Abstract The fossil record of Marsilea is challenging to assess, due in part to unreliable reports and conflicting opinions regarding the proper application of the names Marsilea and Marsileaceaephyllum to fossil leaves and leaflets similar to those of modern Marsilea . Specimens examined for this study include material assigned to Marsileaceaephyllum johnhallii , purportedly the oldest fossil record of a Marsilea -like sporophyte from the Lower Cretaceous of the Dakota Formation, Kansas, U.S.A.; leaves and leaf whorls of the extinct aquatic angiosperm Fortuna from several Late Cretaceous and Paleocene localities in western North America; and leaves and leaflets resembling Marsilea from the Eocene Green River Formation, Colorado and Utah, U.S.A. Literature on the fossil record of Marsilea was also reviewed. As a result, several taxonomic changes are proposed. Marsileaceaephyllum johnhallii is reinterpreted as an aquatic angiosperm that shares some architectural features with the genus Fortuna , although Marsileaceaephyllum is here maintained as a distinct genus with an emended diagnosis; under this reinterpretation, the name Marsileaceaephyllum can no longer be applied to sporophyte organs with affinities to Marsileaceae. Three valid fossil Marsilea species are recognized on the basis of sporophyte material that includes characteristic quadrifoliolate leaves and reticulate-veined leaflets: Marsilea campanica (J. Kvaček & Herman) Hermsen, comb. nov., from the Upper Cretaceous Grünbach Formation, Austria; Marsilea mascogos Estrada-Ruiz et al., from the Upper Cretaceous Olmos Formation, Mexico; and Marsilea sprungerorum Hermsen, sp. nov., from the Eocene Green River Formation, U.S.A. The species are distinguished from one another based on leaflet dimensions. Leaves from the Eocene Wasatch Formation, U.S.A., are transferred from Marsileaceaephyllum back to Marsilea , although not assigned to a fossil species. Finally, an occurrence of Marsilea from the Oligocene of Ethiopia is reassigned to Salvinia . A critical evaluation of the fossil record of Marsilea thus indicates that (1) the oldest fossil marsileaceous sporophytes bearing Marsilea -like leaves are from the Campanian; (2) only four credible records of sporophyte material attributable to Marsilea are known; and (3) the oldest dispersed Marsilea spores are known from the Oligocene.
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Late Cretaceous angiosperm woods from the McRae Formation, south-central New Mexico, USA: Part 2
Premise of research. Over the past 3 decades, angiosperm woods have been reported from the Campanian to the Maastrichtian of southern Laramidia, including Coahuila and Chihuahua, Mexico; Big Bend National Park, Texas; and the San Juan Basin, New Mexico. Recent investigations of the upper Campanian (76.5 to >72.5 Ma) Jose Creek Member of the McRae Formation, south-central New Mexico, indicate an abundance of well-preserved silicified woods, representing one of the most diverse Cretaceous wood floras in the world.
In this report, we describe four new angiosperm wood types.
Methodology. The fossil woods described here were collected from the upper Campanian of south-central New Mexico, along the northeastern flank of the Caballo Mountains and in the adjacent Cutter Sag, and were
studied using thin sections. The potential affinities of these McRae woods were determined by comparison with fossil and extant woods.
Pivotal results. The woods reported here comprise one magnoliid and three eudicots with varying levels of
comparability to extant taxa. Laurinoxylon rennerae sp. nov. belongs to Lauraceae and has a combination of features found in multiple extant genera variously referred to as Cinnamomeae Nees, Laureae Maout & Decaisne, or Lauroideae Burnett/core Lauraceae. Turneroxylon newmexicoense gen. et sp. nov. is a eudicot with many similarities to Dilleniaceae but differs in having narrower rays. Mcraeoxylon waddellii gen. et sp. nov. has a suite of features seen in several families of Malpighiales, Myrtales, and Oxalidales. McRae angiosperm wood type 1 has a suite of features found in genera of Dilleniales, Ericales, and Malpighiales.
Conclusions. All wood types, with the exception of M. waddellii, have minimum axis diameters of 110 cm (12–50 cm), indicating that they represent trees. This reinforces previous evidence for the presence of small to large angiosperm trees in the Jose Creek Member and underscores the importance of woody angiosperms in vegetation of the southern Western Interior during the Campanian-Maastrichtian.
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- Award ID(s):
- 1655985
- NSF-PAR ID:
- 10052013
- Date Published:
- Journal Name:
- International Journal of Plant Sciences
- Volume:
- 179
- Issue:
- 2
- ISSN:
- 0973-1547
- Page Range / eLocation ID:
- 136 - 150
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Premise Solanaceae is a scientifically and economically important angiosperm family with a minimal fossil record and an intriguing early evolutionary history. Here, we report a newly discovered fossil lantern fruit with a suite of features characteristic of Physalideae within Solanaceae. The fossil comes from the early Eocene Laguna del Hunco site (ca. 52 Ma) in Chubut, Argentina, which previously yielded the only other physaloid fruit fossil,
Physalis infinemundi .Methods The fruit morphology and calyx venation pattern of the new fossil were compared with
P. infinemundi and extant species of Solanaceae.Results Physalis hunickenii sp. nov. is clearly distinct fromP. infinemundi in its fruiting calyx with wider primary veins, longer and thinner lobes, and especially in its venation pattern with high density, transverse tertiary veins; these features support its placement in a new species. In comparison with extant physaloid genera, the calyx venation pattern and other diagnostic traits reinforce placement of the new fossil, likeP. infinemundi , within the tribe Physalideae of Solanaceae.Conclusions Both species of fossil nightshades from Laguna del Hunco represent crown‐group Solanaceae but are older than all prior age estimates of the family. Although at least 20 transoceanic dispersals have been proposed as the driver of range expansion of Solanaceae, the Patagonian fossils push back the diversification of the family to Gondwanan times. Thus, overland dispersal across Gondwana is now a likely scenario for at least some biogeographic patterns, in light of the ancient trans‐Antarctic land connections between South America and Australia.
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Novel species of fungi described in this study include those from various countries as follows: Antartica , Cladosporium austrolitorale from coastal sea sand. Australia , Austroboletus yourkae on soil, Crepidotus innuopurpureus on dead wood, Curvularia stenotaphri from roots and leaves of Stenotaphrum secundatum and Thecaphora stajsicii from capsules of Oxalis radicosa. Belgium , Paraxerochrysium coryli (incl. Paraxerochrysium gen. nov.) from Corylus avellana. Brazil , Calvatia nordestina on soil, Didymella tabebuiicola from leaf spots on Tabebuia aurea, Fusarium subflagellisporum from hypertrophied floral and vegetative branches of Mangifera indica and Microdochium maculosum from living leaves of Digitaria insularis. Canada , Cuphophyllus bondii fromagrassland. Croatia , Mollisia inferiseptata from a rotten Laurus nobilis trunk. Cyprus , Amanita exilis oncalcareoussoil. Czech Republic , Cytospora hippophaicola from wood of symptomatic Vaccinium corymbosum. Denmark , Lasiosphaeria deviata on pieces of wood and herbaceousdebris. Dominican Republic , Calocybella goethei among grass on a lawn. France (Corsica) , Inocybe corsica onwetground. France (French Guiana) , Trechispora patawaensis on decayed branch of unknown angiosperm tree and Trechispora subregularis on decayed log of unknown angiosperm tree. Germany , Paramicrothecium sambuci (incl. Paramicrothecium gen. nov.)ondeadstemsof Sambucus nigra. India , Aureobasidium microtermitis from the gut of a Microtermes sp. termite, Laccaria diospyricola on soil and Phylloporia tamilnadensis on branches of Catunaregam spinosa . Iran , Pythium serotinoosporum from soil under Prunus dulcis. Italy , Pluteus brunneovenosus on twigs of broad leaved trees on the ground. Japan , Heterophoma rehmanniae on leaves of Rehmannia glutinosa f. hueichingensis. Kazakhstan , Murispora kazachstanica from healthy roots of Triticum aestivum. Namibia , Caespitomonium euphorbiae (incl. Caespitomonium gen. nov.)from stems of an Euphorbia sp. Netherlands , Alfaria junci, Myrmecridium junci, Myrmecridium juncicola, Myrmecridium juncigenum, Ophioceras junci, Paradinemasporium junci (incl. Paradinemasporium gen. nov.), Phialoseptomonium junci, Sporidesmiella juncicola, Xenopyricularia junci and Zaanenomyces quadripartis (incl. Zaanenomyces gen. nov.), fromdeadculmsof Juncus effusus, Cylindromonium everniae and Rhodoveronaea everniae from Evernia prunastri, Cyphellophora sambuci and Myrmecridium sambuci from Sambucus nigra, Kiflimonium junci, Saro cladium junci, Zaanenomyces moderatricis academiae and Zaanenomyces versatilis from dead culms of Juncus inflexus, Microcera physciae from Physcia tenella, Myrmecridium dactylidis from dead culms of Dactylis glomerata, Neochalara spiraeae and Sporidesmium spiraeae from leaves of Spiraea japonica, Neofabraea salicina from Salix sp., Paradissoconium narthecii (incl. Paradissoconium gen. nov.)from dead leaves of Narthecium ossifragum, Polyscytalum vaccinii from Vaccinium myrtillus, Pseudosoloacrosporiella cryptomeriae (incl. Pseudosoloacrosporiella gen. nov.)fromleavesof Cryptomeria japonica, Ramularia pararhabdospora from Plantago lanceolata, Sporidesmiella pini from needles of Pinus sylvestris and Xenoacrodontium juglandis (incl. Xenoacrodontium gen. nov. and Xenoacrodontiaceae fam. nov.)from Juglans regia . New Zealand , Cryptometrion metrosideri from twigs of Metrosideros sp., Coccomyces pycnophyllocladi from dead leaves of Phyllocladus alpinus, Hypoderma aliforme from fallen leaves Fuscopora solandri and Hypoderma subiculatum from dead leaves Phormium tenax. Norway , Neodevriesia kalakoutskii from permafrost and Variabilispora viridis from driftwood of Picea abies. Portugal , Entomortierella hereditatis from abio film covering adeteriorated limestone wall. Russia , Colpoma junipericola from needles of Juniperus sabina, Entoloma cinnamomeum on soil in grasslands, Entoloma verae on soil in grasslands, Hyphodermella pallidostraminea on a dry dead branch of Actinidia sp., Lepiota sayanensis onlitterinamixedforest, Papiliotrema horticola from Malus communis , Paramacroventuria ribis (incl. Paramacroventuria gen. nov.)fromleaves of Ribes aureum and Paramyrothecium lathyri from leaves of Lathyrus tuberosus. South Africa , Harzia combreti from leaf litter of Combretum collinum ssp. sulvense, Penicillium xyleborini from Xyleborinus saxesenii , Phaeoisaria dalbergiae from bark of Dalbergia armata, Protocreopsis euphorbiae from leaf litter of Euphorbia ingens and Roigiella syzygii from twigs of Syzygium chordatum . Spain , Genea zamorana on sandy soil, Gymnopus nigrescens on Scleropodium touretii, Hesperomyces parexochomi on Parexochomus quadriplagiatus, Paraphoma variabilis from dung, Phaeococcomyces kinklidomatophilus from a blackened metal railing of an industrial warehouse and Tuber suaveolens in soil under Quercus faginea. Svalbard and Jan Mayen , Inocybe nivea associated with Salix polaris. Thailand , Biscogniauxia whalleyi oncorticatedwood. UK , Parasitella quercicola from Quercus robur. USA , Aspergillus arizonicus from indoor air in a hospital, Caeliomyces tampanus (incl. Caeliomyces gen. nov.)fromoffice dust, Cippumomyces mortalis (incl. Cippumomyces gen. nov.)fromatombstone, Cylindrium desperesense from air in a store, Tetracoccosporium pseudoaerium from air sample in house, Toxicocladosporium glendoranum from air in a brick room, Toxicocladosporium losalamitosense from air in a classroom, Valsonectria portsmouthensis from airinmen'slockerroomand Varicosporellopsis americana from sludge in a water reservoir. Vietnam , Entoloma kovalenkoi on rotten wood, Fusarium chuoi inside seed of Musa itinerans , Micropsalliota albofelina on soil in tropical evergreen mixed forest sand Phytophthora docyniae from soil and roots of Docynia indica. Morphological and culture characteristics are supported by DNA barcodes.more » « less
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Our understanding of the earliest stages of crown bird evolution is hindered by an exceedingly sparse avian fossil record from the Mesozoic era. The most ancient phylogenetic divergences among crown birds are known to have occurred in the Cretaceous period but stem-lineage representatives of the deepest subclades of crown birds—Palaeognathae (ostriches and kin), Galloanserae (landfowl and waterfowl) and Neoaves (all other extant birds)—are unknown from the Mesozoic era. As a result, key questions related to the ecology, biogeography and divergence times of ancestral crown birds remain unanswered. Here we report a new Mesozoic fossil that occupies a position close to the last common ancestor of Galloanserae and fills a key phylogenetic gap in the early evolutionary history of crown birds. Asteriornis maastrichtensis, gen. et sp. nov., from the Maastrichtian age of Belgium (66.8–66.7 million years ago), is represented by a nearly complete, three-dimensionally preserved skull and associated postcranial elements. The fossil represents one of the only well-supported crown birds from the Mesozoic era, and is the first Mesozoic crown bird with well-represented cranial remains. Asteriornis maastrichtensis exhibits a previously undocumented combination of galliform (landfowl)-like and anseriform (waterfowl)-like features, and its presence alongside a previously reported Ichthyornis-like taxon from the same locality provides direct evidence of the co-occurrence of crown birds and avialan stem birds. Its occurrence in the Northern Hemisphere challenges biogeographical hypotheses of a Gondwanan origin of crown birds, and its relatively small size and possible littoral ecology may corroborate proposed ecological filters that influenced the persistence of crown birds through the end-Cretaceous mass extinction.more » « less
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null (Ed.)Xiphosurans are aquatic chelicerates with a fossil record extending into the Early Ordovician and known from a total of 88 described species, four of which are extant. Known for their apparent morphological conservatism, for which they have gained notoriety as supposed ‘living fossils’, recent analyses have demonstrated xiphosurans to have an ecologically diverse evolutionary history, with several groups moving into non-marine environments and developing morphologies markedly different from those of the modern species. The combination of their long evolutionary and complex ecological history along with their paradoxical patterns of morphological stasis in some clades and experimentation among others has resulted in Xiphosura being of particular interest for macroevolutionary study. Phylogenetic analyses have shown the current taxonomic framework for Xiphosura—set out in the Treatise of Invertebrate Paleontology in 1955—to be outdated and in need of revision, with several common genera such as Paleolimulus Dunbar, 1923 and Limulitella Størmer, 1952 acting as wastebasket taxa. Here, an expanded xiphosuran phylogeny is presented, comprising 58 xiphosuran species as part of a 158 taxon chelicerate matrix coded for 259 characters. Analysing the matrix under both Bayesian inference and parsimony optimisation criteria retrieves a concordant tree topology that forms the basis of a genus-level systematic revision of xiphosuran taxonomy. The genera Euproops Meek, 1867, Belinurus König, 1820, Paleolimulus , Limulitella , and Limulus are demonstrated to be non-monophyletic and the previously synonymized genera Koenigiella Raymond, 1944 and Prestwichianella Cockerell, 1905 are shown to be valid. In addition, nine new genera ( Andersoniella gen. nov. , Macrobelinurus gen. nov. , and Parabelinurus gen. nov. in Belinurina; Norilimulus gen. nov. in Paleolimulidae; Batracholimulus gen. nov. and Boeotiaspis gen. nov. in Austrolimulidae; and Allolimulus gen. nov., Keuperlimulus gen. nov., and Volanalimulus gen. nov. in Limulidae) are erected to accommodate xiphosuran species not encompassed by existing genera. One new species, Volanalimulus madagascarensis gen. et sp. nov., is also described. Three putative xiphosuran genera— Elleria Raymond, 1944, Archeolimulus Chlupáč, 1963, and Drabovaspis Chlupáč, 1963—are determined to be non-xiphosuran arthropods and as such are removed from Xiphosura. The priority of Belinurus König, 1820 over Bellinurus Pictet, 1846 is also confirmed. This work is critical for facilitating the study of the xiphosuran fossil record and is the first step in resolving longstanding questions regarding the geographic distribution of the modern horseshoe crab species and whether they truly represent ‘living fossils’. Understanding the long evolutionary history of Xiphosura is vital for interpreting how the modern species may respond to environmental change and in guiding conservation efforts.more » « less
- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/DOI: 10.1086/695503
