scholarly journals Preface to 'Evolution, Extinction and Biogeography in Gondwana'

2001 ◽  
Vol 49 (3) ◽  
pp. I
Author(s):  
Robert S. Hill

The macrofossil record of the plant family Cunoniaceae in Australia is summarised and reviewed where necessary by using detailed studies of the morphology of extant genera. Eleven of the 26 Cunoniaceae genera are represented in the Australian macrofossil record and include leaves and leaf fragments, foliar cuticle and reproductive structures, and range from Late Paleocene to Quaternary in age. Macrofossils show that some genera had a different or more widespread distribution in Australia during the Cenozoic, with two genera (Weinmannia and Codia) having become extinct from the continent. Changes in climate, including increasing cold, frost, dryness, seasonality, or some combination of these, or a reduction in vegetation disturbance regimes (e.g. volcanism, uplifting, landslips), may be implicated in the regional or continental extinctions demonstrated by the macrofossil record. Many extant genera (Schizomeria, Vesselowskya, Callicoma, Ceratopetalum, Acsmithia, Codia) had evolved by the Early Oligocene or earlier (Eucryphia, Late Paleocene; Ceratopetalum, Middle Eocene), perhaps with generic diversification more or less complete by the end of the Early Cenozoic or earlier. A Cretaceous origin of the family is possible, and may account for its widespread distribution on Southern Hemisphere landmasses, although long-distance dispersal events are required to explain some modern geographic disjunctions.

2001 ◽  
Vol 49 (3) ◽  
pp. 301 ◽  
Author(s):  
Richard W. Barnes ◽  
Robert S. Hill ◽  
Jason C. Bradford

The macrofossil record of the plant family Cunoniaceae in Australia is summarised and reviewed where necessary by using detailed studies of the morphology of extant genera. Eleven of the 26 Cunoniaceae genera are represented in the Australian macrofossil record and include leaves and leaf fragments, foliar cuticle and reproductive structures, and range from Late Paleocene to Quaternary in age. Macrofossils show that some genera had a different or more widespread distribution in Australia during the Cenozoic, with two genera (Weinmannia and Codia) having become extinct from the continent. Changes in climate, including increasing cold, frost, dryness, seasonality, or some combination of these, or a reduction in vegetation disturbance regimes (e.g. volcanism, uplifting, landslips), may be implicated in the regional or continental extinctions demonstrated by the macrofossil record. Many extant genera (Schizomeria, Vesselowskya, Callicoma, Ceratopetalum, Acsmithia, Codia) had evolved by the Early Oligocene or earlier (Eucryphia, Late Paleocene; Ceratopetalum, Middle Eocene), perhaps with generic diversification more or less complete by the end of the Early Cenozoic or earlier. A Cretaceous origin of the family is possible, and may account for its widespread distribution on Southern Hemisphere landmasses, although long-distance dispersal events are required to explain some modern geographic disjunctions.


2005 ◽  
Vol 42 (2) ◽  
pp. 243-257 ◽  
Author(s):  
Alexander P Wolfe ◽  
Mark B Edlund

A new centric diatom genus is described from laminated freshwater sediments of Middle Eocene age near Horsefly, British Columbia, Canada. This diatom, Eoseira wilsonii gen. et sp. nov., grew in filaments that constitute dense monospecific sub-horizons within the white couplets that represent summer deposition in the varved sequence. Although Eoseira clearly belongs within the Family Aulacoseiraceae, several features distinguish its valve structure from Aulacoseira. Gigantism of spines and the lack of geometric relationships between spine position and mantle areolae are the most conspicuous features of the genus. Eoseira is among the oldest freshwater diatoms known and one of relatively few extinct freshwater genera. In addition to serving as a potential biostratigraphic marker, Eoseira is a cornerstone to undertanding the evolutionary trajectory of the Aulacoseiraceae, likely the oldest family of freshwater diatoms. As such, it refines our understanding of early radiations from the marine realm in western North America. Furthermore, paleoecological inferences based on Eoseira life strategy pertain directly to limnological conditions during early Cenozoic hot-house conditions.


Author(s):  
Olga B. Kuzmina ◽  
◽  
Natalia K. Lebedeva ◽  

The Upper Cretaceous and Paleogene sediments exposed in Borehole 9 (Troizk, Chelyabinsk Area) in the south of the Trans-Ural Region (Western Siberia) are studied by palynological methods. The BH9 has uncovered the Fadyushinskaya and Gan’kino formations of Upper Cretacious age and the Talitsa, Serov, Irbit, Chegan and Kurtamysh formations of Paleogene age. Nine dinocysts assemblages and nine spores and pollen assemblages were revealed. The Campanian, Maastrichtian, Late Paleocene, Low-Middle Eocene and Early Oligocene age of the sediments were substantiated.


Crustaceana ◽  
2017 ◽  
Vol 90 (7-10) ◽  
pp. 953-967 ◽  
Author(s):  
Sebastian Klaus ◽  
Célio Magalhães ◽  
Rodolfo Salas-Gismondi ◽  
Martin Gross ◽  
Pierre-Olivier Antoine

We describe claw fragments of fossil primary freshwater crabs from three areas in the Amazon basin, Tarapoto (Early Oligocene) and Contamana (Middle Eocene to early Late Miocene) in Peru, and Eirunepé (Late Miocene) in Brazil. All these fragments most likely belong to the family Trichodactylidae. We show a continuous presence of primary freshwater crabs in proto-Amazonian lowlands from the Middle Eocene to the Late Miocene and can thus shift the earliest appearance date of freshwater-adapted brachyurans into the Eocene, at least in the Neotropics.


1992 ◽  
Vol 6 ◽  
pp. 12-12
Author(s):  
Marie-Pierre Aubry

Calcareous nannoplankton diversity varied greatly during the Paleogene. From extremely reduced values (~10 species) in the early Paleocene (circa 66.4 to 66 Ma, age estimates from Berggren, Kent and Flynn, 1985) following the terminal Cretaceous extinctions, diversity increased progressively throughout the late Paleocene and early Eocene and reached a maximum (~120 species) in the early middle Eocene (circa 52–48 Ma). This was followed by a step-like decrease until the early Oligocene (circa 35 Ma) when minimal values (~37 species) were reached once again. After a stable low during the remainder of the early Oligocene, a moderate, increase occurred near the early/late Oligocene boundary (circa 30 Ma).Temperature has been regarded as the most important factor controlling the distribution of the calcareous nannoplankton following the characterisation of five temperature-controlled assemblages of living Coccolithophoridae in the Atlantic Ocean. Studies relative to variations in diversity in the calcareous nannoplankton throughout the Mesozoic and Cenozoic and among the extinct late Paleocene to Pliocene group Discoaster, and to changing biogeographic patterns during the Cenozoic have revealed an apparent relationship between composition of calcareous nannofossil assemblages and temperature as deduced from isotopic studies. This relationship, which is currently used to infer Paleogene climatic and oceanographic evolution from quantitative analyses of calcareous nannofossil assemblages, is however not a simple one as indicated by the fact that maximum diversity during the Paleogene (i.e., the early middle Eocene) did not occur during (but subsequently to) the warmest time (i.e., the latest Paleocene-earliest Eocene).Diversity changes in the Paleogene calcareous nannoplankton are strikingly similar to diversity changes in the Paleogene planktonic foraminifera, which have been shown to reflect fluctuations in nutrient availibility as indicated by oxygen and carbon isotopes. The parallel evolution in the two groups thus suggests that trophic levels in the photic zone played an important role in the Paleogene diversification of the calcareous nannoplankton. In the present day ocean, the calcareous nannoplankton (Coccolithophoridae) dominate the phytoplankton under oligotrophic conditions and tropical waters are characterized by highly diversified associations with strong vertical specific stratification. Only few species occur under meso- and eutrophic conditions, and there is no vertical stratification. Extremely low diversity during the earliest Paleocene followed by increasing diversity through the Paleocene and earliest Eocene is interpreted as reflecting the change from an essentially mesotrophic to an oligotrophic ocean, increased rates of speciation resulting from niche partitioning occasioned by increased oligotrophy, leading to strong vertical stratification of species in the photic zone. Decrease in diversity from middle Eocene to early Oligocene reflects, on the other hand, progressive eutrophication of the ocean as a result of climatic deterioration.


Geosciences ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 34
Author(s):  
Santiago Moliner-Aznar ◽  
Manuel Martín-Martín ◽  
Tomás Rodríguez-Estrella ◽  
Gregorio Romero-Sánchez

The Cenozoic Malaguide Basin from Sierra Espuña (Internal Betic Zone, S Spain) due to the quality of outcropping, areal representation, and continuity in the sedimentation can be considered a key-basin. In the last 30 years, a large number of studies with very different methodological approaches have been done in the area. Models indicate an evolution from passive margin to wedge-top basin from Late Cretaceous to Early Miocene. Sedimentation changes from limestone platforms with scarce terrigenous inputs, during the Paleocene to Early Oligocene, to the deep basin with huge supplies of turbidite sandstones and conglomerates during the Late Oligocene to Early Miocene. The area now appears structured as an antiformal stack with evidence of synsedimentary tectonics. The Cenozoic tectono-sedimentary basin evolution is related to three phases: (1) flexural tectonics during most of the Paleogene times to create the basin; (2) fault and fold compartmentation of the basin with the creation of structural highs and subsiding areas related to blind-fault-propagation folds, deforming the basin from south to north during Late Oligocene to Early Aquitanian times; (3) thin-skin thrusting tectonics when the basin began to be eroded during the Late Aquitanian-Burdigalian. In recent times some works on the geological heritage of the area have been performed trying to diffuse different geological aspects of the sector to the general public. A review of the studies performed and the revisiting of the area allow proposing different key-outcrops to follow the tectono-sedimentary evolution of the Cenozoic basin from this area. Eight sites of geological interest have been selected (Cretaceous-Cenozoic boundary, Paleocene Mula Fm, Lower Eocene Espuña-Valdelaparra Fms, Middle Eocene Malvariche-Cánovas Fms, Lowermost Oligocene As Fm, Upper Oligocene-Lower Aquitanian Bosque Fm, Upper Oligocene-Aquitanian Río Pliego Fm, Burdigalian El Niño Fm) and an evaluation has been performed to obtain four parameters: the scientific value, the educational and touristic potential, and the degradation risk. The firsts three parameters obtained values above 50 being considered of “high” or “very high” interest (“very high” in most of the cases). The last parameter shows always values below 50 indicating a “moderate” or “low” risk of degradation. The obtained values allow us considering the tectono-sedimentary evolution of this basin worthy of being proposed as a geological heritage.


Author(s):  
Ümitcan Erbil ◽  
Aral I. Okay ◽  
Aynur Hakyemez

AbstractLate Cenozoic was a period of large-scale extension in the Aegean. The extension is mainly recorded in the metamorphic core complexes with little data from the sedimentary sequences. The exception is the Thrace Basin in the northern Aegean, which has a continuous record of Middle Eocene to Oligocene marine sedimentation. In the Thrace Basin, the Late Oligocene–Early Miocene was characterized by north-northwest (N25°W) shortening leading to the termination of sedimentation and formation of large-scale folds. We studied the stratigraphy and structure of one of these folds, the Korudağ anticline. The Korudağ anticline has formed in the uppermost Eocene–Lower Oligocene siliciclastic turbidites with Early Oligocene (31.6 Ma zircon U–Pb age) acidic tuff beds. The turbidites are underlain by a thin sequence of Upper Eocene pelagic limestone. The Korudağ anticline is an east-northeast (N65°E) trending fault-propagation fold, 9 km wide and 22 km long and with a subhorizontal fold axis. It is asymmetric with shallowly-dipping northern and steeply-dipping southern limbs. Its geometry indicates about 1 km of shortening in a N25°W direction. The folded strata are unconformably overlain by Middle Miocene continental sandstones, which constrain the age of folding. The Korudağ anticline and other large folds in the Thrace Basin predate the inception of the North Anatolian Fault (NAF) by at least 12 myr. The Late Oligocene–Early Miocene (28–17 Ma) shortening in the Thrace Basin and elsewhere in the Balkans forms an interlude between two extensional periods, and is probably linked to changes in the subduction dynamics along the Hellenic trench.


2006 ◽  
Vol 80 (20) ◽  
pp. 10055-10063 ◽  
Author(s):  
Adrian Valli ◽  
Ana Montserrat Martín-Hernández ◽  
Juan José López-Moya ◽  
Juan Antonio García

ABSTRACT The P1 protein of viruses of the family Potyviridae is a serine proteinase, which is highly variable in length and sequence, and its role in the virus infection cycle is not clear. One of the proposed activities of P1 is to assist HCPro, the product that viruses of the genus Potyvirus use to counteract antiviral defense mediated by RNA silencing. Indeed, an HCPro-coding region is present in all the genomes of members of the genera Potyvirus, Rymovirus, and Tritimovirus that have been sequenced. However, it was recently reported that a sequence coding for HCPro is lacking in the genome of Cucumber vein yellowing virus (CVYV), a member of the genus Ipomovirus, the fourth monopartite genus of the family. In this study, we provide further evidence that P1 enhances the activity of HCPro in members of the genus Potyvirus and show that it is duplicated in the ipomovirus CVYV. The two CVYV P1 copies are arranged in tandem, and the second copy (P1b) has RNA silencing suppression activity. CVYV P1b suppressed RNA silencing induced either by sense green fluorescent protein (GFP) mRNA or by a GFP inverted repeat RNA, indicating that CVYV P1b acts downstream of the formation of double-stranded RNA. CVYV P1b also suppressed local silencing in agroinfiltrated patches of transgenic Nicotiana benthamiana line 16c and delayed its propagation to the neighboring cells. However, neither the short-distance nor long-distance systemic spread of silencing of the GFP transgene was completely blocked by CVYV P1b. CVYV P1b and P1-HCPro from the potyvirus Plum pox virus showed very similar behaviors in all the assays carried out, suggesting that evolution has found a way to counteract RNA silencing by similar mechanisms using very different proteins in viruses of the same family.


1998 ◽  
Vol 11 (6) ◽  
pp. 711 ◽  
Author(s):  
Robert S. Hill ◽  
Leonie J. Scriven

A re-investigation of macrofossils previously referred to the extantpodocarpaceous genus Falcatifolium Laubenfels shows thatno records can be sustained. Falcatifolium australisD.R.Greenwood from Middle Eocene sediments in Victoria bears littleresemblance to extant species in the genus and is transferred to the newfossil genus Sigmaphyllum R.S.Hill & L.J.Scriven.Specimens from Early Oligocene sediments in Tasmania previously assigned toFalcatifolium are described as a second species ofSigmaphyllum, S. tasmanensisR.S.Hill & L.J.Scriven, and specimens from mid to late Eocene sediments inTasmania previously assigned to Falcatifolium do notbelong to that genus, although their true generic affinities are uncertain.Dispersed cuticle specimens from Late Eocene–Oligocene sediments inSouth Australia referred to Falcatifolium are notreliable records of the genus and require further investigation. However,Dacrycarpus eocenica D.R.Greenwood, from Middle Eocenesediments in Victoria is transferred to Falcatifolium,and is similar to the extant species F. angustumLaubenfels, which has a leaf morphology unusual for the genus.Falcatifolium eocenica (D.R.Greenwood) R.S.Hill & L.J.Scriven is the only reliable record of the genus in the Australian fossilrecord to date.


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