“共同演化”的版本间的差异
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− | + | ===Fig reproduction and fig wasps=== | |
− | + | [[File:Ficus plant.jpg|thumb|left|A [[Common fig|fig]] exposing its many tiny matured, seed-bearing [[gynoecia]]. These are pollinated by the fig wasp, ''[[Blastophaga psenes]]''. In the cultivated fig, there are also asexual varieties.<ref name=Suleman/>|链接=Special:FilePath/Ficus_plant.jpg]] | |
− | [[File: | + | {{Main|Reproductive coevolution in Ficus}} |
− | {{ | + | The genus ''[[Ficus]]'' is composed of 800 species of vines, shrubs, and trees, including the cultivated fig, defined by their [[syconium]]s, the fruit-like vessels that either hold female flowers or pollen on the inside. Each fig species has its own [[fig wasp]] which (in most cases) pollinates the fig, so a tight mutual dependence has evolved and persisted throughout the genus.<ref name=Suleman>{{cite journal |last1=Suleman |first1=Nazia |last2=Sait |first2=Steve |last3=Compton |first3=Stephen G. |title=Female figs as traps: Their impact on the dynamics of an experimental fig tree-pollinator-parasitoid community |journal=Acta Oecologica |volume=62 |year=2015 |pages=1–9 |doi=10.1016/j.actao.2014.11.001 |bibcode=2015AcO....62....1S|url=http://eprints.whiterose.ac.uk/85568/7/Female%20plants%20as%20traps%20paper%20%283%29.pdf }}</ref> |
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− | + | The genus Ficus is composed of 800 species of vines, shrubs, and trees, including the cultivated fig, defined by their syconiums, the fruit-like vessels that either hold female flowers or pollen on the inside. Each fig species has its own fig wasp which (in most cases) pollinates the fig, so a tight mutual dependence has evolved and persisted throughout the genus. | |
− | + | 榕属植物由800种藤本植物、灌木和乔木组成,其中包括栽培的无花果。每一种榕树都有自己的榕小蜂(在大多数情况下)为榕小蜂授粉,所以这个属中形成了一种紧密的相互依赖关系。 | |
− | + | [[File:Ant - Pseudomyrmex species, on Bull Thorn Acacia (Acacia cornigera) with Beltian bodies, Caves Branch Jungle Lodge, Belmopan, Belize - 8505045055.jpg|thumb|right|''Pseudomyrmex'' ant on bull thorn acacia (''[[Vachellia cornigera]]'') with Beltian bodies that provide the ants with protein<ref name="Hölldobler-532"/>|链接=Special:FilePath/Ant_-_Pseudomyrmex_species,_on_Bull_Thorn_Acacia_(Acacia_cornigera)_with_Beltian_bodies,_Caves_Branch_Jungle_Lodge,_Belmopan,_Belize_-_8505045055.jpg]] | |
− | + | ===Acacia ants and acacias=== | |
− | + | ===Acacia ants and acacias=== | |
− | + | = = = 相思蚂蚁和金合欢 = = | |
− | + | {{Main|Pseudomyrmex ferruginea}} | |
− | + | The [[acacia ant]] (''Pseudomyrmex ferruginea'') is an obligate plant ant that protects at least five species of "Acacia" (''[[Vachellia]]''){{efn|The acacia ant protects at least 5 species of "Acacia", now all renamed to ''Vachellia'': ''[[Vachellia chiapensis|V. chiapensis]]'', ''[[Vachellia collinsii|V. collinsii]]'', ''[[Vachellia cornigera|V. cornigera]]'', ''[[Vachellia hindsii|V. hindsii]]'', and ''[[Vachellia sphaerocephala|V. sphaerocephala]]''.}} from preying insects and from other plants competing for sunlight, and the tree provides nourishment and shelter for the ant and its larvae.<ref name="Hölldobler-532">{{cite book |last1=Hölldobler |first1=Bert |last2=Wilson |first2=Edward O. |title=The ants |publisher=Harvard University Press |year=1990 |url=https://archive.org/details/ants0000hlld |url-access=registration |isbn=978-0-674-04075-5 |pages=[https://archive.org/details/ants0000hlld/page/532 532]–533}}</ref><ref>{{cite web|last=National Geographic|title=Acacia Ant Video|url=http://video.nationalgeographic.com/video/player/animals/bugs-animals/ants-and-termites/ant_acaciatree.html|url-status=dead|archive-url=https://web.archive.org/web/20071107085438/http://video.nationalgeographic.com/video/player/animals/bugs-animals/ants-and-termites/ant_acaciatree.html|archive-date=2007-11-07}}</ref> Such mutualism is not automatic: other ant species exploit trees without reciprocating, following different [[evolutionary strategy|evolutionary strategies]]. These cheater ants impose important host costs via damage to tree reproductive organs, though their net effect on host fitness is not necessarily negative and, thus, becomes difficult to forecast.<ref>{{cite journal |doi=10.1073/pnas.1006872107 |vauthors=Palmer TM, Doak DF, Stanton ML, Bronstein JL, Kiers ET, Young TP, Goheen JR, Pringle RM |year=2010 |title=Synergy of multiple partners, including freeloaders, increases host fitness in a multispecies mutualism |journal=Proceedings of the National Academy of Sciences of the United States of America |volume=107 |issue=40 |pages=17234–9 |pmid=20855614 |pmc=2951420 |bibcode=2010PNAS..10717234P|doi-access=free }}</ref><ref>{{cite journal |title=Kinship and incompatibility between colonies of the acacia ant ''Pseudomyrex ferruginea'' |journal=Behavioral Ecology and Sociobiology |first=Alex |last=Mintzer |author2=Vinson, S.B. |volume=17 |issue=1 |pages=75–78 |doi=10.1007/bf00299432 |jstor=4599807 |year=1985|s2cid=9538185 }}</ref> | |
− | + | The acacia ant (Pseudomyrmex ferruginea) is an obligate plant ant that protects at least five species of "Acacia" (Vachellia) from preying insects and from other plants competing for sunlight, and the tree provides nourishment and shelter for the ant and its larvae. Such mutualism is not automatic: other ant species exploit trees without reciprocating, following different evolutionary strategies. These cheater ants impose important host costs via damage to tree reproductive organs, though their net effect on host fitness is not necessarily negative and, thus, becomes difficult to forecast. | |
− | + | 金合欢蚂蚁(相思树蚁)是一种专性植物蚂蚁,它能保护至少5种金合欢树(Vachellia)免受捕食昆虫和其他植物争夺阳光的伤害,并为蚂蚁及其幼虫提供营养和庇护。这种互利共生并不是自然而然的: 其他蚂蚁种类遵循不同的进化策略,不作回报地利用树木。这些骗子蚂蚁通过破坏树木的生殖器官给寄主造成重大损失,但它们对寄主适合度的净影响并不一定是负面的,因此难以预测。 | |
− | == | + | ==Hosts and parasites== |
− | {{Main| | + | {{Main|Host–parasite coevolution}} |
− | + | ===Parasites and sexually reproducing hosts=== | |
+ | [[Host–parasite coevolution]] is the coevolution of a [[host (biology)|host]] and a [[parasite]].<ref name="Woolhouse">{{cite journal |doi=10.1038/ng1202-569 |last1=Woolhouse |first1=M. E. J. |last2=Webster |first2=J. P. |last3=Domingo |first3=E. |last4=Charlesworth|first4=B. |last5=Levin |first5=B. R. |title=Biological and biomedical implications of the coevolution of pathogens and their hosts |journal=[[Nature Genetics]] |date=December 2002 |pmid=12457190 |volume=32 |issue=4 |pages=569–77 |url=http://www.era.lib.ed.ac.uk/bitstream/1842/689/2/Charlesworth_Woolhouse.pdf|hdl=1842/689 |s2cid=33145462 |hdl-access=free }}</ref> A general characteristic of many viruses, as [[obligate parasite]]s, is that they coevolved alongside their respective hosts. Correlated mutations between the two species enter them into an evolution arms race. Whichever organism, host or parasite, that cannot keep up with the other will be eliminated from their habitat, as the species with the higher average population fitness survives. This race is known as the [[Red Queen hypothesis]].<ref>{{cite journal |author=Van Valen, L. |date=1973 |title=A New Evolutionary Law |journal=Evolutionary Theory |volume=1 |pages=1–30}} cited in: [http://pespmc1.vub.ac.be/REDQUEEN.html The Red Queen Principle]</ref> The Red Queen hypothesis predicts that sexual reproduction allows a host to stay just ahead of its parasite, similar to the [[Red Queen's race]] in ''[[Through the Looking-Glass]]'': "it takes all the running ''you'' can do, to keep in the same place".<ref>{{cite book |last=Carroll |first=Lewis |author-link=Lewis Carroll |orig-year=1871 |title=Through the Looking-glass: And what Alice Found There |url=https://books.google.com/books?id=cJJZAAAAYAAJ |publisher=Macmillan |date=1875 |page=42 |quote=it takes all the running ''you'' can do, to keep in the same place.}}</ref> The host reproduces sexually, producing some offspring with immunity over its parasite, which then evolves in response.<ref>{{cite journal |doi=10.1038/srep10004 |last=Rabajante |first=J. |display-authors=etal |title=Red Queen dynamics in multi-host and multi-parasite interaction system |journal=[[Scientific Reports]] |year=2015 |volume=5 |pages=10004 |pmid=25899168 |pmc=4405699|bibcode=2015NatSR...510004R}}</ref> | ||
− | + | Host–parasite coevolution is the coevolution of a host and a parasite. A general characteristic of many viruses, as obligate parasites, is that they coevolved alongside their respective hosts. Correlated mutations between the two species enter them into an evolution arms race. Whichever organism, host or parasite, that cannot keep up with the other will be eliminated from their habitat, as the species with the higher average population fitness survives. This race is known as the Red Queen hypothesis. cited in: The Red Queen Principle The Red Queen hypothesis predicts that sexual reproduction allows a host to stay just ahead of its parasite, similar to the Red Queen's race in Through the Looking-Glass: "it takes all the running you can do, to keep in the same place". The host reproduces sexually, producing some offspring with immunity over its parasite, which then evolves in response. | |
− | + | = = = 寄生虫和有性生殖的宿主 = = = 宿主-寄生虫的共同进化是宿主和寄生虫的共同进化。许多病毒作为专性寄生虫的一个普遍特征是它们与各自的宿主共同进化。这两个物种之间的相关突变使它们进入了进化的军备竞赛。无论是哪种生物、宿主或寄生物,如果不能跟上其他生物的步伐,就会从它们的栖息地消失,因为平均适合度较高的物种会幸存下来。这一种族被称为红皇后假说。红皇后原则红皇后假说预测有性生殖可以让寄主在寄生虫之前保持领先,就像爱丽丝镜中奇遇的红皇后比赛一样: “你可以尽你所能地跑,保持在同一个地方。”。宿主进行有性繁殖,产生一些对寄生虫具有免疫力的后代,然后进化为应对措施。 | |
− | === | + | The parasite–host relationship probably drove the prevalence of sexual reproduction over the more efficient asexual reproduction. It seems that when a parasite infects a host, sexual reproduction affords a better chance of developing resistance (through variation in the next generation), giving sexual reproduction variability for fitness not seen in the asexual reproduction, which produces another generation of the organism susceptible to infection by the same parasite.<ref>{{cite web |title=Sexual reproduction works thanks to ever-evolving host, parasite relationships |website=PhysOrg |url=https://phys.org/news/2011-07-sexual-reproduction-ever-evolving-host-parasite.html |date=7 July 2011}}</ref><ref>{{cite journal |author1=Morran, L.T. |author2=Schmidt, O.G. |author3=Gelarden, I.A. |author4=Parrish, R.C. II |author5= Lively, C.M. |title=Running with the Red Queen: Host-Parasite Coevolution Selects for Biparental Sex |journal=Science |volume=333 |issue=6039 |pages=216–8 |date=8 July 2011 |id=Science.1206360 |bibcode=2011Sci...333..216M |doi=10.1126/science.1206360 |pmid=21737739 |pmc=3402160}}</ref><ref>{{cite encyclopedia |author=Hogan, C. Michael |date=2010 |url=https://editors.eol.org/eoearth/wiki/Virus |title=Virus |encyclopedia=Encyclopedia of Earth |editor=Cutler Cleveland |editor2=Sidney Draggan}}</ref> Coevolution between host and parasite may accordingly be responsible for much of the genetic diversity seen in normal populations, including blood-plasma polymorphism, protein polymorphism, and histocompatibility systems.<ref>{{cite journal |author1=Anderson, R. |author2=May, R. |date=October 1982 |title=Coevolution of hosts and parasites |journal=Parasitology |volume=85 |issue=2 |pages=411–426 |doi=10.1017/S0031182000055360 |pmid=6755367}}</ref> |
− | + | The parasite–host relationship probably drove the prevalence of sexual reproduction over the more efficient asexual reproduction. It seems that when a parasite infects a host, sexual reproduction affords a better chance of developing resistance (through variation in the next generation), giving sexual reproduction variability for fitness not seen in the asexual reproduction, which produces another generation of the organism susceptible to infection by the same parasite. Coevolution between host and parasite may accordingly be responsible for much of the genetic diversity seen in normal populations, including blood-plasma polymorphism, protein polymorphism, and histocompatibility systems. | |
− | + | 寄生虫与宿主的关系可能导致了有性生殖的流行,而不是更有效率的无性生殖。看起来,当寄生虫感染宿主时,有性生殖提供了一个更好的机会来发展抗药性(通过下一代的变异) ,使得适应性的有性生殖变异性在无性生殖中看不到,这就产生了另一代的有机体,易受同一寄生虫的感染。宿主和寄生虫之间的共同进化可能相应地导致了正常人群中的许多遗传多样性,包括血浆多态性、蛋白多态性和组织相容性系统。 | |
− | + | [[File:Reed warbler cuckoo.jpg|upright|thumb|[[Brood parasite]]: [[Eurasian reed warbler]] raising a [[common cuckoo]]<ref name=Weiblen/>|链接=Special:FilePath/Reed_warbler_cuckoo.jpg]] | |
− | + | ===Brood parasites=== | |
+ | {{Main|Brood parasitism}} | ||
− | + | [[Brood parasite|Brood parasitism]] demonstrates close coevolution of host and parasite, for example in some [[cuckoo]]s. These birds do not make their own nests, but lay their eggs in nests of other species, ejecting or killing the eggs and young of the host and thus having a strong negative impact on the host's reproductive fitness. Their eggs are camouflaged as eggs of their hosts, implying that hosts can distinguish their own eggs from those of intruders and are in an evolutionary arms race with the cuckoo between camouflage and recognition. Cuckoos are counter-adapted to host defences with features such as thickened eggshells, shorter incubation (so their young hatch first), and flat backs adapted to lift eggs out of the nest.<ref name=Weiblen>{{cite web |last1=Weiblen |first1=George D. |title=Interspecific Coevolution |url=http://geo.cbs.umn.edu/Weiblen2003.pdf |publisher=Macmillan |date=May 2003}}</ref><ref>{{cite journal |last1=Rothstein |first1=S.I |year=1990 |title=A model system for coevolution: avian brood parasitism |journal=Annual Review of Ecology and Systematics |volume=21 |pages=481–508 |doi=10.1146/annurev.ecolsys.21.1.481}}</ref><ref>{{Cite book|title=Cuckoo : cheating by nature|last=Davies, N. B. (Nicholas B.), 1952-|others=McCallum, James (Wildlife artist)|date=7 April 2015|isbn=978-1-62040-952-7|edition=First U.S.|location=New York, NY|oclc=881092849}}</ref> | |
− | + | Brood parasitism demonstrates close coevolution of host and parasite, for example in some cuckoos. These birds do not make their own nests, but lay their eggs in nests of other species, ejecting or killing the eggs and young of the host and thus having a strong negative impact on the host's reproductive fitness. Their eggs are camouflaged as eggs of their hosts, implying that hosts can distinguish their own eggs from those of intruders and are in an evolutionary arms race with the cuckoo between camouflage and recognition. Cuckoos are counter-adapted to host defences with features such as thickened eggshells, shorter incubation (so their young hatch first), and flat backs adapted to lift eggs out of the nest. | |
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− | + | 巢寄生证明了宿主和寄生虫的密切共同进化,例如在一些杜鹃中。这些鸟不自己筑巢,而是在其他物种的巢中产卵,排出或杀死寄主的卵和幼鸟,从而对寄主的生殖适应性产生严重的负面影响。它们的卵伪装成它们寄主的卵,这意味着寄主能够区分自己的卵和入侵者的卵,并且处于一种进化的军备竞赛中,杜鹃介于伪装和识别之间。杜鹃与寄主相反,具有加厚的蛋壳、较短的孵化期(所以它们的幼鸟先孵化)以及适于将蛋提出巢外的平背等特征。 | |
− | + | ===Antagonistic coevolution=== | |
− | + | ===Antagonistic coevolution=== | |
− | + | = = = 对抗性共同进化 = = | |
− | + | Antagonistic coevolution is seen in the [[harvester ant]] species ''[[Pogonomyrmex barbatus]]'' and ''[[Pogonomyrmex rugosus]]'', in a relationship both parasitic and mutualistic. The queens are unable to produce worker ants by mating with their own species. Only by crossbreeding can they produce workers. The winged females act as parasites for the males of the other species as their sperm will only produce sterile hybrids. But because the colonies are fully dependent on these hybrids to survive, it is also mutualistic. While there is no genetic exchange between the species, they are unable to evolve in a direction where they become too genetically different as this would make crossbreeding impossible.<ref name="Herrmann Cahan pp. 20141771–20141771">{{cite journal |last1=Herrmann |first1=M. |last2=Cahan |first2=S. H. |title=Inter-genomic sexual conflict drives antagonistic coevolution in harvester ants |journal=Proceedings of the Royal Society B: Biological Sciences |volume=281 |issue=1797 |date=29 October 2014 |doi=10.1098/rspb.2014.1771 |pmid=25355474 |pages=20141771 |pmc=4240986}}</ref> | |
− | + | Antagonistic coevolution is seen in the harvester ant species Pogonomyrmex barbatus and Pogonomyrmex rugosus, in a relationship both parasitic and mutualistic. The queens are unable to produce worker ants by mating with their own species. Only by crossbreeding can they produce workers. The winged females act as parasites for the males of the other species as their sperm will only produce sterile hybrids. But because the colonies are fully dependent on these hybrids to survive, it is also mutualistic. While there is no genetic exchange between the species, they are unable to evolve in a direction where they become too genetically different as this would make crossbreeding impossible. | |
− | + | 拮抗性的共同进化在收获蚂蚁种类 Pogonomyrmex barbatus 和 Pogonomyrmex rugosus 中可以看到,它们之间既有寄生关系也有互惠关系。蚁后无法通过与同类交配来繁殖工蚁。只有通过杂交,他们才能生产工人。有翅膀的雌性像寄生虫一样为其他物种的雄性服务,因为它们的精子只会产生不育的杂种。但由于殖民地完全依赖这些杂交种生存,这也是互惠互利的。虽然两个物种之间没有基因交换,但它们无法朝着基因差异太大的方向进化,因为这将使杂交繁殖变得不可能。 | |
− | + | ==Predators and prey== | |
+ | [[File:Leopard kill - KNP - 001.jpg|thumb|left|Predator and prey: a [[leopard]] killing a [[bushbuck]]|链接=Special:FilePath/Leopard_kill_-_KNP_-_001.jpg]] | ||
+ | {{Main|Predation}} | ||
− | + | [[Predator]]s and prey interact and coevolve: the predator to catch the prey more effectively, the prey to escape. The coevolution of the two mutually imposes [[selective pressure]]s. These often lead to an [[evolutionary arms race]] between prey and predator, resulting in [[anti-predator adaptation]]s.<ref>{{cite web|title=Predator-Prey Relationships|url=https://necsi.edu/predator-prey-relationships|publisher=New England Complex Systems Institute|access-date=17 January 2017}}</ref> | |
− | + | Predators and prey interact and coevolve: the predator to catch the prey more effectively, the prey to escape. The coevolution of the two mutually imposes selective pressures. These often lead to an evolutionary arms race between prey and predator, resulting in anti-predator adaptations. | |
− | + | 捕食者和猎物相互作用并共同进化: 捕食者更有效地捕捉猎物,猎物逃跑。两者的共同进化相互施加选择压力。这往往导致进化的军备竞赛之间的猎物和捕食者,导致反捕食适应。 | |
− | + | The same applies to [[herbivore]]s, animals that eat plants, and the plants that they eat. [[Paul R. Ehrlich]] and [[Peter H. Raven]] in 1964 proposed the theory of [[escape and radiate coevolution]] to describe the evolutionary diversification of plants and butterflies.<ref>{{cite journal |last1=Ehrlich |first1=Paul R. |author1-link=Paul R. Ehrlich |last2=Raven |first2=Peter H. |author2-link= Peter H. Raven |year=1964 |title=Butterflies and Plants: A Study in Coevolution |journal=Evolution |volume=18 |issue=4 |pages=586–608 |doi=10.2307/2406212 |jstor=2406212}}</ref> In the [[Rocky Mountains]], [[red squirrel]]s and [[crossbill]]s (seed-eating birds) compete for seeds of the [[lodgepole pine]]. The squirrels get at pine seeds by gnawing through the cone scales, whereas the crossbills get at the seeds by extracting them with their unusual crossed mandibles. In areas where there are squirrels, the lodgepole's cones are heavier, and have fewer seeds and thinner scales, making it more difficult for squirrels to get at the seeds. Conversely, where there are crossbills but no squirrels, the cones are lighter in construction, but have thicker scales, making it more difficult for crossbills to get at the seeds. The lodgepole's cones are in an evolutionary arms race with the two kinds of herbivore.<ref name="Berkeley">{{cite web |title=Coevolution |url=https://evolution.berkeley.edu/evolibrary/article/evo_33 |publisher=University of California Berkeley |access-date=17 January 2017}} and the two following pages of the web article.</ref> | |
− | + | The same applies to herbivores, animals that eat plants, and the plants that they eat. Paul R. Ehrlich and Peter H. Raven in 1964 proposed the theory of escape and radiate coevolution to describe the evolutionary diversification of plants and butterflies. In the Rocky Mountains, red squirrels and crossbills (seed-eating birds) compete for seeds of the lodgepole pine. The squirrels get at pine seeds by gnawing through the cone scales, whereas the crossbills get at the seeds by extracting them with their unusual crossed mandibles. In areas where there are squirrels, the lodgepole's cones are heavier, and have fewer seeds and thinner scales, making it more difficult for squirrels to get at the seeds. Conversely, where there are crossbills but no squirrels, the cones are lighter in construction, but have thicker scales, making it more difficult for crossbills to get at the seeds. The lodgepole's cones are in an evolutionary arms race with the two kinds of herbivore. and the two following pages of the web article. | |
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− | + | 这同样适用于食草动物,吃植物的动物,以及它们吃的植物。1964年,Paul r. Ehrlich 和 Peter h. Raven 提出了逃逸辐射共同进化理论来描述植物和蝴蝶的进化多样性。在落基山脉,红松鼠和斑鸠(食种子的鸟)争夺海滩松的种子。松鼠通过啃咬松果鳞片来获取松子,而交喙则通过它们不寻常的交叉下颚来获取松子。在有松鼠的地方,海滩鱼的球果更重,种子更少,鳞片更薄,这使得松鼠更难获得种子。相反,如果有交喙,但没有松鼠,球果的结构较轻,但有较厚的鳞片,使交喙更难以获得种子。海滩上的锥形细胞与这两种食草动物进行着一场进化中的军备竞赛。以及接下来两页的网络文章。 | |
− | + | [[File:Drosophila.melanogaster.couple.2.jpg|thumb|upright|[[Sexual conflict]] has been studied in ''[[Drosophila melanogaster]]'' (shown mating, male on right).|链接=Special:FilePath/Drosophila.melanogaster.couple.2.jpg]] | |
− | + | ==Competition== | |
+ | {{Main|Intraspecific competition|Interspecific competition}} | ||
− | + | Both [[intraspecific competition]], with features such as [[sexual conflict]]<ref>{{cite journal |doi=10.1098/rstb.2005.1785 |title=Sexual conflict over mating and fertilization: An overview |year=2006 |last1=Parker |first1=G. A. |journal=Philosophical Transactions of the Royal Society B: Biological Sciences |volume=361 |issue=1466 |pages=235–59 |pmid=16612884 |pmc=1569603}}</ref> and [[sexual selection]],<ref name="UCL">{{cite web|title=Biol 2007 - Coevolution|url=https://www.ucl.ac.uk/~ucbhdjm/courses/b242/Coevol/Coevol.html|publisher=[[University College, London]]|access-date=19 January 2017}}</ref> and [[interspecific competition]], such as between predators, may be able to drive coevolution.<ref>{{cite journal |last1=Connell |first1=Joseph H. |s2cid=5576868 |title=Diversity and the Coevolution of Competitors, or the Ghost of Competition Past |journal=Oikos |date=October 1980 |volume=35 |issue=2 |pages=131–138 |doi=10.2307/3544421 |jstor=3544421}}</ref> | |
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− | + | Both intraspecific competition, with features such as sexual conflict and sexual selection, and interspecific competition, such as between predators, may be able to drive coevolution. | |
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− | + | 无论是具有如性冲突和性选择等特征的种内竞争,还是具有如食肉动物之间的种间竞争,都可能推动共同进化。 | |
− | + | == Multispecies == | |
+ | [[File:Amegilla cingulata on long tube of Acanthus ilicifolius flower.jpg|thumb|upright|Long-tongued bees and long-tubed flowers coevolved, whether pairwise or "diffusely" in groups known as guilds.<ref name=Juenger/>|链接=Special:FilePath/Amegilla_cingulata_on_long_tube_of_Acanthus_ilicifolius_flower.jpg]] | ||
− | + | thumb|upright|Long-tongued bees and long-tubed flowers coevolved, whether pairwise or "diffusely" in groups known as guilds. | |
− | + | 多种蜂和长舌蜜蜂共同进化,不论是成对的还是“广泛”进化的,都被称为公会。 | |
− | + | The types of coevolution listed so far have been described as if they operated pairwise (also called specific coevolution), in which traits of one species have evolved in direct response to traits of a second species, and vice versa. This is not always the case. Another evolutionary mode arises where evolution is reciprocal, but is among a group of species rather than exactly two. This is variously called guild or diffuse coevolution. For instance, a trait in several species of [[flowering plant]], such as offering its [[nectar]] at the end of a long tube, can coevolve with a trait in one or several species of pollinating insects, such as a long proboscis. More generally, flowering plants are pollinated by insects from different families including [[bee]]s, [[fly|flies]], and [[beetle]]s, all of which form a broad [[guild (ecology)|guild]] of [[pollinator]]s which respond to the nectar or pollen produced by flowers.<ref name=Juenger>Juenger, Thomas, and [[Joy Bergelson]]. "Pairwise versus diffuse natural selection and the multiple herbivores of scarlet gilia, Ipomopsis aggregata." Evolution (1998): 1583–1592.</ref><ref>{{cite book |author1=Gullan, P. J. |author2=Cranston, P. S. |date=2010 |title=The Insects: An Outline of Entomology |url=https://archive.org/details/insectsoutlineen00pjgu |url-access=limited |publisher=Wiley |edition=4th |isbn=978-1-118-84615-5 |pages=[https://archive.org/details/insectsoutlineen00pjgu/page/n315 291]–293}}</ref><ref>{{cite journal |last1=Rader |first1=Romina |last2=Bartomeus |first2=Ignasi |display-authors=etal |title=Non-bee insects are important contributors to global crop pollination |journal=PNAS |date=2016 |volume=113 |issue=1 |doi=10.1073/pnas.1517092112 |pmid=26621730 |pmc=4711867 |pages=146–151 |bibcode=2016PNAS..113..146R|doi-access=free }}</ref> | |
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− | + | The types of coevolution listed so far have been described as if they operated pairwise (also called specific coevolution), in which traits of one species have evolved in direct response to traits of a second species, and vice versa. This is not always the case. Another evolutionary mode arises where evolution is reciprocal, but is among a group of species rather than exactly two. This is variously called guild or diffuse coevolution. For instance, a trait in several species of flowering plant, such as offering its nectar at the end of a long tube, can coevolve with a trait in one or several species of pollinating insects, such as a long proboscis. More generally, flowering plants are pollinated by insects from different families including bees, flies, and beetles, all of which form a broad guild of pollinators which respond to the nectar or pollen produced by flowers.Juenger, Thomas, and Joy Bergelson. "Pairwise versus diffuse natural selection and the multiple herbivores of scarlet gilia, Ipomopsis aggregata." Evolution (1998): 1583–1592. | |
− | + | 到目前为止,所列出的共同进化类型被描述为是两两运作的(也称为特定共同进化) ,其中一个物种的特征是直接响应第二个物种的特征而进化的,反之亦然。但事实并非总是如此。另一种进化模式出现在进化是相互的,但是是在一组物种之间而不是两个物种之间。这被称为公会或漫反射共同进化。例如,几种开花植物的一个特征,例如在长管的末端提供花蜜,可以与一种或几种传粉昆虫的特征共同进化,例如长喙。更一般地说,被子植物是由来自不同科的昆虫授粉的,包括蜜蜂、苍蝇和甲虫,所有这些昆虫形成了一个广泛的授粉者协会,它们对花朵产生的花蜜或花粉作出反应。朱恩格、托马斯和乔伊 · 贝尔格森。成对自然选择与扩散自然选择以及猩红吉利亚的多种食草动物——绿芽菜(Ipomopsis aggregata)进化(1998) : 1583-1592。 | |
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2022年1月9日 (日) 14:03的版本
Fig reproduction and fig wasps
The genus Ficus is composed of 800 species of vines, shrubs, and trees, including the cultivated fig, defined by their syconiums, the fruit-like vessels that either hold female flowers or pollen on the inside. Each fig species has its own fig wasp which (in most cases) pollinates the fig, so a tight mutual dependence has evolved and persisted throughout the genus.[1]
The genus Ficus is composed of 800 species of vines, shrubs, and trees, including the cultivated fig, defined by their syconiums, the fruit-like vessels that either hold female flowers or pollen on the inside. Each fig species has its own fig wasp which (in most cases) pollinates the fig, so a tight mutual dependence has evolved and persisted throughout the genus.
榕属植物由800种藤本植物、灌木和乔木组成,其中包括栽培的无花果。每一种榕树都有自己的榕小蜂(在大多数情况下)为榕小蜂授粉,所以这个属中形成了一种紧密的相互依赖关系。
Acacia ants and acacias
Acacia ants and acacias
= = 相思蚂蚁和金合欢 =
The acacia ant (Pseudomyrmex ferruginea) is an obligate plant ant that protects at least five species of "Acacia" (Vachellia)模板:Efn from preying insects and from other plants competing for sunlight, and the tree provides nourishment and shelter for the ant and its larvae.[2][3] Such mutualism is not automatic: other ant species exploit trees without reciprocating, following different evolutionary strategies. These cheater ants impose important host costs via damage to tree reproductive organs, though their net effect on host fitness is not necessarily negative and, thus, becomes difficult to forecast.[4][5]
The acacia ant (Pseudomyrmex ferruginea) is an obligate plant ant that protects at least five species of "Acacia" (Vachellia) from preying insects and from other plants competing for sunlight, and the tree provides nourishment and shelter for the ant and its larvae. Such mutualism is not automatic: other ant species exploit trees without reciprocating, following different evolutionary strategies. These cheater ants impose important host costs via damage to tree reproductive organs, though their net effect on host fitness is not necessarily negative and, thus, becomes difficult to forecast.
金合欢蚂蚁(相思树蚁)是一种专性植物蚂蚁,它能保护至少5种金合欢树(Vachellia)免受捕食昆虫和其他植物争夺阳光的伤害,并为蚂蚁及其幼虫提供营养和庇护。这种互利共生并不是自然而然的: 其他蚂蚁种类遵循不同的进化策略,不作回报地利用树木。这些骗子蚂蚁通过破坏树木的生殖器官给寄主造成重大损失,但它们对寄主适合度的净影响并不一定是负面的,因此难以预测。
Hosts and parasites
Parasites and sexually reproducing hosts
Host–parasite coevolution is the coevolution of a host and a parasite.[6] A general characteristic of many viruses, as obligate parasites, is that they coevolved alongside their respective hosts. Correlated mutations between the two species enter them into an evolution arms race. Whichever organism, host or parasite, that cannot keep up with the other will be eliminated from their habitat, as the species with the higher average population fitness survives. This race is known as the Red Queen hypothesis.[7] The Red Queen hypothesis predicts that sexual reproduction allows a host to stay just ahead of its parasite, similar to the Red Queen's race in Through the Looking-Glass: "it takes all the running you can do, to keep in the same place".[8] The host reproduces sexually, producing some offspring with immunity over its parasite, which then evolves in response.[9]
Host–parasite coevolution is the coevolution of a host and a parasite. A general characteristic of many viruses, as obligate parasites, is that they coevolved alongside their respective hosts. Correlated mutations between the two species enter them into an evolution arms race. Whichever organism, host or parasite, that cannot keep up with the other will be eliminated from their habitat, as the species with the higher average population fitness survives. This race is known as the Red Queen hypothesis. cited in: The Red Queen Principle The Red Queen hypothesis predicts that sexual reproduction allows a host to stay just ahead of its parasite, similar to the Red Queen's race in Through the Looking-Glass: "it takes all the running you can do, to keep in the same place". The host reproduces sexually, producing some offspring with immunity over its parasite, which then evolves in response.
= = = 寄生虫和有性生殖的宿主 = = = 宿主-寄生虫的共同进化是宿主和寄生虫的共同进化。许多病毒作为专性寄生虫的一个普遍特征是它们与各自的宿主共同进化。这两个物种之间的相关突变使它们进入了进化的军备竞赛。无论是哪种生物、宿主或寄生物,如果不能跟上其他生物的步伐,就会从它们的栖息地消失,因为平均适合度较高的物种会幸存下来。这一种族被称为红皇后假说。红皇后原则红皇后假说预测有性生殖可以让寄主在寄生虫之前保持领先,就像爱丽丝镜中奇遇的红皇后比赛一样: “你可以尽你所能地跑,保持在同一个地方。”。宿主进行有性繁殖,产生一些对寄生虫具有免疫力的后代,然后进化为应对措施。
The parasite–host relationship probably drove the prevalence of sexual reproduction over the more efficient asexual reproduction. It seems that when a parasite infects a host, sexual reproduction affords a better chance of developing resistance (through variation in the next generation), giving sexual reproduction variability for fitness not seen in the asexual reproduction, which produces another generation of the organism susceptible to infection by the same parasite.[10][11][12] Coevolution between host and parasite may accordingly be responsible for much of the genetic diversity seen in normal populations, including blood-plasma polymorphism, protein polymorphism, and histocompatibility systems.[13]
The parasite–host relationship probably drove the prevalence of sexual reproduction over the more efficient asexual reproduction. It seems that when a parasite infects a host, sexual reproduction affords a better chance of developing resistance (through variation in the next generation), giving sexual reproduction variability for fitness not seen in the asexual reproduction, which produces another generation of the organism susceptible to infection by the same parasite. Coevolution between host and parasite may accordingly be responsible for much of the genetic diversity seen in normal populations, including blood-plasma polymorphism, protein polymorphism, and histocompatibility systems.
寄生虫与宿主的关系可能导致了有性生殖的流行,而不是更有效率的无性生殖。看起来,当寄生虫感染宿主时,有性生殖提供了一个更好的机会来发展抗药性(通过下一代的变异) ,使得适应性的有性生殖变异性在无性生殖中看不到,这就产生了另一代的有机体,易受同一寄生虫的感染。宿主和寄生虫之间的共同进化可能相应地导致了正常人群中的许多遗传多样性,包括血浆多态性、蛋白多态性和组织相容性系统。
Brood parasites
Brood parasitism demonstrates close coevolution of host and parasite, for example in some cuckoos. These birds do not make their own nests, but lay their eggs in nests of other species, ejecting or killing the eggs and young of the host and thus having a strong negative impact on the host's reproductive fitness. Their eggs are camouflaged as eggs of their hosts, implying that hosts can distinguish their own eggs from those of intruders and are in an evolutionary arms race with the cuckoo between camouflage and recognition. Cuckoos are counter-adapted to host defences with features such as thickened eggshells, shorter incubation (so their young hatch first), and flat backs adapted to lift eggs out of the nest.[14][15][16]
Brood parasitism demonstrates close coevolution of host and parasite, for example in some cuckoos. These birds do not make their own nests, but lay their eggs in nests of other species, ejecting or killing the eggs and young of the host and thus having a strong negative impact on the host's reproductive fitness. Their eggs are camouflaged as eggs of their hosts, implying that hosts can distinguish their own eggs from those of intruders and are in an evolutionary arms race with the cuckoo between camouflage and recognition. Cuckoos are counter-adapted to host defences with features such as thickened eggshells, shorter incubation (so their young hatch first), and flat backs adapted to lift eggs out of the nest.
巢寄生证明了宿主和寄生虫的密切共同进化,例如在一些杜鹃中。这些鸟不自己筑巢,而是在其他物种的巢中产卵,排出或杀死寄主的卵和幼鸟,从而对寄主的生殖适应性产生严重的负面影响。它们的卵伪装成它们寄主的卵,这意味着寄主能够区分自己的卵和入侵者的卵,并且处于一种进化的军备竞赛中,杜鹃介于伪装和识别之间。杜鹃与寄主相反,具有加厚的蛋壳、较短的孵化期(所以它们的幼鸟先孵化)以及适于将蛋提出巢外的平背等特征。
Antagonistic coevolution
Antagonistic coevolution
= = 对抗性共同进化 =
Antagonistic coevolution is seen in the harvester ant species Pogonomyrmex barbatus and Pogonomyrmex rugosus, in a relationship both parasitic and mutualistic. The queens are unable to produce worker ants by mating with their own species. Only by crossbreeding can they produce workers. The winged females act as parasites for the males of the other species as their sperm will only produce sterile hybrids. But because the colonies are fully dependent on these hybrids to survive, it is also mutualistic. While there is no genetic exchange between the species, they are unable to evolve in a direction where they become too genetically different as this would make crossbreeding impossible.[17]
Antagonistic coevolution is seen in the harvester ant species Pogonomyrmex barbatus and Pogonomyrmex rugosus, in a relationship both parasitic and mutualistic. The queens are unable to produce worker ants by mating with their own species. Only by crossbreeding can they produce workers. The winged females act as parasites for the males of the other species as their sperm will only produce sterile hybrids. But because the colonies are fully dependent on these hybrids to survive, it is also mutualistic. While there is no genetic exchange between the species, they are unable to evolve in a direction where they become too genetically different as this would make crossbreeding impossible.
拮抗性的共同进化在收获蚂蚁种类 Pogonomyrmex barbatus 和 Pogonomyrmex rugosus 中可以看到,它们之间既有寄生关系也有互惠关系。蚁后无法通过与同类交配来繁殖工蚁。只有通过杂交,他们才能生产工人。有翅膀的雌性像寄生虫一样为其他物种的雄性服务,因为它们的精子只会产生不育的杂种。但由于殖民地完全依赖这些杂交种生存,这也是互惠互利的。虽然两个物种之间没有基因交换,但它们无法朝着基因差异太大的方向进化,因为这将使杂交繁殖变得不可能。
Predators and prey
Predators and prey interact and coevolve: the predator to catch the prey more effectively, the prey to escape. The coevolution of the two mutually imposes selective pressures. These often lead to an evolutionary arms race between prey and predator, resulting in anti-predator adaptations.[18]
Predators and prey interact and coevolve: the predator to catch the prey more effectively, the prey to escape. The coevolution of the two mutually imposes selective pressures. These often lead to an evolutionary arms race between prey and predator, resulting in anti-predator adaptations.
捕食者和猎物相互作用并共同进化: 捕食者更有效地捕捉猎物,猎物逃跑。两者的共同进化相互施加选择压力。这往往导致进化的军备竞赛之间的猎物和捕食者,导致反捕食适应。
The same applies to herbivores, animals that eat plants, and the plants that they eat. Paul R. Ehrlich and Peter H. Raven in 1964 proposed the theory of escape and radiate coevolution to describe the evolutionary diversification of plants and butterflies.[19] In the Rocky Mountains, red squirrels and crossbills (seed-eating birds) compete for seeds of the lodgepole pine. The squirrels get at pine seeds by gnawing through the cone scales, whereas the crossbills get at the seeds by extracting them with their unusual crossed mandibles. In areas where there are squirrels, the lodgepole's cones are heavier, and have fewer seeds and thinner scales, making it more difficult for squirrels to get at the seeds. Conversely, where there are crossbills but no squirrels, the cones are lighter in construction, but have thicker scales, making it more difficult for crossbills to get at the seeds. The lodgepole's cones are in an evolutionary arms race with the two kinds of herbivore.[20]
The same applies to herbivores, animals that eat plants, and the plants that they eat. Paul R. Ehrlich and Peter H. Raven in 1964 proposed the theory of escape and radiate coevolution to describe the evolutionary diversification of plants and butterflies. In the Rocky Mountains, red squirrels and crossbills (seed-eating birds) compete for seeds of the lodgepole pine. The squirrels get at pine seeds by gnawing through the cone scales, whereas the crossbills get at the seeds by extracting them with their unusual crossed mandibles. In areas where there are squirrels, the lodgepole's cones are heavier, and have fewer seeds and thinner scales, making it more difficult for squirrels to get at the seeds. Conversely, where there are crossbills but no squirrels, the cones are lighter in construction, but have thicker scales, making it more difficult for crossbills to get at the seeds. The lodgepole's cones are in an evolutionary arms race with the two kinds of herbivore. and the two following pages of the web article.
这同样适用于食草动物,吃植物的动物,以及它们吃的植物。1964年,Paul r. Ehrlich 和 Peter h. Raven 提出了逃逸辐射共同进化理论来描述植物和蝴蝶的进化多样性。在落基山脉,红松鼠和斑鸠(食种子的鸟)争夺海滩松的种子。松鼠通过啃咬松果鳞片来获取松子,而交喙则通过它们不寻常的交叉下颚来获取松子。在有松鼠的地方,海滩鱼的球果更重,种子更少,鳞片更薄,这使得松鼠更难获得种子。相反,如果有交喙,但没有松鼠,球果的结构较轻,但有较厚的鳞片,使交喙更难以获得种子。海滩上的锥形细胞与这两种食草动物进行着一场进化中的军备竞赛。以及接下来两页的网络文章。
Competition
Both intraspecific competition, with features such as sexual conflict[21] and sexual selection,[22] and interspecific competition, such as between predators, may be able to drive coevolution.[23]
Both intraspecific competition, with features such as sexual conflict and sexual selection, and interspecific competition, such as between predators, may be able to drive coevolution.
无论是具有如性冲突和性选择等特征的种内竞争,还是具有如食肉动物之间的种间竞争,都可能推动共同进化。
Multispecies
thumb|upright|Long-tongued bees and long-tubed flowers coevolved, whether pairwise or "diffusely" in groups known as guilds.
多种蜂和长舌蜜蜂共同进化,不论是成对的还是“广泛”进化的,都被称为公会。
The types of coevolution listed so far have been described as if they operated pairwise (also called specific coevolution), in which traits of one species have evolved in direct response to traits of a second species, and vice versa. This is not always the case. Another evolutionary mode arises where evolution is reciprocal, but is among a group of species rather than exactly two. This is variously called guild or diffuse coevolution. For instance, a trait in several species of flowering plant, such as offering its nectar at the end of a long tube, can coevolve with a trait in one or several species of pollinating insects, such as a long proboscis. More generally, flowering plants are pollinated by insects from different families including bees, flies, and beetles, all of which form a broad guild of pollinators which respond to the nectar or pollen produced by flowers.[24][25][26]
The types of coevolution listed so far have been described as if they operated pairwise (also called specific coevolution), in which traits of one species have evolved in direct response to traits of a second species, and vice versa. This is not always the case. Another evolutionary mode arises where evolution is reciprocal, but is among a group of species rather than exactly two. This is variously called guild or diffuse coevolution. For instance, a trait in several species of flowering plant, such as offering its nectar at the end of a long tube, can coevolve with a trait in one or several species of pollinating insects, such as a long proboscis. More generally, flowering plants are pollinated by insects from different families including bees, flies, and beetles, all of which form a broad guild of pollinators which respond to the nectar or pollen produced by flowers.Juenger, Thomas, and Joy Bergelson. "Pairwise versus diffuse natural selection and the multiple herbivores of scarlet gilia, Ipomopsis aggregata." Evolution (1998): 1583–1592.
到目前为止,所列出的共同进化类型被描述为是两两运作的(也称为特定共同进化) ,其中一个物种的特征是直接响应第二个物种的特征而进化的,反之亦然。但事实并非总是如此。另一种进化模式出现在进化是相互的,但是是在一组物种之间而不是两个物种之间。这被称为公会或漫反射共同进化。例如,几种开花植物的一个特征,例如在长管的末端提供花蜜,可以与一种或几种传粉昆虫的特征共同进化,例如长喙。更一般地说,被子植物是由来自不同科的昆虫授粉的,包括蜜蜂、苍蝇和甲虫,所有这些昆虫形成了一个广泛的授粉者协会,它们对花朵产生的花蜜或花粉作出反应。朱恩格、托马斯和乔伊 · 贝尔格森。成对自然选择与扩散自然选择以及猩红吉利亚的多种食草动物——绿芽菜(Ipomopsis aggregata)进化(1998) : 1583-1592。
- ↑ 1.0 1.1 Suleman, Nazia; Sait, Steve; Compton, Stephen G. (2015). "Female figs as traps: Their impact on the dynamics of an experimental fig tree-pollinator-parasitoid community" (PDF). Acta Oecologica. 62: 1–9. Bibcode:2015AcO....62....1S. doi:10.1016/j.actao.2014.11.001.
- ↑ 2.0 2.1 Hölldobler, Bert; Wilson, Edward O. (1990). The ants. Harvard University Press. pp. 532–533. ISBN 978-0-674-04075-5. https://archive.org/details/ants0000hlld.
- ↑ National Geographic. "Acacia Ant Video". Archived from the original on 2007-11-07.
- ↑ Palmer TM, Doak DF, Stanton ML, Bronstein JL, Kiers ET, Young TP, Goheen JR, Pringle RM (2010). "Synergy of multiple partners, including freeloaders, increases host fitness in a multispecies mutualism". Proceedings of the National Academy of Sciences of the United States of America. 107 (40): 17234–9. Bibcode:2010PNAS..10717234P. doi:10.1073/pnas.1006872107. PMC 2951420. PMID 20855614.
- ↑ Mintzer, Alex; Vinson, S.B. (1985). "Kinship and incompatibility between colonies of the acacia ant Pseudomyrex ferruginea". Behavioral Ecology and Sociobiology. 17 (1): 75–78. doi:10.1007/bf00299432. JSTOR 4599807. S2CID 9538185.
- ↑ Woolhouse, M. E. J.; Webster, J. P.; Domingo, E.; Charlesworth, B.; Levin, B. R. (December 2002). "Biological and biomedical implications of the coevolution of pathogens and their hosts" (PDF). Nature Genetics. 32 (4): 569–77. doi:10.1038/ng1202-569. hdl:1842/689. PMID 12457190. S2CID 33145462.
- ↑ Van Valen, L. (1973). "A New Evolutionary Law". Evolutionary Theory. 1: 1–30. cited in: The Red Queen Principle
- ↑ Carroll, Lewis (1875). Through the Looking-glass: And what Alice Found There. Macmillan. p. 42. https://books.google.com/books?id=cJJZAAAAYAAJ. "it takes all the running you can do, to keep in the same place."
- ↑ Rabajante, J.; et al. (2015). "Red Queen dynamics in multi-host and multi-parasite interaction system". Scientific Reports. 5: 10004. Bibcode:2015NatSR...510004R. doi:10.1038/srep10004. PMC 4405699. PMID 25899168.
- ↑ "Sexual reproduction works thanks to ever-evolving host, parasite relationships". PhysOrg. 7 July 2011.
- ↑ Morran, L.T.; Schmidt, O.G.; Gelarden, I.A.; Parrish, R.C. II; Lively, C.M. (8 July 2011). "Running with the Red Queen: Host-Parasite Coevolution Selects for Biparental Sex". Science. 333 (6039): 216–8. Bibcode:2011Sci...333..216M. doi:10.1126/science.1206360. PMC 3402160. PMID 21737739. Science.1206360.
- ↑ Hogan, C. Michael (2010). "Virus". In Cutler Cleveland; Sidney Draggan (eds.). Encyclopedia of Earth.
- ↑ Anderson, R.; May, R. (October 1982). "Coevolution of hosts and parasites". Parasitology. 85 (2): 411–426. doi:10.1017/S0031182000055360. PMID 6755367.
- ↑ 14.0 14.1 Weiblen, George D. (May 2003). "Interspecific Coevolution" (PDF). Macmillan.
- ↑ Rothstein, S.I (1990). "A model system for coevolution: avian brood parasitism". Annual Review of Ecology and Systematics. 21: 481–508. doi:10.1146/annurev.ecolsys.21.1.481.
- ↑ Davies, N. B. (Nicholas B.), 1952- (7 April 2015). Cuckoo : cheating by nature. McCallum, James (Wildlife artist) (First U.S. ed.). New York, NY. ISBN 978-1-62040-952-7. OCLC 881092849.
- ↑ Herrmann, M.; Cahan, S. H. (29 October 2014). "Inter-genomic sexual conflict drives antagonistic coevolution in harvester ants". Proceedings of the Royal Society B: Biological Sciences. 281 (1797): 20141771. doi:10.1098/rspb.2014.1771. PMC 4240986. PMID 25355474.
- ↑ "Predator-Prey Relationships". New England Complex Systems Institute. Retrieved 17 January 2017.
- ↑ Ehrlich, Paul R.; Raven, Peter H. (1964). "Butterflies and Plants: A Study in Coevolution". Evolution. 18 (4): 586–608. doi:10.2307/2406212. JSTOR 2406212.
- ↑ "Coevolution". University of California Berkeley. Retrieved 17 January 2017. and the two following pages of the web article.
- ↑ Parker, G. A. (2006). "Sexual conflict over mating and fertilization: An overview". Philosophical Transactions of the Royal Society B: Biological Sciences. 361 (1466): 235–59. doi:10.1098/rstb.2005.1785. PMC 1569603. PMID 16612884.
- ↑ "Biol 2007 - Coevolution". University College, London. Retrieved 19 January 2017.
- ↑ Connell, Joseph H. (October 1980). "Diversity and the Coevolution of Competitors, or the Ghost of Competition Past". Oikos. 35 (2): 131–138. doi:10.2307/3544421. JSTOR 3544421. S2CID 5576868.
- ↑ 24.0 24.1 Juenger, Thomas, and Joy Bergelson. "Pairwise versus diffuse natural selection and the multiple herbivores of scarlet gilia, Ipomopsis aggregata." Evolution (1998): 1583–1592.
- ↑ Gullan, P. J.; Cranston, P. S. (2010). The Insects: An Outline of Entomology (4th ed.). Wiley. pp. 291–293. ISBN 978-1-118-84615-5. https://archive.org/details/insectsoutlineen00pjgu.
- ↑ Rader, Romina; Bartomeus, Ignasi; et al. (2016). "Non-bee insects are important contributors to global crop pollination". PNAS. 113 (1): 146–151. Bibcode:2016PNAS..113..146R. doi:10.1073/pnas.1517092112. PMC 4711867. PMID 26621730.