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Aim Many subtropical organisms exhibit an East Asian‐Tethyan disjunction, a distribution split between East Asia and the Mediterranean. The underlying mechanisms and timing have remained unclear to date. The evolutionary history of Quercus section Ilex Loudon, a representative East Asian‐Tethyan disjunct lineage with a rich and widespread fossil record, was investigated to understand the key drivers of this disjunction. Location Eurasia. Methods The phylogeny of Quercus section Ilex was reconstructed using RAD‐seq. Divergence times were estimated based on three fossil calibrations. Ancestral range and niche were reconstructed on the calibrated tree to infer the timing of transitions in geographic distributions and niche. Convergence in ecological space was estimated by fitting alternative multiple‐regime Ornstein‐Uhlenbeck models. Leaf shape affinities among extant and fossil taxa of section Ilex were assessed using geometric morphometric approaches. Results Six clades were well resolved in section Ilex. Ancestral range reconstruction and divergence time dating suggest a wide distribution along the East Tethys seaway, with initial divergence at the mid‐Eocene, and all six clades originating before the Miocene. The section dispersed from East Asia to the Mediterranean at the Eocene‐Oligocene boundary. A shift toward higher elevations was detected in the Himalayan clade during the middle or late Miocene. European fossil lineages during the early Miocene differ in leaf morphology from later lineages, which we infer to be a consequence of adaptive differentiation or species turnover. Main conclusions Quercus section Ilex was widespread along the East Tethys seaway from the middle Eocene onward. The European holly oaks originated from an East Asian ancestral lineage that dispersed to Europe via the Tibet‐Himalaya corridor in the Oligocene. Lowlands along the margins of the Himalayas and through an Oligocene Tibetan valley served as the dispersal route(s) for these species. Changing climates drove Miocene extinction and local adaptation of European lineages.

Within the Field and lab work strategy subsection, information regarding two samples from the study is incorrect. Individual 1 and individual 2 from la Zaida were collected by S. López and C. Fabregat (20-08-2014) and the samples are herbarium specimens obtained from the Jardí Botànic de la Universitat de València (VAL-221325).

Valvular heart disease is a leading cause of cardiovascular morbidity and mortality and a major contributor of symptoms and functional disability. Knowledge of valvular heart disease epidemiology and a deep comprehension of the geographical and temporal trends are crucial for clinical advances and the formulation of effective health policy for primary and secondary prevention. This review mainly focuses on the epidemiology of primary (organic, related to the valve itself) valvular disease and its management, especially emphasizing the importance of heart valve centers in ensuring the best care of patients through a multidisciplinary team.

Aim The biogeographical and habitat history of the species‐rich angiosperm genus Artabotrys is reconstructed to assess hypotheses relating to processes that underlie palaeotropical intercontinental disjunction (PID) and regional diversification patterns. Location Palaeotropics. Taxon Artabotrys (Annonaceae). Methods Phylogenetic relationships were estimated based on 53 Artabotrys species, using four chloroplast and 10 nuclear markers (c. 15.7 kb). Divergence times were estimated using two fossil calibrations and an uncorrelated lognormal relaxed clock model. Ancestral range estimation was performed under a dispersal–extinction–cladogenesis model while ancestral habitat reconstruction was conducted using the BAYAREALIKE model. Results Artabotrys is unequivocally monophyletic, with a species‐rich main Artabotrys clade (MAC) comprising distinct African and Asian sister clades, and an early divergent grade (EDG) comprising two African species. An ancestral range in Africa is inferred, with a single dispersal to Asia. The PID at the MAC crown occurred in the Miocene. A broad habitat tolerance spanning rain forests and seasonally dry forests/savannas was inferred at the MAC stem and crown nodes. Several shifts from rain forests to seasonally dry habitats were inferred, but there is no indication of a reverse transition. Main conclusions The most plausible explanation for the PID involves overland migration across Arabia in the Miocene, prior to subsequent climate deterioration. Long‐standing differences in climatic niche may have resulted in a significant yet porous biogeographical divide at the Isthmus of Kra, but Wallace's line does not reflect differences in climatic niches. Niche conservatism is an underlying pattern in Artabotrys, with local niche shifts occurring rather recently.

Carya , in the Juglandiodeae subfamily, is to a typical temperate-subtropical forest-tree genus for studying the phylogenetic evolution and intercontinental disjunction between eastern Asia (EA) and North America (NA). Species of the genus have high economic values worldwide for their high-quality wood and the rich healthy factors of their nuts. Although previous efforts based on multiple molecular markers or genome-wide SNPs supported the monophyly of Carya and its two EA and NA major subclades, the maternal phylogeny of Carya still need to be comprehensively evaluated. The variation of Carya plastome has never been thoroughly characterized. Here, we novelly present 19 newly generated plastomes of congeneric Carya species, including the recently rediscovered critically endangered C. poilanei . The overall assessment of plastomes revealed highly conservative in the general structures. Our results indicated that remarkable differences in several plastome features are highly consistent with the EA-NA disjunction and showed the relatively diverse matrilineal sources among EA Carya compared to NA Carya . The maternal phylogenies were conducted with different plastome regions and full-length plastome datasets from 30 plastomes, representing 26 species in six genera of Juglandoideae and Myrica rubra (as root). Six out of seven phylogenetic topologies strongly supported the previously reported relationships among genera of Juglandoideae and the two subclades of EA and NA Carya , but displayed significant incongruencies between species within the EA and NA subclades. The phylogenetic tree generated from full-length plastomes demonstrated the optimal topology and revealed significant geographical maternal relationships among Carya species, especially for EA Carya within overlapping distribution areas. The full-length plastome-based phylogenetic topology also strongly supported the taxonomic status of five controversial species as separate species of Carya . Historical and recent introgressive hybridization and plastid captures might contribute to plastome geographic patterns and inconsistencies between topologies built from different datasets, while incomplete lineage sorting could account for the discordance between maternal topology and the previous nuclear genome data-based phylogeny. Our findings highlight full-length plastomes as an ideal tool for exploring maternal relationships among the subclades of Carya , and potentially in other outcrossing perennial woody plants, for resolving plastome phylogenetic relationships.

If we go through the literature, one can find many matrices that are derived for a given simple graph. The one among them is the anti-adjacency matrix which is given as follows; The anti-adjacency matrix of a simple undirected graph $G$ with vertex set   $V (G) \\,= \\,\\{\\,v_1,\\,v_2,\\\ \\dots, v_n\\}$   is an $n \\times n$ matrix $B(G) = (b_{ij} )$, where $b_{ij} = 0$ if there exists an edge between $v_i$ and $v_j$ and $1$ otherwise. In this paper, we try to bring out an expression, which establishes a connection between the anti-adjacency matrices of the two graphs $G_1$ and $G_2$ and the   anti-adjacency matrix of their tensor product, $G_1 \\otimes G_2$. In addition, an expression for the anti-adjacency matrix of the disjunction of two graphs, $G_1\\lor G_2$, is obtained in a similar way. Finally, we obtain an expression for the anti-adjacency matrix for the generalized tensor product and generalized disjunction of two graphs.  Adjacency and anti-adjacency matrices are square matrices that are used to represent a finite graph in graph theory and computer science. The matrix elements show whether a pair of vertices in the graph are adjacent or not.

The liquorice genus, Glycyrrhiza L. (Leguminosae), is a medicinal herb with great economic importance and an intriguing intercontinental disjunct distribution in Eurasia, North Africa, the Americas, and Australia. Glycyrrhiza , along with Glycyrrhizopsis Boiss. and Meristotropis Fisch. & C.A.Mey., comprise Glycyrrhiza s.l. Here we reconstructed the phylogenetic relationships and biogeographic history in Glycyrrhiza s.l. using sequence data of whole chloroplast genomes. We found that Glycyrrhiza s.l. is sister to the tribe Wisterieae and is divided into four main clades. Clade I, corresponds to Glycyrrhizopsis and is sister to Glycyrrhiza sensu Meng. Meristotropis is embedded within Glycyrrhiza sensu Meng, and these two genera together form Clades II–IV. Based on biogeographic analyses and divergence time dating, Glycyrrhiza s.l. originated during the late Eocene and its most recent common ancestor (MRCA) was distributed in the interior of Eurasia and the circum-Mediterranean region. A vicariance event, which was possibly a response to the uplifting of the Turkish-Iranian Plateau, may have driven the divergence between Glycyrrhiza sensu Meng and Glycyrrhizopsis in the Middle Miocene. The third and fourth main uplift events of the Qinghai-Tibetan Plateau may have led to rapid evolutionary diversification within Glycyrrhiza sensu Meng. Subsequently, the MRCA of Clade II might have migrated to North America ( G. lepidota ) via the Bering land bridge during the early Pliocene, and reached temperate South America ( G. astragalina ) by long-distance dispersal (LDD). Within Clade III, the ancestor of G. acanthocarpa arrived at southern Australia through LDD after the late Pliocene, whereas all other species (the SPEY clade) migrated to the interior of Eurasia and the Mediterranean region in the early Pleistocene. The MRCA of Clade IV was restricted in the interior of Eurasia, but its descendants have become widespread in temperate regions of the Old World Northern Hemisphere during the last million years.

Aim: Arctic plant phylogeography has largely focused on seed plants, and studies on other plant groups are necessary for comparison. Bryophytes have a unique life cycle and can be resistant to extreme conditions, suggesting that their phylogeographic patterns may differ from those of vascular plants. We address the history of the bryophyte genus Cinclidium in order to assess: (1) interspecific relationships, (2) whether its current broad circumarctic distribution results from recent dispersal or has been maintained by long-term local survival under severe glacial conditions, and (3) the origin of its bipolar disjunction. Location: Arctic/boreal and bipolar. Methods: We sequenced three plastid regions (atpH-atpl, rpl32-trnL and clpP1.1–clpP1.2) in 129 accessions covering the entire geographical range of all four described species, and inferred phylogenetic relationships and phylogeographical patterns using maximum parsimony, statistical parsimony and Bayesian inference. Results: Cinclidium subrotundum was inferred to be monophyletic, in agreement with its distinct morphology and ecology. The three remaining known species (the haploids C. latifolium and C. arcticum, and the diploid C. stygium) shared a number of closely related or identical haplotypes despite their clear morphological differentiation. In all species, identical haplotypes occurred across the entire circumpolar region, including North Atlantic islands. In the bipolar species C. stygium, the haplotype observed in South America (Tierra del Fuego) was identical to one found in Iceland. Three populations originally referred to C. latifolium harboured highly divergent haplotypes and may represent a new species. Main conclusions: The extensive haplotype sharing suggests a polyploid origin of C. stygium from C. arcticum, as well as incomplete lineage sorting and/or hybridization between the two haploids C. arcticum and C. latifolium. We interpret the finding of identical haplotypes over vast areas, including isolated islands, as a result of recent dispersal causing the circumpolar distribution of all species in the Northern Hemisphere and the extreme bipolar disjunction in C. stygium. The patterns in the bryophyte genus Cinclidium resemble those previously documented in arctic-alpine and bipolar vascular plants, suggesting that similar mechanisms have shaped species distributions in bryophytes and higher plants.

Mitral annular disjunction (MAD) is routinely diagnosed by cardiac imaging, mostly by echocardiography, and shown to be a risk factor for ventricular arrhythmias. While MAD is associated with mitral valve (MV) prolapse (MVP), it is unknown which patients with MAD are at higher risk and which additional imaging features may help identify them. The value of cardiac computed tomography (CCT) for the diagnosis of MAD is unknown. Accordingly, we aimed to: (1) develop a standardized CCT approach to identify MAD in patients with MVP and severe mitral regurgitation (MR); (2) determine its prevalence and identify features that are associated with MAD in this population. We retrospectively studied 90 patients (age 63 ± 12 years) with MVP and severe MR, who had pre-operative CCT (256-slice scanner) of sufficient quality for analysis. The presence and degree of MAD was assessed by rotating the view plane around the MV center to visualize disjunction along the annulus. Additionally, detailed measurements of MV apparatus and left heart chambers were performed. Univariate logistic regression analysis was performed to determine which parameters were associated with MAD. MAD was identified in 18 patients (20%), and it was typically located adjacent to a prolapsed or flail mitral leaflet scallop. Of these patients, 75% had maximum MAD distance > 4.8 mm and 90% > 3.8 mm. Female gender was most strongly associated with MAD (p = 0.04). Additionally, smaller end-diastolic mitral annulus area (p = 0.045) and longer posterior leaflet (p = 0.03) were associated with greater MAD. No association was seen between MAD and left ventricular size and function, left atrial size, and papillary muscle geometry. CCT can be used to readily detect MAD, by taking advantage of the 3D nature of this modality. A significant portion of MVP patients referred for mitral valve repair have MAD. The presence of MAD is associated with female gender, smaller annulus size and greater posterior leaflet length.