Early Eudicot flower and fruit: Dakotanthus gen. nov. from the Cretaceous Dakota Formation of Kansas and Nebraska, USA
 
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1
Florida Museum of Natural History, University of Florida, 1659 Museum Road, Dickinson Hall, Gainesville, Florida, 32611-7800, USA
 
2
Department of Earth and Atmospheric Sciences, Indiana University, 1001 East 10th Street, Bloomington, Indiana 47405-1405, USA
 
3
Department of Biology, University of Florida, 213 Carr Hall, Newell Dr., Gainesville, Florida, 32611-8525, USA
 
4
Department of Geological Sciences, University of Saskatchewan, 114 Science Place, Saskatoon, SK S7N 5E2, Canada
 
 
Online publication date: 2018-06-19
 
 
Publication date: 2018-06-19
 
 
Acta Palaeobotanica 2018; 58(1): 27-40
 
ABSTRACT
An extinct plant that populated the eastern margin of the Cretaceous Midcontinental Seaway of North America about 100 million years ago has attracted interest as one of the earliest known bisexual flowers in the fossil record. Reexamination of the type specimen of Carpites cordiformis Lesq., and corresponding specimens from sandstones and clays of the Dakota Formation of Kansas and Nebraska and the correlative Woodbine Sandstone of Texas, with both light microscopy and micro CT scanning, leads to a revised concept of the morphology and affinities of the “Rose Creek flower”. The moderately large flowers (22–30 mm diameter) have two perianth whorls: five basally fused sepals and five free spatulate petals. The gynoecium is pentacarpellate with five styles. A crescent-shaped nectariferous pad occurs at the base of the gynoecium aligned with each sepal. Ten stamens are inserted at the level of the nectaries, one whorl organized opposite the sepals and another opposite the petals. In situ pollen is oblate, brevitricolporate and finely verrucate. The fruits are loculicidal capsules with persistent calyx and disk. Comparing the full suite of observed characters with those of extant angiosperms indicates particularly close similarity to the monogeneric fabalean family Quillajaceae, with shared features of perianth number and morphology, nectary position and morphology, stamen number and morphology, and gynoecium merosity, although the fossil differs from extant Quillaja in fruit type (capsule vs basally syncarpous follicles) and especially in pollen morphology (10 μm oblate, microverrucate, vs 30–40 μm prolate, striate).
 
REFERENCES (37)
1.
ANDREWS H.N, JR. 1970. Index of generic names of fossil plants, 1820–1965. U.S. Geol. Surv. Bull., 1300: 1–354.
 
2.
Barclay R.S., Rioux M., Meyer L.B., Bowring S.A., Johnson K.R. & Miller I.M. 2015. High precision U–Pb zircon geochronology for Cenomanian Dakota Formation floras In Utah. Cret. Res., 52: 213–237.
 
3.
Basinger J.F. & Dilcher D.L. 1984. Ancient bisexual flowers. Science, 224(4648): 511–513.
 
4.
Bello M.A., Hawkins J.A., Rudall P.J., Bello M.A., Hawkins J.A. & Rudall P.J. 2008. Floral morphology and development in Quillajaceae and Surianaceae (Fabales), the species-poor relatives of Leguminosae and Polygalaceae. Ann. Bot., 101: 483–483.
 
5.
BRENNER R.L., LUDVIGSON G.A., WITZKE B.J., ZAWISTOSKI A.N., KVALE E.P., RAVN R.L. & JOECKEL R.M. 2000. Late Albian Kiowa–Skull Creek marine transgression, lower Dakota Formation, eastern margin of Western Interior Seaway, USA. J. Sed. Res., 70: 868–878.
 
6.
Claxton F., Banks H., Klitgaard B.B. & Crane P.R. 2005. Pollen morphology of families Quillajaceae and Surianaceae (Fabales). Rev. Palaeobot. Palynol., 133: 221–233.
 
7.
CRANE P.R. & DILCHER D.L. 1984. Lesqueria: an early angiosperm fruiting axis from the mid-Cretaceous. Ann. Missouri Bot. Gard., 71: 384–402.
 
8.
Crane P.R., Manchester S.R. & Dilcher D.L. 1991. Reproductive and vegetative structure of Nordenskioldia (Trochodendraceae), a vesselless dicotyledon from the Early Tertiary of the Northern Hemisphere. Am. J. Bot., 78: 1311–1334.
 
9.
CREPET W.L., NIXON K.C. & GANDOLFO M.A. 2004. Fossil evidence and phylogeny: the age of major angiosperm clades based on mesofossil and macrofossil evidence from Cretaceous deposits. Am. J. Bot., 91: 1666–1682.
 
10.
Díaz-Forestier J., Gómez M. & Montenegro G. 2009. Nectar volume and floral entomofauna as a tool for the implementation of sustainable apicultural management plans in Quillaja saponaria Mol. Agroforestry Systems, 76: 149–162.
 
11.
DILCHER D.L. 1979. Early angiosperm reproduction: an introductory report. Rev. Palaeobot. Palynol., 27: 291–328.
 
12.
DILCHER D.L. & CRANE P.R. 1984a. In pursuit of the first flower. Nat. Hist. Mag., 93: 56–61.
 
13.
DILCHER D.L. & CRANE P.R. 1984b. Archaeanthus: An early angiosperm from the Cenomanian of the Western Interior of North America. Ann. Missouri Bot. Gard., 71: 351–383.
 
14.
FRIIS E.M., CRANE P.R. & PEDERSEN K.R. 2011. Early flowers and angiosperm evolution. Cambridge University Press, Cambridge, New York.
 
15.
FRIIS E.M., CRANE P.R. & PEDERSEN K.R. 2016. The emergence of core eudicots: new floral evidence from the earliest Late Cretaceous. Proc. R. Soc. B, 283: 20161325.
 
16.
GRÖCKE D.R., LUDVIGSON G.A., WITZKE B.L., ROBINSON S.A., JOECKEL R.M., UFNAR D.F. & RAVN R.S. 2006. Recognizing the Albian-Cenomanian (OAE1d) sequence boundary using plant carbon isotopes: Dakota Formation, Western Interior Basin, USA. Geology, 34: 193–196.
 
17.
HEER O. 1869. Miocene baltische Flora. Beiträge zur Naturkunde Preussens, Volume 2. Koch, Königsberg.
 
18.
HEER O. 1870. Die Miocene Flora und Fauna Spitzbergens. Kungliga Svenska Vetenskapsakademien Handlingar 8(7): 1–98 (Reprinted as Flora Fossilis Arctica 2[3], 1871).
 
19.
LESQUEREUX L. 1874. Contributions to the fossil flora of the Western Territories, Part I. The Cretaceous flora. Rep. (Annual) U.S. Geol. Geogr. Surv. Territ., 6: 1–136.
 
20.
LESQUEREUX L. 1892. The flora of the Dakota Group: a posthumous work. Monogr. U.S. Geol. Surv., 17: 1–287.
 
21.
LUDVIGSON G.A., WITZKE B.J., JOECKEL R.M., RAVN R.L., PHILLIPS P.L., GONZÁLEZ L.A., & BRENNER R.L. 2010. New insights on the sequence stratigraphic architecture of the Dakota Formation in Kansas-Nebraska-Iowa from a decade of sponsored research activity. Current Research in Earth Sciences: Kansas Geol. Surv. Bull. 258, part 2, 35 pp.
 
22.
MACNEAL D.L. 1958. The flora of the Upper Cretaceous Woodbine sand in Denton County, Texas. Monogr. Acad. Nat. Sci., 10: 1–152.
 
23.
MCNEILL J., Chairman Editor. 2012. International code of nomenclature for algae, fungi, and plants (Melbourne Code). Regnum Vegetabile, 154: 1–208. Koeltz Scientific Books, Königstein, Germany.
 
24.
MANCHESTER S.R. & O’LEARY E.L. 2010. Phylogenetic distribution and identification of fin-winged fruits. Bot. Rev., 76: 1–82.
 
25.
RETALLACK G. & DILCHER D.L. 1981a. Coastal hypothesis for the dispersal and rise to dominance of flowering plants: 27–77. In: K.J. Niklas (ed.), Paleobotany, Paleoecology, and Evolution, vol. 2, Praeger Publishers, New York.
 
26.
RETALLACK G. & DILCHER D.L. 1981b. Early angio­sperm reproduction: Prisca reynoldsii, gen. et sp. nov. from mid-Cretaceous coastal deposits in Kansas, USA. Palaeontographica, B, 179: 103–137.
 
27.
RETALLACK G. & DILCHER D.L. 1986. Cretaceous angiosperm invasion of North America. Cret. Res., 7: 227–252.
 
28.
RETALLACK G. & DILCHER D.L. 2012. Outcrop versus core and geophysical log interpretation of mid-Cretaceous paleosols from the Dakota Formation of Kansas. Palaeogeogr., Palaeoclim., Palaeoecol. 329–330: 47–63.
 
29.
RICHARDSON J.E., FAY M.F., CRONK Q.C., BOWMAN D. & CHASE M.W. 2000. A phylogenetic analysis of Rhamnaceae using rbcL and trnL-F plastid DNA sequences. Am. J. Bot., 87: 1309–1324.
 
30.
RICHARDSON J.E., CHATROU L.W., MOLS J.B., ERKENS R.H.J. & PIRIE M.D. 2004. Historical biogeography of two cosmopolitan families of flowering plants: Annonaceae and Rhamnaceae. Philos. Trans. R. Soc. Lond. B, 359: 1495–1508.
 
31.
RONSE De CRAENE L.P. 2010. Floral Diagrams: an Aid to Understanding Flower Morphology and Evolution. Cambridge University Press, Cambridge, New York.
 
32.
SCHÖNENBERGER J. & von BALTHAZAR M. 2006. Reproductive structures and phylogenetic framework of the rosids – progress and prospects. Plant Syst. Evol., 260: 87–106.
 
33.
SLATTERY J.S., COBBAN W.A., MCKINNEY K.C., HARRIES P.J. & SANDNESS A.L. 2015. Early Cretaceous to Paleocene paleogeography of the Western Interior Seaway: the interaction of eustasy and tectonism. Wyoming Geological Association Guidebook, 2015: 22–60.
 
34.
SOLTIS D., SOLTIS P., ENDRESS P., CHASE M., MANCHESTER S., JUDD W., MAJURE L. & MAVRODIEV E. 2018. Phylogeny and Evolution of the Angiosperms, revised and updated edition. University of Chicago Press, Chicago.
 
35.
Upchurch G.R. & Dilcher D.L. 1990. Cenomanian angiosperm leaf megafossils, Dakota Formation, Rose Creek locality, Jefferson County, southeastern Nebraska. U.S. Geol. Surv. Bull., 1915: 1–55.
 
36.
Wang H., Dilcher D.L., Schwarzwalder R.N. & Kvaček J. 2011. Vegetative and reproductive morphology of an extinct Early Cretaceous member of Platanaceae from the Braun’s Ranch locality, Kansas, USA. Int. J. Plant Sci., 172: 139–157.
 
37.
Whitehead D.R. 1983. Wind pollination: some ecological and evolutionary perspectives: 97–108. In: L. Real (ed.), Pollination Biology, Academic Press.
 
 
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