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1 bundant birds, fishes, burrowing shrimps and polychaetes.
2 ro-dimer formation in the GKs from these two polychaetes.
3  loss from animal tissues were 20% d(-1) for polychaetes, 10% d(-1) for crabs, and 6% d(-1) for fish
4     We estimate that up to 18,500 ornamental polychaetes (16,980 sabellids and 1,018 serpulids) are s
5                     The Hb from the deep-sea polychaete Alvinella exhibited in addition, peaks at app
6   Dehaloperoxidase (DHP) from the terebellid polychaete Amphitrite ornata is a bifunctional enzyme th
7  dehaloperoxidase (DHP), from the terebellid polychaete Amphitrite ornata is designed to catalyze the
8                               The terebellid polychaete Amphitrite ornata produces no detectable vola
9 (DHP), found in the coelom of the terebellid polychaete Amphitrite ornata, is a dual-function protein
10 gen transport hemoglobin from the terebellid polychaete Amphitrite ornata, is the first globin identi
11 e (DHP), discovered in the marine terebellid polychaete Amphitrite ornata, is the first heme-containi
12 al function protein found in the terrebellid polychaete Amphitrite ornata.
13 (Hb) originally isolated from the terebellid polychaete Amphitrite ornata.
14 rect contribution of two macrofaunal groups, polychaetes and bivalves, to methane and nitrous oxide f
15 ssemblages differed, with significantly less polychaetes and more oligochaetes in treatments exposed
16 ylsiloxane (PDMS), and organisms ranged from polychaetes and oligochaetes to bivalves, aquatic insect
17 solated mineral-free exception (e.g., marine polychaetes and squids), minerals are thought to be indi
18             The Annelida, which includes the polychaetes and the clitellates, has long held the taxon
19 shima sediment, up to 55% in crabs ingesting polychaetes, and about 80% in fish ingesting worms.
20 c organisms, including bacteria, seagrasses, polychaetes, and corals.
21 sufficiently bioavailable to deposit-feeding polychaetes, and macrofauna assimilate Cs from these pol
22            However, unlike the case found in polychaete annelid and soil nematode embryos, there is n
23 g/Wnt1) in larval and juvenile stages of the polychaete annelid Capitella sp. I and en in a second po
24 uring larval and juvenile development in the polychaete annelid Capitella sp. I., a member of the thi
25 x genes in embryos of a lophotrochozoan, the polychaete annelid Chaetopterus sp.
26        In the equally cleaving embryo of the polychaete annelid Hydroides, MAPK activation was not de
27 d along the proximodistal axis of developing polychaete annelid parapodia, onychophoran lobopodia, as
28 u hybridization in larvae of Chaetopterus, a polychaete annelid with a tagmatized axial body plan.
29  interpreted as a primitive mollusc and as a polychaete annelid worm.
30                                              Polychaete annelids and arthropods are both segmented pr
31 erns which suggest that both sea urchins and polychaete annelids use Hox genes in a very similar fash
32 complex, segmented vertebrates, insects, and polychaete annelids with jointed appendages.
33 complex, segmented vertebrates, insects, and polychaete annelids with jointed appendages.
34 od molluscs, brachyuran decapod crustaceans, polychaete annelids, and macroalgae.
35 e arthropods and the nonganglionic brains of polychaete annelids, polyclad planarians, and nemerteans
36                                Free-swimming polychaetes are common in marine habitats and exhibit a
37                                              Polychaetes are frequented in toxicological studies, one
38 esponses in early life history stages of the polychaete Arenicola marina and found both synergistic a
39                Here we describe a new fossil polychaete (bristle worm) from the early Cambrian Cangla
40  provides the first assessment of ornamental polychaetes but more importantly highlights the issues s
41 Part of this rich diversity includes annelid polychaetes but unfortunately, our understanding of such
42 f a segmentation gene homologue in the basal polychaete Capitella capitata using a pan-annelid cross-
43 l life-history traits in the deposit-feeding polychaete Capitella teleta and extrapolate these to pos
44 holine-binding protein (AChBP) in the marine polychaete Capitella teleta, from the annelid phylum.
45             To determine the identity of the polychaete causing these blisters, we obtained Pacific o
46  creatine kinase (CK) from a protostome, the polychaete Chaetopterus variopedatus, were elucidated an
47  gene engrailed (en) in a basal annelid, the polychaete Chaetopterus.
48  groups of benthic invertebrates (amphipods, polychaetes, chironomids, and bivalves).
49  were 45% d(-1), 14% d(-1), and 5% d(-1) for polychaetes, crabs, and fish, respectively.
50 similar to each other than to microbiomes of polychaetes, decapods and fish.
51 s including barnacles, decapods, gastropods, polychaetes, etc.) were more universally present in muss
52                          Echinoderms and the polychaete Eunice norvegica occupy the same trophic guil
53 hey display many characteristics atypical of polychaete eyes, such as ciliary photoreceptors [3,4] th
54 eatures seen in several different Palaeozoic polychaete families.
55          The synergistic effects between the polychaete feeding and the eyestalk ablation in the proc
56 hat without having proper nutrients from the polychaetes, female broodstock might not be ready to dev
57 oodstock must be fed with live feeds such as polychaetes for this practice to be effective.
58 ids from Vancouver Island, and amphipods and polychaetes from Ojo de Liebre Lagoon.
59 r and possessed the largest jaws recorded in polychaetes from the fossil record, with maxillae reachi
60 in and it has been compared with nemerteans, polychaetes, gastropods, conodonts, and the stem arthrop
61                       This demonstrates that polychaete gigantism was already a phenomenon in the Pal
62                      A re-description of the polychaete groups traded using a combination of molecula
63 e provision of live feed supplement (such as polychaetes) has not been emphasized in previous studies
64                                          The polychaete Hox complex is shown not to be expressed duri
65                       Larvae of the serpulid polychaete Hydroides elegans can be induced to settle by
66 he molecular mechanism suggested for another polychaete, Hydroides elegans, highlighting likely molec
67 e annelid Capitella sp. I and en in a second polychaete, Hydroides elegans.
68                   is unique amongst Cambrian polychaetes in possessing the rod-like supports of the p
69  providing evidence of the presence of these polychaetes in the Late Jurassic.
70 ed by dwelling traces of marine bivalves and polychaetes in the upper layers and sea anemones at the
71 ehaloperoxidase activities in other infaunal polychaetes, including halometabolite-producing species.
72                                              Polychaetes indirectly enhance methane efflux through bi
73 ic analyses, belonging to two main lineages: polychaete-infecting (5 species) and oligochaete-infecti
74 ssimilation efficiency of (137)Cs was 16% in polychaetes ingesting Fukushima sediment, up to 55% in c
75                                       In the polychaete jaws, HIS-rich sequences are expanded into a
76 n two noncellular tissues, mussel byssus and polychaete jaws, recent studies suggest that one natural
77  contains small molecules that mimic natural polychaete mating pheromones, evoking the mating phenoty
78        E1 is longer and E2 is shorter in the polychaete MiCK gene than the counterpart sarcomeric and
79                                  We compared polychaete morphology to original descriptions, extracte
80 lopsis oscura and the chlorocruorin from the polychaete Myxicola infundibulum, over the pH range 3.5-
81        Prior work has shown that GK from the polychaete Neanthes (Nereis) diversicolor exits as a het
82 ly with tissue residue in the marine benthic polychaete Neanthes arenaceodentata exposed in the same
83  We have been studying one population of the polychaete Nereis (Hediste) diversicolor exhibiting inhe
84 which is released by swimming females of the polychaete Nereis succinea to activate spawning behavior
85  was significantly accumulated in the marine polychaete Nereis virens (N. virens) in the AgNP-citrate
86            In contrast with vertebrate MiCK, polychaete octamers are very stable indicating that dime
87 g) in Washington State suggest a new spionid polychaete outbreak.
88 s are found at hydrothermal vents, where the polychaete Paralvinella sulfincola lives on vent sulfide
89                                Acid-tolerant polychaetes (Polynoidae) live in this environment, appar
90 mber and provenance of species of ornamental polychaetes (sabellids and serpulids) traded was underta
91  quantity of MeHg in benthic chironomids and polychaetes seems to be driven by MeHg accumulation via
92 fluid dynamics for three species of swimming polychaetes, spanning two orders of magnitude in size.
93 and molecular analyses show that two further polychaete species are shared with vents beyond the Indi
94                    Invasions by shell-boring polychaetes such as Polydora websteri Hartman have resul
95 time of AP pattern formation in leech and in polychaete suggests that the anterior organizing functio
96  worm, Sabellaria alveolata, a reef-building polychaete that supports high biodiversity, we carried o
97  To our knowledge, Dannychaeta is the oldest polychaete that unambiguously belongs to crown annelids,
98 , which inhabits estuary mudflats with other polychaetes that secrete a range of toxic brominated phe
99 Fan worms (Annelida: Sabellidae) are sessile polychaetes that spend their adult lives in tubes and pr
100  low oxygen levels on the feeding ecology of polychaetes, the dominant macrofaunal animals in deep-se
101 tes, and macrofauna assimilate Cs from these polychaetes to account for >90% of their body burden.
102  intermixed with detrital debris composed of polychaete tubes, and sand, gravel, and/or rocks.
103 umbricus terrestris and Tubifex tubifex, the polychaetes Tylorrhynchus heterochaetus, Arenicola marin
104 nd I provide examples for insects, molluscs, polychaetes, vertebrates and flowering plants.
105             Here we describe a new eunicidan polychaete, Websteroprion armstrongi gen.
106                                        These polychaetes were thermotaxic, preferring temperatures of
107                    High copper levels in the polychaete worm Glycera dibranchiata recently were attri
108 ette filter toxicants and microfibres on the polychaete worm Hediste diversicolor (ragworm), a widesp
109                              Inspired by the polychaete worm jaw, we report a novel approach to gener
110 of zinc also occur in the jaws of the marine polychaete worm Nereis sp.
111 cone snail, Conus imperialis Using the model polychaete worm Platynereis dumerilii, we demonstrate th
112  the dominance and distribution of the known polychaete worm species living in a naturally acidic sea
113 on metals zinc and copper in the jaws of two polychaete worm species Nereis and Glycera, respectively
114                          The vent-associated polychaete worm, Alvinella pompejana, is host to a visib
115 e known to trigger larval metamorphosis in a polychaete worm.
116 n vent ecosystems in other oceans, including polychaete worms (Siboglinidae), bathymodiolid mussels,
117                  Whilst the fossil record of polychaete worms extends to the early Cambrian, much dat
118  bioeroding sea urchins and burrowing fauna (polychaete worms, bivalve mollusks) increased from N to
119 ined them for blisters and burrows caused by polychaete worms.
120 ct undamaged cryptic respiring prey, such as polychaete worms.

 
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