2009
DOI: 10.1127/1863-9135/2009/0175-0307
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Nitrogen stable isotope ratios of lake macrophytes in relation to growth form and nutrient-limitation

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Cited by 10 publications
(9 citation statements)
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“…Hawassa, Ziway and Koka showed a wide variation in δ 13 C, δ 34 S and δ 15 N values. The δ 15 N values of macrophyte taxa were variable with a range of about 12‰, which, however, is in accordance with several studies (King et al, 2009;and cited therein). Similarly, the δ 13 C of macrophytes were much more variable reaching differences up to 20‰ (Table 1), which appears large as freshwater macrophytes belong to the C3 group of plants (Beer & Wetzel, 1982).…”
Section: Stable Isotope Compositionsupporting
confidence: 92%
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“…Hawassa, Ziway and Koka showed a wide variation in δ 13 C, δ 34 S and δ 15 N values. The δ 15 N values of macrophyte taxa were variable with a range of about 12‰, which, however, is in accordance with several studies (King et al, 2009;and cited therein). Similarly, the δ 13 C of macrophytes were much more variable reaching differences up to 20‰ (Table 1), which appears large as freshwater macrophytes belong to the C3 group of plants (Beer & Wetzel, 1982).…”
Section: Stable Isotope Compositionsupporting
confidence: 92%
“…The nitrogen nutrition of the primary producers in Lake Koka could be NH4+ (162.4 ± 49.4 μg/L, ± SD ), the primary form of nitrogen in the lake, leading to high δ 15 N values in successive trophic levels. In contrary, in phosphorus‐limited system, where N is in excess of demand, plant uptake of N exhibits fractionation against the heavier 15 N isotope leading to lower plant δ 15 N values (King et al., ; Montoya, ), a possible cause for Lake Hawassa lower delta values (Table ; Lake Hawassa soluble reactive phosphorus, 6.00 ± 1.23 μg/L, was low compared to Lake Koka 34.36 ± 5.53 μg/L, ± SD ). Nevertheless, the studied rift valley lakes have high δ 15 N values compared to other lakes (Rao et al., ).…”
Section: Discussionmentioning
confidence: 99%
“…Species that exclusively use nitrogen from the water column (e.g., rootless vascular plants such as Utricularia spp. and mosses) show lower average δ 15 N values than species that use nitrogen from the sediment pore water (King et al., ). No differences were seen among functional groups in our dataset due to a lack of species primarily using nitrogen from the water column, since most species also obtained nitrogen from the sediment pore water, and probably to a large and uncoupled δ 15 N variability of DIN in water and pore water.…”
Section: Discussionmentioning
confidence: 99%
“…One reason could be that most samples were from rooted aquatic plants, which mainly used DIN from the sediment pore water (Barko et al, 1991), whose concentration did not necessarily correlate with water column DIN (Gacia, Chappuis, Lumbreras, Riera, & Ballesteros, 2009). The concentration of other nutrients and their stoichiometry can also be important factors (King et al, 2009;Pastor et al, 2013). For example, plants thriving in phosphorus limited ecosystems tend to have a lower demand relative to the nitrogen source and discrimination is likely to occur, which results in low plant d 15 N (King et al, 2009).…”
Section: Variation Of D 15 N In Aquatic Plants From Stagnant Water mentioning
confidence: 99%
“…in ULC and LLC which leads to the assumption that the δ 15 N values are related to differences in nutrient loads. [35] Chara spp. can utilize nitrogen from sediment or from the water column.…”
mentioning
confidence: 99%