scispace - formally typeset
Search or ask a question
Author

Patrick S. Herendeen

Bio: Patrick S. Herendeen is an academic researcher from George Washington University. The author has contributed to research in topics: Caesalpinioideae & Genus. The author has an hindex of 40, co-authored 134 publications receiving 10630 citations. Previous affiliations of Patrick S. Herendeen include Royal Botanic Gardens & University of California, Davis.


Papers
More filters
01 Jan 2012
TL;DR: This book is intended to provide a jumping-off point for future generations of plant taxonomists to assess the phytochemical properties ofruits and vegetables in the context of E.coli.

2,578 citations

BookDOI
26 Jun 2018
TL;DR: The International Association for Plant Taxonomy (IApt-Taxon) as mentioned in this paper provides a taxonomic overview of the plant taxonomy and its relationships with plant taxa and its taxa.
Abstract: © 2018, International Association for Plant Taxonomy. All rights reserved. No part of this book may be reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, or by any information storage and retrieval system, or be translated into any other language, without written permission from the copyright holder. https://www.iapt-taxon.org/nomen/main.php

1,190 citations

Book
01 Jan 1981
TL;DR: An examination of the phylogenetic relationships of Papilionoideae and the relationships in Caesalpinioidae and Mimosoideae is examined.
Abstract: An examination of the phylogenetic relationships of Papilionoideae and the relationships in Caesalpinioideae and Mimosoideae

956 citations

Journal ArticleDOI
TL;DR: Tertiary macrofossils of the flowering plant family Leguminosae were used as time constraints to estimate ages of the earliest branching clades identified in separate plastid matK and rbcL gene phylogenies, pointing to a rapid family-wide diversification, and predict few if any legume fossils prior to the Cenozoic.
Abstract: Tertiary macrofossils of the flowering plant family Leguminosae (legumes) were used as time constraints to estimate ages of the earliest branching clades identified in separate plastid matK and rbcL gene phylogenies. Penalized likelihood rate smoothing was performed on sets of Bayesian likelihood trees generated with the AIC-selected GTR+ Gamma +I substitution model. Unequivocal legume fossils dating from the Recent continuously back to about 56 million years ago were used to fix the family stem clade at 60 million years (Ma), and at 1-Ma intervals back to 70 Ma. Specific fossils that showed distinctive combinations of apomorphic traits were used to constrain the minimum age of 12 specific internal nodes. These constraints were placed on stem rather than respective crown clades in order to bias for younger age estimates. Regardless, the mean age of the legume crown clade differs by only 1.0 to 2.5 Ma from the fixed age of the legume stem clade. Additionally, the oldest caesalpinioid, mimosoid, and papilionoid crown clades show approximately the same age range of 39 to 59 Ma. These findings all point to a rapid family-wide diversification, and predict few if any legume fossils prior to the Cenozoic. The range of the matK substitution rate, 2.1-24.6 x 10(-10) substitutions per site per year, is higher than that of rbcL, 1.6- 8.6 x 10(-10), and is accompanied by more uniform rate variation among codon positions. The matK and rbcL substitution rates are highly correlated across the legume family. For example, both loci have the slowest substitution rates among the mimosoids and the fastest rates among the millettioid legumes. This explains why groups such as the millettioids are amenable to species-level phylogenetic analysis with these loci, whereas other legume groups are not.

848 citations

Journal ArticleDOI
Nasim Azani1, Marielle Babineau2, C. Donovan Bailey3, Hannah Banks4, Ariane R. Barbosa5, Rafael Barbosa Pinto6, James S. Boatwright7, Leonardo Maurici Borges8, Gillian K. Brown9, Anne Bruneau2, Elisa Silva Candido6, Domingos Cardoso10, Kuo-Fang Chung11, Ruth Clark4, Adilva de Souza Conceição, Michael D. Crisp12, Paloma Cubas13, Alfonso Delgado-Salinas14, Kyle G. Dexter, Jeff J. Doyle15, Jérôme Duminil16, Ashley N. Egan17, Manuel de la Estrella4, Marcus J. Falcao, Dmitry A. Filatov18, Ana Paula Fortuna-Perez19, Renee Hersilia Fortunato20, Edeline Gagnon2, Peter Gasson4, Juliana Gastaldello Rando21, Ana Maria Goulart de Azevedo Tozzi6, Bee F. Gunn12, David Harris22, Elspeth Haston22, Julie A. Hawkins23, Patrick S. Herendeen, Colin E. Hughes24, João Ricardo Vieira Iganci25, Firouzeh Javadi26, Sheku Alfred Kanu27, Shahrokh Kazempour-Osaloo28, Geoffrey C. Kite4, Bente B. Klitgaard4, Fabio J. Kochanovski6, Erik J. M. Koenen24, Lynsey Kovar3, Matt Lavin29, M. Marianne le Roux30, Gwilym P. Lewis4, Haroldo Cavalcante de Lima, Maria Cristina Lopez-Roberts5, Barbara A. Mackinder22, Vitor Hugo Maia31, Valéry Malécot32, Vidal de Freitas Mansano, Brigitte Marazzi, Sawai Mattapha23, Joseph T. Miller33, Chika Mitsuyuki26, Tania M. Moura34, Daniel J. Murphy4, Madhugiri Nageswara-Rao3, Bruno Nevado18, Danilo M. Neves4, Dario I. Ojeda16, R. Toby Pennington22, Darirn E. Prado35, Gerhard Prenner4, Luciano Paganucci de Queiroz5, Gustavo Ramos10, Fabiana L. Ranzato Filardi, Pétala Gomes Ribeiro5, María de Lourdes Rico-Arce4, Michael J. Sanderson36, Juliana Santos-Silva, Wallace M. B. São-Mateus37, Marcos J. S. Silva38, Marcelo F. Simon39, Carole Sinou2, Cristiane Snak5, Élvia R. de Souza, Janet I. Sprent40, Kelly P. Steele41, Julia E. Steier42, Royce Steeves2, Charles H. Stirton43, Shuichiro Tagane26, Benjamin M. Torke44, Hironori Toyama26, Daiane Trabuco da Cruz5, Mohammad Vatanparast17, Jan J. Wieringa45, Michael Wink46, Martin F. Wojciechowski42, Tetsukazu Yahara26, Ting-Shuang Yi47, Erin Zimmerman2 
01 Feb 2017-Taxon
TL;DR: The classification of the legume family proposed here addresses the long-known non-monophyly of the traditionally recognised subfamily Caesalpinioideae, by recognising six robustly supported monophyletic subfamilies and reflects the phylogenetic structure that is consistently resolved.
Abstract: The classification of the legume family proposed here addresses the long-known non-monophyly of the traditionally recognised subfamily Caesalpinioideae, by recognising six robustly supported monophyletic subfamilies. This new classification uses as its framework the most comprehensive phylogenetic analyses of legumes to date, based on plastid matK gene sequences, and including near-complete sampling of genera (698 of the currently recognised 765 genera) and ca. 20% (3696) of known species. The matK gene region has been the most widely sequenced across the legumes, and in most legume lineages, this gene region is sufficiently variable to yield well-supported clades. This analysis resolves the same major clades as in other phylogenies of whole plastid and nuclear gene sets (with much sparser taxon sampling). Our analysis improves upon previous studies that have used large phylogenies of the Leguminosae for addressing evolutionary questions, because it maximises generic sampling and provides a phylogenetic tree that is based on a fully curated set of sequences that are vouchered and taxonomically validated. The phylogenetic trees obtained and the underlying data are available to browse and download, facilitating subsequent analyses that require evolutionary trees. Here we propose a new community-endorsed classification of the family that reflects the phylogenetic structure that is consistently resolved and recognises six subfamilies in Leguminosae: a recircumscribed Caesalpinioideae DC., Cercidoideae Legume Phylogeny Working Group (stat. nov.), Detarioideae Burmeist., Dialioideae Legume Phylogeny Working Group (stat. nov.), Duparquetioideae Legume Phylogeny Working Group (stat. nov.), and Papilionoideae DC. The traditionally recognised subfamily Mimosoideae is a distinct clade nested within the recircumscribed Caesalpinioideae and is referred to informally as the mimosoid clade pending a forthcoming formal tribal and/or cladebased classification of the new Caesalpinioideae. We provide a key for subfamily identification, descriptions with diagnostic charactertistics for the subfamilies, figures illustrating their floral and fruit diversity, and lists of genera by subfamily. This new classification of Leguminosae represents a consensus view of the international legume systematics community; it invokes both compromise and practicality of use.

697 citations


Cited by
More filters
01 Jun 2012
TL;DR: SPAdes as mentioned in this paper is a new assembler for both single-cell and standard (multicell) assembly, and demonstrate that it improves on the recently released E+V-SC assembler and on popular assemblers Velvet and SoapDeNovo (for multicell data).
Abstract: The lion's share of bacteria in various environments cannot be cloned in the laboratory and thus cannot be sequenced using existing technologies. A major goal of single-cell genomics is to complement gene-centric metagenomic data with whole-genome assemblies of uncultivated organisms. Assembly of single-cell data is challenging because of highly non-uniform read coverage as well as elevated levels of sequencing errors and chimeric reads. We describe SPAdes, a new assembler for both single-cell and standard (multicell) assembly, and demonstrate that it improves on the recently released E+V-SC assembler (specialized for single-cell data) and on popular assemblers Velvet and SoapDeNovo (for multicell data). SPAdes generates single-cell assemblies, providing information about genomes of uncultivatable bacteria that vastly exceeds what may be obtained via traditional metagenomics studies. SPAdes is available online ( http://bioinf.spbau.ru/spades ). It is distributed as open source software.

10,124 citations

Journal ArticleDOI
TL;DR: A revised and updated classification for the families of the flowering plants is provided in this paper, which includes Austrobaileyales, Canellales, Gunnerales, Crossosomatales and Celastrales.

7,299 citations

Journal ArticleDOI
14 Jan 2010-Nature
TL;DR: An accurate soybean genome sequence will facilitate the identification of the genetic basis of many soybean traits, and accelerate the creation of improved soybean varieties.
Abstract: Soybean (Glycine max) is one of the most important crop plants for seed protein and oil content, and for its capacity to fix atmospheric nitrogen through symbioses with soil-borne microorganisms. We sequenced the 1.1-gigabase genome by a whole-genome shotgun approach and integrated it with physical and high-density genetic maps to create a chromosome-scale draft sequence assembly. We predict 46,430 protein-coding genes, 70% more than Arabidopsis and similar to the poplar genome which, like soybean, is an ancient polyploid (palaeopolyploid). About 78% of the predicted genes occur in chromosome ends, which comprise less than one-half of the genome but account for nearly all of the genetic recombination. Genome duplications occurred at approximately 59 and 13 million years ago, resulting in a highly duplicated genome with nearly 75% of the genes present in multiple copies. The two duplication events were followed by gene diversification and loss, and numerous chromosome rearrangements. An accurate soybean genome sequence will facilitate the identification of the genetic basis of many soybean traits, and accelerate the creation of improved soybean varieties.

3,743 citations

Journal ArticleDOI
TL;DR: Angiosperm divergence times are estimated using non–parametric rate smoothing and a three–gene dataset covering ca.
Abstract: Growing evidence of morphological diversity in angiosperm flowers, seeds and pollen from the mid Cretaceous and the presence of derived lineages from increasingly older geological deposits both imply that the timing of early angiosperm cladogenesis is older than fossil-based estimates have indicated. An alternative to fossils for calibrating the phylogeny comes from divergence in DNA sequence data. Here, angiosperm divergence times are estimated using non-parametric rate smoothing and a three-gene dataset covering ca. 75% of all angiosperm families recognized in recent classifications. The results provide an initial hypothesis of angiosperm diversification times. Using an internal calibration point, an independent evaluation of angiosperm and eudicot origins is performed. The origin of the crown group of extant angiosperms is indicated to be Early to Middle Jurassic (179-158 Myr), and the origin of eudicots is resolved as Late Jurassic to mid Cretaceous (147-131 Myr). Both estimates, despite a conservative calibration point, are older than current fossil-based estimates.

1,522 citations

Journal ArticleDOI
01 Feb 1987-Taxon

1,361 citations