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opencc-by-4.0Apr 2019View details →

Data: Trans-saccadic integration is dominated by early, independent noise

Data for "Trans-saccadic integration is dominated by early, independent noise"

Fig. 4 in Divergent Morphology among Populations of the New Guinea Crocodile, Crocodylus novaeguineae (Schmidt, 1928): Diagnosis of an Independent Lineage and Description of a New Species

Fig. 4. Ventral cranial shape variation depicted using transformation grids with corresponding example specimen among drainages in Papua New Guinea. Solid points indicate consensus landmarks for all individuals, and lines extending from points indicate the extent (length) and direction of shape change exhibited by that classifier. Populations in northern drainages (i.e., Sepik; FMNH 14048; Crocodylus novaeguineae) exhibit an extended maxilla and reduced postcranial elements relative to southern populations from Lake Murray/Binaturi (C. halli; LSUMZ 44740) and the Aramia River (C. halli; USNM 211290), exhibiting strikingly shorter maxilla and enlarged postcranial elements.

Fig. 3 in Divergent Morphology among Populations of the New Guinea Crocodile, Crocodylus novaeguineae (Schmidt, 1928): Diagnosis of an Independent Lineage and Description of a New Species

Fig. 3. Dorsal cranial shape variation depicted using transformation grids with corresponding example specimen among drainages in Papua New Guinea. Solid points indicate consensus landmarks for all individuals, and lines extending from points indicate the extent (length) and direction of shape change exhibited by that classifier. Populations in northern drainages (i.e., Sepik River; FMNH 14048; Crocodylus novaeguineae) exhibit an extended maxilla and reduced postcranial elements relative to southern populations from Lake Murray/Binaturi (C. halli; LSUMZ 44740), exhibiting strikingly shorter maxilla and enlarged postcranial elements, or Aramia River (C. halli; USNM 211290), exhibiting a morphology closer to consensus.

Fig. 1 in Divergent Morphology among Populations of the New Guinea Crocodile, Crocodylus novaeguineae (Schmidt, 1928): Diagnosis of an Independent Lineage and Description of a New Species

Fig. 1. Homologous landmarks used in geometric morphometric analysis for dorsal (top, n ¼ 15 landmarks) and ventral (bottom, n ¼ 13 landmarks) views. LSUMZ 44740.

Fig. 2 in Divergent Morphology among Populations of the New Guinea Crocodile, Crocodylus novaeguineae (Schmidt, 1928): Diagnosis of an Independent Lineage and Description of a New Species

Fig. 2. Map of localities for specimens examined; Crocodylus novaeguineae from the Sepik (circle) and Hunstein (pentagon) drainages, and Crocodylus halli from Lake Murray (square), Binaturi (triangle), and Aramia (star) rivers.

Fig. 5 in Divergent Morphology among Populations of the New Guinea Crocodile, Crocodylus novaeguineae (Schmidt, 1928): Diagnosis of an Independent Lineage and Description of a New Species

Fig. 5. Canonical variates analysis exhibiting position in morphospace among specimens from SCN (Lake Murray, Binaturi, and Aramia; Crocodylus halli) and NCN (Sepik; Crocodylus novaeguineae) from dorsal (A; CV1 ¼ 75% variance, CV2 ¼ 13.7% variance) and ventral (B; CV1 ¼ 49% variance, CV2 ¼ 27.4% variance) perspectives.

opencc-by-nc-sa-4.0Oct 2019View details →

Twitter network of independent publishers

Nodes and edges data of independent publishers following relationships on Twitter.

opencc-by-4.0Nov 2019View details →

Seismic dataset in "Source-Independent Passive Seismic Reverse-time Structure Imaging with Grouping Imaging Condition: Method and Application to Microseismic Events Induced by Hydraulic Fracturing"

This dataset contains the seismic data and the velocity model used in the manuscript entitled "Source-Independent Passive Seismic Reverse-time Structure Imaging with Grouping Imaging Condition: Method and Application to Microseismic Events Induced by Hydraulic Fracturing" submitted to Journal of Geophysical Research-Solid Earth.

opencc-by-4.0Nov 2019View details →

Data for "Magnetic field independent sub-gap states in hybrid Rashba nanowires"

Data for the publication "Magnetic field independent sub-gap states in hybrid Rashba nanowires"

Fig. 3 in Morphological dissection of behavior: thoracic musculature clarifies independent development of jumping mechanisms between sister groups, planthoppers and leafhoppers (Insecta: Hemiptera: Auchenorrhyncha)

Fig. 3 Flight and jumping muscles of Auchenorrhyncha, lateral (left) and posterior (right) views. A, B, Ricania japonica (Fulgoromorpha: Fulgoroidea: Ricaniidae); C, D, Cicadella viridis (Cicadomorpha: Membracoidea: Cicadellidae); E, F, Aphrophora pectoralis (Cercopoidea: Aphrophoridae); G, H, Graptopsaltria nigrofuscata (Cicadidae: Cicadoidea). See Fig. 2 for terminology, colors, and abbreviations. The right side of posterior images shows muscles (colored shadows) and muscle attachment regions (black dots). The border of mesophragma is highlighted by green line

Fig. 5 in Morphological dissection of behavior: thoracic musculature clarifies independent development of jumping mechanisms between sister groups, planthoppers and leafhoppers (Insecta: Hemiptera: Auchenorrhyncha)

Fig. 5 Metathoracic endoskeletons and attachment regions of IIIpcm5, lateral view. See Fig. 2 for terminology and abbreviations. a Ricania japonica (Fulgoromorpha: Fulgoroidea: Ricaniidae). b Cicadella viridis (Cicadomorpha: Membracoidea: Cicadellidae). IIIpcm5 is indicated by gray shadow. Dotted areas indicate muscle attachment regions

Fig. 4 in Morphological dissection of behavior: thoracic musculature clarifies independent development of jumping mechanisms between sister groups, planthoppers and leafhoppers (Insecta: Hemiptera: Auchenorrhyncha)

Fig. 4 Enlarged view of left metatrocanteral tendons and attachments point of muscles. a Ricania japonica (Fulgoromorpha: Fulgoroidea: Ricaniidae). b Cicadella viridis (Cicadomorpha: Membracoidea: Cicadellidae). c Aphrophora pectoralis (Cercopoidea: Aphrophoridae). d Graptopsaltria nigrofuscata (Cicadoidea: Cicadidae). See Fig. 2 for

Fig. 6 in Morphological dissection of behavior: thoracic musculature clarifies independent development of jumping mechanisms between sister groups, planthoppers and leafhoppers (Insecta: Hemiptera: Auchenorrhyncha)

Fig. 6 Most parsimonious reconstruction of character states scored in this study (Appendix) onto the phylogeny of Auchenorrhyncha estimated by Misof et al. (2014), Cryan and Urban (2012), and Urban and Cryan (2007). Out-groups are omitted. Character and character state changes reconstructed on the branches are indicated by black (gain) and white bars (reversal). For some characters (e.g., Character 5), an

opennotspecifiedAug 2015View details →

Fig. 1 in Sex or no sex? Group I introns and independent marker genes reveal the existence of three sexual but reproductively isolated biospecies in Trichia varia (Myxomycetes)

Fig. 1 Three-gene phylogeny of Trichia varia. a Associations between partial SSU and partial COI genotypes within the three groups (1, 2a, 2b). Dotted lines indicate associations found in one specimen, dashed lines in two to five specimens, and solid lines more than five specimens. b Bayesian majority-rule consensus tree of combined partial sequences of

opennotspecifiedDec 2014View details →

Fig. 3 in Phylogenetic evidence for multiple independent origins of functional kleptoplasty in Sacoglossa (Heterobranchia, Gastropoda)

Fig. 3 Phylogeny of the Sacoglossa based on Bayesian analysis (50 % majority rule consensus tree). Numbers at nodes indicate Posterior Probability (PP), black circles indicate PP=100, and black asterisks indicate PP=95–99. The inner dark gray circle borders functional-retention information of taxa, the outer food sources (displayed are only three major food sources per species). The scale bar displays substitutions per site. Yellow highlighted is the "outgroup", pink the Oxynoacea, purple the Platyhedylidae, green the " Limapontioidea ", and blue the

opennotspecifiedDec 2014View details →

Fig. 2 in Phylogenetic evidence for multiple independent origins of functional kleptoplasty in Sacoglossa (Heterobranchia, Gastropoda)

Fig. 2 Maximum quantum yield measurements (Fv/Fm) of Elysia clarki. Specimens of E. clarki were either starved under 40 μmol quanta m−2 s−1 (diamonds) or in complete darkness (rectangles) over a period of 49 days. Error bars indicate standard deviation between different specimens for each measuring point. Because specimens were fixed at certain intervals, finally only one individual was left at day 49

Fig. 4 in Independent acquisition of sulfide tolerance in a population of tubificine worms: a habitat extension for the Limnodrilus hoffmeisteri complex

Fig. 4 Maximum likelihood gene trees based on BSP1 and available mitochondrial COI, 12S, and nuclear ITS Limnodrilus sequences (see Fig. 5 left, 16 SrRNA). L. hoffmeisteri taxa are labeled and colored according to the clades numbered I–X described earlier. Abbreviations on taxon labels are: Lsu (L. sulphurensis), Lu (L. udekemianus), Lg (L. grandisetosus), Lr (L. rubripenis), Lc-c (L. claparedianus-cervix), Lc' (L. claparedianus isolate), Lm (L. maumeesis), Lp (L. profundicola), Ls

Fig. 1 A in Independent acquisition of sulfide tolerance in a population of tubificine worms: a habitat extension for the Limnodrilus hoffmeisteri complex

Fig. 1 A The layout of the springs and their effluents. Spring numbering (red circles) is based on Fuller (1905). Springs 1, 2, 3, and 6 produce sulfidic water. The larger stream to the northeast (broad, dark blue line) is non-sulfidic as is the effluent from spring 4. Remnants of the old rock wall are shown as a dotted brown line. This map represents the position of the streams in mid-summer, 2022. The dark blue dashed line shows the position of a now dry alternate route of the stream in the summer of 2017. "Lh" indicates where populations of the Blount Springs L. hoffmeisteri were abundant in late summer. Arrows indicated the direction of water flow. The locations of worm colonies of specimens used for morphological and molecular analysis are indicated by green circles. Specimens 213, 215, and 216 were from C21; specimens 273, 274, and 276 were from C27; specimens 362, 364, 365, and 366 were from C36; specimens 371, 372, 373, 374, 375, and 376 were from C37; specimen BSP1 was from C1, while all others used for morphology were from C1 or just downstream of that colony. B Dark substrate material in the gut just below the dorsal blood vessel in a live worm. C A cluster of tubificine worms found at Blount Springs with their heads buried in the black, fluffy substrate

Fig. 5 in Independent acquisition of sulfide tolerance in a population of tubificine worms: a habitat extension for the Limnodrilus hoffmeisteri complex

Fig. 5 Left: Maximum likelihood gene tree estimated from the taxonomically rich 16S rDNA sequence alignment of L. hoffmeisteri and related species. Of seven gene trees used infer the evolution relationship of the Blount Springs specimen, only this gene contained enough phylogenetically informative signal to resolve deep nodes of the tree. Resolution of these nodes shows that the 10-species complex of L. hoffmeisteri may not be monophyletic. This is consistent with the

Fig. 3 in Independent acquisition of sulfide tolerance in a population of tubificine worms: a habitat extension for the Limnodrilus hoffmeisteri complex

Fig. 3 Drawings of chaetae and reproductive structures, from a mature Blount Springs L. hoffmeisteri. A Ventral chaetal bundle, segment IV. B Penis sheath. C Male reproductive organs, showing (from