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Assets for 'Phase correlation on the edge for estimating cloud motion' submitted to Atmospheric Measurement Techniques
<p>1. CMV-26-07-2016_ARM-SGP.gif Sample cloud motion vectors from TSI camera images over the United States Atmospheric Radiation Measurement user facility’s Southern Great Plains site.</p> <p>2. raindrop_02-01-2017_ARM-SGP.gif Rotation of cloud motion vectors from raindrop contaminated TSI camera.</p>
SUBATOMIC analysis of Homo sapiens integrated multi-edge networks
<p>We applied SUBATOMIC (https://github.com/CBIGR/SUBATOMIC/) to analyze a composite <em>H. sapiens</em> network containing transcription factor-target gene, miRNA-target gene, protein-protein, homologous and co-functional interactions from three different databases. We derived and annotated 5586 modules with diverse topological, regulatory and functional properties.</p>
Edge effects and vertical stratification of aerial insectivorous bats across the interface of primary-secondary Amazonian rainforest
<p><span>Edge effects - abiotic and biotic changes associated with habitat boundaries - are key drivers of community change in fragmented landscapes. Their influence is heavily modulated by matrix composition. With over half of the world's tropical forests predicted to become forest edge by the end of the </span><span>century, it is paramount that conservationists gain a better understanding of how tropical biota is impacted by edge gradients. Bats comprise a large fraction of tropical mammalian fauna and are demonstrably sensitive to habitat modification. Yet, </span><span>knowledge about how bat assemblages are affected by edge effects remains scarce</span><span>. Capitalizing on a whole-ecosystem manipulation in the Central Amazon, the aims of this study were to i) assess the consequences of edge effects for twelve aerial insectivorous bat species across the interface of primary and secondary forest and ii) investigate if the activity levels of these species differed between the understory and canopy and if they were modulated by distance from the edge</span><span>. Acoustic surveys were conducted along four 2-km transects each traversing equal parts of primary and ca. 30-year-old secondary forest. Five models were used to assess the changes in the relative activity of forest specialists (three species), flexible forest foragers (three species), and edge foragers (six species). Modelling results revealed no evidence of edge effects, except for forest specialists in the understory. No significant differences in activity were found between the secondary or primary forest but most species exhibited pronounced vertical stratification. Our study highlights that forest specialist bats are more edge-sensitive than both flexible forest and edge foraging bats and suggests that the influence of edge effects on aerial insectivorous bats may exceed 2 km. The absence of pronounced edge effects and the comparable activity levels between primary and old secondary forests indicates that old secondary forest can help ameliorate the consequences of fragmentation on tropical aerial insectivorous bats. </span></p>
Joint analysis of microsatellites and flanking sequences enlightens complex demographic history of interspecific gene flow and vicariance in rear-edge oak populations
<p><span>Inference of recent population divergence requires fast evolving markers and necessitates to differentiate shared genetic variation caused by ancestral polymorphism and gene flow. Theoretical research shows that the use of compound marker systems integrating linked polymorphisms with different mutational dynamics, such as a microsatellite and its flanking sequences, can improve estimation of population structure and inference of demographic history, especially in the case of complex population dynamics. However, empirical application in natural populations has so far been limited by lack of suitable methods for data collection. A solution comes from the development of sequence-based microsatellite genotyping which we used to study molecular variation at 36 sequenced nuclear microsatellites in seven <em>Quercus canariensis</em> and four <em>Q. faginea</em> rear-edge populations across Algeria. We aim to decipher their taxonomic relationship, past evolutionary history and recent demographic trajectory. First, we compare the estimation of population genetics parameters and simulation-based inference of demographic history from microsatellite sequence alone, flanking sequence alone or the combination of linked microsatellite and flanking sequence variation. Second, we apply random forest approximate Bayesian computation to identify which of these sequence types is most informative. Whereas analysing microsatellite variation alone indicates recent interspecific gene flow, additional information gained by integrating nucleotide variation in flanking sequences, by reducing homoplasy, suggests ancient interspecific gene flow followed by drift in isolation instead. The weight of each polymorphism in the inference also demonstrates the value of linked variations with contrasted mutation dynamic to improve estimation of both demographic and mutational parameters.</span></p>
Dataset for "Quantification of Muscle Fiber Malformations Using Edge Detection to Investigate Chronic Wound Healing"
<p>Primary images, spreadsheets and files for "Quantification of Muscle Fiber Malformations Using Edge Detection to Investigate Chronic Wound Healing"</p>
Text-fig. 12. Paramblypterus cf. rohani. Arrows indicate directio cranialis. a, b: photograph and drawing of four ridge scales in front of the dorsal fin base, locality Otovice "Chmelnice", P 80178, scale bars 5 mm; c: scale rows from the area between the pectoral and pelvic fins, outer surfaces of the scales bear fine ridges terminating as denticles on the posterior edge of the scales, locality Otovice "Chmelnice", NM-M 4916, scale bar 5 mm; d: isolated scale, from anterior area of the lateral side of the body, with denticulated posterior edge, locality Otovice "Chmelnice", P 30945, scale bar 2 mm; e: isolated scale from the pelvic area of the body, locality Otovice "Chmelnice", P 30945, scale bar 2 mm; f, g: drawing and photograph of the postcleithrum and the scales behind the pectoral girdle (the scales bear conspicuous ridges on their outer surface; well preserved large postcleithrum is without ridges.), locality Otovice "Chmelnice", NM-M 4915, scale bars 5 mm. Abbreviations: Cl – cleithrum, Pcl – postcleithrum, Scl – supracleithrum. in Actinopterygians Of The Broumov Formation (Permian) In The Czech Part Of The Intra-Sudetic Basin (The Czech Republic)
Text-fig. 12. Paramblypterus cf. rohani. Arrows indicate directio cranialis. a, b: photograph and drawing of four ridge scales in front of the dorsal fin base, locality Otovice "Chmelnice", P 80178, scale bars 5 mm; c: scale rows from the area between the pectoral and pelvic fins, outer surfaces of the scales bear fine ridges terminating as denticles on the posterior edge of the scales, locality Otovice "Chmelnice", NM-M 4916, scale bar 5 mm; d: isolated scale, from anterior area of the lateral side of the body, with denticulated posterior edge, locality Otovice "Chmelnice", P 30945, scale bar 2 mm; e: isolated scale from the pelvic area of the body, locality Otovice "Chmelnice", P 30945, scale bar 2 mm; f, g: drawing and photograph of the postcleithrum and the scales behind the pectoral girdle (the scales bear conspicuous ridges on their outer surface; well preserved large postcleithrum is without ridges.), locality Otovice "Chmelnice", NM-M 4915, scale bars 5 mm. Abbreviations: Cl – cleithrum, Pcl – postcleithrum, Scl – supracleithrum.
Text-fig. 5. Paramblypterus vratislaviensis (AGASSIZ, 1833). Scale bars 5 mm. a: drawing of the skull roof in dorsal view, locality Olivětín, NM-M 2213; b, c: photograph and drawing of the left maxila in lateral view, locality Ruprechtice, NM-M 64696; d: right parietal in dorsal view, locality Ruprechtice "Pod Světlinou", P 64741; e: left maxilla in lateral view, locality Ruprechtice "Pod Světlinou", P 64738; f, g: photograph and drawing of the left mandible in medial view, locality Ruprechtice "Pod Světlinou", P 64738. Abbreviations: ap – anterior pit line, Dpt – dermopterotic, Dsph – dermosphenotic, eo – edge overlapped by surrounding bones, Fr – frontal, mp – medial pit line, Na – nasal, Pa – parietal, pp – posterior pit line, Ptr – postrostral, soc – supraorbital canal, socp – pores of the supraorbital canal. in Actinopterygians Of The Broumov Formation (Permian) In The Czech Part Of The Intra-Sudetic Basin (The Czech Republic)
Text-fig. 5. Paramblypterus vratislaviensis (AGASSIZ, 1833). Scale bars 5 mm. a: drawing of the skull roof in dorsal view, locality Olivětín, NM-M 2213; b, c: photograph and drawing of the left maxila in lateral view, locality Ruprechtice, NM-M 64696; d: right parietal in dorsal view, locality Ruprechtice "Pod Světlinou", P 64741; e: left maxilla in lateral view, locality Ruprechtice "Pod Světlinou", P 64738; f, g: photograph and drawing of the left mandible in medial view, locality Ruprechtice "Pod Světlinou", P 64738. Abbreviations: ap – anterior pit line, Dpt – dermopterotic, Dsph – dermosphenotic, eo – edge overlapped by surrounding bones, Fr – frontal, mp – medial pit line, Na – nasal, Pa – parietal, pp – posterior pit line, Ptr – postrostral, soc – supraorbital canal, socp – pores of the supraorbital canal.
Text-fig. 17. Aeduellidae. Scale bars 5 mm. a: the scales of oblong shape on the lateral side of the body, locality Otovice "Stěnava", DP 4307, whitened; b: drawing of the scales with fine denticles on their posterior edge, locality Otovice "Stěnava", DP 4307; c, d: drawing and photograph (whitened) of the scales of lateral side of the body, two times large scales occur in the rows 14, 16, 17, 19 (they are marked with arrows), locality Otovice "Černý potok", NM-M 4912; e: lepidotrichia of the anal fin with sigmoidal sutures between the segments (marked by arrows), locality Otovice, NM-M 4931, whitened; f: anterior edge of the dorsal fin and lepidotrichia with sigmoidal sutures between the segments, locality Otovice "Stěnava", DP 4307, whitened; g: anterior edge of the ventral lobe of the caudal fin, locality Otovice, NM-M 4931, whitened; h: the caudal peduncle with begin of bifurcation of the dorsal and ventral lobes of the caudal fin, locality Otovice, NM-M 4931. in Actinopterygians Of The Broumov Formation (Permian) In The Czech Part Of The Intra-Sudetic Basin (The Czech Republic)
Text-fig. 17. Aeduellidae. Scale bars 5 mm. a: the scales of oblong shape on the lateral side of the body, locality Otovice "Stěnava", DP 4307, whitened; b: drawing of the scales with fine denticles on their posterior edge, locality Otovice "Stěnava", DP 4307; c, d: drawing and photograph (whitened) of the scales of lateral side of the body, two times large scales occur in the rows 14, 16, 17, 19 (they are marked with arrows), locality Otovice "Černý potok", NM-M 4912; e: lepidotrichia of the anal fin with sigmoidal sutures between the segments (marked by arrows), locality Otovice, NM-M 4931, whitened; f: anterior edge of the dorsal fin and lepidotrichia with sigmoidal sutures between the segments, locality Otovice "Stěnava", DP 4307, whitened; g: anterior edge of the ventral lobe of the caudal fin, locality Otovice, NM-M 4931, whitened; h: the caudal peduncle with begin of bifurcation of the dorsal and ventral lobes of the caudal fin, locality Otovice, NM-M 4931.
Text-fig. 10. Progyrolepis heyleri POPLIN, 1999. a: dorsal lobe of the caudal fin with the fulcral scales along the dorsal edge of the lobe, GMC 55, whitened, scale bar 5 mm; b: basal fulcral scales from the dorsal edge of the caudal peduncle, G 123, whitened, scale bar 5 mm; c: fragment of the body of juvenile specimen with dorsal and anal fins, GMC 11, whitened, scale bar 5 mm; d: isolated scales from lateral side of the body, G 123, whitened, scale bar 5 mm; e: ridges on the scale surface, the frame delineates the area illustrated in (f) at higher magnification, G 123, scale bar 500 µm; f: details of the surface with microtubercles, scale bar 50 µm; g: isolated lepidotrichium of an adult specimen with very short and wide segments and with unsegmented basal part, GMC 101, whitened, scale bar 5 mm; h: large conical teeth from the internal row of the maxilla, G 123, scale bar 2 mm; i: microsculpture formed by elliptical proximo-distally elongated protuberances on the large conical tooth, G 123, scale bar 100 µm; j: large conical tooth from the internal row of the maxilla, G 123, scale bar 2 mm; k: microsculpture formed by elliptical proximo-distally elongated protuberances on the large conical tooth, G 123, scale bar 100 µm. in New Actinopterygians From The Permian Of The Brive Basin, And The Ichthyofaunas Of The French Massif Central
Text-fig. 10. Progyrolepis heyleri POPLIN, 1999. a: dorsal lobe of the caudal fin with the fulcral scales along the dorsal edge of the lobe, GMC 55, whitened, scale bar 5 mm; b: basal fulcral scales from the dorsal edge of the caudal peduncle, G 123, whitened, scale bar 5 mm; c: fragment of the body of juvenile specimen with dorsal and anal fins, GMC 11, whitened, scale bar 5 mm; d: isolated scales from lateral side of the body, G 123, whitened, scale bar 5 mm; e: ridges on the scale surface, the frame delineates the area illustrated in (f) at higher magnification, G 123, scale bar 500 µm; f: details of the surface with microtubercles, scale bar 50 µm; g: isolated lepidotrichium of an adult specimen with very short and wide segments and with unsegmented basal part, GMC 101, whitened, scale bar 5 mm; h: large conical teeth from the internal row of the maxilla, G 123, scale bar 2 mm; i: microsculpture formed by elliptical proximo-distally elongated protuberances on the large conical tooth, G 123, scale bar 100 µm; j: large conical tooth from the internal row of the maxilla, G 123, scale bar 2 mm; k: microsculpture formed by elliptical proximo-distally elongated protuberances on the large conical tooth, G 123, scale bar 100 µm.
Text-fig. 2. Briveichthys chantepieorum gen. et sp. nov. a, b: whitened photograph and drawing of the skull, GMC 15, scale bars 5 mm; c: anterior part of the left and right frontal in dorsal view, a conspicuous concave anterior edge of the bones is demonstrated, GMC 18, whitened, scale bar 5 mm. Abbreviations: Clei – cleithrum, De – dentalosplenial, Dpt – dermopterotic, Dsph – dermosphenotic, Ext? – extrascapular?, Fr – frontal, Gul – lateral gular, Hy – hyomandibula, Mx – maxilla, Na – nasal, Pa – parietal, Pop – preoperculum, ppl – parietal pit lines, Pt – posttemporal, Rbr – branchiostegal rays, Scl – supracleithrum, soc – supraorbital canal, Sop – suboperculum, sr – sclerotic ring. in New Actinopterygians From The Permian Of The Brive Basin, And The Ichthyofaunas Of The French Massif Central
Text-fig. 2. Briveichthys chantepieorum gen. et sp. nov. a, b: whitened photograph and drawing of the skull, GMC 15, scale bars 5 mm; c: anterior part of the left and right frontal in dorsal view, a conspicuous concave anterior edge of the bones is demonstrated, GMC 18, whitened, scale bar 5 mm. Abbreviations: Clei – cleithrum, De – dentalosplenial, Dpt – dermopterotic, Dsph – dermosphenotic, Ext? – extrascapular?, Fr – frontal, Gul – lateral gular, Hy – hyomandibula, Mx – maxilla, Na – nasal, Pa – parietal, Pop – preoperculum, ppl – parietal pit lines, Pt – posttemporal, Rbr – branchiostegal rays, Scl – supracleithrum, soc – supraorbital canal, Sop – suboperculum, sr – sclerotic ring.
Text-fig. 4. Briveichthys chantepieorum gen. et sp. nov. a, b: photograph and drawing of the parasphenoid in dorsal view, GMC 15, whitened, scale bars 5 mm; c: maxillary plate in medial view with horizontal lamina along the ventral edge of the bone, segment of the lower jaw with assembly of large slender teeth of the inner row and coronoids with small teeth, GMC 15, whitened, scale bar 5 mm; d: detail of the sculpture on the maxilla and dentalosplenial, GMC 126, whitened, scale bar 5 mm; e: detail of the teeth of the inner and outer row and coronoids on the lower jaw, the frame delineates the area illustrated in (f) at higher magnification, GMC 15, scale bar 2 mm; f: microsculpture formed by elliptical proximo-distally elongated protuberances on the large conical teeth, GMC 15, scale bar 100 µm; g: small fringing fulcra tightly attached to the anterior edge of a lepidotrichium, individual fulcral scales are indicated by arrows, GMC 18, scale bar 2 mm. Abbreviation: bhf – bucco-hypophysial foramen, Cor – coronoids, cp – corpus parasphenoidis, De – dentalosplenial, hl – horizontal lamina, mc – pores of the mandibular sensory canal, Mx – maxilla, paa – processus ascendens anterior, pap – processus ascendens posterior. in New Actinopterygians From The Permian Of The Brive Basin, And The Ichthyofaunas Of The French Massif Central
Text-fig. 4. Briveichthys chantepieorum gen. et sp. nov. a, b: photograph and drawing of the parasphenoid in dorsal view, GMC 15, whitened, scale bars 5 mm; c: maxillary plate in medial view with horizontal lamina along the ventral edge of the bone, segment of the lower jaw with assembly of large slender teeth of the inner row and coronoids with small teeth, GMC 15, whitened, scale bar 5 mm; d: detail of the sculpture on the maxilla and dentalosplenial, GMC 126, whitened, scale bar 5 mm; e: detail of the teeth of the inner and outer row and coronoids on the lower jaw, the frame delineates the area illustrated in (f) at higher magnification, GMC 15, scale bar 2 mm; f: microsculpture formed by elliptical proximo-distally elongated protuberances on the large conical teeth, GMC 15, scale bar 100 µm; g: small fringing fulcra tightly attached to the anterior edge of a lepidotrichium, individual fulcral scales are indicated by arrows, GMC 18, scale bar 2 mm. Abbreviation: bhf – bucco-hypophysial foramen, Cor – coronoids, cp – corpus parasphenoidis, De – dentalosplenial, hl – horizontal lamina, mc – pores of the mandibular sensory canal, Mx – maxilla, paa – processus ascendens anterior, pap – processus ascendens posterior.
Text-fig. 5. Mastixiopsis nyssoides KIRCHH. a, b, g–n: Organic preservation. a, b: Lignitic, unpermineralized, early Eocene Dorset Pipe clays at Arne, V. 40762. a: Ventral view (original illustration from pl. 18, fig. 1 of Chandler 1962). b: Transverse fracture, somewhat distorted by compression. c–f: Pyrite permineralization. c: Ventral view, V. 22963(1) from Sheppey, originally listed as Mastixia cantiensis. d: Lateral view, V. 22969 from Sheppey (identified as Mastixia grandis by Reid and Chandler 1933: pl. 25, fig. 8). e: Equatorial transverse physical section from (c). f: Equatorial transverse physical section from (d). g: Detail of pericarp from (e), showing endocarp formed of dense fibrous tissue, surrounded by mesocarp of anticlinally oriented larger cells. h: Detail of pericarp from (f). i–n: Type material from Eocene of Riestadt, Germany, MNB. i: Ventral view. j, k: Ventral and apical views of holotype. l: View of the transversely fractured surface from (j) showing horseshoe shaped locule. m: Equatorial transverse physical cut of the specimen in (i); note yellow resin cavity (arrow). n: Scanning electron microscopy of pericarp from (l) with locule lining at lower edge of image. Note dense endocarp tissue composed of small cells (fibres and sclereids), extending about 3/5 of distance to periphery, surrounded by mesocarp of larger, anticlinally oriented cells. Scale bars 1 cm in (a–f), (i–k), 1 mm in (g), 2 mm in (h), 3 mm in (l), m, 250 Μm in (n). Bar in (d) applies also to (c). Bar in (l) also applies to (m). Bar in (i) also applies to (j) and (k). in Mastixioid Fruits (Cornales) From The Early Eocene London Clay Flora: Morphology, Anatomy And Nomenclatural Revision
Text-fig. 5. Mastixiopsis nyssoides KIRCHH. a, b, g–n: Organic preservation. a, b: Lignitic, unpermineralized, early Eocene Dorset Pipe clays at Arne, V. 40762. a: Ventral view (original illustration from pl. 18, fig. 1 of Chandler 1962). b: Transverse fracture, somewhat distorted by compression. c–f: Pyrite permineralization. c: Ventral view, V. 22963(1) from Sheppey, originally listed as Mastixia cantiensis. d: Lateral view, V. 22969 from Sheppey (identified as Mastixia grandis by Reid and Chandler 1933: pl. 25, fig. 8). e: Equatorial transverse physical section from (c). f: Equatorial transverse physical section from (d). g: Detail of pericarp from (e), showing endocarp formed of dense fibrous tissue, surrounded by mesocarp of anticlinally oriented larger cells. h: Detail of pericarp from (f). i–n: Type material from Eocene of Riestadt, Germany, MNB. i: Ventral view. j, k: Ventral and apical views of holotype. l: View of the transversely fractured surface from (j) showing horseshoe shaped locule. m: Equatorial transverse physical cut of the specimen in (i); note yellow resin cavity (arrow). n: Scanning electron microscopy of pericarp from (l) with locule lining at lower edge of image. Note dense endocarp tissue composed of small cells (fibres and sclereids), extending about 3/5 of distance to periphery, surrounded by mesocarp of larger, anticlinally oriented cells. Scale bars 1 cm in (a–f), (i–k), 1 mm in (g), 2 mm in (h), 3 mm in (l), m, 250 Μm in (n). Bar in (d) applies also to (c). Bar in (l) also applies to (m). Bar in (i) also applies to (j) and (k).
Text-fig. 2. Nymphaea sp. from the Miocene Clarkia Lake flora, Locality P-33. a: Photograph of the fossil leaf. b: Sketch of leaf showing the salient features of shape, basal lobes and margin, eccentric insertion point of the abaxial petiole, and primary actinodromous venation. Dashed lines represent torn edge of lamina; dotted line is outline of right basal lobe. Line drawing by P. Martin Sander. Scale bar applies to both photo and drawing. in First Water Lily, A Leaf Of Nymphaea Sp., From The Miocene Clarkia Flora, Northern Idaho, Usa: Occurrence, Taphonomic Observations, Floristic Implications
Text-fig. 2. Nymphaea sp. from the Miocene Clarkia Lake flora, Locality P-33. a: Photograph of the fossil leaf. b: Sketch of leaf showing the salient features of shape, basal lobes and margin, eccentric insertion point of the abaxial petiole, and primary actinodromous venation. Dashed lines represent torn edge of lamina; dotted line is outline of right basal lobe. Line drawing by P. Martin Sander. Scale bar applies to both photo and drawing.
Text-fig. 10. Carpolithes (a–j). a–d: Carpolithes sp. 10. USNM PAL 772375. Scale bar = 5 mm, reflected light, palladium coated. a: Lateral view of one face of structure; note adherent mineral material. Longitudinal groove is to right. b: Lateral view of one edge of the structure. c: Opposite view from (b), note groove in upper half of the specimen, facing viewer. d: Apical view. e–j: Carpolithes sp. 11. USNM PAL 772376. Scale bar = 5 mm, micro-CT scan surface views. e: Structure in face view showing central protuberance. f: Same, lateral view. g: Opposite face from (e). h: Opposite face from (f). i: View from one end. j: View from opposite end from (i). in The Early Middle Eocene Wagon Bed Carpoflora Of Central Wyoming, U.S.A.
Text-fig. 10. Carpolithes (a–j). a–d: Carpolithes sp. 10. USNM PAL 772375. Scale bar = 5 mm, reflected light, palladium coated. a: Lateral view of one face of structure; note adherent mineral material. Longitudinal groove is to right. b: Lateral view of one edge of the structure. c: Opposite view from (b), note groove in upper half of the specimen, facing viewer. d: Apical view. e–j: Carpolithes sp. 11. USNM PAL 772376. Scale bar = 5 mm, micro-CT scan surface views. e: Structure in face view showing central protuberance. f: Same, lateral view. g: Opposite face from (e). h: Opposite face from (f). i: View from one end. j: View from opposite end from (i).
Figure 2. HMM with weights and necessary conditions on top of edges-Neuroevolution Mechanism for Hidden Markov Model
<p>Based on the HMM structure in Figure 2, we can perform the following steps:<br> 1. Make the number of nodes of inputs in the input layer of the NN as the number of states<br> (visible states not the observations). Each input node represents one state.<br> 2. Number of nodes in the output layer in the NN is equal to the number of states and<br> observations (visible and invisible states), where each node corresponds to one state (visible<br> or invisible).<br> 3. We construct a hidden layer in NN with n number of nodes, where n is the same number of<br> nodes in the input layer.<br> 4. We make a connection from every input to every hidden layer node with a very negligible<br> weight.<br> 5. Connect every hidden node in the hidden layer to every node in the output layer.<br> 6. Assign weights from the hidden layer to output layer in a way that as every node in the<br> hidden layer corresponding to input state. The weight on top of the link between the hidden<br> node to the output node is the probability value between the states in the HMM.<br> In our proposed structure, we injected a hidden layer to have a multilayer perceptron which<br> is more efficient than single layer perceptron.<br> To make this process clear, Figure 3 shows the neural networks for the HMM presented in<br> Figure 2.</p>
Evolutionary potential under heat and drought stress at the southern range edge of North American Arabidopsis lyrata
<p>The warm edges of species' distributions are vulnerable to global warming. Evidence is the recent range retraction from there found in many species. It is unclear why populations cannot easily adapt to warmer, drier, or combined hot and dry conditions and locally persist. Here, we assessed the ability to adapt to these stressors in the temperate species <em>Arabidopsis lyrata</em>. We grew plants from replicate seed families of a central population with high genetic diversity under a temperature and precipitation regime typical of the low-latitude margin or under hotter and/or drier conditions within naturally occurring amplitudes. We then calculated genetic variance-covariance (G-) matrices of traits depicting growth and allocation as well as selection vectors to compare the predicted adaptation potential under the different climate-stress regimes. We found that the sum of genetic variances and genetic correlations were not significantly different under stress as compared to benign conditions. However, under drought and heat drought, the predicted ability to adapt was severely constrained due to strong selection and selection pointing in a direction with less multivariate genetic variation. The much-reduced ability to adapt to dry and hot-dry conditions is likely to reduce the persistence of populations at the low-latitude margin of the species' distribution and contribute to the local extinction of the species under further warming.</p>
Рис. 5. Дополнительные структуры, служаЩие укреплению Замочного краЯ и раковины у Laternula elliptica: А – дополнительнаЯ поддерживаюЩаЯ пластинка прикрывает макушечную Щель; Б – утолЩение ранее поврежденного краЯ раковины; В – пример воЗникновениЯ двух поддерживаюЩих пластинок. ОбоЗначениЯ: мщ – макушечнаЯ Щель; хр – хондрофор; ппЛ – поддерживаюЩаЯ пластинка; дпЛ – дополнительные пластинки; уКр – утолЩениЯ Задне-дорсального краЯ и краЯ сифонального ЗиЯниЯ. Fig. 5. Additional structures serving for consolidation of hinge margin and for restoration of shell edge in Laternula elliptica: А – the umbonal crack covered by additional buttress; Б – thickening of damaged edge; В – appearance of two supporting plates. Notes: мщ – umbonal crack; хр – chondrophore; ппЛ – buttress; дпЛ – additional supporting plate; уКр – thickening of posterior-dorsal margin. in Species of warm-water origin Laternula elliptica (King, 1832) (Mollusca: Bivalvia: Laternulidae), a widespread mollusk in recent Antarctica
Рис. 5. Дополнительные структуры, служаЩие укреплению Замочного краЯ и раковины у Laternula elliptica: А – дополнительнаЯ поддерживаюЩаЯ пластинка прикрывает макушечную Щель; Б – утолЩение ранее поврежденного краЯ раковины; В – пример воЗникновениЯ двух поддерживаюЩих пластинок. ОбоЗначениЯ: мщ – макушечнаЯ Щель; хр – хондрофор; ппЛ – поддерживаюЩаЯ пластинка; дпЛ – дополнительные пластинки; уКр – утолЩениЯ Задне-дорсального краЯ и краЯ сифонального ЗиЯниЯ. Fig. 5. Additional structures serving for consolidation of hinge margin and for restoration of shell edge in Laternula elliptica: А – the umbonal crack covered by additional buttress; Б – thickening of damaged edge; В – appearance of two supporting plates. Notes: мщ – umbonal crack; хр – chondrophore; ппЛ – buttress; дпЛ – additional supporting plate; уКр – thickening of posterior-dorsal margin.
Fig. 2 in Surviving at the edge of land: finding of the limnetic snail Sibirenauta sibirica (Gastropoda: Physidae) on the coast of the Laptev Sea (Eastern Siberia)
Fig. 2. Shell and anatomy of Sibirenauta sibirica, Tyulahk-Kuel Lake. A – shell, B – body extracted from the shell, C – copulatory apparatus, D, E – female reproductive system. A–D – organs of the same specimen. ag – albumen gland, bc – bursa copulatrix, с – caecum, o – oviduct, v – vagina. Scale bars: 5 mm (A–B), 2 mm (C–E).
Fig. 1 in Surviving at the edge of land: finding of the limnetic snail Sibirenauta sibirica (Gastropoda: Physidae) on the coast of the Laptev Sea (Eastern Siberia)
Fig. 1. Collecting sites of Sibirenauta sibiraca. A – Tyulahk-Kuel Lake, B – small pool on the coast of Tiksi Bay. Photographs by A. Nekhaeva.
Propagation, dissipation and breakdown in quantum anomalous Hall edge states probed by microwave edge plasmons
<p>Here we upload the raw data from the manuscript entitled “Propagation, dissipation and breakdown in quantum anomalous Hall edge states probed by microwave edge plasmons ”, by T. Röper, H. Thomas, D. Rosenbach, A. Uday, G. Lippertz, A. Denis, P. Morfin, A.A. Taskin, Y. Ando and E. Bocquillon. We provide Jupyter notebooks to load, process, and plot all results. The datasets contain measurements on 4 devices. Each device has its own Jupyter notebook. The necessary Python packages are listed in the file called "requirements.txt". <br><br><br></p>
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.