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1 iny freshwater invertebrates called bdelloid rotifers.
2 idy and gene conversion in asexual, bdelloid rotifers.
3 hment (biomagnification) was observed in the rotifers.
4 s in the putatively ancient asexual bdelloid rotifers.
5 e groundwork for future evolution studies in rotifers.
6 ly among species and are present in bdelloid rotifers.
7 overed last(3), which is the sister group to rotifers(4)(,)(5).
8 ylogenies have instead recovered them within rotifers(5-10), suggesting acanthocephalans are derived
9 etic, and genomic data suggest that bdelloid rotifers, a clade of microscopic animals, have persisted
10                                     Bdelloid rotifers, a class of freshwater invertebrates, are extra
11 sequence data from eight species of bdelloid rotifers, a class of invertebrates in which males are th
12 ics during the ingestion of microplastics by rotifers, a commonly found and globally distributed surf
13      We confirmed the finding by identifying rotifer actin gene sequences in a metagenome obtained fr
14 f 11 wild-caught individuals of the bdelloid rotifer Adineta vaga and present evidence that some patt
15 ir study of genetic exchange in the bdelloid rotifer Adineta vaga, Debortoli et al. [1] conclude that
16 omain of the N4CMT protein from the bdelloid rotifer Adineta vaga.
17                            In predator-prey (rotifer-alga) microcosms, cyclical changes in predator a
18 onstrated that predator-prey oscillations in rotifer-algal laboratory microcosms are qualitatively al
19                                        Using rotifer-algal microcosms, we tracked rapid evolution res
20 A fully specified mathematical model for the rotifer-algal population and evolutionary dynamics predi
21 ting predator density affects predator-prey (rotifer-algal) cycles in laboratory microcosms.
22 tly shown to promote lifespan in C. elegans, rotifer and yeast through a mechanism which has remained
23  c oxidase subunit 1 (cox1) gene of bdelloid rotifers and amplified and cloned sequences using a nest
24 g metazoan phyla such as sponges, jellyfish, rotifers and flatworms.
25  members of gnathiferans (which also include rotifers and several other microscopic phyla)(5,6), chae
26  bridging the evolutionary gap between jawed rotifers and the obligate parasitic, jawless acanthoceph
27    An interesting observation about bdelloid rotifers and their reversion to asexual reproduction as
28 ngly clear that the biodiversity of bdelloid rotifers (and other less easily dispersed microbes) is m
29                                     Bdelloid rotifers are ancient, apparently asexual animals, and la
30                                              Rotifers are free-living animals usually smaller than 1
31                                     Bdelloid rotifers are freshwater invertebrates that abandoned sex
32                                     Bdelloid rotifers are important contributors to biogeochemical cy
33 to reject the hypothesis that communities of rotifers are the same across even fairly small geographi
34                                     Bdelloid rotifers are well known for their abilities to survive l
35 ing with high efficiency, to further advance rotifers as a model system for biological discovery.
36   Relative-rate tests, using acanthocephalan rotifers as an outgroup, showed slightly higher rates of
37 port that a subset of PLEs found in bdelloid rotifers, basidiomycete fungi, stramenopiles, and plants
38 ant to IR than that of Euchlanis dilatata, a rotifer belonging to the desiccation-intolerant and facu
39 ogical and molecular markers, the discovered rotifer belongs to the genus Adineta, and aligns with a
40 on experiments with the facultatively sexual rotifer Brachionus calyciflorus, we test how environment
41 ISPR-mediated gene editing in the monogonont rotifer Brachionus manjavacas by microinjection of Cas9
42 eption exists in the invertebrate monogonont rotifer Brachionus manjavacas, suggesting an ancient ori
43 ic structure of the cyclical parthenogenetic rotifer Brachionus plicatilis by following populations e
44 icity tests (48-h LC50) using the euryhaline rotifer Brachionus plicatilis were performed to assess t
45 redictable) in laboratory populations of the rotifer Brachionus plicatilis.
46                                In the clonal rotifer Brachionus, low food conditions delay reproducti
47  The effect of feeding low, medium, and high rotifer (Brachionus rotundiformis) DHA levels (2.0, 3.6
48 s a source of maternal age effects using the rotifer, Brachionus manjavacas, an aquatic invertebrate.
49       After 48 hours of algal growth, marine rotifers, Brachionus plicatilis, were added to the algae
50                         Facultatively sexual rotifers can develop adaptive responses to fluctuating e
51 uggested by the recent finding that bdelloid rotifers can recover and resume reproduction after suffe
52 he remarkable freezing tolerance of bdelloid rotifers can thus be at least partially attributed to ho
53 Nanoindentation studies of the trophi of the rotifer chitinous mastax revealed a Young's modulus of 1
54 at Acanthocephala is the sister group of the rotifer class Bdelloidea.
55   It has been known for several decades that rotifers colonizing the schistosome's snail intermediate
56                                     Bdelloid rotifers constitute a class of microscopic animals livin
57 f the carotenoid-derived VOCs increased with rotifer consumption of algae.
58                   Both marine and freshwater rotifers could rapidly grind polystyrene, polyethylene a
59 erior competitor dominated initially, but as rotifer densities increased, the more predator-resistant
60 nsmitted nuclear parasites and that bdelloid rotifers evolved asexually.
61 to test, for example, MNP toxicity in marine rotifers, freshwater mussels, daphnids and earthworms.
62                        Marine and freshwater rotifers generated over 3.48 x 10(5) and 3.66 x 10(5) su
63 DNA sequencing has shown individual bdelloid rotifer genomes to contain two or more diverged copies o
64 find that chaetognaths cluster together with rotifers, gnathostomulids, and micrognathozoans within a
65                                              Rotifers have been studied in the laboratory and field f
66                             In recent years, rotifers have emerged as a model system for modern studi
67 in Drosophila virilis and Athena in bdelloid rotifers, have proliferated as copies containing introns
68 and 3.66 x 10(5) submicrometre particles per rotifer in a day, respectively, from photo-aged micropla
69  have contributed to the success of bdelloid rotifers in avoiding the early extinction suffered by mo
70  Recently sequenced genomes of some bdelloid rotifers in England were found to encode several protein
71               Furthermore, multiple bdelloid rotifers in the algal patch were revived in less than an
72 s in an animal, Adineta steineri, a bdelloid rotifer indigenous to freshwater environments.
73  identify volatiles emitted from healthy and rotifer infested cultures of Microchloropsis salina.
74                    Here, I describe bdelloid rotifers inhabiting an algal patch in Antarctica that ha
75 e that the great radioresistance of bdelloid rotifers is a consequence of an unusually effective syst
76 traordinary radiation resistance of bdelloid rotifers is a consequence of their evolutionary adaptati
77 refore that "Genetic exchange among bdelloid rotifers is more likely due to horizontal gene transfer
78 enetic test of this indication that bdelloid rotifers may have evolved without sexual reproduction or
79 ogical conflict and DNA transfer in bdelloid rotifers, microscopic animals whose genomes show elevate
80 e of the most striking examples are bdelloid rotifers, microscopic freshwater invertebrates believed
81                                     Bdelloid rotifers, microscopic multicellular animals, are known f
82 anhydrobiosis and cryobiosis, as do bdelloid rotifers, nematodes, and other animals of the water film
83 plants, and many types of animals, including rotifers, nematodes, insects, and mites.
84                                              Rotifers of class Bdelloidea are common invertebrate ani
85                                              Rotifers of class Bdelloidea have evolved for millions o
86                                              Rotifers of class Bdelloidea, a group of aquatic inverte
87                                              Rotifers of the asexual class Bdelloidea are unusual in
88  patterns of evolution of DNA transposons in rotifers of the class Bdelloidea, a group of basal tripl
89 d positive for reverse transcriptases except rotifers of the class Bdelloidea, the largest eukaryotic
90 ene in bdelloids and in facultatively sexual rotifers of the class Monogononta, employing distance ba
91 ce barcodes with rates especially high among rotifers, oligochaetes, and mites.
92 our copies of the hsp82 gene of the bdelloid rotifer Philodina roseola, each of which is on a separat
93 population dynamics by modeling a structured rotifer population that preys on a dynamic food supply.
94                                              Rotifer populations established rapidly after first floo
95 xperimentally evolved 32 pairs of monogonont rotifer populations under either unidimensional divergen
96  ingesting increasing levels of DHA in their rotifer prey.
97  macrophytes) and smaller (microcrustaceans, rotifers, protists and phytoplankton) groups of aquatic
98 ival of an obligate parthenogenetic bdelloid rotifer, recovered from northeastern Siberian permafrost
99  We find that genomes of individual bdelloid rotifers, representing four different species, appear to
100 a novel tetracyclic alkaloid produced by the rotifer Rotaria rotatoria.
101 lids, nemerteans, phoronids, brachiopods and rotifers-show that at least one of these, lophotrochin,
102 he R2 clade in the 28S RNA genes of bdelloid rotifers, small freshwater invertebrate animals best kno
103 e of microplastic fragmentation by different rotifer species in natural aquatic environments of both
104 on of these clusters in a pathogen-resistant rotifer species was nearly ten times stronger than in a
105            A new study of a group of asexual rotifers supports the idea that selection for a common e
106 his constitutes the longest reported case of rotifer survival in a frozen state.
107 ng a set of genomes for 144 bacteria and one rotifer that constituted the abundant community in both
108                                     Bdelloid rotifers therefore offer an advantageous system for inve
109  be transferred to higher trophic organisms (rotifers) through dietary uptake of ciliated protozoans.
110                                     Bdelloid rotifers, tiny freshwater invertebrates with transposon-
111                     By contrast, in bdelloid rotifers we found many genes that appear to have origina
112 n an asexual microinvertebrate, the bdelloid rotifer, we have observed a mechanism by which such orga
113 lation and the creation of reporter lines in rotifers, we developed a protocol for highly efficient,
114                                         When rotifers were challenged with a fungal pathogen, horizon
115                                  In general, rotifers were more abundant in riverine environments tha
116    Experiments demonstrated that the ancient rotifer withstands slow cooling and freezing (~1 C min(-
117      Similar trends occurred for copepod and rotifer zooplankton.

 
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