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1 s, prompted the suggestion that the genus is carnivorous.
2 ibalism among insects that typically are not carnivorous.
3 did barnacle (>1,500 individuals m(-2)), and carnivorous actinostolid anemone (>30 individuals m(-2))
4  and confirms the close relationship between carnivorous action and plant defense mechanisms.
5 nterpreted as the diversification of various carnivorous and cursorial taxa, whereas the acquisition
6 systems [5], due to community respiration of carnivorous and detritivorous zooplankton.
7             Plants in the genus Genlisea are carnivorous and feed on microorganisms that live in soil
8 ng hyperopic foraging manoeuvres, exhibiting carnivorous and insectivorous diets, and displaying noct
9 w to be one of the most enormous terrestrial carnivorous animals ever.
10 re a separate phylum (Chaetognatha) of small carnivorous animals, dominantly pelagic, and a major com
11  is a very important process, especially for carnivorous animals.
12 hemical mimicry of the food sources of adult carnivorous animals.
13 e) in H. monstrosus may have facilitated the carnivorous aspect of its diet.
14 d development of the orofacial region in the carnivorous Australian marsupial, the fat-tailed dunnart
15 herbivorous arthropods, and indirectly serve carnivorous (beneficial) arthropods by providing food an
16 ting high-lipid diets (e.g., polar bears and carnivorous birds) were predicted to be able to biomagni
17                  However, unlike mammals and carnivorous birds, expected broad relationships between
18 s, I found that are territorial solitary and carnivorous carnivorans exhibited selection towards incr
19 nd a shift towards smaller phytoplankton and carnivorous copepods, associated with the seasonal impac
20     Triconodontidae are considered the first carnivorous crown mammals.
21 e transition from an omnivorous to primarily carnivorous diet during polar bear evolution.
22 s associated with an obligate herbivorous or carnivorous diet in 31 placental mammals.
23 ranging apex felid predators with a strictly carnivorous diet, could also be effective secondary long
24            Humans are not fully adapted to a carnivorous diet; human consumption of meat is limited b
25     The combination of traits linked to both carnivorous diets (e.g. fore-aft cutting edges) and inse
26 ike that of extant bears with omnivorous and carnivorous diets.
27 d natural endocranial cast (endocast) from a carnivorous dinosaur of the late Jurassic period, Allosa
28 s did, in fact, evolve from certain types of carnivorous dinosaur.
29 nt to our knowledge of the feeding habits of carnivorous dinosaurs and for accurate reconstruction th
30 s, but until now the evidence in relation to carnivorous dinosaurs has been sparse and anecdotal.
31                   Prey-capture strategies in carnivorous dinosaurs have been inferred from the biomec
32        Tyrannosaurids--the familiar group of carnivorous dinosaurs including Tyrannosaurus and Albert
33                                        Giant carnivorous dinosaurs such as Tyrannosaurus rex and abel
34 tionary history of Maniraptora, the clade of carnivorous dinosaurs that includes birds and the sickle
35                    Tyrannosaurids were large carnivorous dinosaurs that underwent major changes in sk
36 rannosauridae, the best known group of large carnivorous dinosaurs, and determine the developmental m
37  final two stages of the Cretaceous, whereas carnivorous dinosaurs, mid-sized herbivores, and some As
38 test gait and speed of the largest theropod (carnivorous) dinosaurs, such as Tyrannosaurus, is contro
39 st that the mechanism of prey recognition in carnivorous Droseraceae evolved by co-opting ancestral m
40                                              Carnivorous eating habits are linked to TMAO levels in t
41 ponds to the cues of a distant predator, the carnivorous elephant mosquito larva.
42 also regulates volatile signals that attract carnivorous enemies of herbivores or warn neighboring pl
43        Our results demonstrate that strictly carnivorous, felid predators could have broad and overlo
44 uscle samples of Plagioscion squamosissimus (carnivorous fish) and Colossoma macropomum (omnivorous f
45 CE across 3 trophic levels (phytoplankton to carnivorous fish) was highest under low light and high n
46 iency that can be especially detrimental for carnivorous fish.
47 s evolved independently from a plesiomorphic carnivorous form.
48              Constricting ring (CR) cells of carnivorous fungi triple in size within 0.1-1 s to captu
49 ology of the predatory lifestyle switch in a carnivorous fungus and provide frameworks for other fung
50 ete oyster mushroom Pleurotus ostreatus is a carnivorous fungus that preys on nematodes to supplement
51                  Here, we investigated how a carnivorous fungus, Drechslerella dactyloides, executes
52 ic analyses support ctenophores, a phylum of carnivorous, gelatinous marine organisms, as the sister
53 e report a species in which caterpillars are carnivorous inhabitants of spider's webs, feeding on the
54 ous mammals have a relatively high slope and carnivorous, insectivorous, and nectarivorous birds have
55 tophagous early larvae, intermediate larvae, carnivorous late larvae) was analyzed by using 16S rRNA-
56 ldiaceae) represents a previously overlooked carnivorous lineage that captures insects on sticky infl
57 ncer mortality is associated with diet, with carnivorous mammals (especially mammal-consuming ones) f
58 s in scaling exponents among herbivorous and carnivorous mammals and birds.
59 to their mother of origin and concluded that carnivorous mammals can be better dispersers than birds.
60                                         Most carnivorous mammals can pulverize skeletal elements by g
61 50 million years, successive clades of large carnivorous mammals diversified and then declined to ext
62 FMRs and desert birds have low FMRs; and (g) carnivorous mammals have a relatively high slope and car
63 fornianus) are members of a diverse clade of carnivorous mammals known as pinnipeds.
64 mirrored differences between herbivorous and carnivorous mammals, reflecting trade-offs between carbo
65 D event risk does not seem to occur in other carnivorous mammals.
66 ng other reptiles, fish, and herbivorous and carnivorous mammals.
67 phan in peptides recovered from the venom of carnivorous marine cone snails (Conus).
68         The Tasmanian devil is an endangered carnivorous marsupial threatened by devil facial tumor d
69 asmanian tiger, is the largest of modern-day carnivorous marsupials and was hunted to extinction by E
70  of the Plantaginaceae, a family in which no carnivorous members are otherwise known.
71  that controls prey capture reactions in the carnivorous mollusc Clione limacina.
72 ative phylogenetic analyses to show that two carnivorous Nepenthes pitcher plant species independentl
73 f-contained pools that form in leaves of the carnivorous northern pitcher plant, Sarracenia purpurea.
74 pulations, where L. humile is among the most carnivorous of ants, Argentine ants from California occu
75 esentative genomes from across Mammalia with carnivorous, omnivorous, and herbivorous dietary special
76 cantly longer in herbivorous species than in carnivorous ones (p = 0.008), presumably allowing the ex
77                   However, the production of carnivorous organs can be a phenotypically plastic trait
78 tic costs associated with the maintenance of carnivorous organs.
79 nsect communities, that harvesting of single carnivorous parasitoid species led to a significant incr
80 lated Scaphiopus tadpoles do not induce this carnivorous phenotype.
81 repeatable, passive-dynamic motion used by a carnivorous pitcher plant to catch prey.
82                            Extracts from the carnivorous pitcher plant, Sarracenia purpurea, have pre
83 munities collected from wild pitchers of the carnivorous pitcher plant, Sarracenia purpurea, we test
84                                              Carnivorous pitcher plants (Nepenthes) are a striking ex
85                                              Carnivorous pitcher plants capture prey with modified le
86 y, it was shown that aspartic proteases from carnivorous pitcher plants of the genus Nepenthes are ac
87 nteresting group of proteolytic enzymes from carnivorous pitcher plants of the genus Nepenthes.
88  In order to evaluate interactions between a carnivorous plant (greater bladderwort, Utricularia vulg
89 imentally demonstrate interactions between a carnivorous plant and a fish.
90 teine protease from the digestive fluid of a carnivorous plant and confirms the close relationship be
91                     A new study shows that a carnivorous plant attracts bats by possessing modified p
92 ed and recorded by Darwin, the leaves of the carnivorous plant Drosera capensis L. slowly fold around
93 the uptake of N via roots versus prey of the carnivorous plant Drosera rotundifolia growing in ombrot
94 ed arthropods) represent a crucial aspect of carnivorous plant ecology, yet remain poorly studied.
95 logical features with extant Roridulaceae, a carnivorous plant family that is today endemic to the Ca
96 significant investment of the resources of a carnivorous plant is committed to producing the traps, a
97 ple of convergent evolution across unrelated carnivorous plant lineages.
98 ouch-sensing cells of Cape sundew, a related carnivorous plant of the Droseraceae family.
99  new method facilitated accurate analyses of carnivorous plant prey spectra (even of heavily digested
100                                   No case of carnivorous plant traps has so far been reported from th
101                    Here, we show that in the carnivorous plant Utricularia gibba, the upper leaf (ada
102 ergenic regions in the compact genome of the carnivorous plant Utricularia gibba, we investigated its
103 e the development of cup-shaped traps of the carnivorous plant Utricularia gibba.
104 ocument both a unique capturing strategy for carnivorous plants and a case of a plant that traps and
105 share a common prey could exist than between carnivorous plants and animals.
106 e considered inter-Kingdom competition among carnivorous plants and animals.
107  organs, such as the prey-capturing traps of carnivorous plants and nectary-bearing petals of ranuncu
108     Modern Roridula species are unique among carnivorous plants as they digest prey in a complex mutu
109                                              Carnivorous plants consume animals for mineral nutrients
110 pitcher secretions of the Nepenthes genus of carnivorous plants contain a proteolytic activity that i
111 es between simple and complex leaves and how carnivorous plants form three-dimensional insect traps.
112                     Triantha is unique among carnivorous plants in capturing prey solely with sticky
113 ase (COX) from an active-trapping lineage of carnivorous plants is caused by positive Darwinian selec
114                         The fossil record of carnivorous plants is very scarce and macrofossil eviden
115                        Our data suggest that carnivorous plants may actively promote or reduce animal
116                                              Carnivorous plants primarily use aspartic proteases duri
117                   In response to touch, some carnivorous plants such as the Venus flytrap have evolve
118 ng stems secrete phosphatase, as seen in all carnivorous plants that directly digest prey.
119               Charles Darwin recognized that carnivorous plants thrive in nutrient-poor soil by captu
120 t similarities of Philcoxia to those of some carnivorous plants, along with recent observations of ne
121 ical, and physiological) and mutualisms with carnivorous plants, and the ecological and agricultural
122 e growth and local growth repression, and in carnivorous plants, by modifying the relative growth of
123 the Venus flytrap as a representative of the carnivorous plants, we summarize the molecular mechanism
124  sensitive to increasing nutrient input, and carnivorous plants, which are characteristic of these wi
125 been shown to control leaf peltation in some carnivorous plants, yet the mechanisms underlying the ge
126 en active and passive trapping mechanisms in carnivorous plants.
127  insufficient to explain the movement of all carnivorous polar bears.
128 from RLB was more omnivorous than the highly carnivorous populations from the Northwest.
129 well as for homologous toxin peptides from a carnivorous predator.
130                               Prey shifts in carnivorous predators are events that can initiate the a
131 ction in repelling herbivores and attracting carnivorous predators in green tissues, the presumed pri
132        Sampled fish species comprised 48% of carnivorous reef fish biomass.
133 rgy channels may buffer nominally generalist carnivorous reef fishes from some negative effects of ch
134                                  Conversely, carnivorous reptiles have non-occluding dentitions that
135                        Oxygen consumption by carnivorous reptiles increases enormously after they hav
136 homys leucogaster) are among the most highly carnivorous rodents in North America.
137 rements in the pelagic prey-predator system (carnivorous sculpins and top-predator seals).
138 on of an alien biological control agent: the carnivorous snail Euglandina rosea[3].
139 salpa are consistent with those reported for carnivorous Sparidae species.
140 he late Pleistocene, during which many large carnivorous species coexisted as predators and competito
141                                 Aquacultured carnivorous species consume most of the world's fishmeal
142 effect is of particular interest because two carnivorous species of sea turtles-hawksbills, Eretmoche
143                                      Farming carnivorous species requires large inputs of wild fish f
144 anism, and they demonstrate the ability of a carnivorous species to respond to the availability of re
145                                Leaves of the carnivorous sundew plants (Drosera spp.) secrete mucilag
146 e origin, distribution, and frequency of the carnivorous syndrome in angiosperms and, more generally,
147 erstanding of the traits associated with the carnivorous syndrome, from trap leaf development and pre
148 s Spea, where an invertebrate diet induces a carnivorous tadpole morph capable of consuming live cons
149 trophic webs with a seeming overabundance of carnivorous taxa and the evolution of entirely new preda
150                               In the case of carnivorous taxa, Late Miocene pre-GABI endemic sparasso
151 for an emblematic and ecologically important carnivorous taxa, the Felidae family.
152 rnivores in a community and low diversity of carnivorous taxa, whereas higher oxygen levels support m
153 g a stream productivity gradient, as well as carnivorous terrestrial invertebrates, in a forested wat
154 his technique to the long skull of the large carnivorous theropod dinosaur Allosaurus fragilis.
155 logy of Megaraptora, a group of large-clawed carnivorous theropod dinosaurs known from Cretaceous dep
156                         Indications are that carnivorous theropods may have had dispersals that were
157 saurs nested within a clade of predominantly carnivorous theropods, are known to have had teeth, wher
158 re much smaller than published estimates for carnivorous theropods, being more similar to the herbivo
159            Feeding, for example, ranges from carnivorous, through subaquatic and terrestrial omnivoro
160 ated with the grass carp's adaptation from a carnivorous to an herbivorous diet.
161 m associated with electrical activity in the carnivorous Venus flytrap, Dionaea muscipula, was record
162 t evidence for the presence of a terrestrial carnivorous vertebrate from the Middle Permian of South
163 light may enable predation of zooplankton by carnivorous zooplankters, fish, and birds now known to f

 
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