ライフサイエンスコーパス: cod

1 [(cod)Ir(I)(chelate)] precursors bearing the same chelate

2 m a 93-year survey of juvenile (age 0 and 1) cod sampled along >200 km of the Norwegian Skagerrak coa

3 When 3 was allowed to react with Ni(cod)(2) (cod = 1,5-cyclooctadiene), the unique {[Si(II)(Xant)Si(I

4 zed by the combination of [Ir(cod)(OMe)](2) (cod=1,5-cyclooctadiene) and a phenanthroline ligand or a

5 n with the homochelate analogues [Rh( L 2a )(cod)]BF 4 and [Rh(dppe)(cod)]BF 4.

6 complexes [Si(II)(Xant)Si(II)]Ni(eta(2)-1,3-cod) and [Si(II)(Xant)Si(II)]Ni(PMe3)2 were synthesized

7 [Si(II)(Xant)Si(II)]Ni(eta(2)-1,3-cod) is a strikingly efficient precatalyst for homogeneo

8 Exposing [Si(II)(Xant)Si(II)]Ni(eta(2)-1,3-cod) to 1 bar H2 at room temperature quantitatively gene

9 ing a chiral bicyclic NHC ligand, [RhCl(3az)(cod)] 4az, was synthesized and fully characterized by X-

10 ing/dehydrogenation of 7 with [Rh(mu-Cl)(1,5-cod)](2) (2) as the catalyst at 20 degrees C, a reaction

11 with antioxidative activity obtained from a cod protein hydrolysate.

12 pagate to higher trophic levels (capelin and cod).

13 undwater, wastewater, herring, cormorant and cod tissues, pig kidney, lobster, tobacco, scallion, cel

14 ated with willow (Salix sp) bark extract and cod liver oil are compared in this study using both MRI

15 and TBA-reactive substances in herring- and cod-derived products increased rapidly during ice storag

16 of plastic-associated PCBs for lugworms and cod ranged from 14 to 42% and 45-83% respectively.

17 se mackerel, haddock, atlantic mackerel, and cod.

18 flower seed oil, rapeseed oil, olive oil and cod liver oil.

19 n-enriched products from herring, salmon and cod backbones was investigated.

20 declines of its predators such as seals and cod, resulted in a strong increase for this stock under

21 ze glycoprotein fractions 1-5 from Antarctic cod have been assigned, and the dynamics have been measu

22 Weddell seals stalked large Antarctic cod and the smaller subice fish Pagothenia borchgrevinki

23 splayed a positive correlation with the anti-cod PAV polyclonal antibody, but no correlation with the

24 In 2012, Arctic cod (Boreogadus saida) were collected from offshore regi

25 In the 1930s, northeast Arctic cod (Gadus morhua), currently the world's largest cod st

26 requent skipped spawning in Northeast Arctic cod (NEAC) in a massive field and laboratory effort from

27 lop a bioeconomic model for Northeast Arctic cod to compare the economic yield in a model in which li

28 and length at maturation in northeast Arctic cod, while mimicking the stock's historical harvesting r

29 AFGP genes from notothenioids and the Arctic cod show that their AFGPs are both encoded by a family o

30 ginate from a pancreatic trypsinogen, Arctic cod AFGP genes share no sequence identity with the tryps

31 red Hg isotope ratios in zooplankton, Arctic cod, total gaseous Hg, sediment, seawater, and snowpack

32 e large, generalist, motile species, such as cod and haddock.

33 ipids in different complex matrixes, such as cod liver oil.

34 tems are relying on similar features such as cod on usage and as a result the predictions are often c

35 d or short footprints (56 bp for the site at cod) with less DNA bending.

36 Atlantic cod (Gadus morhua) and the Tvedestrand fjord on the Norw

37 Atlantic cod (Gadus morhua) has recently emerged as a model organ

38 Atlantic cod (Gadus morhua) possesses two Ahr proteins, Ahr1a and

39 X-cell xenomas of blue whiting and Atlantic cod and assembled 63 X-cell protein-coding genes for a e

40 er species like walleye pollock and Atlantic cod will be less impacted but may struggle at high latit

41 raced back to the North East Arctic Atlantic cod population that has supported the Lofoten fisheries

42 subsequent medieval (1066-1280 CE) Atlantic cod (Gadus morhua) specimens from excavation sites in Ge

43 of a population complex of coastal Atlantic cod (Gadus morhua).

44 Farmed Atlantic cod were subjected to a combination of stressors in a ho

45 tment dynamics in the highly fecund Atlantic cod.

46 has been studied in juvenile female Atlantic cod ( Gadus morhua).

47 and edible crab); and teleost fish (Atlantic cod, European place, and Lemon sole).

48 and ecologically important fishes, Atlantic cod (Gadus morhua) and haddock (Melanogrammus aeglefinus

49 For Atlantic cod, an historically dominant piscivore in the region, w

50 kagerrak will become ill-suited for Atlantic cod.

51 ivo precision-cut liver slices from Atlantic cod (Gadus morhua) to investigate whether BPA and 11 BPA

52 In this study, tropomyosin from Atlantic cod fillets (Gadus morhua, C(TM)) was purified using a t

53 killifish (Fundulus heteroclitus), Atlantic cod, and three-spined stickleback.

54 to show that MeHg concentrations in Atlantic cod (Gadus morhua) increased by up to 23% between the 19

55 ins three extensive "supergenes" in Atlantic cod, linking these genes to species persistence and ecol

56 in many teleost species, including Atlantic cod (Gadus morhua) and three-spined stickleback (Gastero

57 ent and management of Gulf of Maine Atlantic cod caused overfishing.

58 phalus (Pacific cod) and G. morhua (Atlantic cod).

59 spawning stock biomass of 22 North Atlantic cod (Gadus morhua) stocks revealed that both the tempora

60 Here, we track 80 years of Atlantic cod (Gadus morhua) population dynamics in West Greenland

61 mpare whole-genome sequence data of Atlantic cod (Gadus morhua) that were collected before (early 20t

62 D) assays for the identification of Atlantic cod (Gadus morhua), Pacific cod (Gadus macrocephalus), A

63 stinguishing fillets and patties of Atlantic cod (n=80) from those of haddock (n=90), in comparison w

64 onstruct the population dynamics of Atlantic cod, one of the world's most harvested fish species, fro

65 tion limits and the central role of Atlantic cod, which is the main target species but cannot be pers

66 increased mortality in the region's Atlantic cod (Gadus morhua) stock.

67 and salt distribution in dry salted Atlantic cod (Gadus morhua) fillets was studied with proton and s

68 We also screened Atlantic cod populations for xenomas and residual pathologies and

69 e authentication of gadoid species: Atlantic cod (Gadus morhua), Pacific cod (Gadus macrocephalus), A

70 movement behavior of free-swimming Atlantic cod (Gadus morhua).

71 The Atlantic cod (Gadus morhua L.) has been overexploited in the Nort

72 The Atlantic cod (Gadus morhua) has historically been highly abundant

73 t functional specializations of the Atlantic cod Ahr's.

74 ed to assess the sensitivity of the Atlantic cod Ahrs to 31 polycyclic aromatic compounds (PACs), inc

75 le only BPC2 and BPAF activated the Atlantic cod androgen receptor alpha (gmAra), several bisphenols

76 ogenic properties by activating the Atlantic cod estrogen receptor alpha (gmEra).

77 ealed two Ahr-encoding genes in the Atlantic cod genome, gmahr1a and gmahr2a.

78 e study, we provide examples of the Atlantic cod genome, whose sequencing and assembly were hindered

79 typical pause-travel predator (the Atlantic cod larva), does predict the existence of an optimal rat

80 locus among five populations of the Atlantic cod, Gadus morhua.

81 Freitas et al. () tracked Atlantic cod within a Norwegian fjord using electronic acoustic t

82 imilar at the amino acid level to the Baltic cod ADH8 (previously named ADH1), the human ADH1B2, the

83 imilar at the amino acid level to the Baltic cod ADH8, the human ADH1B2, the mouse ADH1, and the rat

84 Using Baltic cod otolith chemical proxies of hypoxia, salinity, and f

85 to the Lotidae family, while among battered cod chunks labelled as bocconcini di baccala, the post-s

86 cod fillets shown as baccala and on battered cod chunks labelled as bocconcini di baccala.

87 with (bpy)Ni(cod) (2; bpy = 2,2'-bipyridine; cod = 1,5-cyclooctadiene) or (bpy)NiEt(2) (3) results in

88 80 (see scheme, Boc = tert-butyloxycarbonyl, cod = 1,5-cyclooctadiene, TFA = trifluoroacetic acid).

89 Four fish species were examined: pike, carp, cod, and herring.

90 l and temporal dynamics of Skagerrak coastal cod.

91 chlorinated n-alkanes (PCAs) from commercial cod liver oil samples.

92 The complex [(cod)Ru(3-methallyl)2] reacts with benzophenone imine or

93 The SEAD comprised cod, other fresh fish, red meat and pork products, dairy

94 ic analysis of a mutant that lacks crystals, cod 5, did not reveal any difference in plant growth and

95 induction of cyp1a in exposed precision-cut cod liver slices confirmed the activation of the Ahr sig

96 ant association for walleye pollock, and (d) cod and pollock will likely have reduced recruitment giv

97 e for tissue from calcium oxalate-defective (cod) mutant lines cod5 and cod6 in choice test compariso

98 (Pollachius virens,n = 40) and the demersal cod (Gadus morhua,n = 40), along a south-north gradient

99 A pilot study evaluated three different cod loin samples: one of high-quality, one of medium-qua

100 nalogues [Rh( L 2a )(cod)]BF 4 and [Rh(dppe)(cod)]BF 4.

101 s on a relatively inexpensive Ni(cod)2/dppf (cod = 1,5-cyclooctadiene; dppf = 1,1'-bis(diphenylphosph

102 rformed to six study foods (cow's milk, egg, cod, wheat, sesame, and peanut).

103 ed significantly better on fresh Hb-enriched cod mince than Brown's and Drabkin's methods; recovery w

104 Furthermore, during the exposure, cod decreased their activity, with time spent being "loc

105 ve fillet gaping score and texture of farmed cod (Gadus morhua L.) harvested during summer.

106 as a tool to improve flesh texture of farmed cod with a low gaping score, but with compromise of incr

107 S (BPS) was investigated in water and fish (cod, basa) fillets.

108 otal volatiles of high n-3 oils (flax, fish, cod liver) were 120-170 mg/kg while low n-3 vegetable oi

109 pothesis are borne out in oceanic fisheries (cod and pollock) that have experienced substantial incre

110 For cod and tuna, almost 70% of patients demonstrated the st

111 The Gulf of Riga can be considered for cod a "true sink" habitat, where in the absence of immig

112 n hydrolysates (FPHs) as cryoprotectants for cod fish mince subjected to freeze-thaw abuse.

113 opulation sizes shows continued declines for cod in the North Sea-Skagerrak-Kattegat system through t

114 he establishment of a recovery programme for cod (Gadus morhua) will alter the amount of fish discard

115 sum, the decline in the ecological role for cod that began with overfishing in this ecosystem will l

116 culated and found to rarely exceed unity for cod (Gadus morhua), a fish species with a TL of approxim

117 specific real-time PCR probes were used for cod (Gadus morhua) and haddock (Melanogrammus aeglefinus

118 ft processing was studied using Hb-fortified cod mince.

119 (AsHC) mentioned for the first time in fresh cod liver.

120 total concentration of arsenic in the fresh cod liver was analysed by ICP-MS to be 1.53+/-0.02 mg As

121 nteractions, we purified a glycopeptide from cod (designated TFD100) that binds gal3 with picomolar a

122 nsaturated fatty acids (PUFAs) prepared from cod liver oil.

123 al xenomas had previously been reported from cod in the Atlantic [2] and Pacific Oceans [3].

124 Antifreeze glycoproteins from the Greenland cod Boreogadus saida were dimethylated at the N-terminus

125 lyfluoroalkyl substances (PFASs) in herring, cod, eelpout, and guillemot covering four decades and mo

126 Protease P "Amano" 6 was used to hydrolyze cod protein in the presence and absence of pro-oxidants

127 Enrichment of omega-3 fatty acids in cod liver oil via alternate operation of solvent winteri

128 tests run by FAPAS for vitamin A analysis in cod liver oil were observed to give rise to multi-modal

129 However, in highly oxidised samples and in cod protein isolates made with acid pH-shift processing,

130 ankton have resulted in long-term changes in cod recruitment in the North Sea (bottom-up control).

131 nd as main water-soluble arsenic compound in cod liver followed by higher molecular mass arsenic-cont

132 cern has been expressed about the decline in cod biomass and recruitment.

133 The highest frequency (>33%) was found in cod from the English Channel.

134 s from south to north, especially for OCs in cod: i.e. the relative importance of low-chlorinated pol

135 -nonenal (HNE), and 4-oxo-2-nonenal (ONE) in cod liver-, anchovy-, krill-, and algae oil during in vi

136 es of compensatory mechanisms or pathways in cod and stickleback in the absence of pxr.

137 ime, that of vitamin A, naturally present in cod liver oil.

138 ent response to hypoxanthine which increased cod expression in K. pneumoniae but decreased it in E. c

139 Phenanthroline ligands and [Ir(cod)(OMe)](2) form complexes that catalyze the silylatio

140 4,4'-di-tert-butylbipyridine (dtbpy) and [Ir(cod)Cl]2 has typically been governed by steric effects.

141 ) was isolated from the reaction between [Ir(cod)Cl]2, rac-BINAP, and benzyl alcohol.

142 functionalization reactions catalyzed by [Ir(cod)Cl](2) (4 mol %) to provide 2-substituted indoles (u

143 Reported herein is the use of catalytic [{Ir(cod)Cl}2 ] to facilitate hydrogen-borrowing reactions of

144 isphosphine molecular precatalyst, [(dmpe)Ir(cod)CH(3)], onto amorphous silica dramatically enhances

145 anePhos complexes generated in situ from [Ir(cod)Cl](2) and (R)-PhanePhos catalyze 2-propanol-mediate

146 iridium catalyst generated in situ from [Ir(cod)Cl](2), 4-cyano-3-nitrobenzoic acid and the chiral p

147 l iridium precatalyst (R)-I derived from [Ir(cod)Cl](2), 4-cyano-3-nitrobenzoic acid, (R)-SEGPHOS, an

148 lated iridium complex (S)-I derived from [Ir(cod)Cl](2), 4-cyano-3-nitrobenzoic acid, allyl acetate,

149 iral iridium complex formed in situ from [Ir(cod)Cl]2 and (R)-H8-BINAP is found to catalyze the direc

150 benzoate complex (R)-Ir-VIb derived from [Ir(cod)Cl]2, allyl acetate, 4-cyano-3-nitro-benzoic acid, a

151 iridium catalyst generated in situ from [Ir(cod)Cl]2, chiral phosphine ligand (R)-BINAP or (R)-Cl,Me

152 ity when catalyzed by the combination of [Ir(cod)(OMe)](2) (cod=1,5-cyclooctadiene) and a phenanthrol

153 The combination of [Ir(cod)(OMe)](2) and 2,9-Me(2)-phenanthroline (2,9-Me(2)-ph

154 roarenes catalyzed by the combination of [Ir(cod)(OMe)]2 and 2,4,7-trimethylphenanthroline occurs wit

155 ary benzylic alcohols in the presence of [Ir(cod){(R)-segphos}]OTf (cod = 1,5-cyclooctadiene, segphos

156 ity of the most common iridium precursor [Ir(cod)OMe](2), and, particularly on small scale, the chall

157 An [IrCl(cod)(NHC)] (cod = 1,5-cyclooctadiene, NHC = N-heterocycl

158 ce of an iridium catalyst derived from [IrCl(cod)]2 and (-)-TMBTP delivers identical products of C-al

159 ce of an iridium catalyst derived from [IrCl(cod)]2 and (R)-BINAP delivers products of C-allylation 2

160 ies of more than 100,000 individual juvenile cod lengths from surveys that began in 1919 along the No

161 mer springs have resulted in larger juvenile cod, with less variation in lengths within a cohort, pos

162 cts of spring and summer warming on juvenile cod lengths.

163 Gadus morhua), currently the world's largest cod stock, experienced a shift from a traditional spawni

164 hua), which is currently the world's largest cod stock, over six decades (1949-2009), and identify a

165 ch variability in temperature affects larval cod survival and conclude that rising temperature since

166 Survival of larval cod is shown to depend on three key biological parameter

167 Mechanized harvesting of bottom fishes like cod set off a series of trophic cascades that eliminated

168 iconic groundfish fishery for Gulf of Maine cod has endured several dramatic reductions in annual ca

169 waters reduce growth rates in Gulf of Maine cod.

170 e, squid muscle, crab claw meat, whale meat, cod muscle, Greenland halibut muscle and dogfish liver (

171 bits across time, and Ba/Sr ratios in modern cod otoliths indicate increasing use of a more saline ha

172 We call these mutants cod mutants for the control of HMG-CoA reductase degrada

173 The Newfoundland cod fishery is expected to rebuild to an ecologically st

174 An [IrCl(cod)(NHC)] (cod = 1,5-cyclooctadiene, NHC = N-heterocyclic carbene)

175 Ni(cod)(2) was used as a catalyst without any ligands or ba

176 nch selectivity, even in the absence of a Ni(cod)(2) cocatalyst.

177 Me; 1c, R = n-Bu; 1d, R = i-Pr) with (bpy)Ni(cod) (2; bpy = 2,2'-bipyridine; cod = 1,5-cyclooctadiene

178 It relies on a relatively inexpensive Ni(cod)2/dppf (cod = 1,5-cyclooctadiene; dppf = 1,1'-bis(di

179 atalyst with free bidentate phosphines is Ni(cod)(2), which accounts for ~50% of the reports surveyed

180 hed with pinacolborane in the presence of Ni(cod)(2) and PCy(3).

181 ess of this reaction relies on the use of Ni(cod)2 as the catalyst and NaOMe as a uniquely effective

182 first-row catalytic system comprised of [Ni(cod)2 ] and dppf was used in this process, thus constitu

183 t particles that form from a solution of [Ni(cod)2].

184 ender the catalyst resting state as [(P-P)Ni(cod)].

185 a catalyst system of a Ni(0) precursor ([Ni(cod)2]), N-heterocyclic carbene (NHC) ligand (IPr), and

186 ion, as the use of the very air-sensitive Ni(cod)2 is avoided.

187 c investigations reveal that the tailored Ni(cod)(BQ(iPr)) precatalyst modulates the electronic prope

188 osed the modified catalytic cycle for the Ni(cod)(dcype)-catalyzed C-H/C-O coupling of benzoxazole an

189 biological applications, are prepared via Ni(cod)(2)/IPr-catalyzed cross-couplings between 4-chloro-1

190 When 3 was allowed to react with Ni(cod)(2) (cod = 1,5-cyclooctadiene), the unique {[Si(II)(

191 he usage and efficacy of each ligand with Ni(cod)(2) and other nickel sources.

192 The HSn(9)(3-) cluster reacts with Ni(cod)(2) to give the Ni@HSn(9)(3-) ion containing a hydri

193 Analysis of cod otoliths recovered during archaeological excavations

194 ing most susceptible to oxidation in case of cod.

195 They approached to within centimeters of cod without startling the fish.

196 was demonstrated via the characterization of cod liver oil and other vegetable oils.

197 Collapses of cod stocks have been observed on both sides of the Atlan

198 0.2 uM HNE) were detected after digestion of cod liver oil, while the lowest levels were detected in

199 ance and wide spatiotemporal distribution of cod eggs.

200 r (bpy)NiEt(2) (3) results in elimination of cod or butane from 2 and 3, respectively, and oxidative

201 The extent of cod liver oil hydrolysis and oxidation during in vitro g

202 of arsenic species in methanolic extracts of cod liver.

203 uctures of the Ca-bound and Ca-free forms of cod parvalbumin.

204 pid oxidation during enzymatic hydrolysis of cod proteins was investigated.

205 pod Calanus finmarchicus, a key food item of cod, and led to significantly lower projected abundances

206 led that the current distribution pattern of cod - mostly in the deeper, northern- and north-easternm

207 c Sea hypoxia and Mn/Ca ratios in regions of cod (Gadus morhua) otoliths corresponding to year 1 of l

208 Historically, important stocks of cod and whiting showed declining trends caused by high f

209 A complex of commercial [Ir(OMe)(cod)](2) and 4,4-di-tert-butyl-2,2-bipyridine (dtbpy) ca

210 med IgE-mediated fish allergy, with focus on cod, tuna and salmon extracts.

211 analyses of a spatially resolved data set on cod eggs covering a period (1959-1993) with large change

212 ailure to recognize the impact of warming on cod contributed to overfishing.

213 estimated the effects of climate warming on cod lengths and length variability using a unique 91-y t

214 n the presence of [Ir(cod){(R)-segphos}]OTf (cod = 1,5-cyclooctadiene, segphos = 5,5'-bis(diphenylpho

215 Neolithic (4500 B.P.) cod otoliths (n = 12) had low levels of Mn/Ca ratios, co

216 Gulf of Alaska Pacific cod (Gadus macrocephalus) larval, juvenile, and adult ab

217 d-of-century (2075-2100) pollock and Pacific cod fisheries collapse in >70% and >35% of all simulatio

218 inability) for two exploited fishes (Pacific cod Gadus macrocephalus and walleye pollock G. chalcogra

219 rs are statistically significant for Pacific cod and walleye pollock recruitment, (c) separately anal

220 We examined the response of larval Pacific cod (Gadus macrocephalus) to MHWs in the Gulf of Alaska

221 d exclusively from G. macrocephalus (Pacific cod) and G. morhua (Atlantic cod).

222 tion of Atlantic cod (Gadus morhua), Pacific cod (Gadus macrocephalus), Alaska pollock (Gadus chalcog

223 pecies: Atlantic cod (Gadus morhua), Pacific cod (Gadus macrocephalus), Alaska pollock (Theragra chal

224 Partial cod decoordination or chloride loss is thus required for

225 counterions ([Rh(cod)2X]; X = OTf, BF4, PF6; cod = 1,5-cyclooctadiene).

226 ined more TGs than did predatory ones (pike, cod).

227 l during summer, demonstrated here for polar cod.

228 Embryos and larvae of polar cod (Boreogadus saida), a key Arctic forage fish species

229 pelin and the practical extirpation of polar cod from the system, the two most abundant species in th

230 periods of warmer waters, will reduce polar cod survival in the fall and restrict habitats in these

231 hat transitory spillover of the top-predator cod from its main distribution area produces cascading e

232 phosphino)ethynyl)benzene (dppeb, 1) with Pt(cod)Cl2 followed by treatment with N2H4 yields the reduc

233 octadiene derivative (1,2,4-C(5)Ph(3)H(2))Rh(cod) (2) were developed.

234 enation catalysis carried out with M and [Rh(cod) 2]BF 4 is controlled by the dominant and most effic

235 plexes [Rh(cod)(PMePh 2) 2]BF 4 ( 6) and [Rh(cod)( L 1a ) 2]BF 4 ( 7) in the ratio 2:1:1.

236 )] ( 1a, b), [PtCl 2( L A,B )] ( 2a, b), [Rh(cod)( L A,B )]BF 4 ( 3a, b) and [Rh( L A,B ) 2]BF 4 ( 4a

237 2]BF 4 to give the heteroligand complex [Rh(cod)(PMePh 2)( L 1a )]BF 4 ( 5) and homoligand complexes

238 The derived rhodium complex, [Rh(cod)(2)]BF(4), serves as an effective catalyst for asymm

239 1a )]BF 4 ( 5) and homoligand complexes [Rh(cod)(PMePh 2) 2]BF 4 ( 6) and [Rh(cod)( L 1a ) 2]BF 4 (

240 containing noncoordinating counterions ([Rh(cod)2X]; X = OTf, BF4, PF6; cod = 1,5-cyclooctadiene).

241 with loss of CO2 has been calculated for Rh(cod)Cl.

242 ion or chloride loss is thus required for Rh(cod)Cl.

243 By immobilization of 6 mol % [Rh(cod)Cl]2 within a hydrophobic silica sol-gel matrix we w

244 The reaction of M with 0.5 equiv of [Rh(cod) 2]BF 4 gives exclusively the heteroligand complex c

245 '-bi-2-naphthol), reacts with 1 equiv of [Rh(cod) 2]BF 4 to give the heteroligand complex [Rh(cod)(PM

246 ally aqueous media, a catalyst system of [Rh(cod)(OH)](2) and DPPBenzene ligand effectively promotes

247 nt enantioselectivity in the presence of [Rh(cod)Cl]2 and a chiral bisphosphine ligand.

248 ) cycloaddition in benzaldehyde by using [Rh(cod)Cl](2) as the catalyst in the presence of rac-BINAP.

249 t, were investigated in combination with [Rh(cod)2]BArF (1 mol %) in the asymmetric hydrogenation of

250 at low temperature, in the presence of [RhCl(cod)]2 and [(Me2S)AuCl] lead to air-stable rhodium and g

251 y of a series of X-ray structures of rhodium(cod)chloride/phosphoramidite complexes, we have formulat

252 5; in 1), (Ga(2)Bi(16))(4-) (in 2), and [{Ru(cod)}(4)Bi(18)](4-) (in 3).

253 In the presence of [Ru(cod)(H(2)CC(Me)CH(2))(2)], yet another reaction pathway

254 , which are Bi-Bi linked dimers of two "[{Ru(cod)}(2)Bi(9)](2-)" subunits.

255 e reaction of ene-cyclopropenes with Cp*RuCl(cod) leads to alkenyl bicyclo[3.1.0]hexanes, bicyclo[4.1

256 eat and fish samples (chicken, pork, salmon, cod) over several days was also demonstrated.

257 e sequences revealed that 55/65 dried salted cod fillet samples were detected as belonging to the fam

258 y, its concordance with the labels on salted cod fillets shown as baccala and on battered cod chunks

259 ed two models: one which assumes all sampled cod belong to one larger population, and a second which

260 e of social dynamics in the 1980s Baltic Sea cod boom and collapse.

261 nd size in the spawning stock of Barents Sea cod (Gadus morhua) is positively associated with high ab

262 The Barents Sea cod (Gadus morhua) stock has recently increased markedly

263 the multivariate development of Barents Sea cod (Gadus morhua), which is currently the world's large

264 ationship between vital rates of Barents Sea cod stock productivity (recruitment, growth, and mortali

265 of the suitable feeding area for Barents Sea cod, likely offering a release from density-dependent ef

266 For North Sea cod, we show for the first time and in great spatial det

267 cies: causing severe declines in grey seals, cod, herring and haddock, while eurythermal species were

268 At varying population size, cod expand/contract their distribution range and invade/

269 f three commercially important fish species: cod, herring, and sprat.

270 .5% and 35.4 +/- 1.2% in incurred and spiked cod, respectively; and the degradation percentage of BPS

271 We found that cod did not leave the detection area more than expected

272 We propose that cod exhibiting enhanced Mn/Ca ratios were exposed to dis

273 We propose that cod liver oil, a commonly used food supplement in Norway

274 celandic fish processing sites revealed that cod in the 10th to 12th centuries were 25% larger and up

275 enetic populations, and eventually drove the cod fishery to a collapse in the early 1970s.

276 ted both to the temporary persistence of the cod boom and to its subsequent collapse.

277 e source areas of the central Baltic Sea the cod population goes extinct due to the absence of suitab

278 pase inhibitor (orlistat) and tocopherols to cod liver oil, lipolysis and oxidation was also studied.

279 ently consumed by humans (for example, tuna, cod and swordfish) have not been considered when setting

280 in-water (O/W) emulsion composed of 5% (w/v) cod liver oil (CLO) and metmyoglobin (metMb) in 50mM pho

281 y showed that when surface waters were warm, cod occupied the cold deep non-vegetated habitats.

282 Different variants of a washed cod model system, containing different combinations of h

283 lipid oxidation were investigated in washed cod muscle (WCM).

284 ) and their pro-oxidant activities in washed cod muscle mince (WCM) were studied using simple pH-shif

285 onic HbI with insoluble components of washed cod mince under different pH and salt conditions.

286 nsistent effect on lipid oxidation of washed cod mince.

287 Higher binding of HbI to washed cod mince occurred compared to HbIV, yet HbIV better pro

288 al and oxidative stability of 5% (by weight) cod liver oil-in-water emulsions fortified with common c

289 active peaks at dusk and dawn, periods when cod are known to actively feed.(11)(,)(12) The combined

290 t, hard-boiled hen's egg, sesame, whitefish (cod), and wheat; the standard introduction group followe

291 the simultaneous intake of antioxidants with cod liver oil should be considered, in order to increase

292 onsumption, respectively, of test meals with cod or lean beef.

293 in a way that reduces the survival of young cod.