scholarly journals Paleobiology of early angiosperms: evidence from sedimentological associations in the Early Cretaceous Potomac Group of the eastern U.S.A.

1992 ◽  
Vol 6 ◽  
pp. 128-128 ◽  
Author(s):  
Leo J. Hickey ◽  
David W. Taylor

Lately, we proposed a hypothesis that the ancestral angiosperm was a diminutive, rhizomatous to scrambling perennial herb with small simple flowers. Our phylogenetic studies suggest that arborescent to shrubby magnolialians with large, multiparted, complex flowers are derived, rather ancestral as commonly thought. We suggest that the early angiosperm, due to its rhizomatous habit, would have been able to survive in more ephemeral habitats. A test of this idea would be to examine the sedimentological context of early angiosperms.Despite a number of reports of early angiosperm megafossils from Barremian to middle Albian (mid- to late Early Cretaceous) age sediments, only the Potomac Group of the eastern U.S.A. has provided a stratigraphic sequence of early angiosperm diversification. Furthermore, study of this sequence has also linked observations on floristic assemblages to the lithofacies in which they occur, leading Doyle and Hickey to report an ecological expansion of early angiosperms from relatively near-channel environments to a much broader range of flood plain sites during the Barremian/Aptin to latest Albian/early Cenomanian interval represented by Potomac Group deposition. From this those authors inferred that the early angiosperms were “riparian weeds” that grew on moderately unstable, near-channel sites subject to periodic flooding and episodes of alluviation.We recently expanded on these inferences by examining the sedimentology of Dutch Gap, an early angiosperm site at the earliest level of the Potomac Group (Barremain/Aptian-Pollen Zone I) near Richmond, VA. Sediments here appear to represent the meander belt of a fluvial setting. A series of multi-storied channel units at the site are filled with arkosic, medium to coarse, sub-angular sand with pebble- to boulder-size clasts of gneiss, claystone and mudstone concentrated at channel bases, reactivation surfaces, and on lateral accretion surfaces. These channels are cut into inferred levee and splay deposits that consist of thin interbeds of sand and silt alternating with dark grey, micaceous mudstone to claystone. This sequence fines in an inferred distal direction from the channels and the mudstone/claystone interbeds thicken at the expense of the coarser units until they coalesce into relatively thick, dark grey clay beds with only thin silty laminae. These beds are thought to represent floodbasin deposits.The megafossil plants recovered from our studies at Dutch Gap exhibit a clear pattern of association with each other and with these lithofacies. Angiosperms (Celastrophyllum, Rogersia, and an unnamed new form) together with ferns are found in relatively silty interbeds that lie in what appear to be distal levee settings, while the backswamp was dominated by the bennittitalean Dioonites buchianus. Conifers of diverse kinds are dominant only in pinkish, silty clay clasts that are inferred to have been transported from drier flood-plain environments.This study provides added evidence of an association between early angiosperms and moderately unstable, channel-margin sites and, in addition, calls attention to the potential that detailed sedimentological investigations have of providing important evidence on early angiosperm paleoecology.

2021 ◽  
Vol 77 (2) ◽  
pp. 231-255
Author(s):  
Lina Golovneva ◽  
Eugenia Bugdaeva ◽  
Elena Volynets ◽  
Yuewu Sun ◽  
Anastasia Zolina

The Partizansk and Razdolnaya coal basins of Primorye, Far East of Russia, contain diverse early angiosperm fossils (pollen, leaves, and fruits). In this paper, we revise the previous data on early angiosperms of this region and summarize the results of our latest research. Age of the plant-bearing deposits was clarified using isotopic U-Th-Pb LA-ICP-MS and U-Pb ID-TIMS methods. Age of the upper part of the Lipovtsy Formation is 118 ± 1.4 Ma, which corresponds to the late Aptian. The early Albian age (109 ± 1 Ma) is assigned to the upper part of the Frentsevka Formation. The diversification of angiosperms in the Early Cretaceous of Primorye region and their systematic affinity are analyzed. Early representatives of Laurales, Ranunculales, Platanaceae, and probable Cercidiphyllaceae are revealed. New combination Pandanites ahnertii (Krysht.) Golovn., comb. nov. is created, and new species Araliaephyllum vittenburgii Golovn. et Volynets, sp. nov. is described. Reconstructions of herbaceous angiosperms from autochthonous locality Bolshoy Kuvshin are proposed.


Paleobiology ◽  
2011 ◽  
Vol 37 (2) ◽  
pp. 195-213 ◽  
Author(s):  
Taylor S. Feild ◽  
Garland R. Upchurch ◽  
David S. Chatelet ◽  
Timothy J. Brodribb ◽  
Kunsiri C. Grubbs ◽  
...  

The photosynthetic gas exchange capacities of early angiosperms remain enigmatic. Nevertheless, many hypotheses about the causes of early angiosperm success and how angiosperms influenced Mesozoic ecosystem function hinge on understanding the maximum capacity for early angiosperm metabolism. We applied structure-functional analyses of leaf veins and stomatal pore geometry to determine the hydraulic and diffusive gas exchange capacities of Early Cretaceous fossil leaves. All of the late Aptian—early Albian angiosperms measured possessed low vein density and low maximal stomatal pore area, indicating low leaf gas exchange capacities in comparison to modern ecologically dominant angiosperms. Gas exchange capacities for Early Cretaceous angiosperms were equivalent or lower than ferns and gymnosperms. Fossil leaf taxa from Aptian to Paleocene sediments previously identified as putative stem-lineages to Austrobaileyales and Chloranthales had the same gas exchange capacities and possibly leaf water relations of their living relatives. Our results provide fossil evidence for the hypothesis that high leaf gas exchange capacity is a derived feature of later angiosperm evolution. In addition, the leaf gas exchange functions of austrobaileyoid and chloranthoid fossils support the hypothesis that comparative research on the biology of living basal angiosperm lineages reveals genuine signals of Early Cretaceous angiosperm ecophysiology.


Paleobiology ◽  
1993 ◽  
Vol 19 (2) ◽  
pp. 141-167 ◽  
Author(s):  
James A. Doyle ◽  
Michael J. Donoghue

Approaches to patterns of diversification based on counting taxa at a given rank can be misleading, even when all taxa are monophyletic. Such “rank-based” approaches are unable to reflect a hierarchy of evolutionary events because taxa of the same rank cannot be nested within one another. Phylogenetic trees specify an order of origination of characters and clades and can therefore be used in some cases to test hypotheses on causal relationships between characters and changes in diversity. “Tree-thinking” also clarifies discussions of the age of groups, by distinguishing between splitting of the stem-lineage from its sister group and splitting of the crown-group into extant clades.Cladistic evidence that Pentoxylon, Bennettitales, and Gnetales are the sister group of angiosperms implies that the angiosperm line (angiophytes) existed by the Late Triassic. The presence of primitive members of five basic angiosperm clades indicates that the crown-group (angiosperms) had begun to diversify by the mid-Early Cretaceous (Barremian-Aptian), but not necessarily much earlier. The greatest unresolved issue raised by cladistic analyses concerns the fact that the angiosperm tree can be rooted in two almost equally parsimonious positions. Trees rooted near Magnoliales (among “woody magnoliids”) suggest that the angiosperm radiation may have been triggered by the origin of intrinsic traits, e.g., a fast-growing, rhizomatous habit in the paleoherb and eudicot subgroup. However, trees rooted among paleoherbs, which are favored by rRNA data, imply that these traits are basic for angiosperms as a whole. This could mean that the crown-group originated not long before its radiation, or, if it did originate earlier, that its radiation was delayed due to extrinsic factors. Such factors could be a trend from environmental homogeneity and stability in the Jurassic to renewed tectonic activity and disturbance in the Early Cretaceous. Potentially relevant pre-Cretaceous fossils cannot be placed with confidence, but may be located along the stem-lineage (stem angiophytes); their generally paleoherb-like features favor the paleoherb rooting. The history of angiophytes may parallel that of Gnetales: some diversification of the stem-lineage in the Late Triassic, near disappearance in the Jurassic, and vigorous radiation of the crown-group in the Early Cretaceous.


2010 ◽  
Vol 365 (1539) ◽  
pp. 369-382 ◽  
Author(s):  
Else Marie Friis ◽  
Kaj Raunsgaard Pedersen ◽  
Peter R. Crane

In the second half of the nineteenth century, pioneering discoveries of rich assemblages of fossil plants from the Cretaceous resulted in considerable interest in the first appearance of angiosperms in the geological record. Darwin's famous comment, which labelled the ‘rapid development’ of angiosperms an ‘abominable mystery’, dates from this time. Darwin and his contemporaries were puzzled by the relatively late, seemingly sudden and geographically widespread appearance of modern-looking angiosperms in Late Cretaceous floras. Today, the early diversification of angiosperms seems much less ‘rapid’. Angiosperms were clearly present in the Early Cretaceous, 20–30 Myr before they attained the level of ecological dominance reflected in some mid-Cretaceous floras, and angiosperm leaves and pollen show a distinct pattern of steadily increasing diversity and complexity through this interval. Early angiosperm fossil flowers show a similar orderly diversification and also provide detailed insights into the changing reproductive biology and phylogenetic diversity of angiosperms from the Early Cretaceous. In addition, newly discovered fossil flowers indicate considerable, previously unrecognized, cryptic diversity among the earliest angiosperms known from the fossil record. Lineages that today have an herbaceous or shrubby habit were well represented. Monocotyledons, which have previously been difficult to recognize among assemblages of early fossil angiosperms, were also diverse and prominent in many Early Cretaceous ecosystems.


HortScience ◽  
1992 ◽  
Vol 27 (11) ◽  
pp. 1168a-1168
Author(s):  
Dan Chapman ◽  
Laurence Sistrunk ◽  
J. Benton Storey

In 1990, a randomized design was set up in a 33 year old orchard on Westwood silty clay loam with 4 main treatment factors: 1990 nut size, chiseling, aeration, and cultivar. Location for this experiment was the Adriance Orchard on the Texas A&M Plantation – Brazos River flood plain. Nut quality was determined by the % kernel and # nuts / kg. Yield was measured per tree and calculated for g/cm2 cross-sectional trunk area. The soil bulk density for each treatment was 1.53 g/cm3 and found to be statistically uniform at the start of the experiment. Results after one year showed that aeration increased the nut size and % kernel of `Mahan' but not of `Desirable' and `Stuart'. Chiseling increased the yield of `Stuart' and `Desirable' and nut size of all 3 cultivars but not % kernel. Aeration increased the % kernel from a mean 48.6% to 56.8% and nut size from 129 nuts/kg to 102 nuts/kg of the 1990 small-nut-size trees but did not significantly increase nut quality for the 1990 normal-nut-size trees.


2018 ◽  
Vol 74 (3-4) ◽  
pp. 317-326 ◽  
Author(s):  
Mário Miguel Mendes ◽  
Mário Pedro Dinis ◽  
Jiří Kvaček

Several mesofossil floras discovered in the Early Cretaceous rocks from the Lusitanian Basin of western Portugal comprise numerous well-preserved conifer remains. Here we report the occurrence of four conifer types in the mesofossil flora from the Catefi ca locality, about 4 km south of Torres Vedras in the Estremadura region on the western Portuguese Basin. The specimens were recovered from rocks belonging to the Almargem Formation, interpreted to be of late Aptian - early Albian age. It includes three Cheirolepidiaceae genera Frenelopsis SCHENK, Pseudofrenelopsis NATH. and Watsoniocladus V.SRINIV., and one conifer twig of Pagiophyllum-type. These conifers, which co-occurred in the same depositional bed with a well-diversified early angiosperm assemblage including flowers, seeds, fruits and dispersed stamens with pollen in situ, provide new insights into Early Cretaceous palaeoecology.


Author(s):  
Mary Jane West-Eberhard

Recurrent phenotypes are similar or identical phenotypic traits with discontinuous phylogenetic distributions, which owe their similarity to common ancestry (homology). A recurrent trait may be found as a fixed trait, as an alternative phenotype (one morph of a polymorphism or polyphenism), or as a low-frequency developmental anomaly. Recurrence, then, is the phyletically disjunct appearance of homologous traits. An example is the repeated evolution of larviform (paedomorphic) adults in salamanders. The larviform morph is characterized by retention in the reproductive stage of homologous larval traits such as external gills and a tail. This has involved changes at various points in the hormonal mechanism that controls metamorphosis in all salamanders (chapter 25), perhaps under selection for accelerated reproduction in stressful environments (Whiteman, 1994). As is characteristic of recurrent phenotypes, the occurrence of the reproductive larviform adult morph varies in frequency from one species of salamander to another: it can be absent, an anomaly (<5% of population), a common (>5%) alternative to complete metamorphosis, or a predominant or fixed form. Even within the genus Ambystoma, the unmetamorphosed larviform adult occurs as an occasional anomaly in some populations, as a facultatively expressed alternative phenotype in others (e.g., A. tigrinum) and as a fixed form in others (e.g., A. dumerilii; Collins et al., 1993). All atavisms and reversions (see chapter 12) are examples of recurrence. Discontinuity of expression is expected in combinatorial evolution, where traits are turned off and on and expressed in different combinations due to regulatory change. The growing evidence of homoplasy in phylogenetic studies is important evidence that combinatorial evolution occurs and that homoplasy itself is worthy of study, not just a source of “noise” in cladistics (Wake, 1996a). Homoplasy has been defined as “possession by two or more taxa of a character derived not from the nearest common ancestor but through convergence, parallelism, or reversal”. More simply, homoplasy is the recurrence of similarity in evolution (Sanderson and Hufford, 1996).


Palaeoworld ◽  
2008 ◽  
Vol 17 (2) ◽  
pp. 142-152 ◽  
Author(s):  
Marc Philippe ◽  
Bernard Gomez ◽  
Vincent Girard ◽  
Clément Coiffard ◽  
Véronique Daviero-Gomez ◽  
...  

2013 ◽  
Vol 48 ◽  
pp. 97-105 ◽  
Author(s):  
Valeria S. Perez Loinaze ◽  
Ezequiel I. Vera ◽  
Mauro G. Passalia ◽  
Magdalena Llorens ◽  
Richard Friedman ◽  
...  

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