Street, Lorna E; Shaver, Gauis R; Rastetter, Edward B; van Wijk, Mark T; Kaye, Brooke A; Williams, Mathew (2012): (Table 3) Leaf area and leaf nitrogen for deciduous, evergreen, forb and graminoid species at Barrow, Svalbard and Zackenberg [dataset]. PANGAEA, https://doi.org/10.1594/PANGAEA.837943, Supplement to: Street, LE et al. (2012): Incident radiation and the allocation of nitrogen within Arctic plant canopies: implications for predicting gross primary productivity. Global Change Biology, 18(9), 2838-2852, https://doi.org/10.1111/j.1365-2486.2012.02754.x
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Abstract:
Arctic vegetation is characterized by high spatial variability in plant functional type (PFT) composition and gross primary productivity (P). Despite this variability, the two main drivers of P in sub-Arctic tundra are leaf area index (LT) and total foliar nitrogen (NT). LT and NT have been shown to be tightly coupled across PFTs in sub-Arctic tundra vegetation, which simplifies up-scaling by allowing quantification of the main drivers of P from remotely sensed LT. Our objective was to test the LT-NT relationship across multiple Arctic latitudes and to assess LT as a predictor of P for the pan-Arctic. Including PFT-specific parameters in models of LT-NT coupling provided only incremental improvements in model fit, but significant improvements were gained from including site-specific parameters. The degree of curvature in the LT-NT relationship, controlled by a fitted canopy nitrogen extinction co-efficient, was negatively related to average levels of diffuse radiation at a site. This is consistent with theoretical predictions of more uniform vertical canopy N distributions under diffuse light conditions. Higher latitude sites had higher average leaf N content by mass (NM), and we show for the first time that LT-NT coupling is achieved across latitudes via canopy-scale trade-offs between NM and leaf mass per unit leaf area (LM). Site-specific parameters provided small but significant improvements in models of P based on LT and moss cover. Our results suggest that differences in LT-NT coupling between sites could be used to improve pan-Arctic models of P and we provide unique evidence that prevailing radiation conditions can significantly affect N allocation over regional scales.
Project(s):
Coverage:
Median Latitude: 74.891020 * Median Longitude: -53.069833 * South-bound Latitude: 71.300000 * West-bound Longitude: -156.667000 * North-bound Latitude: 78.900000 * East-bound Longitude: 18.010000
Minimum Elevation: 7.0 m * Maximum Elevation: 7.0 m
Event(s):
Comment:
Data extracted in the frame of a joint ICSTI/PANGAEA IPY effort, see http://doi.pangaea.de/10.1594/PANGAEA.150150
Parameter(s):
# | Name | Short Name | Unit | Principal Investigator | Method/Device | Comment |
---|---|---|---|---|---|---|
1 | Area/locality | Area | Street, Lorna E | |||
2 | Latitude of event | Latitude | ||||
3 | Longitude of event | Longitude | ||||
4 | Species | Species | Street, Lorna E | |||
5 | Sample amount | N | # | Street, Lorna E | ||
6 | Vegetation type | Vegetation type | Street, Lorna E | D = deciduous, E = evergreen, F = forb, G = graminoid | ||
7 | Nitrogen per area | N area | g/m2 | Street, Lorna E | per leaf area | |
8 | Nitrogen, standard deviation | N std dev | ± | Street, Lorna E | N/area | |
9 | Nitrogen, organic | N org | mg/kg | Street, Lorna E | per leaf mass | |
10 | Nitrogen, standard deviation | N std dev | ± | Street, Lorna E | N/mass | |
11 | Leaf area, specific, per mass dry weight | LA spec DW | mm2/mg | Street, Lorna E | ||
12 | Standard deviation | Std dev | ± | Street, Lorna E | leaf area |
License:
Creative Commons Attribution 3.0 Unported (CC-BY-3.0)
Size:
300 data points
Data
1 Area | 2 Latitude | 3 Longitude | 4 Species | 5 N [#] | 6 Vegetation type (D = deciduous, E = evergreen,...) | 7 N area [g/m2] (per leaf area) | 8 N std dev [±] (N/area) | 9 N org [mg/kg] (per leaf mass) | 10 N std dev [±] (N/mass) | 11 LA spec DW [mm2/mg] | 12 Std dev [±] (leaf area) |
---|---|---|---|---|---|---|---|---|---|---|---|
Barrow | 71.30 | -156.67 | Salix phlebophylla | 7 | D | 1.76 | 0.09 | 23300 | 1800 | 13.2 | 0.3 |
Barrow | 71.30 | -156.67 | Stellaria species | 9 | F | 1.43 | 0.17 | 22400 | 1600 | 17.4 | 2.2 |
Barrow | 71.30 | -156.67 | Saxifraga cernua | 8 | F | 0.95 | 0.07 | 19400 | 1300 | 20.6 | 1.0 |
Barrow | 71.30 | -156.67 | Dupontia fisheri | 15 | G | 2.21 | 0.17 | 23100 | 1000 | 11.2 | 0.8 |
Barrow | 71.30 | -156.67 | Eriophorum scheuchzeri | 10 | G | 2.51 | 0.23 | 30300 | 1900 | 12.5 | 0.6 |
Barrow | 71.30 | -156.67 | Other grasses | 9 | G | 1.73 | 0.14 | 19300 | 1000 | 11.5 | 0.6 |
Svalbard | 78.90 | 18.01 | Salix polaris | 34 | D | 1.75 | 0.05 | 24200 | 800 | 13.9 | 0.4 |
Svalbard | 78.90 | 18.01 | Dryas octopetala | 21 | E | 2.68 | 0.13 | 20200 | 600 | 8.1 | 0.8 |
Svalbard | 78.90 | 18.01 | Cassiope tetragona | 6 | E | 2.16 | 0.20 | 19800 | 1200 | 4.6 | 0.2 |
Svalbard | 78.90 | 18.01 | Polygonum viviparum | 35 | F | 2.06 | 0.07 | 30800 | 300 | 15.5 | 0.5 |
Svalbard | 78.90 | 18.01 | Other forbs | 20 | F | 1.88 | 0.20 | 24900 | 1100 | 15.1 | 1.3 |
Svalbard | 78.90 | 18.01 | Equisetum species | 30 | P | 3.14 | 0.18 | 28400 | 1300 | 9.5 | 0.5 |
Svalbard | 78.90 | 18.01 | Carex species | 9 | G | 1.90 | 0.17 | 19300 | 1300 | 10.6 | 0.9 |
Svalbard | 78.90 | 18.01 | Dupontia fisheri | 5 | G | 2.09 | 0.20 | 16100 | 1300 | 7.8 | 0.2 |
Svalbard | 78.90 | 18.01 | Other graminoids | 32 | G | 2.32 | 0.10 | 21600 | 600 | 9.7 | 0.3 |
Zackenberg | 74.47 | -20.55 | Salix arctica | 58 | D | 2.18 | 0.08 | 30900 | 1000 | 14.4 | 0.6 |
Zackenberg | 74.47 | -20.55 | Arctostaphylos alpina | 14 | D | 2.87 | 0.20 | 31100 | 2000 | 11.1 | 0.6 |
Zackenberg | 74.47 | -20.55 | Vaccinium uliginosum | 14 | D | 1.44 | 0.05 | 24600 | 1300 | 16.2 | 1.5 |
Zackenberg | 74.47 | -20.55 | Dryas species | 23 | E | 2.12 | 0.09 | 16000 | 700 | 8.0 | 0.5 |
Zackenberg | 74.47 | -20.55 | Cassiope tetragona | 22 | E | 2.15 | 0.19 | 23200 | 600 | 5.8 | 0.4 |
Zackenberg | 74.47 | -20.55 | Polygonum viviparum | 37 | F | 4.01 | 1.09 | 38300 | 1000 | 15.9 | 1.3 |
Zackenberg | 74.47 | -20.55 | Stellaria species | 16 | F | 2.15 | 0.57 | 27000 | 1500 | 17.6 | 1.9 |
Zackenberg | 74.47 | -20.55 | Pedicularis species | 8 | F | 2.40 | 0.23 | 36200 | 3700 | 16.1 | 2.5 |
Zackenberg | 74.47 | -20.55 | Equisetum species | 12 | P | 2.62 | 0.10 | 27300 | 1900 | 10.4 | 0.5 |
Zackenberg | 74.47 | -20.55 | Carex species | 8 | G | 2.17 | 0.22 | 24900 | 1900 | 11.8 | 0.8 |
Zackenberg | 74.47 | -20.55 | Dupontia species | 6 | G | 2.45 | 0.21 | 21300 | 2700 | 8.6 | 0.7 |
Zackenberg | 74.47 | -20.55 | Eriophorum species | 6 | G | 2.47 | 0.12 | 25900 | 1600 | 10.7 | 0.9 |
Zackenberg | 74.47 | -20.55 | Other graminoids | 28 | G | 4.47 | 2.03 | 24900 | 1400 | 11.1 | 1.1 |
Zackenberg | 74.47 | -20.55 | Other grasses | 18 | G | 5.07 | 1.69 | 28600 | 1600 | 8.2 | 0.9 |
Zackenberg | 74.47 | -20.55 | Other sedges | 5 | G | 2.25 | 0.26 | 24900 | 2100 | 11.5 | 1.2 |