Peter C. Hoch’s research while affiliated with Missouri Botanical Garden and other places

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Publications (71)


Novel Perspectives on Plastome Evolution in Onagraceae
  • Article

April 2025

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11 Reads

AoB Plants

Chia-Ying Ou

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Ting-Yu Yeh

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Previous systematic studies have generated abundant information on plants in family Onagraceae Juss., making this taxonomic group a model for understanding plant evolution. The chloroplast genome is widely used to provide valuable insights into how plant lineages evolved. In the present study, we employed shotgun sequencing to assemble new plastomes from Onagraceae. Plastomes of ten species and one genus, Fuchsia, are reported for the first time. We characterize and compare the plastome features of six genera (Chamaenerion, Circaea, Epilobium, Fuchsia, Ludwigia, and Oenothera), allowing us to reconstruct their phylogenies and explore inter- and infra-generic evolutionary relationships, inverted repeat (IR) expansion, plastome size increases, and correlations among repeat elements, genetic variations, and evolutionary events. Our findings indicate that each of the tribes and subfamilies we assessed exhibits unique plastome features. Our phylogenetic tree supports previous findings, but also reveals that some clades need further systematic analyses. We show that increased plastome size within subfamily Onagroideae coincides with IR expansion, which is not the case for subfamily Ludwigioideae. In addition, our results indicate that higher repeat numbers and greater genetic variation can serve as indicators of evolutionary events, such as gene loss and gain, IR boundary shifts, and inversions, but they may not have arisen universally across all members of Onagraceae. Our study provides some novel insights into plastome evolution in the Onagraceae. Further studies should aim to elucidate how plastome size has evolved in Ludwigioideae and explore the evolutionary roles of regions in Onagraceae plastomes exhibiting high repeat numbers and genetic variations.


Conceptual overview of how phenological shifts can affect pairwise overlap of sympatric species. (a) Pairwise overlap can be affected by changes in phenological duration or interspecific variability in the magnitude and/or direction of phenological shifts. (b) Illustrative example of change in pairwise flowering overlap analyses. For each species, Bayesian quantile regressions were performed at the 10th and 90th quantiles to describe changes to the beginning and ending of flowering, respectively, across the past century. Changes to flowering duration are taken as changes in the 10th–90th interquantile range from 1940 to 2010. Change in flowering overlap between two species is calculated as the difference in the proportion of the focal species' flowering duration that is overlapped by the nonfocal species' duration from 1940 to 2010. In this example, change in overlap is greater when Conoclinium coelestinum (pink) is focal and Rudbeckia hirta (blue) is nonfocal (c. 100% increase), than vice versa (c. 70% increase).
Flowering duration (i.e. the 10th–90th interquantile range) per species in 1940 (blue) and 2010 (red), ordered by the beginning of flowering in 1940. The 10th and 90th quantiles were obtained through Bayesian quantile regressions that tested how flowering time has changed over years.
Phenological shifts and climatic sensitivities. (a) Changes to the beginning of flowering from 1940 to 2010 (ΔDOY10,Y). (b) Mean spring temperature sensitivity of the beginning of flowering (ΔDOY10,T). (c) Total spring precipitation sensitivity of the beginning of flowering (ΔDOY10,P). (d) Changes to the ending of flowering from 1940 to 2010 (ΔDOY90,Y). (e) Mean spring temperature sensitivity of the ending of flowering (ΔDOY90,T). (f) Total spring precipitation sensitivity of the ending of flowering (ΔDOY90,P). In each panel, points give the mean of the posterior distribution, thick lines give the 50% CI, and thin lines give the 80% CI. Dark colors indicate a > 90% probability, light colors a > 75% probability, and gray a ≤ 75% probability of phenological shifts (gold) and sensitivities to mean spring temperature (red) and total spring precipitation (blue). Species are arranged in each panel by ΔDOY10,Y (top) or ΔDOY90,Y (bottom) in descending order.
Changes to flowering duration (i.e. the 10th–90th interquantile range) from 1940 to 2010. (a) Absolute shifts (ΔIQRY). (b) Shifts relative to 1940 duration (ΔRIQRY). Points give the mean of the posterior distribution, thick lines give the 50% CI, and thin lines give the 80% CI. Dark green indicates a > 90% probability, light green a > 75% probability, and gray a ≤ 75% probability of changes to duration.
Correlations between phenological shifts from 1940 to 2010 and climatic sensitivities. Changes to the beginning of flowering (10th quantile) from 1940 to 2010 (ΔDOY10,Y) are (a) positively correlated with changes to the beginning of flowering for 1°C increase in mean spring temperature (ΔDOY10,T; P < 0.0005) and (b) negatively correlated with changes to the beginning of flowering for 100 mm increase in total spring precipitation (ΔDOY10,P; P < 0.0001). Changes to the ending of flowering (90th quantile) from 1940 to 2010 (ΔDOY90,Y) are (c) positively correlated with changes to the ending of flowering for 1°C increase in mean spring temperature (ΔDOY90,T; P < 0.0001) and (d) not correlated with changes to the ending of flowering for 100 mm increase in total spring precipitation (ΔDOY90,P; P = 0.93). Negative values indicate shifts to earlier flowering dates; positive values indicate shifts to later‐flowering dates. P‐values generated from Pearson correlations.

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Climate change increases flowering duration, driving phenological reassembly and elevated co‐flowering richness
  • Article
  • Full-text available

July 2024

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329 Reads

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4 Citations

Changes to flowering phenology are a key response of plants to climate change. However, we know little about how these changes alter temporal patterns of reproductive overlap (i.e. phenological reassembly). We combined long‐term field (1937–2012) and herbarium records (1850–2017) of 68 species in a flowering plant community in central North America and used a novel application of Bayesian quantile regression to estimate changes to flowering season length, altered richness and composition of co‐flowering assemblages, and whether phenological shifts exhibit seasonal trends. Across the past century, phenological shifts increased species' flowering durations by 11.5 d on average, which resulted in 94% of species experiencing greater flowering overlap at the community level. Increases to co‐flowering were particularly pronounced in autumn, driven by a greater tendency of late season species to shift the ending of flowering later and to increase flowering duration. Our results demonstrate that species‐level phenological shifts can result in considerable phenological reassembly and highlight changes to flowering duration as a prominent, yet underappreciated, effect of climate change. The emergence of an autumn co‐flowering mode emphasizes that these effects may be season‐dependent.

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Fig. 1 Onagraceae. subfamily Ludwigioideae. A Ludwigia octovalvis. Flower and immature capsule. Baldwin Co., Alabama (image Warren Wagner in 2003). Subfamily Onagroideae B-L. B Tribe Hauyeae. Hauya elegans subsp. lucida. Branch with flower at anthesis and in bud. Cultivated at San Diego Zoo (image Wikipedia in 2008). C, D Tribe Circaeeae. C. Fuchsia inflata. Inflorescence. Cusco, Peru (image P. Berry in 1978). D Circaea pacifica. Inflorescence and young fruit. Benton Co Oregon (image G. Carr-4162b in 2006). E, F Tribe Lopezieae. E Lopezia racemosa subsp racemosa. Flower with inflorescence and leaves. Puebla, Mexcio (image Jon Amith in 2007). F Megacorax gracielanus. Chasmogamous flower with bud and stem with leaves. Sierra de Coneto, Durango, Mexico (image M. Socorro Gonzalez-Elizondo in 2021). G Tribe Gongylocarpeae. Gongylocarpus fruticulosus. Stem with flowers and gall-like mature fruit embedded in pith of stem, indehiscent, and inset showing flower closeup. Isla Magdalena, Baja California Sur, Mexico (images Jon Rebman in 2016). Tribe Epilobieae H-J H. Chamaenerion angustifolium subsp. circumvagum. Stem with inflorescence with open flowers and maturing capsules. MN (image Peter M. Dziuk, Minnesota Wildflowers in 2002). I Epilobium nankotaizanense. Habit with flower. Taiwan (image Ching-I Peng in 2008). J Epilobium canum subsp latifolium. Stem with flowers and some dispersed seeds. Curry Co., OR (image Gerry Carr 6317b in 2015). Tribe Onagreae. K, L K. Xylonagra arborea. Stem with flowers and very young fruit. Cultivated at Missouri Botanical Garden, originally from Baja California, Mexico (image Ching-I Peng in 1982). L. Taraxia ovata. Habit with flowers. Monterey, CA (image Christian Schwarz)
Fig. 2 Tribe Onagreae. A-L. A Clarkia rhomboidea. Stem with flower and immature capsule. Jefferson Co., OR (image Gerry Carr 6468b in 2006). B Chylismiella pterosperma. Stem with leaves, flower, and buds. Inyo Co., CA (image Larry Blakely in 2001). C Gayophytum diffusum subsp. diffusum. Stem with flowers and buds. Tulare CA (image Peter Raven collection). D Eremothera boothii susbp. boothii. Flowers and buds. Mono Co., CA (image Michael Moore 3260 in 2015). E Camissonia contorta. Plant with flowers and young capsules. Klickitat Co., WA (image Gerry Carr 0356b in 2009). F Neoholmgrenia andina. Plant with fading flower and immature capsule. Harney Co., OR (image Gerry Carr 0996b in 2011). G Tetrapteron graciliflorum. Plant with flower and immature capsule. Marin Co., CA (image David Greenberger in 2018). H Camissoniopsis cheiranthifolia subsp. cheiranthifolia. Stem with flowers and immature capsules. San Mateo Co., CA (image Leslie Flint in 2015). Inset of immature capsule. Monterey, CA (image Steve Rovell in 2016). I Eulobus californicus. Stem with flowers. San Diego Co., CA (image Ron King in 2021). J Chylismia eastwoodiae. Flowers and buds with capsules in background. Emery Co., UT (image Rob Raguso in 2001). K Oenothera tetraptera. Plant with flower (from Oageng Modise) and immature capsule. South Africa (image Behrens in 2021). Inset of dehisced capsule with seeds clustered inside. South Africa (image Warren Wagner in 2008). L Oenothera toumeyi. Stem with flowers. Cochise Co., AZ (image Rob Raguso in 1996)
Fig. 3 Best-scoring ASTRAL-II tree (displayed as a cladogram) based on 303 input best-scoring maximum likelihood gene trees from RAxML. Numbers above branches represent the number of gene trees in concordance with a particular clade in the species tree (blue in pie chart), whereas those below indicate gene trees in conflict (red/green in pie chart). Pie charts were constructed using 206 genes, and additionally represent the portion of conflicting gene trees that support the main alternative (green), those that support all remaining alternatives (red), and finally those with no information (gray), which could be due to bootstrap support < 50% for the branch in question or missing data (Fig. S1, Additional file 2). The ASTRAL tree and concatenated ML tree are represented with branch lengths (with the exception of tip branch lengths) in Figure S2 (Additional file 2) and individual tree files are provided in the Dryad repository that accompanies this study
Fig. 4 Distribution of support for the monophyly of 17 of 22 genera (x-axis) in Onagraceae among 303 gene trees using DiscoVista. Gene trees (y-axis) are shown to strongly support (dark green), weakly support (teal), weakly reject (pink), or strongly reject (maroon) genera. Shown in blue are gene trees that do not contain any data for a certain genus
Fig. 5 Alternative topologies for clades within Onagraceae. The relative frequency of gene trees is shown for quartets of taxa (bar graphs). Green bars indicate the RAxML-ASTRAL topology, teal and light blue bars indicate alternative topologies. Dotted lines indicate 1/3 of the total gene trees for each quartet; roughly equal proportions for the three possible topologies indicate a polytomy within the present dataset. a Early-diverging Onagraceae; b Placement of Hauya; c Monophyly of Circaea and Fuchsia; d Monophyly of Megacorax and Lopezia; e Early-diverging Onagreae, where clades X and Y refer to the following groups: clade X comprises Camissoniopsis, Eremothera, Camissonia, Tetrapteron, and Neoholmgrenia; clade Y comprises Clarkia, Chylismiella, and Gayophytum; f Clades within Oenothera, the quartet at node I is ((Lineage B, sect. Pachylophus), Lineage A + sect. Calylophus) Outgroup) and node II is ((Lineage A, sect. Calylophus), (Lineage B + sect. Pachylophus) Outgroup), the mode common alternative topology for node I is shown
A phylogeny of the evening primrose family (Onagraceae) using a target enrichment approach with 303 nuclear loci

November 2023

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610 Reads

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1 Citation

BMC Ecology and Evolution

Background The evening primrose family (Onagraceae) includes 664 species (803 taxa) with a center of diversity in the Americas, especially western North America. Ongoing research in Onagraceae includes exploring striking variation in floral morphology, scent composition, and breeding system, as well as the role of these traits in driving diversity among plants and their interacting pollinators and herbivores. However, these efforts are limited by the lack of a comprehensive, well-resolved phylogeny. Previous phylogenetic studies based on a few loci strongly support the monophyly of the family and the sister relationship of the two largest tribes but fail to resolve several key relationships. Results We used a target enrichment approach to reconstruct the phylogeny of Onagraceae using 303 highly conserved, low-copy nuclear loci. We present a phylogeny for Onagraceae with 169 individuals representing 152 taxa sampled across the family, including extensive sampling within the largest tribe, Onagreae. Deep splits within the family are strongly supported, whereas relationships among closely related genera and species are characterized by extensive conflict among individual gene trees. Conclusions This phylogenetic resource will augment current research projects focused throughout the family in genomics, ecology, coevolutionary dynamics, biogeography, and the evolution of characters driving diversification in the family.


Fig. 6 Boxplots showing the estimated migration rates (M, migration rates per gene copy per generation) between ploidy levels in Ludwigia sect. Isnardia based on (a) atpB-rbcL and (b) ITS data. Groups on the x axial are coded, showing the direction of the migration rates, e.g., 2 × > 4 × indicates the migration rates from diploids to tetraploids. Letters above each boxplot indicate pairwise statistical differences (p-values < 0.05) between 2 × > 2 × and other groups. The asterisks indicate pairwise statistical differences (p-values < 0.05) between the two groups. The complete details for the statistical analysis are shown in Additional file 8. The estimated migration rates among taxa are available in Additional file 7
New insights into polyploid evolution and dynamic nature of Ludwigia section Isnardia (Onagraceae)

June 2023

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101 Reads

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1 Citation

Botanical Studies

Background: While polyploids are common in plants, the evolutionary history and natural dynamics of most polyploid groups are still unclear. Owing to plentiful earlier systematic studies, Ludwigia sect. Isnardia (comprising 22 wetland taxa) is an ideal allopolyploid complex to investigate polyploid evolution and natural dynamics within and among taxa. With a considerable sampling, we concentrated on revisiting earlier phylogenies of Isnardia, reevaluating the earlier estimated age of the most recent common ancestor (TMRCA), exploring the correlation between infraspecific genetic diversity and ploidy levels, and inspecting interspecific gene flows among taxa. Results: Phylogenetic trees and network concurred with earlier phylogenies and hypothesized genomes by incorporating 192 atpB-rbcL and ITS sequences representing 91% of Isnardia taxa. Moreover, we detected three multi-origin taxa. Our findings on L. repens and L. sphaerocarpa were consistent with earlier studies; L. arcuata was reported as a multi-origin taxon here, and an additional evolutionary scenario of L. sphaerocarpa was uncovered, both for the first time. Furthermore, estimated Isnardia TMRCA ages based on our data (5.9 or 8.9 million years ago) are in accordance with earlier estimates, although younger than fossil dates (Middle Miocene). Surprisingly, infraspecific genetic variations of Isnardia taxa did not increase with ploidy levels as anticipated from many other polyploid groups. In addition, the exuberant, low, and asymmetrical gene flows among Isnardia taxa indicated that the reproductive barriers may be weakened owing to allopolyploidization, which has rarely been reported. Conclusions: The present research gives new perceptions of the reticulate evolution and dynamic nature of Isnardia and points to gaps in current knowledge about allopolyploid evolution.


Plastome evolution in Onagraceae

April 2023

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21 Reads

https://twsps.wordpress.com/category/2023%e5%b9%b4%e6%9c%83%e6%9a%a8%e7%a0%94%e8%a8%8e%e6%9c%83/ Earlier systematic studies have accumulated abundant knowledge of Onagraceae plants, making this family a model group for understanding plant evolution. In the present study, we applied next-generation sequencing techniques and comparative analyses to give new perceptions on Onagraceae evolution. Totally, 12 newly assembled and 17 published plastomes representing six genera in Onagraceae were analyzed. Onagraceae plastomes are ca. 159,942 bp in length and contain 132-137 genes. Gene arrangement in Onagraceae is conserved except for some Oenothera taxa, while gene numbers, region sizes and boundaries, and nucleotide variations vary among genera. Moreover, most repeats are located in LSC as in many other plant groups. Onagraceae is similar to Lythraceae in the relative synonymous codon usage. In addition, our phylogeny mainly agrees with earlier research but suggests that Epilobium amurense and clades B3 and B4 in Ludwigia need further systematic studies.


Molecular Phylogenetics Reveals Multiple Transitions to Self-Compatibility in a Primary Subclade of Oenothera (Onagraceae)

August 2022

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110 Reads

Annals of the Missouri Botanical Garden

Evolutionary shifts in breeding system are thought to have played key roles in the diversification of many lineages of plants, including the evening primrose family (Onagraceae), which includes the genus Oenothera L. Diversification in Oenothera has been accompanied by frequent breeding system shifts, but it is not clear whether these differences are due to shared evolutionary history or reflect repeated independent adaptations to varying ecological conditions. In this study, we focus on “Subclade B,” one of two primary clades within Oenothera, and combine phylogenetic reconstructions and breeding system data to evaluate evidence for multiple transitions to self-compatibility. This study includes 46 of the 58 named taxa (species and subspecies) of Oenothera Subclade B. Some taxa were sequenced in earlier analyses, available from GenBank, one was resampled here to add new sequences, and 28 taxa are newly sequenced here. We base our phylogeny on sequencing of portions of four chloroplast markers (rps16, ndhF, trnL-F, and rbcL) and two nuclear genes (ITS and ETS). We used pollination tests to verify or determine the breeding system of these taxa. Our phylogeny supports the current classification of Oenothera with minor changes and provides greater insight and clarity to the relationships of these species. Our results provide support for the monophyly of most of the sections in Oenothera Subclade B, as well as greater resolution for topology within sections Gaura (L.) W. L. Wagner & Hoch, Hartmannia (Spach) Walpers, Kneiffia (Spach) Walpers, and Megapterium (Spach) Walpers. Relationships among these monophyletic lineages, and the placement of sections Paradoxus W. L. Wagner and Peniophyllum (Pennell) Munz, and of the allopolypoid O. hispida (Benth.) W. L. Wagner, Hoch & Zarucchi, are not uniformly well-supported and need further clarification, but these phylogenetic uncertainties had minimal impact on the inference of transitions in self-compatibility in Subclade B. We use maximum likelihood, Bayesian inference and stochastic character mapping to estimate the minimum and maximum number of transitions necessary to explain the phylogenetic distribution of self-compatible lineages. Our results confirm at least 12 and possibly up to 15 independent transitions from self-incompatibility to self-compatibility in Oenothera Subclade B. This lability in breeding system, which is also seen broadly across Oenothera, lends strong support to the hypothesis that this trait plays a key role in the diversification of the genus.



FIGURE 4. Exons coalescent ASTRAL (A) versus coalescent supercontigs ASTRAL (B) topology comparison in major families and subclades. Annotations above and below branches are respectively as described for Figs. 1A and 3A-C.
FIGURE 6. Topological contrast of two controversial clades of Myrtales. (A) Relationships between Combretaceae, Lythraceae and Onagraceae. CAP = Crypteroniaceae, Alzateaceae, Penaeaceae. (B) The BKMMT clade (Myrtaceae) and the position of Syzygieae. Support values (when available) are reported from this study or from the relevant publications. Supports above branches are bootstrap support or quartet score values for each node (as described in Figs. 1A and 3A-C). Local posterior probability values are presented below branches. BKMMST = Backhousieae, Kanieae, Metrosidereae, Myrteae, Syzygieae, Tristanieae in Myrtaceae (BKMMT excludes Syzygieae).
A nuclear phylogenomic study of the angiosperm order Myrtales, exploring the potential and limitations of the universal Angiosperms353 probe set

July 2021

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895 Reads

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91 Citations

American Journal of Botany

Premise To further advance the understanding of the species-rich, economically and ecologically important angiosperm order Myrtales in the rosid clade, comprising nine families, approximately 400 genera and almost 14,000 species occurring on all continents (except Antarctica), we tested the Angiosperms353 probe kit. Methods We combined high-throughput sequencing and target enrichment with the Angiosperms353 probe kit to evaluate a sample of 485 species across 305 genera (76% of all genera in the order). Results Results provide the most comprehensive phylogenetic hypothesis for the order to date. Relationships at all ranks, such as the relationship of the early-diverging families, often reflect previous studies, but gene conflict is evident, and relationships previously found to be uncertain often remain so. Technical considerations for processing HTS data are also discussed. Conclusions High-throughput sequencing and the Angiosperms353 probe kit are powerful tools for phylogenomic analysis, but better understanding of the genetic data available is required to identify genes and gene trees that account for likely incomplete lineage sorting and/or hybridization events.


The End of Botany

December 2020

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952 Reads

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51 Citations

Trends in Plant Science

Biologists unable to recognize common plants, and a decline in botany students, faculty, courses, university departments, and herbaria, highlight the current erosion of botany. How did we reach this crisis, knowing that plants form the basis for life? What are the causes? What can we do to reverse it?


Floristic patterns in New Guinea
a, Map of the study area of mainland New Guinea and surrounding islands, showing the number of digitized collections per grid cell of 25 × 25 km. b, The five plant families that comprise 35% of the flora. c, Families with highest species endemism in angiosperms (orange), gymnosperms (blue) and ferns and lycophytes (green), arranged by increasing number of endemic species. Black bars depict the number of non-endemic species.
Representatives of species-rich genera with more than 80 species in New Guinea
a, Bulbophyllum; b, Dendrobium; c, Crepidium; d, Taeniophyllum; e, Oberonia; f, Phreatia; g, Glomera; h, Syzygium; i, Rhododendron; j, Cyrtandra; k, Timonius; l, Freycinetia; m, Saurauia; n, Begonia; o, Medinilla; p, Ficus; q, Myristica; r, Psychotria; s, Vaccinium. Photograph credits: A.S. (a–f), W.J.B. (g, s), Y.W.L. (h), T.U. (i–l, o, q), M.S.A. (m, n) and Z.E. (p, r).
Breakdown of the New Guinea flora by life form
Fraction of species that are trees (pink), herbs (dark blue), epiphytes (orange), shrubs (green), climbers (light blue), non-climbing palms (yellow) and tree ferns (mid blue).
Species described per decade in New Guinea
The number of plant species (basionyms) described per decade from 1753 to 2019, grouped into tree species (red bars) and non-tree species (blue bars); and the cumulative number of verified species of trees (red dotted line), non-trees (blue dotted line) and total (black dotted line).
New Guinea has the world's richest island flora

August 2020

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4,016 Reads

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213 Citations

Nature

New Guinea is the world’s largest tropical island and has fascinated naturalists for centuries. Home to some of the best-preserved ecosystems on the planet and to intact ecological gradients—from mangroves to tropical alpine grasslands—that are unmatched in the Asia-Pacific region, it is a globally recognized centre of biological and cultural diversity. So far, however, there has been no attempt to critically catalogue the entire vascular plant diversity of New Guinea. Here we present the first, to our knowledge, expert-verified checklist of the vascular plants of mainland New Guinea and surrounding islands. Our publicly available checklist includes 13,634 species (68% endemic), 1,742 genera and 264 families—suggesting that New Guinea is the most floristically diverse island in the world. Expert knowledge is essential for building checklists in the digital era: reliance on online taxonomic resources alone would have inflated species counts by 22%. Species discovery shows no sign of levelling off, and we discuss steps to accelerate botanical research in the ‘Last Unknown’.


Citations (38)


... It is well documented that phenological data extracted from herbarium specimens covering a wide range of plant taxa at local scales can often provide comparable information to field-based phenology surveys in temperate regions (e.g. Davis et al., 2015;Austin et al., 2024). Using simulations, Park et al. (2024) found that herbarium data accurately predicted the timing and duration of flowering phenology at the population level. ...

Reference:

The promise of digital herbarium specimens in large‐scale phenology research
Climate change increases flowering duration, driving phenological reassembly and elevated co‐flowering richness

... Of the three strategies we used here: (1) coalescent species tree reconstruction from all loci, (2) coalescent species tree reconstruction from single-copy loci, and (3) phylogenetic analysis of concatenated loci (all loci or single-copy loci only), the first one produced the 'best' species tree for Myosotis, but there was nevertheless congruent signal to varying degrees in the 25-loci single copy coalescent and concatenated analyses. Although concatenation can be useful for shallow phylogenies where combining all information from all available loci may increase phylogenetic signal (Chen et al., 2023), as a method that is not "ILS-aware", it may also lead to erroneously reconstructed relationships for rapid radiations (Thureborn et al., 2022) especially those that are also mainly polyploid (e.g., Nicol et al., 2024;Overson et al., 2023). This may have occurred in the current study, in which many of the branches of the concatenated trees were highly supported but were highly inconsistent with other morphological or geographic data, and with previous taxonomic or other biological knowledge, and were likely erroneous. ...

A phylogeny of the evening primrose family (Onagraceae) using a target enrichment approach with 303 nuclear loci

BMC Ecology and Evolution

... hexapetala, forming a phylogenetic group corresponding to subsect Jussiaea (in green, Figure 8). . The sections are based on the works of Raven (1963), Wagner et al. (2007) and Liu et al. (2023). The scale bar indicates the branch length. ...

New insights into polyploid evolution and dynamic nature of Ludwigia section Isnardia (Onagraceae)

Botanical Studies

... We conducted our phylogenomic data analyses on the collaborative high-performance computing resource UKCropDiversity-HPC (Percival-Alwyn et al., 2024). We followed the workflow described by Maurin et al. (2021) for sequence assembly but using HybPiper version 2.2.0 (Johnson et al., 2016). Recovery statistics for exons and their flanking regions (supercontigs), including ENA accession are provided in ENA_IDs_For (Supplementary Data S2). ...

A nuclear phylogenomic study of the angiosperm order Myrtales, exploring the potential and limitations of the universal Angiosperms353 probe set

American Journal of Botany

... Besides the demonstration of strong floristic changes across a 500-year timespan, plausibly reflecting variations of climate and land use, our study warns about the risk of ceasing to collect herbarium specimens and keep herbaria active [78,79]. This would cause irreparable gaps to our botanical memory, hindering our ability to document biodiversity and predicting its trajectories just during decades of fast global changes. ...

The End of Botany
  • Citing Article
  • December 2020

Trends in Plant Science

... This result is novel for birds but consistent with previous studies on island endemism in monocotyledonous plants, which also exhibit superendemism in New Guinea (and neoendemism in Australia, see below) (Veron et al. 2019). New Guinea superendemism unifies signatures of this region as both a museum of low diversity lineages with relatively long histories (Cámara-Leret et al. 2020;Jønsson et al. 2011;McCullough et al. 2022;Oliver et al. 2023), and also a cradle of diversification in the last 15 Ma (Hill et al. 2023;Oliver et al. 2018;Roycroft et al. 2022;Toussaint et al. 2021). These results point to the confluence of geological and macroevolutionary processes that underpin the contemporary megadiversity of many components of the New Guinea biota (Cámara-Leret et al. 2020-plants; Kennedy et al. 2022;Prasetya et al. 2023)birds;Oliver et al. 2023-frogs), including initial colonization and insular diversification in the proto-Papuan region FIGURE 6 | Phylogenetic diversity (PD), phylogenetic endemism (PE), relative phylogenetic diversity, and relative phylogenetic endemism for passerine birds in different areas in the IAA calculated from three different supermatrix phylogenetic datasets, namely our phylogenetic tree, the Jetz (genetic) tree; and the Jetz (imputed) tree. ...

New Guinea has the world's richest island flora

Nature

... mitochlondrial and nuclear genomes. Finally, the three new Ludwigia plastomes generated by our study make it possible to extend the phylogenetic study of the Onagraceae family and to compare it with previously published analyses [4,27,28]. ...

Disentangling Reticulate Evolution of North Temperate Haplostemonous Ludwigia (Onagraceae)

Annals of the Missouri Botanical Garden

... Aloe vera Anti-infammatory, antibacterial, choleretic, anti-burn, and wound healing properties [58] 8 Filipendula Immunomodulatory, bracing efect, diuretic [59,60], diaphoretic activity [61][62][63][64][65], anti-infammatory, antioxidant, and gastroprotective activity [66] proven in studies [77][78][79]. According to recent data, black cumin can be used as a new drug against COVID-19. ...

Nomenclatural changes in Onagraceae

... Some recent studies on other Ludwigia clade and other plant groups (e.g. Liu et al. 2018;Duvall et al. 2020;Simmonds et al. 2021) have shown that the nextgeneration sequencing (NGS) data would provide complete plastome sequences and improve the understanding of maternal evolutionary inferences. Further studies with NGS data will be called on to uncover maternal phylogeny in Isnardia thoroughly. ...

Genome skimming provides new insight into the relationships in Ludwigia section Macrocarpon, a polyploid complex
  • Citing Article
  • May 2018

American Journal of Botany

... [2][3][4] Ludwigia has received in-depth investigations into cytology, 5 morphology, [6][7][8] reproductive traits, 9 wood and leaf anatomy, 10 environment adaptation, 11 chemical isolation, 12,13 biological activities of antitumor and antibacterial properties, [14][15][16] environmental water improvement, 17 and molecular data. [18][19][20][21][22][23][24][25][26] Chloroplast (cp) is a vital organelle in plant cells, responsible for carrying out photosynthesis. This process harnesses the sunlight energy and converts it into high-energy molecules, which are then used to synthesize macro-biomolecules in living cells. ...

Multi-locus phylogeny of Ludwigia (Onagraceae): Insights on infra- generic relationships and the current classification of the genus

Taxon