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Fig. 5. A in Resurrection of nominal species previously regarded as junior synonyms of Thrissina baelama (Fabricius, 1775) and their re-descriptions (Teleostei: Clupeiformes: Engraulidae)
Fig. 5. A, Holotype of Anchovia evermanni, USNM 51719, 105.0 mm, and B, paratype of Anchovia evermanni, USNM 451580, 98.3 mm SL, Apia, Samoa.
Fig. 4 in Resurrection of nominal species previously regarded as junior synonyms of Thrissina baelama (Fabricius, 1775) and their re-descriptions (Teleostei: Clupeiformes: Engraulidae)
Fig. 4. Distributional records of Thrissina baelama (triangles), T. evermanni (squares), T. polynemoides (diamonds), T. samam (circles), and T. tuberculosa (star), based on specimens examined in this study.
Fig. 2 in Resurrection of nominal species previously regarded as junior synonyms of Thrissina baelama (Fabricius, 1775) and their re-descriptions (Teleostei: Clupeiformes: Engraulidae)
Fig. 2. Scatter plots of principal component 2 and 3 scores on 26 measurements and counts of total gill rakers on first to fourth gill arches for specimens of Thrissina baelama (triangles), T. evermanni (squares), T. polynemoides (diamonds), T. samam (circles), and T. tuberculosa (stars).
FIG. 3 in Resurrection of Plocamium pusillum Sonder (Plocamiaceae, Rhodophyta) from Australia
FIG. 3. — Morphology of recently collected Plocamium pusillum (all PERTH 09316647): A, pressed specimen showing habit; B, detail of apex showing origin of lateral branches in groups of three; C, section of young branch; D, section of older branch; E, surface view of living material showing prominent refringent vacuoles. These are not visible in preserved or dried material; F, tetrasporangia borne in groups near apices of lateral branches (arrows), not or only slightly distending the bearing branch; G, closer view of tetrasporangia showing biseriate arrangement. Scale bars: A, 1 cm; B, F, 300 µm; C, E, 30 µm; D, G, 60 µm.
FIG. 1 in Resurrection of Plocamium pusillum Sonder (Plocamiaceae, Rhodophyta) from Australia
FIG. 1. — Maximum likelihood phylogeny generated for the concatenated alignment. Bootstrap values>70% are provided; *, indicates 100% support. Plocamium pusillum is highlighted in bold text. Scale bar: substitutions per site.
Figure 6. Pseudophycis bachus. A, B, NMNZ P.054828 in A review of the Australasian genus Pseudophycis (Gadiformes: Moridae), redescribing its four species and resurrecting the name Physiculus palmatus Klunzinger, 1872, for the Australian Red Cod
Figure 6. Pseudophycis bachus. A, B, NMNZ P.054828, neotype, 351 mm SL, 2.5 km off coast from Whanganui River bar, Whanganui, New Zealand, fresh specimen, lateral view of body and anterior body showing black pectoral blotch respectively (photographs C. Struthers, NMNZ); C, unpublished line drawing by S. Parkinson of Enchelyopus bachus Forster in Bloch and Schneider, 1801 (reproduced from Whitehead, 1969: pl. 31).
Figure 5 in A review of the Australasian genus Pseudophycis (Gadiformes: Moridae), redescribing its four species and resurrecting the name Physiculus palmatus Klunzinger, 1872, for the Australian Red Cod
Figure 5. Scatter plot of canonical analysis of principal coordinates scores on the first and second canonical axes for 124 specimens of Pseudophycis, including types.
Figure 2. Pseudophycis palmata. A, B, CSIRO H 7366-01, 265 in A review of the Australasian genus Pseudophycis (Gadiformes: Moridae), redescribing its four species and resurrecting the name Physiculus palmatus Klunzinger, 1872, for the Australian Red Cod
Figure 2. Pseudophycis palmata. A, B, CSIRO H 7366-01, 265 mm SL, Storm Bay, east of Variety Bay on North Bruny Island, Tasmania, Australia, fresh specimen, lateral view of body and lateral view of head and anterior body with black pectoral blotch, respectively, (photographs C. Devine, CSIRO); C, SMNS 1589, holotype, 172 mm SL, Port Phillip, Hobsons Bay, Victoria, Australia (photograph C. Struthers, NMNZ).
Figure 8. Pseudophycis breviuscula. A, CSIRO H 4384-01, 110 in A review of the Australasian genus Pseudophycis (Gadiformes: Moridae), redescribing its four species and resurrecting the name Physiculus palmatus Klunzinger, 1872, for the Australian Red Cod
Figure 8. Pseudophycis breviuscula. A, CSIRO H 4384-01, 110 mm SL, Albany, Western Australia (photograph compliments CSIRO Marine Research); B, BMNH 1855.9.19.1182, holotype of Lota breviuscula, 152 mm SL, Bay of Islands, New Zealand (photograph © The Trustees of the Natural History Museum, London).
Figure 1 in A review of the Australasian genus Pseudophycis (Gadiformes: Moridae), redescribing its four species and resurrecting the name Physiculus palmatus Klunzinger, 1872, for the Australian Red Cod
Figure 1. Hasegawa-Kishino-Yano maximum likelihood tree of 65 COI sequences from four purported species of Pseudophycis, along with seven sequences for an outgroup species, Auchenoceros punctatus. Percentage bootstrap values followed by bootstrap values in p-distance neighbour joining and maximum parsimony trees are given for all well supported nodes (2 of 3 exceeding 80%). Specimen numbers are those of registered museum vouchers or sequence numbers in the Barcode of Life Database (BOLD, http://www.barcodinglife.org/).
Resurrecting Ancient Antibiotics: Unveiling the Origins of Modern Lipid II Targeting Glycopeptides
<p>Data supporting the publication "Resurrecting Ancient Antibiotics: Unveiling the Origins of Modern Lipid II Targeting Glycopeptides"</p>
FIG. 3 in Passiflora tinifolia Juss. (Passiflora subgenus Passiflora): resurrection and synonymies
FIG. 3. — Pictures and drawings of P. laurifolia L., P. oblongifolia Pulle, P. gabrielleana Vanderpl. and P. favardensis Kuethe: A, P. laurifolia from Guadeloupe (photograph F. Booms); B, C, P. gabrielleana from Montsinery, near its locus classicus in French Guiana (photograph M. Rome); D, drawing of P. oblongifolia from the holotype Versteeg 652 (from Pulle 1906); E, drawing of P. gabrielleana by J. Vanderplank in Vanderplank & Laurens (2006); F, picture of P. favardensis by Christian Houel in Kuethe (2011). Scale bars: 1 cm.
Phylogenomics and Intergenomic Conflict in a Challenging Orchid Clade (Calypsoinae): Monophyly of Corallorhiza, Paraphyly of Oreorchis, and Resurrection of Kitigorchis
<p>Dataset S1: Concatenated nuclear sequence capture data (Angiosperms353) for Calypsoinae. This nexus file contains a partition block, which can be used to plit the data into individual alignments (in R, Trifusion, SequenceMatrix, etc.).</p> <p>Dataset S2: Concatenated nuclear sequence capture data (Angiosperms353) for Calypsoinae without partition block.</p> <p>Dataset S3: Concatenated mitochondrial sequence data for Calypsoinae.</p> <p>Dataset S4: Concatenated plastid gene sequence data for Calypsoinae.</p> <p> </p>
Data from: Resurrected seeds from herbarium specimens reveal rapid evolution of drought resistance in a selfing annual
Open the record for dataset details and reuse information.
Monitoring demography of resurrected populations of locally extinct and extant species to investigate drivers of species loss
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Data from: A resurrection study reveals limited evolution of thermal performance in response to recent climate change across the geographic range of the scarlet monkeyflower
<p>Evolutionary rescue can prevent populations from declining under climate change, and should be more likely at high-latitude, "leading" edges of species' ranges due to greater temperature anomalies and gene flow from warm-adapted populations. Using a resurrection study with seeds collected before and after a seven-year period of record warming, we tested for thermal adaptation in the scarlet monkeyflower <i>Mimulus</i> <i>cardinalis</i>. We grew ancestors and descendants from northern-edge, central, and southern-edge populations across eight temperatures. Despite recent climate anomalies, populations showed limited evolution of thermal performance curves. However, one southern population evolved a narrower thermal performance breadth by 1.31 °C, which matches the direction and magnitude of the average decrease in seasonality experienced. Consistent with the climate variability hypothesis, thermal performance breadth increased with temperature seasonality across the species' geographic range. Inconsistent with performance trade-offs between low and high temperatures across populations, we did not detect a positive relationship between thermal optimum and mean temperature. These findings fail to support the hypothesis that evolutionary response to climate change is greatest at the leading edge, and suggest that the evolution of thermal performance is unlikely to rescue most populations from the detrimental effects of rapidly changing climate.</p>
Resurrection of a global, metagenomically defined gokushovirus
<p>Gokushoviruses are single-stranded, circular DNA bacteriophages found in metagenomic datasets from diverse ecosystems wordwide, including human gut microbiomes. Despite their ubiquity and abundance, little is known about their biology or host range: isolates are exceedingly rare, known only from three obligate intracellular bacterial genera. By synthesizing circularized phage genomes from prophages embedded in diverse enteric bacteria, we produced gokushoviruses in an experimentally tractable model system, allowing us to investigate their features and biology. We demonstrate <a>that virions can reliably</a> infect and lysogenize hosts by hijacking a conserved chromosome-dimer resolution system. Sequence motifs required for lysogeny are detectable in other metagenomically defined gokushoviruses; however, we show that even partial motifs enable phages to persist cytoplasmically without leading to collapse of their host culture. This ability to employ multiple, disparate survival strategies is likely key to the long-term persistence and global distribution of <em>Gokushovirinae</em>.</p>
St Mary-at-Hill Resurrection Panel
A Resurrection Panel which probably once stood at the entrance to the churchyard of St Mary-at-Hill Church, Lovat Lane, London. Now located in the interior western vestibule area of the same church. The panel depicts the Last Judgement. Christ is trampling Satan under foot whilst the dead emerge from their coffins to be judged. Date: 1670s https://www.stmary-at-hill.org/ 262 photos taken in September 2021 with a Sony a7R III and processed in Reality Capture. Source: Objaverse 1.0 / Sketchfab
Fig. 1 in Resurrection Of The Genus Micherdzinskiiobovella Hirschmann, 1989, With The Description Of M. Petofii Sp. N. From Singapore (Acari: Mesostigmata: Urodinychidae)
Fig. 1. Micherdzinskiiobovella petofii sp. n., holotype, female, dorsal view
Fig. 2 in Resurrection Of The Genus Micherdzinskiiobovella Hirschmann, 1989, With The Description Of M. Petofii Sp. N. From Singapore (Acari: Mesostigmata: Urodinychidae)
Fig. 2. Micherdzinskiiobovella petofii sp. n., holotype, female, ventral view
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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.