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230 results for “species presence”
FIGURES 104–109. 104–105 in A review of the monophyly and composition of the Bengaliinae with the description of a new genus and species, and new evidence for the presence of Melanomyinae in the Afrotropical Region (Diptera, Calliphoridae) 2964
FIGURES 104–109. 104–105. Adichosina eos Zumpt (CNC). Male genitalia. 104. Epandrium, cerci, surstyli and bacilliform sclerites, left lateral view. 105. Aedeagus, pre- and postgonites, left lateral view. 106–109. Adichosina munroi (Curran) (MZLU). Female ovipositor. 106. Dorsal intersegmental membrane 6–7 (behind T6). 107. Segment 6, right lateral view. Pink arrows point to spiracles 6 and 7. 108. Segment 7, with segment 8 and cerci telescoped within it, right lateral view. 109. Dorsal view of T8+epiproct telescoped within segment 7. Note tooth-like microtrichiae on intersegmental membrane 7–8 superimposed on the compound T8+epiproct sclerite; these are pointing towards hind end of T7. They seem to be pointing backwards, but if segment 8 had been drawn out from segment 7, they would have been be pointing forwards.
FIGURES 124–133 in A review of the monophyly and composition of the Bengaliinae with the description of a new genus and species, and new evidence for the presence of Melanomyinae in the Afrotropical Region (Diptera, Calliphoridae) 2964
FIGURES 124–133. Onesihoplisa umbrosa Villeneuve (CNC). 124–126. Male genitalia. 127–133. Female ovipositor. 124. Epandrium, cerci and surstyli, posterior (dorsal) view. 125. Hypandrium, phallapodeme and gonites, left lateral view. 126. Aedeagus, left lateral view. 127. Fully extended ovipositor, left lateral view. Pink arrows point to spiracles 6 and 7. 128. Segment 6, left lateral view. Pink arrow points to spiracle 7. 129. Intersegmental membrane 6–7, left lateral view. 130. Segment 7, left lateral view. 131. Intersegmental membrane 7–8, left lateral view. 132. T8+epiproct, cerci and hypoproct, left lateral view. 133. T8+epiproct and cerci, dorsal view.
FIGURES 116–123 in A review of the monophyly and composition of the Bengaliinae with the description of a new genus and species, and new evidence for the presence of Melanomyinae in the Afrotropical Region (Diptera, Calliphoridae) 2964
FIGURES 116–123. Ochromelinda thoracica Villeneuve (CNC). First instar uterine larva. 116–119. Photomicrographs. 120–123. Scanning electron micrographs (SEM). 116. Whole mount in Hoyer's medium, left lateral view. Inset: posterior spiracles. 117. Pseudocephalon and first thoracic segment, lateral view. 118. Cephalopharyngeal skeleton, left lateral view. 119. Cephalopharyngeal skeleton, ventral view. 120. Pseudocephalon, ventral view (SEM). 121. Spines from anterior spinose band on second thoracic segment. 122. Spines from anterior spinose band on third thoracic segment. 123. Spines from anterior spinous band on third thoracic segment, enlarged. [All photographs by Krzysztof Szpila]. Abbreviations, see Material and methods chapter.
FIGURES 79–84 in A review of the monophyly and composition of the Bengaliinae with the description of a new genus and species, and new evidence for the presence of Melanomyinae in the Afrotropical Region (Diptera, Calliphoridae) 2964
FIGURES 79–84. Tricyclea semicinerea Bezzi, male (specimen no. 13747, BMSA). 79. Epandrium, cerci and surstyli, dorsal (posterior) view. 80. Epandrium, cerci, surstyli and bacilliform sclerites, oblique left antero-lateral view. 81. Epandrium, cerci, surstyli and bacilliform sclerites, oblique ventral (internal) view. 82. Aedeagus, left lateral view. 83. Aedeagus, oblique dorsal view. 84. Aedeagus, apical view.
FIGURE 14 in The presence of Homoeoneuria s.s. (Ephemeroptera: Oligoneuriidae) in South America with the description of a new species
FIGURE 14. The most parsimonious cladograma showing only unambiguous characters. Length: 33 steps; consistency index: 72 (66 without autapomorphic characters); retention index: 60. Black circles corresponds to synapomorphies and white circles to homoplasies. Bremer support represented at nodes.
FIGURES 3–10 in The presence of Homoeoneuria s.s. (Ephemeroptera: Oligoneuriidae) in South America with the description of a new species
FIGURES 3–10. Homoeoneuria (H.) watu sp. n., nymph. 3, lateral view of nymph; 4, Antenna. 5, Galea-lacinia. 6, Hypopharynx. 7, Fore leg (long and pectinated setae on inner margin of femur and tibia omitted). 8, Detail of apex of fore leg. 9, Detail of mid tarsal claw. 10, Detail of hind tarsal claw.
FIGURES 11–13 in The presence of Homoeoneuria s.s. (Ephemeroptera: Oligoneuriidae) in South America with the description of a new species
FIGURES 11–13. Homoeoneuria (H.) watu sp. n., nymph. 11, Head (frontal view); 12, Head (lateral view); 13, Abdomen (dorsal view).
Figs. 1–6. Dichotomius species. D in Presence of Dichotomius (dichotomius) centralis (Harold) in Mexico and a New State Record for Dichotomius amplicollis (Harold) (Coleoptera: Scarabaeidae: Scarabaeinae)
Figs. 1–6. Dichotomius species. D. centralis: 1) Parameres, dorsal view; 2) Paramere, apex; 3) Elytral striae. D. amplicollis: 4) Parameres, dorsal view; 5) Paramere, apex; 6) Elytral striae.
Figure 4 in Uncovering species boundaries in the Neotropical ant complex Ectatomma ruidum (Ectatomminae) under the presence of nuclear mitochondrial paralogues
Figure 4. Digital photographs showing the head (full face) and pronotal hump of representative specimens belonging to the four delimited morphospecies originally assigned to Ectatomma ruidum: A, E. gibbum; B, E. sp. 'ruidum 1'; C, E. sp. 'ruidum 2'; D, E. sp. 'ruidum 3'; E, E. sp. 'ruidum 4'; F, E. sp. 'ruidum 2 X sp. ruidum 3'.
Figure 3 in Uncovering species boundaries in the Neotropical ant complex Ectatomma ruidum (Ectatomminae) under the presence of nuclear mitochondrial paralogues
Figure 3. Phylogram derived from the Bayesian concatenated (COI + cyt b) analysis excluding all potential numts and hybrids. Black circles near branches are Bayesian posterior probabilities ≥0.95. Coloured lines refer to the main lineages recovered. Taxon names refer to the delimited morphospecies.
Figure 1 in Uncovering species boundaries in the Neotropical ant complex Ectatomma ruidum (Ectatomminae) under the presence of nuclear mitochondrial paralogues
Figure 1. Map showing the sampled localities for the specimens assigned to Ectatomma ruidum and Ectatomma gibbum. The taxon names refer to the delimited morphospecies.
Figure 5 in The common bottlenose dolphin (Tursiops truncatus) ecotypes of the western North Atlantic revisited: an integrative taxonomic investigation supports the presence of distinct species
Figure 5. Worldwide morphological analyses of bottlenose dolphins. Scatter plot of the principal component 1 (PC1) and 2 (PC2) scores from the analysis of 18 skull measurements and 316 bottlenose dolphin skulls. Ellipses correspond to the 95% confidence interval. Samples are differentiated by type classification and geographical region. The holotype Tursiops truncatus is represented by an open triangle.
Figure 2 in The common bottlenose dolphin (Tursiops truncatus) ecotypes of the western North Atlantic revisited: an integrative taxonomic investigation supports the presence of distinct species
Figure 2. Traditional morphometric analyses of bottlenose dolphins of the western North Atlantic. A, scatter plot of the principal component 1 (PC1) and 2 (PC2) scores from the analysis of 25 cranial variables and 147 samples. Ellipses correspond to the 95% confidence interval. The shape of the data points represents the ecotype (coastal or offshore) as defined based on random forest (RF) results. The colour of the data points represents the clustering classifications according to density clustering (DC) results: black, samples follow the same classification (coastal or offshore) as RF and the a priori stratification; orange, 'cluster-3' identified only by DC (see main text). B, violin plot of the total external body length (TL) differentiated per sex (F, female; M, male) and ecotype.
Figure 4. A, B in The common bottlenose dolphin (Tursiops truncatus) ecotypes of the western North Atlantic revisited: an integrative taxonomic investigation supports the presence of distinct species
Figure 4. A, B, genetic clustering and relationship of bottlenose dolphins of the western North Atlantic. Membership probabilities of bottlenose dolphins in the western North Atlantic were based on 19 nuclear microsatellite loci and inferred using TESS (A) and STRUCTURE (B). Each column represents one individual, with colours representing the proportional membership to each of the clusters: white, coastal cluster; black, offshore cluster. C, median joining network of mitochondrial DNA haplotypes of bottlenose dolphins of the western North Atlantic. Haplotypes found in samples identified as the coastal ecotype are shown in white and those identified as the offshore ecotype in black. The size of the circles is proportional to the haplotype frequency in each group. Red diamonds indicate either extinct or unsampled haplotypes. Small red numbers on the branches represent the step mutations; branches without numbers represent one step mutation. The unique heteroplasmic haplotypes were not included in this analysis owing to program limitations to deal with ambiguous bases. The haplotype (Ttr2) obtained for the holotype Tursiops erebennus is in red.
Figure 1 in The common bottlenose dolphin (Tursiops truncatus) ecotypes of the western North Atlantic revisited: an integrative taxonomic investigation supports the presence of distinct species
Figure 1. Map of the western North Atlantic study area showing the sampling locations of samples with only morphological data available (brown), with morphological and genetic data available (cyan) or with only genetic data available (gold). The 200 m isobath line is shown in bold black. Thin black lines represent the 2000 and 4000 m isobaths.
Figure 3 in The common bottlenose dolphin (Tursiops truncatus) ecotypes of the western North Atlantic revisited: an integrative taxonomic investigation supports the presence of distinct species
Figure 3. Three-dimensional geometric morphometric (GM) analyses of bottlenose dolphins of the western North Atlantic. A, allometry plot of predicted lines based on fitted values (unique allometries model) to visualize how shape allometry varies by ecotype. The PredLine method calculates fitted values from the procD.lm fit and plots the first principal component of the predicted values against size, i.e. lnCS (see Adams & Nistri, 2010). B, scatter plot of the principal component 1 (PC1) and 2 (PC2) scores based on 23 cranial landmarks and 90 samples. Ellipses correspond to the 95% confidence interval. Samples are differentiated by sex (F, female; M, male; U, unknown) and ecotype. The mean specific shape variation along PC1 (bottom right) and PC2 (top left) is also shown. Grey represents the mean shape, whereas black represents the change in shape from the mean shape. Sample 1, USNM504096; sample 2, USNM572261.
Figure 7 in The common bottlenose dolphin (Tursiops truncatus) ecotypes of the western North Atlantic revisited: an integrative taxonomic investigation supports the presence of distinct species
Figure 7. Assembled portions of the postcranial skeleton of the holotype Tursiops erebennus (Cope, 1865) deposited in the Academy of Natural Sciences of Drexel University (museum number ANSP 3020).
Figure 6 in The common bottlenose dolphin (Tursiops truncatus) ecotypes of the western North Atlantic revisited: an integrative taxonomic investigation supports the presence of distinct species
Figure 6. Compressed phylogenetic tree of bottlenose dolphins based on maximum likelihood. For sample information and the full tree, see the Supporting Information (Table S7; Fig. S11, respectively). The clade formed by seven haplotypes from this study found as the wNA coastal ecotype (and two GenBank haplotypes of the Bahamas and Cuba, respectively) is coloured in white, whereas the clade composed of three coastal haplotypes of the Gulf of Mexico, 15 of the Bahamas and Caribbean Sea, and Ttr2 (wNA coastal haplotype; Tursiops erebennus haplotype; GOMx coastal haplotype) is coloured in red. Most the haplotypes forming the Tursiops truncatus offshore clade (N = 192; including haplotypes from the present study found in the wNA offshore ecotype, in addition to GenBank haplotypes found in T. truncatus worldwide) are coloured in black. Highlighted inside the offshore clade are the haplotypes found in T. t. gephyreus (green) and 'Tursiops australis' (purple). The clade composed of coastal T. truncatus from Ecuador and Peru is coloured in light blue, whereas Tursiops aduncus clades are coloured in orange (one clade composed of haplotypes from Bangladesh/African waters and another of haplotypes from Chinese/Australian waters and one haplotype found in Bangladesh). The haplotype found in the holotype T. aduncus is shown in bold. Bootstrap values (UFBoot) cut-off ≥ 80, because UFBoot achieves more unbiased support values. Shimodaira–Hasegawa-like approximate likelihood ratio test (SH-aLRT; first value) and UFBoot (second value) bootstrap values are represented on the tree branches (see also Supporting Information, Fig. S11). Abbreviations: AFR, western Indian Ocean–African coast; AUS, Australian coast; BGD, Bangladeshi coast; CHN, Chinese coast; eNA, eastern North Atlantic; eSP, eastern South Pacific; MED, Mediterranean Sea; wNA, western North Atlantic; wNP, western North Pacific; wSA, western South Atlantic; wSP, western South Pacific.
Presence of gastrointestinal parasite species of baboons reported in literature
<p>A spreadsheet of the presence (or absence) of parasite species at all study sites that have published data on baboon (<em>Papio</em>) spp. parasite communities. The first tab '2023_Helminths_PrevData' are a list of the macroparasites that have been reported. The second tab '2023_Protozoa_PrevData' are a list of the macroparasites that have been reported. For both these sheets, '1' indicates that a parasite is present, and '0' indicates that a parasite species was not recorded at that study site.</p> <p>The data provided here are collated from all published journal articles and degree theses on baboon parasites up the start of 2023. A list of the publications that contributed are provided in the reference information. </p>
Data from: Mitochondrial genomes of Australian chicken Eimeria support the presence of ten species with low genetic diversity among strains
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
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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.