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Wikipedia / Insular dwarfism

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").

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

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 ratss, 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

Example

Species

Range

Time frame

Continental relative

Ampelosaurus

A. atacis

Ibero-Armorican Island

Late Cretaceous / Maastrichtian

Nemegtosaurids

Europasaurus

E. holgeri

Lower Saxony

Late Jurassic / Middle Kimmeridgian

Brachiosaurs

Magyarosaurus

M. dacus

Hațeg Island

Late Cretaceous / Maastrichtian

Rapetosaurus

Lirainosaurus

L. astibiae

Ibero-Armorican Island

Late Cretaceous

Paludititan

P. nalatzensis

Hațeg Island

Late Cretaceous / Maastrichtian

Epachthosaurus

Other

Example

Species

Range

Time frame

Continental relative

Langenberg Quarrytorvosaur (blue)

Unnamed

Lower Saxony

Late Jurassic / Middle Kimmeridgian

Torvosaurus

Struthiosaurus

S. austriacus

Ibero-Armorican, Australoalpine, and Hațeg Islands

Late Cretaceous

Edmontonia

S. transylvanicus

S. languedocensis

Telmatosaurus

T. transsylvanicus

Hațeg Island

Hadrosaurids

Thecodontosaurus

T. antiquus

Southern England

Late Triassic / Rhaetian

Plateosaurs

Zalmoxes (purple)

Z. robustus

Hațeg Island

Late Cretaceous

Tenontosaurus

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

Example

Binomial name

Native range

Status

Continental relative

Insular / mainlandlength or mass ratio

Hawaiian flightless ibises

Apteribis glenos

Molokai

Extinct (Late Quaternary)

American ibises

Apteribis brevis

Maui

Cozumel curassow

Crax rubra griscomi

Cozumel

Unknown

Great curassow

Kangaroo Island emu

Dromaius novaehollandiae baudinianus

Kangaroo Island, South Australia

Extinct (c. AD 1827)

Emu

King Island emu (black)

Dromaius novaehollandiae minor

King Island, Tasmania

Extinct (AD 1822)

LR ≈ 0.48

Dwarf yellow eyed penguin

Megadyptes antipodes richdalei

Chatham Islands, New Zealand

Extinct (after 1300 AD)

Yellow-eyed penguin

Cozumel thrasher

Toxostoma gluttatum

Cozumel

Critically endangered

Other thrashers

SquamatesSquamates

Example

Binomial name

Native range

Status

Continental relative

Insular / mainlandlength or mass ratio

Madagascar dwarf chameleon

Brookesia minima

Nosy Be island, Madagascar

Endangered

Madagascar leaf chameleons

Nosy Hara chameleon

Brookesia micra

Nosy Hara island, Madagascar

Vulnerable

Roxby Island tiger snake

Notechis scutatus

Roxby Island, South Australia

Unknown

Tiger snake

Dwarf Burmese python

Python bivittatus progschai

Java, Bali, Sumbawa and Sulawesi, Indonesia

Burmese python

LR ≈ 0.44

Tanahjampea reticulated python

Python reticulatus jampeanus

Tanahjampea, between Sulawesi and Flores

Reticulated python

LR ≈ 0.41, malesLR ≈ 0.49, females

Mammals

Pilosans of the CaribbeanPilosans

Example

Binomial name

Native range

Status

Continental relative

Pygmy three-toed sloth

Bradypus pygmaeus

Isla Escudo de Veraguas, Panama

Critically endangered

Brown-throated sloth

Acratocnus

A. antillensis

Cuba, Hispaniola and Puerto Rico

Extinct (c. 3000 BC)

Continental ground sloths

A. odontrigonus

A. ye

Imagocnus

I. zazae

Cuba

Extinct (Early Miocene)

Megalocnus

M. rodens

Cuba and Hispaniola

Extinct (c. 2700 BC)

M. zile

Neocnus

Neocnus spp.

Extinct (c. 3000 BC)

ProboscideanProboscideans

Example

Binomial name

Native range

Status

Continental relative

Sulawesi dwarf elephant

Elephas celebensis

Sulawesi

Extinct (Early Pleistocene)

Asian elephant

Cabarruyan dwarf elephant

Elephas beyeri

Luzon

Extinct

Cretan dwarf mammoth

Mammuthus creticus

Crete

Mammuthus

Channel Islands mammoth

Mammuthus exilis

Santa Rosae island

Extinct (Late Pleistocene)

Columbian mammoth

Sardinian mammoth

Mammuthus lamarmorai

Sardinia

Steppe mammoth

Taiwan mammoth

Mammuthus trogontherii taiwanicus

Taiwan

Extinct

Saint Paul Island woolly mammoth

Mammuthus primigenius

Saint Paul Island, Alaska

Extinct (c. 3750 BC)

Woolly mammoth

Siculo-Maltese elephants

Palaeoloxodon antiquus leonardi

Sicily and Malta

Extinct

Straight-tusked elephant(left)

P. mnaidriensis

P. melitensis

P. falconeri

Cretan elephants

P. creutzburgi

Crete

Cyprus dwarf elephant

Palaeoloxodon cypriotes

Cyprus

Extinct (c. 9000 BC)

Naxos dwarf elephant

Palaeoloxodon sp.

Naxos

Extinct

Tilos dwarf elephant

Palaeoloxodon tiliensis

Tilos

Rhodes dwarf elephant

Palaeoloxodon sp.

Rhodes

Bumiayu dwarf sinomastodont

Sinomastodon bumiajuensis

Bumiayu Island (now part of Java)

Extinct (Early Pleistocene)

Sinomastodon

Japanese stegodont

Stegodon miensis

Japan (Also Taiwan for S. aurorae)

Chinese Stegodon

Stegodon protoaurorae

Stegodon aurorae

Greater Flores dwarf stegodont

Stegodon florensis

Flores

Extinct (Late Pleistocene)

Sundaland Stegodon

Javan dwarf stegodonts

Stegodon hypsilophus

Java

Extinct (Quaternary)

S. semedoensis

S. sp.

Mindanao pygmy stegodont

Stegodon mindanensis

Mindanao and Sulawesi

Extinct (Middle Pleistocene)

Sulawesi dwarf stegodont

Stegodon sompoensis

Sulawesi

Extinct

Lesser Flores dwarf stegodont

Stegodon sondaari

Flores

Extinct (Middle Pleistocene)

Sumba dwarf stegodont

Stegodon sumbaensis

Sumba, Indonesia

Timor dwarf stegodont

Stegodon timorensis

Timor

Extinct

Dwarf stegolophodont

Stegolophodon pseudolatidens

Japan

Extinct (Miocene)

Stegolophodon

PrimatesPrimates

Example

Binomial name

Native range

Status

Continental relative

Nosy Hara dwarf lemur

Cheirogaleus sp.

Nosy Hara island off Madagascar

Unknown

Dwarf lemurs

Flores Man

Homo floresiensis

Flores

Extinct (Late Pleistocene)

Homo erectus

Callao Man

Homo luzonensis

Luzon, Philippines

Modern pygmies of Flores

Homo sapiens

Flores

Extant

other members of Homo sapiens

Early Palau modern humans (disputed)

Palau

Extinct (?)

Andamanese

Andaman Islands

Extant

Sardinian macaque

Macaca majori

Sardinia

Extinct (Pleistocene)

Barbary macaque

Zanzibar red colobus

Piliocolobus kirkii

Unguja

Endangered

Udzungwa red colobus

CarnivoransCarnivorans

Example

Binomial name

Native range

Status

Continental relative

Insular / mainlandlength or mass ratio

Sicilian wolf

Canis lupus cristaldii

Sicily

Extinct (AD 1970)

Gray wolf

Japanese wolf

Canis lupus hodophilax

Japan (excluding Hokkaido)

Extinct (AD 1905)

Sardinian dhole(forward)

Cynotherium sardous

Corsica and Sardinia

Extinct (c. 8300 BC)

Xenocyon

Trinil dog

Mececyon trinilensis

Java

Extinct (Pleistocene)

Cozumel coati

Nasua narica nelsoni

Cozumel

Critically endangered

Yucatan white-nosed coati

Zanzibar leopard

Panthera pardus pardus

Unguja

Critically endangered or Extinct

African leopard

Taiwan leopard

Panthera pardus

Taiwan

Extinct (Pleistocene)

Amur leopard

Bali tiger

Panthera tigris sondaica

Bali

Extinct (c. AD 1940)

Sumatran tiger

Javan tiger

Java

Extinct (c. AD 1975)

Cozumel raccoon

Procyon pygmaeus

Cozumel

Critically endangered

Raccoon

Island fox

Urocyon littoralis

Six of the Channel Islands of California

Near Threatened

Gray fox

LR ≈ 0.84 LR ≈ 0.75

Cozumel fox

Urocyon sp.

Cozumel

Critically endangered or Extinct

Non-ruminant ungulateungulates

Example

Binomial name

Native range

Status

Continental relative

Eumaiochoerus

Eumaiochoerus etruscus

Baccinello, Montebamboli

Extinct (Miocene)

Microstonyx

Malagasy dwarf hippopotamuseses

Hippopotamus laloumena

Madagascar

Extinct (c. AD 1000)

Hippopotamus

H. lemerlei

H. madagascariensis

Bumiayu dwarf hippopotamus

Hexaprotodon simplex

Bumiayu Island (now Java)

Extinct (Early Pleistocene)

Asian hippopotamuses

Cretan dwarf hippopotamus

Hippopotamus creutzburgi

Crete

Extinct (Middle Pleistocene)

Hippopotamus antiquus

Maltese dwarf hippopotamus

Hippopotamus melitensis

Malta

Extinct (Pleistocene)

Hippopotamus (H. amphibius)

Sicilian dwarf hippopotamus

Hippopotamus pentlandi

Sicily

Cypriot pygmy hippopotamus

Hippopotamus minor

Cyprus

Extinct (c. 8000 BC)

Unclear, either H. amphibius or H. antiquus.

Cozumel collared peccary

Pecari tajacu nanus

Cozumel

Unknown

Collared peccary

BovidBovids

Example

Binomial name

Native range

Status

Continental relative

Sicilian bison

Bison priscus siciliae

Sicily

Extinct (Late Pleistocene)

Steppe bison

Sicilian aurochs

Bos primigenius siciliae

Eurasian aurochs

Cebu tamaraw

Bubalus cebuensis

Cebu, Philippines

Extinct

Wild water buffalo

Lowland anoa

Bubalus depressicornis

Sulawesi and Buton, Indonesia

Endangered

Bubalus grovesi

Bubalus grovesi

Sulawesi, Indonesia

Extinct

Tamaraw

Bubalus mindorensis

Mindoro, Philippines

Critically endangered

Mountain anoa

Bubalus quarlesi

Sulawesi and Buton, Indonesia

Endangered

Balearic Islands cave goat

Myotragus balearicus

Mallorca and Menorca

Extinct (after 3000 BC)

Gallogoral

Nesogoral

Nesogoral spp.

Sardinia

Extinct

Dahlak Kebir gazelle

Nanger soemmerringi ssp.

Dahlak Kebir island, Eritrea

Vulnerable

Soemmerring's gazelle

Tyrrhenotragus

Tyrrhenotragus gracillimus

Baccinello

Extinct

Antilopinae sp.

CervidCervids and relatives

Example

Binomial name

Native range

Status

Continental relative

Cretan deer

Candiacervus spp.

Crete

Extinct (Pleistocene)

Unknown

Sardinian deer

Praemegaceros cazioti

Sardinia

Extinct (c. 5500 BC)

Praemegaceros

Ryukyu dwarf deer

Cervus astylodon

Ryukyu Islands

Extinct

Sika deer (?)

Cervus praenipponicus (?)

Jersey red deer population

Cervus elaphus jerseyensis

Jersey

Extinct (Pleistocene)

Red deer

Corsican red deer

Cervus elaphus corsicanus

Corsica and Sardinia

Near Threatened

Sicilian red deer

Cervus siciliae

Sicily

Extinct (Late Pleistocene)

Hoplitomeryx

Hoplitomeryx spp.

Gargano Island

Extinct (Early Pliocene)

Pecorans

Sicilian fallow deer

Dama carburangelensis

Sicily

Extinct (Late Pleistocene)

Fallow deer

Florida Key deer

Odocoileus virginianus clavium

Florida Keys

Endangered

Virginia deer

Svalbard reindeer

Rangifer tarandus platyrhynchus

Svalbard

Vulnerable

Reindeer

Philippine deer

Rusa marianna

Philippines

Sambar deer

PlantPlants

Possible example

Binomial name

Native range

Status

Continental relative

Insular elephant cacti

Pachycereus pringlei

Remote islands in the Sea of Cortez (e.g. Santa Cruz, San Pedro Mártir)

Not evaluated

Mainland elephant cacti

See also

Notes

References