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Fig. 12 in Brachiopods and their response to the Early-Middle Frasnian biogeochemical perturbations on the South Polish carbonate shelf

Fig. 12. Scatter diagrams of shell width to shell length (A), shell thickness to shell length (B), sulcus width to shell width (C), and number of costae on fold to shell width (D) ratios in Flabellulirostrum rackii sp. nov. from Wietrznia.

Fig. 11 in Brachiopods and their response to the Early-Middle Frasnian biogeochemical perturbations on the South Polish carbonate shelf

Fig. 11. Serial sections of two shells of Flabellulirostrum rackii sp. nov., ZPAL Bp 60/30 (A) and ZPAL Bp 60/31 (B), middle Wietrznia Beds of Wietrznia Ie. Numbers refer to distance in mm from ventral umbo.

Fig. 13 in Brachiopods and their response to the Early-Middle Frasnian biogeochemical perturbations on the South Polish carbonate shelf

Fig. 13. Serial sections of two shells of Coeloterorhynchus dillanus (Schmidt, 1941), ZPAL Bp 60/32 (A) and ZPAL Bp 60/33 (B), middle Wietrznia Beds of Wietrznia Ie. Numbers refer to distance in mm from ventral umbo.

Fig. 15 in Brachiopods and their response to the Early-Middle Frasnian biogeochemical perturbations on the South Polish carbonate shelf

Fig. 15. Serial sections of the shell of Coeloterorhynchus schucherti (Stainbrook, 1945), ZPAL Bp 60/34, middle Wietrznia Beds of Wietrznia Ie. Numbers refer to distance in mm from ventral umbo.

Fig. 8 in Brachiopods and their response to the Early-Middle Frasnian biogeochemical perturbations on the South Polish carbonate shelf

Fig. 8. Rhynchonellid brachiopods from the Frasnian of Wietrznia and Dębnik. A. Flabellulirostrum guerichi (Baliński, 1979), ZPAL Bp 60/15, complete shell from the Nodular Limestone (Palmatolepis hassi Zone) of Dębnik in dorsal (A1), ventral (A2), lateral (A3), posterior (A4), and anterior (A5) views. B–D. Flabellulirostrum kielcensis sp. nov., ZPAL Bp 60/1 (B), ZPAL Bp 60/2 (C), and GIUS 4−273 Wt/IM−1 (D), three shells (C—holotype) from the middle Wietrznia Beds of Wietrznia Ie (B, C) and Id−W (D), in dorsal (B1, C1, D1), ventral (B2, C2, D2), lateral (B3, C3, D3), posterior (B4, C4, D4), and anterior (B5, C5, D5) views. E–G. Flabellulirostrum rackii sp. nov., ZPAL Bp 60/11 (E), GIUS 4−273 Wt/IM−9 (F), and ZPAL Bp 60/12 (G), three shells (G—holotype) from the middle Wietrznia Beds of Wietrznia Ie (E, G) and Id−W (F) in dorsal (E1, F1, G1) ventral (E2, F2, G2), lateral (E3, F3, G3), posterior (E4, F4, G4), and anterior (E5, F5, G5) views.

Fig. 10 in Brachiopods and their response to the Early-Middle Frasnian biogeochemical perturbations on the South Polish carbonate shelf

Fig. 10. Scatter diagrams of shell width to shell length (A), shell thickness to shell length (B), sulcus width to shell width (C), and number of costae on fold to shell width ratios in Flabellulirostrum kielcensis sp. nov. from Wietrznia Id−W and Ie Wietrznia (solid diamonts) and Flabellulirostrum guerichi (Baliński, 1979) from Dębnik (open diamonts).

Fig. 9 in Brachiopods and their response to the Early-Middle Frasnian biogeochemical perturbations on the South Polish carbonate shelf

Fig. 9. Serial sections of Flabellulirostrum kielcensis sp. nov., ZPAL Bp 60/29, middle Wietrznia Beds of Wietrznia Ie. Numbers refer to distance in mm from ventral umbo.

Fig. 7 in Brachiopods and their response to the Early-Middle Frasnian biogeochemical perturbations on the South Polish carbonate shelf

Fig. 7. Rhynchonellid brachiopods from the Frasnian of Wietrznia and Dębnik. A, B. Hypothyridina sp., ZPAL Bp 60/28 (A) and GIUS 4−273 Wt/IM−4 (B), two complete shells from the middle Wietrznia Beds of Wietrznia Ie and Id−W, respectively, in dorsal (A1, B1), ventral (A2, B2), lateral (A3, B3), posterior (A4, B4), and anterior (A5, B5) views. C. Fitzroyella alata Biernat, 1969, GIUS 4−273 Wt/GR−1, complete shell from the middle Wietrznia Beds of Wietrznia Id−W. D, E. Fitzroyella sp. from the middle Wietrznia Beds of Wietrznia Id−W. D. Incomplete specimen GIUS 4−273 Wt/IM−7 in dorsal (D1) and ventral (D2) views. E. Complete shell GIUS 4−273 Wt/GR−2 in dorsal (E1), ventral (E2), lateral (E3), posterior (E4), and anterior (E5) views. F, G. Plionoptycherhynchus cracoviensis (Gürich, 1903) from the Nodular Limestone (Palmatolepis hassi Zone) of Dębnik. F. ZPAL Bp 60/17, fragment of a large shell in ventral view. G. ZPAL Bp 60/4, complete shell in dorsal (G1), ventral (G2), lateral (G3), posterior (G4), and anterior (G5) views. H. Phlogoiderhynchus polonicus (Roemer, 1866) from the middle Wietrznia Beds of Wietrznia Id−W, shell GIUS 4−273 Wt/IM−8 in dorsal (H1), ventral (H2), lateral (H3), posterior (H4), and anterior (H5) views.

Fig. 6 in Brachiopods and their response to the Early-Middle Frasnian biogeochemical perturbations on the South Polish carbonate shelf

Fig. 6. Orthid, strphomenid, productid, and pentamerid brachiopods from the Frasnian of Wietrznia and Dębnik. A. Schizophoria (Schizophoria) sp., ZPAL Bp 60/1, exterior of dorsal valve from the middle Wietrznia Beds of Wietrznia Ie. B, C. Corbicularia cracoviensis Baliński, 1979, ZPAL Bp 60/18 (B) and ZPAL Bp 60/19 (C), two specimens embedded in rock from the Nodular Limestone (Pa. hassi Zone) of Dębnik. D. Devonoproductus sp., GIUS 4−273 Wt/IM−2, incomplete ventral valve from the middle Wietrznia Beds of Wietrznia Ie. E. Douvillina sp., ZPAL Bp 60/13, two shells embedded in rock from the Nodular Limestone (Pa. hassi Zone) of Dębnik. F. Gypidula sp., ZPAL Bp 60/23, ventral (F1) and lateral (F2) views of the ventral valve from the middle Wietrznia Beds of Wietrznia Ie.

Fig. 5 in Brachiopods and their response to the Early-Middle Frasnian biogeochemical perturbations on the South Polish carbonate shelf

Fig. 5. Discinoid Roemerella? sp. from middle Szydłówek Beds, Kostomłoty II. A. ZPAL Bp 60/27−10, nine specimens adhered to large shell of Phlogoiderhynchus polonicus (Roemer, 1866). B. ZPAL Bp 60/27−9, strongly flattened specimen adhered in the sulcus of a shell of Phlogoiderhynchus polonicus. C. ZPAL Bp 60/27−6, enlargement of flattened and crushed specimen showing details of surface ornamentation.

Fig. 4 in Brachiopods and their response to the Early-Middle Frasnian biogeochemical perturbations on the South Polish carbonate shelf

Fig. 4. Succession of brachiopod assemblages in studied sections during the Early–Middle Frasnian (Palmatolepis transitans–Pa. hassi conodont zones) against carbon isotope record; the δ13C curve generalised from detailed records of Pisarzowska et al. (2006). Abbreviation: Pa., Palmatolepis.

Fig. 1 in Brachiopods and their response to the Early-Middle Frasnian biogeochemical perturbations on the South Polish carbonate shelf

Fig. 1. Location of collecting sites. A. General map of Poland. B. Geological sketch−map of the western part of the Holy Cross Mountains (after Racki et al. 2004; modified). C. Sketch map of Wietrznia quarries and location of the studied sections (after Makowski in Racki et al. 1993, simplified). D. Geological sketch−map of the Dębnik vicinity (after Szulczewski and Dvořák 1995; modified).

MITgcm simulations of sea level response to freshwater injected at the surface and at depth in southern high latitudes: Model output and analysis code

Model output (netcdf) and python code (included in both py and ipynb formats) to create the figures in Eisenman et al. (2024). <div> See https://eisenman-group.github.io for further details. </div>

opencc-by-4.0Jun 2024View details →

Simulation data for Response of the Thermosphere-Ionosphere System to an X-Class Solar Flare: March 30, 2022 Case Study

GITM simulation results for the research article titled "Response of the Thermosphere-Ionosphere System to an X-Class Solar Flare: March 30, 2022 Case Study" submitted to JGR: Space Weather

Plant responses to urban gradients: extinction, plasticity, adaptation

Individual functional traits (LMA – leaf mass per area, plant height and flower length), population performance traits (seed mass and germination rate), as well as species frequency in the plant community, of four herbaceous plant species present in the metropolitan area of Strasbourg: Dactylis glomerata, Medicago lupulina, Plantago lanceolata, Trifolium pratense. Traits were measured in situ at 60 mesophilic herbaceous sites, and ex situ in a common garden experiment in the Botanical Garden of the University of Strasbourg. Environmental data include mowing frequency, soil characteristics (composition and structure), air temperature, air humidity, and surrounding landscape variables: mean building height, population density, NDVI, road density, and distance to the city center.

Supplementary Data: Data Imbalance in Drug Response Prediction: Multi-Objective Optimization Approach in Deep Learning Setting

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Dataset: Biological Responses of Oyster Crassostrea gasar Exposed to Different Concentrations of Biofloc

Dataset related to the following article and poster presentation <ul> <li>COSTA, Léa Carolina de Oliveira et al. Biological Responses of Oyster Crassostrea gasar Exposed to Different Concentrations of Biofloc. Fishes, v. 8, n. 12, p. 586, 2023.</li> <li>Je Nam Jun Junior, Lea Costa, Silvia Botelho, Shaw Bamber, Marcelo Pias, Paulo Drews, Nelson Duarte Filho, Luis Poersch, Wilson Wasielesky, Bård Henriksen, Gilles Orazi, & Bruna Guterres. (2022). Biosensor technology for oysters behaviour assessment in biofloc environment. Aquaculture Europe 2022, Rimini (Italy). Zenodo. https://doi.org/10.5281/zenodo.7362702</li> </ul>

openSep 2024View details →

Interferon-induced activation of dendritic cells and monocytes by yellow fever vaccination correlates with early antibody responses

Bulk RNA-seq analysis of sorted subpopulations isolated from PBMC of yellow fever vaccinees from before and 3, 7, 14 and 28 days after vaccination and single cell RNA-seq analysis of sorted DC and monocytes fractions isolated from PBMC of of yellow fever vaccinees from before and 3 and 7 days after vaccination.

Resources for "BMF CP 97: The roles of health information-seeking ability and e-health literacy in illness response capability and health checkup frequency"

The current study is conducted to examine the following research questions: <ul> <li>How are health information-seeking ability and e-health literacy associated with illness response capability?</li> <li>How are health information-seeking ability and e-health literacy associated with the frequency of health checkups?</li> </ul>