371 results on '"Escudero, Marcial"'
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2. Convergent evolutionary patterns of heterostyly across angiosperms support the pollination-precision hypothesis
3. Phylogenomics and the rise of the angiosperms
4. Genome constitution and evolution of Elymus atratus (Poaceae: Triticeae) inferred from cytogenetic and phylogenetic analysis
5. Chromosomal evolution in Cryptangieae Benth. (Cyperaceae): Evidence of holocentrism and pseudomonads
6. Phylogenetic, cytogenetic and morphological evidences are critical for recognizing a new genus: Valdesiana, an Iberian intergeneric allopolyploid between Schenkia and Exaculum
7. Sierra Nevada, a Mediterranean Biodiversity Super Hotspot
8. A holocentric twist to chromosomal speciation?
9. Spatial patterns of genus-level phylogenetic endemism in the tree flora of Mediterranean Europe
10. Genomic hotspots of chromosome rearrangements explain conserved synteny despite high rates of chromosome evolution in a holocentric lineage.
11. The holocentric chromosome microevolution: From phylogeographic patterns to genomic associations with environmental gradients.
12. Holocentric repeat landscapes: From micro‐evolutionary patterns to macro‐evolutionary associations with karyotype evolution.
13. The grand sweep of chromosomal evolution in angiosperms
14. Isolation and characterization of microsatellites markers in Centaurium grandiflorum ssp. boissieri
15. Cladogenesis
16. Polyploidy and hybridization in the Mediterranean: unravelling the evolutionary history of Centaurium (Gentianaceae).
17. Chorological and nomenclatural notes on Peruvian Carex (Cyperaceae)
18. Author Correction: WOODIV, a database of occurrences, functional traits, and phylogenetic data for all Euro-Mediterranean trees
19. WOODIV, a database of occurrences, functional traits, and phylogenetic data for all Euro-Mediterranean trees
20. Inferring hypothesis-based transitions in clade-specific models of chromosome number evolution in sedges (Cyperaceae)
21. Founder events and subsequent genetic bottlenecks underlie karyotype evolution in the Ibero-North African endemic Carex helodes.
22. Global analysis of Poales diversification – parallel evolution in space and time into open and closed habitats
23. Vicariance versus dispersal across Beringian land bridges to explain circumpolar distribution: A case study in plants with high dispersal potential
24. Niche shifts after long-distance dispersal events in bipolar sedges ( Carex , Cyperaceae)
25. Bipolar distributions in vascular plants : A review
26. Long-distance dispersal explains the bipolar disjunction in Carex macloviana
27. The holocentric chromosome microevolution: From phylogeographic patterns to genomic associations with environmental gradients
28. Global analysis of Poales diversification - parallel evolution in space and time into open and closed habitats
29. Detecting shifts in the mode of chromosomal speciation across the cosmopolitan plant lineageCarex
30. Holocentric repeat landscapes: From micro‐evolutionary patterns to macro‐evolutionary associations with karyotype evolution
31. Global analysis of Poales diversification – parallel evolution in space and time into open and closed habitats.
32. Founder events and subsequent genetic bottlenecks underlie karyotype evolution in the Ibero-North African endemic Carex helodes
33. The holocentric chromosome microevolution: from phylogeographic patterns to genomic associations with environmental gradients
34. Chromosomal rearrangements in holocentric organisms lead to reproductive isolation by hybrid dysfunction: The correlation between karyotype rearrangements and germination rates in sedges
35. Specimens at the Center: An Informatics Workflow and Toolkit for Specimen-level analysis of Public DNA database data
36. Megaphylogenetic Specimen-level Approaches to the Carex (Cyperaceae) Phylogeny Using ITS, ETS, and matK Sequences: Implications for Classification
37. The Phylogenetic Origins and Evolutionary History of Holocentric Chromosomes
38. Carex camposii subsp. tejedensis (Cyperaceae), a new taxon for Southern Iberian Peninsula based on molecular, morphological and ecological differentiation.
39. A non‐homogeneous model of chromosome‐number evolution to reveal shifts in the transition patterns across the phylogeny
40. Highly conserved synteny despite massive chromosome fusion and fission suggest fragile sites in holocentric plants
41. Addressing inconsistencies in Cyperaceae and Juncaceae taxonomy: Comment on Brožová et al. (2022)
42. Long-distance dispersal during the middle—late Pleistocene explains the bipolar disjunction of Carex maritima (Cyperaceae)
43. Direct long-distance dispersal best explains the bipolar distribution of Carex arctogena (Carex sect. Capituligerae, Cyperaceae)
44. Phylogeny, systematics, and trait evolution of Corex section Glareosae
45. Phylogenetic congruence of parasitic smut fungi (Anthracoidea, Anthracoideaceae) and their host plants (Carex, Cyperaceae): Cospeciation or host-shift speciation?
46. Genome size stability despite high chromosome number variation in Carex gr. laevigata
47. Karyotypic diversity: a neglected trait to explain angiosperm diversification?
48. Carex camposii subsp. tejedensis (Cyperaceae), a new taxon for Southern Iberian Peninsula based on molecular, morphological and ecological differentiation.
49. Chromosome size matters: genome evolution in the cyperid clade
50. Genotyping-by-sequencing as a tool to infer phylogeny and ancestral hybridization: A case study in Carex (Cyperaceae)
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