Plant assemblages from the Shafer Peak Formation (Lower Jurassic), north Victoria Land, Transantarctic Mountains

2010 ◽  
Vol 23 (2) ◽  
pp. 188-208 ◽  
Author(s):  
Benjamin Bomfleur ◽  
Christian Pott ◽  
Hans Kerp

AbstractThe Jurassic plant fossil record of Gondwana is generally meagre, which renders phytogeographic and palaeoclimatic interpretations difficult to date. Moreover, plant fossil assemblages mainly consist of impressions/compressions with rather limited palaeobiological and palaeoecological significance. We here present a detailed survey of new Early Jurassic plant assemblages from the Pliensbachian Shafer Peak Formation, north Victoria Land, Transantarctic Mountains. Some of the well-preserved fossils yield cuticle. The floras consist of isoetalean lycophytes, sphenophytes, several ferns, bennettitaleans, and conifers. In addition, three distinct kinds of conifer shoots and needles were obtained from bulk macerations. The composition of the plant communities is typical for Jurassic macrofloras of Gondwana, which underscores the general homogeneity of Southern Hemisphere vegetation during the mid-Mesozoic. Altogether, the plant fossil assemblages indicate humid and warm temperate conditions, which is in contrast to recent palaeoclimatic models that predict cool temperate climates for the continental interior of southern Gondwana during the Jurassic. However, there is no evidence for notable soil development or peat accumulation. The environmental conditions were apparently very unstable due to intense volcanic activity that resulted in frequent perturbation of landscape and vegetation, hampering the development of long-lived climax communities. Cuticles of bennettitaleans and conifers show xeromorphic features that may have been beneficial for growth in this volcanic environment.

1989 ◽  
Vol 63 (1) ◽  
pp. 47-52 ◽  
Author(s):  
Robert B. Blodgett ◽  
David M. Rohr

Two new spine-bearing gastropods, Chlupacispira spinosa n. gen. and sp. and Spinulrichospira cheeneetnukensis n. gen. and sp., are described from the late Early Devonian (Emsian) and early Middle Devonian (Eifelian), respectively, of west-central Alaska. These represent the earliest reported spiny pleurotomariacean gastropods. Otherwise, spinose pleurotomariaceans are known from strata no older than Carboniferous age. Spinulrichospira cheeneetnukensis n. gen. and sp. appears to represent a more highly ornamented derivative of Ulrichospira Donald. Both new genera are part of the more highly ornamented fauna which occurred in warm equatorial waters of the Old World Realm during the Early and Middle Devonian, in contrast to more weakly ornamented shells of the Eastern Americas Realm and even more weakly ornamented (almost totally “plain”) shells of the Malvinokaffric Realm. The latter two realms are thought to represent subtropical to warm temperate and cool temperate to cool polar conditions, respectively.


Author(s):  
Jean-Claude Dauvin ◽  
Denise Bellan-Santini

A recent inventory of the benthic Gammaridea: Amphipoda species on the French continental coastline catalogued 495 species. An analysis of the biodiversity and the biogeographic relationships that exist between the French Amphipoda: Gammaridea, living on the coastline that extends along 10° latitude range in the temperate region between 41° and 51° North and the other gammaridean faunas living in the north-eastern Atlantic has drawn the pattern of diversity in this marine invertebrate group on a large biogeographical scale. Gammaridean amphipods exhibit a latitudinal gradient over the total number of species, including the continental shelf species and the bathyal species. There are four main fauna groups, which correspond to the biogeographical zones of the north-eastern Atlantic: (1) a cold arctic and cool-temperate Svalbard and Norwegian coastal fauna; (2) a cool-temperate boreal and Boreal–Lusitanian United Kingdom, Irish and English Channel shallow fauna; (3) a warm-temperate Lusitanian Bay of Biscay and subtropical central Atlantic fauna; and (4) a subtropical Mediterranean fauna. The French fauna appears particularly rich, presenting 44% of the 1119 species recorded in the north-eastern Atlantic along the 50° latitude range (30°N–80°N).  This is obviously due to France's intermediate latitudinal location within the Lusitanian temperate biogeographical zone, which produces a biogeographical cross between the boreal fauna in the north and the warm temperate and sub-tropical fauna in the south.


2021 ◽  
Author(s):  
Daniela Roehnert ◽  
Frank Lisker ◽  
Maria Laura Balestrieri ◽  
Luca Grewe ◽  
Evandro Balbi ◽  
...  

<p>Northern Victoria Land constitutes the Pacific terminus of the Transantarctic Mountains (TAM) on the western shoulder of the Cenozoic West Antarctic Rift System. It is characterised by a distinct morphological transition from an elevated peneplain that dominates throughout most of the TAM to a strongly undulating relief with prominent narrow crests and alpine peaks. This contrast is associated with a lithological change from high-grade metamorphics and granitoids to low-grade metasedimentary rocks that contain only few scattered igneous bodies.</p><p>New high-resolution thermochronological data (fission-track and (U-Th-Sm)/He) from more than 60 locations in the Southern Cross Mountains and Mountaineer Range of northern Victoria Land provide the basis for studying regional exhumation and uplift with particular focus on the establishment of landscape contrasts. In an integrated approach, differences in topography are examined with respect to regional and local controls including tectonics, lithology and climate to identify differential trends and quantify the morphological evolution of the TAM and West Antarctic Rift System.</p><p> </p><p>Two coastal profiles covering 2 to 3 km in elevation reveal apatite fission track ages from 23 to 45 Ma with mean track lengths of 13.3 – 14.7 μm. Corresponding (U-Th-Sm)/He apatite and zircon data range between 19 – 32 Ma and 24 – 27 Ma, respectively. The dates show distinctive spatial trends of increasing ages from north to south and at greater distance to the coast whereby younger cooling ages correlate with stronger terrain segmentation and higher topographic relief.</p><p>Thermal history modelling of the combined data indicates that accelerated cooling commencing at 35 Ma proceeded at progressively higher rates reaching >25°C/Ma in late stages. This cooling episode continued until at least 20 Ma and refers to exhumation from burial depths of more than 5 km, clearly exceeding the calculated overburden on adjacent crustal blocks to the south. Although rapid upper lithospheric cooling is a generic feature of northern Victoria Land, the current data demonstrates that Cenozoic exhumation dynamics were highly differential. Understanding these patterns requires thorough balancing of structural against isostatic factors, lithological against climate parameters and focussed local incision against large-scale denudation and levelling processes.</p>


1986 ◽  
Vol 15 ◽  
pp. 10-26 ◽  
Author(s):  
Robert A. Spicer ◽  
Anthony G. Greer

Plant fossil assemblages are biased samples of the capacity of the once living source vegetation to produce litter (leaves, flowers, pollen, spores, fruits, seeds, twigs, branches, trunks, roots etc.). The “image” that the depositional system “sees” of the vegetation is in terms of isolated plant organs (or parts of organs) that are produced in greater or lesser quantities depending on the organ type. For instance throughout the life of a tree hundreds of thousands of leaves, many millions of pollen grains but only one trunk are produced. Only very rarely do plant fossil assemblages consist of entire or nearly entire plants. Instead assemblages consist of a mixture of organs in various states of completeness derived from a number of different taxa (each of which produces different organs in different relative amounts) growing at various distances from the depositional site.


2001 ◽  
Vol 49 (3) ◽  
pp. 223 ◽  
Author(s):  
Detlef H. Rohr ◽  
Brian S. Malone

Local climatic conditions influence the way in which ectotherms regulate their body temperature and activity. We examined correlations between local climatic conditions, body temperature and activity in adult, basking lowland copperheads (Austrelaps superbus) from two localities (warm-temperate versus cool-temperate) in south-eastern Australia. We also collected data from highland copperheads (Austrelaps ramsayi) at a locality with cold-temperate climate. We found that across the active season, mean body temperatures were similar among localities (approximately 27˚C) irrespective of species. In contrast, activity times differed. Cool-temperate A. superbus emerged earlier in spring and in the morning and retreated earlier in the evening and in autumn than their conspecifics from the warm-temperate locality. Spring emergence was correlated with yearly fluctuations in thermal conditions, suggesting that activity times depend on environmental temperatures. Predator–prey interactions influenced body temperature and activity to some extent in spring when warm-temperate A. superbus with relatively low body temperatures (as low as 18.5˚C) were captured around ponds in which they had been foraging for frogs. Austrelaps ramsayi from the cold-temperate locality not only displayed a later emergence in spring and reduced daily activity times compared with warm and cool-temperate A. superbus but also compared with A. ramsayi, as reported from a warmer locality in eastern Australia. These data indicate that activity times vary on a geographic basis while snake body temperatures largely remain inflexible. The surprising exception was that cold-temperate A. ramsayi retreated later in autumn than cool-temperate A. superbus, and at that time they showed body temperatures as low as 12.5˚C, well below those we had recorded for A. superbus. We suggest that A. ramsayi retreat later in autumn because they need to extend their reproductive season and that this is mediated via adaptive changes in the critical minimum body temperature, as has been reported for other snakes.


Geology ◽  
1982 ◽  
Vol 10 (12) ◽  
pp. 641 ◽  
Author(s):  
Hermann W. Pfefferkorn ◽  
Margaret C. Thomson

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