David Dilcher’s research while affiliated with Indiana University Bloomington and other places

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Publications (4)


Fig. 1. P. wuhaia J. Wang et al. sp. nov. from the early Permian Taiyuan Formation of Wuda Coalfield, Inner Mongolia. (A) Holotype with an entire crown consisting of pseudostrobili and leaves. (B) Once-pinnate compound leaf with both large and small pinnules visible. Reprinted with permission from ref. 15. (C) Cross-section of a crown illustrating pseudostrobili around the stem. (D) Cross-section of pseudostrobilus with microsporangia around the axis with bilateral, inversed Ω-shaped vascular bundle. (E) Cross-section of a leaf rachis showing the same form of vascular bundle as that of pseudostrobili axes. (F-H) Partial cross, radial, and tangential sections of the stem showing the secondary xylem (wood). (I) Tangential section of pseudostrobilus showing sporangial arrangement with single line of megasporangia along with the axis (middle-right pseudostrobilus of the fragmental crown illustrated SI Appendix, Fig. S8; specimen PB22132; magnified in SI Appendix, Fig. S21C.) (J) Radial section of pseudostrobilus showing adaxial sporangia and axis lacking nodes (upmost-left pseudostrobilus of the fragmental crown in SI Appendix, Fig. S8; magnified in SI Appendix, Fig. S21A). (K) Tangential section showing adaxial sporangia and a single line of megasporangia along with the axis (SI Appendix, Fig. S7; specimen PB22131, second up-right pseudostrobilus). (L) Tangential section through same specimen as K showing megasporangial arrangement (magnified in SI Appendix, Figs. S21B and S23A). (M) Detail of the middle part of L showing the megasporangia and microsporangia. (N) Single spore macerated from the holotype. (Scale bars: A, 10 cm; B, 3 cm; C-E, 1 cm; F, 100 μm; G and H, 200 μm; I-L, 5 mm; M, 2 mm; N, 10 μm.)
Fig. 2. Reconstruction of the aerial parts of P. wuhaia J. Wang et al. sp. nov. from the early Permian of China (based on the holotype). Image credit: Yugao Ren and Sijia Tang (artists).
Fig. 3. Diagrammatic reconstruction of the key features of P. wuhaia J. Wang et al. (A) Stem bears pseudostrobili and once-pinnate compound leaves; pseudostrobili are attached to the fertile zone, above which the leaves are shown from the abaxial side, and below which the leaves are shown from the adaxial side. (B) A pseudostrobilus shown its longitudinal surface. (C) Cross-section of a pseudostrobilus showing both megasporangia and microsporangia, the bilateral symmetrical Ω-shaped vascular bundle and sporophylls; noting the relative position of the presumed two megasporangia and the orientation of the opening of the vascular bundle. (D) Partial longitudinal section through the central axis of the pseudostrobilus and the symmetric axis of the vascular bundle, approximately corresponding to the dashed line in C; (E) partial of the leaf showing the arrangement of the small and big pinnules, seen from the abaxial (Upper) and adaxial (Lower) sides, respectively; (F) a pair of small and big pinnules showing the radiate venation; (G and H) cross-section of the stem showing the anatomy; H is the magnification of a part (within the dashed line) of the stem in G. CT, cortex; LT, leaf trace; MEG, megasporangium; MIG, microsporangium; PD, periderm; PT, pith; PX, primary xylem; SP, sporophyll; SX, secondary xylem; VB, vascular bundle.
Fig. 4. Single most parsimonious 102 step tree resolving Noeggerathiales (Paratingia and Dorsalistachya) as the most derived members of a heterosporous progymnosperm clade that is immediate sister group to seed plants. The heterosporous progymnosperm clade and seed plants diverge from the stem after the homosporous Aneurophytales clade. Bootstrap values above branches, decay values below. Traditionally identified paraphyletic plant groups shown with dashed lines and their names in bounding commas.
Ancient noeggerathialean reveals the seed plant sister group diversified alongside the primary seed plant radiation
  • Article
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March 2021

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839 Reads

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20 Citations

Proceedings of the National Academy of Sciences

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David Dilcher

Significance There were two heterosporous lignophyte lineages of which only one, the seed plants, survived the Permian–Triassic mass extinction. Based on exceptionally complete fossil trees from a 300-My-old volcanic ash, the enigmatic Noeggerathiales are now recognized as belonging to the other lineage. They diversified alongside the primary seed plant radiation and constitute seed plants’ closest relatives. Noeggerathiales are reconstructed as members of a plexus of free-sporing woody plants called progymnosperms, extending their age range by 60 My. Following the origin of seed plants, progymnosperms were previously thought to have become gradually less abundant before dying out in Carboniferous. We show they diversified and evolved complex morphologies including cone-like structures from modified leaves before going extinct at the Permian–Triassic extinction.

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Fig. 1. Cretaceous tumbling flower beetle A. burmitina. (A) Habitus. (B) Drawing. (C) Prothorax and pronotum highlighted by red dashed lines. (D) Microtomographic reconstruction of the head. Maxillary palpi highlighted in yellow. (E) Abdomen, I−IV represent first to fifth abdominal ventrites. (F) Hind leg, I−IV represent first to fourth metatarsomeres. an, antennae; cl, claw; mp, maxillary palp; py, pygidium; sp, spines on metatibiae and metatarsi; tr, trochanter.
Fig. 2. A. burmitina and tricolpate pollen grains. (A) Habitus. Pollen grains attached to the body are indicated by red dots, unattached are indicated by yellow dots, clumped pollen are indicated by blue squares. (B−H) Locations are highlighted in A. (B and C) Pollen grains near the body. Yellow arrows point to colpi. (D and E) Pollen grains on the body. (F−H) Clumped pollen grains. (G and H) Locations are highlighted in F and G, respectively. Blue arrows point to colpi.
Fig. 3. Ecological reconstruction of A. burmitina. These tumbling flower beetles are feeding on eudicot flowers. The color and morphology of flowers are artistic only.
Pollination of Cretaceous flowers

November 2019

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1,605 Reads

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69 Citations

Proceedings of the National Academy of Sciences

Insect pollination of flowering plants (angiosperms) is responsible for the majority of the world’s flowering plant diversity and is key to the Cretaceous radiation of angiosperms. Although both insects and angiosperms were common by the mid-Cretaceous, direct fossil evidence of insect pollination is lacking. Direct evidence of Cretaceous insect pollination is associated with insect-gymnosperm pollination. Here, we report a specialized beetle-angiosperm pollination mode from mid-Cretaceous Burmese amber (99 mega-annum [Ma]) in which a tumbling flower beetle (Mordellidae), Angimordella burmitina gen. et sp. nov., has many tricolpate pollen grains attached. A. burmitina exhibits several specialized body structures for flower-visiting behavior including its body shape and pollen - feeding mouthparts revealed by X-ray microcomputed tomography (micro-CT). The tricolpate pollen in the amber belongs to the eudicots that comprise the majority of extant angiosperm species. These pollen grains exhibit zoophilous pollination attributes including their ornamentation, size, and clumping characteristics. Tricolpate pollen grains attached to the beetle’s hairs are revealed by confocal laser scanning microscopy, which is a powerful tool for investigating pollen in amber. Our findings provide direct evidence of insect pollination of Cretaceous angiosperms, extending the range insect-angiosperm pollination association by at least 50 million years. Our results support the hypothesis that specialized insect pollination modes were present in eudicots 99 million years ago.


Fig. 1. Geological and paleogeographic maps of Burmese amber. (A) Geological map showing the position of Burmese amber in Hukawng Valley, northern Myanmar. (B) Paleogeographic map showing the position (red triangle) of Burmese amber site during Late Albian (14, 17).
Fig. 2. Ammonite Puzosia (Bhimaites) Matsumoto. (A) Lateral view under light microscopy. (B) Flattened sutures reconstructed by microtomography. (C) Microtomographic reconstruction, apparent view. (D) Microtomographic reconstruction, surface rendering; (E) Microtomographic reconstruction, virtual section. (Scale bars, 2 mm.)
Fig. 3. Isopods of uncertain taxonomic affinity, but generally consistent with littoral or supralittoral taxa. (A) Isopod 1. (B) Isopod 2. (C) Isopod 3. (D) Circular structure attached to the dorsal surface of isopod 2. (Scale bars, 1 mm in A and C. Scale bar, 0.5 mm in B and D.)
Fig. 4. Gastropods. (A) Mathilda sp. (B) Mathilda sp. (C) Undetermined specimen. (D) Undetermined specimen. (Scale bars, 1 mm.)
An ammonite trapped in Burmese amber

May 2019

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2,178 Reads

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336 Citations

Proceedings of the National Academy of Sciences

Significance Aquatic organisms are rarely found in amber, but when they occur they provide invaluable evidence for the better understanding of amber taphonomy and past ecosystems. We report an ammonite and several marine gastropods alongside a mixed assemblage of intertidal and terrestrial forest floor organisms in mid-Cretaceous Burmese amber. Our discovery indicates that the Burmese amber forest was living near a dynamic and shifting coastal environment. The ammonite also provides supporting evidence for the age of the amber, which is still debated, and represents a rare example of dating using fossils present inside the amber.

Citations (4)


... Leary, 1980;Wang et al. 2004;Taylor et al. 2009). Recently, the finding and description of whole specimens found within a Permian ash-tuff with articulated foliage, (pseudo-like)strobili and stem with anatomical preservation, allowed the elucidation of the Noeggerathiales as members of the progymnosperms clade, a sister group to the seed plants (Wang et al. 2021;Yang et al. 2023). ...

Reference:

Palaeopteridium andrenelii sp. nov., a new noeggerathialean species from the Middle Pennsylvanian of Portugal with new insights on the Noeggerathiales
Ancient noeggerathialean reveals the seed plant sister group diversified alongside the primary seed plant radiation

Proceedings of the National Academy of Sciences

... The marked increase in angiosperm diversity is closely linked to their evolution of reproductive and ecophysiological innovations (Leslie et al., 2021;William, 2008). Key floral traits evolved associated with specialized modes of insect pollination, including bilateral symmetry, prolonged calyx tubes, fused petals (sympetaly), and the production of nectar and resin rewards (Crepet, 1996;Bao et al., 2019). Additionally, by the Cenomanian, angiosperms had evolved highly efficient leaves with vein densities significantly surpassing those of non-angiosperms, marking a major advancement in photosynthetic capacity and ecological competitiveness (Feild et al., 2011;Brodribb & Feild, 2010). ...

Pollination of Cretaceous flowers

Proceedings of the National Academy of Sciences

... Zygogrylloblatta inhabited warm, humid tropical environments [56], a stark contrast to the high-latitude, high-elevation habitats of extant Grylloblattidae in the Northern Hemisphere [7,30]. The divergence time of the extant Grylloblattidae is unknown, dated to 30−115 Ma [57], but it may overlap with the age of the Burmese amber, which could suggest that the ice-crawlers preserved in Burmese amber are from the early period of divergence of the extant linages. ...

An ammonite trapped in Burmese amber

Proceedings of the National Academy of Sciences