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CONTENT - International Society of Zoological Sciences

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S7 ICZ2008 - Abstracts<br />

S8 - Biodiversity and ecology <strong>of</strong> Protists S9 – Genomics and cell biology <strong>of</strong> Protists<br />

A global perspective <strong>of</strong> the biodiversity <strong>of</strong> heterotrophic<br />

nan<strong>of</strong>lagellates as the most abundant heterotrophic eukaryotes<br />

Harmut Arndt 1* , Frank Nitsche 1 , Frank Scheckenbach 1 and Claudia<br />

Wylezich 1,2<br />

1 Department <strong>of</strong> General Ecology, <strong>Zoological</strong> Institute, University <strong>of</strong><br />

Cologne, D-50968 Koeln (Cologne), Germany<br />

2 Institute for Baltic Sea Research, D-18119 Rostock, Germany<br />

Protist diversity is still controversially discussed. One group <strong>of</strong><br />

protistologists assumes a relatively low number <strong>of</strong> protistan species<br />

compared to their low size due to assumed high rates <strong>of</strong> dispersal<br />

and low speciation rates. Another group <strong>of</strong> protistologists assumes<br />

high protistan diversity similar to other groups <strong>of</strong> eukaryotes claiming<br />

a high number <strong>of</strong> cryptic species behind each nominal species. We<br />

will summarise investigations <strong>of</strong> heterotrophic nan<strong>of</strong>lagellates<br />

regarding their diversity and distribution patterns. We will include<br />

samples from the largest, though seldom investigated parts <strong>of</strong> the<br />

biosphere, deep sea, groundwater and polar regions. There seems<br />

to exist biogeographies in nan<strong>of</strong>lagellates. The endemic and<br />

cosmopolitan distribution <strong>of</strong> certain taxa will be discussed. Regarding<br />

the knowledge <strong>of</strong> nan<strong>of</strong>lagellate biodiversity, we are still at the<br />

beginning and we will point to several problems associated with a<br />

current estimate <strong>of</strong> biodiversity patterns. According to our recent<br />

estimates, protists as the most abundant eukaryotic key players in<br />

most ecosystems and as the evolutionary oldest and<br />

phylogenetically most diverse eukaryotes should account for a large<br />

proportion <strong>of</strong> Earth’s eukaryotic diversity. The knowledge <strong>of</strong><br />

biogeographic characteristics <strong>of</strong> nanoprotists is also important from<br />

the viewpoint <strong>of</strong> overall biological theory. Are small organisms<br />

different from large organisms? At least regarding their importance<br />

for the matter transfer in both aquatic and terrestrial ecosystems<br />

protists are much more important than larger eukaryotes. The<br />

knowledge <strong>of</strong> diversity patterns <strong>of</strong> nanoprotists seems to be<br />

fundamental for understanding the Earth’s biodiversity patterns and<br />

ecosystem functioning and may give us also a hint for a better<br />

understanding <strong>of</strong> evolutionary processes.<br />

The genome <strong>of</strong> Paramecium<br />

Jean Cohen<br />

Centre de Génétique Moléculaire, CNRS, 91198 Gif-sur-Yvette<br />

cedex.<br />

Ciliates such as Paramecium are the only unicellular eukaryotes<br />

known to separate germinal and somatic functions. Diploid but silent<br />

micronuclei transmit the genetic information to the next sexual<br />

generation. Polyploid macronuclei express the genetic information<br />

from a streamlined version <strong>of</strong> the genome but are replaced at each<br />

sexual generation through reproducible rearrangements <strong>of</strong> the<br />

zygotic genome involving elimination <strong>of</strong> repeated sequences, precise<br />

excision <strong>of</strong> unique-copy internal eliminated sequences (IES), and<br />

amplification <strong>of</strong> the cellular genes to high copy number. The<br />

macronuclear genome <strong>of</strong> Paramecium tetraurelia was recently<br />

sequenced by a shotgun approach, providing access to the gene<br />

repertoire. The 72-Mb assembly represents a consensus sequence<br />

for the somatic DNA which revealed the presence <strong>of</strong> nearly 40,000<br />

genes, most <strong>of</strong> them arising through at least three successive wholegenome<br />

duplications, which is produced after sexual. An overview <strong>of</strong><br />

genomic and postgenomic data obtained with the Paramecium<br />

genome will be presented.<br />

Aury et al. 2006. Global trends <strong>of</strong> whole-genome duplications<br />

revealed by the ciliate Paramecium tetraurelia. Nature 444, 171-178.<br />

Duret et al. 2008. Analysis <strong>of</strong> sequence variability in the<br />

macronuclear DNA <strong>of</strong> Paramecium tetraurelia: a somatic view <strong>of</strong> the<br />

germ line. Genome Research, 18, 585-596.<br />

- 28 -<br />

Bacterial Endocytobionts Variety in Ciliophora<br />

Sergei I. Fokin<br />

Department <strong>of</strong> Invertebrate Zoology, St. Petersburg State University,<br />

199034, Russia<br />

Different bacteria, which could be considered facultative or,<br />

sometimes, permanent endocytobionts (Eb) can occupy ciliate’s cell.<br />

Till now over 230 ciliate species were recorded as hosts <strong>of</strong> different<br />

intracellular bacteria. However, approximate number <strong>of</strong> species <strong>of</strong><br />

free-living ciliated protists is about 9000-20000. Thus the number <strong>of</strong><br />

recorded Eb is, apparently, just a small part <strong>of</strong> the real biodiversity <strong>of</strong><br />

this mostly undiscovered world. In the presentation is mentioned<br />

some new material concerning Eb variety, its categories and<br />

interaction with a host cell. Special attention is paid to the<br />

endocytobiosis between some ciliates and highly infectious bacteria<br />

Holospora or other alpha-proteobacteria, as well as to life cycles and<br />

strategies <strong>of</strong> Eb <strong>of</strong> different ciliates. From ecological point <strong>of</strong> view we<br />

can assume that association with Eb sometimes is useful for the host<br />

cell, especially in unstable environment like littoral marine zone or<br />

river’s estuary. However, quite low percentage <strong>of</strong> bacteria infection in<br />

most ciliate’ populations, revealed so far, appears to indicate that<br />

majority <strong>of</strong> Eb are either parasites or commensals, but not true<br />

symbionts. Dynamic <strong>of</strong> some bacterial infections, first <strong>of</strong> all infectious<br />

ones, in natural ciliate’ populations looks epidemic. In some years<br />

and places the number <strong>of</strong> infected populations increases and then<br />

infected cells become rare for a long time. There is a great need for a<br />

more extensive field-based research in this key sub-discipline <strong>of</strong><br />

symbiosis.<br />

Rare ciliate species (Ciliophora, Protista) revealed from<br />

brackish water habitats with oxygen deficiency.<br />

Sergei I. Fokin 1,2 , Letizia Modeo 1 , Ilaria Andreoli 1 , Filippo Ferrantini 1 ,<br />

Franco Verni 1 and Giulio Petroni 1<br />

1<br />

Department <strong>of</strong> Biology, University <strong>of</strong> Pisa, 56126, Italy<br />

2 Department <strong>of</strong> Invertebrate Zoology, St. Petersburg State<br />

University, 199034, Russia<br />

Sonderia pharyngea. Cell size 80-130 μm; all ventral ciliary rows<br />

extending from posterior end; cytopharynx is almost tubular,<br />

sometimes as long as a half <strong>of</strong> the body; there are few trichocysts.<br />

Found in salinity 5-12‰.<br />

Parablepharisma bacteriophora. Cell size 70-110 μm; has about 50<br />

membranelles on the left side <strong>of</strong> the large vestibulum; undulated<br />

membrane is very conspicuous – up to 30 μm long; 2 micronuclei;<br />

contractile vacuole closed to posterior end; According to SSrRNA<br />

sequence it clustered with Spirotrichea, very basal to the group.<br />

Found in salinity 22‰. All body surfaces <strong>of</strong> both mentioned species<br />

are covered with sulfur bacteria.<br />

Copemetopus sp. (subsalsus?). Cell size 150-300 μm; has about 50<br />

membranelles on the left side <strong>of</strong> large vestibulum (up to half <strong>of</strong> the<br />

body) and additional 8-12 units <strong>of</strong> very long cirri (up to 80 μm)<br />

decorate external apical-left part <strong>of</strong> the mouth area. Cilia tuff in<br />

anterial part <strong>of</strong> dorsal side; macronucleus has dumbbell shape;<br />

micronuclei are numerous (9-13). According to SSrRNA sequence it<br />

is clustered with Spirotrichea, very basal to the group. Found in<br />

salinity 5-8‰.<br />

All mentioned rare species were isolated in Italy. Probably previous<br />

single finds <strong>of</strong> the cilates connected with insufficient investigation <strong>of</strong><br />

the habitats.

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