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1 s the first genetic map of neurogenesis in a cephalopod.
2 e increment in daily intake of shellfish and cephalopods.
3 ized cells in the skin of squids and related cephalopods.
4 al pupils that are characteristic of coleoid cephalopods.
5 ectin proteins drives dynamic iridescence in cephalopods.
6 dynamic body patterning for communication in cephalopods.
7 nderstanding the peculiar brain evolution in cephalopods.
8  color-changing abilities of animals such as cephalopods.
9  different phyla, including S-crystallins of cephalopods.
10 ns that support learning and memory in other cephalopods.
11  known how moray eels swallow large fish and cephalopods.
12 the presence of a single Hox gene cluster in cephalopods.
13  patterns, is ubiquitous among all unshelled cephalopods.
14 lly feed near the seafloor on small fish and cephalopods [1-3].
15           To investigate long-term trends in cephalopod abundance, we assembled global time-series of
16                                              Cephalopods also have at least two taxon-specific crysta
17 agonitic structures from other aquatic taxa (cephalopods and coral) were also analyzed.
18 vegetables and pulses, fruits, shellfish and cephalopods, and fish, and the weekly mean intake (servi
19                                              Cephalopods are a diverse group of highly derived mollus
20 udies demonstrate that soft-bodied (coleoid) cephalopods are adept at learning and remembering featur
21                             Evolution of the cephalopod body plan from a monoplacophoran-like ancesto
22        To investigate the molecular bases of cephalopod brain and body innovations, we sequenced the
23 e neural controls of these components in the cephalopod brain thus reflects the versatility of the in
24 s relevant to the developmental evolution of cephalopods by using the sepiolid squid Euprymna scolope
25                                              Cephalopods can display dazzling patterns of colours by
26 ontrol of stretchable surfaces; for example, cephalopods can project hierarchical structures from the
27 bundance, we assembled global time-series of cephalopod catch rates (catch per unit of fishing or sam
28 ctions and is perceived by insects, spiders, cephalopods, crustaceans, and some vertebrates.
29 of photoreceptive organs, we established the cephalopod Doryteuthis pealeii as a lophotrochozoan mode
30 ially emerge early and simultaneously during cephalopod embryogenesis but no data exist on the proces
31                                   In nature, cephalopods employ unique dynamic camouflage mechanisms.
32  which these genes have been co-opted during cephalopod evolution provides insight to the nature of t
33 a perception fuelled by increasing trends in cephalopod fisheries catch [4,5].
34 al control of the dynamic body patterning of cephalopods for camouflage and intraspecies communicatio
35                                              Cephalopods, for example, achieve amazing feats of manip
36      Some animals, such as the chameleon and cephalopod, have the remarkable capability to change the
37 signated ALDH1A9) is 55-56% identical to its cephalopod homologues, while it is 67 and 64% identical
38                                              Cephalopods in nature undergo highly dynamic skin colora
39 mpared with only three crustaceans and three cephalopods in Spain.
40     Gonatus onyx is one of the most abundant cephalopods in the Pacific and Atlantic Oceans and is an
41 vation of eumelanin in two > 160 Ma Jurassic cephalopod ink sacs and to confirm its chemical similari
42 s for the design and development of advanced cephalopod-inspired functional materials.
43 anging optical conditions in two mesopelagic cephalopods, Japetella heathi and Onychoteuthis banksii.
44  nautilus brain is the simplest among extant cephalopods, lacking dedicated neural regions that suppo
45           This has fostered the opinion that cephalopods may experience pain, leading some government
46                                              Cephalopod molluscs are the most neurally and behavioral
47                                              Cephalopod molluscs, and in particular Octopus vulgaris,
48 near to mammals - birds - and one quite far -cephalopod molluscs.
49  the light-interacting tissues of a range of cephalopod mollusks, arthropods, and cubozoan cnidarians
50 , played a critical role in the evolution of cephalopod morphological innovations, including their la
51                                  Inspired by cephalopod muscular morphology, we developed synthetic t
52 udy shows that avoidance conditioning in the cephalopod Octopus vulgaris is mediated by long-term pot
53                                      Coleoid cephalopods (octopus, squid and cuttlefish) are active,
54 ted a computer model of the visual system of cephalopods (octopus, squid, and cuttlefish) that have a
55 contrast to mammalian ALDH1 and -2 and other cephalopod Omega-crystallins, which are tetrameric prote
56  acid sequence shares greatest homology with cephalopod opsins.
57 olarities than are typical in seawater or in cephalopods, partially accounting for the bacterium's lo
58      There has been growing speculation that cephalopod populations are proliferating in response to
59  This study presents the first evidence that cephalopod populations have increased globally, indicati
60                                 We show that cephalopod populations have increased over the last six
61                 It is not known, however, if cephalopods possess nociceptors, or whether their somati
62                                         Many cephalopods produce complex body patterns and visual sig
63                               Films from the cephalopod protein reflectin demonstrate multifaceted fu
64 s to Omega-crystallin, a minor crystallin in cephalopods related to aldehyde dehydrogenase (ALDH) cla
65                Unlike vertebrate rhodopsins, cephalopod rhodopsin is arranged in an ordered lattice i
66 chemical similarity to the ink of the modern cephalopod, Sepia officinalis.
67                                              Cephalopods show behavioral parallels to birds and mamma
68                This is also true for pelagic cephalopods, some of which are very abundant in oceanic
69 eater in Egypt, with nine crustacean and two cephalopod species found compared with only three crusta
70 mpared with those in hatchlings of two other cephalopod species.
71                    We identified hundreds of cephalopod-specific genes, many of which showed elevated
72                                    The major cephalopod (squid, octopus, and cuttlefish) crystallins
73 brate rods and cones, visual transduction in cephalopod (squid, octopus, cuttlefish) invertebrates is
74                                              Cephalopods (squid, cuttlefish and octopuses) have a uni
75                  These data indicate that in cephalopod statocysts an inhibitory NO-cGMP and an excit
76                  These data indicate that in cephalopod statocysts, a cGMP and a cAMP signal transduc
77 ffect on the RA of afferent crista fibers in cephalopod statocysts.
78 vity for thin films composed of reflectin, a cephalopod structural protein.
79  times and in many ways in the origin of new cephalopod structures.
80 ysiological data that has been obtained from cephalopod studies and offers a possible solution to the
81                                              Cephalopods such as octopuses have a combination of a st
82                                              Cephalopods, such as cuttlefish, demonstrate remarkable
83                                              Cephalopods, such as octopus and squid, can change their
84  by shells and practically immobile; and the cephalopods, such as the octopus, cuttlefish and squid.
85 ly consistent across a highly diverse set of cephalopod taxa.
86 formation about the location of an injury in cephalopods than it does in mammals.
87             Ammonites are a group of extinct cephalopods that garner tremendous interest over a range
88 ifferent regions of Portugal, being fish and cephalopods the main captures in the Northern ports.
89 tal program are seen in some molluscs (i.e., cephalopods), the findings presented here indicate that
90 aused by a predatory attack, presumably by a cephalopod; these were most likely, the top predators of
91 tion from self-assembled structures found in cephalopods to fabricate tunable biomimetic camouflage c
92 -containing amino acids, are used by certain cephalopods to manage and manipulate incident light in t
93 ined two switchable camouflage strategies in cephalopods: transparency and dark pigmentation.
94 ce pain, leading some governments to include cephalopods under animal welfare laws.
95 eaches an exceptional level of complexity in cephalopods, where the typical molluscan ganglia become
96 placophorans to the complex body plan of the cephalopods with highly developed sensory organs, a comp
97 common in behaviorally sophisticated coleoid cephalopods, with tens of thousands of evolutionarily co

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