ライフサイエンスコーパス: allelopathic

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1 The allelopathic activity of naturally occurring quinones an

2 en bromide (BrCN), which exhibits pronounced allelopathic activity.

3 polyacetylenes, whose major constituent was allelopathic against a heterospecific competitor, Poa pr

4 s a number of phytoalexins, and at least one allelopathic agent, from syn-copalyl diphosphate (CPP),

5 ay-guided fractionation of extracts from two allelopathic algae led to identification of two loliolid

6 corals varied markedly in susceptibility to allelopathic algae, with globally declining corals such

7 Allelopathic chemicals released by plants into the rhizo

8 and the quinone head of sorgoleone, the main allelopathic component of the oily root exudate of Sorgh

9 Allelopathic compounds appear to target multiple physiol

10 o be mediated by the increased production of allelopathic compounds in S. altissima.

11 invasion success is partially attributed to allelopathic compounds release and more benefits from AM

12 anipulation to ablate production of putative allelopathic compounds, but such an approach previously

13 Sorghum bicolor is considered to be an allelopathic crop species, producing phytotoxins such as

14 Sorghum is considered to be one of the more allelopathic crop species, producing phytotoxins such as

15 ill suppress seaweeds and lower frequency of allelopathic damage to corals if reefs retain intact foo

16 unity dynamics should A. petiolata (which is allelopathic) decline.

17 We show that allelopathic effects are H(2)O(2) dependent and link BrC

18 oplankton, presumably through the release of allelopathic exotoxins that offer advantages for Prymnes

19 oid corals that had been in contact with the allelopathic Galaxaura filamentosa, suggesting that chem

20 Allelopathic interactions and resource competition have

21 d light has been studied for many years, but allelopathic interactions between them have been more di

22 highlight the importance of competitive and allelopathic interactions in regulating the occurrence o

23 that an McC-like molecule is involved in the allelopathic interactions with CC9605.

24 regularly applied either green leaves of the allelopathic invader Alliaria petiolata, a nonsystemic f

25 f native species in ecosystems challenged by allelopathic invaders: RFS mutualism disruption drives c

26 rial parts on their chemical composition and allelopathic potential, assessed on lettuce germination

27 olor), is likely responsible for much of the allelopathic properties of sorghum root exudates against

28 leone, which likely accounts for many of the allelopathic properties of Sorghum spp.

29 in T. versicolor root tips treated with the allelopathic quinone 2,6-dimethoxybenzoquinone (DMBQ).

30 parasitic plant Triphysaria treated with the allelopathic quinone 2,6-dimethoxybenzoquinone (DMBQ).

31 hat TvQR2-like proteins function to detoxify allelopathic quinones in the rhizosphere, while TvQR1 ha

32 a primary response to treatment with various allelopathic quinones.

33 These patterns suggest that allelopathic seaweed-coral interactions can be important

34 genetic variation in the concentration of an allelopathic secondary compound in Brassica nigra is nec

35 nutrients, many plant species have developed allelopathic strategies to suppress competitors.

36 quency of seaweed-coral contacts, increasing allelopathic suppression of remaining corals, and contin

37 K. brevis is variably allelopathic to multiple competitors, typically causing

38 anges likely stem in part from reductions in allelopathic traits in the invader and evolution of tole

39 l agents, enhancement of crop competition or allelopathic traits, and production of cover crops that

40 allelopathy, and (iii) that one macroalga is allelopathic under conditions of elevated CO2, but not a

41 Rankings of macroalgae from most to least allelopathic were similar across the three coral genera

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