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5,931 results for “laterality”
FIGURES 19–23. Plumolepilius antonioi. Female. 19, Dorsal habitus. 20, Lateral habitus. 21, Frontal view. 22 in Taxonomy of the weevil genus Plumolepilius Barrios-Izás & Anderson (Coleoptera Curculionidae: Molytinae: Conotrachelini): new species from Central America
FIGURES 19–23. Plumolepilius antonioi. Female. 19, Dorsal habitus. 20, Lateral habitus. 21, Frontal view. 22, Genitalia and associated sclerites. 23, Spermatheca.
FIGURES 95–98. Plumolepilius monzoni. Female. 95, Dorsal habitus. 96, Lateral habitus. 97, Frontal view. 98 in Taxonomy of the weevil genus Plumolepilius Barrios-Izás & Anderson (Coleoptera Curculionidae: Molytinae: Conotrachelini): new species from Central America
FIGURES 95–98. Plumolepilius monzoni. Female. 95, Dorsal habitus. 96, Lateral habitus. 97, Frontal view. 98, Genitalia and associated sclerites.
FIGURES 7–12. Plumolepilius andersoni. Female. 7, Dorsal habitus. 8, Lateral habitus. 9, Frontal view. 10 in Taxonomy of the weevil genus Plumolepilius Barrios-Izás & Anderson (Coleoptera Curculionidae: Molytinae: Conotrachelini): new species from Central America
FIGURES 7–12. Plumolepilius andersoni. Female. 7, Dorsal habitus. 8, Lateral habitus. 9, Frontal view. 10, Genitalia and associated sclerites. 11, Pygidium. 12, Spermatheca.
FIGURES 44–48. Plumolepilius guaimacaensis. Female. 44, Dorsal habitus. 45, Lateral habitus. 46, Frontal view. 47, Genitalia. 48 in Taxonomy of the weevil genus Plumolepilius Barrios-Izás & Anderson (Coleoptera Curculionidae: Molytinae: Conotrachelini): new species from Central America
FIGURES 44–48. Plumolepilius guaimacaensis. Female. 44, Dorsal habitus. 45, Lateral habitus. 46, Frontal view. 47, Genitalia. 48, Genitalia associated sclerites.
FIGURES 145–150. Plumolepilius velizi. Male. 145, Dorsal habitus. 146, Lateral habitus. 147, Frontal view. 148, Abdominal ventrites I–V. 149, Aedeagus dorsal view. 150 in Taxonomy of the weevil genus Plumolepilius Barrios-Izás & Anderson (Coleoptera Curculionidae: Molytinae: Conotrachelini): new species from Central America
FIGURES 145–150. Plumolepilius velizi. Male. 145, Dorsal habitus. 146, Lateral habitus. 147, Frontal view. 148, Abdominal ventrites I–V. 149, Aedeagus dorsal view. 150, Aedeagus lateral view.
FIGURES 1–6. Plumolepilius andersoni. Male. 1, Dorsal habitus. 2, Lateral habitus. 3, Frontal view. 4, Abdominal ventrites I–V. 5, Aedeagus dorsal view. 5 in Taxonomy of the weevil genus Plumolepilius Barrios-Izás & Anderson (Coleoptera Curculionidae: Molytinae: Conotrachelini): new species from Central America
FIGURES 1–6. Plumolepilius andersoni. Male. 1, Dorsal habitus. 2, Lateral habitus. 3, Frontal view. 4, Abdominal ventrites I–V. 5, Aedeagus dorsal view. 5, Aedeagus lateral view.
FIGURES 5–6. Nonnus spp., lateral habitus. 5. N in First record of Nesomesochorinae (Hymenoptera: Ichneumonidae) from America north of Mexico with descriptions of two new species of Nonnus Cresson
FIGURES 5–6. Nonnus spp., lateral habitus. 5. N. barnesae Wahl & Bennett, paratype male (USA: Arizona); AEI photo vouch- er specimen #1069. 6. N. spurius Wahl & Bennett, holotype female; AEI photo voucher specimen #1074.
Three needle Sorter 1 element, effect of the lateral needles on the probe
<p>In this Dataset it is possible to observe the effect of the lateral needles, or stigmators, of the Sorter1 on a slightly out of focus probe.</p> <p>The theory behind this device can be found at <strong><a href="https://doi.org/10.1016/j.ultramic.2019.112861">10.1016/j.ultramic.2019.112861</a></strong></p>
Electroencephalography of completely locked-in state patients with amyotrophic lateral sclerosis
<p>The data set includes raw EEG data for 10 completely locked-in state (CLIS) patients with amyotrophic lateral sclerosis (ALS) and 6 healthy participants. The EEG data were recorded during resting state and the reference was right mastoid. This data was used in the publication https://doi.org/10.1016/j.neures.2020.01.013.</p>
Sheep brain lateral view
Drawing uploaded to scidraw.io on: 04 June 2020
The legacy of stress: coral bleaching impacts reproduction years later
1. The extent to which populations persist under environmental stress depends on the reproductive output of individuals that survive the stress. In coral systems, corals bleach in response to stress from elevated water temperature. However, little is known of the extent to which thermal stress impairs the reproductive capacity of the survivors over the following years, limiting the capacity to predict how populations will persist in the Anthropocene. 2. Using histology to quantify the abundance and size of oocytes and spermaries per polyp, we tested how bleaching impairs the reproductive response of the coral <i>Pocillopora meandrina</i> over two reproductive seasons following the 2015 mass bleaching event in the Hawaiian Islands. 3. We found that smaller colonies not only had a greater probability of bleaching but also suffered greater reproductive impacts over a longer time. In contrast, larger colonies generated comparable reproductive output regardless of bleaching severity, although bleached colonies generated smaller oocytes the year after bleaching. 4. These results show that reproductive impacts of bleaching are more complex and size-specific than commonly assumed. Therefore, estimates of bleaching mortality may underestimate the true impact of thermal stress on populations, especially as populations lose larger individuals from repeated and co-occurring stressors.
FIGS. 173–189. Brunsonia spp. Figs. 173–179. Brunsonia chelanomagna. Fig. 173. Right anterior gonopod, lateral view. Fig. 174. Left posterior gonopod coxite, posterior view. Figs. 175–179. Male legs 3–7, respectively. Figs. 180, 181. Brunsonia selwayana. Fig. 180. Right anterior gonopod, posteriolateral view. Fig. 181. Left posterior gonopod coxite, posterior view. Figs. 182–189. Brunsonia benewah. Fig. 182. Anterior gonopods, posterior view. Fig. 183 in The millipede family Conotylidae in northwestern North America, with a complete bibliography of the family (Diplopoda, Chordeumatida, Heterochordeumatidea, Conotyloidea)
FIGS. 173–189. Brunsonia spp. Figs. 173–179. Brunsonia chelanomagna. Fig. 173. Right anterior gonopod, lateral view. Fig. 174. Left posterior gonopod coxite, posterior view. Figs. 175–179. Male legs 3–7, respectively. Figs. 180, 181. Brunsonia selwayana. Fig. 180. Right anterior gonopod, posteriolateral view. Fig. 181. Left posterior gonopod coxite, posterior view. Figs. 182–189. Brunsonia benewah. Fig. 182. Anterior gonopods, posterior view. Fig. 183. Tip of left anterior gonopod, posterior view. Fig. 184. Left posterior gonopod coxite, posterior view. Figs. 185–189. Male legs 3–7, respectively.
FIGS. 141–143. Brunsonia pulchra. Fig. 141. Posterior gonopod coxites, posterior view. Fig. 142. Right anterior gonopod, lateral view. Fig. 143 in The millipede family Conotylidae in northwestern North America, with a complete bibliography of the family (Diplopoda, Chordeumatida, Heterochordeumatidea, Conotyloidea)
FIGS. 141–143. Brunsonia pulchra. Fig. 141. Posterior gonopod coxites, posterior view. Fig. 142. Right anterior gonopod, lateral view. Fig. 143. Detail of left anterior gonopod, mesal view.
FIGURE 34. Metasoma, A lateral view, B in Revisited morphology applied for Systematics of flat wasps (Hymenoptera, Bethylidae)
FIGURE 34. Metasoma, A lateral view, B dorsal view; C–D ventral view. A, D. Pristocera ♂; B. Dissomphalus ♂; C. Zimankos ♂.
FIGURE 33. Metasoma, A–B lateral view, C in Revisited morphology applied for Systematics of flat wasps (Hymenoptera, Bethylidae)
FIGURE 33. Metasoma, A–B lateral view, C dorsal view; D ventral view. A, C–D. Pristocera ♂; B. Pseudisobrachium ♀.
FIGURE 6. Head, A–B ventral view, C–F lateral view. A, F in Revisited morphology applied for Systematics of flat wasps (Hymenoptera, Bethylidae)
FIGURE 6. Head, A–B ventral view, C–F lateral view. A, F. Zimankos ♂; B. Pristocera ♂; B. Pristocera ♂; D. Proplastanoxus ♀; E. Anisepyris ♂.
Data from: Lipids, apolipoproteins, and prognosis of amyotrophic lateral sclerosis
<p><span><b>Objective</b> To determine whether lipids and apolipoproteins predict prognosis of patients with amyotrophic lateral sclerosis in a cohort study of 99 amyotrophic lateral sclerosis patients who were diagnosed during 2015-2018 and followed until October 31, 2018, at the Neurology Clinic in Karolinska University Hospital in Stockholm, Sweden. </span></p> <p><span><b>Methods</b> Total cholesterol, low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, triglyceride, apolipoprotein A-I, apolipoprotein B, and lipid ratios were measured at the time of amyotrophic lateral sclerosis diagnosis or shortly thereafter. Death after amyotrophic lateral sclerosis diagnosis was used as the main outcome. Cox model was used to estimate hazard ratios with 95% confidence intervals of death after amyotrophic lateral sclerosis diagnosis, after controlling for sex, age at diagnosis, site of symptoms onset, diagnostic delay, body mass index, Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised, and progression rate.</span></p> <p><span><b>Results </b>One-standard deviation increase of total cholesterol (hazard ratio, 0.60; 95% confidence interval, 0.41-0.89; P=0.01), low-density lipoprotein cholesterol (hazard ratio, 0.64; 95% confidence interval, 0.44-0.92; P=0.02), low-density lipoprotein cholesterol/high-density lipoprotein cholesterol ratio (hazard ratio, 0.65; 95% confidence interval, 0.46-0.92; P=0.02), apolipoprotein B (hazard ratio, 0.62; 95% confidence interval, 0.44-0.88; P=0.01), or apolipoprotein B/apolipoprotein A-I ratio (hazard ratio, 0.61; 95% confidence interval, 0.43-0.86; P<0.01) were all associated with a lower risk of death after amyotrophic lateral sclerosis diagnosis. A dose-response relationship was also noted when analyzing these biomarkers as categorical variables. </span></p> <p><span><b>Conclusions </b>Lipids and apolipoproteins are important prognostic indicators for amyotrophic lateral sclerosis and should be monitored at the diagnosis of amyotrophic lateral sclerosis.</span></p>
Data and R code used in Delory et al (2020) Soil chemical legacies trigger species-specific and context-dependent root responses in later arriving plants
<p>This repository contains the data and R markdown files supporting the findings presented in Delory et al (2020) Soil chemical legacies trigger species-specific and context-dependent root responses in later arriving plants.</p>
Thalamic encoding of lexical status is lateralized during reading aloud
<p>To explore whether the thalamus participates in lexical status encoding, local field potentials were recorded in patients undergoing deep brain stimulation lead implantation while they read aloud single-syllable words and nonwords. Bilateral decreases in thalamic beta (12-30Hz) activity were preferentially locked to stimulus presentation, and these decreases were greater when nonwords were read. Increased broadband gamma (70-150Hz) activity also was locked preferentially to speech onset bilaterally, but greater nonword-related increases in this activity were observed only on the left, demonstrating lateralization of thalamic broadband gamma selectivity for lexical status. In addition, this lexical status effect was strongest in more anterior thalamic locations, regions which are more likely to receive pallidal than cerebellar afferents. These results provide evidence from intracranial thalamic recordings for the lateralization and topography of subcortical lexical status processing.</p>
FIGURES8-11. L. sichuanensis Maetal,1994 8.Tegmen in lateral viewƋ; 9. Mesosternum ventral view Ƌ; 10. Epiphallus; 11. Epiproct in dorsal view Ƌ. (Figs.8-11 after Ma et al, 1994) in --A--new--species--and--a--key--to--10--species--of--the--genus Lemba--Huang,--1983--(Orthoptera Catantopidae)--from--China--
FIGURES8-11. L. sichuanensis Maetal,1994 8.Tegmen in lateral viewƋ; 9. Mesosternum ventral view Ƌ; 10. Epiphallus; 11. Epiproct in dorsal view Ƌ. (Figs.8-11 after Ma et al, 1994)
ScienceDex guides
Understand access before you commit
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.