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1 onate is not known to be a direct source for autotrophy.
2  that minerals could directly supply CO2 for autotrophy.
3 c signatures consistent with mineral-sourced autotrophy.
4 779 during the transition from quiescence to autotrophy.
5 opmental program that promotes the switch to autotrophy.
6 oxygenic phototrophs that are not capable of autotrophy.
7 constrained by simultaneous energy-intensive autotrophy.
8 but is rather an investment in readiness for autotrophy.
9  heterotrophy and shifting metabolism toward autotrophy.
10 t the dominant metabolism at depth indeed is autotrophy (83%), whereas heterotrophic consumption of m
11 in Sulfolobus acidocaldarius DSM639, but not autotrophy, although earlier reports indicate this strai
12 DH dehydrogenase genes, as well as genes for autotrophy and aromatic compound degradation.
13 stoichiometry, relative to a system in which autotrophy and heterotrophy are mutually exclusive.
14         Mixotrophic bacteria can employ both autotrophy and heterotrophy for growth.
15 ol to quantify the relative contributions of autotrophy and heterotrophy in planktonic protists.
16 location of carbon from adults to gametes by autotrophy and heterotrophy in previously bleached and n
17 e prevalence of mixotrophy (relative to pure autotrophy and heterotrophy), and to ask whether observe
18 P05 clade that has the genetic potential for autotrophy and heterotrophy.
19 ost through feedbacks that reduced mistletoe autotrophy and improved resource availability for the re
20                               Restoration of autotrophy and leaf pigmentation following aadA-based tr
21 ce microbes and reinforced the importance of autotrophy and the preferential utilization of dissolved
22 ng a widespread potential for MGI to perform autotrophy and transport and degrade organic nitrogen.
23 ms of RubisCO, forms I and II participate in autotrophy, and form III so far has been associated only
24 ow CA and Ci uptake improve growth, we model autotrophy as colimited by CO(2) and HCO(3)(-), as both
25 us maintaining favourable conditions for net autotrophy at the hole floors.
26  developing seedling must reach the state of autotrophy before the nutrients stored in the seed are e
27 sonal shift from heterotrophy (%DO < 100) to autotrophy (%DO > 100) and dramatic shifts in aragonite
28 ere regions of both extreme heterotrophy and autotrophy exist.
29       Our study highlights the importance of autotrophy for carbon allocation from adult corals to ga
30 n its source (mine tailings) and metabolism (autotrophy) from those of previous studies.
31 explored, and the ecological implications of autotrophy in attine ant- and plant root-associated Pseu
32 iquely sensitive to heterotrophy relative to autotrophy in plants and bacteria.
33                   In this study, we examined autotrophy in Pseudonocardia dioxanivorans CB1190, which
34 m net heterotrophy in the inner fjord to net autotrophy in the coastal shelf waters.
35 lfur starvation under heterotrophy and photo-autotrophy in the green alga (Chlamydomonas reinhardtii)
36 drive the shift between net heterotrophy and autotrophy in the oligotrophic ocean.
37  may have for the organism in the context of autotrophy in the RNA world.
38 hat at least 51% of the RNA was derived from autotrophy, in close agreement with the RNA-Seq data, wh
39                                    Synthetic autotrophy is a promising avenue to sustainable bioprodu
40                                              Autotrophy is prominent across the West and is sensitive
41 nvestigated how trophic strategies along the autotrophy-mixotrophy spectrum vary in importance over t
42 est that it results in remarkably robust net autotrophy on the Greenland Ice Sheet.
43 ained by differences in trophic preferences (autotrophy or heterotrophy).
44                            Either to sustain autotrophy, or as a prelude to heterotrophy, organic syn
45  acquire carbon-based resources through both autotrophy (photosynthesis) and heterotrophy (obtaining
46 he genomes did not indicate any capacity for autotrophy, phototrophy, or trace gas metabolism.
47  relative abundance of genes associated with autotrophy (rbc, coxL), nor increased relative abundance
48 ph Optimal Contributions to Heterotrophy and Autotrophy) that predicts the optimal (growth-maximizing
49 ional constraints during the transition from autotrophy to a nonphotosynthetic parasitic lifestyle.
50 vealed that both species: (1) relied only on autotrophy to allocate carbon to gametes, while heterotr
51 eterotrophy and endosymbiotic dinoflagellate autotrophy to meet their metabolic needs.
52 ganic iron and sulfur biotransformations, to autotrophy, to chemoheterotrophy in less acidophilic spe
53 sion support heterotrophy, which succumbs to autotrophy under groundwater discharge.
54 , at some point, must make the transition to autotrophy via the initiation of photosynthesis.
55 lysis of cells grown under strict H(2)-CO(2) autotrophy was consistent with the involvement of Msed_0
56 c TABs are caused by mixotrophs that augment autotrophy with organic nutrient sources, including comp
57  cycle and, thus, the delayed acquisition of autotrophy within the Chlorobiaceae.