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Bushveld elephant shrews Elephantulus intufi occur on Kalahari sands

Dwarf Sperm Whale

Kogia sima

2025 Red list status

Data Deficient

Decline
Regional Population Trend

Unknown

Change compared
to 2016

No Change

Overview
Red list assessment
Regional Distribution and Occurrence
Climate change
Population information
Population genetics
Habitats and ecology
Use and Trade
Threats
Conservation
Bibliography

Overview

Kogia sima – (Owen, 1866)

ANIMALIA – CHORDATA – MAMMALIA – ARTIODACTYLA – KOGIIDAE – Kogia – sima 

Common Names: Dwarf Sperm Whale, Owen’s Pygmy Sperm Whale (English), Miniatuurpotvis (Afrikaans), Cachalot nain (French), Cachalote enano (Spanish; Castilian)
Synonyms: Physeter simus Owen, 1866; Kogia simus Owen, 1866 

Taxonomic Note: 
The genus Kogia contains two species, the Dwarf Sperm Whale (Kogia sima) and Pygmy Sperm Whale (Kogia breviceps), with no subspecies recognised (Committee on Taxonomy 2021). The cryptic behaviour and similar external morphology of the two species mean that records are often not displayed at the species level and are instead combined into Kogia spp. It has been suggested that K. sima may consist of two parapatric species occupying the Atlantic and Indo-Pacific Oceans, based on evidence from the mitochondrial cytochrome b gene (Chivers et al. 2005). K. breviceps and K. sima are clearly distinguished genetically, but full recognition of a putative third Kogia spp. awaits further supporting evidence (Plön et al. 2023; Chivers et al. 2005). 

Red List Status: DD– Data Deficient 

Assessment Information

Assessors: Plön, S.1 & da Silva, J.2 

Reviewers: Patel, T.3

Institutions: 1University of Cape Town, 2South African National Biodiversity Institute, 3Endangered Wildlife Trust 

Previous Assessors & Reviewers: Plön, S. & Relton, C. 

Previous Contributors: Elwen, S., Findlay, K., Meÿer, M., Oosthuizen, H., Child, MF. & Taylor et al. (2008a, 2008b)  

Assessment Rationale 

K.sima is naturally uncommon and there are no regional estimates of population size or trends (Plön 2022). However, as they are a deep-diving species (up to 800 m), the effects of marine noise pollution should be monitored (although thus far no strandings have been linked to this threat), and we urge more research into the severity of this threat within South African waters. Additionally, plastic pollution should be recognised as an increasing emerging threat, as they are known to fatally ingest plastic bags mistaken for squid. While their offshore distributions do not overlap with many major threats in the assessment region, their natural scarcity and presumed low population numbers make them vulnerable to minor threats, which may be increasing in severity in the assessment region. Thus, in line with the global assessments, we list this species as Data Deficient and urge more systematic monitoring and analysis to determine population sizes and trends within the assessment 

Regional population effects: Dwarf Sperm Whales occur extensively across pelagic waters of tropical and temperate regions, and although their movement patterns are largely unknown, no barriers to dispersal have been recognised (Plön et al. 2023), thus rescue effects are considered possible. 

Reasons for Change 

Reason(s) for Change in Red List Category from the Previous Assessment: No change 

Red List Index 

Red List Index: No change 

Recommended citation: Plön S & da Silva JM. 2025. A conservation assessment of Kogia sima. In Patel T, Smith C, Roxburgh L, da Silva JM & Raimondo D, editors. The Red List of Mammals of South Africa, Eswatini and Lesotho. South African National Biodiversity Institute and Endangered Wildlife Trust, South Africa.

Regional Distribution and occurrence

Geographic Range

Dwarf Sperm Whales are widely distributed and inhabit deep tropical, subtropical and temperate waters throughout all oceans (Plön 2022; Plön and Baird 2022; McAlpine 2002). They seem to prefer warmer waters, compared to the Pygmy Sperm Whale (Plön 2022; Plön and Baird 2022; Caldwell & Caldwell 1989). The distributional ranges of Kogia spp. are poorly known, and most records originate from strandings or occasionally as individuals captured in small fisheries, rather than live sightings at sea (Plön 2022; Nagorsen 1985; Caldwell & Caldwell 1989; McAlpine 2002). This may, however, be attributed to their cryptic nature and affiliation for pelagic regions, rather than low population abundances, particularly since a number of recent studies report extensive observations of K. sima in the wild off Hawaii (Baird et al. 2022), Reunion (Dulau et al. 2024) and in the Eastern Caribbean (Kiszka et al. 2024). The Dwarf Sperm Whale is thought to predominantly reside in waters over the continental shelf edge and slope (Plön and Baird 2022; Ross 1979). Ballance & Pitman (1998) recorded a number of sightings of Dwarf Sperm Whales in extremely deep waters (over 3,000 m) in the western Indian equatorial zone.

Within the assessment region, stranding records of Dwarf Sperm Whales suggest that this species occurs from 22°42’S on the west coast of southern Africa (Elwen et al. 2013) to 29°51’S on the east coast (Plön et al. 2023). Prior to 1977, Ross (1979) documented strandings of 42 Dwarf Sperm Whales along South Africa’s coastline from Saldanha Bay to East London. There appears to be no seasonal variation in the occurrence of either Dwarf or Pygmy Sperm Whales within the assessment region (Skinner & Chimimba 2005), and their movement patterns are largely unknown. 

Elevation / Depth / Depth Zones 

Elevation Lower Limit (in metres above sea level): (Not specified) 

Elevation Upper Limit (in metres above sea level): (Not specified) 

Depth Lower Limit (in metres below sea level): (Not specified) 

Depth Upper Limit (in metres below sea level): (Not specified) 

Depth Zone: (Not specified) 

Map

Figure 1. Distribution records for Dwarf Sperm Whale (Kogia sima) within the assessment region (South Africa, Eswatini and Lesotho). Note that distribution data is obtained from multiple sources and records have not all been individually verified.

Biogeographic Realms 

Biogeographic Realm: Afrotropical, Australasian, Indomalayan, Nearctic, Neotropical, Oceanian, Palearctic 

Occurrence 

Countries of Occurrence 

Country  Presence  Origin  Formerly Bred  Seasonality 
American Samoa  Extant  Native    Resident 
Angola  Extant  Native    Resident 
Anguilla  Extant  Native    Resident 
Antigua and Barbuda  Extant  Native    Resident 
Argentina  Extant  Native    Resident 
Aruba  Extant  Native    Resident 
Australia  Extant  Native    Resident 
Bahamas  Extant  Native    Resident 
Bahrain  Extant  Native    Resident 
Bangladesh  Extant  Native    Resident 
Barbados  Extant  Native    Resident 
Belize  Extant  Native    Resident 
Benin  Extant  Native    Resident 
Bermuda  Extant  Native    Resident 
Bonaire, Sint Eustatius and Saba  Extant  Native    Resident 
Brazil  Extant  Native    Resident 
Brazil -> Rio Grande do Sul  Extant  Native    Resident 
British Indian Ocean Territory  Extant  Native    Resident 
Brunei Darussalam  Extant  Native    Resident 
Cabo Verde  Extant  Native    Resident 
Cambodia  Extant  Native    Resident 
Cameroon  Extant  Native    Resident 
Canada  Extant  Native    Resident 
Canada -> British Columbia  Extant  Native    Resident 
Cayman Islands  Extant  Native    Resident 
Chile  Extant  Native    Resident 
Chile -> Valparaíso  Extant  Native    Resident 
China  Extant  Native    Resident 
Christmas Island  Extant  Native    Resident 
Cocos (Keeling) Islands  Extant  Native    Resident 
Colombia  Extant  Native    Resident 
Comoros  Extant  Native    Resident 
Congo  Extant  Native    Resident 
Congo, The Democratic Republic of the  Extant  Native    Resident 
Cook Islands  Extant  Native    Resident 
Costa Rica  Extant  Native    Resident 
Cuba  Extant  Native    Resident 
Curaçao  Extant  Native    Resident 
Côte d’Ivoire  Extant  Native    Resident 
Djibouti  Extant  Native    Resident 
Dominica  Extant  Native    Resident 
Dominican Republic  Extant  Native    Resident 
Ecuador  Extant  Native    Resident 
Ecuador -> Galápagos  Extant  Native    Resident 
Egypt  Presence Uncertain  Native    Seasonal Occurrence Uncertain 
El Salvador  Extant  Native    Resident 
Equatorial Guinea  Extant  Native    Resident 
Eritrea  Presence Uncertain  Native    Seasonal Occurrence Uncertain 
Fiji  Extant  Native    Resident 
French Guiana  Extant  Native    Resident 
French Polynesia  Extant  Native    Resident 
Gabon  Extant  Native    Resident 
Gambia  Extant  Native    Resident 
Ghana  Extant  Native    Resident 
Gibraltar  Extant  Native    Resident 
Grenada  Extant  Native    Resident 
Guadeloupe  Extant  Native    Resident 
Guam  Extant  Native    Resident 
Guatemala  Extant  Native    Resident 
Guinea  Extant  Native    Resident 
Guinea-Bissau  Extant  Native    Resident 
Guyana  Extant  Native    Resident 
Haiti  Extant  Native    Resident 
Honduras  Extant  Native    Resident 
Hong Kong  Extant  Native    Resident 
India  Extant  Native    Resident 
Indonesia  Extant  Native    Resident 
Iran, Islamic Republic of  Extant  Native    Resident 
Iraq  Presence Uncertain  Native    Seasonal Occurrence Uncertain 
Jamaica  Extant  Native    Resident 
Japan  Extant  Native    Resident 
Japan -> Honshu  Extant  Native    Resident 
Kenya  Extant  Native    Resident 
Kiribati  Extant  Native    Resident 
Korea, Democratic People’s Republic of  Extant  Native    Resident 
Korea, Republic of  Extant  Native    Resident 
Kuwait  Extant  Native    Resident 
Liberia  Extant  Native    Resident 
Madagascar  Extant  Native    Resident 
Malaysia  Extant  Native    Resident 
Maldives  Extant  Native    Resident 
Marshall Islands  Extant  Native    Resident 
Martinique  Extant  Native    Resident 
Mauritania  Extant  Native    Resident 
Mauritius  Extant  Native    Resident 
Mayotte  Extant  Native    Resident 
Mexico  Extant  Native    Resident 
Micronesia, Federated States of  Extant  Native    Resident 
Montserrat  Extant  Native    Resident 
Morocco  Extant  Native    Resident 
Mozambique  Extant  Native    Resident 
Myanmar  Extant  Native    Resident 
Namibia  Extant  Native    Resident 
Nauru  Extant  Native    Resident 
New Caledonia  Extant  Native    Resident 
New Zealand  Extant  Native    Resident 
New Zealand -> Kermadec Is.  Extant  Native    Resident 
New Zealand -> North Is.  Extant  Native    Resident 
Nicaragua  Extant  Native    Resident 
Nigeria  Extant  Native    Resident 
Niue  Extant  Native    Resident 
Norfolk Island  Extant  Native    Resident 
Northern Mariana Islands  Extant  Native    Resident 
Oman  Extant  Native    Resident 
Pakistan  Extant  Native    Resident 
Palau  Extant  Native    Resident 
Panama  Extant  Native    Resident 
Papua New Guinea  Extant  Native    Resident 
Peru  Extant  Native    Resident 
Philippines  Extant  Native    Resident 
Pitcairn  Extant  Native    Resident 
Portugal  Extant  Native    Resident 
Portugal -> Azores  Extant  Native    Resident 
Portugal -> Madeira  Extant  Native    Resident 
Puerto Rico  Extant  Native    Resident 
Qatar  Extant  Native    Resident 
Réunion  Extant  Native    Resident 
Saint Barthélemy  Extant  Native    Resident 
Saint Helena, Ascension and Tristan da Cunha  Extant  Native    Resident 
Saint Kitts and Nevis  Extant  Native    Resident 
Saint Lucia  Extant  Native    Resident 
Saint Martin (French part)  Extant  Native    Resident 
Saint Vincent and the Grenadines  Extant  Native    Resident 
Samoa  Extant  Native    Resident 
Sao Tome and Principe  Extant  Native    Resident 
Saudi Arabia  Presence Uncertain  Native    Seasonal Occurrence Uncertain 
Senegal  Extant  Native    Resident 
Seychelles  Extant  Native    Resident 
Sierra Leone  Extant  Native    Resident 
Singapore  Extant  Native    Resident 
Sint Maarten (Dutch part)  Extant  Native    Resident 
Solomon Islands  Extant  Native    Resident 
Somalia  Extant  Native    Resident 
South Africa  Extant  Native    Resident 
Spain  Extant  Native    Resident 
Spain -> Canary Is.  Extant  Native    Resident 
Sri Lanka  Extant  Native    Resident 
Sudan  Presence Uncertain  Native    Seasonal Occurrence Uncertain 
Suriname  Extant  Native    Resident 
Taiwan, Province of China  Extant  Native    Resident 
Tanzania, United Republic of  Extant  Native    Resident 
Thailand  Extant  Native    Resident 
Timor-Leste  Extant  Native    Resident 
Togo  Extant  Native    Resident 
Tokelau  Extant  Native    Resident 
Tonga  Extant  Native    Resident 
Trinidad and Tobago  Extant  Native    Resident 
Turks and Caicos Islands  Extant  Native    Resident 
Tuvalu  Extant  Native    Resident 
United Arab Emirates  Extant  Native    Resident 
United States of America  Extant  Native    Resident 
United States of America -> Hawaiian Is.  Extant  Native    Resident 
Uruguay  Extant  Native    Resident 
Vanuatu  Extant  Native    Resident 
Venezuela, Bolivarian Republic of  Extant  Native    Resident 
Viet Nam  Extant  Native    Resident 
Virgin Islands, British  Extant  Native    Resident 
Virgin Islands, U.S.  Extant  Native    Resident 
Wallis and Futuna  Extant  Native    Resident 
Western Sahara  Extant  Native    Resident 
Yemen  Extant  Native    Resident 

Large Marine Ecosystems (LME) Occurrence 

Large Marine Ecosystems: (Not specified) 

FAO Area Occurrence 

  Presence  Origin  Formerly Bred  Seasonality 
21. Atlantic – northwest  Extant  Native    Resident 
27. Atlantic – northeast  Extant  Native    Resident 
31. Atlantic – western central  Extant  Native    Resident 
34. Atlantic – eastern central  Extant  Native    Resident 
41. Atlantic – southwest  Extant  Native    Resident 
47. Atlantic – southeast  Extant  Native    Resident 
51. Indian Ocean – western  Extant  Native    Resident 
57. Indian Ocean – eastern  Extant  Native    Resident 
61. Pacific – northwest  Extant  Native    Resident 
67. Pacific – northeast  Extant  Native    Resident 
71. Pacific – western central  Extant  Native    Resident 
77. Pacific – eastern central  Extant  Native    Resident 
81. Pacific – southwest  Extant  Native    Resident 
87. Pacific – southeast  Extant  Native    Resident 

Climate change

The impact of global climate change, and the associated effects of increased water temperature and CO2 concentration on Kogia spp. is largely unknown; however, it is likely to have cascading effects on the movements and feeding ecology of these species (Learmonth et al. 2006). 

Population information

Abundance estimates of this species are often underestimated due to their offshore habitats, long and deep-diving behaviour and inconspicuous nature at the surface (Barlow 1999). For example, they lie very low in the water when on the surface and can only be seen when wind speeds are between 0 and 2 on the Beaufort scale. Additionally, Pygmy and Dwarf Sperm Whales are often confused during sightings, which further complicates any population assessments. No global population size estimates are available for this species.

The 3-generation period of the species is calculated as 36 years (Taylor et al. 2007), and, globally, a 30% reduction over three generations cannot be ruled out (Taylor et al. 2008a, 2008b). 

Current population trend: Unknown 

Continuing decline in mature individuals? Unknown 

Extreme fluctuations in the number of subpopulations: (Not specified) 

Continuing decline in number of subpopulations: (Not specified) 

All individuals in one subpopulation: (Not specified) 

Number of mature individuals in population: Unknown 

Number of mature individuals in largest subpopulation: Unknown 

Number of Subpopulations: Unknown 

Severely fragmented: No 

Quantitative Analysis 

Probability of extinction in the wild within 3 generations or 10 years, whichever is longer, maximum 100 years: (Not specified) 

Probability of extinction in the wild within 5 generations or 20 years, whichever is longer, maximum 100 years: (Not specified) 

Probability of extinction in the wild within 100 years: (Not specified) 

Population genetics

Molecular evidence examining individuals across its range (South Africa, Australia, New Zealand, South America) have found extensive mixing (interbreeding) between locations, indicating individuals belong to a single metapopulation in the Southern Hemispher(Plön et al. 2023). Given that no estimates of population size are available and no measure of effective population size (Ne) was conducted using the available genetic information, it is not possible to quantify the Ne 500 indicator 

Habitats and ecology

Dwarf Sperm Whales inhabit deep waters over the continental shelf and slope (Plön and Baird 2022; Best 2007; Ross 1979). Although some studies document some division between K. breviceps and Ksima in their preference for water depth, largely based on the analysis of stomach contents (Plön 2004; Ross 1979), Mullin et al. (1994) using aerial observations noted that in the Gulf of Mexico, both species occurred in waters between 400–600 m deep. These depths constituted the upper regions of the continental slope, which exhibited high concentrations of zooplankton (Baumgartner et al. 2001). Both species appear to feed over the deeper continental shelf and slope (Plön 2022; Plön and Baird 2022; Ross 1979).

Ross (1979) reported that Dwarf Sperm Whales occur in socially structured schools of up to ten individuals and they lie very low in the water (Leatherwood & Reeves 1983).

The stomach contents of stranded Dwarf Sperm Whales contained the remains of deep-water cephalopods, suggesting that this species feeds at depths of up to 600 m, possibly even deeper, and is mostly found over the continental shelf (Plön and Baird 2022; Ross 1979The majority of the diet of Kogia spp. consists of cephalopods, but they may also consume other prey, for example deep-sea fishes and shrimps (McAlpine et al. 1997; dos Santos & Haimovici 2001; S. Plön pers. comm.). In South African waters, Pygmy and Dwarf Sperm Whales consumed at least 67 and 38 different prey species, respectively, and Pygmy Sperm Whales are likely to feed in deeper waters compared to Dwarf Sperm Whales (Plön 2004; Ross 1979).

Although little is known about the reproductive biology of Kogia spp., and no seasonality can be inferred, female and male K. sima from South Africa are estimated to reach sexual maturity at 2.15 m and 1.97 m, respectively (Plön 2004). Dwarf Sperm Whale calves are born at an approximate length of 1.03 m (Plön 2004).

Ecosystem and cultural services: Marine mammals integrate and reflect ecological variation across large spatial and long temporal scales, and therefore they are prime sentinels of marine ecosystem change (Moore 2008). 

IUCN Habitats Classification Scheme 

Habitat  Season  Suitability  Major Importance? 
10.1. Marine Oceanic -> Marine Oceanic – Epipelagic (0-200m)    Suitable  Yes 
10.2. Marine Oceanic -> Marine Oceanic – Mesopelagic (200-1000m)    Suitable  Yes 
10.3. Marine Oceanic -> Marine Oceanic – Bathypelagic (1000-4000m)    Suitable  Yes 

Life History 

Generation Length: (Not specified) 

Age at Maturity: Female or unspecified: 5 yrs (Plön 2004) 

Age at Maturity: Male: 2.6-3 yrs (Plön 2004) 

Size at Maturity (in cms): Female: 215 cm (Plön 2004) 

Size at Maturity (in cms): Male: 197 cm (Plön 2004) 

Longevity: 21.5 yrs for females, 17 yrs for males (Plön 2004) 

Average Reproductive Age: (Not specified) 

Maximum Size (in cms): 274.3cm in females, 260.4 cm in males (Plön 2004) 

Size at Birth (in cms): 103 cm (Plön 2004) 

Gestation Time: (Not specified) 

Reproductive Periodicity: (Not specified) 

Average Annual Fecundity or Litter Size: (Not specified) 

Natural Mortality: (Not specified) 

Does the species lay eggs? No 

Does the species give birth to live young: Yes 

Does the species exhibit parthenogenesis: (Not specified) 

Does the species have a free-living larval stage? (Not specified) 

Does the species require water for breeding? (Not specified) 

Movement Patterns 

Movement Patterns: (Not specified) 

Congregatory: (Not specified) 

Systems 

System: Marine 

General Use and Trade Information

Although this species is hunted at low levels in some parts of their range, there is no trade or use of the species within the assessment region. In other parts of the world, such as the Philippines, Kogia spp. are hunted for bait to be used in fisheries or meat for human consumption (Leatherwood et al. 1992; Anonymous 1996). Additionally, where they are caught accidentally in fisheries, such as gillnets, they may also be utilised for human consumption (Klinowska 1991; Muñoz-Hincapié et al. 1998). 

Subsistence:  Rationale:  Local Commercial:  Further detail including information on economic value if available: 
Yes       

National Commercial Value: Yes 

International Commercial Value: No 

End Use  Subsistence  National  International  Other (please specify) 
1. Food – human  true  true     

Is there harvest from captive/cultivated sources of this species? (Not specified) 

Harvest Trend Comments: (Not specified) 

Threats

Although no major threats have been recognised for Kogia spp. within the assessment region, and the threats listed below are not likely to cause drastic population reduction on their own, they may result in slow, significant declines in the future, especially if the threats synergise. 
 
Kogia spp. were not historically hunted commercially but are currently hunted on a small-scale in regions such as Japan, Taiwan, Sri Lanka, Indonesia and the Lesser Antilles (Jefferson et al. 1993). Dwarf Sperm Whales are occasionally caught as bycatch in many areas of their range (including southern Brazil; Zerbini & Kotas 1998). No direct or indirect catches of this species has been reported from South African waters. 
 
The ingestion of plastic bags (which the animals possibly mistake for squid) is common among squid-eating cetaceans and has been documented for both Kogia species (Plön 2022; Plön and Baird 2022) and is considered to be relatively common among these species. Plastic pollution in the stomachs of cetaceans frequently hinders natural digestion of food resources, leading to gut-blockage, starvation, strandings and death (Caldwell & Caldwell 1989; Laist et al. 1999; S. Plön pers. obs.).  
 
As deep-diving species (similar to beaked whales), Dwarf Sperm Whales are presumably vulnerable to anthropogenic noise pollution, for example those produced by seismic surveys and sonar generated during naval operations (Cox et al. 2006; Wang & Yang 2006; Yang et al. 2008). A number of stranding events, which included Kogia spp., have been documented in Taiwan (Wang & Yang 2006; Yang et al. 2008), the Gulf of Mexico and off the east coast of Florida (Waring et al. 2006). Although, anthropogenic noise pollution is a possible cause of these stranding incidents, due to spatial and temporal associations, this assumption has not been confirmed (Hohn et al. 2006; Wang & Yang 2006; Yang et al. 2008). Marine noise pollution is thought to be intensifying within South African waters (Koper & Plön 2012). 

Conservation

K. sima is listed in Appendix II of the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES). In the absence of further data, no specific conservation measures can be recommended for this species within the assessment region at present. Continued research is necessary into the impact of and interactions between threats, such as plastic and noise pollution, climate change and incidental bycatches in pelagic fisheries. Management plans should be developed as such data become available.

Recommendations for managers and practitioners: 

  • The interaction between Kogia spp. and gillnet, purse seine and longline fisheries requires ongoing monitoring, and regular records of bycatch should be collected by fishing operations. 

Research priorities: 

  • Population size, distribution and trends of these species in South African waters. 
  • Investigations into threats to these species, such as the impacts and severity of marine pollution (both plastics and noise) on populations. 

Encouraged citizen actions: 

  • Use information dispensed by the South African Sustainable Seafood Initiative to make good choices when buying fish in shops and restaurants, e.g. FishMS 0794998795. 
  • Save electricity and fuel to mitigate CO2 emissions and hence, the rate of climate change. 
  • Sightings data from pelagic commercial tourism operators may be valuable. 
  • Report any strandings to the relevant local authorities. 

Bibliography

Baird, R. W., Nelson, D., Lien, J. and Nagorsen, D. W. 1996. The status of the pygmy sperm whale, Kogia breviceps, in Canada. Canadian Field-Naturalist 110: 525-532. 

Baird, R. W., Mahaffy, S. D., & Lerma, J. K. 2022. Site fidelity, spatial use, and behavior of dwarf sperm whales in Hawaiian waters: using small-boat surveys, photo-identification, and unmanned aerial systems to study a difficult-to-study species. Marine Mammal Science, 38(1), 326-348. 

Ballance, L. T. and Pitman, R. L. 1998. Cetaceans of the western tropical Indian Ocean: distribution, relative abundance, and comparisons with cetacean communities of two other tropical ecosystems. Marine Mammal Science 14: 429-459. 

Barlow, J. 1999. Trackline detection probability for long-diving whales. In: G. W. Garner, S. C. Amstrup, J. L. Laake, B. J. F. Manley, L. L. McDonald and D. G. Robertson (eds), Marine mammal survey and assessment methods, pp. 209-221. Balkema Press, Netherlands. 

Barlow, J., Forney, K. A., Hill, K. A., Brownell Jr., R. L., Caretta, R. L., Demaster, D. P., Julian, D. P., Lowry, M. S., Ragen, M. S. and Reeves, R. R. 1997. U.S. Pacific marine mammal stock assessments: 1996. NOAA Technical Memorandum NMFS-SWFSC 248: 223 pp. 

Baumgartner, M. F., Mullin, K. D., May, L. N. and Leming, T. D. 2001. Cetacean habitats in the northern Gulf of Mexico. Fishery Bulletin 99: 219-239. 

Best, P. B. B. 2007. Whales and Dolphins of the Southern African Subregion. Cambridge University Press, Cape Town. 338pp. 

Caldwell, D. K. and Caldwell, M. C. 1989. Pygmy sperm whale Kogia breviceps (de Blainville, 1838): Dwarf sperm whale Kogia simus Owen, 1866. In: S. H. Ridgway and R. Harrison (eds), Handbook of marine mammals, Vol. 4: River dolphins and the larger toothed whales, pp. 234-260. Academic Press. 

Chivers, S.J., Leduc, A.E., Robertson, K.M., Barros, N.B. and Dizon, A.E. 2005. Genetic variation in Kogia spp., with preliminary evidence for two species of Kogia simaMarine Mammal Science 21(4): 619-634. 

Cox, T.M., Ragen, T.J., Read, A.J., Vos, E., Baird, R.W., Balcomb, K., Barlow, J., Caldwell, J., Cranford, T., Crum, L., D’Amico, A., D’Spain, A., Fernández, J., Finneran, J., Gentry, R., Gerth, W., Gulland, F., Hildebrand, J., Houser, D., Hullar, T., Jepson, P.D., Ketten, D., Macleod, C.D., Miller, P., Moore, S., Mountain, D., Palka, D., Ponganis, P., Rommel, S., Rowles, T., Taylor, B., Tyack, P., Wartzok, D., Gisiner, R., Mead, J. and Benner, L. 2006. Understanding the impacts of anthropogenic sound on beaked whales. Journal of Cetacean Research and Management 7(3): 177-187. 

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