
An annotated collection of pointers
to information on palaeobotany
or to WWW resources which may be of use to palaeobotanists
(with an Upper Triassic bias).
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What´s New on Links for Palaeobotanists?
C.A. Meyer et al. (2026):
Sedimentology
and palaeoecology of a Rhaetian bone bed in Northern Switzerland formed during transgression
of a muddy coastal plain setting with fluvial-estuarine channels. In PDF,
Swiss Journal of Geosciences, 119: 85-110. DOI 10.3897/sjg.119.187486.
"... Palynological assemblages dominated by hygrophilous spores and characteristic Rhaetian
dinoflagellates constrain the age to the middle Rhaetian and document a diverse
lowland vegetation adapted to a humid environment
[...] This study reconciles earlier conflicting interpretations by demonstrating that the bone
bed records a complex interplay
of terrestrial, freshwater and marine influences rather than a fully marine or
purely continental setting ..."
N. De Leo et al. (2026):
Open
access and digital morphology data in evolutionary biology: expanding frontiers
of knowledge. Open access, BMC Ecology and Evolution.
https://doi.org/10.1186/s12862-026-02522-yhttps://doi.org/10.1186/s12862-026-02522-y.
See likewise here
(in PDF).
"... This review synthesizes technical, legal, and
behavioural perspectives on open data in digital morphology, building on prior
work to address the specific
challenges of the current AI era. By advocating for the adoption of
FAIR principles [Findable, Accessible, Interoperable, and Reusable],
the use of persistent digital
identifiers, and the implementation of digital watermarking, we offer
recommendations for establishing minimum standards in data publication. ..."
Paul R. Janke,
Pan Terra Inc., Hill City, SD:
History
of Geology.
Retrieved from the Internet Archive's Wayback Machine.
J.S. Ferraz and J.R.I. Ribeiro (2026):
Quantitative
patterns of vegetative versus reproductive fossil preservation in Permian
palaeoflorae: a meta-analysis and network approach. Open access,
Brazilian Journal of Botany, 49. See here
as well (in PDF).
"... Reproductive and vegetative organs may be preserved
in systematically different proportions, potentially biasing our understanding of
past plant communities and leading to over or underestimation of diversity depending on
the fossils available in different regions, climates, or time intervals. We thus
investigate whether vegetative or reproductive elements reported in 37 studies spanning
1945 to 2024 are more abundant in the Permian fossil record and how different geographic
scales influence the diversity of these elements ..."
J. McElwain et al. (2026):
The
geological history of plant mass extinction and terrestrial ecosystem collapse. In PDF,
https://doi.org/10.21203/rs.3.rs-9282628/v1.
See here
as well.
"... we briefly review the magnitudes and abiotic drivers of past plant extinction events,
examine their global climatic context compared to today and critically evaluate metrics used to define
fossil plant mass extinction
[...] We show that
ecosystem collapse during four of the five examined events is characterized by a transition to a novel
ecosystem post-collapse rather than by an expansion of the antecedent ecospace ..."
! E.M. Dowding et al. (2026):
The
billion-dollar case for sustaining palaeontology's digital databases. Open access,
Nature Ecology & Evolution, 10: 594–605.
See here
as well (in PDF).
"... we conducted a survey of 118 palaeontological and allied Earth science
databases, analysing their diversity dynamics, including origination and
extinction rates. We show that approximately 85% of all community-curated
databases have lifespans of less than 15 years, putting decades of investment
at risk. We show that database creation effort has increased in the past
30 years, with peaks in database loss related to 5-year funding cycles.
[...] The path forward requires a collective effort, sustained funding and
a commitment to collaboration, ensuring that palaeontological data
remain valuable resources for future generations ..."
!
L. Portailler and L. Luthardt (2026):
Shoot
apical meristem and initial vascular development of a late Palaeozoic spermatophyte
(order Medullosales). Free access,
Annals of Botany, https://doi.org/10.1093/aob/mcaf336.
"... We re-examine historical sections of a stem apex of Medullosa stellata Cotta, 1832
[...] The complex vascular system of M. stellata results from the primary stem thickening and
the corresponding position of the leaf primordia. The comparison with extant cycads demonstrates
that similar stem anatomical features of both clades are likely to be referred to functional
analogies of the vascular systems ..."
J.B. Riding and M.J. Pound (2026): Michael Charles Boulter (1942–2025). In PDF, Palynology, 50. DOI: 10.1080/01916122.2026.2634553. Note likewise here (Wikipedia).
A.M.C. Bowles and J. Paps (2025):
The
genomes of flowering plants reveal contrasting evolutionary paths in
monocots and eudicots. In PDF,
https://doi.org/10.21203/rs.3.rs-7464600/v1.
See here
as well.
"... starting with 1,181 genomes, we have selected and analysed 273 archaeplastid genomes,
to produce a novel, robustly supported angiosperm phylogeny
[...] The origin of monocots was accompanied by a period of reductive
genome evolution while the first eudicot genomes experienced modest rates of gene duplication
[...] angiosperms reached a core genomic
diversity early in their evolutionary history, corresponding to their high floral diversity ..."
!
C. Strullu-Derrien et al. (2026):
An
arbuscular mycorrhiza from the 407-million-year-old Windyfield Chert identified through
advanced fluorescence and Raman imaging. Open access,
New Phytologist, 249: 448-459. oi: 10.1111/nph.70655.
See likewise
here.
"... we combine confocal laser scanning microscopy and fluorescence lifetime imaging
microscopy (FLIM) to investigate a newly identified fungus and cellular structures of a
407-Myr-old plant from the Windyfield Chert
[...] These findings expand our understanding of ancient and extremely rare plant–fungal sym-
bioses and highlight the potential of confocal-FLIM for advancing palaeobotanical research. ..."
J. Ma (2003): The Chronology of the "living fossil" Metasequoia glyptostroboides (Taxodiaceae): A Review (1943-2003). In PDF, Harvard Papers in Botany, 8: 9-18. See here as well.
P. Kenrick and E.J. Long (2026):
Transfer
cells in Horneophyton lignieri illuminate the origin of vascular tissues
in land plants. Free access,
New Phytologist, 249: 3149-3164.
Note figure 1: Horneophyton lignieri habit and sampling of vascular tissues.
"... We show that the vascular system of H. lignieri lacks distinct xylem and phloem tissues,
contrary to prior assumptions. Instead, tissues with transfer cell-like structures are prominent ..."
M.P. D'antonio and C.K. Boyce (2026):
Structural
and physiological constraints on arborescent lycopsid establishment and growth. Free access,
New Phytologist, 249: 1605–1617.
"... a fossil specimen preserving both proximal and distal vascular
anatomy of a single lycopsid tree was studied to compare proximal
and distal trunk hydraulic conductivity
[...] We propose a new model that, despite its unusual nature, agrees
with all available evidence: sequentially larger stigmarian rooting
axes must have been serially produced as the unipolar plant body
grew upward and expanded its primary body during early ontogeny,
thereby bypassing the proximal shoot ..."
W.E. Piller (2026):
Biostratigraphy–interrelationship
between evolution, paleoecology and paleogeography. In PDF,
Newsletters on Stratigraphy, 59: 1–37.
"... The principles of biostratigraphy are reevaluated here and considered generally valid as
described in the ISG [International Stratigraphic Guide] and in general use ..."
!
O.T. Akinsanpe et al. (2025):
Biomarkers
in terrestrial organic matter from the Lower Devonian to
Oligocene: Evidence from selected regions of the laurasian supercontinent. Open access,
Evolving Earth, 3.
Note figure 4: Evolution of terrestrial plants [...] and sample ages where authors have
previously detected terrestrial plant biomarkers.
"... Biomarkers and biomarker-based parameters have been employed in
this paper as a geochemical tracer to understand the Laurasian Super
continent geological and paleoenvironmental processes, and to recon
struct paleobotanic (paleovegetation) evolution via their structural
configurations (carbon skeletons)
[...] The study has enhanced our understanding of the organic matter provenance,
terrestrialisation process, and spatiotemporal
evolution of higher plants across different geological settings ...
D. Quiroz-Cabascango et al. (2025):
Earliest
Jurassic plant assemblages from Sweden reveal a low-diversity ginkgoalean and cheirolepid
flora dominating the post-extinction landscape. Free access,
Annals of Botany, mcaf143. https://doi.org/10.1093/aob/mcaf143.
"... typical Lower Jurassic macrofloral and palynological assemblages that provide
a glimpse into the recovery flora following the end-Triassic mass extinction in a middle–high
latitude setting. This pioneer flora, dominated by Ginkgoopsida and cheirolepid conifers (well
preserved Brachyphyllum and abundant Classopollis minor), has features in
common with coeval recovery ecosystems ..."
X. Zhao et al. (2025):
Climate–carbon-cycle
interactions and spatial heterogeneity of the late Triassic Carnian pluvial episode. In PDF,
Nature Communications. See likewise
here
Note figure 4: Simulated climate states before and during the Carnian Pluvial Episode (CPE).
"... We find that the rapid CPE [Carnian Pluvial Episode] onset
(~15.8 kyr) could have been the result of volcanism and subsequent surface
carbon-cycle feedbacks.
[...] The CPE hydrological cycle was typified by
increased aridification in continental interiors and multiple precipitation
centres at low-latitude eastern regions of Pangea and at the poles ..."
M. Viney et al. (2026):
Fossil
Forests Kits: A Hands-on Approach to Paleobotany & Paleoclimate. Free access,
The American Biology Teacher, 88: 117–126.
See here
as well (in PDF).
!
H. Nakayama and N.R. Sinha (2025):
Leaf
evolution: integrating phylogenetics, developmental dynamics, and genetic insights across
land plants. Free access,
New Phytologist, 248: 2205-2220.
Note figure 2: Plant diversification and leaf evolution in the context of the fossil record
of land plants.
"... In this review, we focus on the current understanding of leaf evolution by integrating
phylogenetic relationships, the developmental dynamics of the shoot apical meristem –
the site of leaf initiation – and comparative analyses of leaf morphogenesis ..."
X. Liu et al. (2026): Multiple paths to recovery after the Permian-Triassic mass extinction. Abstract, Current Biolgy, 38.
J. van Konijnenburg-van Cittert et al. (2022):
Plant
macrofossils from the Rhaetian of Einberg near Coburg (Bavaria, Germany). Part 2.
Cycadophyta and Ginkgophyta. In PDF,
Neues Jahrbuch für Geologie und Paläontologie. Abhandlungen, 305: 109–130.
Note here
as well.
!
A.P. Storari et al. (2025):
Taphonomy
of aquatic insects from the Crato Formation Lagerstätte (Aptian, Lower Cretaceous) under an
actualistic look. Open access,
Plos one, 20. https://doi.org/10.1371/journal.pone.0331656.
"... we analyze the preservation of mayflies (Ephemeroptera) and
dragonflies (Odonata) from this formation using experimental taphonomy on 253
extant Ephemeroptera and 236 Odonata, alongside 306 fossil specimens. Disarticulation
experiments showed that the thorax of modern mayfly larvae disarticulated
first
[...] Dragonfly carcasses exhibited a characteristic leg posture in death
[...] we can safely propose with experimental data
that microbial biofilms on the surface of the water were acting during carcass sinking ..."
J. Rust and V.E. McCoy (2026):
Fossilisation
ecology – a more complete concept of taphonomy
Trends in Ecology & Evolution, 40: 942-944. Free access,
Note the given explanations in the glossary.
"... In many cases, the fossil assemblages that comprise a Fossil-Lagerstätte show
patterns that cannot be understood when considered only through the traditional taphonomic lens
[...] we propose the concept of fossilisation ecology, which extends taphonomy
by formalising the idea that the ecology of an organism may
affect its fossilisation ..."
!
R. Spiekermann et al. (2026):
Charcoalified
wood remains from the Madygen Fossil-Lagerstätte (SW Kyrgyzstan): Evidence of wildfire
in the Triassic (Ladinian–Carnian) mid-northern latitudes. Free access,
Review of Palaeobotany and Palynology, 351.
Note figure 13: Palaeogeographical distribution of published palaeo-wildfire records for
the Ladinian–Carnian interval.
"... In this study, we present a detailed description of charcoalified gymnosperm wood remains
[...] This finding extends the current wildfire record for the studied interval and, together with the
updated database of palaeo-wildfire proxies presented herein, suggests that such a phenomenon
eventually occurred throughout the entire Ladinian and Carnian time span ..."
Nan Crystal Arens (2025; illustrated by Julius Csotonyl, Sante Mazzei, Shuyu Hsu):
The
Princeton Field Guide to Mesozoic Plants. Google books.
See here
as well.
University of Vermont
Burlington, VT:
Origins of Life.
Diversity:
The Main Groups & How They are Connected. Lecture notes, Powerpoint presentation.
Speciation:
The Origin of New Species.
Lecture notes, Powerpoint presentation.
!
J. Chen et al. (2026):
Triassic–Jurassic
environmental instability on the subtropical eastern Tethyan margin linked to low-latitude dinosaur
dispersal. Free access, Communication Earth & Environ, 7. https://doi.org/10.1038/s43247-025-03083-6.
See here as well.
! Note figure 3: Stratigraphic correlation across the
Triassic–Jurassic boundary (TJB) between the
studied WK23-1 drill core from the Wande section and globally recognized reference sections.
"... we present an integrated dataset of chemostratigraphic and astrochronological records for a continental drill core
[...] Three negative carbon isotope excursions coupled with volcanogenic mercury anomalies
confirm pulsed volcanism-induced environmental impacts on this subtropical
terrestrial setting and placement of the Triassic–Jurassic boundary
[...] Large-scale volcanism-induced stressors, potentially coupled with increased climate seasonality,
likely created ecological opportunities facilitating dinosaur expansion in the Earliest Jurassic ..."
T.B. dos Santos et al. (2026):
An
early Permian Euramerican plant assemblage in northwestern Gondwana: The plant-arthropod
interactions of the Costela Mine locality, northeastern Brazil. Open access,
Palaeogeography, Palaeoclimatology, Palaeoecology, 690.
"...The Costela Mine plant assemblage of the Pedra de Fogo Formation
includes representatives from the Euramerican Floristic Realm, such
as the callipterid peltasperms Rhachiphyllum sp. and Auritifolia-like foliage
[...] Herbivory recorded at the Costela Mine plant assemblage is represented by eight
functional feeding groups, 15 damage types, and 72 recorded feeding event occurrences ..."
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This index is compiled and maintained by
Klaus-Peter Kelber, Würzburg, e-mail kp-kelber@t-online.de Last updated June 08, 2026 |
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