2007
DOI: 10.1016/j.soilbio.2007.05.013
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Methane emissions from stems of Fraxinus mandshurica var. japonica trees in a floodplain forest

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Cited by 103 publications
(94 citation statements)
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“…However, microbial production of CH 4 in the wet heartwood of trees has been known for at least 40 yr (Zeikus and Ward, 1974). Furthermore, trees can transport and release CH 4 from soil water (Gauci et al, 2010;Terazawa et al, 2007). Laboratory studies have shown that aerobic CH 4 emissions from vegetation could be triggered by UV radiation and heating (Vigano et al, 2008), but emissions in the absence of UV have also been measured, although at much lower rates (Bruhn et al, 2009).…”
Section: Impact Of Vegetationmentioning
confidence: 99%
See 1 more Smart Citation
“…However, microbial production of CH 4 in the wet heartwood of trees has been known for at least 40 yr (Zeikus and Ward, 1974). Furthermore, trees can transport and release CH 4 from soil water (Gauci et al, 2010;Terazawa et al, 2007). Laboratory studies have shown that aerobic CH 4 emissions from vegetation could be triggered by UV radiation and heating (Vigano et al, 2008), but emissions in the absence of UV have also been measured, although at much lower rates (Bruhn et al, 2009).…”
Section: Impact Of Vegetationmentioning
confidence: 99%
“…Even if CH 4 emissions are sporadic and limited to restricted areas, their occurrence frequency and source strength might turn a forest from a net sink to a net source of CH 4 (Fiedler et al, 2005;Sakabe et al, 2012). The capacity of plants with roots in CH 4 -rich water-saturated soils, even woody plants, to transport and release CH 4 (Terazawa et al, 2007;Gauci et al, 2010) adds another level of the complexity to the analyses.…”
Section: Introductionmentioning
confidence: 99%
“…In a very wet forest with thick moss mats, epiphytes, and termites in the canopy, anaerobic microbial emission is possible (do Carmo et al, 2006), but our forest has a dry canopy except immediately after rain events, and no similar organic microbial habitat within the canopy or termites. The possibility exists for deep soil anaerobic microbial CH 4 production, followed by transport through the stem and out through the stomata, but this mechanism is highly speculative at present except for flood-adapted species that possess aerenchyma (Rusch and Rennenberg, 1998;Terazawa et al, 2007;Megonigal and Guenther, 2008). The evening wind direction reversal from somewhat-polluted to relatively-cleaner flow at Niwot Ridge (Fig.…”
Section: Within-canopy Gradients Daytime Excess and Canopy Fluxesmentioning
confidence: 99%
“…Until recently, the role of living plants in the methane cycle was thought to be limited to transport of microbiallyproduced CH 4 through aerenchyma in herbaceous wetland plants and some woody plants (Schimel, 1995;Rusch and D. R. Bowling et al: Soil, plant, and transport influences on methane Rennenberg, 1998;Terazawa et al, 2007). A recent paper by Keppler et al (2006) suggested the intriguing possibility that vascular plants emit CH 4 directly, under aerobic conditions, and without the involvement of microorganisms.…”
Section: Introductionmentioning
confidence: 99%
“…Although a large amount of CH 4 has been shown to come through emergent wetland plants (Shannon et al, 1996), physiological correlations for tree emission of CH 4 have been studied very little and the role that woody vegetation has in wetland emission of CH 4 is still poorly understood (Vann 25 and Megonigal, 2003;Terazawa et al, 2007). It should be mentioned that more recently, Pangala et al (2014) did find a strong correlation between lenticel density and CH 4 flux from stems in the tree species Alnus glutinosa.…”
mentioning
confidence: 99%