Geographic variability in expression of the sex-linkedAAT-1 gene of the bell-ring frog,Buergeria buergeri

2004 ◽  
Vol 302B (2) ◽  
pp. 182-194 ◽  
Author(s):  
Masayuki Sumida ◽  
Shigeru Ohta ◽  
Shigeru Atsumi ◽  
Tamotsu Fujii
1989 ◽  
Vol 16 (2) ◽  
pp. 169-190 ◽  
Author(s):  
INGO KRUMBIEGEL ◽  
GUNTER G. SEHM

The subspecific division of the Plains Bison by one of the authors (Krumbiegel, 1980) into a Southern Plains Bison Bison bison bison (Linnaeus, 1758) and a Northern Plains Bison Bison bison montanae Krumbiegel, 1980, is here corroborated by reference to early illustrations and reports unknown to mammalogists, thereby proving that the authors' historiographical approach can be used in establishing taxonomic reconstructions of recently exterminated species or subspecies.


Molecules ◽  
2021 ◽  
Vol 26 (15) ◽  
pp. 4534
Author(s):  
Taitusi Taufa ◽  
Ramesh Subramani ◽  
Peter Northcote ◽  
Robert Keyzers

The islands of the South Pacific Ocean have been in the limelight for natural product biodiscovery, due to their unique and pristine tropical waters and environment. The Kingdom of Tonga is an archipelago in the central Indo-Pacific Ocean, consisting of 176 islands, 36 of which are inhabited, flourishing with a rich diversity of flora and fauna. Many unique natural products with interesting bioactivities have been reported from Indo-Pacific marine sponges and other invertebrate phyla; however, there have not been any reviews published to date specifically regarding natural products from Tongan marine organisms. This review covers both known and new/novel Marine Natural Products (MNPs) and their biological activities reported from organisms collected within Tongan territorial waters up to December 2020, and includes 109 MNPs in total, the majority from the phylum Porifera. The significant biological activity of these metabolites was dominated by cytotoxicity and, by reviewing these natural products, it is apparent that the bulk of the new and interesting biologically active compounds were from organisms collected from one particular island, emphasizing the geographic variability in the chemistry between these organisms collected at different locations.


Apidologie ◽  
1978 ◽  
Vol 9 (4) ◽  
pp. 363-381 ◽  
Author(s):  
F. RUTTNER ◽  
Lucienne TASSENCOURT ◽  
J. LOUVEAUX

1984 ◽  
Vol 59 (4) ◽  
pp. 490-491
Author(s):  
Glenn D. Prestwich
Keyword(s):  

2013 ◽  
Vol 109 (1) ◽  
pp. 219-228 ◽  
Author(s):  
E Crocetti ◽  
◽  
R De Angelis ◽  
C Buzzoni ◽  
A Mariotto ◽  
...  

1996 ◽  
Vol 143 (5) ◽  
pp. 487-495 ◽  
Author(s):  
J. M. Soucie ◽  
R. J. Coates ◽  
W. McClellan ◽  
H. Austin ◽  
M. Thun

Paleobiology ◽  
2015 ◽  
Vol 41 (4) ◽  
pp. 610-632 ◽  
Author(s):  
Phoebe A. Cohen ◽  
Francis A. Macdonald

AbstractProterozoic strata host evidence of global “Snowball Earth” glaciations, large perturbations to the carbon cycle, proposed changes in the redox state of oceans, the diversification of microscopic eukaryotes, and the rise of metazoans. Over the past half century, the number of fossils described from Proterozoic rocks has increased exponentially. These discoveries have occurred alongside an increased understanding of the Proterozoic Earth system and the geological context of fossil occurrences, including improved age constraints. However, the evaluation of relationships between Proterozoic environmental change and fossil diversity has been hampered by several factors, particularly lithological and taphonomic biases. Here we compile and analyze the current record of eukaryotic fossils in Proterozoic strata to assess the effect of biases and better constrain diversity through time. Our results show that mean within assemblage diversity increases through the Proterozoic Eon due to an increase in high diversity assemblages, and that this trend is robust to various external factors including lithology and paleogeographic location. In addition, assemblage composition changes dramatically through time. Most notably, robust recalcitrant taxa appear in the early Neoproterozoic Era, only to disappear by the beginning of the Ediacaran Period. Within assemblage diversity is significantly lower in the Cryogenian Period than in the preceding and following intervals, but the short duration of the nonglacial interlude and unusual depositional conditions may present additional biases. In general, large scale patterns of diversity are robust while smaller scale patterns are difficult to discern through the lens of lithological, taphonomic, and geographic variability.


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