© 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 51 sur 116<br />
JUBERTHIE (C.), <strong>2010</strong>. Mesovoid shallow substratum<br />
(MSS):25-26. In: 20 th International Conference on<br />
Subterranean Biology, Postojna, Slovenia, 29 August-3<br />
September <strong>2010</strong>, ICSB <strong>2010</strong> Abstract Book, edited by:<br />
Ajda MOŠKRIČ and Peter TRONTELJ, ISBN 978-961-<br />
269-286-5. ABS: The MSS was discovered by Juberthie et al. (1980,<br />
1981) in the French Pyrenees, then in 1981 in Carpathian Mountains in<br />
Romania (Juberthie et al.). At the same time Ueno described in Japan the<br />
Upper Hypogean Habitat. In 1986, Oromi et al. described from Canary<br />
Islands a Volcanic MSS type found also in Hawaii by Howarth. The MSS<br />
is present in mountains of the temperate zone. The MSS is recorded at<br />
least from: Canary Islands, Spain, France, Italy, Austria, Czech Republic,<br />
Slovenia, Romania, Bulgaria, Greece, Turkey, Japan, Taiwan, China,<br />
Hawaii. The MSS is located beneath the last mineral horizon of soil and<br />
the compact bedrock. The more frequent MSS is composed of a network<br />
of small voids in screes covered by soil. When a soil has covered the<br />
scree, a climatic subterranean habitat, similar to the climate of caves is<br />
generated and a new MSS is available for colonization. The difference<br />
consists in the greater range of seasonal temperature variations. In karstic<br />
areas the MSS lies at the foot of carbonated cliffs; it can be connected<br />
with caves. The second type is very superficial cracks of the rocks,<br />
covered by soil. The third type is the Volcanic MSS in scoriaceous layers<br />
or in some types of lava flow, or in combination of the first and the<br />
second. The MSS extends the subterranean habitat. It is present in karstic<br />
areas but mainly in other types of rocks, without caves. Trophic resources<br />
consist in organic matters introduced by meteoric waters, and soil animals<br />
which penetrate passively or actively. Two fauna communities inhabit the<br />
MSS: one specific to the MSS, and the other composed of selected soil<br />
dwellers. The specific community is composed of troglophile and<br />
troglobiotic species, the same as in caves, or specific to MSS. Dominant<br />
group, the Coleoptera Trechinae and Leptodirinae: around 120 troglobitic<br />
species, and 46 genera. Also found are: Isopoda, Pseudoscorpiones,<br />
Araneae, Chilopoda, Diplopoda, Collembola, Campodea, Blattaria,<br />
Orthoptera, Diptera. In Pyrenees, a scree on a slope of a glacial valley<br />
was formed at the end of the last glacial period, from 24000 to 12000 BP,<br />
the genesis of the MSS began 12000-13000 years ago when climate<br />
changed, and a soil covered the scree. It was colonized by Coleoptera<br />
Aphaenops and Speonomus migrating from small populations surviving<br />
in limestone caves in the neighbouring karstic massif. The MSS is really<br />
a permanent subterranean habitat similar to caves.<br />
http://www.icsb<strong>2010</strong>.net/<br />
JUGOVIC (J.), <strong>2010</strong>. Vrstna in rasna morfološka<br />
diferenciacija jamskih kozic Troglocaris aggr.<br />
anophthalmus (Crustacea: Decapoda: Atyidae) na<br />
Dinarskem krasu [Cave shrimps Troglocaris aggr.<br />
anophthalmus (Crustacea: Decapoda: Atyidae), species<br />
and racial morphological differentiation in the dinaric<br />
karst]. Doktorska disertacija [Doctoral dissertation],<br />
Univerza v Ljubljani, Biotehniška fakulteta, Oddelek za<br />
biologijo, Ljubljana, <strong>2010</strong>, 173 p.<br />
JUGOVIC (J.), PREVORČNIK (S.), ALJANČIČ (G.) &<br />
SKET (B.), <strong>2010</strong>. The shrimp rostrum between phylogeny<br />
and adaptation:118, poster presentation. In: 20 th<br />
International Conference on Subterranean Biology,<br />
Postojna, Slovenia, 29 August-3 September <strong>2010</strong>, ICSB<br />
<strong>2010</strong> Abstract Book, edited by: Ajda MOŠKRIČ and Peter<br />
TRONTELJ, ISBN 978-961-269-286-5. ABS: Cave shrimps of<br />
the subgenus Troglocaris (Crustacea: Decapoda: Atyidae), exhibit high<br />
variability in rostral length and dentition. In the shrimp populations that<br />
are co-occurring with its amphibian predator Proteus anguinus, longer<br />
rostra armed with more numerous teeth are recorded. These shrimps are<br />
also larger than the ones living in the presumably Proteus-free<br />
environment. Discrepancies between the molecularly established<br />
phylogenetic relations and distributions of rostral length, as well as body<br />
size, directed our search towards possible environmental influences and<br />
possible defence mechanisms of cave shrimps. Although there are some<br />
exceptions, the common use of the rostral length is disputable in the<br />
diagnoses of the Atyid taxa. In preliminary laboratory observations no<br />
successful frontal attack of Proteus was recorded on shrimps with long<br />
rostra. Also, a handling time of Proteus feeding on shrimps with long<br />
rostra was longer. http://www.icsb<strong>2010</strong>.net/<br />
Bernard LEBRETON & Jean-Pierre BESSON<br />
Créé le : 01.01.<strong>2010</strong><br />
Modifié le : 30.06.<strong>2010</strong><br />
JUGOVIC (J.), PREVORČNIK (S.), BLEJEC (A.) &<br />
SKET (B.), <strong>2010</strong>. Linking molecular phylogeny to<br />
morphological evolution in Troglocaris (Crustacea:<br />
Decapoda: Atyidae):58. In: 20 th International Conference<br />
on Subterranean Biology, Postojna, Slovenia, 29 August-3<br />
September <strong>2010</strong>, ICSB <strong>2010</strong> Abstract Book, edited by:<br />
Ajda MOŠKRIČ and Peter TRONTELJ, ISBN 978-961-<br />
269-286-5. ABS: Ever since first species of Troglocaris (Dormitzer,<br />
1853) was described the taxonomy of the genus has been unresolved.<br />
Only after the phylogenetic reconstruction (COI, 16S rRNA and 28S<br />
rRNA) of the putative Troglocaris taxa from three separated distribution<br />
areas - from the Dinarides (Western Balkan Peninsula), S France and<br />
Caucasus - their phylogenetic relationships were revealed. The only<br />
French species was relocated into a new genus as Gallocaris inermis Sket<br />
& Zakšek, 2009, being more closely related to the epigean Dugastella<br />
valentina (Ferrer Galdiano, 1924) than to its supposed congeners. The<br />
taxa from the other two areas constitute a monophylum comprising the<br />
Caucasian Xiphocaridinella Sadovsky, 1930, and three Dinaric<br />
subgenera: sg. Troglocaris (= Troglocaris s. str.), sg. Spelaeocaris<br />
Matjašič, 1956 and sg. Troglocaridella Babić, 1922. Eleven species and<br />
phylogroups of the Dinaric subgenera were morphometrically analysed.<br />
The accordance of morphology and molecular data is demonstrated by<br />
multivariate statistical analyses. Although already a set of non-sexual<br />
characters enables distinct separation of all subgenera, optimal<br />
accordance of morphological and molecular data is achieved by the<br />
consideration of sexual characters in adult males. At the subgeneric level,<br />
both phylogenetic subclades of the subgenus Spelaeocaris are<br />
morphologically recognized, together with most of their species. In<br />
Troglocaris s. str., however, only a combination of numerous characters<br />
can separate phylogroups to some extent. A few characters, inappropriate<br />
for the multivariate statistics support the separation additionally. While<br />
the majority of the morphometric characters seem to be a subject of a<br />
phylogenetic patrimony, rostral characteristics and body size may be a<br />
result of adaptation. Eventually, the molecular approach remains the most<br />
appropriate for a reliable determination of the most Troglocaris s. str.<br />
species and phylogroups. http://www.icsb<strong>2010</strong>.net/<br />
JURADO (V.), PORCA (E.), CUEZVA (S.),<br />
FERNANDEZ-CORTES (A.), SÁNCHEZ-MORAL<br />
(S.) & SÁIZ-JIMÉNEZ (C.), <strong>2010</strong>. Fungal outbreak in a<br />
show cave. Science of the Total Environment 408(17,<br />
August 1 st ):3632-3638. DOI:<br />
http://dx.doi.org/10.1016/j.scitotenv.<strong>2010</strong>.04.057. ABS:<br />
Castañar de Ibor Cave (Spain) was discovered in 1967 and declared a<br />
Natural Monument in 1997. In 2003 the cave was opened to public visits.<br />
Despite of extensive control, on 26 August 2008 the cave walls and<br />
sediments appeared colonized by long, white fungal mycelia. This event<br />
was the result of an accidental input of detritus on the afternoon of 24<br />
August 2008. We report here a fungal outbreak initiated by Mucor<br />
circinelloides and Fusarium solani and the methods used to control it.<br />
KW: Show caves, Fungal outbreak, Control of fungi, Mucor<br />
circinelloides, Fusarium solani.<br />
JUSTINIANO (E. D.), NIEVES-RIVERA (Á. M.) &<br />
SANTOS-FLORES (C. J.), <strong>2010</strong>. Preliminary Survey of<br />
Copepods from Cueva Clara, Río Camuy Caves Park,<br />
Puerto Rico. Espeleorevista Puerto Rico 3(Junio-<br />
Diciembre):13-16. ABS: Recent surveys have recorded cosmopolitan<br />
cyclopoid copepods such as Macrocyclops albidus, Mesocyclops<br />
aspericorni, Microcyclops varicans and Eucyclops agilis from Cueva<br />
Clara de Empalme (or Cueva Clara) in the Río Camuy Caves Park of the<br />
Río Camuy Cave System (RCCS) in the northern karst of Puerto Rico.<br />
Our findings do not support the widely accepted notion that cave<br />
dwelling organisms are for the most part endemic and/or highly<br />
specialized species, leading to the conclusion that not all cave fauna is<br />
necessarily endemic. Further detailed examination of cave-dwelling<br />
copepod fauna using molecular techniques would prove beneficial in<br />
determining whether species found are indeed individuals of a particular<br />
species with a wide distribution, or if the presence of cryptic species is a<br />
viable explanation. KW: Copepoda, Cyclopoidea, microcrustaceans,<br />
karst, caverns, Caribbean. http://www.cuevaspr.org/<br />
KAJI (T.) & TSUKAGOSHI (A.), <strong>2010</strong>. Heterochrony and<br />
modularity in the degeneration of maxillopodan nauplius<br />
eyes. Biological Journal of the Linnean Society 99(3,