© Biospeologica Bibliographia - Publications 2010-2
© Biospeologica Bibliographia - Publications 2010-2
© Biospeologica Bibliographia - Publications 2010-2
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<strong>©</strong> <strong>Biospeologica</strong> <strong>Bibliographia</strong><br />
<strong>Publications</strong> <strong>2010</strong>-1<br />
Page 50 sur 116<br />
embryos, which increases mouth and taste bud development at the<br />
expense of eyes via pleiotropic Shh signaling. Cavefish lack melanin<br />
synthesis in regressed pigment cells due to loss-of-function mutations in<br />
oca2, which normally regulates the supply of L-DOPA precursor during<br />
melanin synthesis. The block in cavefish pigmentation occurs at a<br />
metabolic branch point in which L-tyrosine is normally converted either<br />
(1) to L-DOPA, DOPAquinone, and melanin by tyrosinase or (2) to L-<br />
DOPA, dopamine, and related catecholamines by tyrosine hydroxylase<br />
and other enzymes. A similar block in the initial step of melanin synthesis<br />
has evolved independently in the cave plant hopper Oliarus polyphemus<br />
and other diverse cave animals. In Astyanax cavefish, the benefit of lost<br />
melanin pigment appears to be the production of excess L-DOPA and its<br />
derivative dopamine by the second alternative pathway, which promotes<br />
constructive development of dopaminergic neurons and enhances the<br />
magnitude of adaptive feeding behavior. We conclude that the evolution<br />
of beneficial constructive traits could have driven regressive traits via<br />
developmental tradeoffs encoded in pleiotropic genes, which adapt cave<br />
animals to life in darkness. http://www.icsb<strong>2010</strong>.net/<br />
JEFFERY (W. R.) & STRICKLER (A. G.), <strong>2010</strong>. Chapter<br />
6. Development as an Evolutionary Process in Astyanax<br />
Cavefishes:141-182. DOI:<br />
http://dx.doi.org/10.1201/EBK1578086702-c6. In:<br />
TRAJANO (E.), BICHUETTE (M. E.) & KAPOOR (B.<br />
G.), Biology of Subterranean Fishes. Edited by TRAJANO<br />
(E.), BICHUETTE (M. E.) & KAPOOR (B. G.). ISBN:<br />
978-1-57808-670-2. eBook ISBN: 978-1-4398-4048-1.<br />
Science Publishers <strong>2010</strong>. 460 p.<br />
JIANG (T.), LIU (R.), METZNER (W.), YOU (Y.), LI (S.),<br />
LIU (S.) & FENG (J.), <strong>2010</strong>. Geographical and individual<br />
variation in echolocation calls of the intermediate leafnosed<br />
bat, Hipposideros larvatus. Ethology 116(8,<br />
August):691-703. DOI: http://dx.doi.org/10.1111/j.1439-<br />
0310.<strong>2010</strong>.01785.x. ABS: The cause and significance of variation in<br />
echolocation call frequency within hipposiderid bats is not well<br />
understood despite an increasing number of allopatric and sympatric<br />
examples being documented. We examined variation patterns in the<br />
resting frequency (RF) of echolocation calls emitted by the intermediate<br />
leaf-nosed bat, Hipposideros larvatus, on a broad geographical scale.<br />
Data mining technology and Kruskal-Wallis test both showed substantial<br />
variation with a longitudinal pattern in RF in H. larvatus among colonies,<br />
and this variation was associated with geographical distance and not body<br />
size. In addition, we found that a high degree of variability between<br />
individuals was hidden under the geographical variation. The results<br />
support an effect of random cultural drift, and challenge the prey<br />
detection hypothesis. Moreover, an acoustic difference among local<br />
island colonies may be indicative of a vocal dialect. We found that each<br />
colony of H. larvatus seems to maintain a "private bandwidth", which<br />
could be used for colony identity and individual communication thus<br />
helping individuals and colonies to get a number of fitness benefits.<br />
JOCHUM (A.), WEIGAND (A. M.), SLAPNIK (R.) &<br />
KLUSSMANN-KOLB (A.), <strong>2010</strong>. Zospeum: Luminaries<br />
of the Dark - Barcoding highlights an old taxonomic<br />
conundrum besetting microsnails (Pulmonata, Ellobioidea,<br />
Carychiidae). Abstract. The Malacological Society of<br />
London Molluscan Forum, Nov. 30, <strong>2010</strong>, NHM London,<br />
UK.<br />
JOHNSON (J. B.), FORD (W. M.), RODRIGUE (J. L.),<br />
EDWARDS (J. W.) & JOHNSON (C. M.), <strong>2010</strong>. Roost<br />
selection by male Indiana myotis following forest fires in<br />
Central Appalachian Hardwoods Forests. Journal of Fish<br />
and Wildlife Management 1(2):111-121; e1944-687X.<br />
DOI: http://dx.doi.org/10.3996/04<strong>2010</strong>-JFWM-007.<br />
JONES (B.), <strong>2010</strong>. Microbes in caves: agents of calcite<br />
corrosion and precipitation:7-30. DOI:<br />
http://dx.doi.org/10.1144/SP336.2. In: PEDLEY (H. M.) &<br />
ROGERSON (M.), Tufas and Speleothems: Unravelling<br />
the Microbial and Physical Controls, Edited by: PEDLEY<br />
(H. M.) & ROGERSON (M.), University of Hull, UK.<br />
Geological Society, London, Special <strong>Publications</strong>, 336.<br />
Bernard LEBRETON & Jean-Pierre BESSON<br />
Créé le : 01.01.<strong>2010</strong><br />
Modifié le : 30.06.<strong>2010</strong><br />
ABS: Diverse biogenic and abiogenic processes produce calcite<br />
speleothems. From a biogenic perspective, cave microbes mediate a wide<br />
range of destructive and constructive processes that collectively influence<br />
the growth of calcite speleothems and their internal fabrics. Destructive<br />
processes include substrate breakdown by dissolution, boring and residue<br />
micrite production, whereas constructive processes include microbe<br />
calcification, trapping and binding of detrital particles to substrates, and<br />
microbial induced calcite precipitation. Biogenesis can be established<br />
from: (1) the presence of mineralized microbes; (2) fabrics, such as<br />
stromatolite-like structures, that can be attributed to microbial activity;<br />
and/or (3) geochemical proxies (carbon and oxygen isotopes, lipid<br />
biomarkers) considered indicative of microbe activity. Such criteria have,<br />
for example, been used to demonstrate microbial involvement in the<br />
formation of pool fingers, stalactites/stalagmites, cave pisoliths and<br />
moonmilk. Nevertheless, absolute proof of microbial biogenesis in<br />
calcitic speleothems is commonly difficult because taphonomic processes<br />
and/or diagenetic processes commonly mask evidence of microbial<br />
activity. The assumption that calcitic speleothems are abiogenic, which<br />
has been tacitly assumed in many studies, is dangerous as there is clear<br />
evidence that microbes thrive in most caves and can directly and<br />
indirectly influence calcite precipitation in many different ways.<br />
JONES (D. S.), TOBLER (D.), SCHAPERDOTH (I.),<br />
MAINIERO (M.) & MACALADY (J. L.), <strong>2010</strong>.<br />
Community structure of subsurface biofilms from the<br />
thermal sulfidic caves of Acquasanta Terme, Italy. Applied<br />
and Environmental Microbiology 76(17, September):5902-<br />
5910. DOI: http://dx.doi.org/10.1128/AEM.00647-10.<br />
JUAN (C.) & EMERSON (B. C.), <strong>2010</strong>. Evolution<br />
underground: shedding light on the diversification of<br />
subterranean insects. Journal of Biology 9(3):17, 5 p. DOI:<br />
http://dx.doi.org/10.1186/jbiol227. ABS: A recent study in BMC<br />
Evolutionary Biology has reconstructed the molecular phylogeny of a<br />
large Mediterranean cave-dwelling beetle clade, revealing an ancient<br />
origin and strong geographic structuring. It seems likely that<br />
diversification of this clade in the Oligocene was seeded by an ancestor<br />
already adapted to subterranean life. See research article<br />
http://www.biomedcentral.com/1471-2148/10/29 webcite.<br />
JUAN (C.), GUZIK (M. T.), JAUME (D.) & COOPER (S.<br />
J. B.), <strong>2010</strong>. Evolution in caves: Darwin's "wrecks of<br />
ancient life" in the molecular era. Molecular Ecology<br />
19(18, September):3865-3880. DOI:<br />
http://dx.doi.org/10.1111/j.1365-294X.<strong>2010</strong>.04759.x. ABS:<br />
Cave animals have historically attracted the attention of evolutionary<br />
biologists because of their bizarre "regressive" characters and convergent<br />
evolution. However, understanding of their biogeographic and<br />
evolutionary history, including mechanisms of speciation, has remained<br />
elusive. In the last decade, molecular data have been obtained for<br />
subterranean taxa and their surface relatives, which have allowed some of<br />
the classical debates on the evolution of cave fauna to be revisited. Here,<br />
we review some of the major studies, focusing on the contribution of<br />
phylogeography in the following areas: biogeographic history and the<br />
relative roles of dispersal and vicariance, colonization history, cryptic<br />
species diversity and modes of speciation of cave animals. We further<br />
consider the limitations of current research and prospects for the future.<br />
Phylogeographic studies have confirmed that cave species are often<br />
cryptic, with highly restricted distributions, but have also shown that their<br />
divergence and potential speciation may occur despite the presence of<br />
gene flow from surface populations. Significantly, phylogeographic<br />
studies have provided evidence for speciation and adaptive evolution<br />
within the confines of cave environments, questioning the assumption<br />
that cave species evolved directly from surface ancestors. Recent<br />
technical developments involving "next generation" DNA sequencing and<br />
theoretical developments in coalescent and population modelling are<br />
likely to revolutionize the field further, particularly in the study of<br />
speciation and the genetic basis of adaptation and convergent evolution<br />
within subterranean habitats. In summary, phylogeographic studies have<br />
provided an unprecedented insight into the evolution of these unique<br />
fauna, and the future of the field should be inspiring and data rich. KW:<br />
Cave animals, cryptic species, phylogeography, speciation, subterranean,<br />
vicariance and dispersal.<br />
JUBERTHIE (C.), <strong>2010</strong>. Jacques Pierre DURAND, 12 Juillet<br />
1936 - 13 Avril 2007. SIBIOS-ISSB Newsletter 7(2006-<br />
<strong>2010</strong>):26-34.