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1 idy and gene conversion in asexual, bdelloid rotifers.
2 hment (biomagnification) was observed in the rotifers.
3 s in the putatively ancient asexual bdelloid rotifers.
4 ly among species and are present in bdelloid rotifers.
5 etic, and genomic data suggest that bdelloid rotifers, a clade of microscopic animals, have persisted
7 ir study of genetic exchange in the bdelloid rotifer Adineta vaga, Debortoli et al. [1] conclude that
9 onstrated that predator-prey oscillations in rotifer-algal laboratory microcosms are qualitatively al
11 A fully specified mathematical model for the rotifer-algal population and evolutionary dynamics predi
13 c oxidase subunit 1 (cox1) gene of bdelloid rotifers and amplified and cloned sequences using a nest
14 An interesting observation about bdelloid rotifers and their reversion to asexual reproduction as
15 ngly clear that the biodiversity of bdelloid rotifers (and other less easily dispersed microbes) is m
19 to reject the hypothesis that communities of rotifers are the same across even fairly small geographi
20 Relative-rate tests, using acanthocephalan rotifers as an outgroup, showed slightly higher rates of
21 port that a subset of PLEs found in bdelloid rotifers, basidiomycete fungi, stramenopiles, and plants
22 ant to IR than that of Euchlanis dilatata, a rotifer belonging to the desiccation-intolerant and facu
23 on experiments with the facultatively sexual rotifer Brachionus calyciflorus, we test how environment
24 eption exists in the invertebrate monogonont rotifer Brachionus manjavacas, suggesting an ancient ori
25 ic structure of the cyclical parthenogenetic rotifer Brachionus plicatilis by following populations e
26 icity tests (48-h LC50) using the euryhaline rotifer Brachionus plicatilis were performed to assess t
27 uggested by the recent finding that bdelloid rotifers can recover and resume reproduction after suffe
29 erior competitor dominated initially, but as rotifer densities increased, the more predator-resistant
31 DNA sequencing has shown individual bdelloid rotifer genomes to contain two or more diverged copies o
32 in Drosophila virilis and Athena in bdelloid rotifers, have proliferated as copies containing introns
33 have contributed to the success of bdelloid rotifers in avoiding the early extinction suffered by mo
34 e that the great radioresistance of bdelloid rotifers is a consequence of an unusually effective syst
35 traordinary radiation resistance of bdelloid rotifers is a consequence of their evolutionary adaptati
36 refore that "Genetic exchange among bdelloid rotifers is more likely due to horizontal gene transfer
37 enetic test of this indication that bdelloid rotifers may have evolved without sexual reproduction or
38 anhydrobiosis and cryobiosis, as do bdelloid rotifers, nematodes, and other animals of the water film
43 patterns of evolution of DNA transposons in rotifers of the class Bdelloidea, a group of basal tripl
44 d positive for reverse transcriptases except rotifers of the class Bdelloidea, the largest eukaryotic
45 ene in bdelloids and in facultatively sexual rotifers of the class Monogononta, employing distance ba
47 our copies of the hsp82 gene of the bdelloid rotifer Philodina roseola, each of which is on a separat
48 population dynamics by modeling a structured rotifer population that preys on a dynamic food supply.
50 We find that genomes of individual bdelloid rotifers, representing four different species, appear to
51 he R2 clade in the 28S RNA genes of bdelloid rotifers, small freshwater invertebrate animals best kno
53 ng a set of genomes for 144 bacteria and one rotifer that constituted the abundant community in both
55 be transferred to higher trophic organisms (rotifers) through dietary uptake of ciliated protozoans.
57 n an asexual microinvertebrate, the bdelloid rotifer, we have observed a mechanism by which such orga
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