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539 results for “disentangling”
Supplementary material 1 from: Lefort M, Wratten S, Cusumano A, Varennes Y, Boyer S (2017) Disentangling higher trophic level interactions in the cabbage aphid food web using high-throughput DNA sequencing. Metabarcoding and Metagenomics 1: e13709. https://doi.org/10.3897/mbmg.1.13709
OSR aphid mummy collection. Sampling location and size / Amplification success of mummies' DNA extracts by Illumina sequencing.
Disentangling forced trends in the North Atlantic jet from natural variability using deep learning
<p>Code used to train the LLAE to obtain forced trends in the North Atlantic jet stream and to produce plots.</p>
Delayed dichromatism as a convenient tool to disentangle the effects of survival and productivity on the population dynamics in waterfowl
<p>Data and R codes necessary to replicate the analyses presented in the paper entitled "Delayed dichromatism as a convenient tool to disentangle the effects of survival and productivity on the population dynamics in waterfowl", submitted for review in Peer Community in Ecology.</p>
Disentangling drivers of mudflat intertidal DOM chemodiversity using ecological models
<p><span><span>Microorganisms consume and transform dissolved organic matter (DOM) into various forms.</span></span><span><span> </span><span>However, it remains unclear whether the ecological patterns and drivers of DOM chemodiversity are analogous to those of microbial communities. </span></span><span>Here, a large-scale investigation was conducted along the Chinese coasts to resolve </span><span>the intrinsic linkages among the complex intertidal DOM pools, microbial communities and environmental heterogeneity</span><span>. The abundance of DOM molecular formulae best fitted log-normal distribution and followed Taylor’s Law. </span><span>Distance-decay relationships were observed for labile molecular formulae, while latitudinal diversity gradients were noted for recalcitrant molecular formulae.</span><span> </span><span>Latitudinal patterns were also observed for DOM molecular features. </span><span>Negative cohesion, bacterial diversity, and molecular traits were the main drivers of DOM chemodiversity. Stochasticity analyses demonstrated that determinism dominantly shaped the DOM compositional variations. This study unveils the intrinsic mechanisms underlying the intertidal DOM chemodiversity and microbial communities from ecological perspectives, deepening our understanding of microbially driven chemical ecology.</span></p>
Disentangling Heat-or-Eat Dilemma: Data and Code
<p>Data and code used to conduct research about the risk of energy poverty, particularly on the heat-or-eat dilemma.</p> <p>"_Metadata" files contain all needed info to read and run the respective code and data to reproduce authors' results and conduct research on the topic.</p> <p> </p>
Fig. 6 in Disentangling morphological variation in metapodials of giraffids: Modern and traditional approaches
Fig. 6 Shape variation grids illustrating the extreme values of PC1 for the metacarpals a and the metatarsals b. For both skeletal elements, extreme positive PC1 values depict robust metapodials, whereas extreme negative PC1 values depict gracile ones
Fig. 4 in Disentangling morphological variation in metapodials of giraffids: Modern and traditional approaches
Fig. 4 PC1 vs. PC2 scatter plots of the results of the geometric morphometrics with projected phylogeny analysis for the metacarpals a and the metatarsals b
Fig. 3 in Disentangling morphological variation in metapodials of giraffids: Modern and traditional approaches
Fig. 3 PC1 vs. PC2 scatter plots of the results of the geometric morphometrics analysis for the metacarpals a and the metatarsals b
FIGURE 1 in Disentangling Astraea lobata: three new names in Astraea based on previous varieties of Croton lobatus (Euphorbiaceae)
FIGURE 1. Morphological characters of Astraea digitata, A. gracilis and A. manihot. A–D: Astraea digitata. A. abaxial surface of leaf, B. pistillate flowers, C. immature fruit, D. cymules with staminate flowers in bud. E–I: Astraea gracilis. E. herborized branch with inflorescences, F. abaxial surface of herborized leaf, G. staminate cymule, H. pistillate flower, I. herborized inflorescences with immature fruit. J–N: Astraea manihot. J. habit with inflorescences, K. abaxial surface of leaf, L. pistillate flower, M. staminate cymules with one mature flower, N. immature fruits with mature staminate flowers. Photos: O.L.M. Silva.
FIGURE 12. A in Disentangling the diversity and taxonomy of Hymenophyllaceae (Hymenophyllales, Polypodiidae) in the Mascarene archipelago, with ecological implications
FIGURE 12. A. Didymoglossum barklyanum (Baker) J.P.Roux, as lithophyte (Mauritius, 'Vallée d'Osterlog'). B. D. lorencei (Tardieu) Ebihara & Dubuisson, as lithophyte (La Réunion, 'Grand Etang'). C. D. lorencei, detail of frond with marginal trichomes (photographs. A–C: J.-Y. Dubuisson; D: J.-M. Tamon).
FIGURE 15. A in Disentangling the diversity and taxonomy of Hymenophyllaceae (Hymenophyllales, Polypodiidae) in the Mascarene archipelago, with ecological implications
FIGURE 15. A. Hymenophyllum capillare Desv., typical form, as epiphyte (La Réunion, 'Forêt de Bon Accueil, Les Makes'). B. H. capillare, typical form, detail of fronds. C. H. capillare f. nanum Hennequin & Dubuisson, f. nov., as epiphyte (La Réunion, 'Pitons Mare à Boue'). D. H. capillare f. nanum, habit, type individual, scale = 0.5 cm (La Réunion, 'Forêt de Bon Accueil, Les Makes', J.-Y. Dubuisson & L. Bauret HR 2016-10, P). E. H. digitatum (Sw.) Forsberg, as epiphyte (La Réunion, 'Forêt de Bon Accueil, Les Makes'). F. H. digitatum, detail of laminar margin showing minute dark trichomes. G. H. digitatum, detail of fronds and sori with tubular bases (s) (photographs. A–B: L. Bauret; C–G: J.-Y. Dubuisson).
FIGURE 9. A in Disentangling the diversity and taxonomy of Hymenophyllaceae (Hymenophyllales, Polypodiidae) in the Mascarene archipelago, with ecological implications
FIGURE 9. A. Crepidomanes fallax (Christ) Ebihara & Dubuisson, as lithophyte on wet rock (La Réunion, 'Rivière des Marsouins'). B. C. fallax, habit (from Madagascar, F. Rakotondrainibe 6467, P00248564). C. C. frappieri (Cordem.) J.P.Roux, covering a rock in a wet ravine (La Réunion, 'Ravine Rivière Ste Anne'). D. C. frappieri, habit, type specimen (Bédier s.n., P00477825). E. C. frappieri, detail of long branched rhizome trichomes. F. C. frappieri, detail of sori (photographs. A, C & F: J.-M. Tamon).
FIGURE 18. A in Disentangling the diversity and taxonomy of Hymenophyllaceae (Hymenophyllales, Polypodiidae) in the Mascarene archipelago, with ecological implications
FIGURE 18. A. Polyphlebium diaphanum (Kunth) Ebihara & Dubuisson, as epiphyte (La Réunion, 'Forêt de Bon Accueil, Les Makes'). B. P. diaphanum, detail of a frond and sori. C. Vandenboschia gigantea (Bory ex Willd.) Pic.Serm., climbing on a tree trunk (La Réunion, 'Mare Longue'). D. V. gigantea, terrestrial parts (La Réunion, 'Grand Etang'). E. V. gigantea, detail of a long-creeping climbing rhizome (photographs. A: L. Bauret; B–E: J.-Y. Dubuisson).
FIGURE 19 in Disentangling the diversity and taxonomy of Hymenophyllaceae (Hymenophyllales, Polypodiidae) in the Mascarene archipelago, with ecological implications
FIGURE 19. Importance of gametophyte ecology and biology for the sporophyte settlement on distant islands according to Dassler & Farrar's (2001) hypothesis. The long-lived and colonial epiphytic gametophytes (above) would have the possibilities to realize fertilization many seasons/years (T) after the spore germination, whereas short-lived and non-colonial terrestrial gametophytes (below) would fail in realizing the fertilization if they are not close enough, and die at the end of the season (red crosses). Hence, the epiphytic taxa with longlived and colonial gametophytes would have a higher probability of establishment than terrestrial taxa. Hymenophyllaceae and the genus Ctenitis (Dryopteridaceae) illustrate such contrasts in the Mascarene archipelago, explaining the difference in the level of endemicity (see text for an in-depth discussion).
FIGURE 7 in Disentangling the diversity and taxonomy of Hymenophyllaceae (Hymenophyllales, Polypodiidae) in the Mascarene archipelago, with ecological implications
FIGURE 7. Abrodictyum tamarisciforme (Jacq.) Ebihara & Dubuisson. A. A dense population of many individuals covering a trunk (La Réunion, 'Grand Etang'). B. Single individual as epiphytic on a tree-fern trunk, which is also covered here by Didymoglossum cuspidatum (La Réunion, 'Mare Longue'). C. Lithophytic individual, the little individual at the bottom right is A. parviflorum (Poir.) Bauret & Dubuisson (La Réunion, 'Grand Etang'). D. Detail of segments with typical distinct marginal row of cells (mc) (photographs. A, C: J.-Y. Dubuisson; B: C. Chaussidon; D: L. Bauret).
FIGURE 6 in Disentangling the diversity and taxonomy of Hymenophyllaceae (Hymenophyllales, Polypodiidae) in the Mascarene archipelago, with ecological implications
FIGURE 6. Abrodictyum parviflorum (Poir.) Bauret & Dubuisson. A. typical habit, here as terrestrial (La Réunion, 'Mare Longue'). B. Brush-like 'meifolium' form (La Réunion, 'Grand Etang'). C. Plane 'parviflorum' form (La Réunion, 'Grand Etang'). D. Detail of subcapillary ultimate segments and sori (photographs. A: C. Chaussidon; B, D: L. Bauret; C: J.-Y. Dubuisson).
FIGURE 5 in Disentangling the diversity and taxonomy of Hymenophyllaceae (Hymenophyllales, Polypodiidae) in the Mascarene archipelago, with ecological implications
FIGURE 5. Distribution of Hymenophyllaceae species richness in relation to elevations, here on the windward side of La Réunion and on Mauritius (data are reported in Appendices 1 & 2). The range of each taxon is assumed to correspond to the range between the minimum and the maximum elevation at which they have been observed, even if the taxon has not been observed in all intermediate localities between such limits.
FIGURE 14. A in Disentangling the diversity and taxonomy of Hymenophyllaceae (Hymenophyllales, Polypodiidae) in the Mascarene archipelago, with ecological implications
FIGURE 14. A. Hymenophyllum fumarioides Bory ex. Willd, as epiphyte (La Réunion, 'Mare Longue'). B. H. fumarioides, detail of curled/crisped segments and sori with toothed margins. C. H. peltatum (Poir.) Desv., as epiphyte (La Réunion, 'Pitons Mare à Boue'). D. H. peltatum, detail of toothed/serrulate laminar margins. E. H. sibthorpioides (Bory ex Willd.) Mett. ex Kuhn, as epiphytic (La Réunion, 'Vallée Heureuse'). F. H. sibthorpioides, fertile frond and sori with toothed margins (photographs. A, E: C. Chaussidon; B, F: L. Bauret; C: J.-Y. Dubuisson; D: J.-M. Tamon).
FIGURE 4. Mauritian ecosystems. A in Disentangling the diversity and taxonomy of Hymenophyllaceae (Hymenophyllales, Polypodiidae) in the Mascarene archipelago, with ecological implications
FIGURE 4. Mauritian ecosystems. A. Lowland Sapotaceae rainforest, here invaded by the exotic Malagasy traveller's trees Ravenala madagascariensis (Strelitziaceae) ('Vallée d'Osterlog' forest, ~260 m). B. 'Pétrin' locality showing particular habitat with thickets of the endemic Erica brachyphylla (Ericaceae) (~670 m) (photographs by J.-Y. Dubuisson).
FIGURE 11 in Disentangling the diversity and taxonomy of Hymenophyllaceae (Hymenophyllales, Polypodiidae) in the Mascarene archipelago, with ecological implications
FIGURE 11. Crepidomanes trinerve (Baker) Dubuisson & Ebihara. A. As lithophyte in a wet ravine of the western side of La Réunion ('Les Canots'; photograph by J.-M. Tamon). B. Habit (from Comores, F. Rakotondrainibe 6651, P00310478; modified from Dubuisson et al. 2013).
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