Sarah Z. Ficinski’s research while affiliated with Royal Botanic Gardens, Kew and other places

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Publications (8)


Figure 1: Phylogeny of 1,153 Poaceae accessions inferred from 331 nuclear genes, including paralogs, using a multi-species coalescent approach. Branch colours reflect local posterior support for the quartet configuration displayed. Hollow circles indicate supported conflict among nuclear gene trees at 48 internal branches, where two alternative quartet configurations each have >1/3 local posterior support. Subfamilies and larger tribes (abbreviated) are labelled according to the most recent Poaceae classification (Soreng et al., 2022). The coloured lines link taxonomic outliers at tribe to subfamily level to their nominal taxa. Silhouettes show representatives for large subfamilies (from top): Maize or corn, Zea mays (Panicoideae); Dactyloctenium radulans (Chloridoideae); oat, Avena sativa (Pooideae); Bambusa textilis (Bambudoideae); rice, Oryza sativa (Oryzoideae). See Fig. S5 for a detailed version of the tree.
Figure 3: Comparison of nuclear and plastome topologies for the Poaceae. The 1,153-tip nuclear tree is shown on the left, the 910-tip plastome tree on the right. Plastome support (transfer bootstrap expectation, TBE) was summarised for branches present in both trees (814 shared species). Grey branches in the nuclear tree had no equivalent for comparison in the plastome tree. Hollow circles indicate strong signals of conflict, i.e. high support in the nuclear tree (local posterior probability > 0.8) but poor support (TBE < 0.3) in the plastome tree. Tribes are matched between the two in both trees, and larger tribes are labelled for orientation. The inset plots plastome support against a measure of conflict between nuclear gene trees (local posterior support for the second-most supported quartet per branch), which are negatively correlated. The blue line is a simple linear trend line.
Taxonomic discrepancies in the nuclear tree at subfamily to tribe level. Taxa listed here will need follow-up studies to validate their placement. An asterisk (*) denotes genera whose type species was sampled.
Nuclear phylogenomics of grasses (Poaceae) supports current classification and reveals repeated reticulation
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May 2024

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Grasses (Poaceae) comprise around 11,800 species and are central for human livelihoods and terrestrial ecosystems. Knowing their relationships and evolutionary history is key to comparative research and crop breeding. Advances in genome-scale sequencing allow for increased breadth and depth of phylogenomic analyses, making it possible to infer a new reference species tree of the family. We inferred a comprehensive species tree of grasses by combining new and published sequences for 331 nuclear genes from genome, transcriptome, target enrichment and shotgun data. Our 1,153-tip tree covers 79% of grass genera (including 21 genera sequenced for the first time) and all but two small tribes. We compared it to a 910-tip plastome tree. The nuclear phylogeny matches that of the plastome at most deep branches, with only a few instances of incongruence. Gene tree–species tree reconciliation suggests that reticulation events occurred repeatedly in the history of grasses. We provide a robust framework for the grass tree of life to support research on grass evolution, including modes of reticulation, and genetic diversity for sustainable agriculture.

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Phylogenomics and the rise of the angiosperms

April 2024

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3,801 Reads

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56 Citations

Nature

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.


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

December 2021

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221 Reads

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16 Citations

Annals of Botany

Background and Aims Diploid and polyploid Urochloa (including Brachiaria, Panicum and Megathyrsus species) C4 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 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 U. 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 will assist in measuring and conserving biodiversity in grasslands.


Number of analyzed accessions and their distribution in the various levels of ploidy. 1
Complex polyploid and hybrid species in an apomictic and sexual tropical forage grass group: genomic composition and evolution in Urochloa ( Brachiaria ) species

February 2021

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97 Reads

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2 Citations

Background and Aims Diploid and polyploid Urochloa (including Brachiaria , Panicum and Megathyrsus species) C 4 tropical forage grasses originating from Africa and now planted worldwide are important for food security and the environment, often being planted in marginal lands. 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 determined using an optimized flow cytometry method. Whole-genome survey sequencing and molecular cytogenetic analysis with in situ hybridization to chromosomes were used to identify chromosomes and genomes in Urochloa accessions belonging to the different agamic complexes. 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 U. brizantha, U. decumbens , and U. ruziziensis . 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 will assist in measuring and conserving biodiversity in grasslands.


Global patterns of plant extinction and rediscovery. (a) Proportions of native plant species which are presumed extinct. Low proportions (%) in blue, through greens, yellows and to high proportions (%) in red. Only small, isolated island regions are colored red or yellow. Gray indicates no record of a globally extinct plant. (b) Numbers of extinct (non‐rediscovered) and rediscovered species. The colors illustrate the number of extinct and rediscovered plant species recorded in each area: pink indicates extinctions, green indicates rediscoveries, and mixed shades indicate both extinction and rediscovery. Dark gray indicates more than one extinction as well as more than one rediscovery. Light gray indicates no record of a globally extinct plant. Data from Humphreys et al. (2019) and WCSP (2018)
(a) Change in the Human Development Index placements across global regions 2000–2018, and for the United Kingdom and Madagascar (data from Sustainable Development Solutions Network, 2019). (b) Comparative timeline of publications on the biodiversity and biogeography of Malagasy vertebrates published 1959–2019 and recorded in Noe4D biodiversity database, by first authors based in a Malagasy versus foreign institution, 8,720 publications updated and modified from Waeber et al. (2016)
Grass (Poaceae) distribution patterns, based on the number of species in each TDWG level 3 region. (a) Global diversity (green): The World Checklist of Selected Plant Families (WCSP, 2018) contains 77,166 records for native distributions of Poaceae, representing 11,454 species in 368 out of the 369 regions. Bouvet Island between Africa and Antarctica is the only place in the world where no grasses are recorded, but they are likely to have been overlooked. (b) Global Poaceae endemism (pale blue). Endemic grasses are found on all nine continents, with top continents being temperate Asia (1,048 species), South America (991 species), and Africa (800 species). (c, d) Global distribution of all species in Madagascar (dark blue) and the British Isles (pink, see also Figure S2)
Geographic distribution, life form and species description patterns of grasses compared to all seed plants and extinct seed plants. (a) Proportion of species among continental regions, on islands, with small range sizes (presence in a single TDWG level 3 area), climate zones, and life forms for all grasses (green), compared to random draws of 500 species of all seed plants (gray boxes) and extinct seed plants (red). (b) Cumulative number of species described over time
Inequality in plant diversity knowledge and unrecorded plant extinctions: An example from the grasses of Madagascar

June 2020

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931 Reads

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18 Citations

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.


Distribution of extinct and rediscovered seed plant species among geographical regions, climate zones and life forms
a, The geographical pattern of modern extinction in seed plants. Hawaii stands out as having the most recorded extinctions (79), followed by the Cape Provinces of South Africa (37) and Mauritius (32), with Australia, Brazil, India and Madagascar also being among the top regions. Seventeen extinctions are of cultivated plants that have never been known in the wild (Supplementary Dataset 1). b, The geographical pattern of rediscovery of seed plants that have been erroneously declared extinct. Australia stands out for contributing the most rediscovered species overall (133). About half of the regions with the most recorded extinctions also have the most rediscovered species (Supplementary Information). c, Comparison of the proportions of extinct and rediscovered species on different continents, on islands versus continental regions, in a single geographical area versus multiple, in different climate zones and life forms, compared to the global distribution of seed plants. Boxplots show the range of proportions calculated across 500 random draws of 500 species from a database of 269,441 seed plant species (World Checklist of Selected Plant Families²³). Upper and lower box bounds represent the 75th and 25th percentiles, respectively, and the horizontal line represents the median value and circles denote outliers. Numbers along the x axis represent the total number of seed plant species known in each category. Observed values are shown with asterisks (pink, extinct; green, rediscovered).
Phylogenetic distribution of seed plant families with extinct and rediscovered species
a, Extinction and b, rediscovery of species. There is no phylogenetic signal to what families contain species that a, have been declared extinct in recent centuries or b, have subsequently been rediscovered. This finding is robust to whether extinction is analysed as a proportion of species per family or the presence/absence of at least one extinct/rediscovered species. Families with at least one extinct/rediscovered species are shown in pink (extinct) or green (rediscovered), and proportions of extinct/rediscovered species are shown as filled circles. Note that the proportion of extinct/rediscovered species per family is vanishingly small in most cases (≤ 3.7% for extinct and ≤8.3% for rediscovered species; Supplementary Fig. 1), and circles have been scaled for visibility.
Rates of modern extinction in seed plants compared to vertebrates
Global dataset shows geography and life form predict modern plant extinction and rediscovery

July 2019

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6,910 Reads

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362 Citations

Nature Ecology & Evolution

Most people can name a mammal or bird that has become extinct in recent centuries, but few can name a recently extinct plant. We present a comprehensive, global analysis of modern extinction in plants. Almost 600 species have become extinct, at a higher rate than background extinction, but almost as many have been erroneously declared extinct and then been rediscovered. Reports of extinction on islands, in the tropics and of shrubs, trees or species with narrow ranges are least likely to be refuted by rediscovery. Plant extinctions endanger other organisms, ecosystems and human well-being, and must be understood for effective conservation planning.



Citations (6)


... Similarly, UK-based students have made use of the facility for biodiversity research, for example, investigation into the evolutionary history of the antelope genus Hippotragus using degraded museum specimens (Plaxton et al., 2023). The resource has enabled the large-scale (and thus computationally demanding) analysis of flowering plants as a whole: for example, in a phylogenetic study which provided new insights into their evolutionary history (Zuntini et al., 2024); and in the automated prediction of extinction risk for every flowering plant species (Bachman et al., 2024). 4. AI-powered trait analysis: The use of AI technologies is emerging as an important tool for the plant sciences, for example enabling scientists to gain a deeper understanding of complex trait interactions (SDG 9: Industry, Innovation, and Infrastructure). ...

Reference:

UKCropDiversity‐HPC: A collaborative high‐performance computing resource approach for sustainable agriculture and biodiversity conservation
Phylogenomics and the rise of the angiosperms

Nature

... Chromosome number is of great importance for the study of speciation and evolution (Wei et al. 2011;Oginuma and Tobe 2021;Tomaszewska et al. 2023). The present study recovers potential polyploidization in Strobilanthes species and lays a foundation for speciation and evolutionary research. ...

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

Annals of Botany

... Recently, the ploidy and relatedness of 280 of Urochloa spp. accessions from the CIAT genebank have been defined for the first time (Tomaszewska et al., 2021). ...

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

... Conservative estimates indicate that only 13-18% of species are known and described, and the probability of discovering new species and taxonomic uncertainties of already described species are concentrated mainly in tropical regions 10,11 . However, taxonomists frequently report that the tropics are the region from which numerous NBT were collected and sent abroad, mainly to NHBC in Europe and North America, hampering the effort to catalog and describe the yet-to-be-discovered diversity 12,13 . In this study, we argue that a fairer distribution of NBT is necessary if we aim to effectively fill the gaps in biological knowledge by cataloging, organizing, and describing biodiversity in the coming years. ...

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

... To increase the rate of assessment, families with high endemism or those restricted to threatened habitats should be prioritised (Drummond et al., 2009;Humphreys et al., 2019;Ruslandi et al., 2011;Schatz, 2009), namely, Calophyllaceae, Oleaceae, and Pandanaceae for trees and Orchidaceae, Palmae, and Zingiberaceae for nontrees. For species with limited data, the ENM approach, using a variety of high-resolution spatial data to develop models and refining these through ground surveys, will be used ( Figure 10). ...

ESM: Global dataset shows geography and life form predict modern plant extinction

... This configuration creates a closed-loop graph within the layer, which minimizes geodesic distance between similar superpixels, enhancing similarity measurements and ranking accuracy [48]. s ∈ [1,3] with dimension n × m , with n, m ∈ N denote the number of nodes of layers k and s respectively, is defined as: ...

Global dataset shows geography and life form predict modern plant extinction and rediscovery

Nature Ecology & Evolution