Map of the Agulhas Bank centred on the Outeniqua Basin
|Ecozone||Temperate Southern Africa|
|Area||116,000 km2 (45,000 sq mi)|
|Elevation||-50 to -200 m|
|Oceans or seas||Atlantic Ocean, Indian Ocean|
The Agulhas Bank (//, from Portuguese for Cape Agulhas, Cabo das Agulhas, "Cape of Needles") is a broad, shallow part of the southern African continental shelf which extends up to 250 km (160 mi) south of Cape Agulhas before falling steeply to the abyssal plain.
It is the ocean region where the warm Indian Ocean and the cold Atlantic Ocean meet. This convergence leads to treacherous sailing conditions, accounting for numerous wrecked ships in the area over the years. However the meeting of the oceans here also fuels the nutrient cycle for marine life, making it one of the best fishing grounds in South Africa.
- 1 Extent and characteristics
- 2 Oceanography
- 3 Geology
- 4 Human evolution
- 5 Commercial importance
- 6 Biodiversity
- 7 References
Extent and characteristics
The Agulhas Bank stretches approximately 800 km (500 mi) along the African coast, from off Cape Peninsula (18°E) to Port Alfred (26°E), and up to 250 km (160 mi) from it. The bank is 50 m (160 ft) deep near the coast and reaches 200 m (660 ft) before dropping steeply to 1,000 m (3,300 ft) on its southern edge. The shelf spans an area of 116,000 km2 (45,000 sq mi) with a mean depth slightly over 100 m (330 ft).
The National Spatial Biodiversity Assessment 2004 recognised 34 biozones nested within 9 bioregions (of which four were offshore). The National Biodiversity Assessment 2011 replaced these ecozones and biozones with the terms ecoregions and ecozones. In 2011, the Agulhas Ecoregion was divided into four distinct ecozones: Agulhas inshore, Agulhas inner shelf, Agulhas outer shelf, and Agulhas shelf edge. 33 different benthic habitats types were identified on the Agulhas Bank.
There are dozens of warm temperate reefs along the coast of the Agulhas Ecoregion spanning from 5–30 m (16–98 ft) below sea level. Many rocky sub-tidal reefs are of aeolianite or sandstone origin, but granite, quartzite and siltstone reefs are also present. The Agulhas reefs are very heterogeneous and include several possible different sub-types. Some of the reefs are within protected areas, but only a few of those protected areas include protection from fishing.
The Agulhas Current flows south along the African east-coast and along the south-eastern edge of the bank. It then retroflects back into the Indian Ocean south-west of the bank. This retroflection results in intense eddy activities such as meanders, eddies, and filaments. In upper layer water, the Agulhas rings and eddies move warm and salty water into the large South Atlantic gyre, which exports it to the tropics. In the lower ocean layers water is transported in the opposite direction.
Cyclonic eddies is another source of edge upwelling west of Port Elisabeth. Plumes of warm surface water migrate onto the bank along its eastern edge, providing subtropical surface water from the Indian Ocean. In summer, easterly winds can intermittently drive coastal upwelling along the South African south coast. The Agulhas Bank is dominated by westerly winds and most of the upwelling on the bank is related to the interaction of the Agulhas Current on the eastern edge, but easterly winds do occur, especially in summer and fall, and can generate local upwelling cells.
As the current is diverged away from the coast, dynamic processes draws an onshore Ekman layer of cold water from below the warm shelf-edge flow. In spring and summer, at a depth of 100 m (330 ft), a semi-permanent ridge of cold water is present on the eastern and central shelf.
In summer, there is mixture of subtropical water separated by thermoclines from cool waters, but there is a considerable seasonal variation. On the shelf, bottom waters exhibit characteristics of the central Indian Ocean in the east and central Atlantic Ocean waters in the west.
Agulhas meanders and Natal pulses
As the Agulhas Current flows south along the African east coast, it tends to bulge inshore frequently, a deviation from the current's normal path known as Agulhas Current meanders (ACM). These bulges are occasionally (1-7 times per year) followed by a much larger offshore bulge, known as Natal pulses (NP). Natal pulses move along the coast at 20 km (12 mi) per day. An ACM can bulge up to 20 km (12 mi) and a NP up to 120 km (75 mi) from the current's mean position. The AC passes 34 km (21 mi) offshore and an ACM can reach 123 km (76 mi) offshore. When the AC meanders, its width broadens from 88 km (55 mi) to 125 km (78 mi) and its velocity weakens from 208 cm/s (82 in/s) to 136 cm/s (54 in/s). An ACM induces a strong inshore counter-current.
Large-scale cyclonic meanders known as Natal pulses are formed as the Agulhas Current reaches the continental shelf on the South African east-coast (i.e. the eastern Agulhas Bank off Natal). As these pulses moves along the coast on the Agulhas Bank, they tend to pinch off Agulhas rings from the Agulhas Current. Such a ring shedding can be triggered by a Natal pulse alone, but sometimes meanders on the Agulhas Return Current merge to contribute to the shedding of an Agulhas ring.
Agulhas leakage and rings
Agulhas rings are large anticyclonic eddies or warm core rings of ocean water that are pinched off the Agulhas Current along the eastern edge of the Agulhas Bank from where they move into the South Atlantic. As the Agulhas Current reaches the east coast of South Africa, large solitary meanders known as Natal pulses form at irregular intervals. 165 days after the appearance of a Natal pulse, an Agulhas ring is formed off Durban. The Agulhas rings are among the largest eddies in the world and play an important role in the Agulhas Leakage, the transport of warm water from the Indian Ocean to the Atlantic Ocean, which affects the global climate.
The average diameter of the Agulhas rings is 320 km (200 mi), but they can reach 500 km. They extend down to the ocean floor; circulate at 0.3–1.5 m/s (0.98–4.92 ft/s); and move into the South Atlantic at 4–8 km (2.5–5.0 mi)/day. Only half of the Agulhas eddies that leave the Cape Basin manage to cross the Walvis Ridge and those who do tend to lose half their energy before reaching the ridge within six month. The Agulhas rings transport an estimated 1-5 Sv (millions m²/s) of water from the Indian Ocean to the South Atlantic.
The Agulhas rings are thought to be of global climatic importance. Their delivery of warm water from the Indian to the Atlantic ocean can control the rate of thermohaline overturning of the entire Atlantic. Other factors contribute to various extent to the inter-ocean exchanges in the region, including filaments from the Agulhas Current and intrusions of water from Antarctica. Cold, cyclonic eddies have been observed in the southwestern Atlantic. Based on model simulations, researchers have found that the interaction of the Agulhas Current and the eastern edge of the bank can result in the Agulhas rings.
The provenance of ocean sediments can be determined by analysing terrigenous strontium isotope ratios in deep ocean cores. Sediments underlying the Agulhas Current and Return Current have significantly higher ratios than surrounding sediments. Analyses of cores in the South Atlantic deposited during the Last Glacial Maximum (LGM, 20 000 years ago), show that the Agulhas leakage (shedding of Agulhas rings) was significantly reduced. It has been hypothesised that the reason for this was that the Agulhas Current was stronger which resulted in a more eastward retroflection and therefore less leakage. However, analyses of such cores south of Africa show that the trajectory of the current was the same during the LGM and that the reduced leakage must be explained by a weaker current. Consequently, it can be predicted that a stronger Agulhas Current will result in its retroflection occurring more eastward and an increased Agulhas leakage.
Compared to the Agulhas Current, the Benguela Current on the west and south-west coast of Africa is more intense and steadier. Its dynamic southern upwelling system is driven by the prevailing northward winds that produce an intense off-shore Ekman transport. Most of this upwelling is concentrated to a few upwelling cells in the southern region: Namaqua (30°S), Cape Columbine (32.5°S), and Cape Peninsula (34°S). The wind is most intense from October to February, and the contrast in sea surface temperature between the open sea and the shelf is most prominent during summer.
Coastal upwelling s also common on the western bank, but the more stable atmospheric condition results in larger cold water plumes that sometimes merge to form a continuous upwelling regime along the South African south-west coast. This upwelling zone is the southernmost extension of the Benguela Current Large Maritime Ecosystem. The Agulhas Current regularly flows around the southern tip of the bank and brings warm water to the western bank along the bank's western edge. Regularly, the mesoscale eddies from the east interact with the Benguela upwelling system on the African west coast.
Deep water eddies
Floating south along the South American continental slope, the Deep Western Boundary Current (DWBC) carries North Atlantic Deep Water (NADW) into the South Atlantic. At about 8°S and at a depth of 2,200–3,500 m (7,200–11,500 ft), the DWBC breaks into anticyclonic eddies during periods of strong meridional overturning circulation. One such NADW eddy was observed in 2003 and the researchers speculated that a deeply penetrating Agulhas ring pinched it off the NADW slope current. Spinning at 20 cm/s (7.9 in/s), these deep-water eddies move around the southern tip of the Agulhas Bank and into the Indian Ocean. Most of the NADW flow (more than 7 Sv) meanders east around the Agulhas Plateau together with the surface Agulhas Return Current, but a smaller portion (3 Sv) continue north along the African east-coast as the Agulhas Undercurrent. Of 89.5 Sv released from the North Atlantic, 3.6 Sv leaves the South Atlantic south of the Agulhas Bank. However, 0.9 Sv recirculate in the basin north of the Walvis Ridge for centuries, of which 50-90% end up flowing south of the Agulhas Bank within 300 years, increasing the net inter-oceanic exchange with 4.1-4.5 Sv.
The oldest rock found along the coastline of the Agulhas Bank are eugeosynclinal sediments of the up to 3 km (1.9 mi) thick Kaaimans group deposited during continental rifting some 900 million years ago (Mya). The proto-South Atlantic closed during the Saldanian orogeny to form part of the supercontinent Gondwana (700-600 Mya). The Cape granites were emplaced and the Kaaimans Group rocks were folded and thermally metamorphosed during this period. The formation of the main basin in the Cape Province commenced 570 Mya and lasted for 200 My. The Table Mountain Group is 4 km (2.5 mi) thick and an erosional unconformity marking its base is composed of both terrestrial and marine sediments. Synclines along the coast of the southern Cape contains sediments from the Bokkveld Group.
The Cape Fold Belt (CFB) rocks and the Karoo Basin were deposited 450 Mya; the Cape Supergroup 450-300 Mya during a series of transgression-regression cycles. Pan-African thrusts were reactivated 270-215 Mya to form the CFB which was then part of a continuous fold belt that developed during the Gondwanide orogeny together with Sierra de la Ventana (Argentina), Pensacola Mountains (East Antarctica), and Ellsworth Mountains (West Antarctica). In the late Carboniferous and early Jurassic, the Karoo Supergroup was deposited in the Karoo Basin where the CFB is located today.
Basaltic lavas were extruded 183 Mya to form the Karoo large igneous province; a volcanism caused by the Bouvet hotspot which is linked to the Gondwana break-up. The Bouvet hotspot was located in or near present-day South Africa from the late Triassic 220 mya and until the Africa-Antarctica breakup 120 mya. The Bouvet hotspot track stretches south-east from the African continent, near the South Africa-Mozambique border, and east of the AFFZ down to Bouvet Island/Bouvet Triple Junction in the South Atlantic. 100 Mya, the region where the triple junction was located passed over the hotspot, resulting in a continuous eruption that lasted to about 94 Mya and the seafloor spreading that still separates Antarctica, Africa, and South America.
The Agulhas-Falkland Fracture Zone (AFFZ) stretches 1,200 kilometres (750 mi) across the South Atlantic. It is one of the largest and most spectacular fracture zones on Earth. It developed during the Early Cretaceous as West Gondwana (=South America) broke up from Africa. The AFFZ is characterized by a pronounced topographic anomaly, the Agulhas Ridge (41°S,16°E-43°S,9°E) which rises more than 2 km above the surrounding sea floor. The only equivalent in size are the neighbouring Diaz Ridge and the Falkand Escarpment. The Agulhas Ridge is unique because it was not formed during the continental breakup during the Cretaceous and because it separates oceanic crusts of different age, and not oceanic crust (~14 km thick) from continental crust (25 km thick).
North of the (AFFZ) is the Outeniqua Basin which is a complex system of sub-basins separated from each other by faults and basement arches; there are several smaller fault-bounded sub-basins in the north (Bredasdorp, Infanta, Pletmos, Gamtoos, and Algoa) and a distinctively deeper sub-basin in the south (the South Outeniqua Basin.) The sedimentary fill of the these basins developed as the northern edge of the Falkland Plateau separated from the South African southern margin during the early Cretaceous.
The Diaz Marginal Ridge (DMR) separates these basins from the AFFZ. The DMR is buried under 200–250 m (660–820 ft) of sediments and sedimentary rocks and 150–200 m (490–660 ft) of this sedimentary material is undisturbed Cretaceous sediments younger than the oldest Cretaceous sedimentary rocks in the Southern Outeniqua Basin. The DMR must therefore have formed after the initial West Gondwana breakup 130-90 Mya. The DMR probably formed when new, hot oceanic crust slid past old, cold continental crust and the contrast in temperatures induced a thermal uplift.
As West Gondwana drifted away from Africa roughly 125 Myr, the South Atlantic seafloor formed between them and magnetic anomalies north of the AFFZ reflects phase of the seafloor spreading. South of the AFFZ traces can be found of how the Falkland Plateau and the Agulhas Bank moved relative to each other. On a modern map, the Falkland Plateau can still be rotated and fitted into the Natal Valley in the Indian Ocean east of South Africa. The Agulhas Plateau is located southeast of the shelf, separated from it by the Agulhas Passage (through which the Agulhas Current flows.)
One of the largest known slumps occurred on the south-eastern edge of the Agulhas Bank in the Pliocene or more recently. Stretching from a depth of 190–700 m (620–2,300 ft), the so-called Agulhas slump is 750 km (470 mi) long, 106 km (66 mi) wide, and has a volume of 20,000 km3 (4,800 cu mi). It is a composite slump with proximal and distal allochthonous sediment masses separated by a large glide plane scar. In the western part, the sediments are dammed by basement ridges, but, in the eastern part, they have spread into the Transkei Basin. A series of slump scarps along the western edge of the shelf are 18–2 Mya, but covered by younger sediments brought there by the Benguela upwelling.
Anatomically modern humans evolved around 200 kya. The genetic diversity in the human lineage is relatively low, which indicate one or several population bottlenecks late in our lineage. It has been estimated that the population was limited to maybe 600 individuals during the MIS 6 glacial stage (195-125 kya), one of the longest cold periods in the Quaternary of Africa. A technological and behavioural revolution that occurred globally about 50 kya led to a cultural complexity which happened in South Africa around 120-70 kya.
The Cape Floral Region is a thin coastal strip and a botanic hotspot which developed at the confluence of the Benguela Upwelling and Agulhas Current. According to what professor Curtis Marean call the "Cape Floral Region – South Coast Model" for the origins of modern humans, the early hunter-gatherers survived on shellfish, as well as geophytes, fur seal, fish, seabirds, and wash-ups found on the exposed Agulhas Bank. The bank slopes into the sea and a reconstruction of how the coastline has changed over 440 kya shows that the coast during the Pleistocene was located as far as 90 km (56 mi) from the present coast.
The present South African southern coastal plain (SCP) is still separated from the rest of Africa by the Cape Fold Belt. During glacial maxima the sea-level dropped 120 metres (390 ft). This not only left large parts of the Agulhas Bank exposed, which greatly expanded the area of the SCP, but it also reconnected the SCP to the rest of Africa by the shallow water shelves, which broke the isolation of the SCP. Modern humans evolved on the SCP and the fluctuation in sea-levels would have resulted in a significant variation in selective pressure. No fossil records are known from the now submerged shelf, but a series of key fossil sites along the costal margin of the present SCP provide earliest traces of anatomically modern humans and the use of marine resources.
South Africa began oil exploration on the Agulhas Bank in the 1980s. Of more than 200 offshore wells in South Africa, most are found on Bredasdorp Basin on the Agulhas Bank.
The Agulhas Bank is also significant for fisheries who use demersal trawling, demersal longline fishing, and midwater trawl fishing on the bank. Squid and small pelagic fishes are also caught. Before the introduction of the EEZ, foreign fisheries used roch-hopper gear trawling on the bank.
Most of the catches are short-lived shelf-zone pelagic species and more long-lived deep-water species. The large populations of sardine and anchovy also present on the shelf follow an annual cycle. Anchovy spawn on the western Agulhas Bank in early summer while the sardines span over a broader season and area — eggs are transported by currents to the nursery area in the St Helena Bay on the South African west coast from where juvenile then migrate back to the Agulhas Bank to spawn.
South Africa has a relatively large fishing industry mostly catching pelagic pilchard and anchovy and demersal Hake on the south and western coasts. Though the east coast has fewer commercial fisheries, the large human population along there has resulted in overexploitation of coastal fish and invertebrate stocks by recreational and subsistence fishers. A small aquaculture industry produces mussles and oysters offshore.
Several pelagic species are heavily harvested by the commercial fleet: purse-seine fishery is used to catch sardines, anchovies, and round herring; mid-water trawl fishery to catch horse mackerel and chub mackerel; pelagic longline and pole fishery to catch tunas and swordfish; while hook and line are used inshore to catch squid and teleost species, including snoek and geelbek. All these species are relatively common and are considered having an important role in the ecosystem.
There are at least 12,914 marine species in South Africa, but small bodied species are poorly documented and the abyssal zone is almost completely unexplored. Almost a quarter of South Africa's coast line is protected, excluding deeper water. A third of the marine species are endemic to South Africa (though poor levels of taxonomic research in adjoining countries probably affects the apparent endemism.) The degree of endemism varies considerably among taxa: Bryozoa 64%, Mollusca 56%, Echinodermata 3.6%, Porifera 8.8%, Amphipoda 33%, Isopoda 85%, or Cumacea 71%. Fisheries are one of the major threats to the biodiversity of the Agulhas Bank.
Copepods comprise 90% of the zooplankton carbon on the Agulhas Bank, and are thus an important source of food for pelagic fish and juvenile squids. The population of Calanus agulhensis, a large species that dominates the copepod community in terms of biomass, has a center of distribution on the central Agulhas Bank. Since 1997 the copepod biomass on the central Agulhas Bank has declined significantly while the biomass of pelagic fish has increased significantly. While it is likely that predation has played an important role in the copepod decline, global warming (sea surface temperature and Cholorphyll A abundance) is believed to have contributed to a smaller population.
The shelf edge along the bank's southern tip is subject to sporadic upwelling. This slope and its surrounding seamounts are the spawning ground for sardine, anchovy, and horse mackerel. Eddies help transport water inshore and link the spawning habitat with important nursery areas. Eggs and larvae laid by the anchovy are transported via the Good Hope Jet to Africa's southwestern coast where they mature. Young anchovies then return to the Agulhas Bank to spawn. Young sardine and anchovy congregate along the west coast between March and September before they migrate to their spawning grounds on the Agulhas Bank. Sardines of intermediate age are present on the western Agulhas Bank between January and April before migrating to KwaZulu-Natal for winter. The spawning on the Agulhas Bank takes place 30–130 km (19–81 mi) offshore from September to February.
The bank is the spawning area of deep reef fish species, including the threatened endemic red steenbras (Petrus rupestris). Other species have been overexploited, including daggerhead seabream (Chrysoblephus cristiceps), black musselcracker (Cymatoceps nasutus), and silver kob (Argyrosomus inodorus).
The main food source for African penguins (Spheniscus demersus) is anchovy and sardine which they forage between Cape Columbine and the central Agulhas Bank. The birds have colonies on Dassen Island, on the South African west coast, and Bird Island, on the south coast. African penguins breed opportunistically, following the anchovy and sardine: from February to September on the Western Cape but from January to July on St Croix Island off Eastern Cape. After breeding, the birds forage further offshore: 10–15 km (6.2–9.3 mi) off the western coast and up to 40 km (25 mi) from their colonies off Eastern Cape.
In 2005, when Korean and Philippine vessels started longline fishing along the edges of the Agulhas Bank, seabird bycatch became a huge problem. Large numbers of albatrosses and petrels were killed — in average 0.6 birds per 1000 hooks, but up to 18 birds per 1000 hooks were reported. Since 2007, however, more restrictive permit conditions for foreign-flagged fleets and the use of birds scaring lines have decreased the number of killed birds by 85%.
Cape fur seals are present along the South African coast. Fur seals are protected in South Africa since 1893 although a small number are occasionally culled to protect sea birds. Many seals are caught in fishery nets and boat propellers, but the seals are also regularly accused of stealing fish from the fisheries. Sharks are known to prey on them, but in 2012 a cape fur seal was observed preying on and consuming a mid-sized blue shark.
51 species, or more than 50%, of the recognized species of cetaceans are present in the southern African subregion (between the equator and the Antarctic ice edge), of which 36 have been sighted in South African and Namibian waters.
A vulnerable population of fish-eating killer whales are present offshore on the Agulhas Bank. Observations peak in January while few are sighted in April and May. The killer whales move in pods of 1-4 individuals and are mostly sited over the shelf edge off the south-east coast. An analysis of killer whale mtDNA has shown that there was a peak inter-oceanic migration events during the Eemian interglacial period, 131-114 kya. This peak coincides with a period of maximal Agulhas leakage which promoted a rapid and episodic interchange of killer whale lineages. During this period killer whales and other marine top predators, such as the great white shark, colonised the North Atlantic and Mediterranean by following their prey — bluefin tuna and swordfish.
A vagrant Commerson's dolphin — a species with two isolated populations, one along the southern coast of Argentina and the other around the Kerguelen Islands — was sighted on the Agulhas Bank in 2004. It is not known from which population the sighted individual stems. The Kerguelen Islands are located 4,200 km (2,600 mi) and South America 6,300 km (3,900 mi) from the Agulhas Bank, but the west-ward direction of the Antarctic Circumpolar Current would force the dolphin to swim against the current from the Kerguelen Islands.
- Gyory et al. 2004
- "Sea Atlas - Agulhas Bank". Bayworld Centre For Research & Education. Retrieved January 2015.
- Blanke et al. 2009, Introduction, pp. 1-2
- Whittle 2012, Introduction
- Sink et al. 2012, Fig. 4, pp. 50-51
- Sink et al. 2012, Fig. 5, p. 53
- Sink et al. 2012, pp. 66-67
- Ruijter et al. 2003, p. 45
- Jackson et al. 2012
- Leber & Beal 2012
- Leeuwen, Ruijter & Lutjeharms 2000, Abstract
- Leeuwen, Ruijter & Lutjeharms 2000, Introduction
- Ruijter et al. 2003, p. 46
- Penven et al. 2001, Introduction, p. 1055
- Penven et al. 2001, Conclusion, p. 1057
- Franzese, Goldstein & Skrivanek 2012
- Casal, Beal & Lumpkin 2006, Abstract, Introduction, pp. 1718-1719; Fig. 7, p. 1727
- Sebille, Johns & Beal 2012, 3.1. Connectivity Between the DWBC and the Agulhas Region
- Durrheim 1987, Geological evolution of the Agulhas Bank, pp. 395-396
- Parsiegla et al. 2009, Geological and Tectonic Background, pp. 2-4
- Golonka & Bocharova 2000, Figs. 3-8
- Gohl & Uenzelmann-Neben 2012, Figs. 1, 5
- Uenzelmann-Neben & Gohl 2003, Abstract
- Bird 2001, p. 152
- Parsiegla et al. 2009, Introduction , p. 2; Geological and Tectonic Background , p. 3; Fig. 3, p.5
- Parsiegla et al. 2009, The Diaz Marginal Ridge, pp. 12-14
- Goodlad, Martin & Hartnay 1982
- Parsiegla et al. 2009, Fig. 1
- Uenzelmann-Neben & Huhn 2009, pp. 66, 76
- Marean 2011, pp. 421–423
- Marean 2011, pp. 423–425
- Compton 2011, p. 508
- "Assessment of Offshore Benthic Biodiversity on the Agulhas Bank and the Potential Role of Petroleum". WWF. November 2008. Retrieved January 2015.
- Jury 2011, pp. 1–2
- Griffith et al. 2010, p. 1
- Grantham et al. 2011, p. 2
- Griffith et al. 2010, pp. 6, 8
- Huggett et al. 2012
- Sink et al. 2012b
- Crawford et al. 2006, Introduction
- Sink et al. 2012a
- Ebert, Compagno & Cowley 1992, Introduction
- Harding 2013, Abstract
- Ryan 2006
- "Albatross Task Force". BirdLife South Africa. Retrieved March 2015.
- "South African Fur Seal". Seal Conservation Society. 2011. Retrieved March 2015.
- Nuwer, Rachel (March 2015). "Fur Seals Caught Preying on Sharks Off South Africa". Smithsonian Magazine. Retrieved March 2015.
- Elwen et al. 2011, p. 470
- Williams et al. 2009, Abstract
- Foote et al. 2011, p. 5
- Bruyn, Hofmeyr & Villiers 2006
- Bianucci, Lambert & Post 2007, Abstract
- Elwen et al. 2013, Introduction
- Bianucci, G.; Lambert, O.; Post, K. (2007). "A high diversity in fossil beaked whales (Mammalia, Odontoceti, Ziphiidae) recovered by trawling from the sea floor off South Africa" (PDF). Biodiversitas 29 (4). Retrieved February 2015.
- Bird, D. (2001). "Shear margins: Continent-ocean transform and fracture zone boundaries" (PDF). The Leading Edge 20 (2): 150–159. doi:10.1190/1.1438894. Retrieved January 2015.
- Blanke, B.; Penven, P.; Roy, C.; Chang, N.; Kokoszka, F. (2009). "Ocean variability over the Agulhas Bank and its dynamical connection with the southern Benguela upwelling system" (PDF). Journal of Geophysical Research 114 (C12028). doi:10.1029/2009JC005358. Retrieved January 2015.
- Bruyn, P. J. N., de; Hofmeyr, G. J. G.; Villiers, M. S., de (2006). "First record of a vagrant Commerson’s dolphin, Cephalorhynchus commersonii, at the southern African continental shelf" (PDF). African Zoology 41 (1). Retrieved February 2015.
- Casal, T. G. D.; Beal, L. M.; Lumpkin, R. (2006). "A North Atlantic deep-water eddy in the Agulhas Current system". Deep-Sea Research I 53: 1718–1728. doi:10.1016/j.dsr.2006.08.007.
- Compton, J. S. (2011). "Pleistocene sea-level fluctuations and human evolution on the southern coastal plain of South Africa" (PDF). Quaternary Science Reviews 30: 506–527. doi:10.1016/j.quascirev.2010.12.012. Retrieved January 2015.
- Crawford, R. J. M.; Hemming, M.; Kemper, J.; Klage, N. T. W.; Randall, R. M.; Underhill, L. G.; Venter, A. D.; Wolfaardt, A. C. (2006). "S24-2 Molt of the African penguin, Spheniscus demersus, in relation to its breeding season and food availability" (PDF). Acta Zoologica Sinica 52 (Supplement): 444–447. Retrieved March 2015.
- Durrheim, R. J. (1987). "Seismic reflection and refraction studies of the deep structure of the Agulhas Bank". Geophysical Journal International 89 (1): 395–398. doi:10.1111/j.1365-246X.1987.tb04437.x.
- Ebert, D. A.; Compagno, L. J. V.; Cowley, P. D. (1992). "A preliminary investigation of the feeding ecology of squaloid sharks off the west coast of southern Africa". South African Journal of Marine Science 12 (1): 601–609. doi:10.2989/02577619209504727.
- Elwen, S. H.; Findlay, K. P.; Kiszka, J.; Weir, C. R. (2011). "Cetacean research in the southern African subregion: a review of previous studies and current knowledge" (PDF). African Journal of Marine Science 33 (3): 469–493. doi:10.2989/1814232x.2011.637614. Retrieved March 2015.
- Elwen, S. H.; Gridley, T.; Roux, J.-P.; Best, P. B.; Smale, M.J. (2013). "Records of kogiid whales in Namibia, including the first record of the dwarf sperm whale (Kogia sima)" (PDF). Marine Biodiversity Records 6 (e45). doi:10.1017/S1755267213000213. Retrieved February 2015.
- Foote, A. D.; Morin, P. A.; Durban, J. W.; Willerslev, E.; Orlando, L.; Gilbert, : T. P. (2011). "Out of the Pacific and Back Again: Insights into the Matrilineal History of Pacific Killer Whale Ecotypes" (PDF). PLoS ONE 6 (9): e24980. doi:10.1371/journal.pone.0024980. Retrieved March 2015.
- Franzese, A. M.; Goldstein, S. L.; Skrivanek, A. L. (2012). "Assessing the role of the Subtropical Front in regulating Agulhas leakage at the Last Glacial Termination" (PDF). American Geophysical Union Chapman Conference. Retrieved February 2015.
- Gohl, K.; Uenzelmann-Neben, G. (2012). "The Southeast African Large Igneous Province: a model of its crustal growth and plate-kinematic dispersal". Large Igneous Provinces Commission. Retrieved February 2015.
- Golonka, J.; Bocharova, N. Y. (2000). "Hot spot activity and the break-up of Pangea" (PDF). Palaeogeography, Palaeoclimatology, Palaeoecology 161: 49–69. doi:10.1016/s0031-0182(00)00117-6. Retrieved February 2015.
- Goodlad, S. W.; Martin, A. K.; Hartnay, C. J. H. (1982). "Mesozoic magnetic anomalies in the southern Natal Valley" (PDF). Nature 295 (25): 686–688.
- Grantham, H. S.; Game, E. T.; Lombard, A. T.; Hobday, A. J.; Richardson, A. J.; Beckley, L. E.; Pressey, R. L.; Huggett, J. A.; Coetzee, J. C.; van der Lingen, C. D.; Petersen, S. L.; Merkle, D.; Possingham, H. P. (2011). "Accommodating Dynamic Oceanographic Processes and Pelagic Biodiversity in Marine Conservation Planning". PLoS ONE 6 (2): e16552. doi:10.1371/journal.pone.0016552. Retrieved March 2015.
- Griffith, C. L.; Robinson, T. B.; Lange, L.; Mead, A. (2010). "Marine Biodiversity in South Africa: An Evaluation of Current States of Knowledge". PLoS One 5 (8): e12008. doi:10.1371/journal.pone.0012008.
- Gyory, J.; Beal, L. M.; Bischof, B.; Mariano, A. J.; Ryan, E. H. (2004). "The Agulhas Current". RSMAS. Retrieved April 2015.
- Harding, C. T. (2013). Tracking African penguins (Spheniscus demersus) outside of the breeding season: Regional effects and fishing pressure during the pre-moult period (MSc). Percy FitzPatrick Institute of African Ornithology, University of Cape Town. Retrieved March 2015.
- Huggett, J.; Lamont, T.; Coetzee, J.; Lingen, Carl, van der (2012). "Are Changes in the Copepod Community on the Agulhas Bank over the Last Two Decades Mediated by Environmental factors or Predation?" (PDF). American Geophysical Union Chapman Conference. Retrieved February 2015.
- Jackson, J. M.; Rainville, L.; Roberts, M. J.; McQuald, C. D.; Porri, F.; Durgadoo, J.; Blastoch, A. (2012). "Mesoscale bio-physical interactions between the Agulhas Current and Agulhas Bank, South Africa" (PDF). American Geophysical Union Chapman Conference. Retrieved February 2015.
- Jury, Mark R. (2011). "Environmental Influences on South African Fish Catch: South Coast Transition". International Journal of Oceanography 2011 (920414). doi:10.1155/2011/920414. Retrieved January 2015.
- Leber, G.; Beal, L. (2012). "Velocity Structure and Transport of the Meandering vs. Non-Meandering Agulhas Current" (PDF). RSMAS. Retrieved April 2015.
- Leeuwen, P. J., van; Ruijter, W. P. M., de; Lutjeharms, J. R. E. (2000). "Natal pulses and the formation of Agulhas rings". Journal of Geophysical Research 105 (C3): 6425–6436. doi:10.1029/1999jc900196. Retrieved February 2015.
- Marean, C. W. (2011). "Coastal South Africa and the Coevolution of the Modern Human Lineage and the Coastal Adaptation" (PDF). In Bicho, N. F.; Haws, J. A.; Davis, L. G. Trekking the Shore: Changing Coastlines and the Antiquity of Coastal Settlement. Interdisciplinary Contributions to Archaeology. Springer. pp. 421–440. ISBN 978-1-4419-8219-3. Retrieved January 2015.
- Parsiegla, N.; Stankiewicz, J.; Gohl, K.; Ryberg, T.; Uenzelmann-Neben, G. (2009). "Southern African continental margin: Dynamic processes of a transform margin". Geochemistry, Geophysics, Geosystems 10 (3). doi:10.1029/2008GC002196.
- Penven, P.; Lutjeharms, J. R. E.; Marchesiello, P.; Roy, C.; Weeks, S. J. (2001). "Generation of cyclonic eddies by the Agulhas Current in the lee of the Agulhas Bank". Geophysical Research Letters 28 (6): 1055–1058. doi:10.1029/2000gl011760. Retrieved January 2015.
- Ruijter, W. P. M., de; Cunningham, S. A.; Gordon, A. L.; Lutjeharms, J. R. E.; Matano, R. P.; Piola, A. R. (2003). "On the South Atlantic Climate Observing System (SACOS)" (PDF). Report of the CLIVAR/OOPC/IAI workshop (NOAA). Retrieved January 2015.
- Ryan, P. (2006). "The long haul: a decade of conserving albatrosses and petrels" (PDF). Africa - birds and birding 11 (2): 52–59. Retrieved March 2015.
- Sebille, Erik, van; Johns, W. E.; Beal, L. M. (2012). "Does the vorticity flux from Agulhas rings control the zonal pathway of NADW across the South Atlantic?". Journal of Geophysical Research 117 (C5). doi:10.1029/2011JC007684. Retrieved April 2015.
- Sink, K.; Holness, S.; Harris, L.; Majiedt, P.; Atkinson, L.; Robinson, T.; Kirkman, S.; Hutchings, L.; Leslie, R.; Lamberth, S.; Kerwath, S.; von der Heyden, S.; Lombard, A.; Attwood, C.; Branch, G.; Fairweather, T.; Taljaard, S.; Weerts, S.; Cowley, P.; Awad, A.; Halpern, B.; Grantham, H.; Wolf, T. (2012). "National Biodiversity Assessment 2011: Technical Report." (PDF). 4: Marine and Coastal Component. Pretoria: South African National Biodiversity Institute. Retrieved March 2015.
- Sink, K.; Leslie, R.; Samaal, T.; Attwood, C. (2012a). "Agulhas Bank, South Africa" (PDF). Southern Indian Ocean Regional Workshop to Facilitate the Description of Ecologically or Biologically Significant Marine Areas (EBSAs) (Convention on Biological Biodiversity). Retrieved March 2015.
- Sink, K.; Leslie, R.; Samaal, T.; Attwood, C. (2012b). "Agulhas slope and seamounts" (PDF). Southern Indian Ocean Regional Workshop to Facilitate the Description of Ecologically or Biologically Significant Marine Areas (EBSAs) (Convention on Biological Biodiversity). Retrieved March 2015.
- Uenzelmann-Neben, G.; Gohl, K. (2003). "Agulhas Ridge, South Atlantic: the peculiar structure of a transform fault". Workshop on East-West Antarctic Tectonics and Gondwana Breakup 60W to 60E as part of the 9th International Symposium on Antarctic Earth Sciences (ISAES) (Potsdam, Germany).
- Uenzelmann-Neben, G.; Huhn, K. (2009). "Sedimentary deposits on the southern South African continental margin: Slumping versus non-deposition or erosion by oceanic currents?". Marine Geology 266: 65–79. doi:10.1016/j.margeo.2009.07.011.
- Whittle, C. P. (2012). "Characterization of Agulhas Bank upwelling variability from satellite-derived sea surface temperature and ocean colour products" (PDF). American Geophysical Union Chapman Conference. Retrieved January 2015.
- Williams, A. J.; Petersen, S. L.; Goren, M.; Watkins, B. P. (2009). "Sightings of killer whales Orcinus orca from longline vessels in South African waters, and consideration of the regional conservation status". African Journal of Marine Science 31 (1): 81–86. doi:10.2989/AJMS.2009.31.1.7.778.