2016-2020

Katelin D Pearson, Gil Nelson, Myla FJ Aronson, Pierre Bonnet, Laura Brenskelle, Charles C Davis, Ellen G Denny, Elizabeth R Ellwood, Hervé Goëau, Mason J Herberling, Alexis Joly, Titouan Lorieul, Susan J Mazer, Emily K Meineke, Brian J Stucky, Patrick Sweeney, Alexander E White, and Pamela S Soltis. 5/13/2020. “Machine Learning Using Digitized Herbarium Specimens to Advance Phenological Research.” BioScience.Abstract
Machine learning (ML) has great potential to drive scientific discovery by harvesting data from images of herbarium specimens—preserved plant material curated in natural history collections—but ML techniques have only recently been applied to this rich resource. ML has particularly strong prospects for the study of plant phenological events such as growth and reproduction. As a major indicator of climate change, driver of ecological processes, and critical determinant of plant fitness, plant phenology is an important frontier for the application of ML techniques for science and society. In the present article, we describe a generalized, modular ML workflow for extracting phenological data from images of herbarium specimens, and we discuss the advantages, limitations, and potential future improvements of this workflow. Strategic research and investment in specimen-based ML methods, along with the aggregation of herbarium specimen data, may give rise to a better understanding of life on Earth.
Rebecca A. Povilus, Jeffrey M. DaCosta, Christopher Grassa, Prasad R. V Satyaki, Morgan Moeglein, Johan Jaenisch, Zhenxiang Xi, Sarah Mathews, Mary Gehring, Charles C. Davis, and William E. Friedman. 4/14/2020. “Water lily (Nymphaea thermarum) genome reveals variable genomic signatures of ancient vascular cambium losses.” PNAS, 117, 15, Pp. 8649-8656.Abstract
For more than 225 million y, all seed plants were woody trees, shrubs, or vines. Shortly after the origin of angiosperms ∼140 million y ago (MYA), the Nymphaeales (water lilies) became one of the first lineages to deviate from their ancestral, woody habit by losing the vascular cambium, the meristematic population of cells that produces secondary xylem (wood) and phloem. Many of the genes and gene families that regulate differentiation of secondary tissues also regulate the differentiation of primary xylem and phloem, which are produced by apical meristems and retained in nearly all seed plants. Here, we sequenced and assembled a draft genome of the water lily Nymphaea thermarum, an emerging system for the study of early flowering plant evolution, and compared it to genomes from other cambium-bearing and cambium-less lineages (e.g., monocots and Nelumbo). This revealed lineage-specific patterns of gene loss and divergence. Nymphaea is characterized by a significant contraction of the HD-ZIP III transcription factors, specifically loss of REVOLUTA, which influences cambial activity in other angiosperms. We also found the Nymphaea and monocot copies of cambium-associated CLE signaling peptides display unique substitutions at otherwise highly conserved amino acids. Nelumbo displays no obvious divergence in cambium-associated genes. The divergent genomic signatures of convergent loss of vascular cambium reveals that even pleiotropic genes can exhibit unique divergence patterns in association with independent events of trait loss. Our results shed light on the evolution of herbaceousness—one of the key biological innovations associated with the earliest phases of angiosperm evolution.
Jianquan Liu, Charles C Davis, Xiyin Wang, Zhenxiang Xi, Zhiji Qin, Qinfeng Wang, Man Liu, Lanxing Shan, Beibei Jiao, Fanbo Meng, Xingxing Shen, Lei Zhang, Tao Ma, Ying Li, Dafu Ru, Donglei Wang, Leke Lv, Pengchuan Sun, and Yongzhi Yang. 2/24/2020. “Prickly waterlily and rigid hornwort genomes shed light on early angiosperm evolution.” Nature Plants, 2020, Pp. 1-8.Abstract
Angiosperms represent one of the most spectacular terrestrial radiations on the planet 1, but their early diversification and phylogenetic relationships remain uncertain 2, 3, 4, 5. A key reason for this impasse is the paucity of complete genomes representing early-diverging angiosperms. Here, we present high-quality, chromosomal-level genome assemblies of two aquatic species—prickly waterlily (Euryale ferox; Nymphaeales) and the rigid hornwort (Ceratophyllum demersum; Ceratophyllales)—and expand the genomic representation for key sectors of the angiosperm tree of life. We identify multiple independent polyploidization events in each of the five major clades (that is, Nymphaeales, magnoliids, monocots, Ceratophyllales and eudicots). Furthermore, our phylogenomic analyses, which spanned multiple datasets and diverse methods, confirm that Amborella and Nymphaeales are successively sister to all other …
Brandon Hedrick, Mason Heberling, Emily Meineke, Kathryn Turner, Christopher Grassa, Daniel Park, Jonathan Kennedy, Julia A. Clarke, Joseph Cook, David Blackburn, Scott V. Edwards, and Charles C. Davis. 3/1/2020. “Digitization and the future of natural history collections.” BioScience, 70, 3, Pp. 243-251. Publisher's VersionAbstract
Natural history collections (NHCs) are the foundation of historical baselines for assessing anthropogenic impacts on biodiversity. Along these lines, the online mobilization of specimens via digitization–the conversion of specimen data into accessible digital content–has greatly expanded the use of NHC collections across a diversity of disciplines. We broaden the current vision of digitization (Digitization 1.0)–whereby specimens are digitized within NHCs–to include new approaches that rely on digitized products rather than the physical specimen (Digitization 2.0). Digitization 2.0 builds upon the data, workflows, and infrastructure produced by Digitization 1.0 to create digital-only workflows that facilitate digitization, curation, and data linkages, thus returning value to physical specimens by creating new layers of annotation, empowering a global community, and developing automated approaches to advance biodiversity discovery and conservation. These efforts will transform large-scale biodiversity assessments to address fundamental questions including those pertaining to critical modern issues of global change.
Xiaoqing Liu, Weirui Fu, Yiwei Tang, Wenju Zhang, Zhiping Soonog, Linfeng Li, Ji Yang, Hong Ma, Jianhua Yang, Chan Zhou, Charles C. Davis, and Yugu Wang. 1/23/2020. “Diverse trajectories of plastome degradation in holoparasitic Cistanche and the whereabouts of the lost plastid genes.” Journal of Experimental Botany, 71, 3, Pp. 877-892. Publisher's VersionAbstract
The plastid genomes (plastomes) of non-photosynthetic plants generally undergoes gene loss and pseudogenization. Despite massive plastomes reported in different parasitism types of the broomrape family (Orobanchaceae), more plastomes representing different degradation patterns in a single genus are expected to be explored. Here, we sequenced and assembled the complete plastomes of three holoparasitic Cistanche species (C. salsaC. tubulosa and C. sinensis) and compared them with the available plastomes of Orobanchaceae. We identified that the diverse degradation trajectories under purifying selection existed among three Cistanche clades, showing obvious size differences on entire plastome, long single copy region and non-coding region, and different patterns of the retention/loss of functional genes. With few exception of putatively functional genes, massive plastid fragments which have been lost and transferred into the mitochondrial or nuclear genomes are nonfunctional. In contrast with the equivalents of the Orobanche species, some plastid-derived genes with diverse genomic locations are found in Cistanche. The early and initially diverged clades in different genera such as Cistanche and Aphyllon possess obvious patterns of plastome degradation, suggesting that such key lineages should be considered prior to comparative analysis of plastome evolution, especially in the same genus.
Rebecca A Povilus, Jeffery M DaCosta, Christopher Grassa, Prasad RV Satyaki, Morgan Moeglein, Johan Jaenisch, Zhenxiang Xi, Sarah Mathews, Mary Gehring, Charles C Davis, and William E Friedman. 1/1/2019. “Water lily (Nymphaea thermarum) draft genome reveals variable genomic signatures of ancient vascular cambium losses.” bioRxiv.Abstract
For more than 225 million years, all seed plants were woody trees, shrubs, or vines (1,2,3,4). Shortly after the origin of angiosperms ~135 million years ago (MYA) (5), the Nymphaeales (water lilies) became one of the first lineages to deviate from their ancestral, woody habit by losing the vascular cambium (6), the meristematic population of cells that produces secondary xylem (wood) and phloem. Many of the genes and gene families that regulate differentiation of secondary tissues also regulate the differentiation of primary xylem and phloem (7,8,9), which are produced by apical meristems and retained in nearly all seed plants. Here we sequence and assemble a draft genome of the water lily Nymphaea thermarum, an emerging system for the study of early flowering plant evolution, and compare it to genomes from other cambium-bearing and cambium-less lineages (like monocots and Nelumbo). This reveals lineage-specific patterns of gene loss and divergence. Nymphaea is characterized by a significant contraction of the HD-ZIP III transcription factors, specifically loss of REVOLUTA, which influences cambial activity in other angiosperms. We also find the Nymphaea and monocot copies of cambium-associated CLE signaling peptides display unique substitutions at otherwise highly conserved amino acids. Nelumbo displays no obvious divergence in cambium-associated genes. The divergent genomic signatures of convergent vascular cambium loss reveals that even pleiotropic genes can exhibit unique divergence patterns in association with independent trait loss events. Our results shed light on the evolution of herbaceousness,which is one …

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