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1 gests that an ancestor was a nitrogen-fixing autotroph.
2 coccus is the smallest-known oxygen-evolving autotroph.
3 h weaker contributions from bacterivores and autotrophs.
4 gens--strictly anaerobic, hydrogen-dependent autotrophs.
5 ganic matter is recycled to plants and other autotrophs.
6 ggests that these microfossils were probably autotrophs.
7 nsforming other heterotrophic organisms into autotrophs.
8 documented cascades in that it includes only autotrophs.
9 isphosphatase (SBPase) is expressed in photo-autotrophs and catalyzes the hydrolysis of sedoheptulose
10         H2 is a favorable electron donor for autotrophs and causes fixation of organic carbon that co
11  spatial patterns of nutrient limitation for autotrophs and habitat availability for other members of
12                   The classification between autotrophs and heterotrophs achieved an overall accuracy
13 rease in abundance at lower latitudes, while autotrophs and heterotrophs do not, and that this may be
14  the marine archaeal community includes both autotrophs and heterotrophs or is a single population wi
15 trient and energy exchange between microbial autotrophs and heterotrophs, highlighting the importance
16 as well as tightly coupled exchanges between autotrophs and heterotrophs.
17  in mediating ecosystem services provided by autotrophs and outline scenarios in which infection may
18                                We found that autotrophs and slower-grazing mixotrophs tended to preva
19 how that simple regulatory feedbacks between autotrophs and their environment when embedded within co
20 tional separation between primary producers (autotrophs) and consumers (heterotrophs) at the base of
21 es in the C:N:P ratios of primary producers (autotrophs) and invertebrate primary consumers (herbivor
22 tosynthetic and growth rates of marine macro-autotrophs are likely to increase under elevated [CO2 ]
23 can have particularly strong effects because autotrophs are responsible for a wide range of provision
24                                              Autotrophs assimilated a significantly higher amount (me
25 webs are built on an extremely nutrient-poor autotroph base with C:P and C:N ratios higher than in la
26 inobacter, Halanaerobium, and Halomonas, and autotrophs belonging to Arcobacter.
27                         While some estuarine autotrophs benefit from elevated pCO2, the benefit can c
28 f most reef organisms to ocean warming, some autotrophs benefit from ocean acidification.
29      In this review, we examine marine macro-autotroph biochemistry and physiology relevant to their
30 ssimilatory and dissimilatory utilisation of autotroph biomass by heterotrophs is a fundamental mecha
31  model to study heterotrophic utilisation of autotroph biomass using elementary flux mode analysis an
32  in mass-specific net primary production and autotroph biomass, supported by (i) combined increases i
33                                However, many autotrophs can also grow mixotrophically, a strategy tha
34 , methane-producing archaeon and facultative autotroph capable of biosynthesizing all the amino acids
35                        The size structure of autotroph communities - the relative abundance of small
36 tely underlie the emergent size structure of autotroph communities, divergent aspects of body size (v
37 terotroph, and Chlamydomonas reinhardtii, an autotroph) consumed by a generalist predator Euplotes eu
38   Here we show how microbial phototrophs and autotrophs contribute to this exceptional productivity.
39 ow tens of metres deeper than obligate photo-autotrophs, deepening the nutricline by ~20 m.
40 no acids (AroAAs) are biosynthesized in this autotroph either by the de novo pathway, with chorismate
41                                              Autotrophs from cold streams had higher photosynthetic r
42 ical phenomena, including demonstrating that autotrophs grow more slowly than heterotrophs because of
43                          Many photosynthetic autotrophs have evolved responses that adjust their meta
44 ria, blue-green algae, are the most abundant autotrophs in aquatic environments and form the base of
45 ria, blue-green algae, are the most abundant autotrophs in aquatic environments and form the base of
46 jor lineages of land plants and the dominant autotrophs in most terrestrial ecosystems.
47 hemical cues synthesized by plants and other autotrophs in response to stress.
48                 If archaea live primarily as autotrophs in the natural environment, a large ammonia-o
49                          Both mixotrophs and autotrophs increase greatly in productive coastal enviro
50 type of interaction varied by trophic level (autotrophs: interactive; heterotrophs: additive) and phy
51       The core of intermediary metabolism in autotrophs is the citric acid cycle.
52 e structure of unicellular and multicellular autotrophs is, however, unknown.
53 h and without environmental feedbacks at the autotroph level.
54                   The extent to which marine autotrophs may benefit from elevated CO2 will be a funct
55 Using this method, eight independent acetate autotrophs of Methanococcus maripaludis were isolated.
56                                    Bacterial autotrophs often rely on CO(2) concentrating mechanisms
57 he diverse ODP-encoding microbes, an oxalate autotroph, Oxalobacter formigenes, dominates this functi
58  for nitrogen also shaped interactions among autotrophs, particularly Ulva.
59 w of >100 species revealed that marine macro-autotroph photosynthesis is overwhelmingly C3 (>/= 85%)
60 ough seagrasses and marine macroalgae (macro-autotrophs) play critical ecological roles in reef, lago
61 diverse microbial community of heterotrophs, autotrophs, predators, and symbionts, a community we ref
62 es, paving the way for artificial simplified-autotroph protocells (ASAPs).
63 astal and open ocean systems, the biomass of autotrophs scales non-linearly with the size of the ecos
64 ptolyngbya and the H2-oxidizing denitrifying autotroph Sulfuritalea.
65 s have occupied the Earth to date, that more autotrophs than heterotrophs have ever existed, and that
66 res of Acidimicrobium sp. strain A6 (A6), an autotroph that oxidizes ammonium to nitrite while reduci
67 symbionts appear to be metabolically capable autotrophs underscores the extent to which the host depe
68 ycolate recycling in these nonphotosynthetic autotrophs, we suggest the more general term "phosphogly
69     This review explores the interactions of autotrophs with solid electron donors and their importan
70  growth efficiencies (10-30%) when consuming autotrophs with typical carbon-to-nutrient ratios.