Complex polyploid and hybrid species in an apomictic and sexual tropical forage grass group: genomic composition and evolution in Urochloa (Brachiaria) species

Background and Aims Diploid and polyploid Urochloa (including Brachiaria, Panicum and Megathyrsus species) C-4 tropical forage grasses originating from Africa are important for food security and the environment, often being planted in marginal lands worldwide. We aimed to characterize the nature of their genomes, the repetitive DNA and the genome composition of polyploids, leading to a model of the evolutionary pathways within the group including many apomictic species. Methods Some 362 forage grass accessions from international germplasm collections were studied, and ploidy was determined using an optimized flow cytometry method. Whole-genome survey sequencing and molecular cytogenetic analysis were used to identify chromosomes and genomes in Urochloa accessions belonging to the 'brizantha' and 'humidicola' agamic complexes and U. maxima. Key Results Genome structures are complex and variable, with multiple ploidies and genome compositions within the species, and no clear geographical patterns. Sequence analysis of nine diploid and polyploid accessions enabled identification of abundant genome-specific repetitive DNA motifs. In situ hybridization with a combination of repetitive DNA and genomic DNA probes identified evolutionary divergence and allowed us to discriminate the different genomes present in polyploids. Conclusions We suggest a new coherent nomenclature for the genomes present. We develop a model of evolution at the whole-genome level in diploid and polyploid accessions showing processes of grass evolution. We support the retention of narrow species concepts for Urochloa brizantha, U. decumbens and U. ruziziensis, and do not consider diploids and polyploids of single species as cytotypes. The results and model will be valuable in making rational choices of parents for new hybrids, assist in use of the germplasm for breeding and selection of Urochloa with improved sustainability and agronomic potential, and assist in measuring and conserving biodiversity in grasslands

Inequality in plant diversity knowledge and unrecorded plant extinctions: An example from the grasses of Madagascar

Societal impact statement Plants are essential for all life, providing the infrastructure and energy for our ecosystems. A recent report indicates that more than 500 plant species are already presumed extinct and many more could have been lost without anyone being aware, especially in species‐rich areas with high levels of human impact, and where botanical knowledge is poor. Inequality in the availability and accessibility of biodiversity data, professional expertise, and funding interact to produce chronic differences in knowledge between countries. Here, we illustrate this using an example from Madagascar. Understanding these knowledge inequalities will strengthen our ability to improve the situation for people as well as for plants. Summary In order to understand geographic differences in our knowledge of plant extinction, species occurrence knowledge is compared for the grasses (Poaceae) of Madagascar and the British Isles. Poaceae are a useful model system for exploring extinction because they are globally diverse and present interesting characteristics compared with plants as a whole: grasses have a similar species description curve and percentage assessed as threatened, but they have broader and more continental distribution ranges. Historical and current factors affecting the documentation of the Malagasy and British floras are reviewed with regard to science funding, human capital, accessibility, and existing records. Knowledge of Poaceae is compared in the light of these constraints. Global patterns of grass diversity are examined and future extinction rates for Malagasy grasses are estimated. Multiple factors interact to shape a set of constraints on species distribution knowledge. The flora of Madagascar has been described largely by foreigners, science funding is external, and Malagasy botanists face difficult challenges. Spatial data for Madagascar are more limited and less even. We demonstrate that unrecorded extinctions are more likely among Malagasy than British and Irish grasses: they were described later, have smaller ranges, and are more threatened. It is possible that extinction rates of Malagasy grasses will increase tenfold in the next century. Differences in our knowledge of the Malagasy and British floras are long‐standing, deep, and perpetuated by numerous modern‐day factors. We urge researchers to understand and acknowledge these differences, and we provide recommendations for future work

Phylogenomics and the rise of the angiosperms

Angiosperms are the cornerstone of most terrestrial ecosystems and human livelihoods1,2. A robust understanding of angiosperm evolution is required to explain their rise to ecological dominance. So far, the angiosperm tree of life has been determined primarily by means of analyses of the plastid genome3,4. Many studies have drawn on this foundational work, such as classification and first insights into angiosperm diversification since their Mesozoic origins5,6,7. However, the limited and biased sampling of both taxa and genomes undermines confidence in the tree and its implications. Here, we build the tree of life for almost 8,000 (about 60%) angiosperm genera using a standardized set of 353 nuclear genes8. This 15-fold increase in genus-level sampling relative to comparable nuclear studies9 provides a critical test of earlier results and brings notable change to key groups, especially in rosids, while substantiating many previously predicted relationships. Scaling this tree to time using 200 fossils, we discovered that early angiosperm evolution was characterized by high gene tree conflict and explosive diversification, giving rise to more than 80% of extant angiosperm orders. Steady diversification ensued through the remaining Mesozoic Era until rates resurged in the Cenozoic Era, concurrent with decreasing global temperatures and tightly linked with gene tree conflict. Taken together, our extensive sampling combined with advanced phylogenomic methods shows the deep history and full complexity in the evolution of a megadiverse clade

Phylogenomics and the rise of the angiosperms.

Angiosperms are the cornerstone of most terrestrial ecosystems and human livelihoods1,2. A robust understanding of angiosperm evolution is required to explain their rise to ecological dominance. So far, the angiosperm tree of life has been determined primarily by means of analyses of the plastid genome3,4. Many studies have drawn on this foundational work, such as classification and first insights into angiosperm diversification since their Mesozoic origins5-7. However, the limited and biased sampling of both taxa and genomes undermines confidence in the tree and its implications. Here, we build the tree of life for almost 8,000 (about 60%) angiosperm genera using a standardized set of 353 nuclear genes8. This 15-fold increase in genus-level sampling relative to comparable nuclear studies9 provides a critical test of earlier results and brings notable change to key groups, especially in rosids, while substantiating many previously predicted relationships. Scaling this tree to time using 200 fossils, we discovered that early angiosperm evolution was characterized by high gene tree conflict and explosive diversification, giving rise to more than 80% of extant angiosperm orders. Steady diversification ensued through the remaining Mesozoic Era until rates resurged in the Cenozoic Era, concurrent with decreasing global temperatures and tightly linked with gene tree conflict. Taken together, our extensive sampling combined with advanced phylogenomic methods shows the deep history and full complexity in the evolution of a megadiverse clade