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951 results for “places”
FIGURE 5. Aphanius iconii, IUSHM 2017-1272, 25 in Neotype designation of Aphanius iconii, first reviser action to stabilise the usage of A. fontinalis and A. meridionalis and comments on the family group names of fishes placed in Cyprinodontidae (Teleostei: Cyprinodontiformes)
FIGURE 5. Aphanius iconii, IUSHM 2017-1272, 25 mm SL, neotype; Turkey: Karaot.
FIGURE 2. Aphanius meridionalis, FSJF 2460 in Neotype designation of Aphanius iconii, first reviser action to stabilise the usage of A. fontinalis and A. meridionalis and comments on the family group names of fishes placed in Cyprinodontidae (Teleostei: Cyprinodontiformes)
FIGURE 2. Aphanius meridionalis, FSJF 2460, female, 38 mm SL, male, 33 mm SL; Turkey: Söğüt.
FIGURE 1. Aphanius fontinalis, FSJF 3456 in Neotype designation of Aphanius iconii, first reviser action to stabilise the usage of A. fontinalis and A. meridionalis and comments on the family group names of fishes placed in Cyprinodontidae (Teleostei: Cyprinodontiformes)
FIGURE 1. Aphanius fontinalis, FSJF 3456, male, 42 mm SL; Turkey: Yarışlı.
Data and R code for cluster analysis and machine learning modelling of favourite places for outdoor recreation
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FIGURE 3 in Taxonomy of the Brazilian species previously placed in Mantispa Illiger, 1798 (Neuroptera: Mantispidae), with the description of three new species
FIGURE 3. Buyda phthisica: fore and hindwing.
ISOMORPHIC AND ALLOMORPHIC FEATURES OF COMPLEX SENTENCES WITH ADVERBIAL CLAUSES OF PLACE IN ENGLISH AND UZBEK LANGUAGES.
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Fig. 7 in A Revised Catalog of the Species ofStenocratesBurmeister (Coleoptera: Scarabaeidae: Dynastinae: Cyclocephalini), with Descriptions of Three New Species from Peru and Brazil andStenocrates inpaiRatcliffe, 1978 Placed in Junior Synonymy withStenocrates popeiEndrödi, 1971
Fig. 7. Stenocrates celatus, parameres.
Figs. 8– 11 in A Revised Catalog of the Species ofStenocratesBurmeister (Coleoptera: Scarabaeidae: Dynastinae: Cyclocephalini), with Descriptions of Three New Species from Peru and Brazil andStenocrates inpaiRatcliffe, 1978 Placed in Junior Synonymy withStenocrates popeiEndrödi, 1971
Figs. 8– 11. Stenocrates species, parameres.
Figs. 1–2 in A Revised Catalog of the Species ofStenocratesBurmeister (Coleoptera: Scarabaeidae: Dynastinae: Cyclocephalini), with Descriptions of Three New Species from Peru and Brazil andStenocrates inpaiRatcliffe, 1978 Placed in Junior Synonymy withStenocrates popeiEndrödi, 1971
Figs. 1–2. Stenocrates serendipitus, parameres.
FIG. 5 in They are all over the place! The exceptional high biodiversity of dormice in the Early Miocene of the Ribesalbes-Alcora Basin (Spain)
FIG. 5. — Gliridae from the Ribesalbes-Alcora Basin. Bransatoglis cf. infralactorensis: A, right p4 (MAB3-382); B, right m1 (MAB3-399); C, right m1 (MAB11-78); D, left m2 (MAB5-258); E, right m2 (MAB0A-75); F, left m3 (MAB0A-74); G, left M3 (MAB3-295). Peridyromys murinus: H, right d4 (MAB0C-1); I, right p4 (BC1- 15); J, right p4 (BC1-113); K, right p4 (MAB3-380); L, left p4 (MAB13-2); M, right p4 (MTR2-130); N, right m1 (MTR2-133); O, left m1 (MTR2-132); P, right m1 (MTR2-131); Q, left m1 (MCX7-3); R, left m1 (MAB5-608); S, left m1 (MAB3-418); T, left m2 (MTR2-141); U, right m2 (MTR2-139); V, left m2 (MTR2-15); W, right m2 (MAB11-79); X, right m2 (FS1-44); Y, right m2 (BC1-120); Z, left m3 (MTR2-147); AA, right m3 (MTR2-146); AB, left m3 (MTR2-145); AC, right m3 (MAB3-468); AD, left m3 (MAB5-856); AE, right m3 (BC1-140). Scale bar: 1 mm.
IMPROVING THE SYSTEM OF UTILIZING EFFICIENTS FROM PASTURE PLACES
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THE PLACE OF UNIVERSAL HUMAN VALUES IN THE FAMILY
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Enigmas no longer: using Ultraconserved Elements to place several unusual hawk taxa and address the non-monophyly of the genus Accipiter (Accipitriformes: Accipitridae)
<p>Alignment and tree data associated with the paper:<strong> </strong><span>Enigmas no longer: using Ultraconserved Elements to place several unusual hawk taxa and address the non-monophyly of the genus <em>Accipiter </em>(Accipitriformes: Accipitridae)</span></p>
Functional changes in fortified places: Strategy and defensive architecture in the Medieval and Early Modern Era
<p><strong>Data for Scott Kirk's Doctoral Dissertation.</strong></p> <p><strong>Dissertation Abstract:</strong></p> <p>Defined as fortified elite Houses, castles are a cross-cultural phenomenon, best understood by pairing Niche Construction Theory (NCT) with the Lévi-Straussian concept of the House. NCT can be thought of as a theory of the built environment, thus the material configuration of castles and their placement on the landscape reflect elite socio-cultural requirements. My dissertation asks: How do changes in castle morphology and landscape placement reflect broad shifts in function diachronically and cross-culturally?</p> <p>Wherever elites are militarized, castles typically appear. Similarities in castle design and function are best understood through anthropological frameworks and comparative, interdisciplinary approaches. Using a sample of castles from medieval European, western colonial, and nonwestern societies, I hypothesize that: (1) castle building is a common, cross-cultural behavior, (2) geography and the environment constrain castle location, allowing for a landscape-based typology of castles, and (3) changes in castle placement and design reflect large-scale social competition between elites.</p> <p>These hypotheses contradict much of the current regionally-focused work in castle studies, which are often grounded in national ideologies. Early 20th century studies were more aligned with my hypotheses. Revisiting these earlier investigations, my dissertation uses anthropological theories within an interdisciplinary approach. It combines architectural, statistical, and geospatial analyses to quantitatively test how similar castle placement and co-occurring architectural features are cross-culturally, and how these attributes change over time in relation to elite competition.</p> <p>This research has general and theoretical significance for assessing mechanisms of elite status reinforcement, behavior, and decision-making across space and time. Building a typology that characterizes castles as resource control points, examining how similar architectural features appear in disparate cultures, and exploring social change driven by elite competition, my dissertation takes aim at nationalistic policies by illustrating cross-cultural similarities that are applicable to the modern world in terms of increasing wealth disparities and socioeconomic inequality.</p>
Same place, different stories: Disparate evolutionary trends of Mygalomorphae from the peripampasic orogenic arc
<p><b>Aim:</b> Comparative phylogeography seeks to unravel similarities in the population structure and evolutionary processes undergone by co-distributed taxa under the assumption that they will have experienced the same geoclimatic events. However, small differences in functional traits, particularly those related to dispersal abilities, may translate into incongruent evolutionary histories. Here, we used a sequence target multi-locus approach to infer and compare the phylogeographical patterns of three sympatric mygalomorph spiders in the Argentinean peripampasic orogenic arc.</p> <p><b>Location:</b> The mountainous systems of central and northern Argentina.</p> <p><b>Taxon:</b> Mygalomorphae spiders (Araneae)</p> <p><b>Methods:</b> We inferred the phylogeny of three species of mygalomorph spiders based on <i>16</i>S+L1+nad1 and ITS sequences from o<span>ne hundred and thirty-four </span>individuals by using a Bayesian and Maximum likelihood approaches and we also estimated divergence dates. Also, nuclear networks were inferred. Based on our molecular phylogeny, we reconstructed <span>ancestral areas using the the Bayesian Binary MCMC method</span>.</p> <p><b>Results:</b> A deep genetic divergence and highly structured populations was obtained in the pycnothelid <i>Acanthogonatus centralis</i>, whereas the theraphosids <i>Plesiopelma longisternale </i>and <i>Grammostola vachoni </i>showed shallow divergences and poorly structured populations. Additionally, we uncovered potentially overlooked species diversity within <i>G</i>. <i>vachoni</i>, which warrants conducting a full taxonomic revision of <i>Grammostola</i>.</p> <p><b>Main conclusions:</b> We propose that differences in dispersion rates and time of colonization between the theraphosids and the pycnothelid led to divergent lineage history despite common environmental conditions. Our results further corroborate the key role played of the Plio-Pleistocene geoclimatic events in shaping the present-day diversity of mygalomorph spiders along the peripampasic orogenic arc.</p>
Non-invasive recording of EEG from the cervical spinal cord via surface electrodes placed around the neck
<p>Data and scripts used for Chander et al. 2022. EEG data recorded via 10 electrodes placed around the neck of 17 healthy young human individuals, in addition to EEG data recorded from scalp electrodes (numbers of electrodes vary across individuals), an ECG channel, and EOG channels. The reference electrode was placed above the right acromion, the ground electrode above the left acromion. Sampling rate 5000 Hz, online lowpass filter 1000 Hz, online highpass filter .1 Hz (BrainAmp DC amplifier). During recordings, the left median nerve of participants was stimulated using a DS7 Digitimer at ~110% of motor threshold (constant current stimulation, 50-500 µsec pulse width (depending on the participant), square wave) at 3 Hz. 15% of stimuli were pseudo-randomly omitted. Participants counted the number of omissions in each of 3 minute blocks. The montage for neck electrodes is explained in Chander et al. 2022. There are three trigger values: 1 = experimenter pressed a key to start the experiment, or to initiate a new block. 130 = median nerve stimulation. 99 = omission. Further details in Chander et al. 2022. The scripts are mostly aiming at characterizing high-frequency signals (400-1200 Hz) in response to median nerve stimulation (8 to 16 ms), and their dissociation from the evoked response.</p>
conditioned place preference CPP rat
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Data for: Hippocampal place codes are gated by behavioral engagement
<p><span>As animals explore an environment, the hippocampus is thought to automatically form and maintain a place code by combining sensory and self-motion signals. Instead, we observed an extensive degradation of the place code when mice voluntarily disengaged from a virtual-navigation task, remarkably even as they continued to traverse the identical environment. Internal states therefore can strongly gate spatial maps and reorganize hippocampal activity even without sensory and self-motion changes.</span></p>
FIGURE 8 in Taxonomic implications of anatomical characteristics of the genus Tulipa (Liliaceae) in Turkey and their place in the historical subgeneric classifications
FIGURE 8. Results of principle component analysis of subgenus Tulipa.
FIGURE 7 in Taxonomic implications of anatomical characteristics of the genus Tulipa (Liliaceae) in Turkey and their place in the historical subgeneric classifications
FIGURE 7. Results of principle component analysis of subgenus Tulipa+T. clusiana.
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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.