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2,885 results for “Transfers”
Supported data for manuscript NCOMMS-23-54335B: Microdroplets initiate organic-inorganic interactions and mass transfer in thermal hydrous geosystems
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Demonstration of the tunnel transfer method for non-aversive handling used to perform daily dam-pup separation sessions as part of the MSEW protocol on PDs 2-13
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FIGURE. 1 in Aphelandra verticillata transferred to Holographis (Acanthaceae: Acantheae)
FIGURE. 1. Holographis verticillata. Vegetative node showing quaternate leaves (top left). Habit with inflorescence (top right). Inflorescence (center left). Head-on view of floral limb (center). Upper lip of corolla with stamens and style/stigma (center right). Flower and buds on inflorescence with bracts and bracteoles (bottom). Photos courtesy of Dale Denham.
Advanced Iterative Model for Lumpy Skin Disease Prediction Using Fine-grained Feature Fusion and Adaptive Transfer Learning
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ICF_2024: Multielectron transfer and field-induced slow magnetic relaxation in opto-electroactive spin crossover cobalt(II) complexes: structure-function correlations
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Benchmarking DFT-based excited-state methods for intermolecular charge-transfer excitations
<p>Inter-molecular charge-transfer (ICT) excitation energies and density-based descriptors (DCT) computed over a variety of small molecular dimer complexes, computed with DFT-based excited-state electronic structure methods (TD-DFT and OO-DFT with multiple exchange-correlation functionals and basis sets), as well as original reference data computed with equation-of-motion Coupled-Clouster theory (RDA dataset) and from other publications (large dataset).</p> <p>The data used to produce Figures 3, 4, and 5, as well as Tables 1, 2, and 3 in our publication available at</p> <p>https://arxiv.org/abs/2405.01382</p>
Counterintuitive extracellular electron transfer of Shewanella spp. under aerobic conditions
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Nextlasers WP4 - FPGA control for comb-assisted frequency transfer
<p>This dataset contains the VHDL and Matlab code developed in Nextlasers WP4 - frequency transfer using a comb</p> <p> </p> <p>This work was partly supported by the European Metrology Program for Innovation and Research (EMPIR), Project 20FUN08 NextLasers, which received funding from the EMPIR programme cofinanced by the Participating States and from the European Union's Horizon 2020 research and innovation program. </p> <p> </p>
WRF model output used in an ideal model experiment demonstrating the applicability of a channel-synthesizing method for reducing uncertainties in satellite radiance transfer modeling
<p>This repository stores the WRF model output used in the paper "A novel channel-synthesizing method for reducing uncertainties in satellite radiance transfer modeling" submitted to Geophysical Research Letters.</p>
Supplementary material 2 from: Bellati A, Scherz MD, Megson S, Hyde Roberts S, Andreone F, Rosa GM, Noël J, Randrianirina JE, Fasola M, Glaw F, Crottini A (2018) Resurrection and re-description of Plethodontohyla laevis (Boettger, 1913) and transfer of Rhombophryne alluaudi (Mocquard, 1901) to the genus Plethodontohyla (Amphibia, Microhylidae, Cophylinae). Zoosystematics and Evolution 94(1): 109-135. https://doi.org/10.3897/zse.94.14698
PDF-embedded 3D model of the skeleton of Plethodontohyla laevis holotype (SMF 4286) :
Supplementary material 1 from: Bellati A, Scherz MD, Megson S, Hyde Roberts S, Andreone F, Rosa GM, Noël J, Randrianirina JE, Fasola M, Glaw F, Crottini A (2018) Resurrection and re-description of Plethodontohyla laevis (Boettger, 1913) and transfer of Rhombophryne alluaudi (Mocquard, 1901) to the genus Plethodontohyla (Amphibia, Microhylidae, Cophylinae). Zoosystematics and Evolution 94(1): 109-135. https://doi.org/10.3897/zse.94.14698
PDF-embedded 3D model of the skeleton of Plethodontohyla alluaudi holotype (MNHN 1901.235) :
Figure 9 from: Bellati A, Scherz MD, Megson S, Hyde Roberts S, Andreone F, Rosa GM, Noël J, Randrianirina JE, Fasola M, Glaw F, Crottini A (2018) Resurrection and re-description of Plethodontohyla laevis (Boettger, 1913) and transfer of Rhombophryne alluaudi (Mocquard, 1901) to the genus Plethodontohyla (Amphibia, Microhylidae, Cophylinae). Zoosystematics and Evolution 94(1): 109-135. https://doi.org/10.3897/zse.94.14698
Figure 9 The skeleton of Plethodontohyla alluaudi (MNHN 1901.235) rendered via micro-CT scanning. (a–b) Full skeleton in (a) dorsal and (b) ventral view. (c–e) Skull in (c) dorsal, (d) ventral and (e) lateral view. Abbreviations are as in Fig. 7. For a 3D rotational model, see Suppl. material 1.
Figure 6 from: Bellati A, Scherz MD, Megson S, Hyde Roberts S, Andreone F, Rosa GM, Noël J, Randrianirina JE, Fasola M, Glaw F, Crottini A (2018) Resurrection and re-description of Plethodontohyla laevis (Boettger, 1913) and transfer of Rhombophryne alluaudi (Mocquard, 1901) to the genus Plethodontohyla (Amphibia, Microhylidae, Cophylinae). Zoosystematics and Evolution 94(1): 109-135. https://doi.org/10.3897/zse.94.14698
Figure 6 Skull and pectoral girdle morphology of Plethodontohyla alluaudi and P. laevis. Asterisks indicate the holotypes of each species. Arrows on the pectoral girdle of P. alluaudi MNHN 1901.235 indicate the clavicles. Scale bars indicate 1 mm.
Figure 4 from: Bellati A, Scherz MD, Megson S, Hyde Roberts S, Andreone F, Rosa GM, Noël J, Randrianirina JE, Fasola M, Glaw F, Crottini A (2018) Resurrection and re-description of Plethodontohyla laevis (Boettger, 1913) and transfer of Rhombophryne alluaudi (Mocquard, 1901) to the genus Plethodontohyla (Amphibia, Microhylidae, Cophylinae). Zoosystematics and Evolution 94(1): 109-135. https://doi.org/10.3897/zse.94.14698
Figure 4 Individuals of (a) Plethodontohyla alluaudi in dorsolateral and (inset) ventral view (ZSM 89/2004 , until now referred to as P. bipunctata; from Andohahela); (b) P. sp. Ca01 in dorsolateral view (ZCMV 555; from Ambatolahy); (c) P. brevipes in dorsolateral view (ZSM 649/2003; from Ranomafana); and (d) Rhombophryne sp. (formerly identified as R. alluaudi) in lateral view (ZFMK 52765 from Andasibe) (Photos by Frank Glaw and Miguel Vences).
Figure 3 from: Bellati A, Scherz MD, Megson S, Hyde Roberts S, Andreone F, Rosa GM, Noël J, Randrianirina JE, Fasola M, Glaw F, Crottini A (2018) Resurrection and re-description of Plethodontohyla laevis (Boettger, 1913) and transfer of Rhombophryne alluaudi (Mocquard, 1901) to the genus Plethodontohyla (Amphibia, Microhylidae, Cophylinae). Zoosystematics and Evolution 94(1): 109-135. https://doi.org/10.3897/zse.94.14698
Figure 3 Individuals of Plethodontohyla laevis in life, illustrating the diversity of colour patterns from different sites of the species known distribution range: (a) MRSN A6188 from Betampona in dorsolateral and (inset) ventral view; (b) MRSN A6181 from Betampona in dorsolateral view; (c) FAZC 13898 from Betampona in dorsolateral view (Photos by Gonçalo M. Rosa); (d) MRSN A6787 from Anivorano Est in dorsolateral and (inset) ventral view (Photo by Jasmin E. Randrianirina); (e) ZSM 189/2016 from Analalava-Foulpointe in dorsolateral view (Photo by Frank Glaw); (f) individual (not collected) from Ambodiriana in dorsolateral view (Photo by Lauric Reynes).
Figure 2 from: Bellati A, Scherz MD, Megson S, Hyde Roberts S, Andreone F, Rosa GM, Noël J, Randrianirina JE, Fasola M, Glaw F, Crottini A (2018) Resurrection and re-description of Plethodontohyla laevis (Boettger, 1913) and transfer of Rhombophryne alluaudi (Mocquard, 1901) to the genus Plethodontohyla (Amphibia, Microhylidae, Cophylinae). Zoosystematics and Evolution 94(1): 109-135. https://doi.org/10.3897/zse.94.14698
Figure 2 Photographs of the holotypes of (a–b) Phrynocara laeve (SMF 4286), (c–d) Dyscophus alluaudi (MNHN 1901.235) and (e–f) Plethodontohyla laevis tsianovohensis (MNHN 1936.47) in dorsal (a, c, e) and ventral (b, d, f) view.
Figure 1 from: Bellati A, Scherz MD, Megson S, Hyde Roberts S, Andreone F, Rosa GM, Noël J, Randrianirina JE, Fasola M, Glaw F, Crottini A (2018) Resurrection and re-description of Plethodontohyla laevis (Boettger, 1913) and transfer of Rhombophryne alluaudi (Mocquard, 1901) to the genus Plethodontohyla (Amphibia, Microhylidae, Cophylinae). Zoosystematics and Evolution 94(1): 109-135. https://doi.org/10.3897/zse.94.14698
Figure 1 Locality records of Plethodontohyla laevis, P. alluaudi, and P. sp. Ca01, including the uncertain records of two members of this complex (P. cf. laevis and P. sp.) from Blommers-Schlösser (1975).
Figure 8 from: Bellati A, Scherz MD, Megson S, Hyde Roberts S, Andreone F, Rosa GM, Noël J, Randrianirina JE, Fasola M, Glaw F, Crottini A (2018) Resurrection and re-description of Plethodontohyla laevis (Boettger, 1913) and transfer of Rhombophryne alluaudi (Mocquard, 1901) to the genus Plethodontohyla (Amphibia, Microhylidae, Cophylinae). Zoosystematics and Evolution 94(1): 109-135. https://doi.org/10.3897/zse.94.14698
Figure 8 Audiospectrogram and corresponding oscillogram of the advertisement call of Plethodontohyla laevis recorded at Betampona Strict Nature Reserve on 18 November 2007 (22:30 h, 21 °C). Calling male MRSN A6340 (top).
Figure 5 from: Bellati A, Scherz MD, Megson S, Hyde Roberts S, Andreone F, Rosa GM, Noël J, Randrianirina JE, Fasola M, Glaw F, Crottini A (2018) Resurrection and re-description of Plethodontohyla laevis (Boettger, 1913) and transfer of Rhombophryne alluaudi (Mocquard, 1901) to the genus Plethodontohyla (Amphibia, Microhylidae, Cophylinae). Zoosystematics and Evolution 94(1): 109-135. https://doi.org/10.3897/zse.94.14698
Figure 5 a) Bayesian inference tree based on 529 bp of the mitochondrial 16S. Asterisks denote Bayesian posterior probabilities values: one asterisk enclosed in parentheses, ≥ 90%; one asterisk, ≥ 98%; two asterisks, ≥ 99–100%. b) Haplotype network reconstruction for the phased alleles of the nuclear POMC gene fragment in P. laevis from Betampona, Marovato and Anivorano Est, P. alluaudi from Tsitongambarika and Andohahela, P. sp. Ca01 from Ambatolahy and Rhombophryne sp. from Torotorofotsy.
Figure 7 from: Bellati A, Scherz MD, Megson S, Hyde Roberts S, Andreone F, Rosa GM, Noël J, Randrianirina JE, Fasola M, Glaw F, Crottini A (2018) Resurrection and re-description of Plethodontohyla laevis (Boettger, 1913) and transfer of Rhombophryne alluaudi (Mocquard, 1901) to the genus Plethodontohyla (Amphibia, Microhylidae, Cophylinae). Zoosystematics and Evolution 94(1): 109-135. https://doi.org/10.3897/zse.94.14698
Figure 7 The skeleton of Plethodontohyla laevis (SMF 4286) rendered via micro-CT scanning. (a–b) Full skeleton in (a) dorsal and (b) ventral view. (c–e) Skull in (c) dorsal, (d) ventral and (e) lateral view. Abbreviations: angspl, angulosplenial; col, columella; exoc, exoccipital; exoc.oc, occipital condyle of exoccipital; fpar, frontoparietal; fpardop, frontoparietal dorsal process; max, maxilla; max.pf, pars facialis of maxilla; max.parspal, pars palatina of maxilla; mmk, mentomeckelian; npl, neopalatine; pmax, premaxilla; povom, postchoanal vomer; proot, prootic; prsph, parasphenoid; prsph.al, alary process of parasphenoid; prvom, prechoanal vomer; pter, pterygoid; pter.mr, medial ramus of pterygoid; pter.vr, ventral ramus of pterygoid; qj, quadratojugal; qj.pvp, posteroventral process of quadratojugal; smax, septomaxilla; sq.or, otic ramus of squamosal; sq.vr, ventral ramus of squamosal; sq.zr, zygotic ramus of squamosal; spheth, sphenethmoid. For a 3D rotational model, see Suppl. material 2.
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Allen Brain Atlas
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OpenNeuro
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