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Text-fig. 1. D&E tree of Endress and Doyle (2009), from the combined morphological and molecular analysis of Doyle and Endress (2000), with modifications based on more recent data, showing the inferred evolution of the reticulum grading character (39). Boxes under names of taxa indicate their character state; shading of branches indicates their reconstructed state based on parsimony optimization with MacClade (Maddison and Maddison 2003). Nymph = Nymphaeales, Aust = Austrobaileyales, Chlor = Chloranthaceae, Piper = Piperales, Ca = Canellales, Magnol = Magnoliales. in Early Cretaceous Monocots: A Phylogenetic Evaluation
Text-fig. 1. D&E tree of Endress and Doyle (2009), from the combined morphological and molecular analysis of Doyle and Endress (2000), with modifications based on more recent data, showing the inferred evolution of the reticulum grading character (39). Boxes under names of taxa indicate their character state; shading of branches indicates their reconstructed state based on parsimony optimization with MacClade (Maddison and Maddison 2003). Nymph = Nymphaeales, Aust = Austrobaileyales, Chlor = Chloranthaceae, Piper = Piperales, Ca = Canellales, Magnol = Magnoliales.
Text-fig. 5. Most parsimonious trees obtained after addition of the Pennipollis plant to the (A) D&E and (B) J/M trees. Relative parsimony of alternative positions of the Pennipollis plant is indicated as in Text-fig. 2; abbreviations as in Text-fig. 1. in Early Cretaceous Monocots: A Phylogenetic Evaluation
Text-fig. 5. Most parsimonious trees obtained after addition of the Pennipollis plant to the (A) D&E and (B) J/M trees. Relative parsimony of alternative positions of the Pennipollis plant is indicated as in Text-fig. 2; abbreviations as in Text-fig. 1.
Text-fig. 11. Eospondylus cf. primigenius (STÜRTZ) "Prastav" quarry at Praha-Holyně, Třebotov Limestone, Lower Devonian, Dalejan, NM L 36905, x 65. Overlay of proximal and distal articulations. Upper photo is proximal surface with distal bird-like articulation knobs superposed in ink. Lower photo is distal surface with proximal articulation knobs superposed in ink. The architecture of articulation surfaces is both zygospondylous and auluroid. This architecture occurs also in vertebrae of Furcaster and indicates that families Eospondylidae and Furcasteridae are closely related. in Isolated Ossicles Of The Family Eospondylidae Spencer Wright, 1966, In The Lower Devonian Of Bohemia (Czech Republic) And Correction Of The Systematic Position Of Eospondylid Brittlestars (Echinodermata: Ophiuroidea: Oegophiurida)
Text-fig. 11. Eospondylus cf. primigenius (STÜRTZ) "Prastav" quarry at Praha-Holyně, Třebotov Limestone, Lower Devonian, Dalejan, NM L 36905, x 65. Overlay of proximal and distal articulations. Upper photo is proximal surface with distal bird-like articulation knobs superposed in ink. Lower photo is distal surface with proximal articulation knobs superposed in ink. The architecture of articulation surfaces is both zygospondylous and auluroid. This architecture occurs also in vertebrae of Furcaster and indicates that families Eospondylidae and Furcasteridae are closely related.
Text-fig. 2. Eospondylus primigenius (STÜRTZ) Bundenbach, Eschenbach-Bocksberg quarry, Lower Devonian, Lower Emsian (Zlichovian), Hunsrück Slate,, NM S 4764, x 3. Specimen with ventral arm coiling. The specimen is on its dorsum in slate with all five rays curled ventrally inward toward mouth area on underside of disk. Barely visible are tips of two jaws; slightly exposed are proximal parts of rays in oral view extending outward from disk. The location of abrupt ventral bending of rays is indicated by emergence from slate of five rays in aboral view that point inward toward buried disk. Based on ventral bending of rays and intimate association with crinoids Eospondylus has been interpreted as stratigraphic first occurrence of Order Euryalida, which contains epizoic gorgonocephalid and euryalid basket-stars of modern oceans. This status is rejected using new evidence from isolated vertebrae. [Photo by Alexander Glass]. in Isolated Ossicles Of The Family Eospondylidae Spencer Wright, 1966, In The Lower Devonian Of Bohemia (Czech Republic) And Correction Of The Systematic Position Of Eospondylid Brittlestars (Echinodermata: Ophiuroidea: Oegophiurida)
Text-fig. 2. Eospondylus primigenius (STÜRTZ) Bundenbach, Eschenbach-Bocksberg quarry, Lower Devonian, Lower Emsian (Zlichovian), Hunsrück Slate,, NM S 4764, x 3. Specimen with ventral arm coiling. The specimen is on its dorsum in slate with all five rays curled ventrally inward toward mouth area on underside of disk. Barely visible are tips of two jaws; slightly exposed are proximal parts of rays in oral view extending outward from disk. The location of abrupt ventral bending of rays is indicated by emergence from slate of five rays in aboral view that point inward toward buried disk. Based on ventral bending of rays and intimate association with crinoids Eospondylus has been interpreted as stratigraphic first occurrence of Order Euryalida, which contains epizoic gorgonocephalid and euryalid basket-stars of modern oceans. This status is rejected using new evidence from isolated vertebrae. [Photo by Alexander Glass].
Fig. 4 in Assemblages of carabid beetles (Coleoptera: Carabidae) as zoo-indicator of water tourism impact on forest - lake ecotones
Fig. 4. Cluster analysis of the study sites (euclidic distances, Ward˙s method) based on carabid beetle assemblages
Fig. 3 in Assemblages of carabid beetles (Coleoptera: Carabidae) as zoo-indicator of water tourism impact on forest - lake ecotones
Fig. 3. Model of state of carabid beetle assemblages in pine woodlands (B) and alder woodlands (A) in control area (0), medium pressure (1) and high pressure (2).
Fig.2 in Assemblages of carabid beetles (Coleoptera: Carabidae) as zoo-indicator of water tourism impact on forest - lake ecotones
Fig.2. Whittaker diagrams of species-abundance of carabid species in alder woodland (left side) and pine woodlands (right side).
Figure 2 in Trichodinid fauna of freshwater fishes with infestation indices in the Lower Kızılırmak Delta in Turkey and a checklist of trichodinids (Ciliophora: Trichodinidae) in Turkish waters
Figure 2. Trichodinid parasites identified on Lower Kızılırmak Delta fishes: A) T. lepsii, B) T. puytoraci, C) T. domerguei, D) T. heterodentata, E) Paratrichodina corlissi, F) T. domerguei, G) T. modesta, H) Tripartiella macrosoma, I) T. acuta, J) T. lucioperca, K) T. tenuidens, L) Trichodina sp1, M) T. cobitis, N) Trichodina sp2, O) Trichodina sp3.
Figure. Constrained ordination plot as produced from canonical correspondence analysis (CCA). The variability of environmental variables is summarized on Axis 1 and Axis 2 of the constrained biplot, explaining the variability of the trophic groups included in the red fox's diet. Trophic groups are shown with black line (unfilled) pyramids, whereas environmental variables are shown with black filled pyramids. Proximity and distance of response centroids to predictor centroids indicate positive and negative correlations between them, respectively. in Factors affecting the diet of the red fox (Vulpes vulpes) in a heterogeneous Mediterranean landscape
Figure. Constrained ordination plot as produced from canonical correspondence analysis (CCA). The variability of environmental variables is summarized on Axis 1 and Axis 2 of the constrained biplot, explaining the variability of the trophic groups included in the red fox's diet. Trophic groups are shown with black line (unfilled) pyramids, whereas environmental variables are shown with black filled pyramids. Proximity and distance of response centroids to predictor centroids indicate positive and negative correlations between them, respectively.
Figure. Distribution of the recent localities of Lumbricus terrestris on the Balkan Peninsula (plus marks indicate other Balkan countries where L. terrestris also lives). in On the presence of Lumbricus terrestris Linnaeus 1758 (Oligochaeta, Lumbricidae) on the Balkan Peninsula: some aspects of ecology and distribution
Figure. Distribution of the recent localities of Lumbricus terrestris on the Balkan Peninsula (plus marks indicate other Balkan countries where L. terrestris also lives).
Figure 2. Maximum-likelihood trees for J in Mitochondrial evidence indicates a shallow phylogeographic structure for Jaculus blanfordi (Murray, 1884) populations (Rodentia: Dipodidae)
Figure 2. Maximum-likelihood trees for J. blanfordi mtDNA haplotypes in different datasets for cyt b (1110 bp), COI (618 bp), and COI + cyt b (313 bp + 284 bp). The numbers next to the nodes indicate the bootstrap (>50%) and posterior probability (>0.50) values obtained by maximum-likelihood and Bayesian inference, respectively. The trees are rooted with haplotypes from J. orientalis and J. jaculus. See Table 1 and Figure 1 for the haplotype designations and corresponding localities.
Figure 1 in Mitochondrial evidence indicates a shallow phylogeographic structure for Jaculus blanfordi (Murray, 1884) populations (Rodentia: Dipodidae)
Figure 1. Geographical locations of J. blanfordi samples included in the present study. The locality numbers correspond to those in Table 1. The shaded zones in the map correspond to the distribution range of Blanford's jerboa (Shenbrot and Molur, 2008).
Figure 3. Median-joining networks for J in Mitochondrial evidence indicates a shallow phylogeographic structure for Jaculus blanfordi (Murray, 1884) populations (Rodentia: Dipodidae)
Figure 3. Median-joining networks for J. blanfordi mitochondrial DNA haplotypes in the different datasets for cyt b (1110 bp), COI (618 bp) and COI + cyt b (313 bp + 284 bp). The numbers of mutations (greater than 1) between the haplotypes are indicated near the branches and circle sizes are proportional to the number of similar haplotypes. See Table 1 for the haplotype designations.
Figure 4 in Mitochondrial evidence indicates a shallow phylogeographic structure for Jaculus blanfordi (Murray, 1884) populations (Rodentia: Dipodidae)
Figure 4. Observed and expected mismatch distribution of haplotypes for the cyt b (1110 bp), COI (618 bp), and COI + cyt b (313 bp + 284 bp) datasets.
Fig. 3. Rarefaction curves. Solid lines indicate mean and dashed lines indicate 95 in Streetlights attract a broad array of beetle species
Fig. 3. Rarefaction curves. Solid lines indicate mean and dashed lines indicate 95% confidence intervals. Inset shows the full curves for Hg and Na.
Figure 1 in Assessment of the zooplankton community structure of the coastal Uzungöl Lagoon (Kızılırmak Delta, Turkey) based on community indices and physicochemical parameters
Figure 1. Geographical location of study area, coordinates of sampling points. Station 1: 41°32'33.85"N - 36°04'56.80"E; Station 2: 41°33'36.66"N - 36°05'22.24"E; Station 3: 41°34'11.10"N - 36°05'40.67"E; Station 4: 41°34'44.82"N - 36°06'0.14"E; Station 5: 41°35'7.57"N - 36° 06'20.14"E.
Figure 6 in Assessment of the zooplankton community structure of the coastal Uzungöl Lagoon (Kızılırmak Delta, Turkey) based on community indices and physicochemical parameters
Figure 6. Zooplankton community indices (Shannon Diversity, Pielou evenness and Species richness) during the study period.
Figure 3 in Assessment of the zooplankton community structure of the coastal Uzungöl Lagoon (Kızılırmak Delta, Turkey) based on community indices and physicochemical parameters
Figure 3. Seasonal density (ind. m -3) changes of nauplii larvae and copepodit individuals in Uzungöl Lagoon.
Figure 2 in Ecomorphological patterns and shape indices of otoliths in the Pagellus acarne (Actinopterygii, Sparidae) from the Aegean and Marmara Seas
Figure 2. Explanation of morphometric otolith measurements on the proximal otolith surface of Pagellus acarne.
Figure 4 in Ecomorphological patterns and shape indices of otoliths in the Pagellus acarne (Actinopterygii, Sparidae) from the Aegean and Marmara Seas
Figure 4. Principal component analysis (PCA) plot showing similarities/ differences between both Pagellus acarne stocks and left and right side otoliths: (AS) Aegean Sea and (MS) Sea of Marmara.
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Allen Brain Atlas
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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.
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