{"title":"加利福尼亚虎足类局部适应种群的热生态位演化","authors":"C. Willett, C. Son","doi":"10.3160/3712.1","DOIUrl":null,"url":null,"abstract":"Thermal performance is a key component of fitness particularly for ectotherms living in thermally variable environments. Local adaptation can occur within populations of a species that inhabit regions with divergent thermal conditions, but this adaptation may result in trade-offs in other measures of fitness. If these trade-offs affect other aspects of thermal performance, several different patterns are possible (Huey and Kingsolver 1993). One potential pattern from a trade-off is a shift in the thermal niche, meaning that an organism that can handle a new range of higher temperatures can no longer handle colder temperatures as well. A second type of pattern is a generalist/specialist trade-off whereby populations may have broader thermal niches but lower fitness at optimal temperatures [i.e. “a jack-of-all-trades is a master of none” (Huey and Hertz 1984)]. Another possibility is that increased investment associated with local thermal adaptation (i.e. high temperature tolerance) may result in trade-offs in non-thermally dependent traits (Angilletta et al. 2003). The nature and structure of these trade-offs could determine the degree to which organisms will be able to respond to a changing climate. The copepod Tigriopus californicus (Baker, 1912) has become an important system in which to study the evolution of local adaptation to the thermal environment. Geographically distinct populations of this copepod occur in upper intertidal pools along the Pacific coast from central Baja Mexico to Alaska. These populations often show high degrees of genetic divergence from one another indicating that levels of gene flow between populations can be very limited over long periods of time (Burton 1997; Edmands 2001; Willett and Ladner 2009). There is also a clear latitudinal gradient in high temperature survival that is suggestive of local thermal adaptation for this species (Willett 2010; Kelly et al. 2012; Leong et al. 2018). This latitudinal gradient for high temperature tolerance has been seen for nauplii and copepodids as well as adults (Tangwancharoen and Burton 2014). Local thermal adaptation in T. californicus is also suggested by studies of fitness components and competitive fitness under non-extreme temperatures. Hong and Shurin (2015) examined 15 populations of T. californicus from Vancouver Island, BC, Canada, to southern California (CA) for a set of life history traits that contribute to fitness under four different temperature conditions (from 15°C to 30°C). They estimated the net fitness effect of these traits by calculating an intrinsic population growth rate (r) and found a consistent shift in the thermal niche from south to north and also higher r in the northern populations. Willett (2010) also found that for comparisons across a set of moderate temperatures there was a flip in competitive fitness between pairs of southern and central CA T. californicus populations. Central CA populations outcompeted southern populations at 16°C while the opposite pattern was observed in a fluctuating environment with an average temperature of 24°C (a 20°C to 28°C daily cycle). Combined these results suggest that","PeriodicalId":90803,"journal":{"name":"Bulletin (Southern California Academy of Sciences)","volume":"29 1","pages":"150 - 156"},"PeriodicalIF":0.0000,"publicationDate":"2018-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"9","resultStr":"{\"title\":\"The Evolution of the Thermal Niche Across Locally Adapted Populations of the Copepod Tigriopus californicus\",\"authors\":\"C. Willett, C. Son\",\"doi\":\"10.3160/3712.1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Thermal performance is a key component of fitness particularly for ectotherms living in thermally variable environments. Local adaptation can occur within populations of a species that inhabit regions with divergent thermal conditions, but this adaptation may result in trade-offs in other measures of fitness. If these trade-offs affect other aspects of thermal performance, several different patterns are possible (Huey and Kingsolver 1993). One potential pattern from a trade-off is a shift in the thermal niche, meaning that an organism that can handle a new range of higher temperatures can no longer handle colder temperatures as well. A second type of pattern is a generalist/specialist trade-off whereby populations may have broader thermal niches but lower fitness at optimal temperatures [i.e. “a jack-of-all-trades is a master of none” (Huey and Hertz 1984)]. Another possibility is that increased investment associated with local thermal adaptation (i.e. high temperature tolerance) may result in trade-offs in non-thermally dependent traits (Angilletta et al. 2003). The nature and structure of these trade-offs could determine the degree to which organisms will be able to respond to a changing climate. The copepod Tigriopus californicus (Baker, 1912) has become an important system in which to study the evolution of local adaptation to the thermal environment. Geographically distinct populations of this copepod occur in upper intertidal pools along the Pacific coast from central Baja Mexico to Alaska. These populations often show high degrees of genetic divergence from one another indicating that levels of gene flow between populations can be very limited over long periods of time (Burton 1997; Edmands 2001; Willett and Ladner 2009). There is also a clear latitudinal gradient in high temperature survival that is suggestive of local thermal adaptation for this species (Willett 2010; Kelly et al. 2012; Leong et al. 2018). This latitudinal gradient for high temperature tolerance has been seen for nauplii and copepodids as well as adults (Tangwancharoen and Burton 2014). Local thermal adaptation in T. californicus is also suggested by studies of fitness components and competitive fitness under non-extreme temperatures. Hong and Shurin (2015) examined 15 populations of T. californicus from Vancouver Island, BC, Canada, to southern California (CA) for a set of life history traits that contribute to fitness under four different temperature conditions (from 15°C to 30°C). They estimated the net fitness effect of these traits by calculating an intrinsic population growth rate (r) and found a consistent shift in the thermal niche from south to north and also higher r in the northern populations. Willett (2010) also found that for comparisons across a set of moderate temperatures there was a flip in competitive fitness between pairs of southern and central CA T. californicus populations. Central CA populations outcompeted southern populations at 16°C while the opposite pattern was observed in a fluctuating environment with an average temperature of 24°C (a 20°C to 28°C daily cycle). 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引用次数: 9
摘要
热性能是适应性的关键组成部分,特别是对于生活在热变化环境中的变温动物。局部适应可以发生在一个物种的种群中,这些物种居住在具有不同热条件的地区,但这种适应可能导致其他适应度指标的权衡。如果这些权衡影响到热性能的其他方面,则可能有几种不同的模式(Huey和Kingsolver 1993)。这种权衡的一种潜在模式是热生态位的转变,这意味着能够适应更高温度范围的生物不能再适应更冷的温度。第二种模式是通才/专才的权衡,即种群可能有更广泛的热生态位,但在最佳温度下的适应性较低[即“万事通就是样样不精通”(休伊和赫兹,1984)]。另一种可能性是,与局部热适应(即高温耐受性)相关的投资增加可能导致非热依赖性状的权衡(Angilletta et al. 2003)。这些权衡的性质和结构可以决定生物体对气候变化的反应程度。桡足动物Tigriopus californicus (Baker, 1912)已成为研究局部热环境适应进化的重要系统。这种桡足动物在地理上不同的种群分布在太平洋沿岸从下墨西哥中部到阿拉斯加的潮间带上游。这些种群之间经常表现出高度的遗传差异,这表明在很长一段时间内,种群之间的基因流动水平可能非常有限(Burton 1997;Edmands 2001;Willett and Ladner 2009)。在高温生存中也存在明显的纬度梯度,这表明该物种具有局部热适应性(Willett 2010;Kelly et al. 2012;Leong et al. 2018)。这种高温耐受性的纬度梯度在nauplii和桡足类以及成虫中都有发现(Tangwancharoen和Burton 2014)。适应性成分和非极端温度下的竞争适应性的研究也表明加州小蠊的局部热适应性。Hong和Shurin(2015)研究了从加拿大不列颠哥伦比亚省温哥华岛到南加州(CA)的15个加利福尼亚弓形虫种群,研究了一组生活史特征,这些特征有助于在四种不同温度条件下(15°C至30°C)的适应性。他们通过计算固有的种群增长率(r)来估计这些特征的净适应度效应,并发现热生态位从南到北的持续变化,并且北方种群的r更高。威雷特(2010)也发现,跨一组比较温和的温度有一个翻转之间在竞争激烈的健身对CA t . californicus南部和中部的人口。中部CA种群在16°C时优于南部种群,而在平均温度为24°C的波动环境中(每日周期为20°C至28°C)观察到相反的模式。综合这些结果表明
The Evolution of the Thermal Niche Across Locally Adapted Populations of the Copepod Tigriopus californicus
Thermal performance is a key component of fitness particularly for ectotherms living in thermally variable environments. Local adaptation can occur within populations of a species that inhabit regions with divergent thermal conditions, but this adaptation may result in trade-offs in other measures of fitness. If these trade-offs affect other aspects of thermal performance, several different patterns are possible (Huey and Kingsolver 1993). One potential pattern from a trade-off is a shift in the thermal niche, meaning that an organism that can handle a new range of higher temperatures can no longer handle colder temperatures as well. A second type of pattern is a generalist/specialist trade-off whereby populations may have broader thermal niches but lower fitness at optimal temperatures [i.e. “a jack-of-all-trades is a master of none” (Huey and Hertz 1984)]. Another possibility is that increased investment associated with local thermal adaptation (i.e. high temperature tolerance) may result in trade-offs in non-thermally dependent traits (Angilletta et al. 2003). The nature and structure of these trade-offs could determine the degree to which organisms will be able to respond to a changing climate. The copepod Tigriopus californicus (Baker, 1912) has become an important system in which to study the evolution of local adaptation to the thermal environment. Geographically distinct populations of this copepod occur in upper intertidal pools along the Pacific coast from central Baja Mexico to Alaska. These populations often show high degrees of genetic divergence from one another indicating that levels of gene flow between populations can be very limited over long periods of time (Burton 1997; Edmands 2001; Willett and Ladner 2009). There is also a clear latitudinal gradient in high temperature survival that is suggestive of local thermal adaptation for this species (Willett 2010; Kelly et al. 2012; Leong et al. 2018). This latitudinal gradient for high temperature tolerance has been seen for nauplii and copepodids as well as adults (Tangwancharoen and Burton 2014). Local thermal adaptation in T. californicus is also suggested by studies of fitness components and competitive fitness under non-extreme temperatures. Hong and Shurin (2015) examined 15 populations of T. californicus from Vancouver Island, BC, Canada, to southern California (CA) for a set of life history traits that contribute to fitness under four different temperature conditions (from 15°C to 30°C). They estimated the net fitness effect of these traits by calculating an intrinsic population growth rate (r) and found a consistent shift in the thermal niche from south to north and also higher r in the northern populations. Willett (2010) also found that for comparisons across a set of moderate temperatures there was a flip in competitive fitness between pairs of southern and central CA T. californicus populations. Central CA populations outcompeted southern populations at 16°C while the opposite pattern was observed in a fluctuating environment with an average temperature of 24°C (a 20°C to 28°C daily cycle). Combined these results suggest that