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1 eciduous forests are more efficient in using photosynthate.
2 ound linkages by reducing the flow of recent photosynthate.
3 bacterium Mesorhizobium loti in exchange for photosynthate.
4 n source (i.e. insects) with host plants for photosynthate.
5  among mats, originating from cyanobacterial photosynthate.
6  of cells, suggesting an increased supply of photosynthate.
7 urce and excluding contributions from recent photosynthate.
8 a for use by the plant in exchange for plant photosynthate.
9 fungi obtain nutrients in exchange for plant photosynthates.
10 e growth of algal symbionts and retention of photosynthates.
11 ve of N-limited restraints on utilization of photosynthates.
12 e molecular dinitrogen in exchange for plant photosynthates.
13 st obtaining their carbon supply directly as photosynthates.
14 ls simply respond to a diffusing gradient of photosynthate?
15 ositively correlated with photosynthesis and photosynthate accumulation.
16  trend in CUE implies that the proportion of photosynthate allocated to autotrophic respiration is no
17 ipping) to examine the impacts of rice plant photosynthate allocation on paddy N2O emissions.
18                                              Photosynthate allocation to fungi was traced using (14)
19 fore, breeding efforts optimizing rice plant photosynthate allocation to grains, i.e., increasing har
20 ementarity of nutrient pool use and greatest photosynthate allocation to symbiotic fungi.
21                                     Reducing photosynthate allocation to the grain by spikelet clippi
22     Our findings demonstrate that optimizing photosynthate allocation to the grain can reduce paddy N
23                                   Increasing photosynthate allocation to the grain in rice (Oryza sat
24                                              Photosynthate allocation to tree roots and their mycorrh
25 iotropic effect on how the plant distributes photosynthate among fruit.
26                          The partitioning of photosynthate among various forest carbon pools is a key
27               To optimize the utilization of photosynthate and avoid damage that can result from the
28 sed stable isotope enrichment to track plant photosynthate and fungal N.
29 3) C-CO(2) to quantify the capture of recent photosynthate and its transfer below-ground.
30          We found that the exchange ratio of photosynthate and nitrogen between plants and AM fungi i
31                             Sorbitol, a main photosynthate and transport carbohydrate in all tree fru
32 ung leaves non-cellautonomously to available photosynthates and leads to organs constituted of a grea
33 synthesis and unraveling how plants allocate photosynthates and prioritize different carbohydrate syn
34 pattern for efficient distribution of water, photosynthates and signaling molecules.
35 d management modifies the transfer of recent photosynthates and soil nitrogen through plants and soil
36 but it is more strongly controlled by recent photosynthates (and reserve availability) than by total
37 e starch, which restrict the capacity to use photosynthate, and high CO(2), which increases the poten
38 lant vascular network also transports water, photosynthates, and signaling molecules and is essential
39 is conserved across plant species and sugars/photosynthates are crucial for P-deficiency signal trans
40 port tree metabolism and growth when current photosynthates are insufficient, offering resilience in
41       Moreover, we also show that sugars and photosynthates are integrally related to P-deficiency-in
42 tes against (13)CO(2) so that source sugars (photosynthates) are on average (13)C depleted by 20 per
43  also describe how meristems deal with extra photosynthate as a result of exposure to elevated CO2.
44                           Many diatoms store photosynthate as the neutral lipid triacylglycerol (TAG)
45 n used in tree-ring construction can be from photosynthate assimilated the year before ring construct
46 nscriptionally regulated by both nitrate and photosynthate availability.
47            These results are consistent with photosynthate being trapped within anthocyanin-accumulat
48  trees used more than twice as much of their photosynthate belowground and less than half as much abo
49 ast, dominant trees used 27 +/- 19% of their photosynthate belowground, whereas suppressed trees used
50             It also alters the allocation of photosynthates between ribulose 1,5-bisphosphate regener
51  capture and transfer below-ground of recent photosynthate by plants.
52  met by the excess production of carbon-rich photosynthates by their algal symbionts(2,3).
53                      The relative use of new photosynthate compared to stored carbon (C) for the prod
54 fold less than predicted for requirements of photosynthate delivery.
55                                      Besides photosynthates, dodder (Cuscuta spp.) acquires phloem-mo
56                    TaRca1B provides a better photosynthate energy partitioning under HS with a signif
57                 TaRca1beta provides a better photosynthate energy partitioning under HS with a signif
58 se cortical cells are the first to intercept photosynthate exiting the vascular cylinder, transcript
59            Both (11)CO(2) fixation and (11)C-photosynthate export from the labeled source leaf increa
60  affected by the disrupted supply of current photosynthate for over 1 yr; however, carbohydrate conce
61 with many cnidarian hosts requiring symbiont photosynthate for survival-but little is known about how
62 k indicated simultaneous utilization of leaf photosynthates for flowering, rhizome fortification, str
63  They used 25 +/- 10% (mean +/- SD) of their photosynthates for wood production, whereas suppressed t
64 vide a direct pathway for transfer of recent photosynthate from conspecific green orchids to achlorop
65 ns in regulating respiration of recent plant photosynthate from soil.
66  bacteria donated genes that allow export of photosynthate from the plastid and its polymerization in
67 lic exchange (i.e., transfer of fixed carbon photosynthates from symbiont to host) during sensitive e
68 ence for maintained translocation of a major photosynthate, glucose, from the symbiont, but there was
69 oprene is made primarily from recently fixed photosynthate; however, alternate carbon sources play an
70 osystems and account for a large fraction of photosynthate in a wide range of ecosystems; they theref
71 dition to its role as a major translocatable photosynthate in Rosaceae species, sorbitol is a widespr
72  mRNA could be linked to the availability of photosynthate in the plant.
73 hange with the microsymbiont-obtaining plant photosynthates in exchange for mineral nutrients: enhanc
74 al minerals to their plant hosts and receive photosynthates in return.
75 ecifically, G. pallida react to reduced host-photosynthate influx due to concurrent mycorrhizal-host
76                Potential modules for dynamic photosynthate input, wetting-event inputs, freeze-thaw i
77 ate winter, after an extended period with no photosynthate input.
78 n the regrowing forest, plants are investing photosynthate into belowground processes that amplify mi
79 in mind, this study emphasizes the import of photosynthate into developing embryos, its conversion in
80 atalyzes a crucial step in the conversion of photosynthate into oil, suggesting a preferred plastid r
81 n nutrient deprivation, microalgae partition photosynthate into starch and lipids at the expense of p
82 rbon until dawn and modulate partitioning of photosynthate into starch in the light, optimizing the f
83 urements of photosystem II), partitioning of photosynthate into sucrose and starch, and plant growth.
84 es play an important role, particularly when photosynthate is limiting.
85 Deep mixing and rapid turnover indicate most photosynthate is rapidly metabolized.
86                  If growth at night is fast, photosynthate is used for growth at the start of the day
87 from decomposition of surface-derived modern photosynthate, not catotelm C.
88 own to bring about short-term adjustments of photosynthate partitioning between starch and sucrose (S
89 f respiratory CO2 refixation and anaplerotic photosynthate partitioning in support of storage oil and
90 acteria, nematodes and insects intercept the photosynthate produced by plants, and viruses use replic
91 sistent with a defect in chloroplast-derived photosynthate production and are largely rescued by sucr
92 2), which increases the potential to produce photosynthate, provides conditions for strong down-regul
93                      At the same time, (11)C-photosynthate remaining in the aboveground sink tissues
94  Prochlorococcus to synchronize to the daily photosynthate supply from surrounding phytoplankton.
95 e-enhanced and up-/down-regulated in vivo by photosynthate supply from the shoots.
96 anscript (NE-PpcK) is markedly influenced by photosynthate supply from the shoots.
97 t dawn as photosynthesis restored oxygen and photosynthate supply.
98 anoxic stress on soil microbes and decreased photosynthates supply.
99 ulation mechanisms: the symbiont shares only photosynthate that it cannot use itself, and the host de
100                          The mobilization of photosynthate through myo-inositol translocation links r
101 ighlights that capture and rapid transfer of photosynthates through multi-trophic networks are key fo
102 ) C-CO2 was applied to trace (13) C-labelled photosynthate throughout plants, fungi, and soil microbe
103 re the primary recipients of (13) C-labelled photosynthate throughout the system, representing 60-70%
104         Vascular bundles transport water and photosynthate to all organs, and increased bundle number
105 een aboveground production and allocation of photosynthate to belowground processes and the temporal
106 es in skeletal decalcification and providing photosynthate to bleached corals that have lost their di
107 is a preferred route of carbon from imported photosynthate to seed oil in the embryo.
108                            The conversion of photosynthate to seed storage reserves is crucial to pla
109 s closely coordinated with the production of photosynthate to supply nutrients for growth.
110 his is noteworthy since these leaves provide photosynthate to the developing grain.
111 on cycles as plant hosts divert up to 20% of photosynthate to the obligate biotrophic fungi.
112 to SUSIBA2 rice, favouring the allocation of photosynthates to aboveground biomass over allocation to
113 hat NTS and SSS can enhance translocation of photosynthates to grains during the post-anthesis stage.
114 ensitivity of the critical pathway of recent photosynthate transfer from plants to soil organisms to
115 tes to retention of fixed carbon by favoring photosynthate translocation to the host.
116 iologically-driven mechanism associated with photosynthate transport in yielding the observed pattern
117                            Whether increased photosynthates under elevated atmospheric CO(2) could tr
118 cular mycorrhizal fungi (AMF) transfer plant photosynthate underground which can stimulate soil micro
119 led the SGA biosynthetic pathways from CO(2) photosynthates via early precursors to the SGAs.
120 ed quantifying the relative fractions of new photosynthate vs stored C used in root growth and root r
121 n Rsoil suggests that under eCO2, additional photosynthate was produced, transported belowground, and
122 m a closed network that transports essential photosynthates, water and signaling molecules to the dev
123 New fine-root growth was largely from recent photosynthate, while nearly one-quarter of respired C wa
124                    Tomato fruit are sinks of photosynthate, yet unripe green fruit contribute signifi

 
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