Dwarf Sperm Whale
Kogia sima

2025 Red list status
Data Deficient
Regional Population Trend
Unknown
Change compared
to 2016
No Change
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 Hemisphere (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 K. sima 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 sima. Marine 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.
Dulau, V., Estrade, V., Bein, A., Nikolic, N., Fajeau, A., Gancille, J.-M., Martin, J., Leroy, E., and J.-S. Philippe. (2024). Records from visual surveys, strandings and eDNA sampling reveal the regular use of Reunion waters by dwarf sperm whales. Advances in Marine Biology, 99, 65-97.
Findlay KP, Best PB, Ross GJB, Cockcroft VG. 1992. The distribution of small odontocete cetaceans off the coasts of South Africa and Namibia. South African Journal of Marine Science 12: 237-270.
Garrison LP. 2007. Interactions between marine mammals and pelagic longline fishing gear in the US Atlantic Ocean between 1992 and 2004. Fishery Bulletin 105: 408–417.
Handley, C.O. 1966. A synopsis of the genus Kogia (pygmy sperm whales). In: K.S. Norris (ed.), Whales, dolphins, and porpoises, pp. 62-69. University of California Press, Berkeley, California, USA.
Hodge, L. E. W., Baumann-Pickering, S., Hildebrand, J. A., Bell, J. T., Cummings, E. W., Foley, H. J., McAlarney, R. J., McLellan, W. A., Pabst, D. A., Swaim, Z. T., Waples, D. M., & Read, A. J. (2018). Heard but not seen: Occurrence of Kogia spp. along the western North Atlantic shelf break. Marine Mammal Science 34: 1141-1153.
Hohn, A.A., Rotstein, D.S., Harms, C.A. and Southall, B.L. 2006. Multispecies mass stranding of pilot whales (Globicephala macrorhynchus), minke whale (Balaenoptera acutorostrata), and dwarf sperm whales (Kogia sima) in North Carolina on 15-16 January 2005. NOAA Technical Memorandum NMFS-SEFSC-57.
IUCN (International Union for Conservation of Nature). 2012a. Kogia breviceps. Available at: http://www.iucnredlist.org. (Accessed: 21 February 2016).
IUCN (International Union for Conservation of Nature). 2012b.. Kogia sima. Available at: http://www.iucnredlist.org. (Accessed: 21 February 2016).
Jefferson, T. A., Leatherwood, S. and Webber, M. A. 1993. Marine Mammals of the World: FAO Species Identification Guide. United Nation Environment Programme and Food and Agricultural Organization of the UN.
Katona SK, Rough V, Richardson DT. 1983. A field guide to the whales, porpoises and seals of the Gulf of Maine and Eastern Canada, Cape Cod to Newfoundland. Charles Scribners Sons, New York, USA.
Kiszka, J., Maricato, G. and M. Caputo. (2024). Habitat suitability, occurrence, and behavior of dwarf sperm whales (Kogia sima) off St. Vincent and the Grenadines, Eastern Caribbean. Advances in Marine Biology, 99, 1-19.
Koper RP, Plön S. 2012. The potential impacts of anthropogenic noise on marine animals and recommendations for research in South Africa. EWT Research & Technical Paper No. 1. Endangered Wildlife Trust, South Africa.
Laist, D. W., Coe, J. M. and O’Hara, K. J. 1999. Marine debris pollution. In: J. R. Twiss and R. R. Reeves (eds), Conservation and Management of Marine Mammals.
Learmonth, J.A., Macleod, C.D., Santos, M.B., Pierce, G.J., Crick, H.Q.P. and Robinson, R.A. 2006. Potential effects of climate change on marine mammals. Oceanography and Marine Biology: An Annual Review 44: 431-464.
Leatherwood S, Dolar MLL, Wood CJ, Aragones LV, Hill CL. 1992. Marine mammal species confirmed from Philippine waters. Silliman Journal 36: 65–81.
Leatherwood S, Reeves RR. 1983. The Sierra Club Handbook of Whales and Dolphins. Sierra Club Books, San Francisco. USA.
McAlpine, D. F. 2002. Pygmy and dwarf sperm whales Kogia breviceps and K. simus. In: W. F. Perrin, B. Wursig and J. G. M. Thewissen (eds), Encyclopedia of Marine Mammals, pp. 1007-1009. Academic Press.
McAlpine, D. F., Murison, L. D. and Hoberg, E. P. 1997. New records for the pygmy sperm whale, Kogia breviceps (Physeteridae) from Atlantic Canada with notes on diet and parasites. Marine Mammal Science 13(4): 701-704.
Moore SE. 2008. Marine mammals as ecosystem sentinels. Journal of Mammalogy 89: 534-540.
Mullin, K. D., W. Hoggard, C. L. Roden, R. Lohoefener, C. M. Rogers, B. Taggart. 1994. Cetaceans on the upper continental slope in the north-central Gulf of Mexico. Fishery Bulletin 92: 773-786.
Muñoz-Hincapié MF, Mora-Pinto DM, Palacios DM, Secchi ER, Mignucci-Giannoni AA. 1998. First osteological record of the dwarf sperm whale in Colombia, with notes on the zoogeography of Kogia in South America. Revista de la Academia Colombiana de Ciencias 22: 433–44.
Mörzer Bruyns WFJ. 1971. Field Guide to Whales and Dolphins. Mees, Amsterdam.
Nagorsen, D. 1985. Kogia simus. Mammalian Species 239: 1-6.
Perez, C., Lopez, A., Sequeira, M., Silva, M., Herrera, R., Goncalves, J., Valdes, P., Mons, L., Freitag, L., Lens, S. and Cendero, O. 2001. Stranding and by-catch of cetaceans in the northeastern Atlantic during 1996.: 4pp. Copenhagen, Denmark.
Perrin, W. F., Dolar, M. L. L. and Alava, M. N. R. (eds). 1996. Report of the Workshop on the Biology and Conservation of Small Cetaceans and Dugongs of Southeast Asia. UNEP Report UNEP(W)/EAS WG, pp. 101 pp..
Plön, S. 2004. The status and natural history of pygmy (Kogia breviceps) and dwarf (K. sima) sperm whales off Southern Africa. PhD thesis. Department of Zoology & Entomology, Rhodes University, South Africa. 553pp.
Plön, S., Best, P. B., Duignan, P., Lavery, S. D., Bernard, R. T. F., Van Waerebeek, K. and C. S. Baker. 2023. Population structure of pygmy (Kogia breviceps) and dwarf (Kogia sima) sperm whales in the Southern Hemisphere may reflect foraging ecology and dispersal patterns. Advances in Marine Biology 96, Vol. 1: 85-114.
Plön, S. 2022. Pygmy Sperm Whale Kogia breviceps (de Blainville, 1838). In: Hackländer, K., Zachos, F.E. (eds) Handbook of the Mammals of Europe. Handbook of the Mammals of Europe. Springer, Cham. doi.org/10.1007/978-3-319-65038-8_90-1.
Plön, S., Baird, R.W. 2022. Dwarf Sperm Whale, Kogia sima (Owen, 1866). In: Hackländer, K., Zachos, F.E. (eds) Handbook of the Mammals of Europe. Handbook of the Mammals of Europe. Springer, Cham. doi.org/10.1007/978-3-319-65038-8_91-1.
Rice, D.W. 1998. Marine Mammals of the World: Systematics and Distribution. Society for Marine Mammalogy, Special Publication Number 4, Lawrence, Kansas.
Ross GJ. 1984. Smaller cetaceans of the south east coast of southern Africa. Annals of the Cape Provincial Museums. Natural History 16: 309-319.
Ross GJB, Cockcroft VG, Cliff G. 1985. Additions to marine faunas of South Africa and Natal. Lammergeyer 35: 36–40.
Ross, G. J. B. 1979. Records of pygmy and dwarf sperm whales, genus Kogia, from southern Africa, with biological notes and some comparisons. Annals of the Cape Provincial Museums (Natural History) 11(14): 259-327.
Skinner, J.D. and Chimimba, C.T. (eds). 2005. The Mammals of the Southern African Subregion. Cambridge University Press, United Kingdom, Cambridge.
Tarpley, R.J. and Marwitz, S. 1993. Plastic debris ingestion by cetaceans along the Texas coast: two case reports. Aquatic Mammals 19: 93–98.
Taylor, B. L., Baird, R., Barlow, J., Dawson, S. M., Ford, J., Mead, J. G., Notarbartolo di Sciara, G., Wade, P., and Pitman, R. L. 2008. Kogia breviceps. Available at: www.iucnredlist.org. (Accessed: 11 November 2008).
Taylor, B.L., Chivers, S.J., Larese, J. and Perrin, W.F. 2007. Generation length and percent mature estimates for IUCN assessments of cetaceans. NOAA, Southwest Fisheries Science Center Administrative Report LJ-07-01. La Jolla, California.
Wang, J.Y. and Yang, S.C. 2006. Unusual cetacean stranding events of Taiwan in 2004 and 2005. Journal of Cetacean Research and Management 8: 283-292.
Waring, G.T., Josephson, E., Fairfield, C.P. and Maze-Foley, K. 2006. U.S. Atlantic and Gulf of Mexico marine mammal stock assessments – 2005. NOAA Technical Memorandum NMFS-NE-201. 346 p.
Yamada M. 1954. An account of a rare porpoise, Feresa Gray from Japan. Scientific Reports of the Whales Research Institute, Tokyo 9: 59-88.
Yang, W.-C., Chou, L.-S., Jepson, P. D., Brownell Jr., R. L., Cowan, D., Chang, P.-H., Chiou, H.-I., Yao, C.-J., Yamada, T. K., Chiu, J.-T., Wang, P.-J. and Fernandez, A. 2008. Unusual cetacean mortality events in Taiwan, possibly linked to naval activities. Veterinary Record 162: 184-186.
Zerbini, A. N. and Kotas, J. E. 1998. A note on cetacean bycatch in pelagic driftnetting off southern Brazil. Reports of the International Whaling Commission 48: 519-524.
dos Santos, RA. and Haimovici, M. 2001. Cephalopods in the diet of marine mammals stranded or incidentally caught along southeastern and southern Brazil (21- 34º S). Fisheries Research 52: 99-112.
