Early Flowers and Angiosperm Evolution

Author: Else Marie Friis; Peter R. Crane; Kaj Raunsgaard Pedersen  

Publisher: Cambridge University Press‎

Publication year: 2011

E-ISBN: 9781139118255

P-ISBN(Paperback): 9780521592833

Subject: Q914.88 angiosperms

Keyword: 植物学

Language: ENG

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Early Flowers and Angiosperm Evolution

Description

The recent discovery of diverse fossil flowers and floral organs in Cretaceous strata has revealed astonishing details about the structural and systematic diversity of early angiosperms. Exploring the rich fossil record that has accumulated over the last three decades, this is a unique study of the evolutionary history of flowering plants from their earliest phases in obscurity to their dominance in modern vegetation. The discussion provides comprehensive biological and geological background information, before moving on to summarise the fossil record in detail. Including previously unpublished results based on research into Early and Late Cretaceous fossil floras from Europe and North America, the authors draw on direct palaeontological evidence of the pattern of angiosperm evolution through time. Synthesising palaeobotanical data with information from living plants, this unique book explores the latest research in the field, highlighting connections with phylogenetic systematics, structure and the biology of extant angiosperms.

Chapter

3.3 Climate change during the Cretaceous

3.3.1 Early and mid-Cretaceous

3.3.2 Late Cretaceous

3.4 Implications for angiosperm diversification

4 Stratigraphic framework and key areas for Cretaceous angiosperms

4.1 The stratigraphic framework

4.2 Key areas for Cretaceous angiosperms

4.3 Europe

4.3.1 Portugal: Early Cretaceous localities

4.3.2 Portugal, Late Cretaceous localities

4.3.3 Spain

4.3.4 The Czech Republic

4.3.5 Austria

4.3.6 Germany

4.3.7 Great Britain

4.3.8 Sweden

4.3.9 Other parts of Europe

4.4 Eastern North America

4.4.1 Virginia

4.4.2 Maryland and Washington, D.C.

4.4.3 New Jersey

4.4.4 Massachusetts

4.4.5 North Carolina

4.4.6 Georgia

4.4.7. Alabama

4.5 Western interior of the United States and Canada

4.5.1 Kansas and Nebraska

4.5.2 Texas

4.5.3 Colorado, Montana, North and South Dakota and New Mexico

4.5.4 Alberta and British Columbia, Canada

4.6 Alaska

4.7 Greenland

4.8 Israel, Jordan and Lebanon

4.9 North Africa

4.9.1 Egypt and Sudan

4.9.2 Tunisia and Libya

4.10 West Africa and Brazil

4.10.1 West Africa

4.10.2 Brazil

4.11 Asia

4.11.1 Kazakhstan

4.11.2 Transbaikalia

4.11.3 Siberia, Northeastern Russia and the Far East of Russia

4.11.4 Mongolia

4.11.5 China

4.11.6 Japan

4.12 Southern Gondwana and India

4.12.1 Southern Africa

4.12.2 Madagascar

4.12.3 India

4.12.4 Australia

4.12.5 Antarctica

4.12.6 New Zealand

4.12.7 Southern South America

5 Angiosperms in context: extant and fossil seed plants

5.1 Angiosperms among extant and fossil seed plants

5.2 Bennettitales-Erdtmanithecales-Gnetales (BEG) group

5.3 Gnetales

5.3.1 Temporal and spatial patterns of gnetalean radiation

5.3.2 Elaterates

5.3.3 Gnetalean mesofossils and macrofossils

5.4 Erdtmanithecales

5.5 Unassigned dispersed seeds of the BEG group

5.6 Bennettitales (Cycadeoidales)

5.6.1 Permineralised material

5.6.2 Compression material

5.7 Pentoxylales

5.8 Other Palaeozoic and Mesozoic seed plants

5.8.1 Corystospermales and potentially related plants

5.8.2 Caytoniales

5.8.3 Peltaspermales

5.8.4 Glossopteridales

5.8.5 Czekanowskiales

6 Origin and age of angiosperms

6.1 Hypotheses of seed plant relationships

6.1.1 Cladistic hypotheses based on morphology

6.1.2 Cladistic hypotheses based on molecular data

6.1.3 Current status of phylogenetic studies

6.2 Origin of angiosperm structure

6.2.1 The angiosperm flower

6.2.2 The angiosperm stamen

6.2.3 The angiosperm ovule

6.2.4 The angiosperm carpel

6.2.5 Vegetative structure of angiosperms

6.3 The age of angiosperms

6.3.1 Implications of hypotheses of relationships

6.3.2 Age estimates of angiosperms based on molecular data

6.3.3 Angiosperm age based on palaeobotanical data

6.4 Pre-Cretaceous angiosperm-like fossils

7 Phylogenetic framework and the assignment of fossils to extant groups

7.1 Early ideas on angiosperm phylogeny

7.2 Phylogenetic studies of angiosperms based on molecular data

7.3 Angiosperm phylogeny group classification (APGIII)

7.3.1 ANITA grade, Chloranthaceae and Ceratophyllaceae

7.3.2 Eumagnoliids

7.3.3 Monocots

7.3.4 Eudicots

7.4 Angiosperm phylogeny: future directions

7.5 Assignment of fossils to extant groups

8 Fossils near the base of the angiosperm tree

8.1 Early-diverging angiosperm lineages at the ANITA grade

8.1.1 Fossils of uncertain relationships at the ANITA grade

8.2 Amborellaceae

8.3 Nymphaeales

8.3.1 Hydatellaceae

8.3.2 Cabombaceae and Nymphaeaceae

8.4 Austrobaileyales

8.4.1 Austrobaileyaceae

8.4.2 Schisandraceae (including Illiciaceae)

8.4.3 Trimeniaceae

8.5 Chloranthaceae

8.5.1 Asteropollis

8.5.2 Hedyosmum-like flowers

8.5.3 Chloranthistemon

8.6 Ceratophyllaceae

9 Early fossil angiosperms of uncertain relationships

9.1 Putative angiosperms

9.1.1 Bevhalstia

9.1.2 Lappacarpus, Ievlevia, Donlesia and Beipiaoa

9.1.3 Other isolated seeds of uncertain affinity

9.2 Fossil flowers attached to inflorescences and stems

9.2.1 Archaefructus

9.2.2 Xingxueina and Caspiocarpus

9.2.3 The Koonwarra fossil

9.2.4 Myricanthium, Zlatkocarpus and other inflorescences from the Peruc flora

9.2.5 Inflorescences from the Dakota Formation

9.2.6 Other inflorescences

9.3 Isolated flowers and fruits preserved as compressions/impressions

9.3.1 Lesqueria elocata and other isolated reproductive structures

9.4 Permineralised flowers

9.5 Isolated angiosperm mesofossils

9.5.1 Isolated flowers

9.5.2 Isolated fruits and seeds

9.6 Dispersed monoaperturate pollen

9.6.1 Afropollis and Schrankipollis

9.6.2 Asteropollis and Clavatipollenites

9.6.3 Retimonocolpites, Brenneripollis and Pennipollis

9.6.4 Liliacidites and Similipollis

9.6.5 Stellatopollis

9.6.6 Transitoripollis and Tucanopollis

9.6.7 Lethomasites

9.7 Fossil leaves of uncertain relationships

10 Early fossils of eumagnoliids

10.1 Classification of eumagnoliids

10.1.1 Fossil eumagnoliids of uncertain relationships

10.2 Magnoliales

10.2.1 Fossil Magnoliales of uncertain relationships

10.2.2 Myristicaceae

10.2.3 Annonaceae

10.2.4 Eupomatiaceae

10.2.5 Magnoliaceae

10.2.6 Himantandraceae

10.2.7 Degeneriaceae

10.3 Laurales

10.3.1 Fossil Laurales of uncertain relationships

10.3.2 Atherospermataceae

10.3.3 Calycanthaceae

10.3.4 Gomortegaceae

10.3.5 Hernandiaceae

10.3.6 Lauraceae

10.3.7 Monimiaceae

10.3.8 Siparunaceae

10.4 Canellales

10.4.1 Canellaceae

10.4.2 Winteraceae

10.5 Piperales

10.5.1 Fossil Piperales of uncertain relationships

10.5.2 Aristolochiaceae

10.5.3 Lactoridaceae

10.5.4 Piperaceae

10.5.5 Saururaceae

10.5.6 Hydnoraceae

11 Fossils of monocots

11.1 Classification of monocots

11.2 Fossil evidence of monocot diversification

11.3 Putative early monocot fossils

11.3.1 Dispersed leaves

11.3.2 Dispersed pollen

11.3.3 Reproductive structures

11.4 Acorales

11.5 Alismatales

11.5.1 Putative fossil Alismatales

11.5.2 Araceae

11.5.3 Alismataceae

11.5.4 Butomaceae and Hydrocharitaceae

11.5.5 Potamogetonoids

11.6 Dioscoreales

11.7 Pandanales

11.7.1 Pandanaceae

11.7.2 Cyclanthaceae

11.7.3 Stemonaceae

11.7.4 Triuridaceae

11.8 Liliales

11.9 Asparagales

11.9.1 Amaryllidaceae and Asparagaceae

11.9.2 Other Asparagales

11.10 Commelinids

11.10.1 Arecales

11.10.2 Poales

11.10.3 Commelinales

11.10.4 Zingiberales

12 Fossils of eudicots: early-diverging groups

12.1 Classification of eudicots

12.2 Early-diverging eudicots

12.3 Fossil evidence of eudicot diversification

12.4 Fossils of uncertain relationships

12.4.1 Early tricolpate pollen in dispersed palynofloras

12.4.2 Early tricolpate pollen in situ in reproductive structures

12.4.3 Fossil reproductive structures of probable eudicot relationships

12.5 Ranunculales

12.5.1 Berberidaceae

12.5.2 Circaeasteraceae

12.5.3 Eupteleaceae

12.5.4 Lardizabalaceae

12.5.5 Menispermaceae

12.5.6 Papaveraceae

12.5.7 Ranunculaceae

12.6 Proteales

12.6.1 Nelumbonaceae

12.6.2 Platanaceae

12.6.3 Proteaceae

12.7 Sabiaceae

12.8 Buxales

12.8.1 Buxaceae

12.9 Trochodendrales

12.9.1 Trochodendraceae

13 Fossils of core eudicots: basal lineages

13.1 Classification of core eudicots

13.2 Early fossil evidence of core eudicots

13.3 Gunnerales

13.4 Dilleniaceae

13.5 Berberidopsidales

13.6 Santalales

13.7 Caryophyllales

13.8 Saxifragales

13.8.1 Unassigned Saxifragales

13.8.2 Altingiaceae

13.8.3 Cercidiphyllaceae

13.8.4 Hamamelidaceae

13.8.5 Haloragaceae and Crassulaceae

13.8.6 Iteaceae and Pterostemonaceae

13.8.7 Grossulariaceae

13.8.8 Saxifragaceae

13.8.9 Paeoniaceae

14 Fossils of core eudicots: rosids

14.1 Classification of rosids

14.2 Fossil evidence of rosids

14.3 Vitales

14.4 Fabids (Eurosids I)

14.5 The COM clade

14.5.1 Celastrales

14.5.2 Oxalidales

14.5.3 Malpighiales

14.6 The nitrogen-fixing clade

14.6.1 Fabales

14.6.2 Rosales

14.6.3 Cucurbitales

14.6.4 Fagales

14.6.5 Fossil Fagales of uncertain relationships

14.6.6 Normapolles complex

14.6.7 Nothofagaceae and Fagaceae

14.6.8 Ticodendraceae, Betulaceae and Casuarinaceae

14.6.9 Myricaceae, Rhoipteleaceae and Juglandaceae

14.7 Malvids (Eurosids II)

14.7.1 Geraniales

14.7.2 Myrtales

14.7.3 Crossosomatales and Picramniales

14.7.4 Sapindales

14.7.5 Huerteales

14.7.6 Brassicales

14.7.7 Malvales

15 Early fossils of eudicots: asterids

15.1 Classification of asterids

15.1.1 Asterid fossils of uncertain relationships

15.2 Cornales

15.2.1 Fossil Cornales of uncertain relationships

15.2.2 Cornaceae

15.2.3 Nyssaceae

15.3 Ericales

15.3.1 Ericalean fossils of uncertain relationships

15.3.2 Pentaphylacaceae and Theaceae

15.3.3 Core Ericales: Clethraceae, Cyrillaceae and Ericaceae

15.3.4 Core Ericales: Sarraceniaceae, Actinidiaceae and Roridulaceae

15.3.5 Ebenaceae and primuloids

15.3.6 Symplocaceae, Diapensiaceae and Styracaceae

15.4 Lamiids (Euasterids I)

15.4.1 Lamiid fossils of uncertain relationships

15.5 Boraginaceae, Icacinaceae and Vahliaceae

15.6 Garryales

15.7 Gentianales

15.8 Solanales and Lamiales

15.9 Campanulids (Euasterids II)

15.9.1 Campanulid fossils of uncertain relationships

15.10 Aquifoliales, Escalloniales and Asterales

15.11 Bruniales, Apiales, Paracryphiales and Dipsacales

16 Patterns of structural diversification in angiosperm reproductive organs

16.1 Inflorescence structure

16.2 Floral organisation

16.2.1 Sex of flowers

16.2.2 Receptacle, floral phyllotaxis and merism

16.2.3 Position of floral organs

16.2.4 Perianth

16.2.5 Androecium

16.2.6 Pollen

16.2.7 Gynoecium

16.2.8 Ovules and seeds

16.2.9 Nectaries

16.2.10 Floral symmetry

16.3 Other aspects of floral construction

16.3.1 Flower size

16.3.2 Protection in floral bud

16.3.3 Synorganisation of floral parts

17 History and evolution of pollination in angiosperms

17.1 Pollination in extant non-angiosperm seed plants

17.1.1 Pollination in Ginkgo and cycads

17.1.2 Pollination in conifers

17.1.3 Pollination in Gnetales

17.2 Pollination in extant angiosperms

17.2.1 Abiotic versus biotic pollination in early angiosperms

17.2.2 Abiotic pollination

17.2.3 Biotic pollination

17.3 Insects as pollinators

17.3.1 Thrip pollination and the fossil history of Thysanoptera

17.3.2 Beetle pollination and the fossil history of Coleoptera

17.3.3 Bee/wasp pollination and the fossil history of Hymenoptera

17.3.4 Fly pollination and the fossil history of Diptera

17.3.5 Butterfly/moth pollination and the fossil history of Lepidoptera

17.4 Vertebrates as pollinators

17.4.1 Bird pollination and the fossil history of birds

17.4.2 Mammal pollination and the fossil history of mammals

17.5 History of pollination in angiosperms

17.5.1 Pollination in pre-angiosperm vegetation

17.5.2 Pollination in Early Cretaceous angiosperms

17.5.3 Pollination in mid-Cretaceous angiosperms

17.5.4 Pollination in Late Cretaceous angiosperms

17.5.5 Pollination in Cenozoic angiosperms

17.6 Large-scale trends in the history of angiosperm pollination

18 History and evolution of dispersal in angiosperms

18.1 Dispersal in extant non-angiosperm seed plants

18.1.1 Dispersal in cycads

18.1.2 Dispersal in Ginkgo

18.1.3 Dispersal in conifers

18.1.4 Dispersal in Gnetales

18.2 Dispersal in extant angiosperms

18.3 Animal dispersers

18.3.1 Insects

18.3.2 Vertebrates

18.4 History of dispersal in angiosperms

18.4.1 Dispersal in pre-angiosperm vegetation

18.4.2 Dispersal in Early Cretaceous angiosperms

18.4.3 Dispersal in mid-Cretaceous angiosperms

18.4.4 Dispersal in Late Cretaceous angiosperms

18.4.5 Dispersal in Cenozoic angiosperms

18.5 Large-scale trends in the history of angiosperm dispersal

19 Vegetational context of early angiosperm diversification

19.1 Transition to angiosperm-dominated vegetation

19.2 Components of Early Cretaceous vegetation

19.2.1 Free-sporing plants

19.2.2 Bennettitales and Cycadales

19.2.3 Gnetales, Erdtmanithecales and Elaterates

19.2.4 Cheirolepidiaceae

19.2.5 Other conifers

19.2.6 Ginkgoales and Czekanowskiales

19.3 Vegetation during the early diversification of angiosperms

19.4 Early angiosperms: diversity in obscurity

19.5 Mid-Cretaceous vegetation

19.6 Late Cretaceous vegetation and floristic provinces

20 The accumulation of angiosperm diversity

20.1 Large-scale patterns in angiosperm diversification

20.2 Patterns of angiosperm diversification: early lineages

20.2.1 Nymphaeales

20.2.2 Chloranthaceae

20.3 Patterns of angiosperm diversification: eumagnoliids

20.3.1 Canellales-Piperales

20.3.2 Laurales

20.3.3 Magnoliales

20.4 Patterns of angiosperm diversification: monocots

20.5 Patterns of angiosperm diversification: eudicots

20.5.1 Proteales

20.5.2 Fagales

20.6 Angiosperm evolution and global change through the Cenozoic

20.6.1 Angiosperm evolution and the Cretaceous-Palaeogene (K-T) extinction

20.6.2 Palaeogene vegetation

20.6.3 Neogene vegetation and the origin of modern biomes

20.7 Prospects

References

Index

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