Stable oxygen isotope ratios of plant water (sap water) were observed at Spasskaya Pad experimental forest near Yakutsk, Russia in 1997–1999. The δ18O of sap water in larch trees (Larix gmelinii) decreased soon after leaf unfolding every year, indicating that snowmelt water was used in the beginning of summer. During mid to late summer, a clear difference in the water source used by plants was observed between wet summers and severe drought summers. The δ18O values of water in larch trees were high (−17.8 to −16.1‰) in August 1999 (wet summer), but low (−20.4 to −19.7‰) in August 1998 (drought summer). These results indicated that plants used rainwater during a wet summer, but meltwater from permafrost was used by plants during a drought summer. One important role of permafrost is to provide a direct source of water for plants in a severe drought summer; another role is to keep surplus water in the soil until the next summer. If this permafrost system is disturbed by future global warming, unique monotypic stands of deciduous larch trees in east Siberia might be seriously damaged in a severe drought summer.

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Distribution patterns along a slope and vertical root distribution were compared among seven major woody species in a secondary forest of the warm‐temperate zone in central Japan in relation to differences in soil moisture profiles through a growing season among different positions along the slope. Pinus densiflora, Juniperus rigida, Ilex pedunculosa and Lyonia ovalifolia, growing mostly on the upper part of the slope with shallow soil depth had shallower roots. Quercus serrata and Quercus glauca, occurring mostly on the lower slope with deep soil showed deeper rooting. Styrax japonica, mainly restricted to the foot slope, had shallower roots in spite of growing on the deepest soil. These relations can be explained by the soil moisture profile under drought at each position on the slope. On the upper part of the slope and the foot slope, deep rooting brings little advantage in water uptake from the soil due to the total drying of the soil and no period of drying even in the shallow soil, respectively. However, deep rooting is useful on the lower slope where only the deep soil layer keeps moist. This was supported by better diameter growth of a deep‐rooting species on deeper soil sites than on shallower soil sites, although a shallow‐rooting species showed little difference between them.

Laboratory colonies of Capitella sp., which 1s found densely distributed in organically enriched or polluted areas, were cultured in sediments with various levels of organic matter to examine the relationship between level of sediment organic matter and growth of individuals. Growth was independent of absolute levels of sediment organic matter, but was significantly correlated with increases in the level of sediment organic matter on addition of algal powder to the sediment. These results indicate that Capitella species predominating in organically enriched areas have a physiological requirement for organic materials discharged from sources of organic enrichment, e.g, abundant growth of algae, fish farming, industrial effluent, sewage, if they are to grow normally. Although associat~on of some Capitella species with sediment organic enrichment has been previously recognized as a reflection of their opportunistic characteristics, a physiological requirement for organic materials discharged from sources of organic enrichment may be the single factor most responsible for the concentration of CapiteNa species in organically enriched areas. However, it is unlikely that they can directly ingest and assimilate such organic materials. Since the additional organic materials are easily decomposed in the sediment, Capitella species may require either (1) some specific microorganisms, the levels of which increase with levels of the organic materials, or (2) certain substance(s) produced during decomposition of the organic materials.

Variation in stable nitrogen isotope ratios (δ15N) was assessed for plants comprising two wetland communities, a bog‐fen system and a flood plain, in central Japan. δ15N of 12 species from the bog‐fen system and six species from the flood plain were remarkably variable, ranging from −5.9 to +1.1‰ and from +3.1 to +8.7‰, respectively. Phragmites australis exhibited the highest δ15N value at both sites. Rooting depth also differed greatly with plant species, ranging from 5 cm to over 200 cm in the bog‐fen system. There was a tendency for plants having deeper root systems to exhibit higher δ15N values; plant δ15N was positively associated with rooting depth. Moreover, an increasing gradient of peat δ15N was found along with depth. This evidence, together with the fact that inorganic nitrogen was depleted under a deep‐rooted Phragmites australis stand, strongly suggests that deep‐rooted plants actually absorb nitrogen from the deep peat layer. Thus, we successfully demonstrated the diverse traits of nitrogen nutrition among mire plants using stable isotope analysis. The ecological significance of deep rooting in mire plants is that it enables those plants to monopolize nutrients in deep substratum layers. This advantage should compensate for any consequential structural and/or physiological costs. Good evidence of the benefits of deep rooting is provided by the fact that Phragmites australis dominates as a tall mire grass.