Osmundastrum pulchellum

Osmundastrum pulchellum Temporal range: Latest Pliensbachian-Toarcian(?) ~183–180 Ma PreꞒ Ꞓ O S D C P T J K Pg N ↓ Nearby Volcanic neck suggest 176.7 ± 0.5 Ma, Middle-Late Toarcian Age
Holotype rhizome
Scientific classification
Kingdom:	Plantae
Clade:	Tracheophytes
Division:	Polypodiophyta
Class:	Polypodiopsida
Order:	Osmundales
Family:	Osmundaceae
Genus:	Osmundastrum
Species:	†O. pulchellum
Binomial name
†Osmundastrum pulchellum (Bomfleur, B., Grimm, G. W., & McLoughlin, S.) C.Presl
Synonyms
Osmunda pulchella Bomfleur, B., Grimm, G. W., & McLoughlin, S., 2015

Osmundastrum pulchellum is an extinct species of Osmundastrum, leptosporangiate ferns in the family Osmundaceae from the lower Jurassic (Pliensbachian-Toarcian?) Djupadal Formation of Southern Sweden.^[1][2][3][4] It remained unstudied for 40 years.^[5] It is one of the most exceptional fossil ferns ever found, preserving intact tissue with DNA and cells.^[3] Its exceptional preservation has allowed the study of the DNA relationships with extant Osmundaceae ferns, proving a 180-million-year genomic stasis.^[3] It has also preserved its biotic interactions and even ongoing mitosis.^[6][7][1][2]

History and discovery[]

The only known specimen was recovered at the mafic pyroclastic and epiclastic deposits of the Djupadal Formation, dated Pliensbachian-Toarcian(?), that are present near , at the north of Höör, central Skåne, southern Sweden.^[2] The location was studied first by Gustav Andersson, a local farmer, who was a passionate follower of scientific discoveries.^[5] Through his interest in geology, he identified several coeval volcanic plugs, and motivated by the presence of volcanic soils, he excavated a location at the south of the Korsaröd lake.^[5] Initially nothing was found, but a second deeper dig revealed a series of aggregated wood remains on volcanic lahar-derived stones.^[5] Samples taken from the location were sent to the geologist , who carried out palynological research on them, estimating an age of deposition of Late Toarcian-Aalenian(?).^[8] A petrified rhizome was sent to Tralau, who understood the significance of the fossil and intended to publish it formally, but his untimely death in March 1977 made it impossible.^[5] The rhizome, along with the fossil wood, was archived at the Swedish Museum of Natural History, where the geologist tried also to publish it formally, what was also impossible due to her retirement in 1986.^[5] The fossil was lying forgotten in the archives of the museum until 2013, when it was discovered again and studied, finding that it preserved spectacular cellular detail, rarely seen on fossils.^[5] In 2015, it was finally published as Osmunda pulchella by B. Bomfleur, G. W. Grimm and S. McLoughlin.^[2][3][4][9] The specific epithet pulchella (Latin diminutive of pulchra, 'beautiful', 'fair;) was chosen in reference to the exquisite preservation and aesthetic appeal of the holotype specimen.^[2] The name Osmunda pulchella was mostly used in the main publications referring to it until in 2017 a revision of the cladistic status of the fossil Osmundales showed that the fossil was in fact a member of the genus Osmundastrum, so it became Osmundatrum pulchellum.^[1]

Description[]

The Osmundatrum pulchellum holotype is a calcified rhizome fragment about 6 cm long and up to 4 cm in diameter that probably come from a small (aprox. 50 cm tall) fern.^[6] It is composed of a small central stem surrounded by a compact mantle of helically arranged petiole bases and interspersed rootlets that extend outwards perpendicular to the axis, indicating a low rhizomatous rather than arborescent growth.^[2] This, together with the asymmetrical distribution of the roots, points to a creeping habit.^[2] The stem is around about 7.5 mm in diameter and the pith about 1.5 mm in diameter and entirely parenchymatous.^[2] In the pith, cell walls lack the presence of an internal endodermis or internal phloem, considered to be an original feature, rather than a loss due to inadequate preservation.^[2] Traces of leaves and associated rootlets are present traversing the outer cortex.^[2] This specimen is well known for the quality of its preservation, quality revealing cellular and subcellular detail: from tracheids with preserved wall thickenings, to parenchyma cells containing preserved cellular contents.^[2] Some of the parenchyma cells contain oblate particles about 1–5 μm in diameter, interpreted as putative amyloplasts.^[2]

Classification[]

The exceptional preservation of Osmundastrum pulchellum has allowed the establishment of an evolutionary overview of royal ferns since the lower Jurassic.^[2][3][9] At its description as Osmunda pulchella, it was compared with Todea, Leptopteris, Plenasium and Claytosmunda, and found as a bridge in the morphological gap between extant Osmundastrum and the subgenus Osmunda inside Osmunda – the closest species to Osmundastrum.^[2] It was shown that this species and the extant Osmundaceae share the same chromosome count and DNA content.^[3] In 2017, a re-examination of the phylogeny of the fossil Osmundales showed it to be a member of the genus Osmundastrum and a probable precursor of the modern Osmundastrum cinnamomeum.^[1]

Biology[]

Osmundastrum pulchellum Rhizome includes several biotic interactions, including lycopsid roots, possible Peronosporomycetes oogonia, Fungal spores and oribatid mites.

Osmundastrum pulchellum is well known thanks to exceptional preservation of detailed anatomical structures (e.g., pith, stele, petiole base, adventitious roots, and even nuclei). As well is the only known case of fossilized ongoing mitosis.^[7] This is shown by the fact that the chromosomes and cell nuclei show marked structural heterogeneities compared to the cell walls during different stages of the cell cycle.^[7] A rapid calcite permineralization "froze" the organic molecules in time, which suggests the fern rhizome was fossilized probably on a very short time, perhaps even minutes thanks to a fast lahar deposit.^[7] The tissues show cells with nuclei, nucleoli, and chromosomes during the interphase, prophase, prometaphase, and possible anaphase of the cell cycle.^[10] Some cells also show pyknotic nuclei typical of cells undergoing apoptosis (programmed cell death).^[10] The subcelular detail ir nearly unique, as other ferns preserved on similar conditions lack them, for example liaoningensis.^[11] Several biotic interactions were recovered on the rhizome. Exotic roots were recovered on the petiole bases, with a level of preservation that matches that of the whole plant, bearing a similar vasculature as seen in modern lycophytes. They are interpreted as belonging to a small herbaceous epiphytic lycopsid, with its megaspores also linked with the specimen.^[6] Other sporangial fragments from other ferns ( toralis, jurienensis, etc.) were also recovered, known from the nearby deposits.^[12] A similar community was recovered on a Todea rhizome from the early Eocene of Patagonia, but with the epiphytic plants being in Osmundastrum pulchellum exclusively lycopsids and ferns, which may indicate that bryophytes had not yet evolved the epiphytic habit during the Jurassic.^[13] Possible oogonia of Peronosporomycetes are found in a parasitic or saprotrophic relation with the plant. If the identification of the oogonia of Peronosporomycetes is correct, then this implies regularly moist conditions for the growth of Osmundastrum pulchellum.^[6] Thread-like structures were found, identified as derived from a pathogenic or saprotrophic fungus invading necrotic tissues of the host plant. The interaction of the fungus with the plant was probably mycorrhizal.^[6] Excavations up to 715 μm in diameter are evident, filled with pellets that resemble the coprolites of oribatid mites, found also in Paleozoic and Mesozoic woods.^[6]

Paleoenvironment[]

Reconstructed Korsaröd section of the Djupadal Formation

The Djupadal Formation was deposited in the Central Skane region, linked to the late Early Jurassic Volcanism. Several coeval Volcanic necks are recovered on the region, such as Eneskogen (A large hill covered by quaternary sediments. Some few boulders and basalt pillars were exposed), Bonnarp (5–6 m height and covers roughly 5,000 square meters, covered by Jurassic sediments) and Säte (Comprise two basalt pipes, each roughly 6–10 m high and some 10,000 square meters in area).^[14] The Korsaröd member includes a volcanic-derived lagerstatten where this fern was found, probably derived from a fast lahar deposition.^[12] Thanks to the data provided by the fossilized wood rings, it was found that the location of Korsaröd hosted a middle-latitude Mediterranean-type biome in the late Early Jurassic, with low rainfall. Superimposed on this climate were the effects of a local active Strombolian Volcanism and hydrothermal activity.^[12] This location has been compared with modern Rotorua, New Zealand, considered an analogue for the type of environment represented in southern Sweden at this time.^[4] The locality was populated mostly by Cupressaceae trees (including specimens up to 5 m in circunference), known thanks to the great abundance of the wood genus and the high presence of the genus elatoides (also Cupressaceae) and Eucommiidites troedsonii (Erdtmanithecales).^[12] The underlying hosts abundant spp. pollen produced by plants related to cycadophytes, while the Djupadal volcanogenic deposits are dominated by cypress family pollen with an understorey component rich in putative Erdtmanithecales, both representing vegetation of disturbed habitats. The abundance of sp. is also related with a sporadic intraseasonal and multi-year episodes of growth disruption, probably due to the volcanic action.^[12]

References[]