Wittmann, Astrid; Held, Christoph; Pörtner, Hans-Otto; Sartoris, Franz-Josef (2010): Haemolymph inorganic ion composition of crustaceans from the Southern Ocean [dataset]. PANGAEA, https://doi.org/10.1594/PANGAEA.788789, Supplement to: Wittmann, A et al. (2010): Ion regulatory capacity and the biogeography of Crustacea at high southern latitudes. Polar Biology, 33(7), 919-928, https://doi.org/10.1007/s00300-010-0768-1
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Abstract:
Brachyuran and anomuran decapod crabs do not occur in the extremely cold waters of the Antarctic continental shelf whereas caridean and other shrimp-like decapods, amphipods and isopods are highly abundant. Differing capacities for extracellular ion regulation, especially concerning magnesium, have been hypothesised to determine cold tolerance and by that the biogeography of Antarctic crustaceans. Magnesium is known to have a paralysing effect, which is even more distinct in the cold. As only few or no data exist on haemolymph ionic composition of Sub-Antarctic and Antarctic crustaceans, haemolymph samples of 12 species from these regions were analysed for the concentrations of major inorganic ions (Na+, K+, Ca2+, Mg2+, Cl-, SO4 2-) by ion chromatography. Cation relationships guaranteed neuromuscular excitability in all species. Sulphate and potassium correlated positively with magnesium concentration. The Antarctic caridean decapod as well as the amphipods maintained low (6-20% of ambient sea water magnesium concentration), Sub-Antarctic brachyuran and anomuran crabs as well as the Antarctic isopods high (54-96% of ambient sea water magnesium concentration) haemolymph magnesium levels. In conclusion, magnesium regulation may explain the biogeography of decapods, but not that of the peracarids.
Project(s):
Funding:
German Research Foundation (DFG), grant/award no. 5472008: Priority Programme 1158 Antarctic Research with Comparable Investigations in Arctic Sea Ice Areas
Coverage:
Median Latitude: -61.084245 * Median Longitude: -45.113056 * South-bound Latitude: -70.516400 * West-bound Longitude: -70.930000 * North-bound Latitude: -51.686330 * East-bound Longitude: -8.801400
Date/Time Start: 2004-05-29T00:00:00 * Date/Time End: 2008-04-01T00:00:00
Minimum Elevation: -839.1 m * Maximum Elevation: -130.0 m
Event(s):
Icefish2004_19 * Latitude: -51.686330 * Longitude: -57.456000 * Date/Time: 2004-05-29T00:00:00 * Elevation: -130.0 m * Location: South Atlantic Ocean * Campaign: Icefish2004 * Basis: Nathaniel B. Palmer * Method/Device: 2 m Blake Trawl (2mBT)
Icefish2004_26 * Latitude: -53.655830 * Longitude: -40.742500 * Date/Time: 2004-06-05T00:00:00 * Elevation: -410.0 m * Location: South Atlantic Ocean * Campaign: Icefish2004 * Basis: Nathaniel B. Palmer * Method/Device: Trap (TRAP)
Icefish2004_49 * Latitude: -56.319830 * Longitude: -27.450500 * Date/Time: 2004-06-14T00:00:00 * Elevation: -340.0 m * Location: South Atlantic Ocean * Campaign: Icefish2004 * Basis: Nathaniel B. Palmer * Method/Device: 2 m Blake Trawl (2mBT)
Comment:
Paralomis granulosa were obtained from local fishermen in Punta Arenas, Chile in April 2008. Ceratoserolis trilobitoides was sampled at stations PS69/603-5 (Latitude -70.5164, Longitude -8.8014, water depth -297) and PS69/654-1 (Latitude -61.3668, Longitude -56.0158, water depth -353). Glyptonotus antarcticus was sampled at stations PS69/605-3 (Latitude -70.5164, Longitude -8.8014, water depth -297 and PS69/678-1 (Latitude -62.3226, Longitude -60.4517, water depth -109).
Parameter(s):
License:
Creative Commons Attribution 3.0 Unported (CC-BY-3.0)
Size:
1092 data points
Data
| 1 Event | 2 Latitude | 3 Longitude | 4 Elevation [m] | 5 Date/Time | 6 Species | 7 Ha collection | 8 K+ (ha) [mmol/l] | 9 K+ (ha) [%] | 10 Mg2+ (ha) [mmol/l] | 11 Mg2+ (ha) [%] | 12 Na+ (ha) [mmol/l] | 13 Na+ (ha) [%] | 14 Ca2+ (ha) [mmol/l] | 15 Ca2+ (ha) [%] | 16 Cl- (ha) [mmol/l] | 17 Cl- (ha) [%] | 18 [SO4]2- (ha) [mmol/l] | 19 [SO4]2- (ha) [%] |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| PS69/635-1 | -60.9523 | -55.9123 | -231.8 | 2006-12-27T22:35 | Natatolana sp. | laboratory | 12.1 | 125.2 | 39.9 | 79.8 | 412.4 | 92.5 | 10.9 | 110.9 | 361.7 | 69.2 | 10.1 | 37.4 |
| PS69/635-1 | -60.9523 | -55.9123 | -231.8 | 2006-12-27T22:35 | Natatolana sp. | laboratory | 9.8 | 101.2 | 41.0 | 82.0 | 423.3 | 94.9 | 10.7 | 108.9 | 471.7 | 90.2 | 8.4 | 31.3 |
| PS69/635-1 | -60.9523 | -55.9123 | -231.8 | 2006-12-27T22:35 | Natatolana sp. | laboratory | 9.3 | 96.1 | 38.6 | 77.3 | 332.5 | 74.5 | 9.9 | 100.5 | 402.5 | 77.0 | 14.4 | 53.2 |
| PS69/635-1 | -60.9523 | -55.9123 | -231.8 | 2006-12-27T22:35 | Natatolana sp. | laboratory | 12.8 | 131.5 | 44.7 | 89.3 | 431.9 | 96.8 | 11.8 | 120.8 | 500.2 | 95.6 | 15.0 | 55.4 |
| PS69/635-1 | -60.9523 | -55.9123 | -231.8 | 2006-12-27T22:35 | Natatolana sp. | laboratory | 10.1 | 103.9 | 44.3 | 88.5 | 411.1 | 92.2 | 11.5 | 117.4 | 470.6 | 90.0 | 13.8 | 51.2 |
| PS69/635-1 | -60.9523 | -55.9123 | -231.8 | 2006-12-27T22:35 | Natatolana sp. | laboratory | 7.8 | 80.5 | 37.2 | 74.4 | 328.9 | 73.7 | 10.7 | 108.9 | 413.1 | 79.0 | 13.5 | 50.2 |
| PS69/603-5 | -70.5164 | -8.8014 | -297.0 | 2006-12-07T13:38 | Ceratoserolis trilobitoides | laboratory | 8.8 | 90.4 | 26.0 | 52.0 | 407.4 | 91.3 | 10.2 | 104.5 | 460.3 | 88.0 | 16.8 | 62.4 |
| PS69/603-5 | -70.5164 | -8.8014 | -297.0 | 2006-12-07T13:38 | Ceratoserolis trilobitoides | laboratory | 8.3 | 85.9 | 39.8 | 79.5 | 362.3 | 81.2 | 9.1 | 92.9 | 374.0 | 71.5 | 19.2 | 71.0 |
| PS69/603-5 | -70.5164 | -8.8014 | -297.0 | 2006-12-07T13:38 | Ceratoserolis trilobitoides | laboratory | 10.0 | 102.9 | 27.4 | 54.9 | 353.7 | 79.3 | 8.8 | 89.8 | 432.1 | 82.6 | 15.3 | 56.6 |
| PS69/603-5 | -70.5164 | -8.8014 | -297.0 | 2006-12-07T13:38 | Ceratoserolis trilobitoides | laboratory | 9.6 | 98.8 | 29.7 | 59.3 | 383.8 | 86.1 | 8.7 | 88.7 | 492.5 | 94.2 | 21.7 | 80.4 |
| PS69/603-5 | -70.5164 | -8.8014 | -297.0 | 2006-12-07T13:38 | Ceratoserolis trilobitoides | laboratory | 10.7 | 109.9 | 32.4 | 64.8 | 412.3 | 92.4 | 11.3 | 115.7 | 407.4 | 77.9 | 21.8 | 80.8 |
| PS69/603-5 | -70.5164 | -8.8014 | -297.0 | 2006-12-07T13:38 | Ceratoserolis trilobitoides | laboratory | 10.4 | 107.5 | 23.4 | 46.9 | 406.2 | 91.1 | 9.1 | 92.5 | 442.0 | 84.5 | 17.3 | 64.0 |
| PS69/603-5 | -70.5164 | -8.8014 | -297.0 | 2006-12-07T13:38 | Glyptonotus antarcticus | laboratory | 10.3 | 105.8 | 26.1 | 52.1 | 415.4 | 93.1 | 10.0 | 102.1 | 481.1 | 92.0 | 9.1 | 33.6 |
| PS69/603-5 | -70.5164 | -8.8014 | -297.0 | 2006-12-07T13:38 | Glyptonotus antarcticus | laboratory | 13.3 | 137.3 | 28.0 | 56.0 | 413.8 | 92.8 | 9.7 | 98.7 | 491.6 | 94.0 | 8.0 | 29.5 |
| PS69/603-5 | -70.5164 | -8.8014 | -297.0 | 2006-12-07T13:38 | Glyptonotus antarcticus | laboratory | 12.4 | 127.5 | 27.7 | 55.3 | 421.6 | 94.5 | 9.7 | 98.7 | 482.1 | 92.2 | 8.8 | 32.6 |
| PS69/603-5 | -70.5164 | -8.8014 | -297.0 | 2006-12-07T13:38 | Glyptonotus antarcticus | laboratory | 12.0 | 123.5 | 27.3 | 54.7 | 436.3 | 97.8 | 10.8 | 109.7 | 522.0 | 99.8 | 8.8 | 32.5 |
| PS69/603-5 | -70.5164 | -8.8014 | -297.0 | 2006-12-07T13:38 | Glyptonotus antarcticus | laboratory | 13.1 | 134.8 | 25.4 | 50.9 | 390.8 | 87.6 | 9.2 | 94.3 | 468.0 | 89.5 | 7.7 | 28.6 |
| PS69/635-1 | -60.9523 | -55.9123 | -231.8 | 2006-12-27T22:35 | Abyssorchomene plebs | laboratory | 5.9 | 60.5 | 10.0 | 20.0 | 423.2 | 94.9 | 10.5 | 107.2 | 422.0 | 80.7 | 6.9 | 25.5 |
| PS69/635-1 | -60.9523 | -55.9123 | -231.8 | 2006-12-27T22:35 | Abyssorchomene plebs | laboratory | 5.6 | 57.6 | 11.0 | 21.9 | 373.6 | 83.8 | 13.7 | 140.0 | 374.3 | 71.6 | 7.5 | 27.6 |
| PS69/635-1 | -60.9523 | -55.9123 | -231.8 | 2006-12-27T22:35 | Abyssorchomene plebs | laboratory | 5.1 | 52.2 | 8.8 | 17.6 | 377.8 | 84.7 | 9.6 | 98.3 | 389.8 | 74.5 | 7.4 | 27.5 |
| PS69/635-1 | -60.9523 | -55.9123 | -231.8 | 2006-12-27T22:35 | Abyssorchomene plebs | laboratory | 6.5 | 67.4 | 10.2 | 20.4 | 393.9 | 88.3 | 10.8 | 110.6 | 410.2 | 78.4 | 12.2 | 45.2 |
| PS69/635-1 | -60.9523 | -55.9123 | -231.8 | 2006-12-27T22:35 | Abyssorchomene plebs | laboratory | 6.2 | 64.1 | 10.2 | 20.4 | 417.3 | 93.6 | 10.2 | 104.1 | 422.1 | 80.7 | 10.4 | 38.4 |
| PS69/683-1 | -62.9628 | -57.9648 | -839.1 | 2007-01-04T02:14 | Eusirus propeperdentatus | field | 6.5 | 62.4 | 3.8 | 7.0 | 522.3 | 108.6 | 11.2 | 107.1 | 514.1 | 91.3 | 8.7 | 29.9 |
| PS69/683-1 | -62.9628 | -57.9648 | -839.1 | 2007-01-04T02:14 | Eusirus propeperdentatus | field | 5.9 | 56.3 | 3.2 | 5.8 | 624.9 | 129.9 | 9.5 | 90.4 | 743.9 | 132.1 | 10.7 | 36.7 |
| PS69/683-1 | -62.9628 | -57.9648 | -839.1 | 2007-01-04T02:14 | Eurythenes gryllus | field | 7.3 | 69.9 | 11.2 | 20.8 | 503.0 | 104.6 | 6.1 | 58.0 | 579.4 | 102.9 | 1.6 | 5.5 |
| PS69/683-1 | -62.9628 | -57.9648 | -839.1 | 2007-01-04T02:14 | Eurythenes gryllus | field | 7.1 | 68.2 | 11.3 | 21.0 | 518.1 | 107.7 | 9.1 | 86.7 | 568.1 | 100.9 | 1.7 | 5.7 |
| PS69/683-1 | -62.9628 | -57.9648 | -839.1 | 2007-01-04T02:14 | Eurythenes gryllus | field | 7.8 | 74.7 | 11.2 | 20.8 | 494.0 | 102.7 | 6.6 | 62.4 | 548.5 | 97.4 | 2.6 | 9.1 |
| PS69/683-1 | -62.9628 | -57.9648 | -839.1 | 2007-01-04T02:14 | Eurythenes gryllus | field | 7.1 | 68.6 | 9.7 | 18.0 | 508.5 | 105.7 | 6.1 | 58.0 | 523.1 | 92.9 | 1.7 | 5.8 |
| PS69/683-1 | -62.9628 | -57.9648 | -839.1 | 2007-01-04T02:14 | Eurythenes gryllus | field | 7.0 | 67.3 | 12.3 | 22.8 | 500.5 | 104.1 | 4.0 | 37.9 | 549.6 | 97.6 | 2.8 | 9.7 |
| PS69/683-1 | -62.9628 | -57.9648 | -839.1 | 2007-01-04T02:14 | Eurythenes gryllus | field | 6.7 | 64.7 | 10.2 | 18.9 | 464.0 | 96.5 | 13.7 | 130.5 | 524.2 | 93.1 | 1.4 | 4.8 |
| PS69/683-1 | -62.9628 | -57.9648 | -839.1 | 2007-01-04T02:14 | Eurythenes gryllus | field | 7.6 | 73.4 | 9.9 | 18.3 | 458.7 | 95.4 | 12.0 | 113.9 | 489.6 | 87.0 | 1.3 | 4.4 |
| PS69/683-1 | -62.9628 | -57.9648 | -839.1 | 2007-01-04T02:14 | Eurythenes gryllus | field | 6.6 | 63.0 | 11.3 | 20.9 | 449.7 | 93.5 | 12.6 | 120.1 | 517.3 | 91.9 | 2.2 | 7.5 |
| PS69/683-1 | -62.9628 | -57.9648 | -839.1 | 2007-01-04T02:14 | Eurythenes gryllus | field | 7.0 | 67.3 | 12.4 | 23.1 | 468.5 | 97.4 | 16.8 | 159.9 | 511.1 | 90.8 | 1.2 | 4.1 |
| PS69/683-1 | -62.9628 | -57.9648 | -839.1 | 2007-01-04T02:14 | Eurythenes gryllus | field | 7.0 | 67.8 | 11.0 | 20.4 | 475.3 | 98.8 | 12.5 | 118.9 | 560.9 | 99.6 | 2.4 | 8.4 |
| Icefish2004_49 | -56.3198 | -27.4505 | -340.0 | 2004-06-14T00:00 | Paralomis formosa | field | 11.6 | 111.3 | 41.0 | 75.9 | 536.3 | 111.5 | 12.6 | 119.8 | 562.6 | 99.9 | 20.2 | 69.5 |
| Icefish2004_49 | -56.3198 | -27.4505 | -340.0 | 2004-06-14T00:00 | Paralomis formosa | field | 10.0 | 96.2 | 37.6 | 69.6 | 507.1 | 105.4 | 10.1 | 96.4 | 559.1 | 99.3 | 17.5 | 60.3 |
| Icefish2004_49 | -56.3198 | -27.4505 | -340.0 | 2004-06-14T00:00 | Paralomis formosa | field | 11.7 | 112.7 | 41.0 | 75.9 | 533.3 | 110.9 | 7.6 | 72.0 | 531.8 | 94.5 | 26.3 | 90.6 |
| Icefish2004_49 | -56.3198 | -27.4505 | -340.0 | 2004-06-14T00:00 | Paralomis formosa | field | 11.1 | 106.5 | 34.8 | 64.4 | 486.6 | 101.2 | 10.8 | 103.1 | 555.3 | 98.6 | 28.6 | 98.7 |
| Icefish2004_49 | -56.3198 | -27.4505 | -340.0 | 2004-06-14T00:00 | Paralomis formosa | field | 10.7 | 102.9 | 34.8 | 64.5 | 521.8 | 108.5 | 12.7 | 121.3 | 569.4 | 101.1 | 19.9 | 68.6 |
| Icefish2004_49 | -56.3198 | -27.4505 | -340.0 | 2004-06-14T00:00 | Paralomis formosa | field | 9.7 | 93.7 | 44.3 | 81.9 | 470.7 | 97.9 | 10.5 | 99.8 | 572.7 | 101.7 | 21.4 | 73.7 |
| Icefish2004_49 | -56.3198 | -27.4505 | -340.0 | 2004-06-14T00:00 | Paralomis formosa | field | 9.0 | 86.8 | 43.1 | 79.9 | 499.0 | 103.7 | 11.8 | 112.2 | 588.3 | 104.5 | 25.7 | 88.8 |
| Icefish2004_26 | -53.6558 | -40.7425 | -410.0 | 2004-06-05T00:00 | Paralomis spinosissima | field | 10.7 | 102.5 | 38.5 | 71.3 | 483.3 | 100.5 | 12.0 | 113.9 | 533.2 | 94.7 | 18.2 | 62.7 |
| Icefish2004_26 | -53.6558 | -40.7425 | -410.0 | 2004-06-05T00:00 | Paralomis spinosissima | field | 9.5 | 91.2 | 38.0 | 70.3 | 499.0 | 103.7 | 11.5 | 109.4 | 563.7 | 100.1 | 20.7 | 71.4 |
| Icefish2004_26 | -53.6558 | -40.7425 | -410.0 | 2004-06-05T00:00 | Paralomis spinosissima | field | 12.4 | 119.5 | 38.6 | 71.5 | 484.5 | 100.7 | 8.7 | 82.5 | 524.8 | 93.2 | 23.3 | 80.5 |
| Icefish2004_26 | -53.6558 | -40.7425 | -410.0 | 2004-06-05T00:00 | Paralomis spinosissima | field | 12.6 | 120.9 | 41.8 | 77.4 | 460.6 | 95.7 | 12.3 | 116.7 | 556.4 | 98.8 | 19.8 | 68.3 |
| Icefish2004_26 | -53.6558 | -40.7425 | -410.0 | 2004-06-05T00:00 | Paralomis spinosissima | field | 10.6 | 101.6 | 36.7 | 68.0 | 490.7 | 102.0 | 11.0 | 104.5 | 576.8 | 102.5 | 17.8 | 61.4 |
| Icefish2004_26 | -53.6558 | -40.7425 | -410.0 | 2004-06-05T00:00 | Paralomis spinosissima | field | 10.7 | 103.2 | 41.6 | 77.1 | 457.1 | 95.0 | 7.6 | 72.8 | 490.3 | 87.1 | 21.2 | 73.2 |
| Icefish2004_26 | -53.6558 | -40.7425 | -410.0 | 2004-06-05T00:00 | Paralomis spinosissima | field | 10.4 | 99.8 | 42.9 | 79.5 | 454.1 | 94.4 | 11.9 | 112.9 | 494.3 | 87.8 | 17.9 | 61.8 |
| Icefish2004_26 | -53.6558 | -40.7425 | -410.0 | 2004-06-05T00:00 | Paralomis spinosissima | field | 10.0 | 96.3 | 41.9 | 77.6 | 476.3 | 99.0 | 11.5 | 109.4 | 547.9 | 97.3 | 18.9 | 65.1 |
| Icefish2004_26 | -53.6558 | -40.7425 | -410.0 | 2004-06-05T00:00 | Paralomis spinosissima | field | 10.9 | 104.5 | 43.2 | 79.9 | 474.5 | 98.7 | 13.1 | 124.5 | 517.0 | 91.8 | 23.3 | 80.5 |
| Icefish2004_26 | -53.6558 | -40.7425 | -410.0 | 2004-06-05T00:00 | Paralomis spinosissima | field | 11.6 | 111.4 | 44.2 | 81.8 | 474.5 | 98.6 | 12.3 | 117.6 | 522.0 | 92.7 | 24.0 | 82.8 |
| Icefish2004_26 | -53.6558 | -40.7425 | -410.0 | 2004-06-05T00:00 | Lithodes confundens | field | 12.0 | 115.4 | 34.0 | 62.9 | 497.2 | 103.4 | 12.0 | 113.8 | 454.1 | 80.7 | 20.4 | 70.3 |
| Icefish2004_26 | -53.6558 | -40.7425 | -410.0 | 2004-06-05T00:00 | Lithodes confundens | field | 15.6 | 149.7 | 36.6 | 67.8 | 489.1 | 101.7 | 13.9 | 132.0 | 484.5 | 86.1 | 22.6 | 78.0 |
| Icefish2004_26 | -53.6558 | -40.7425 | -410.0 | 2004-06-05T00:00 | Lithodes confundens | field | 13.1 | 125.9 | 31.5 | 58.3 | 487.6 | 101.4 | 10.4 | 99.3 | 468.6 | 83.2 | 18.7 | 64.6 |
| Icefish2004_26 | -53.6558 | -40.7425 | -410.0 | 2004-06-05T00:00 | Lithodes confundens | field | 11.9 | 113.9 | 22.7 | 42.0 | 492.6 | 102.4 | 11.7 | 111.2 | 465.8 | 82.7 | 21.7 | 74.7 |
| Icefish2004_26 | -53.6558 | -40.7425 | -410.0 | 2004-06-05T00:00 | Lithodes confundens | field | 12.2 | 117.6 | 29.9 | 55.3 | 535.7 | 111.4 | 10.7 | 101.5 | 462.5 | 82.1 | 19.3 | 66.6 |
| Icefish2004_26 | -53.6558 | -40.7425 | -410.0 | 2004-06-05T00:00 | Lithodes confundens | field | 17.9 | 172.0 | 40.6 | 75.2 | 436.2 | 90.7 | 13.8 | 131.0 | 534.4 | 94.9 | 30.7 | 105.9 |
| Icefish2004_26 | -53.6558 | -40.7425 | -410.0 | 2004-06-05T00:00 | Lithodes confundens | field | 12.1 | 116.6 | 42.4 | 78.5 | 462.7 | 96.2 | 12.4 | 118.1 | 539.7 | 95.9 | 23.8 | 82.2 |
| Icefish2004_26 | -53.6558 | -40.7425 | -410.0 | 2004-06-05T00:00 | Lithodes confundens | field | 15.6 | 150.3 | 42.8 | 79.3 | 456.1 | 94.8 | 14.1 | 134.2 | 519.5 | 92.3 | 22.3 | 76.9 |
| Icefish2004_26 | -53.6558 | -40.7425 | -410.0 | 2004-06-05T00:00 | Lithodes confundens | field | 14.1 | 135.2 | 48.6 | 90.0 | 452.8 | 94.1 | 14.0 | 133.2 | 547.5 | 97.2 | 20.5 | 70.6 |
| Punta_Arenas_2008c | -53.1600 | -70.9300 | 2008-04-01T00:00 | Paralomis granulosa | laboratory | 10.7 | 110.6 | 42.2 | 84.4 | 423.1 | 94.9 | 11.6 | 117.9 | 477.4 | 91.3 | 14.3 | 52.9 | |
| Punta_Arenas_2008c | -53.1600 | -70.9300 | 2008-04-01T00:00 | Paralomis granulosa | laboratory | 12.9 | 133.3 | 42.4 | 84.7 | 431.0 | 96.6 | 10.8 | 109.9 | 508.8 | 97.3 | 18.7 | 69.1 | |
| Punta_Arenas_2008c | -53.1600 | -70.9300 | 2008-04-01T00:00 | Paralomis granulosa | laboratory | 10.2 | 105.4 | 37.6 | 75.2 | 439.2 | 98.5 | 10.8 | 110.0 | 488.7 | 93.4 | 18.7 | 69.4 | |
| Punta_Arenas_2008c | -53.1600 | -70.9300 | 2008-04-01T00:00 | Paralomis granulosa | laboratory | 9.9 | 102.2 | 36.9 | 73.9 | 451.3 | 101.2 | 10.6 | 108.0 | 486.8 | 93.1 | 18.7 | 69.3 | |
| Punta_Arenas_2008c | -53.1600 | -70.9300 | 2008-04-01T00:00 | Paralomis granulosa | laboratory | 13.5 | 139.5 | 40.3 | 80.5 | 423.0 | 94.8 | 10.6 | 108.1 | 516.7 | 98.8 | 18.6 | 68.8 | |
| Punta_Arenas_2008c | -53.1600 | -70.9300 | 2008-04-01T00:00 | Paralomis granulosa | laboratory | 11.6 | 119.7 | 40.7 | 81.3 | 419.2 | 94.0 | 10.4 | 106.6 | 500.2 | 95.6 | 17.2 | 63.5 | |
| Punta_Arenas_2008c | -53.1600 | -70.9300 | 2008-04-01T00:00 | Paralomis granulosa | laboratory | 10.9 | 112.9 | 40.5 | 80.9 | 423.5 | 94.9 | 10.2 | 103.8 | 475.3 | 90.9 | 13.1 | 48.7 | |
| Punta_Arenas_2008c | -53.1600 | -70.9300 | 2008-04-01T00:00 | Paralomis granulosa | laboratory | 11.3 | 116.7 | 39.7 | 79.4 | 437.0 | 98.0 | 11.3 | 115.4 | 478.1 | 91.4 | 16.0 | 59.4 | |
| PS69/710-6 | -65.5389 | -61.5022 | -490.2 | 2007-01-16T18:58 | Notocrangon antarcticus | field | 4.5 | 43.5 | 4.6 | 8.6 | 459.8 | 95.6 | 14.2 | 134.8 | 521.9 | 92.7 | 8.7 | 29.9 |
| PS69/710-6 | -65.5389 | -61.5022 | -490.2 | 2007-01-16T18:58 | Notocrangon antarcticus | field | 7.4 | 71.0 | 20.8 | 38.5 | 469.3 | 97.6 | 12.3 | 117.0 | 518.5 | 92.1 | 14.6 | 50.4 |
| PS69/710-6 | -65.5389 | -61.5022 | -490.2 | 2007-01-16T18:58 | Notocrangon antarcticus | field | 7.0 | 67.1 | 6.1 | 11.3 | 463.7 | 96.4 | 14.3 | 136.5 | 394.4 | 70.0 | 10.5 | 36.4 |
| PS69/710-6 | -65.5389 | -61.5022 | -490.2 | 2007-01-16T18:58 | Notocrangon antarcticus | field | 8.3 | 79.6 | 5.8 | 10.7 | 470.3 | 97.8 | 14.0 | 133.0 | 470.9 | 83.6 | 8.4 | 29.0 |
| PS69/710-6 | -65.5389 | -61.5022 | -490.2 | 2007-01-16T18:58 | Notocrangon antarcticus | field | 9.4 | 90.3 | 7.5 | 13.8 | 431.1 | 89.6 | 14.6 | 139.3 | 436.7 | 77.6 | 6.4 | 22.0 |
| PS69/710-6 | -65.5389 | -61.5022 | -490.2 | 2007-01-16T18:58 | Notocrangon antarcticus | field | 8.4 | 81.2 | 6.5 | 12.1 | 534.1 | 111.0 | 18.7 | 178.1 | 434.9 | 77.2 | 8.2 | 28.1 |
| Icefish2004_19 | -51.6863 | -57.4560 | -130.0 | 2004-05-29T00:00 | Peltarion spinosulum | field | 9.9 | 95.4 | 50.0 | 92.7 | 449.7 | 93.5 | 5.3 | 50.3 | 511.2 | 90.8 | 29.4 | 101.4 |
| Icefish2004_19 | -51.6863 | -57.4560 | -130.0 | 2004-05-29T00:00 | Peltarion spinosulum | field | 11.9 | 114.0 | 53.1 | 98.3 | 483.6 | 100.5 | 10.3 | 98.6 | 489.3 | 86.9 | 34.5 | 119.0 |
| Icefish2004_19 | -51.6863 | -57.4560 | -130.0 | 2004-05-29T00:00 | Peltarion spinosulum | field | 12.8 | 123.5 | 50.2 | 92.9 | 492.0 | 102.3 | 2.5 | 23.3 | 423.2 | 75.2 | 31.0 | 107.0 |
| Icefish2004_19 | -51.6863 | -57.4560 | -130.0 | 2004-05-29T00:00 | Peltarion spinosulum | field | 11.8 | 113.2 | 53.6 | 99.3 | 482.1 | 100.2 | 3.3 | 31.8 | 493.4 | 87.6 | 26.3 | 90.5 |