ライフサイエンスコーパス: crustacean

1 h a host, in this case a species of ostracod crustacean.

2 ingredient than from those containing other crustaceans.

3 sIgE titres in response to both molluscs and crustaceans.

4 ra) are the most successful group of decapod crustaceans.

5 hts into defining characteristics of decapod crustaceans.

6 going process in the brains of adult decapod crustaceans.

7 ers) is not a proxy for demasculinization in crustaceans.

8 neric avoidance response to large, predatory crustaceans.

9 atopods, a group of highly aggressive marine crustaceans.

10 pendent regulatory mechanisms in insects and crustaceans.

11 the olfactory deutocerebrum of adult decapod crustaceans.

12 uch as male sex determination in branchiopod crustaceans.

13 eject the possible groupings of paraphyletic crustaceans.

14 ression decreased to marginal levels in some crustaceans.

15 ther mechanosensory functions in insects and crustaceans.

16 appears to be conserved between insects and crustaceans.

17 snails, and isopod and barnacle parasites of crustaceans.

18 lobula plate was also found in malacostracan crustaceans.

19 een reported for sampling neuropeptides from crustaceans.

20 s aspects of reproduction and development in crustaceans.

21 ross-reactivity testing on a wide variety of crustaceans.

22 is the chitinous exoskeletons of microscopic crustaceans.

23 iological processes pertaining to molting in crustaceans.

24 Thirty-one patients with anaphylaxis to crustaceans (14 with mollusc allergy and 17 with mollusc

25 in the ventral neuroectoderm of insects and crustaceans accompanied by changes in the morphogenetic

26 assay was developed for detection of crab, a crustacean allergen, in food products.

27 dy investigated the sensitization pattern of crustacean-allergic patients according to tolerance to m

28 protostome invertebrates (mollusk bivalves, crustacean amphipods, branchiopods, copepods and isopods

29 Among patients with crustacean anaphylaxis, patients with mollusc allergy an

30 ction of shellfish-derived tropomyosin in 11 crustacean and 7 mollusc species, and to study the impac

31 e microarray for Daphnia magna, a freshwater crustacean and common indicator species for toxicity, to

32 uroblast selection have been modified during crustacean and insect evolution and if the segregation o

33 LOX6 were more attractive to a detritivorous crustacean and more sensitive to drought, indicating tha

34 ies analyzed was greater in Egypt, with nine crustacean and two cephalopod species found compared wit

35 ces of five ocean-produced demersal fish and crustaceans and 2.5-fold increase of summer chlorophyll-

36 isms, including salamanders, frogs, insects, crustaceans and arachnids.

37 ts the growing number of studies in insects, crustaceans and chelicerates, and is important for the c

38 Malacostracan crustaceans and dicondylic insects possess large second-

39 ging from bacteria to algae, yeasts, plants, crustaceans and fish such as salmon.

40 Astaxanthin (ATX) is a dietary carotenoid of crustaceans and fish that contributes to their coloratio

41 +)-K(+)-ATPase in white skeletal muscle from crustaceans and fishes.

42 or development and survival of salmonids and crustaceans and has been shown to reduce cardiac ischemi

43 opoda, particularly among Tetraconata (i.e., crustaceans and hexapods), and indicate that copepods oc

44 Crustaceans and insects share many similarities of brain

45 birds, mammals, reptiles, amphibians, fish, crustaceans and insects, are known to use the Earth's ma

46 lies and more complete retention within some crustaceans and insects.

47 group that branches basally from myriapods, crustaceans and insects.

48 s was present in the last common ancestor of crustaceans and insects.

49 activity, making specific differentiation of crustaceans and molluscs for food labelling very difficu

50 ives: to develop a global database for fish, crustaceans and molluscs with raw, cooked and processed

51 e developed to differentiate tropomyosins in crustaceans and molluscs.

52 s) that demonstrate recurring consumption of crustaceans and rotted wood by large Late Cretaceous din

53 smaller individuals feeding mainly on small crustaceans and teleost fish, whereas the diet of larger

54 Sunfish fed mainly on crustaceans and teleosts, with cnidarians comprising onl

55 The Y-organ in the cephalothorax of crustaceans and the integument of ticks are sources of s

56 pomyosin is known to be the main allergen in crustaceans and the objective of this study was to inves

57 lopod species found compared with only three crustaceans and three cephalopods in Spain.

58 th functional similarities to certain modern crustaceans and trace these structures through the early

59 inciples in a variety of systems (mammalian, crustacean, and mollusk) to demonstrate the unifying the

60 The conservation of Knickkopf across insect, crustacean, and nematode taxa suggests that its critical

61 ough in several other insect species and one crustacean, and several readthrough candidates in nemato

62 ity of insect species as well as some mites, crustaceans, and filarial nematodes.

63 nters on the question as to whether insects, crustaceans, and myriapods (Mandibulata) share a common

64 hich is used as an energy buffer in insects, crustaceans, and some unicellular organisms.

65 perceived by insects, spiders, cephalopods, crustaceans, and some vertebrates.

66 igh specificity for crab over other types of crustaceans, and yielded much higher signals from commer

67 tantly related animal lineages from insects, crustaceans, annelid worms, and fishes, we find more spe

68 Stomatopod crustaceans appear to have gone one step further in this

69 expression have played a role in generating crustacean appendage diversity and lend general insights

70 expression have generated various aspects of crustacean appendage diversity.

71 within the exocuticle of an impact-resistant crustacean appendage.

72 Here we describe diverse crustacean appendages of Middle and Late Cambrian age fr

73 Crustaceans are evident in the Cambrian fossil record, b

74 Copepod crustaceans are extremely abundant but, because of their

75 of chelicerates and myriapods, while data on crustaceans are fragmentary.

76 sampling neuropeptides in vivo, and decapod crustaceans are important model organisms for studying h

77 Crustaceans are key components of marine ecosystems whic

78 Branchiopod crustaceans are represented by fairy, tadpole, and clam

79 Ostracod crustaceans are the most abundant fossil arthropods and

80 Crustaceans are widely distributed and inhabit very diff

81 p to the Hexapoda, a result confirming that 'crustaceans' are not monophyletic.

82 Simple model systems, such as crustaceans, are often more amenable than vertebrates fo

83 nsects and the hemiellipsoid bodies (HBs) of crustaceans] are homologous structures.

84 iverse group of organisms, are nested within crustaceans, arguably the most abundant group of marine

85 ers of feminization should not be applied to crustaceans, as orthologous genes are not induced in fem

86 We chose the isopod crustacean, Asellus aquaticus, and generated a genome-wi

87 s in mammalian brains, adult neurogenesis in crustacean brains is fueled by neural stem cells that ar

88 xpansions of large-bodied, particle-handling crustaceans by at least one hundred million years, empha

89 ing species (epifaunal echinoderms, infaunal crustaceans) by two to four-fold in areas fished twice a

90 ana, Lucina pectinata, Callinectes sapidus), crustacean (C. sapidus) and fish (Bagre marinus and Diap

91 A small transparent crustacean called Parhyale hawaiensis has become a power

92 e showing hexapods closely related to simple crustaceans called remipedes.

93 Motor neurons of the crustacean cardiac ganglion generate virtually identical

94 channel proteins within motor neurons in the crustacean cardiac ganglion recently revealed correlatio

95 developed a nominal biophysical model of the crustacean cardiac ganglion using biological data.

96 Previous findings suggest that crustacean cardioactive peptide (CCAP) activates the ecd

97 otic defect is circuit-specific by examining crustacean cardioactive peptide (CCAP) and bursicon circ

98 in ecdysis, including Eclosion hormone (EH), Crustacean cardioactive peptide (CCAP) and Bursicon.

99 Crustacean cardioactive peptide (CCAP) and related pepti

100 examine the integrated action of the hormone crustacean cardioactive peptide (CCAP) and the gastropyl

101 subset of Drosophila neurons that expresses crustacean cardioactive peptide (CCAP) has been shown pr

102 Crustacean cardioactive peptide (CCAP) neurons and the p

103 transcript with high sequence similarity to crustacean cardioactive peptide (CCAP) receptors in inse

104 These peptides include allatostatins, crustacean cardioactive peptide (CCAP), calcitonin-like

105 ng the mechanism by which a peptide hormone, crustacean cardioactive peptide (CCAP), modulates the bi

106 ng kinin, FMRFamides, eclosion hormone (EH), crustacean cardioactive peptide (CCAP), myoinhibitory pe

107 Crustacean cardioactive peptide (CCAP)-expressing neuron

108 including the gene encoding the neuropeptide crustacean cardioactive peptide (CCAP).

109 ced wing expansion defects when crossed to a crustacean cardioactive peptide (CCAP)/bursicon neuron-s

110 rotein labeling of burs and pburs as well as crustacean cardioactive peptide in neurons of the ventra

111 In the PNS, MasITPL is coexpressed with crustacean cardioactive peptide in type II link nerve ne

112 se of peptidergic neurons that produce CCAP (crustacean cardioactive peptide), which are key targets

113 beta-pigment-dispersing hormone (beta-PDH), crustacean cardioactive peptide, and red pigment-concent

114 short neuropeptides F, extended FMRFamides], crustacean cardioactive peptide, tachykinin-related pept

115 ed by strict morphological criteria although crustacean centers called hemiellipsoid bodies, which se

116 Life-table response experiments with the crustacean Ceriodaphnia dubia exposed to single and tern

117 l distribution profile within the freshwater crustacean Ceriodaphnia dubia was constructed at a spati

118 In crustaceans, circulating hormones influence many physiol

119 Here, we show that a major part of the crustacean class Malacostraca (which includes lobsters,

120 These new data on a representative of crustaceans complete the arthropod data set on Notch sig

121 ogenetic proximity of insects and stomatopod crustaceans conflicts with genomic evidence showing hexa

122 Cancer pagurus) is one of the most important crustaceans consumed in Southern European countries, eit

123 Thick fragments of laminar crustacean cuticle are scattered within the coprolite co

124 periments with a consumer-resource system of crustacean Daphnia eating algae, Nelson et al. suggest t

125 Accumulation of storage lipids in the crustacean Daphnia magna can be altered by a number of e

126 FPW toxicity to the model freshwater crustacean Daphnia magna was characterized utilizing acu

127 formulations was assessed on the freshwater crustacean Daphnia magna.

128 zed AgNPs (citrate-AgNPs) against a keystone crustacean Daphnia magna.

129 alpha-cypermethrin, on the mortality of the crustacean Daphnia magna.

130 Here we describe a gut parasite of the crustacean Daphnia that despite having remarkable morpho

131 Additionally, crustaceans (Daphnia, Caligus, and Lepeophtheirus) and s

132 rstand the precise roles of Hox genes during crustacean development.

133 Astacin, a crustacean digestive enzyme, has been proposed to carry

134 cea includes three major extant lineages of 'crustaceans', each spanning a significant range of morph

135 fossils indicate profound secular changes in crustacean ecology in terms of body size and environment

136 in arthropods and analyse segmentation in a crustacean embryo.

137 We demonstrate that the intertidal crustacean Eurydice pulchra (Leach) exhibits robust tida

138 In contrast, post-Cambrian crustaceans exhibit a wide diversity of feeding speciali

139 rated that chitosan, a polymer isolated from crustacean exoskeletons, inhibits candidal biofilm forma

140 e, other arthropods such as chelicerates and crustaceans express two dsx genes, both of which are sho

141 s (mantis shrimps) are basal eumalacostracan crustaceans famous for their elaborate visual system, th

142 hat the "base set" of data (EC50s for algae, crustaceans, fish) is available.

143 waters and a wide range of hosts, including crustaceans, fish, mollusks, and humans.

144 er of the Malacostraca clade, which includes crustacean food crop species.

145 Despite the importance of crustaceans for monitoring vulnerable aquatic habitats,

146 In this paper, we describe abundant crustacean fragments, including copepods, from a single

147 demonstrated in a mantis shrimp, a colourful crustacean from tropical reefs.

148 is demonstrated on well-preserved fishes and crustaceans from the Late Cretaceous (ca. 95 million yea

149 The present study with the crustacean Gammarus fossarum, a sentinel species in fres

150 We test this hypothesis with the freshwater crustacean Gammarus pulex and four toxicants that act on

151 one paralog lost in mammals, and a number of crustacean genomes (like Caligus rogercresseyi and Lepeo

152 ete mitochondrial genome from this important crustacean group has not been reported.

153 sted that neuroblasts are present in another crustacean group, the branchiopods, and that they also r

154 leen whales, which prey on animals (fish and crustaceans), harbor unique gut microbiomes with surpris

155 on of the stomatogastric ganglion of decapod crustaceans has been studied extensively biophysically.

156 Previous studies in a wide range of crustaceans have demonstrated a correlation between the

157 In contrast to herbivorous insects, most crustaceans have very broad diets, and the increased ric

158 mine, provides structural rigidity to fungi, crustaceans, helminths and insects.

159 rotein kinase A, specifically label both the crustacean hemiellipsoid bodies and insect mushroom bodi

160 ple correspondences indicate homology of the crustacean hemiellipsoid body and insect mushroom body a

161 the impacts of the invasive freshwater mysid crustacean Hemimysis anomala with a native counterpart M

162 rther study these and other neuropeptides in crustacean hemolymph, complementing current tissue-based

163 in insects may have been acquired within the crustacean-hexapod lineage.

164 f euarthropods (extant arachnids, myriapods, crustaceans, hexapods) has played a major role in unders

165 Mandibular organs, the crustacean homologs of insect corpora allata, produce pr

166 xopolysaccharide production and virulence to crustacean hosts.

167 y a major role in reproductive physiology in crustaceans; however their role in reproductive developm

168 Furthermore, the crustacean hyperglycemia hormones (CHHs, 8.5 kDa) were i

169 idence for the recruitment of genes from the Crustacean Hyperglycemic Hormone (CHH) and arthropod Ion

170 The crustacean hyperglycemic hormone (CHH) is a 72-amino aci

171 to be regulated largely by ecdysteroids and crustacean hyperglycemic hormone (CHH) neuropeptide fami

172 lly related ion transport peptides (ITP) and crustacean hyperglycemic hormones (CHH) are increasingly

173 o follow the same sequence as in insects and crustaceans in both species.

174 Flightin was also found in 14 species of crustaceans in orders Anostraca (water flea), Cladocera

175 diffraction data support a general model for crustaceans in which tails associate together to form 4-

176 FGLamide-type peptides have been isolated in crustaceans, in which they may function to stimulate pro

177 eages of marine, freshwater, and terrestrial crustaceans (including 64 families and 185 genera) have

178 ulthood in the olfactory midbrain of decapod crustaceans, including spiny lobsters, Panulirus argus.

179 orms have been identified in several decapod crustaceans, including the crab Cancer productus, but wh

180 We conclude that crustaceans, insects, and other groups of arthropods sha

181 Although poorly understood, crustacean intersexuality is associated with contaminati

182 ent and immigration of juvenile flatfish and crustaceans into estuaries where they feed and develop.

183 The earliest radiation of crustaceans is largely cryptic in the fossil record, but

184 The early history of crustaceans is obscured by strong biases in fossil prese

185 pelagic species (squid and certain fish and crustaceans) is poorly understood [1].

186 In crustaceans lacking eyestalks, where the entire brain is

187 , distinguishing species that mainly feed on crustaceans; large fish and squid; a mixture of crustace

188 rse as mice and flies, these observations in crustaceans led to the hypothesis that Ubx expression re

189 Crustaceans, like most mineralized invertebrates, adopte

190 ymenoptera; the recognition of hexapods as a crustacean lineage within Pancrustacea; and the elucidat

191 lipeds, from anterior thoracic legs, in many crustacean lineages.

192 waterborne cadmium by the freshwater decapod crustacean Macrobrachium australiense.

193 tals from solution by the freshwater decapod crustacean Macrobrachium australiense.

194 the nervous system in insects and in higher crustaceans (malacostracans); in the remaining euarthrop

195 , mosses, leaves, bark, trunk wood, insects, crustaceans, mammal and human tissues; their association

196 te insect-like mushroom bodies in stomatopod crustaceans (mantis shrimps).

197 iptomes for 19 species of terrestrial isopod crustaceans, many of which are infected by Wolbachia bac

198 l size of a copepod, these mesozooplanktonic crustaceans may serve as hotspots of N2 fixation, at 12.

199 e to time-varying stretches of two different crustacean mechanoreceptors, the gastropyloric receptor

200 layered organization and components of this crustacean medulla and the medullae of insects.

201 lts show that individuals allergic to HDM or crustaceans might be at risk when consuming mealworms, e

202 ected examples of neuropeptide modulation in crustaceans, mollusks, insects, and nematodes, with a pa

203 Ca(2+) stimulates ecdysteroid production by crustacean molting glands (Y-organs).

204 Crustacean molting is known to be regulated largely by e

205 ast common ancestor of Mandibulata (insects, crustaceans, myriapods).

206 of fast transient structural changes in the crustacean nerve during action potential propagation wit

207 ) has been applied to the direct analysis of crustacean neuronal tissues using in-cell accumulation t

208 e report on mass spectral characteristics of crustacean neuropeptides under MALDI-FTMS conditions and

209 f orcokinin peptides, a ubiquitous family of crustacean neuropeptides with a highly conserved N-termi

210 In the crustacean, Notch controlled mechanisms of neuroblast re

211 umerous representatives (fishes, squids, and crustaceans) of their lower trophic level prey sampled f

212 The diet of decayed wood and crustaceans offered a substantial supply of plant polysa

213 this protein could be detected in commercial crustacean oils from Antarctic krill (Euphausia superba)

214 Nevertheless, the neural composition of crustacean optic neuropils deeper than the lamina is mos

215 MALDI-MS/MS analyses revealed that IgE from crustaceans or House dust mite (HDM) allergic patients s

216 ugal neuron hitherto not identified in other crustaceans or insects that probably feeds back informat

217 xample, in urodeles, lizards, arthropods and crustaceans) or permanently lost (such as in mammals).

218 generate about 30 single precursors (insects/crustaceans) or precursor groups (chelicerates/myriapods

219 Stomatopod crustaceans, or mantis shrimp, are renowned for their co

220 idence that the single representative of the crustacean order Amphionidacea is a decapod shrimp and n

221 nse of six Antarctic marine invertebrates: a crustacean Paraceradocus miersi, a brachiopod Liothyrell

222 nships of arachnid orders and the details of crustacean paraphyly with respect to Hexapoda remain the

223 y of the ectoderm and/or the mesoderm in the crustacean Parhyale hawaiensis by ablating either the ec

224 The amphipod crustacean Parhyale hawaiensis has been put forward as a

225 The amphipod crustacean Parhyale hawaiensis is a blossoming model sys

226 ggregations during early gastrulation in the crustacean Parhyale hawaiensis.

227 gene single-minded (Ph-sim) in the amphipod crustacean Parhyale hawaiensis.

228 ssion and use these to misexpress Ubx in the crustacean Parhyale hawaiensis.

229 egeneration at single-cell resolution in the crustacean Parhyale hawaiensis.

230 erated a BAC library for the marine amphipod crustacean, Parhyale hawaiensis.

231 rovilli of the main rhabdom show the typical crustacean pattern of alternating bands of horizontally

232 anisms, including mantis shrimps (stomatopod crustaceans), peaks in the Indo-Australian Archipelago (

233 ding experiments with two herbivorous isopod crustaceans, Porcellio scaber (woodlouse) and Armadillid

234 Crustaceans possess a diverse array of specialized limbs

235 Crustaceans possess remarkably diverse appendages, both

236 No previously described crustacean possesses a mushroom body as defined by stric

237 tive cryoprotectant might be employed during crustacean processing.

238 Two crustaceans producing sharply contrasting bioturbation--

239 including mollusks, nematodes, insects, and crustaceans (referred to here as pigment-dispersing horm

240 eaks appearing in direct tissue spectra from crustaceans result from the metastable decay of aspartat

241 t polysaccharide found in fungal cell walls, crustacean shells, and insect exoskeletons.

242 abundant polysaccharide in nature, found in crustacean shells, insect exoskeletons and fungal cell w

243 ing toughness by using strategies taken from crustacean shells.

244 ostraca: Peracarida), a lineage of marsupial crustaceans, show an interesting variety of brooding str

245 Among crustaceans, shrimps are the most predominant cause of a

246 hophorans, show that, similar to insects and crustaceans, single neural precursors are formed in the

247 staceans; large fish and squid; a mixture of crustaceans, small fish and squid; or carrion.

248 expression boundary of Ubx have resulted in crustacean species with either 0, 1, 2, or 3 pairs of th

249 a pattern reminiscent of that seen in other crustacean species, and these morphological alterations

250 oss-reactive tropomyosin was detected in all crustacean species, with partial detection in molluscs:

251 generated morphological differences between crustacean species.

252 Anatomical studies of the crustacean stomatogastric ganglion (STG) in different sp

253 The crustacean stomatogastric ganglion (STG) is modulated by

254 ly-conserved physiological properties in the crustacean stomatogastric ganglion (STG) of Cancer borea

255 he two motor patterns generated by the adult crustacean stomatogastric ganglion (STG), the gastric mi

256 The pyloric network in the crustacean stomatogastric ganglion generates a rhythmic

257 or model pyloric neurons and networks of the crustacean stomatogastric ganglion, showed that function

258 tes activity in the unmyelinated axon of the crustacean stomatogastric pyloric dilator neuron.

259 For millimeter-scale aquatic crustaceans such as copepods, ensuring reproductive succ

260 The most landed species are crustaceans such as rose shrimp and Norway lobster, alth

261 ill, prawns, lobsters, and other long-tailed crustaceans swim by rhythmically moving limbs called swi

262 Thus, the crustacean swimmeret system serves as a concrete example

263 Given the high metabolic cost of crustacean swimming, our results suggest that natural se

264 of biologically relevant Reynolds numbers in crustacean swimming.

265 e, no consensus has been reached as to which crustacean taxon is the closest relative of hexapods.

266 More than any other crustacean taxon, mantis shrimps display sophisticated b

267 e chelicerate Limulus polyphemus, all isopod crustaceans tested, and the cave shrimp Troglocaris anop

268 d in the last common ancestor of insects and crustaceans (Tetraconata).

269 inearly polarizing reflector in a stomatopod crustacean that consists of 6-8 layers of hollow, ovoid

270 expression of Ubx in Parhyale hawaiensis, a crustacean that normally possesses a single pair of maxi

271 rse and ecologically crucial group of minute crustaceans that are relatively neglected in terms of st

272 e, we show that copepods, abundant migrating crustaceans that graze on phytoplankton, as well as othe

273 perating through the immigration of fish and crustaceans that prey on bivalves, reduce their grazing

274 the dinosaurian defecators consumed sizeable crustaceans that sheltered in rotting logs.

275 g the nervous system, whereas in insects and crustaceans the nervous tissue is produced by stem cells

276 first time the role of Notch signalling in a crustacean, the branchiopod Daphnia magna, and show that

277 otopic organization of the lobula plate in a crustacean, the crab Neohelice granulata using a variety

278 ion trends within a diverse group of aquatic crustaceans, the Anomura.

279 Both in insects and malacostracan crustaceans, the bHLH-PAS transcription factor single-mi

280 Shellfish are classified into mollusks and crustaceans, the latter belonging to the class of arthro

281 f biogenic amines have been characterized in crustaceans, the mechanisms linking these molecules to b

282 Few species of reptant decapod crustaceans thrive in the cold-stenothermal waters of th

283 To increase the relevance of crustaceans to environmental toxicologists, we comprehen

284 standing, will greatly facilitate the use of crustaceans to monitor aquatic habitats.

285 oss evolution, from ancient arthropods, like crustaceans, to humans.

286 ng data from the Vessel Monitoring System of crustacean trawlers along the Portuguese margin, we have

287 ailed immunocytochemical localization of the crustacean type 1 serotonin receptor, 5-HT1crust, throug

288 possess only one, nematodes two, and decapod crustaceans up to three, but their phylogenetic relation

289 New research shows that some midwater crustaceans use antireflection coatings to enhance their

290 no direct evidence that any of these marine crustaceans use this modality to communicate with conspe

291 In insects and crustaceans, ventral midline cells are present that subd

292 ifferences in delta(15) N of potential prey (crustaceans vs. squid vs. fish and carrion), analysis of

293 Here, in stomatopod crustaceans, we describe for the first time a visual sys

294 nisms such as Hyalella azteca, an epibenthic crustacean which forages at the sediment surface, is lik

295 ve this taxon as a probable crown-group (pan)crustacean, while its feeding style, which allowed it to

296 prising diversity of endemic animals (mostly crustaceans) within a highly oligotrophic habitat.

297 ting is a critical developmental process for crustaceans, yet the underlying molecular mechanism is u

298 anipulated lake, to test the hypothesis that crustacean zooplankton production should subsequently de

299 hese increased DOC concentrations may reduce crustacean zooplankton productivity due to reductions in

300 his habitat is the chitinous exoskeletons of crustacean zooplankton.

301 t significant terrestrial support of pelagic crustaceans (zooplankton) is widespread.