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FIGURE 15 in A review of growth form and plant duration (life cycle) in Kalanchoe (Crassulaceae subfam. Kalanchooideae) in an evolutionary and classificatory framework
FIGURE 15. Plants of Kalanchoe crenata are herbaceous-stemmed and develop into shrubby, multi-branched plants. Photograph: Gideon F. Smith.
FIGURE 21 in A review of growth form and plant duration (life cycle) in Kalanchoe (Crassulaceae subfam. Kalanchooideae) in an evolutionary and classificatory framework
FIGURE 21. Virtually all plant parts of Kalanchoe tomentosa are densely tomentose. Photograph: Gideon F. Smith.
Data from: Two forms of asynchronous release with distinctive spatiotemporal dynamics in central synapses
<p>Asynchronous release is a ubiquitous form of neurotransmitter release that persists for tens to hundreds of milliseconds after an action potential. How asynchronous release is organized and regulated at the synaptic active zone (AZ) remains debatable. Using nanoscale-precision imaging of individual release events in rat hippocampal synapses, we observed two spatially distinct subpopulations of asynchronous events, ~75% of which occurred inside the AZ and with a bias towards the AZ center, while ~25% occurred outside of the functionally defined AZ, i.e., ectopically. The two asynchronous event subpopulations also differed from each other in temporal properties, with ectopic events occurring at significantly longer time intervals from synchronous events than the asynchronous events inside the AZ. Both forms of asynchronous release did not, to a large extent, utilize the same release sites as synchronous events. The two asynchronous event subpopulations also differ from synchronous events in some aspects of exo-endocytosis coupling, particularly in the contribution from the fast calcium-dependent endocytosis. These results identify two subpopulations of asynchronous release events with distinctive organization and spatiotemporal dynamics.</p>
Data from: Caveolae and Bin1 form ring-shaped platforms for T-tubule initiation
<p>Excitation-contraction coupling requires a highly specialized membrane structure, the triad, composed of a plasma membrane invagination, the T-tubule, surrounded by two sarcoplasmic reticulum terminal cisternae. Although the precise mechanisms governing T-tubule biogenesis and triad formation remain largely unknown, studies have shown that <span>caveolae participate in T-tubule formation</span> and mutations of several of their constituents induce muscle weakness and myopathies. <span>Here, we demonstrate that, at the plasma membrane, caveolae composed of caveolin-3 and Bin1 assemble into ring-like structures from which emerge tubes enriched in the dihydropyridine receptor. Overexpression of Bin1 leads to the formation of both rings and tubes and we show that Bin1 forms scaffolds on which caveolae accumulate to form the initial T-tubule. Cav3 deficiency caused by either gene silencing or pathogenic mutations causes defective ring formation and perturbed Bin1-mediated tubulation that may explain defective T-tubule organization in mature muscles. Our results uncover new pathophysiological mechanisms that may prove relevant to myopathies caused by Cav3 or Bin1 variants.</span></p>
Data for: Northern crayfish form alternation morphometrics
<p>Complex life histories are frequently associated with biological trade-offs, as the use of one trait can decrease the performance of a second trait due to the need to balance competing demands to maximize fitness. Here, we examine growth patterns in invasive adult male northern crayfish (<em>Faxonius virilis</em>) that are indicative of a potential trade-off between energy allocation for body size versus chelae size growth. Northern crayfish undergo cyclic dimorphism, a process characterized by seasonal morphological changes associated with reproductive status. We measured carapace length and chelae length before and after molting and compared these growth increments between the four morphological transitions of the northern crayfish. Consistent with our predictions, reproductive crayfish molting to the non-reproductive form and non-reproductive crayfish molting within the non-reproductive form experienced a larger carapace length growth increment. Reproductive crayfish molting within the reproductive form and non-reproductive crayfish molting to the reproductive form, on the other hand, experienced a larger growth increment in chelae length. The results of this study support that cyclic dimorphism evolved as a strategy for optimizing energy allocation for body and chelae size growth during discrete periods of reproduction in crayfish with complex life histories.</p>
Portuguese version of Self-Management Ability Questionnaire short-form for periodontitis
<p>Cross-cultural adaptation and validation of the Portuguese version of Self-Management Ability Questionnaire short-form for periodontitis</p>
APPENDIX L - Workshop Attendance Sheet and Informed Consent Form
<p>APPENDIX L - Workshop Attendance Sheet and Informed Consent Form for Memoryscapes in Recto-spection: Visualizing Avenida, Recto, and Carriedo, Manila as Virtual Memoryscapes through immersive mobile technologies and digital heritage interpretation. Thesis Adviser: Dr. Cathe Desiree S. Nadal, Ph. D.</p>
APPENDIX H: Evidence Synthesis Form and APPENDIX I: Extracted Associators
<p>APPENDIX H: Evidence Synthesis Form and APPENDIX I: Extracted Associators for Memoryscapes in Recto-spection: Visualizing Avenida, Recto, and Carriedo, Manila as Virtual Memoryscapes through immersive mobile technologies and digital heritage interpretation. Thesis Adviser: Dr. Cathe Desiree S. Nadal, Ph. D.</p>
Figure 26 in Integrative taxonomy, larval biology and functional morphology of the little known gall-forming coral endoparasite Petrarca (Thecostraca: Ascothoracida)
Figure 26. COI gene tree by maximum likelihood (ML) and species delimitation of Petrarca. Bootstrap support for neighbour-joining (NJ) and ML and posterior probability for Bayesian inference (BI) are presented at the main nodes. Results of species delimitation were presented by vertical bars, and the numbers in the black boxes were as follows: 1–3, results of ASAP with three highest ASAP-score; 4, 5, results of PTP method with maximum likelihood and the highest Bayesian supported solution; 6, result of GMYC.
Figure 25 in Integrative taxonomy, larval biology and functional morphology of the little known gall-forming coral endoparasite Petrarca (Thecostraca: Ascothoracida)
Figure 25. Petrarca rubus sp. nov., paratype, thoracopods and penis, SEM. A, thoracopod 1. B, ctenoid scales on thoracopod 3. C, rudimentary abdomen, ventral side. D, distal end of penis. Abbreviations: pe, penis (base); rab, rudimentary abdomen; thp1, thoracopod 1. Scale bars in µm.
Figure 21 in Integrative taxonomy, larval biology and functional morphology of the little known gall-forming coral endoparasite Petrarca (Thecostraca: Ascothoracida)
Figure 21. Petrarca rubus sp. nov., holotype, thoracopods, penis and abdomen. A, rudimentary setiform thoracopod 1. B, left thoracopods 2–6 (numbered) with groups of seminal receptacles. C, rudimentary abdomen, segments numbered. D, distal part of penis. Scale bars in µm.
Figure 24 in Integrative taxonomy, larval biology and functional morphology of the little known gall-forming coral endoparasite Petrarca (Thecostraca: Ascothoracida)
Figure 24. Petrarca rubus sp. nov., paratype, mouthparts, SEM. A, labrum, lateroventral view. B, C, distal part and cutting edge of mandible respectively (tiny setae on cutting edge indicated by arrowheads). D, dense thin setae on proximal half of outer margin of mandible. E, maxillule. F, G, middle and lower parts of cutting edge of maxillule. H, basal 'pore-field' of maxillule. I, maxillules and maxillae. J, thickened and wrinkled cuticle on distal surface of maxilla. K, ctenoid scale on lateral surface of maxilla. Abbreviations: mx1, maxillules; mx2, maxillae. Scale bars in µm.
Figure 22 in Integrative taxonomy, larval biology and functional morphology of the little known gall-forming coral endoparasite Petrarca (Thecostraca: Ascothoracida)
Figure 22. Petrarca rubus sp. nov., paratypes, general view and mantle (carapace) structures, SEM. A, general view, lateral view, left side. B, external surface of mantle, central part, papillae coloured in magenta. C, external surface of mantle with papillae, ventral side. D, tip of papilla with central micropore. E, habitus with left valve removed (first abdominal segment numbered). F, surface of internal cuticle of mantle with two tiny pores. Abbreviations: oc, oral cone; pe, penis; thp2–6, thoracopods. Scale bars in µm.
Figure 19 in Integrative taxonomy, larval biology and functional morphology of the little known gall-forming coral endoparasite Petrarca (Thecostraca: Ascothoracida)
Figure 19. Petrarca rubus sp. nov., general view, light microscopy (A, B, holotype; C, D, paratypes). A, B, lateral view, right and left sides, respectively. C, adult specimen, right side. D, young specimen, left side. Scale bars in µm.
Figure 20 in Integrative taxonomy, larval biology and functional morphology of the little known gall-forming coral endoparasite Petrarca (Thecostraca: Ascothoracida)
Figure 20. Petrarca rubus sp. nov., holotype, antennules and mouthparts. A, left antennule, segments numbered. B, C, terminal (fifth) segments of left and right antennules, respectively. D, rudimentary seta on fourth antennular segment. E, labrum with mouth structures, lateral view. F, mandible. G, cutting edge of mandible. H, maxillule. I, distal ends of maxillae. Abbreviations: ae, aesthetasc; cl, claw; clg, claw guard; ml, medial languette; mo, mouth opening; oe, oesophagus. Scale bars in µm.
Figure 23 in Integrative taxonomy, larval biology and functional morphology of the little known gall-forming coral endoparasite Petrarca (Thecostraca: Ascothoracida)
Figure 23. Petrarca rubus sp. nov., paratype, antennules, SEM. A, left antennule, segments numbered. B, rudimentary seta on fourth antennular segment. C, tiny pores (circled) on lateral surface of terminal (fifth) antennular segment. D, double pores on lateral surface of terminal (fifth) antennular segment. E, rudimentary setae (indicated by arrowheads) at base of claw, fifth antennular segment. F, aesthetasc on claw guard (rudimentary seta at base of aesthetasc indicated by arrowhead). G, rudimentary subterminal seta (indicated by arrowhead) of aesthetasc of claw guard. H, rudimentary terminal setae of claw guard (indicated by arrowheads). I, wrinkled cuticle with tiny pores on postaxial (ventral) margin of fifth antennular segment. Abbreviations: ae, aesthetasc; cl, claw; clg, claw guard. Scale bars in µm.
Figure 14 in Integrative taxonomy, larval biology and functional morphology of the little known gall-forming coral endoparasite Petrarca (Thecostraca: Ascothoracida)
Figure 14. Petrarca nozaaeai sp. nov., holotype, general view, light microscopy (C–F after treatment with KOH solution). A, B, lateral view, right and left sides, respectively. C–E, lateral, dorsal and ventral views, respectively, ventral papillae from (C) enlarged in oval outline, body proper observed between carapace valves in (E). F, body proper position between carapace valves, lateral view, right valve removed, first abdominal segment numbered. Abbreviations: a1, antennules; oc, oral cone; pa, papillae; pe, penis; rab, rudimentary abdomen; thp, thoracopods. Scale bars in µm.
Figure 16 in Integrative taxonomy, larval biology and functional morphology of the little known gall-forming coral endoparasite Petrarca (Thecostraca: Ascothoracida)
Figure 16. Petrarca nozaaeai sp. nov., holotype, thoracopods, penis and abdomen. A, rudimentary setiform thoracopod 1. B, right thoracopods 2–6 (numbered) with groups of seminal receptacles. C, rudimentary abdomen, segments numbered. D, distal part of penis. Scale bars in µm.
Figure 18 in Integrative taxonomy, larval biology and functional morphology of the little known gall-forming coral endoparasite Petrarca (Thecostraca: Ascothoracida)
Figure 18. Petrarca nozaaeai sp. nov., paratype, oral cone, thoracopods, abdomen and penis, SEM. A, oral cone, ventral view. B, ctenoid scales on labrum and maxilla enlarged from (A). C, rudimentary abdomen, segments numbered. D, thoracopods 3 and 4 (numbered). E, distal part of penis. Abbreviations: lb, labrum; mo, mouth opening; mx2, maxillae. Scale bars in µm.
Figure 17 in Integrative taxonomy, larval biology and functional morphology of the little known gall-forming coral endoparasite Petrarca (Thecostraca: Ascothoracida)
Figure 17. Petrarca nozaaeai sp. nov., paratype, general view and mantle (carapace) structures, SEM. A, left carapace valve, lateral view, external side (anterior end on the left partially destroyed after body proper was removed). B, external surface of mantle with papillae (coloured in magenta), dorsoposterior view. C, papilla on dorsoposterior surface enlarged from (B). D, conspicuous external papillae, anterioventral side. E, external papillae, ventral side. F, tip of external papilla with central micropore (indicated by arrowhead). G, right carapace valve, lateral view, internal side (anterior end on the left partially destroyed after body proper was removed). H, body proper removed from carapace valves (thoracopods numbered in Arabic, first abdominal segment numbered in Roman). Abbreviations: a1, antennule; ad, adductor muscle; oc, oral cone; pe, penis; rab, rudimentary abdomen; thp, thoracopods. Scale bars in µm.
ScienceDex guides
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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.