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Island evolution Evolutionary forces on islands Evolutionary trends on islands Morphology Gigantism and nanism Loss of dispersal abilities Pringleophaga marioni, Marion Island Lepidoptera: Tineidae Paractora dreuxi, Marion Island Diptera: Helcomyzidae Galapaganus, Galapagos Islands Sequiera et al. 2000 winged/apterous mainland/island Naupactus xanthographus Naupactus verecundus Naupactus dissimulator Galapaganus howdenae Galapaganus galapagoensis Galapaganus caroli Galapaganus vandykei Galapaganus collaris Galapaganus conwayensis Galapaganus ashlocki 7.2 Mya Sequiera et al. 2000 Orthoptera Diptera Hemiptera ArcSine-transformed % flightless (mainland areas) Coleoptera 80 60 40 20 0 Thysanoptera 0 Psocoptera 20 40 60 80 ArcSine-transformed % flightless (oceanic islands) Roff 1990 Neuroptera nr of species flightless/total nr of transitions Sphenisciformes 18/18 1 Struthioniformes 15/15 1 Gruiformes 17/122 17 Porzana sandwichiensis (+?1884), Hawaii Islands Porzana atra, Henderson Island Porzana monasa (+1828), Kosrae Island Porzana palmeri (+1920, 1948), Laysan Island Amauornis akoof Amauornis favirostris Porzana monasa Porzana tabuensis Porzana atra Porzana sandwichensis Amauornis bicolor Amauornis olivieri Porzana palmeri 125 000 y Porzana pusilla Porzana parva Porzana fusca Porzana paykullii Porzana carolina Porzana fluminea Porzana porzana Anurolimnas fasciatus Poliolimnas flaviventer Slikas et al. 2002 Kagu, Rhynochetos jubatus, New Caledonia Rodriguez solitaire, Pezophaps solitaria, Rodriguez Dodo, Raphus cucullatus, Mauritius Kakapo, Strigops habroptilus, New Zealand Anas chlorotis, New Zealand Anas nesiotis, Campbell Islands Anas aucklandia, Auckland Islands Cormorant, Phalacrocorax carbo Flightless cormorant, Phalacrocorax harrisi, Galapagos 1cm mandibles Apteribis, Hawaii Islands (+) Chelychelynechen quassus Thambetochen xanion Ptaiochen pau Kauai Oahu Molokai Lanai Maui Hawaii Anas wyviliana Thambetochen chauliodous moa-nalo (+), Hawaiian Islands Sorensen et al. 1999 number of evolutionary transitions number of flightless species Ostriches Rheas Cassowaries Kiwis Emus Moas total number of species 1 2 4 3 1 13 8 9 1 Elephant birds Struthionidae Rheidae Casuariidae Apterygidae Dromaiidae Dinornithidae Dromornithidae Aepyornithidae 1 2 4 3 1 13 8 9 Africa South America Australia, New Guinea New Zealand Australia New Zealand Australia Madagascar Dodos Raphidae 2 2 2 Mascarene Islands Rails Kagus Rallidae Rhynochetidae 17 1 17 1 122 1 Various islands New Caledonia Parrots Psittacidae 1 1 358 New Zealand Ibises Plataleidae 3? ? ? Hawaii Penguins Spheniscidae 18 1 18 Southern hemisphere Cormorants Phalacrocoracidae 1 1 37 Galapagos Islands Grebes Podicipedidae 3 3 21 South America Murres Alcidae 1 1 23 Atlantic Ocean Ducks Anatidae 4 2 148 Various coastlines "There is a very curious point in the astounding proportion of Coleoptera that are apterous; & I think I have grasped the reason, viz that powers of flight wd be injurious to insects inhabiting a confined locality & expose them to be blown to the sea" Darwin, 1855 Loss of dispersal abilities natural selection for energy re-allocation random drift not countered by selection ecological release (lack of predators) Log winglength (cm) 2.0 Gavidae Phasantidae 1.0 Bird families No flightless species Contains flightless species 0 0 1 2 3 Log body mass (g) 4 McCall et al. 1998 Broom stick, Bidens pilosa, Tropics Bog Beggarticks, Bidens conjuncta, Hawaii Islands pappus achene Lactuca muralis, Vancouver Island Cody & Overton 1996 Volume pappus / Volume achenes 2000 1500 1000 500 0 mainland 1-4 5-7 8-9 10+ Age (years) Lactuca muralis, Vancouver Island Cody & Overton 1996 Island evolution Evolutionary forces on islands Evolutionary trends on islands Morphology Gigantism and nanism Loss of dispersal abilities Development of woodiness Cabbage tree, Dendroseris litoralis, Juan Fernandez Islands Sow Thistle, Sonchus fruticosus, Madeira Narrowleaf plantain, Plantago lanceolata, Eurasia Plantago princeps, Hawaii Competition hypothesis growing taller is advantageous Longevity hypothesis woodiness allows extended lifespans, increases chance of sexual reproduction Climate hypothesis islands have milder and moister climates Development of woodiness Island evolution Evolutionary forces on islands Evolutionary trends on islands Morphology Gigantism and nanism Loss of dispersal abilities Development of woodiness Tendency towards melanism lower predation pressure tendency towards melanism thermal advantage Viper, Vipera berus, Swedish islands in the Baltic Sea Melanism frequency (%) 70 60 50 40 30 20 10 0 inland coastal Viper, Vipera berus, Swedish islands in the Baltic Sea insular Forsman 1995 Annual survival rate 0.9 0.7 zigzag males 0.5 melanistic males 1986-87 87-88 88-89 89-90 90-91 Year Viper, Vipera berus, Swedish islands in the Baltic Sea Forsman 1995 Japanese four-lined ratsnake, Elaphe quadrivirgata, Yakushima Island Tanaka 2007 deviation from preferred range (°C) 16 12 melanistic striped 8 4 0 Jul Sep Oct Nov Month Japanese four-lined ratsnake, Elaphe quadrivirgata, Yakushima Island Tanaka 2007