Walter, Hans-Jürgen; Rutgers van der Loeff, Michiel M; Francois, Roger (1999): Compilation of 231Protactinium/230 Thorium excess ratios in various surface sediment samples from the South Atlantic [dataset]. PANGAEA, https://doi.org/10.1594/PANGAEA.55674, Supplement to: Walter, H-J et al. (1999): Reliability of the 231Pa/230Th Activity Ratio as a Tracer for Bioproductivity of the Ocean. In: Fischer, G & Wefer, G (eds.), Use of Proxies in Paleoceanography - Examples from the South Atlantic, Springer, Berlin, Heidelberg, 393-408
Always quote citation above when using data! You can download the citation in several formats below.
Abstract:
In large areas of the world's oceans, there is a relationship between the mass flux of particulate matter and the unsupported 231Pa/230Th (xs231Pa/xs230Th) activity ratio of recent sediments. This observation forms the basis for using the xs231Pa/xs230Th ratio as a proxy for past changes in export productivity. However, a simple relationship between xs231Pa/xs 230Th ratio and particle flux requires that the water residence time in an ocean basin is far in excess of the scavenging residence time of 231Pa, and that the composition of sinking particles maintains a strong preference for the adsorption of 230Th over 231Pa with a constant 230Th/231Pa fractionation factor (F). The best correlation between xs231Pa/xs230Th ratio and mass flux is found in the Pacific Ocean. In the Atlantic, the contrast in the xs231Pa/xs230Th ratios between open ocean (low flux regions) and ocean margins (high flux regions) is much less pronounced due to the shorter residence time of deep water, resulting in less effective boundary scavenging of 231Pa. In the Southern Ocean, south of the Polar Front, there is no more a simple relationship between xs231Pa/xs230Th and particle flux. This is a result of a southward decrease in F, probably reflecting the increased opal content of sinking particles. Opal does not fractionate 231Pa and 230Th significantly. This lack of fractionation results in high xs231Pa/xs230Th ratios in opal-dominated regions, even in areas of very low particle fluxes such as the Weddell Sea. The xs231Pa/xs230Th ratio can therefore only be used as a paleoproductivity proxy if, in the time interval of interest, changes in the basin ventilation rate and differential scavenging of both radionuclides due to changes in the chemical composition of particulate matter can be excluded.
Project(s):
Marine Geochemistry @ AWI (AWI_MarGeoChem)
Coverage:
Median Latitude: -7.143739 * Median Longitude: -121.539218 * South-bound Latitude: -76.413300 * West-bound Longitude: 0.000000 * North-bound Latitude: 77.460000 * East-bound Longitude: -3.206670
Minimum Elevation: 0.0 m * Maximum Elevation: 0.0 m
Event(s):
SURWalter1999 * Elevation Start: 0.0 m * Elevation End: 0.0 m * Campaign: compiled data * Method/Device: Multiple investigations (MULT) * Comment: This is a virtual site to link a compiled data set from ocean bottom sediments
Parameter(s):
# | Name | Short Name | Unit | Principal Investigator | Method/Device | Comment |
---|---|---|---|---|---|---|
1 | Sample code/label | Sample label | data compiled from different sources | |||
2 | LATITUDE | Latitude | Geocode | |||
3 | LONGITUDE | Longitude | Geocode | |||
4 | Depth, top/min | Depth top | m | data compiled from different sources | ||
5 | Depth, bottom/max | Depth bot | m | data compiled from different sources | ||
6 | Protactinium-231/Thorium-230 excess | 231Pa/230Th xs | see reference(s) | data compiled from different sources | ||
7 | Protactinium-231/Thorium-230 excess, standard deviation | 231Pa/230Th xs std dev | ± | see reference(s) | data compiled from different sources | |
8 | Reference/source | Reference | Walter, Hans-Jürgen |
License:
Creative Commons Attribution 3.0 Unported (CC-BY-3.0)
Size:
1917 data points
Data
1 Sample label | 2 Latitude | 3 Longitude | 4 Depth top [m] | 5 Depth bot [m] | 6 231Pa/230Th xs | 7 231Pa/230Th xs std dev [±] | 8 Reference |
---|---|---|---|---|---|---|---|
PS1991-1 | -76.4133 | -30.3533 | 0.000 | 0.050 | 0.080 | 0.009 | Walter et al. (1997) |
PS2011-1 | -71.0950 | -20.7800 | 0.000 | 0.010 | 0.161 | 0.009 | Walter et al. (1997) |
PS1981-1 | -70.1317 | -14.2533 | 0.005 | 0.020 | 0.143 | 0.008 | Walter et al. (1997) |
PS2684-1 | -69.4167 | -95.0233 | 0.000 | 0.005 | 0.172 | 0.004 | Walter (unpubl.) |
PS1979-1 | -69.3667 | -16.4967 | 0.005 | 0.020 | 0.146 | 0.008 | Walter et al. (1997) |
PS2049-3 | -69.0867 | 0.8900 | 0.000 | 0.050 | 0.105 | 0.006 | Walter et al. (1997) |
PS2039-2 | -69.0233 | 6.2283 | 0.000 | 0.050 | 0.151 | 0.009 | Walter et al. (1997) |
PS2040-1 | -68.8417 | 6.2350 | 0.000 | 0.010 | 0.134 | 0.008 | Walter et al. (1997) |
PS1978-1 | -68.8400 | -17.8933 | 0.005 | 0.020 | 0.161 | 0.008 | Walter et al. (1997) |
PS2686-2 | -68.3217 | -89.6267 | 0.000 | 0.005 | 0.175 | 0.006 | Walter (unpubl.) |
PS2055-3 | -68.2900 | 6.2483 | 0.000 | 0.012 | 0.170 | 0.010 | Walter et al. (1997) |
PS1976-1 | -67.8417 | -20.8450 | 0.005 | 0.020 | 0.184 | 0.011 | Walter et al. (1997) |
PS1968-1 | -67.4783 | -31.1100 | 0.000 | 0.005 | 0.161 | 0.010 | Walter et al. (1997) |
PS1974-1 | -67.2217 | -24.1467 | 0.005 | 0.020 | 0.162 | 0.008 | Walter et al. (1997) |
PS2052-2 | -66.8050 | 6.2633 | 0.000 | 0.010 | 0.178 | 0.009 | Walter et al. (1997) |
PS1966-1 | -66.6267 | -27.1250 | 0.000 | 0.005 | 0.174 | 0.009 | Walter et al. (1997) |
PS1964-1 | -66.2767 | -30.2967 | 0.005 | 0.020 | 0.144 | 0.009 | Walter et al. (1997) |
PS2589-2 | -66.0017 | 24.9767 | 0.000 | 0.050 | 0.147 | 0.006 | Walter et al. (1997) |
PS1961-1 | -65.7200 | -35.4483 | 0.005 | 0.020 | 0.136 | 0.008 | Walter et al. (1997) |
PS1957-1 | -65.6717 | -37.7433 | 0.000 | 0.005 | 0.145 | 0.007 | Walter et al. (1997) |
PS1959-1 | -65.4117 | -37.9133 | 0.000 | 0.005 | 0.148 | 0.007 | Walter et al. (1997) |
PS2692-1 | -65.1383 | -90.6833 | 0.000 | 0.005 | 0.139 | 0.006 | Walter (unpubl.) |
E11-11 | -64.8333 | -114.4670 | 0.000 | 0.050 | 0.078 | 0.003 | Ku (1966) |
PS1955-1 | -64.8200 | -42.5033 | 0.000 | 0.005 | 0.160 | 0.010 | Walter et al. (1997) |
PS1954-1 | -64.4067 | -45.8033 | 0.005 | 0.020 | 0.142 | 0.008 | Walter et al. (1997) |
PS2600-2 | -63.1833 | 34.5267 | 0.000 | 0.050 | 0.154 | 0.006 | Walter et al. (1997) |
E17-9 | -63.0833 | -135.1170 | 0.070 | 0.100 | 0.148 | 0.005 | Lao et al. (1992) |
PS2697-1 | -62.9967 | -89.9967 | 0.000 | 0.005 | 0.119 | 0.004 | Walter (unpubl.) |
PS2579-4 | -62.9633 | 7.7733 | 0.000 | 0.050 | 0.163 | 0.009 | Walter et al. (1997) |
PS2578-3 | -62.1233 | 5.0300 | 0.000 | 0.050 | 0.131 | 0.006 | Walter et al. (1997) |
PS2678-2 | -61.5000 | -97.6850 | 0.000 | 0.005 | 0.133 | 0.005 | Walter (unpubl.) |
PS2577-2 | -61.2200 | 2.1950 | 0.000 | 0.005 | 0.095 | 0.004 | Walter et al. (1997) |
PS2072-2 | -60.5650 | 3.9600 | 0.000 | 0.010 | 0.166 | 0.007 | Walter et al. (1997) |
PS2602-3 | -60.3750 | 36.5817 | 0.000 | 0.050 | 0.154 | 0.007 | Walter et al. (1997) |
PS2320-2 | -60.1000 | -44.8467 | 0.000 | 0.010 | 0.125 | 0.007 | Walter et al. (1997) |
E15-6 | -59.9667 | -101.3170 | 0.040 | 0.070 | 0.097 | 0.006 | Lao et al. (1992) |
PS2312-1 | -59.8267 | -39.7050 | 0.000 | 0.010 | 0.188 | 0.012 | Walter et al. (1997) |
PS2283-6 | -59.7350 | -23.2750 | 0.000 | 0.010 | 0.149 | 0.008 | Walter et al. (1997) |
RC 13 271 | -59.6500 | 4.5167 | 0.140 | 0.160 | 0.127 | 0.006 | DeMaster (1979) |
PS2575-1a | -59.4467 | -3.2067 | 0.000 | 0.005 | 0.179 | 0.010 | Walter et al. (1997) |
PS2307-2 | -59.0583 | -35.5767 | 0.000 | 0.010 | 0.142 | 0.008 | Walter et al. (1997) |
PS2331-1a | -59.0400 | -48.9933 | 0.000 | 0.010 | 0.105 | 0.008 | Walter et al. (1997) |
PS2370-4 | -58.4867 | -5.9983 | 0.000 | 0.050 | 0.140 | 0.008 | Walter et al. (1997) |
PS2334-1a | -57.9183 | -52.0000 | 0.000 | 0.010 | 0.090 | 0.005 | Walter et al. (1997) |
PS2675-4 | -57.8817 | -93.5017 | 0.000 | 0.005 | 0.101 | 0.003 | Walter (unpubl.) |
PS2288-1 | -57.7567 | -25.3367 | 0.000 | 0.010 | 0.162 | 0.011 | Walter et al. (1997) |
PS2604-4 | -57.5983 | 38.5900 | 0.000 | 0.050 | 0.161 | 0.009 | Walter et al. (1997) |
PS2299-1 | -57.5100 | -30.2350 | 0.000 | 0.010 | 0.149 | 0.008 | Walter et al. (1997) |
PS2714-6 | -57.4467 | -89.2717 | 0.000 | 0.005 | 0.098 | 0.004 | Walter (unpubl.) |
PS2336-1a | -57.1517 | -53.9883 | 0.000 | 0.010 | 0.123 | 0.006 | Walter et al. (1997) |
PS2371-1 | -57.0550 | -6.0083 | 0.000 | 0.050 | 0.176 | 0.009 | Walter et al. (1997) |
PS2280-1 | -56.8283 | -22.3250 | 0.000 | 0.010 | 0.130 | 0.007 | Walter et al. (1997) |
PS2364-1 | -56.0717 | -6.8433 | 0.000 | 0.050 | 0.130 | 0.008 | Walter et al. (1997) |
PS2339-1a | -56.0317 | -56.9433 | 0.000 | 0.010 | 0.112 | 0.006 | Walter et al. (1997) |
PS2369-4 | -55.8517 | -5.9933 | 0.000 | 0.050 | 0.159 | 0.007 | Walter et al. (1997) |
PS2667-3 | -55.6517 | -89.8150 | 0.000 | 0.005 | 0.096 | 0.003 | Walter (unpubl.) |
PS1772-6 | -55.4583 | 1.1667 | 0.010 | 0.020 | 0.152 | 0.009 | Walter et al. (1997) |
PS2342-1a | -55.2583 | -57.9850 | 0.000 | 0.010 | 0.132 | 0.009 | Walter et al. (1997) |
PS1782-8 | -55.1900 | -18.6100 | 0.000 | 0.050 | 0.155 | 0.008 | Walter et al. (1997) |
PS2365-2 | -55.0083 | -6.0050 | 0.000 | 0.050 | 0.256 | 0.015 | Walter et al. (1997) |
PS2361-1 | -55.0017 | -6.0467 | 0.000 | 0.050 | 0.238 | 0.013 | Walter et al. (1997) |
AII 107-022 | -54.8000 | -3.3333 | 0.030 | 0.040 | 0.231 | 0.014 | Yu (1994) |
PS2276-2 | -54.6350 | -23.9550 | 0.000 | 0.010 | 0.120 | 0.007 | Walter et al. (1997) |
RC 13 255 | -54.5833 | 2.9000 | 0.040 | 0.070 | 0.143 | 0.008 | DeMaster (1979) |
RC 11 76 | -54.3833 | -22.1333 | 0.100 | 0.130 | 0.193 | 0.017 | DeMaster (1979) |
PS2372-1 | -53.9967 | -6.0033 | 0.000 | 0.050 | 0.094 | 0.005 | Walter et al. (1997) |
RC-13-259 | -53.8833 | -4.9333 | 0.230 | 0.230 | 0.213 | 0.009 | Kumar (1994) |
PS2353-2a | -53.6067 | -58.9767 | 0.000 | 0.010 | 0.094 | 0.008 | Walter et al. (1997) |
RC 13 259 | -53.5500 | 4.9333 | 0.050 | 0.080 | 0.294 | 0.026 | DeMaster (1979) |
RC 17-58 | -53.5167 | 36.6333 | 0.070 | 0.090 | 0.111 | 0.007 | DeMaster (1979) |
PS2362-1 | -53.0017 | -5.9983 | 0.000 | 0.050 | 0.172 | 0.010 | Walter et al. (1997) |
AII 76-16 | -53.0000 | 35.6333 | 0.000 | 0.010 | 0.123 | 0.007 | DeMaster (1979) |
PS2273-2 | -52.6567 | -30.5517 | 0.000 | 0.010 | 0.119 | 0.007 | Walter et al. (1997) |
PS1768-1 | -52.5917 | 4.4600 | 0.010 | 0.020 | 0.114 | 0.008 | Walter et al. (1997) |
RC-13-271 | -51.9833 | 4.5167 | 0.310 | 0.310 | 0.110 | 0.004 | Kumar (1994) |
PS1765-1 | -51.8317 | 4.8633 | 0.000 | 0.050 | 0.123 | 0.006 | Walter et al. (1997) |
PS1780-1 | -51.6833 | -15.2733 | 0.000 | 0.050 | 0.151 | 0.008 | Walter et al. (1997) |
PS2271-1 | -51.5317 | -31.3717 | 0.000 | 0.010 | 0.112 | 0.006 | Walter et al. (1997) |
PS2661-4 | -51.4083 | -89.3450 | 0.000 | 0.005 | 0.079 | 0.004 | Walter (unpubl.) |
PS2366-1 | -50.9983 | -6.0000 | 0.000 | 0.050 | 0.147 | 0.010 | Walter et al. (1997) |
PS1775-5 | -50.9517 | -7.5017 | 0.000 | 0.050 | 0.088 | 0.004 | Walter et al. (1997) |
PS1779-3 | -50.3950 | -14.0750 | 0.000 | 0.050 | 0.093 | 0.005 | Walter et al. (1997) |
PS2269-5 | -50.3717 | -33.2450 | 0.000 | 0.010 | 0.116 | 0.006 | Walter et al. (1997) |
PS1759-1 | -50.1533 | 5.7550 | 0.000 | 0.050 | 0.089 | 0.004 | Walter et al. (1997) |
PS2611-3 | -49.5050 | 38.8267 | 0.000 | 0.050 | 0.110 | 0.005 | Walter et al. (1997) |
PS2367-1 | -49.0000 | -6.0017 | 0.000 | 0.050 | 0.084 | 0.004 | Walter et al. (1997) |
RC-13-254 | -48.5667 | 5.1167 | 0.130 | 0.130 | 0.071 | 0.003 | Kumar (1994) |
PS2262-7 | -48.5017 | -37.0050 | 0.000 | 0.010 | 0.098 | 0.007 | Walter et al. (1997) |
PS2376-1 | -48.5017 | -6.0033 | 0.000 | 0.050 | 0.085 | 0.004 | Walter et al. (1997) |
PS1777-7 | -48.2317 | -11.0367 | 0.000 | 0.015 | 0.100 | 0.006 | Walter et al. (1997) |
VM 29-105 | -48.0833 | 18.6833 | 0.030 | 0.060 | 0.090 | 0.003 | DeMaster (1979) |
PS2363-1 | -48.0017 | -6.0017 | 0.000 | 0.050 | 0.069 | 0.003 | Walter et al. (1997) |
RC8-81 | -47.9500 | -159.0500 | 0.030 | 0.040 | 0.074 | 0.003 | Lao et al. (1992) |
PS1755-1 | -47.7883 | 7.1017 | 0.010 | 0.020 | 0.078 | 0.004 | Walter et al. (1997) |
PS2368-1 | -46.8717 | -5.7167 | 0.000 | 0.005 | 0.055 | 0.003 | Walter et al. (1997) |
KH-71-5-24-2 | -46.3217 | -127.7730 | 0.000 | 0.020 | 0.034 | 0.002 | Yang et al. (1986) |
RC-15-93 | -46.1000 | -13.2167 | 0.330 | 0.330 | 0.082 | 0.003 | Kumar (1994) |
PS1752-5 | -45.6200 | 9.6083 | 0.000 | 0.050 | 0.070 | 0.003 | Walter et al. (1997) |
PS2257-1 | -45.0117 | -38.5417 | 0.000 | 0.010 | 0.090 | 0.005 | Walter et al. (1997) |
PS2256-4 | -44.5167 | -44.4517 | 0.000 | 0.010 | 0.085 | 0.008 | Walter et al. (1997) |
PS1751-2 | -44.4883 | 10.4717 | 0.000 | 0.020 | 0.074 | 0.004 | Walter et al. (1997) |
PS2254-1 | -43.9717 | -50.1067 | 0.000 | 0.010 | 0.092 | 0.005 | Walter et al. (1997) |
PS2562-3 | -43.1867 | 31.5867 | 0.000 | 0.050 | 0.073 | 0.003 | Walter et al. (1997) |
V22-108 | -43.1833 | -3.2500 | 0.130 | 0.130 | 0.038 | 0.001 | Kumar (1994) |
RC 15-101 | -42.9833 | -41.5667 | 0.040 | 0.070 | 0.094 | 0.009 | DeMaster (1979) |
RC-15-94 | -42.9000 | -20.8500 | 0.150 | 0.150 | 0.051 | 0.003 | Kumar (1994) |
228KG | -42.0217 | -156.9680 | 0.000 | 0.000 | 0.034 | Schmitz et al. (1986) | |
242KG | -42.0150 | -160.2130 | 0.000 | 0.000 | 0.036 | Schmitz et al. (1986) | |
198KG | -42.0050 | -150.9770 | 0.000 | 0.000 | 0.029 | Schmitz et al. (1986) | |
46KG | -41.9883 | -120.2120 | 0.000 | 0.000 | 0.048 | Schmitz et al. (1986) | |
79KG | -41.9567 | -129.8780 | 0.000 | 0.000 | 0.040 | Schmitz et al. (1986) | |
251KG | -41.9467 | -163.0750 | 0.000 | 0.000 | 0.042 | Schmitz et al. (1986) | |
23KG | -41.6100 | -110.6880 | 0.000 | 0.000 | 0.053 | Schmitz et al. (1986) | |
AII76-3 | -41.5500 | 20.2000 | 0.000 | 0.010 | 0.048 | 0.003 | DeMaster (1979) |
RC15-61 | -40.6167 | -77.2000 | 0.060 | 0.090 | 0.075 | 0.004 | Lao et al. (1992) |
RC 12-294 | -37.2667 | -10.1000 | 0.100 | 0.100 | 0.045 | 0.003 | Yu (1994) |
G972 | -36.2583 | -176.8980 | 0.000 | 0.000 | 0.071 | Schmitz et al. (1986) | |
GPC 5 | -33.6833 | -57.6167 | 0.320 | 0.320 | 0.054 | 0.003 | Bacon and Rosholt (1982) |
AII 107-065 | -32.0333 | -36.1833 | 0.030 | 0.040 | 0.048 | 0.004 | Yu (1994) |
KH-79-4-12 | -31.9950 | 160.6220 | 0.000 | 0.050 | 0.136 | 0.028 | Yang et al. (1986) |
G981 | -31.3767 | -171.2300 | 0.000 | 0.000 | 0.050 | Schmitz et al. (1986) | |
VM 19-240 | -30.5833 | -13.2833 | 0.200 | 0.200 | 0.040 | 0.002 | Yu (1994) |
KH-71-5-42-2 | -27.5800 | -88.0500 | 0.000 | 0.020 | 0.054 | 0.011 | Yang et al. (1986) |
KH-79-4-14 | -24.9533 | 165.1450 | 0.000 | 0.020 | 0.062 | 0.008 | Yang et al. (1986) |
G993 | -23.5350 | -162.9020 | 0.000 | 0.000 | 0.036 | Schmitz et al. (1986) | |
214KG | -21.6000 | -161.5330 | 0.000 | 0.000 | 0.032 | Schmitz et al. (1986) | |
210KG | -21.6000 | -160.5000 | 0.000 | 0.000 | 0.023 | Schmitz et al. (1986) | |
KH-71-5-44-2 | -20.8350 | -93.3533 | 0.060 | 0.080 | 0.025 | 0.002 | Yang et al. (1986) |
KH-71-5-15-2 | -20.3800 | -148.0430 | 0.030 | 0.060 | 0.034 | 0.002 | Yang et al. (1986) |
154-18 | -20.0317 | -113.8570 | 0.000 | 0.020 | 0.199 | 0.012 | Shimmield and Price (1988) |
154-19 | -19.8383 | -116.6300 | 0.000 | 0.010 | 0.076 | 0.006 | Shimmield and Price (1988) |
154-20 | -19.6633 | -117.9670 | 0.000 | 0.010 | 0.057 | 0.003 | Shimmield and Price (1988) |
V18-299 | -16.1167 | -149.6670 | 0.000 | 0.050 | 0.044 | 0.002 | Lao et al. (1992) |
154-4 | -12.6217 | -134.8500 | 0.060 | 0.070 | 0.037 | 0.002 | Shimmield and Price (1988) |
154-5 | -12.3183 | -125.6030 | 0.010 | 0.020 | 0.070 | 0.005 | Shimmield and Price (1988) |
154-6 | -12.0700 | -119.7780 | 0.020 | 0.030 | 0.077 | 0.006 | Shimmield and Price (1988) |
V18-258 | -11.8667 | -165.7500 | 0.000 | 0.050 | 0.036 | 0.002 | Ku (1966) |
KH-71-5-12-3 | -11.0233 | -146.0250 | 0.030 | 0.060 | 0.091 | 0.007 | Yang et al. (1986) |
154-8 | -10.8083 | -113.8680 | 0.000 | 0.010 | 0.110 | 0.008 | Shimmield and Price (1988) |
154-10 | -10.2850 | -111.3280 | 0.000 | 0.010 | 0.160 | 0.009 | Shimmield and Price (1988) |
VM 22-174 | -10.0667 | -12.8167 | 0.080 | 0.080 | 0.050 | 0.001 | Yu (1994) |
KH-71-5-53-2 | -8.2550 | -112.7020 | 0.050 | 0.080 | 0.080 | 0.006 | Yang et al. (1986) |
VNTR01-10GC | -4.5100 | -102.0200 | 0.000 | 0.020 | 0.128 | 0.006 | this study |
V19-29 | -3.5833 | -83.9333 | 0.170 | 0.190 | 0.183 | 0.010 | Lao et al. (1992) |
KH-79-4-10 | -3.3167 | 159.3070 | 0.000 | 0.015 | 0.175 | 0.036 | Yang et al. (1986) |
VNTR01-13GC | -3.0900 | -90.8200 | 0.000 | 0.020 | 0.143 | 0.004 | this study |
VNTR01-12GC | -3.0100 | -95.0700 | 0.000 | 0.020 | 0.119 | 0.003 | this study |
VNTR01-09GC | -3.0000 | -110.5000 | 0.000 | 0.020 | 0.109 | 0.004 | this study |
V19-28 | -2.3667 | -84.6500 | 0.170 | 0.190 | 0.200 | 0.009 | Lao et al. (1992) |
KH-79-4-9 | -0.2917 | 158.1120 | 0.000 | 0.010 | 0.123 | 0.020 | Yang et al. (1986) |
VM 30-040 | -0.2000 | -23.1333 | 0.150 | 0.150 | 0.040 | 0.001 | Yu (1994) |
oj erdc bx88 | -0.0500 | 155.8700 | 0.039 | 0.039 | 0.087 | 0.004 | this study |
oj erdc bx125 | -0.0500 | 161.0000 | 0.043 | 0.043 | 0.053 | 0.003 | this study |
KH-79-4-18 | -0.0117 | 163.9950 | 0.000 | 0.020 | 0.049 | 0.004 | Yang et al. (1986) |
VNTR01-08PC | 0.0400 | -110.4800 | 0.040 | 0.060 | 0.113 | 0.004 | this study |
Y69-071P | 0.0900 | -86.4800 | 0.010 | 0.030 | 0.193 | 0.006 | this study |
VNTR01-11GC | 0.1400 | -95.3400 | 0.010 | 0.030 | 0.137 | 0.006 | this study |
v 9-97 | 0.3833 | -29.8667 | 0.050 | 0.080 | 0.084 | 0.004 | Ku (1966) |
V28-238 | 1.0167 | 160.4830 | 0.000 | 0.080 | 0.067 | 0.003 | Lao et al. (1992) |
VNTR01-07GC | 1.0200 | -110.5700 | 0.000 | 0.020 | 0.116 | 0.003 | this study |
MANOP C | 1.0333 | -138.9330 | 0.015 | 0.021 | 0.064 | 0.002 | Lao et al. (1992) |
KLH 093 | 1.2317 | -102.0630 | 0.075 | 0.075 | 0.161 | 0.028 | Frank et al. (1994) |
KLH 068 | 1.2317 | -101.6120 | 0.025 | 0.025 | 0.071 | 0.025 | Frank et al. (1994) |
VM 25-059 | 1.3667 | -39.4833 | 0.080 | 0.080 | 0.042 | 0.002 | Yu (1994) |
VNTR01-15GC | 1.4900 | -89.8600 | 0.000 | 0.020 | 0.167 | 0.007 | this study |
RC11-210 | 1.8167 | -140.0500 | 0.050 | 0.070 | 0.073 | 0.003 | Lao et al. (1992) |
EN 66-29 | 2.4667 | -19.7667 | 0.020 | 0.120 | 0.047 | 0.003 | Yu (1994) |
VNTR01-16PC | 2.6000 | -89.7300 | 0.000 | 0.020 | 0.106 | 0.004 | this study |
P7 | 2.6050 | -83.9867 | 0.070 | 0.070 | 0.286 | Yang et al. (1995) | |
VNTR01-05GC | 2.7600 | -110.5800 | 0.000 | 0.020 | 0.094 | 0.004 | this study |
VNTR01-06GC | 2.7600 | -110.5500 | 0.000 | 0.020 | 0.092 | 0.004 | this study |
GIK10147-1 | 3.8367 | -145.0280 | 0.000 | 0.020 | 0.044 | 0.006 | Mueller and Mangini (1980) |
GIK10145-1 | 3.9917 | -144.8220 | 0.000 | 0.020 | 0.033 | 0.014 | Mueller and Mangini (1980) |
KNR 110-82 | 4.3333 | -43.4833 | 0.000 | 0.130 | 0.046 | 0.003 | Yu (1994) |
KNR 110-91 | 4.7667 | -43.3000 | 0.000 | 0.000 | 0.029 | 0.002 | Yu (1994) |
EN 66-38 | 4.9167 | -20.5000 | 0.025 | 0.095 | 0.051 | 0.003 | Yu (1994) |
KNR 110-55 | 4.9500 | -42.9000 | 0.040 | 0.170 | 0.052 | 0.004 | Yu (1994) |
KH-79-4-8 | 5.0100 | 156.1430 | 0.000 | 0.015 | 0.026 | 0.007 | Yang et al. (1986) |
KH-79-4-19 | 5.0567 | 165.9220 | 0.000 | 0.020 | 0.042 | 0.003 | Yang et al. (1986) |
KH-79-1-5 | 5.1817 | 130.4650 | 0.000 | 0.015 | 0.095 | 0.015 | Yang et al. (1986) |
VNTR01-04GC | 5.3500 | -110.0900 | 0.000 | 0.020 | 0.093 | 0.004 | this study |
GIK10132-1 | 6.2200 | -148.9550 | 0.000 | 0.040 | 0.038 | 0.004 | Mueller and Mangini (1980) |
VNTR01-03GC | 7.1700 | -109.7400 | 0.000 | 0.020 | 0.089 | 0.002 | this study |
Y71-3-02 | 7.1700 | -85.1500 | 0.000 | 0.020 | 0.121 | 0.005 | this study |
VNTR01-02PC | 7.1900 | -109.7500 | 0.000 | 0.020 | 0.073 | 0.003 | this study |
VNTR01-19PC | 7.9100 | -90.4400 | 0.000 | 0.020 | 0.136 | 0.006 | this study |
KH-78-1-1036 | 8.0050 | 176.9520 | 0.000 | 0.040 | 0.031 | 0.002 | Yang et al. (1986) |
1858 358 bl | 8.0100 | -143.5500 | 0.000 | 0.030 | 0.034 | 0.006 | Mangini and Kuehnel (1987) |
A47-16 | 9.0383 | -151.1900 | 0.000 | 0.010 | 0.028 | 0.002 | Cochran and Krishnaswami (1980) |
Valdivia 10141 | 9.1083 | -148.7780 | 0.000 | 0.020 | 0.028 | 0.004 | Mangini and Sonntag (1977) |
GIK10141-1 | 9.1083 | -148.7780 | 0.000 | 0.020 | 0.035 | 0.005 | Mueller and Mangini (1980) |
GIK10140-1 | 9.2500 | -148.7420 | 0.000 | 0.020 | 0.044 | 0.009 | Mueller and Mangini (1980) |
1858 163 bl | 9.2700 | -146.0300 | 0.000 | 0.030 | 0.027 | 0.005 | Mangini and Kuehnel (1987) |
10175 | 9.3217 | -146.0180 | 0.000 | 0.020 | 0.022 | 0.002 | Mueller and Mangini (1980) |
1858 254 bl | 9.3300 | -146.0900 | 0.000 | 0.030 | 0.031 | 0.004 | Mangini and Kuehnel (1987) |
1858 232 bl | 9.3500 | -146.0500 | 0.000 | 0.030 | 0.034 | 0.008 | Mangini and Kuehnel (1987) |
GIK10149-1 | 9.5083 | -146.1580 | 0.000 | 0.020 | 0.042 | 0.005 | Mueller and Mangini (1980) |
VNTR01-21GC | 9.5900 | -94.6000 | 0.000 | 0.020 | 0.150 | 0.006 | this study |
1858 195 bl | 9.6700 | -146.0900 | 0.000 | 0.030 | 0.023 | 0.008 | Mangini and Kuehnel (1987) |
KH-78-1-1038 | 10.0033 | 176.9880 | 0.000 | 0.040 | 0.027 | 0.002 | Yang et al. (1986) |
KH-79-4-7 | 10.7883 | 153.7180 | 0.000 | 0.010 | 0.033 | 0.005 | Yang et al. (1986) |
MANOP S | 11.0500 | -140.0830 | 0.015 | 0.021 | 0.025 | 0.001 | Lao et al. (1992) |
B52-39 | 11.2467 | -139.0680 | 0.000 | 0.010 | 0.033 | 0.002 | Cochran and Krishnaswami (1980) |
VNTR01-01PC | 11.2500 | -109.6100 | 0.010 | 0.030 | 0.056 | 0.002 | this study |
V18-258 | 11.8667 | -165.7500 | 0.000 | 0.050 | 0.028 | 0.002 | Ku (1965) |
1858 21 bl | 12.3200 | -150.0500 | 0.000 | 0.030 | 0.043 | 0.006 | Mangini and Kuehnel (1987) |
1858 151 bl | 12.3400 | -150.1700 | 0.000 | 0.030 | 0.032 | 0.003 | Mangini and Kuehnel (1987) |
VNTR01-22GC | 13.0100 | -99.3700 | 0.000 | 0.020 | 0.154 | 0.007 | this study |
Valdivia 10127 | 13.6950 | -151.9830 | 0.020 | 0.040 | 0.031 | 0.002 | Mangini and Sonntag (1977) |
CH 75-2-8 | 14.0167 | -54.0167 | 0.020 | 0.040 | 0.031 | 0.002 | Anderson et al. (1983) |
KK1, core1 | 14.1167 | -153.1670 | 0.000 | 0.010 | 0.040 | 0.001 | Anderson et al. (1983) |
VM 22-197 | 14.1667 | -18.5833 | 0.250 | 0.250 | 0.051 | 0.003 | Yu (1994) |
C57-58 | 15.1583 | -125.9070 | 0.000 | 0.010 | 0.034 | 0.002 | Cochran and Krishnaswami (1980) |
KK1, core2 | 15.3333 | -151.5670 | 0.000 | 0.030 | 0.034 | 0.001 | Anderson et al. (1983) |
KNR 64-05 | 16.5167 | -74.8000 | 0.060 | 0.075 | 0.054 | 0.003 | Yu (1994) |
v 12-122 | 17.0000 | -74.4000 | 0.100 | 0.150 | 0.077 | 0.007 | Ku (1966) |
v 16-21 | 17.2833 | -48.4667 | 0.020 | 0.100 | 0.053 | 0.003 | Ku (1966) |
VM 30-049 | 18.4333 | -21.0833 | 0.100 | 0.150 | 0.082 | 0.003 | Yu (1994) |
ktb 14 | 18.4667 | -21.0500 | 0.000 | 0.010 | 0.070 | 0.005 | Legeleux (1994) |
ktb 11 | 18.5000 | -21.0833 | 0.000 | 0.010 | 0.070 | 0.009 | Legeleux (1994) |
KH-79-4-22 | 20.0450 | 158.6000 | 0.000 | 0.020 | 0.040 | 0.003 | Yang et al. (1986) |
ktb 09 | 20.5333 | -18.6000 | 0.000 | 0.010 | 0.160 | 0.037 | Legeleux (1994) |
V21-59 | 20.9167 | -158.1000 | 0.050 | 0.060 | 0.081 | 0.004 | Lao et al. (1992) |
ktb 10 | 21.0500 | -31.2000 | 0.000 | 0.010 | 0.033 | 0.004 | Legeleux (1994) |
ktb 12 | 21.0667 | -31.1500 | 0.000 | 0.010 | 0.032 | 0.004 | Legeleux (1994) |
AII 42-41 | 22.2333 | -56.6500 | 0.000 | 0.050 | 0.039 | 0.004 | Ku et al. (1972) |
VM 23-100 | 22.6833 | -21.3000 | 0.100 | 0.100 | 0.035 | 0.001 | Yu (1994) |
core 12310 | 23.5000 | -18.7167 | 0.020 | 0.040 | 0.102 | 0.013 | Mangini and Dieter-Haass (1983) |
KH-79-4-6 | 23.7917 | 147.6230 | 0.000 | 0.015 | 0.022 | 0.005 | Yang et al. (1986) |
163-9 | 24.2500 | -115.0000 | 0.000 | 0.010 | 0.097 | 0.008 | Shimmield et al. (1986) |
163-10 | 24.6000 | -114.0500 | 0.000 | 0.020 | 0.131 | 0.005 | Shimmield et al. (1986) |
145-7 | 24.7000 | -114.1000 | 0.000 | 0.010 | 0.088 | 0.004 | Shimmield et al. (1986) |
163-14 | 24.7000 | -113.7000 | 0.000 | 0.010 | 0.141 | Shimmield et al. (1986) | |
145-8 | 24.9500 | -113.5000 | 0.000 | 0.010 | 0.120 | 0.005 | Shimmield et al. (1986) |
163-7 | 24.9500 | -113.5000 | 0.000 | 0.020 | 0.145 | 0.010 | Shimmield et al. (1986) |
v 10-95 | 26.5167 | -51.7833 | 0.000 | 0.060 | 0.023 | 0.003 | Ku (1966) |
KH-74-4-21 | 26.7617 | 139.7080 | 0.020 | 0.080 | 0.105 | 0.015 | Yang et al. (1986) |
V21-71 | 27.9000 | 162.5170 | 0.000 | 0.020 | 0.036 | 0.002 | Ku (1966) |
KH-79-4-5 | 29.2800 | 144.0330 | 0.000 | 0.015 | 0.058 | 0.008 | Yang et al. (1986) |
KH-80-2-9 | 30.0000 | -170.0130 | 0.000 | 0.020 | 0.045 | 0.003 | Yang et al. (1986) |
KH-75-3-2-2 | 30.0000 | 143.5130 | 0.000 | 0.025 | 0.091 | 0.007 | Yang et al. (1986) |
KH-80-3-16 | 31.7250 | 157.4450 | 0.000 | 0.015 | 0.195 | 0.032 | Yang et al. (1986) |
SCB QP2 | 32.5833 | -118.1670 | 0.000 | 0.100 | 0.198 | 0.011 | Lao et al. (1992) |
M36/2_192-MUC | 32.9967 | -21.9917 | 0.000 | 0.000 | 0.042 | 0.009 | Scholten, unpublished |
BC31 | 33.7500 | -118.8000 | 0.000 | 0.010 | 0.500 | Huh etal. (1987) | |
KH-75-3-14-2 | 34.3967 | 145.0300 | 0.000 | 0.030 | 0.076 | 0.007 | Yang et al. (1986) |
KH-83-3-D | 34.8667 | 154.7700 | 0.000 | 0.010 | 0.090 | 0.008 | Yang et al. (1986) |
V32-126 | 35.3167 | 174.9000 | 0.070 | 0.080 | 0.064 | 0.003 | Lao et al. (1992) |
PS BC151 | 35.6333 | -121.6170 | 0.000 | 0.010 | 0.157 | 0.015 | Lao et al. (1992) |
VM 26-176 | 36.0000 | -72.0000 | 0.080 | 0.100 | 0.066 | 0.004 | Yu (1994) |
PS BC166 | 36.1000 | -122.6000 | 0.000 | 0.010 | 0.163 | 0.019 | Lao et al. (1992) |
PS BC150 | 36.1833 | -122.3670 | 0.000 | 0.010 | 0.190 | 0.047 | Lao et al. (1992) |
PS BC133 | 36.2000 | -122.2670 | 0.000 | 0.010 | 0.966 | 0.058 | Lao et al. (1992) |
V32-128 | 36.4500 | 177.1500 | 0.080 | 0.100 | 0.062 | 0.005 | Lao et al. (1992) |
EN 187 BC8 | 36.8667 | -74.5733 | 0.010 | 0.020 | 0.053 | 0.015 | Anderson et al. (1994) |
EN 187 BC9 | 36.8700 | -74.5633 | 0.060 | 0.080 | 0.075 | 0.014 | Anderson et al. (1994) |
EN 187 BC10 | 36.8750 | -74.6133 | 0.010 | 0.020 | 0.089 | 0.029 | Anderson et al. (1994) |
EN 187 BC11 | 37.0383 | -74.5717 | 0.020 | 0.030 | 0.062 | 0.023 | Anderson et al. (1994) |
en 187-bc6 | 37.4000 | -73.8283 | 0.000 | 0.010 | 0.055 | 0.007 | Anderson et al. (1991) |
en 179-bc7 | 37.4183 | -73.8233 | 0.000 | 0.010 | 0.051 | 0.006 | Anderson et al. (1991) |
en 179-bc4 | 37.5283 | -74.0383 | 0.010 | 0.020 | 0.071 | 0.011 | Anderson et al. (1991) |
EN 187 BC5 | 37.6183 | -74.1667 | 0.040 | 0.050 | 0.069 | 0.014 | Anderson et al. (1994) |
EN 187 BC4 | 37.6217 | -74.2217 | 0.030 | 0.040 | 0.063 | 0.023 | Anderson et al. (1994) |
EN 179 BC2 | 37.6250 | -74.1667 | 0.040 | 0.050 | 0.050 | 0.011 | Anderson et al. (1994) |
EN 179 BC3 | 37.6400 | -74.1433 | 0.020 | 0.030 | 0.075 | 0.016 | Anderson et al. (1994) |
V21-146 | 37.6833 | 163.0330 | 0.100 | 0.110 | 0.093 | 0.005 | Lao et al. (1992) |
MANOP R | 38.0000 | -158.0000 | 0.000 | 0.050 | 0.043 | 0.002 | Lao et al. (1992) |
KH-80-2-8 | 38.0550 | -179.7620 | 0.000 | 0.010 | 0.073 | 0.005 | Yang et al. (1986) |
KH-84-3-16 | 38.2867 | 135.4920 | 0.000 | 0.015 | 0.413 | 0.055 | Yang et al. (1986) |
KH-80-2-6 | 39.0417 | 166.0050 | 0.020 | 0.030 | 0.113 | 0.011 | Yang et al. (1986) |
oce 152 bc5 | 39.1333 | -70.9333 | 0.000 | 0.005 | 0.063 | 0.003 | Anderson et al. (1991) |
EN 123 BC1 | 39.1367 | -70.9250 | 0.010 | 0.015 | 0.053 | 0.003 | Anderson et al. (1994) |
EN 123 BC3 | 39.5817 | -70.9200 | 0.000 | 0.010 | 0.061 | 0.005 | Anderson et al. (1994) |
RC14-105 | 39.6833 | 157.5500 | 0.100 | 0.120 | 0.090 | 0.005 | Lao et al. (1992) |
OCE 152-BC9 | 39.6983 | -70.9133 | 0.000 | 0.005 | 0.091 | 0.007 | Anderson et al. (1994) |
oce 152 bc8 | 39.7750 | -70.9650 | 0.000 | 0.005 | 0.071 | 0.007 | Anderson et al. (1991) |
EN 123 BC4 | 39.8033 | -70.9283 | 0.010 | 0.015 | 0.076 | 0.008 | Anderson et al. (1994) |
OCE 152-BC1 | 39.8117 | -70.9433 | 0.000 | 0.020 | 0.082 | 0.008 | Anderson et al. (1994) |
EN 123 BC6 | 39.8133 | -70.9233 | 0.000 | 0.010 | 0.066 | 0.006 | Anderson et al. (1994) |
KH-84-3-5 | 39.9583 | 145.4380 | 0.000 | 0.015 | 0.144 | 0.021 | Yang et al. (1986) |
KH-80-2-5 | 40.0033 | 156.0000 | 0.000 | 0.010 | 0.128 | 0.014 | Yang et al. (1986) |
V20-88 | 40.1833 | -151.6500 | 0.000 | 0.000 | 0.044 | 0.002 | Lao et al. (1992) |
VM 30-097 | 41.0000 | -33.9333 | 0.050 | 0.160 | 0.272 | 0.010 | Yu (1994) |
W8709A-1 | 41.5500 | -131.9500 | 0.010 | 0.030 | 0.081 | 0.003 | Lao et al. (1992) |
chn 82-23 | 41.6333 | -27.3333 | 0.000 | 0.050 | 0.057 | 0.003 | Ku et al. (1972) |
chn 82-24 | 41.7167 | -32.8500 | 0.000 | 0.050 | 0.047 | 0.002 | Ku et al. (1972) |
CHN 82-004 | 41.7167 | -32.8500 | 0.020 | 0.040 | 0.065 | 0.005 | Yu (1994) |
chn 82-30 | 41.8500 | -26.4667 | 0.000 | 0.100 | 0.065 | 0.004 | Ku et al. (1972) |
chn 82-28 | 42.0000 | -29.9000 | 0.000 | 0.100 | 0.055 | 0.004 | Ku et al. (1972) |
W8709A-13 | 42.1167 | -125.7500 | 0.040 | 0.050 | 0.217 | 0.036 | Lao et al. (1992) |
chn 82-26 | 42.1667 | -31.6333 | 0.000 | 0.100 | 0.057 | 0.003 | Ku et al. (1972) |
W8709A-8 | 42.2667 | -127.6830 | 0.090 | 0.100 | 0.180 | 0.011 | Lao et al. (1992) |
chn 82-25 | 42.3167 | -28.5833 | 0.000 | 0.060 | 0.041 | 0.003 | Ku et al. (1972) |
chn 82-31 | 42.3833 | -31.8000 | 0.000 | 0.100 | 0.050 | 0.003 | Ku et al. (1972) |
CHN 82-011 | 42.3833 | -31.8000 | 0.035 | 0.050 | 0.053 | 0.004 | Yu (1994) |
chn 82-33 | 42.4833 | -28.6667 | 0.000 | 0.100 | 0.070 | 0.007 | Ku et al. (1972) |
KH-83-3-BC | 43.3000 | 154.7070 | 0.000 | 0.010 | 0.290 | 0.034 | Yang et al. (1986) |
chn 82-42 | 43.3333 | -28.0833 | 0.000 | 0.100 | 0.061 | 0.004 | Ku et al. (1972) |
chn 82-41 | 43.3667 | -28.2333 | 0.000 | 0.100 | 0.093 | 0.005 | Ku et al. (1972) |
CHN 82-015 | 43.3667 | -28.2333 | 0.030 | 0.040 | 0.069 | 0.006 | Yu (1994) |
CHN 82-020 | 43.5000 | -29.8667 | 0.040 | 0.060 | 0.052 | 0.003 | Yu (1994) |
chn 82-32 | 43.7500 | -27.7833 | 0.000 | 0.100 | 0.058 | 0.004 | Ku et al. (1972) |
VM 29-179 | 44.0000 | -24.5333 | 0.160 | 0.160 | 0.044 | 0.002 | Yu (1994) |
V20-85 | 44.9000 | -143.6170 | 0.000 | 0.010 | 0.044 | 0.002 | Lao et al. (1992) |
KH-83-3-C | 45.0250 | 159.9950 | 0.000 | 0.010 | 0.161 | 0.012 | Yang et al. (1986) |
V20-122 | 46.5667 | 161.6830 | 0.080 | 0.100 | 0.145 | 0.007 | Lao et al. (1992) |
KH-78-3-4 | 53.5000 | 177.2580 | 0.000 | 0.025 | 0.219 | 0.027 | Yang et al. (1986) |
M36/2_MC435 | 54.6117 | -21.1500 | 0.000 | 0.000 | 0.073 | 0.013 | Scholten, unpublished |
RC14-121 | 54.8500 | -170.6830 | 0.250 | 0.270 | 0.154 | 0.016 | Lao et al. (1992) |
VM 28-014 | 64.7833 | -29.5667 | 0.130 | 0.130 | 0.108 | 0.004 | Yu (1994) |
VM 27-086 | 66.6000 | 1.1167 | 0.090 | 0.090 | 0.087 | 0.005 | Yu (1994) |
HM-79-26 | 66.9000 | -5.9333 | 0.000 | 0.000 | 0.071 | 0.004 | Yu (1994) |
HM-71-19 | 69.4833 | -9.5167 | 0.000 | 0.000 | 0.077 | 0.006 | Yu (1994) |
GIK17730-2 | 72.1117 | 7.3883 | 0.000 | 0.010 | 0.145 | 0.010 | Scholten et al. (1995) |
23293 | 72.6217 | -6.5917 | 0.000 | 0.010 | 0.079 | 0.011 | Scholten et al. (1995) |
HM-94-18/3 | 73.5000 | 5.6833 | 0.000 | 0.000 | 0.045 | 0.003 | Yu (1994) |
21893 | 74.8683 | -10.1100 | 0.000 | 0.010 | 0.101 | 0.009 | Scholten et al. (1995) |
17729 | 75.0000 | 0.0000 | 0.000 | 0.010 | 0.078 | 0.006 | Scholten et al. (1995) |
21895 | 75.4133 | -7.3100 | 0.000 | 0.010 | 0.076 | 0.008 | Scholten et al. (1995) |
GIK17726-1 | 75.4983 | 3.5617 | 0.000 | 0.010 | 0.072 | 0.006 | Scholten et al. (1995) |
GIK17728-1 | 76.5200 | 3.6250 | 0.000 | 0.010 | 0.105 | 0.009 | Scholten et al. (1995) |
GIK17725-1 | 77.4600 | 4.5800 | 0.000 | 0.010 | 0.077 | 0.005 | Scholten et al. (1995) |