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Supplementary material 6 from: Urfer K, Spasojevic T, Klopfstein S, Baur H, Lasut L, Kropf C (2021) Incongruent molecular and morphological variation in the crab spider Synema globosum (Araneae, Thomisidae) in Europe. ZooKeys 1078: 107-134. https://doi.org/10.3897/zookeys.1078.64116
Morphomatrix of the examined Synema globosum individuals
Supplementary material 2 from: Urfer K, Spasojevic T, Klopfstein S, Baur H, Lasut L, Kropf C (2021) Incongruent molecular and morphological variation in the crab spider Synema globosum (Araneae, Thomisidae) in Europe. ZooKeys 1078: 107-134. https://doi.org/10.3897/zookeys.1078.64116
Genbank and Bold numbers of the Synema globosum specimens that were obtained from these databases
Figure 9 from: Urfer K, Spasojevic T, Klopfstein S, Baur H, Lasut L, Kropf C (2021) Incongruent molecular and morphological variation in the crab spider Synema globosum (Araneae, Thomisidae) in Europe. ZooKeys 1078: 107-134. https://doi.org/10.3897/zookeys.1078.64116
Figure 9 A Shape PC1 plotted against isometric size of 28 males. Colours correspond to the CO1 clades. B PCA Ratio Spectrum for shape PC1. The three specimens with grey symbols could not be included in the molecular analysis and therefore could not be attributed to a clade. Regression lines follow a least-squares model.
Figure 8 from: Urfer K, Spasojevic T, Klopfstein S, Baur H, Lasut L, Kropf C (2021) Incongruent molecular and morphological variation in the crab spider Synema globosum (Araneae, Thomisidae) in Europe. ZooKeys 1078: 107-134. https://doi.org/10.3897/zookeys.1078.64116
Figure 8 Variation in morphology in the male II. A palp with all variable structures B outlines of the palps from two additional males that showadditional variation C–E tips of embolus C Italy, Siena D, E Italy Toskana F–G two out of three individuals where the rta shows a second tip F Greece, Marathonas G Italy, Tuscany. Abbreviations: cy cymbium, et embolus tip, rta retrolateral tibial apophysis, brta base of the retrolateral tibial apophysis, ti tibia, vta ventral tibial apophysis
Supplementary material 1 from: Urfer K, Spasojevic T, Klopfstein S, Baur H, Lasut L, Kropf C (2021) Incongruent molecular and morphological variation in the crab spider Synema globosum (Araneae, Thomisidae) in Europe. ZooKeys 1078: 107-134. https://doi.org/10.3897/zookeys.1078.64116
Coordinates of the collected specimens
Figure 7 from: Urfer K, Spasojevic T, Klopfstein S, Baur H, Lasut L, Kropf C (2021) Incongruent molecular and morphological variation in the crab spider Synema globosum (Araneae, Thomisidae) in Europe. ZooKeys 1078: 107-134. https://doi.org/10.3897/zookeys.1078.64116
Figure 7 Variation in morphology in the male I. A, B habitus males with different colour pattern on femora III and IV A Greece, Marathonas B Portugal C–E Different sizes of palp in ventral view C France, Savoy D Italy, Siena E Greece, Marathonas F–I palp, ventral view, the variation of the retrolateral tibial apophysis and the tibial apophysis F Greece, West Macedonia G Czech Republic, Brno H, I Italy, Tuscany J–M retrolateral view of the palp, variation in the retrolateral tibial apophysis J Czech Republic, Brno K Greece, Attiki L Italy, Siena M Greece, west Macedonia.
Figure 5 from: Urfer K, Spasojevic T, Klopfstein S, Baur H, Lasut L, Kropf C (2021) Incongruent molecular and morphological variation in the crab spider Synema globosum (Araneae, Thomisidae) in Europe. ZooKeys 1078: 107-134. https://doi.org/10.3897/zookeys.1078.64116
Figure 5 CO1 haplotype network of Synema globosum. Nodes represent different haplotypes with the size corresponding to the frequency of the haplotype. The short black lines represent mutations. The colours represent the countries of the origin of the sequences.
Figure 4 from: Urfer K, Spasojevic T, Klopfstein S, Baur H, Lasut L, Kropf C (2021) Incongruent molecular and morphological variation in the crab spider Synema globosum (Araneae, Thomisidae) in Europe. ZooKeys 1078: 107-134. https://doi.org/10.3897/zookeys.1078.64116
Figure 4 ITS2 haplotype network of Synema globosum. Nodes represent haplotypes with the size corresponding to the frequency of the haplotype. The short black lines represent mutations. The colours represent the countries of origin of sequences and have no relation with the CO1 clades.
Figure 3 from: Urfer K, Spasojevic T, Klopfstein S, Baur H, Lasut L, Kropf C (2021) Incongruent molecular and morphological variation in the crab spider Synema globosum (Araneae, Thomisidae) in Europe. ZooKeys 1078: 107-134. https://doi.org/10.3897/zookeys.1078.64116
Figure 3 Bayesian majority rule consensus tree for CO1. The analysis included 72 individuals of Synema globosum and eight outgroup sequences. Node supports represent Bayesian posterior probabilities/ML bootstrap support based on 1,000 replicates; colours correspond to the three distinct clades. The specimen labels contain country information after the specimen number. Four different symbols before each specimen correspond to the states of four scored morphological traits; circles indicate the colour of the opisthosoma, squares the number of teeth on the prolateral claw of leg one, upside triangles the percentage of white colour starting at the base of leg IV in males, downside triangles the entrance state of the vulval hood; black filled symbols indicate a not applicable state (NA).
Figure 1 from: Urfer K, Spasojevic T, Klopfstein S, Baur H, Lasut L, Kropf C (2021) Incongruent molecular and morphological variation in the crab spider Synema globosum (Araneae, Thomisidae) in Europe. ZooKeys 1078: 107-134. https://doi.org/10.3897/zookeys.1078.64116
Figure 1 Map of localities of 72 Synema globosum individuals used for the CO1 phylogeny. The specimens were collected in Portugal, France, Italy, Czech Republic, North Macedonia, Greece, and Turkey. Sequences of specimens from Switzerland, Austria, Germany, and Bulgaria were obtained from BOLD. The colours correspond to the three clades in the CO1 phylogeny of S. globosum.
Supplementary material 3 from: Urfer K, Spasojevic T, Klopfstein S, Baur H, Lasut L, Kropf C (2021) Incongruent molecular and morphological variation in the crab spider Synema globosum (Araneae, Thomisidae) in Europe. ZooKeys 1078: 107-134. https://doi.org/10.3897/zookeys.1078.64116
GenBank accession numbers
Figure 6 from: Urfer K, Spasojevic T, Klopfstein S, Baur H, Lasut L, Kropf C (2021) Incongruent molecular and morphological variation in the crab spider Synema globosum (Araneae, Thomisidae) in Europe. ZooKeys 1078: 107-134. https://doi.org/10.3897/zookeys.1078.64116
Figure 6 Variation in morphology in the female. A–D opisthosoma, dorsal view, colour and black pattern variation E–G white stripe on the ventral side of opisthosoma E Greece, Peloponnese F Italy, Tuscany G Greece, west Macedonia H–J variation in the vulva H Greece, Marathonas I France, Savoy J Greece, west Macedonia K epigyne of the specimen from J with very deep hood. Abbreviations: cd = copulatory duct, rs = receptaculum seminis, fd = fertilisation duct, ho = hood.
Supplementary material 5 from: Urfer K, Spasojevic T, Klopfstein S, Baur H, Lasut L, Kropf C (2021) Incongruent molecular and morphological variation in the crab spider Synema globosum (Araneae, Thomisidae) in Europe. ZooKeys 1078: 107-134. https://doi.org/10.3897/zookeys.1078.64116
Bayesian majority rule consensus tree of ITS2
Supplementary material 4 from: Urfer K, Spasojevic T, Klopfstein S, Baur H, Lasut L, Kropf C (2021) Incongruent molecular and morphological variation in the crab spider Synema globosum (Araneae, Thomisidae) in Europe. ZooKeys 1078: 107-134. https://doi.org/10.3897/zookeys.1078.64116
Input file Mr Bayes and RAxML
Figure 2 from: Urfer K, Spasojevic T, Klopfstein S, Baur H, Lasut L, Kropf C (2021) Incongruent molecular and morphological variation in the crab spider Synema globosum (Araneae, Thomisidae) in Europe. ZooKeys 1078: 107-134. https://doi.org/10.3897/zookeys.1078.64116
Figure 2 Measurements of the palp: Cym.l is the distance of the anterior margin to the tip of the cymbium, cym.b is the maximum breadth of the cymbium, bul.b is the maximum breadth of the genial bulbus and tib.b is the breadth of the tibia at the base of the patella joint.
Data for Interindividual variation in maximum aerobic metabolism varies with gill morphology and myocardial bioenergetics in Gulf killifish
<p>This study asked whether interindividual variation in maximum and standard aerobic metabolic rates of the Gulf killifish, Fundulus grandis, correlate with gill morphology and cardiac mitochondrial bioenergetics, traits reflecting critical steps in the O<sup>2</sup> transport cascade from the environment to the tissues. Maximum metabolic rate (MMR) was positively related to body mass, total gill filament length, and myocardial oxygen consumption during maximum oxidative phosphorylation (multiple R<sup>2</sup> = 0.836). Standard metabolic rate (SMR) was positively related to body mass, total gill filament length, and myocardial oxygen consumption during maximum electron transport system activity (multiple R<sup>2</sup> = 0.717). After controlling for body mass, individuals with longer gill filaments, summed over all gill arches, or greater cardiac respiratory capacity had higher whole-animal metabolic rates. The overall model fit and the explanatory power of individual predictor variables were better for MMR than for SMR, suggesting that gill morphology and myocardial bioenergetics are more important in determining maximum rather than resting metabolism. After controlling for body mass, heart ventricle mass was not related to variation in MMR or SMR, indicating that the quality of the heart (i.e., the capacity for mitochondrial metabolism) was more influential than heart size. Finally, myocardial oxygen consumption required to offset the dissipation of the transmembrane proton gradient in the absence of ATP synthesis was not correlated with either MMR or SMR. The results support the idea that interindividual variation in aerobic metabolism, particularly MMR, is associated with variation in specific steps in the O<sup>2</sup> transport cascade.</p>
FIGURE 7 in Morphological variation and genealogical discordance in Caatinga sand lizards Calyptommatus Rodrigues 1991 (Squamata: Gymnophthalmidae) with the description of a new species
FIGURE 7. Tracks of Calyptommatus frontalis sp. nov. on the sandy soil in Buritirama, Bahia.
Figure 3 in Intraspecific variation in the morphology of Alloxysta fracticornis (Thomson, 1862)(Hymenoptera: Figitidae: Charipinae)
Figure 3. Forms of Alloxysta fracticornis (Thomson, 1862): (a) brachypterous, (b) macropterous.
Supplementary material 2 from: Marcondes RS, Silveira LF (2015) A taxonomic review of Aramides cajaneus (Aves, Gruiformes, Rallidae) with notes on morphological variation in other species of the genus. ZooKeys 500: 111-140. https://doi.org/10.3897/zookeys.500.7685
Recordings examined: Explanation note: A list of tape recordings examined for this study.
Supplementary material 1 from: Marcondes RS, Silveira LF (2015) A taxonomic review of Aramides cajaneus (Aves, Gruiformes, Rallidae) with notes on morphological variation in other species of the genus. ZooKeys 500: 111-140. https://doi.org/10.3897/zookeys.500.7685
Specimens examined: Explanation note: A list of specimens (skins) examined of this study.
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