Soant – supraorbital anterior; Sop – suboperculum; Spi – spiracular; sr – sclerotical ring.
Text-fig. 14. Schema of transversal section of Manilkaroxylon sp. (sample DR2). ap – axial parenchyma, grb – growth ring boundaries, r – rays, v – vessels. in New Fossil Woods From The Paleogene Of Doupovské Hory And České Středohoří Mts. (Bohemian Massif, Czech Republic)
Text-fig. 14. Schema of transversal section of Manilkaroxylon sp. (sample DR2). ap – axial parenchyma, grb – growth ring boundaries, r – rays, v – vessels.
Text-fig. 10. Schema of transversal section of A. tschemrylica (sample 97/04). v – vessel, r – ray, ar – aggregate ray, grb – growth-ring boundary. in New Fossil Woods From The Paleogene Of Doupovské Hory And České Středohoří Mts. (Bohemian Massif, Czech Republic)
Text-fig. 10. Schema of transversal section of A. tschemrylica (sample 97/04). v – vessel, r – ray, ar – aggregate ray, grb – growth-ring boundary.
Text-fig. 2: Microscopic photo of the wood from Kučlín (specimen No. G 4723, NM, transverse section) shoving growth ring boundary with markedly rounded tracheids and abundant axial parenchyma (dark cells) present both in late- and earlywood (scale bar = 100 µm). in Silicified Stem From The Late Eocene Fossil Locality Of Kučlín (Czech Republic): Overview And New Remarks
Text-fig. 2: Microscopic photo of the wood from Kučlín (specimen No. G 4723, NM, transverse section) shoving growth ring boundary with markedly rounded tracheids and abundant axial parenchyma (dark cells) present both in late- and earlywood (scale bar = 100 µm).
Figure. Measurement data plotted for all nestlings as a function of age for the black stork: a) wing length (WL), b) head length (HL), c) bill length (BL), and d) tarsus length. in Age estimation of black stork (Ciconia nigra) nestlings from wing, bill, head, and tarsus lengths at the time of ringing
Figure. Measurement data plotted for all nestlings as a function of age for the black stork: a) wing length (WL), b) head length (HL), c) bill length (BL), and d) tarsus length.
Fig. 1 in DNA barcoding reveals different cestode helminth species in northern European marine and freshwater ringed seals
Fig. 1. (A) Geographic distributions of the three northern European ringed seal subspecies from which cestodes were collected for COI barcoding: Baltic ringed seal (green), Saimaa ringed seal (blue), and Ladoga ringed seal (red). (B) Midpoint-rooted neighbor-joining tree based on K2P distances among COI barcode sequences of 35 cestode individuals collected from the three focal ringed seal subspecies. Individuals are colored according to host subspecies, numbers above or next to branches are bootstrap support values based on 500 resamplings of the data matrix (only values> 70% shown). Cestode species names indicated under the main branches are based on barcode similarity to reference sequences in GenBank. (C) Maximum-likelihood tree based on a 562-bp alignment of the barcode sequences of the focal cestodes and 34 diphyllobothriidean reference taxa obtained from GenBank. Numbers above branches are bootstrap support values based on 100 resamplings of the data (only values> 70% shown). In both trees, individual names include the voucher code or GenBank accession number, seal subspecies abbreviation with seal individual code, barcode-based cestode species name, and name of the host (sub)species from which the cestode specimen was collected. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Fig. 1 in Unveiling a novel parasitosis: Trichostrongylus colubriformis infection in captive ring-tailed lemurs (Lemur catta)
Fig. 1. Morphology of Trichostrongylus colubriformis adult stages: A) anterior end, scale bar 50 μm; B) detail of anterior end of female showing three small lips and a circle of cephalic papillae; C) detail of ovijector, scale bar 50 μm; D) detail of the cuticle; E) posterior end of male showing the structure of bursa, the gubernaculum (g) and short subequal spicules (sp); F) egg, scale bar 50 μm.
Fig. 2 in Unveiling a novel parasitosis: Trichostrongylus colubriformis infection in captive ring-tailed lemurs (Lemur catta)
Fig. 2. The evolutionary history was inferred by using the Maximum Likelihood method based on the Tamura 3-parameter model. The tree is drawn to scale, with branch lengths measured in the number of substitutions per site. The analysis involved 27 nucleotide sequences. There were a total of 684 positions in the final dataset.
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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.