Skeletons of the extinct Palaeoloxodon falconeri, native to Sicily and Malta, it is one of the smallest known species of dwarf elephant. Adult males measured about one meter (3.3 ft) in shoulder height and weighed about 250 kg (550 lb). Females were smaller.

Insular dwarfism, a form of phyletic dwarfism, is the process and condition of large animals evolving or having a reduced body size when their population's range is limited to a small environment, primarily islands. This natural process is distinct from the intentional creation of dwarf breeds, called dwarfing. This process has occurred many times throughout evolutionary history, with examples including various species of dwarf elephants that evolved during the Pleistocene epoch, as well as more ancient examples, such as the dinosaurs Europasaurus and Magyarosaurus. This process, and other "island genetics" artifacts, can occur not only on islands, but also in other situations where an ecosystem is isolated from external resources and breeding. This can include caves, desert oases, isolated valleys and isolated mountains ("sky islands").[citation needed] Insular dwarfism is one aspect of the more general "island effect" or "Foster's rule", which posits that when mainland animals colonize islands, small species tend to evolve larger bodies (island gigantism), and large species tend to evolve smaller bodies. This is itself one aspect of island syndrome, which describes the differences in morphology, ecology, physiology and behaviour of insular species compared to their continental counterparts.

Possible causes

Structure of insular dwarfism web

There are several proposed explanations for the mechanism which produces such dwarfism.

One is a selective process where only smaller animals trapped on the island survive, as food periodically declines to a borderline level. The smaller animals need fewer resources and smaller territories, and so are more likely to get past the break-point where population decline allows food sources to replenish enough for the survivors to flourish. Smaller size is also advantageous from a reproductive standpoint, as it entails shorter gestation periods and generation times.

In the tropics, small size should make thermoregulation easier.

Among herbivores, large size confers advantages in coping with both competitors and predators, so a reduction or absence of either would facilitate dwarfing; competition appears to be the more important factor.

Among carnivores, the main factor is thought to be the size and availability of prey resources, and competition is believed to be less important. In tiger snakes, insular dwarfism occurs on islands where available prey is restricted to smaller sizes than are normally taken by mainland snakes. Since prey size preference in snakes is generally proportional to body size, small snakes may be better adapted to take small prey.

Differences of dwarfism and gigantism

The inverse process, wherein small animals breeding on isolated islands lacking the predators of large land masses may become much larger than normal, is called island gigantism. An excellent example is the dodo, the ancestors of which were normal-sized pigeons. There are also several species of giant rats, one still extant, that coexisted with both Homo floresiensis and the dwarf stegodonts on Flores.

The process of insular dwarfing can occur relatively rapidly by evolutionary standards. This is in contrast to increases in maximum body size, which are much more gradual. When normalized to generation length, the maximum rate of body mass decrease during insular dwarfing was found to be over 30 times greater than the maximum rate of body mass increase for a ten-fold change in mammals. The disparity is thought to reflect the fact that pedomorphism offers a relatively easy route to evolve smaller adult body size; on the other hand, the evolution of larger maximum body size is likely to be interrupted by the emergence of a series of constraints that must be overcome by evolutionary innovations before the process can continue.

Factors influencing the extent of dwarfing

For both herbivores and carnivores, island size, the degree of island isolation and the size of the ancestral continental species appear not to be of major direct importance to the degree of dwarfing. However, when considering only the body masses of recent top herbivores and carnivores, and including data from both continental and island land masses, the body masses of the largest species in a land mass were found to scale to the size of the land mass, with slopes of about 0.5 log(body mass/kg) per log(land area/km2). There were separate regression lines for endothermic top predators, ectothermic top predators, endothermic top herbivores and (on the basis of limited data) ectothermic top herbivores, such that food intake was 7- to 24-fold higher for top herbivores than for top predators, and about the same for endotherms and ectotherms of the same trophic level (this leads to ectotherms being 5 to 16 times heavier than corresponding endotherms).

It has been suggested that for dwarf elephants, competition was an important factor in body size, with islands with competing herbivores having significantly larger dwarf elephants than those where competing herbivores were absent.

Examples

Non-avian dinosaurs

Recognition that insular dwarfism could apply to dinosaurs arose through the work of Ferenc Nopcsa, a Hungarian-born aristocrat, adventurer, scholar, and paleontologist. Nopcsa studied Transylvanian dinosaurs intensively, noticing that they were smaller than their cousins elsewhere in the world. For example, he unearthed six-meter-long sauropods, a group of dinosaurs which elsewhere commonly grew to 30 meters or more. Nopcsa deduced that the area where the remains were found was an island, Hațeg Island (now the Haţeg or Hatzeg basin in Romania) during the Mesozoic era. Nopcsa's proposal of dinosaur dwarfism on Hațeg Island is today widely accepted after further research confirmed that the remains found are not from juveniles.

Sauropods

ExampleSpeciesRangeTime frameContinental relative
AmpelosaurusA. atacisIbero-Armorican IslandLate Cretaceous / MaastrichtianNemegtosaurids
EuropasaurusE. holgeriLower SaxonyLate Jurassic / Middle KimmeridgianBrachiosaurs
MagyarosaurusM. dacusHațeg IslandLate Cretaceous / MaastrichtianRapetosaurus
LirainosaurusL. astibiaeIbero-Armorican IslandLate Cretaceous
PaludititanP. nalatzensisHațeg IslandLate Cretaceous / MaastrichtianEpachthosaurus

Other

ExampleSpeciesRangeTime frameContinental relative
Langenberg Quarry torvosaur (blue)UnnamedLower SaxonyLate Jurassic / Middle KimmeridgianTorvosaurus
StruthiosaurusS. austriacusIbero-Armorican, Australoalpine, and Hațeg IslandsLate CretaceousEdmontonia
S. transylvanicus
S. languedocensis
TelmatosaurusT. transsylvanicusHațeg IslandHadrosaurids
ThecodontosaurusT. antiquusSouthern EnglandLate Triassic / RhaetianPlateosaurs
Zalmoxes (purple)Z. robustusHațeg IslandLate CretaceousTenontosaurus
Z. shqiperorum

In addition, the genus Balaur was initially described as a Velociraptor-sized dromaeosaurid (and in consequence a dubious example of insular dwarfism), but has been since reclassified as a secondarily flightless stem bird, closer to modern birds than Jeholornis (thus actually an example of insular gigantism).

Birds

ExampleBinomial nameNative rangeStatusContinental relativeInsular / mainland length or mass ratio
Hawaiian flightless ibisesApteribis glenosMolokaiExtinct (Late Quaternary)American ibises
Apteribis brevisMaui
Cozumel curassowCrax rubra griscomiCozumelUnknownGreat curassow
Kangaroo Island emuDromaius novaehollandiae baudinianusKangaroo Island, South AustraliaExtinct (c. AD 1827)Emu
King Island emu (black)Dromaius novaehollandiae minorKing Island, TasmaniaExtinct (AD 1822)LR ≈ 0.48
Dwarf yellow eyed penguinMegadyptes antipodes richdaleiChatham Islands, New ZealandExtinct (after 1300 AD)Yellow-eyed penguin
Cozumel thrasherToxostoma gluttatumCozumelCritically endangeredOther thrashers

Squamates

ExampleBinomial nameNative rangeStatusContinental relativeInsular / mainland length or mass ratio
Madagascar dwarf chameleonBrookesia minimaNosy Be island, MadagascarEndangeredMadagascar leaf chameleons
Nosy Hara chameleonBrookesia micraNosy Hara island, MadagascarVulnerable
Roxby Island tiger snakeNotechis scutatusRoxby Island, South AustraliaUnknownTiger snake
Dwarf Burmese pythonPython bivittatus progschaiJava, Bali, Sumbawa and Sulawesi, IndonesiaBurmese pythonLR ≈ 0.44
Tanahjampea reticulated pythonPython reticulatus jampeanusTanahjampea, between Sulawesi and FloresReticulated pythonLR ≈ 0.41, males LR ≈ 0.49, females

Mammals

Pilosans

ExampleBinomial nameNative rangeStatusContinental relative
Pygmy three-toed slothBradypus pygmaeusIsla Escudo de Veraguas, PanamaCritically endangeredBrown-throated sloth
AcratocnusA. antillensisCuba, Hispaniola and Puerto RicoExtinct (c. 3000 BC)Continental ground sloths
A. odontrigonus
A. ye
ImagocnusI. zazaeCubaExtinct (Early Miocene)
MegalocnusM. rodensCuba and HispaniolaExtinct (c. 2700 BC)
M. zile
NeocnusNeocnus spp.Extinct (c. 3000 BC)

Proboscideans

ExampleBinomial nameNative rangeStatusContinental relative
Sulawesi dwarf elephantElephas celebensisSulawesiExtinct (Early Pleistocene)Asian elephant
Cabarruyan dwarf elephantElephas beyeriLuzonExtinct
Cretan dwarf mammothMammuthus creticusCreteMammuthus
Channel Islands mammothMammuthus exilisSanta Rosae islandExtinct (Late Pleistocene)Columbian mammoth
Sardinian mammothMammuthus lamarmoraiSardiniaSteppe mammoth
Taiwan mammothMammuthus trogontherii taiwanicusTaiwanExtinct
Saint Paul Island woolly mammothMammuthus primigeniusSaint Paul Island, AlaskaExtinct (c. 3750 BC)Woolly mammoth
Siculo-Maltese elephantsPalaeoloxodon antiquus leonardiSicily and MaltaExtinctStraight-tusked elephant (left)
P. mnaidriensis
P. melitensis
P. falconeri
Cretan elephantsPalaeoloxodon chaniensisCrete
P. creutzburgi
Cyprus dwarf elephantPalaeoloxodon cypriotesCyprusExtinct (c. 9000 BC)
Naxos dwarf elephantPalaeoloxodon sp.NaxosExtinct
Tilos dwarf elephantPalaeoloxodon tiliensisTilos
Rhodes dwarf elephantPalaeoloxodon sp.Rhodes
Bumiayu dwarf sinomastodontSinomastodon bumiajuensisBumiayu Island (now part of Java)Extinct (Early Pleistocene)Sinomastodon
Japanese stegodontStegodon miensisJapan (Also Taiwan for S. aurorae)Chinese Stegodon
Stegodon protoaurorae
Stegodon aurorae
Greater Flores dwarf stegodontStegodon florensisFloresExtinct (Late Pleistocene)Sundaland Stegodon
Javan dwarf stegodontsStegodon hypsilophusJavaExtinct (Quaternary)
S. semedoensis
S. sp.
Mindanao pygmy stegodontStegodon mindanensisMindanao and SulawesiExtinct (Middle Pleistocene)
Sulawesi dwarf stegodontStegodon sompoensisSulawesiExtinct
Lesser Flores dwarf stegodontStegodon sondaariFloresExtinct (Middle Pleistocene)
Sumba dwarf stegodontStegodon sumbaensisSumba, Indonesia
Timor dwarf stegodontStegodon timorensisTimorExtinct
Dwarf stegolophodontStegolophodon pseudolatidensJapanExtinct (Miocene)Stegolophodon

Primates

ExampleBinomial nameNative rangeStatusContinental relative
Nosy Hara dwarf lemurCheirogaleus sp.Nosy Hara island off MadagascarUnknownDwarf lemurs
Flores ManHomo floresiensisFloresExtinct (Late Pleistocene)Homo erectus
Callao ManHomo luzonensisLuzon, Philippines
Modern pygmies of FloresHomo sapiensFloresExtantother members of Homo sapiens
Early Palau modern humans (disputed)PalauExtinct (?)
AndamaneseAndaman IslandsExtant
Sardinian macaqueMacaca majoriSardiniaExtinct (Pleistocene)Barbary macaque
Zanzibar red colobusPiliocolobus kirkiiUngujaEndangeredUdzungwa red colobus

Carnivorans

ExampleBinomial nameNative rangeStatusContinental relativeInsular / mainland length or mass ratio
Sicilian wolfCanis lupus cristaldiiSicilyExtinct (AD 1970)Gray wolf
Japanese wolfCanis lupus hodophilaxJapan (excluding Hokkaido)Extinct (AD 1905)
Sardinian dhole (forward)Cynotherium sardousCorsica and SardiniaExtinct (c. 8300 BC)Xenocyon
Trinil dogMececyon trinilensisJavaExtinct (Pleistocene)
Cozumel Island coatiNasua narica nelsoniCozumelCritically endangeredYucatan white-nosed coati
Zanzibar leopardPanthera pardus pardusUngujaCritically endangered or ExtinctAfrican leopard
Taiwan leopardPanthera pardusTaiwanExtinct (Pleistocene)Amur leopard
Bali tigerPanthera tigris sondaicaBaliExtinct (c. AD 1940)Sumatran tiger
Javan tigerJavaExtinct (c. AD 1975)
Cozumel raccoonProcyon pygmaeusCozumelCritically endangeredCommon raccoon
Island foxUrocyon littoralisSix of the Channel Islands of CaliforniaNear ThreatenedGray foxLR ≈ 0.84 LR ≈ 0.75
Cozumel foxUrocyon sp.CozumelCritically endangered or Extinct

Non-ruminant ungulates

ExampleBinomial nameNative rangeStatusContinental relative
EumaiochoerusEumaiochoerus etruscusBaccinello, MontebamboliExtinct (Miocene)Microstonyx
Malagasy dwarf hippopotamusesHippopotamus laloumenaMadagascarExtinct (c. AD 1000)Common hippopotamus
H. lemerlei
H. madagascariensis
Bumiayu dwarf hippopotamusHexaprotodon simplexBumiayu Island (now Java)Extinct (Early Pleistocene)Asian hippopotamuses
Cretan dwarf hippopotamusHippopotamus creutzburgiCreteExtinct (Middle Pleistocene)Hippopotamus antiquus
Maltese dwarf hippopotamusHippopotamus melitensisMaltaExtinct (Pleistocene)Common hippopotamus (H. amphibius)
Sicilian dwarf hippopotamusHippopotamus pentlandiSicily
Cyprus dwarf hippopotamusHippopotamus minorCyprusExtinct (c. 8000 BC)Unclear, either H. amphibius or H. antiquus.
Cozumel collared peccaryPecari tajacu nanusCozumelUnknownCollared peccary

Bovids

ExampleBinomial nameNative rangeStatusContinental relative
Sicilian bisonBison priscus siciliaeSicilyExtinct (Late Pleistocene)Steppe bison
Sicilian aurochsBos primigenius siciliaeEurasian aurochs
Cebu tamarawBubalus cebuensisCebu, PhilippinesExtinctWild water buffalo
Lowland anoaBubalus depressicornisSulawesi and Buton, IndonesiaEndangered
Bubalus grovesiBubalus grovesiSulawesi, IndonesiaExtinct
TamarawBubalus mindorensisMindoro, PhilippinesCritically endangered
Mountain anoaBubalus quarlesiSulawesi and Buton, IndonesiaEndangered
Balearic Islands cave goatMyotragus balearicusMallorca and MenorcaExtinct (after 3000 BC)Gallogoral
NesogoralNesogoral spp.SardiniaExtinct
Dahlak Kebir gazelleNanger soemmerringi ssp.Dahlak Kebir island, EritreaVulnerableSoemmerring's gazelle
TyrrhenotragusTyrrhenotragus gracillimusBaccinelloExtinctAntilopinae sp.

Cervids and relatives

ExampleBinomial nameNative rangeStatusContinental relative
Cretan deerCandiacervus spp.CreteExtinct (Pleistocene)Unknown
Sardinian deerPraemegaceros caziotiSardiniaExtinct (c. 5500 BC)Praemegaceros
Ryukyu dwarf deerCervus astylodonRyukyu IslandsExtinctSika deer (?)
Cervus praenipponicus (?)
Jersey red deer populationCervus elaphus jerseyensisJerseyExtinct (Pleistocene)Red deer
Corsican red deerCervus elaphus corsicanusCorsica and SardiniaNear Threatened
Sicilian red deerCervus siciliaeSicilyExtinct (Late Pleistocene)
HoplitomeryxHoplitomeryx spp.Gargano IslandExtinct (Early Pliocene)Pecorans
Sicilian fallow deerDama carburangelensisSicilyExtinct (Late Pleistocene)Fallow deer
Florida Key deerOdocoileus virginianus claviumFlorida KeysEndangeredVirginia deer
Svalbard reindeerRangifer tarandus platyrhynchusSvalbardVulnerableReindeer
Philippine deerRusa mariannaPhilippinesSambar deer

Plants

Possible exampleBinomial nameNative rangeStatusContinental relative
Insular elephant cactiPachycereus pringleiRemote islands in the Sea of Cortez (e.g. Santa Cruz, San Pedro Mártir)Not evaluatedMainland elephant cacti

See also

  • Bones of "small-bodied humans" found in cave

Notes

External links