10.5061/DRYAD.G4Q6PV3
Vőfély, Róza V.
University of Cambridge
Gallagher, Joseph
University of Massachusetts Amherst
Pisano, Grace D.
University of Massachusetts Amherst
Bartlett, Madelaine
University of Massachusetts Amherst
Braybrook, Siobhan A.
University of California Los Angeles
University of Cambridge
Data from: Of puzzles and pavements: a quantitative exploration of leaf
epidermal cell shape
Dryad
dataset
2019
Platycerium elephantotis
Agave sisalana
Paeonia tenuifolia
Stichoneuron caudatum
Guaiacum officinale
Cymbidium gyokuchin
Scrophularia heterophylla
Haloragis erecta
Nephrolepis hirsutula
Sisymbrium austriacum
Ruscus hypoglossum
Todea barbara
Euphorbia flanaganii
Alpinia zerumbet
Angiopteris evecta
Goniopteris
Freycinetia scandens
Cercestis mirabilis
Jasione heldreichii
Alstroemeria aurea
Dicksonia antarctica
Chamaecyparis thyoides
Ceratostigma willmottianum
Eryngium agavifolium
Actiniopteris semiflabellata
Scorzonera hispanica
Aglaonema crispum
Cordia nitida
Veronica petraea
Amaranthus caudatus
Passiflora edulis
Persicaria weyrichii
Senna didymobotrya
Centranthus ruber
Montinia caryophyllacea
Tradescantia spathacea
Carica papaya
Ceratostigma plumbaginoides
Zingiber officinale
Podocarpus macrophyllus
Picea glauca
Zea mays
Galium odoratum
Palisota mannii
Acanthus spinosus
Rumex acetosella
Amaryllis belladonna
Tabernaemontana divaricata
Oncidium sphacelatum
Beta trigyna
Sternbergia lutea
Hydrocleys nymphoides
Pandanus tectorius
Tectaria pseudosinuata
Scabiosa olgae
Plantago afra
Lygodium microphyllum
Clivia miniata
Eriachne pallescens
Mimosa pudica
Pellaea viridis
Asplenium vieillardii
Rhus potaninii
Pollia japonica
Polypodium
Rosa mollis
Danthonia californica
Iris japonica
Asplenium lancifolium
Vanilla planifolia
Polygonum affine
Cuphea ignea
Justicia guttata
Beta vulgaris
Anemone canadensis
Campanula fenestrellata
Tsuga canadensis
Curcuma longa
Microcycas calocoma
Dioscorea bulbifera
Rauvolfia verticillata
Carex morrowii
Lithocarpus henryi
Picea abies
Helminthostachys zeylanica
Aconitum carmichaelii
Euphorbia mellifera
Cycas revoluta
Albuca bracteata
Avena strigosa
epidermal cells
Cephalaria flava
Syringa vulgaris
Marattia attenuata
Citrus limon
Fagraea berteroana
Doodia media
Arum maculatum
Cissus tiliacea
Tricyrtis hirta
Chamaecostus cuspidatus
Penstemon patens
Chenopodium bonus-henricus
Yucca gloriosa
Othonna capensis
Oenothera stricta
Adiantum hispidulum
Saxifraga canaliculata
Lamium orvala
Physalis origanifolia
Angiopteris
Tectaria
Asplenium adiantoides
Rumohra adiantiformis
Aloe vera
Myrrhis odorata
Ceropegia sandersonii
Amaranthus hybridus
Ceiba pentandra
Zamia furfuracea
Helleborus orientalis
Crocus sativus
Mentha spicata
Helminthotheca echioides
Pteris ensiformis
Symphytum caucasicum
Rubia tinctorum
Pastinaca sativa
Veronica missurica
Zamia pumila
Bulbophyllum gracillimum
Setaria italica
Acorus gramineus
Erysimum scoparium
Microsorum pteropus
Berkheya purpurea
Zamia skinneri
Campanula poscharskyana
Araucaria bidwillii
Persicaria polystachya
Eichhornia crassipes
Hiptage benghalensis
Fuchsia magellanica
Calibanus hookeri
Spathiphyllum wallisii
Dorycnium rectum
Veronica rakaiensis
Amorphophallus titanum
Peperomia serpens
Chloranthus holostegius
Globularia trichosantha
Jasminum humile
Symphytum grandiflorum
Anchusa officinalis
Succisella inflexa
Catha edulis
Illicium anisatum
Eustrephus latifolius
Laurus nobilis
Agapanthus praecox
Sabal minor
Lecanopteris sinuosa
Ruscus aculeatus
Danae racemosa
Hordeum vulgare
Leucojum aestivum
Syringa microphylla
Oxalis triangularis
Lygodium japonicum
Clerodendrum thomsoniae
Taxus canadensis
Bergenia purpurascens
Kniphofia caulescens
Bolbitis
Borago officinalis
Diplazium plantaginifolium
Platycerium andinum
Drimys winteri
Carludovica palmata
Elaphoglossum cockscomb
Davallia fejeensis
Pelargonium carnosum
Davallia subsolida
Rumex scutatus
Rohdea japonica
Arabidopsis thaliana
Trifolium pannonicum
Dodonaea viscosa
Gnetum montanum
Impatiens repens
Ercilla spicata
Malva sylvestris
Stachys macrantha
Zantedeschia aethiopica
Stenochlaena palustris
Davallia solida
Phlebodium aureum
Astragalus falcatus
Homalocladium platycladum
Hedera nepalensis
Triraphis mollis
Asarum europaeum
Cissus quadrangularis
Saxifraga hostii
Geum triflorum
Crassula fasciatudform
Annona montana
Macleania insignis
Osmunda banksiifolia
Taxodium distichum
Haworthia retusa
Phanerophlebia
Ilex paraguariensis
Tradescantia virginiana
Bolbitis lonchophora
Oryza sativa
Cyrtomium falcatum
Oxalis valdiviensis
Eryngium bourgatii
Pellaea paradoxa
Callicarpa japonica
Oxyria digyna
Capsicum annuum
Dracunculus canariensis
Bursera schlechtendalii
Smilax bona-nox
Widdringtonia nodiflora
Bupleurum fruticosum
Medicago sativa
Euphorbia pulcherrima
Niphidium crassifolium
Catharanthus roseus
Acanthus hungaricus
Ceratopteris thalictroides
Ginkgo biloba
Murraya koenigii
Monocostus uniflorus
Encephalartos transvenosus
Galium rubioides
Hemerocallis fulva
Centaurea cineraria
Heimia myrtifolia
National Science Foundation
https://ror.org/021nxhr62
IOS-1652380, IOS- 1546837
2019-08-24T00:00:00Z
2019-08-24T00:00:00Z
en
https://doi.org/10.1111/nph.15461
6671887103 bytes
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CC0 1.0 Universal (CC0 1.0) Public Domain Dedication
Epidermal cells of leaves are diverse: tabular pavement cells, trichomes,
and stomatal complexes. Pavement cells from the monocot Zea mays (maize)
and the eudicot Arabidopsis thaliana (Arabidopsis) have highly undulate
anticlinal walls. The molecular basis for generating these undulating
margins has been extensively investigated in these species. This has led
to two assumptions: first, that particular plant lineages are
characterized by particular pavement cell shapes; and second, that
undulatory cell shapes are common enough to be model shapes. To test these
assumptions, we quantified pavement cell shape in epidermides from the
leaves of 278 vascular plant taxa. We found that monocot pavement cells
tended to have weakly undulating margins, fern cells had strongly
undulating margins, and eudicot cells showed no particular undulation
degree. Cells with highly undulating margins, like those of Arabidopsis
and maize, were in the minority. We also found a trend towards more
undulating cell margins on abaxial leaf surfaces; and that highly
elongated leaves in ferns, monocots and gymnosperms tended to have highly
elongated cells. Our results reveal the diversity of pavement cell shapes,
and lays the quantitative groundwork for testing hypotheses about pavement
cell form and function within a phylogenetic context.
SampleTableTable with sampled species name, order, major clade, sample
number (for cell images and outlines), sample ID (for cell images and
outlines), and leaf sideTable S1: Species identifiers and morphometric
meansThis table provides the morphometric means (and standard deviations)
by species reported in the manuscript. It is provided here as an
accompaniment to the data files.Table S1.xlsxLeaf ImagesLeaf image files
as sampled in the manuscript.LeafImages.zipCellCoordinatesThis file
contains cell coordinate files (.txt) per cell, derived from manual
tracing of cell outlines from epidermal images in the accompanying
'CellImages' file. These outlines are designed for import into R
or MatLab for analyses.PhylogeneticResourcesdatamatrix and treefiles used
for phyllogenetic analyses in the manuscript.Cell ImagesThis file contains
all epidermal cell images used in this study. Epidermal peels were stained
with Toludine Blue O. Images are saved as .tiff files.CellImages.zip
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