Evolutionary Stellar Population Synthesis at High Spectral Resolution Optical Wavelengths

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介绍恐龙的演变作文英语

介绍恐龙的演变作文英语

The evolution of dinosaurs is a fascinating subject that has captured the imagination of scientists and enthusiasts alike. Dinosaurs first appeared during the Mesozoic Era, which is often referred to as the Age of Reptiles. This era is divided into three periods: the Triassic, Jurassic, and Cretaceous.The early dinosaurs of the Triassic Period were relatively small, bipedal creatures. They evolved from a group of reptiles known as thecodonts. Over millions of years, these early dinosaurs diversified into a wide variety of species, each adapted to different environments and ecological niches.During the Jurassic Period, dinosaurs reached their peak in terms of diversity and dominance. Herbivorous dinosaurs like the longnecked sauropods, such as Apatosaurus and Diplodocus, roamed the land, while carnivorous dinosaurs like the fearsome Allosaurus and the smaller, agile Velociraptor hunted them. This period also saw the emergence of the first birds, which evolved from small, feathered dinosaurs.The Cretaceous Period marked the final chapter in the history of dinosaurs. This era was characterized by the rise of large, armored herbivores like Ankylosaurus and the massive, carnivorous Tyrannosaurus rex. However, it was also during this period that a catastrophic event occurred, leading to the extinction of all nonavian dinosaurs around 65 million years ago.The exact cause of the dinosaur extinction remains a topic of debate among scientists. The most widely accepted theory is that a massive asteroid impact, combined with volcanic activity, led to a dramatic change in the climate and the collapse of ecosystems, ultimately causing the demise of the dinosaurs.Despite their extinction, the legacy of dinosaurs lives on in the form of birds, which are considered to be the descendants of a group of twolegged dinosaurs known as theropods. Additionally, the study of dinosaur fossils has provided valuable insights into the history of life on Earth and the processes of evolution and adaptation.In conclusion, the evolution of dinosaurs is a captivating journey through time, showcasing the incredible diversity and adaptability of these prehistoric creatures. Their story is a testament to the power of natural selection and the everchanging nature of our planet.。

Population Genetics and Evolution

Population Genetics and Evolution

Population Genetics and EvolutionPopulation genetics is the study of genetic variation within and among populations. It is a field of biology that deals with the genetic makeup of populations, and how genes are passed on from one generation to the next. Evolution, on the other hand, is the process by which species change over time. It is a fundamental principle of biology that explains how organisms adapt to changing environments and how new species arise. In this essay, I will discuss the relationship between population genetics and evolution, and how they are intertwined.Population genetics is the foundation of evolutionary biology. It provides the basic principles that explain how genetic variation arises and how it is maintained within populations. The study of population genetics has revealed that genetic variation is the raw material upon which natural selection acts, and that the frequency of alleles in a population can change over time due to various evolutionary forces. These forces include mutation, genetic drift, migration, and natural selection.Mutation is the ultimate source of genetic variation. It is a random process that introduces new alleles into a population. Mutations can be beneficial, harmful, or neutral, and their effects on the fitness of an organism depend on the environment in which it lives. Genetic drift is a random process that can cause the frequency of alleles in a population to change over time due to chance events. Small populations are more susceptible to genetic drift than large populations, and it can lead to the fixation of alleles that are not necessarily beneficial or harmful.Migration, or gene flow, is the movement of individuals or their genes from one population to another. It can introduce new alleles into a population and prevent genetic differentiation between populations. Natural selection is the process by which organisms with traits that are advantageous in a particular environment have a greater chance of survival and reproduction than those with less advantageous traits. Natural selection can lead to the adaptation of populations to their environment and the evolution of new species.Evolutionary biologists use population genetics to study the patterns and mechanisms of evolution. They use mathematical models to predict how the frequency of alleles in a population will change over time, and to test hypotheses about the causes of evolutionary change. They also use molecular techniques to study the genetic makeup of populations and to reconstruct the evolutionary history of species.One of the most important applications of population genetics is in conservation biology. Many species are threatened with extinction due to habitat loss, climate change, and other human activities. Population genetics can help conservation biologists to understand the genetic diversity of populations, to identify genetically distinct populations, and to develop strategies for conserving genetic diversity. For example, the genetic diversity of captive populations can be maintained by breeding individuals from different populations, and the genetic diversity of wild populations can be enhanced by translocating individuals from other populations.In conclusion, population genetics and evolution are two closely related fields of biology. Population genetics provides the foundation for evolutionary biology by explaining how genetic variation arises and is maintained within populations. Evolutionary biologists use population genetics to study the patterns and mechanisms of evolution, and to develop strategies for conserving genetic diversity. The relationship between population genetics and evolution is a complex and dynamic one, and it is an area of active research in biology. As we continue to study the genetic makeup of populations and the processes that drive evolutionary change, we will gain a better understanding of how life on Earth has evolved and how we can protect it for future generations.。

英语2024年1月六级作文人口老龄化

英语2024年1月六级作文人口老龄化

英语2024年1月六级作文人口老龄化With the advancement of medical technology and improvements in living conditions, the global population is aging at an unprecedented rate. The phenomenon of population aging has become a significant social issue in many countries around the world.There are several reasons contributing to the population aging trend. Firstly, declining birth rates mean that there are fewer young people to support the growing number of elderly individuals. Additionally, advancements in healthcare have led to longer life expectancy, resulting in a larger elderly population. Furthermore, changes in lifestyle and family structures have also played a role in the aging population, with smaller family sizes and increased urbanization leading to fewer children to care for aging parents.The implications of population aging are far-reaching and multifaceted. There are concerns about the economic impact, as a shrinking workforce may lead to labor shortages and increased pressure on social welfare systems. Health care systems will also face challenges in providing quality care for the elderly population. Moreover, theremay be social implications, such as changes in family dynamics and increased demand for elderly care services.In response to the challenges posed by population aging, governments and societies need to develop policies and programs that address the needs of the aging population. This may include measures to support elderly individuals, promote healthy aging, and create a more age-friendly environment. By addressing the challenges of population aging proactively, societies can better prepare for the demographic shift and ensure the well-being of their aging populations.中文翻译:随着医疗技术的进步和生活条件的改善,全球人口正以前所未有的速度老龄化。

雅思og作文有关世界人口的题目

雅思og作文有关世界人口的题目

雅思og作文有关世界人口的题目英文回答:The world's population is a complex and multifaceted issue that has far-reaching implications for our planet and its inhabitants. The growth of the human population has been exponential in recent centuries, and it is estimated that there will be approximately 10 billion people on Earth by 2050. While this growth has the potential to bring many benefits, it also presents a number of challenges that need to be addressed in order to ensure a sustainable future for all.One of the most significant challenges posed by population growth is the strain it puts on the environment. The demand for food, water, and energy is increasing rapidly, and this is putting pressure on natural resources. In order to meet the needs of a growing population, we are forced to exploit the Earth's resources at an unsustainable rate, which is leading to environmental degradation andclimate change.Another challenge posed by population growth is the increased risk of conflict and instability. When resources are scarce, people are more likely to compete for them, which can lead to conflict and violence. This is especially true in areas where there is a high population density and limited access to resources.In addition to these challenges, population growth also has a number of negative consequences for human health and well-being. Overcrowding can lead to poor sanitation and hygiene, which can increase the risk of disease. It canalso lead to increased stress levels and mental health issues.It is clear that the world's population is a majorissue that needs to be addressed in order to ensure a sustainable future for all. There are a number of stepsthat can be taken to slow population growth, including increasing access to education and reproductive health care, and promoting sustainable lifestyles. By working together,we can create a more just and equitable world for all.中文回答:世界人口。

关于人口的英语作文

关于人口的英语作文

When discussing the topic of population,its important to consider various aspects such as growth,distribution,and the impact on society and the environment.Here are some points you might want to include in your essay on population:1.Introduction to Population Growth:Begin by explaining the concept of population growth and its historical context.Discuss how the global population has increased rapidly since the Industrial Revolution,particularly in the last century.2.Causes of Population Growth:Explore the factors contributing to population growth, such as improvements in healthcare,increased life expectancy,and declining infant mortality rates.Also,consider the role of fertility rates and cultural factors that influence family size.3.Geographical Distribution:Discuss how population is not evenly distributed across the globe.Highlight densely populated areas like Asia and Europe,and contrast them with sparsely populated regions like Antarctica and parts of Africa.4.Urbanization:Address the trend of urbanization,where more people are moving to cities in search of better opportunities.Discuss the challenges this presents,such as overcrowding,housing shortages,and increased demand on infrastructure.5.Economic Impact:Analyze the economic implications of population growth.On one hand,a larger workforce can drive economic development,but on the other hand,it can lead to unemployment if there are not enough jobs to accommodate the workforce.6.Social Implications:Discuss how population growth can affect social structures.This includes the potential for increased social stratification,changes in family dynamics,and the strain on social services like education and healthcare.7.Environmental Concerns:Highlight the environmental pressures caused by an increasing population,such as deforestation,loss of biodiversity,pollution,and the depletion of natural resources.ernment Policies and Strategies:Examine the policies that governments around the world have implemented to manage population growth.This could include family planning programs,immigration controls,and incentives for smaller families.9.Future Projections and Challenges:Discuss the projections for future population growth and the potential challenges that lie ahead.Consider the need for sustainable development and the importance of balancing economic growth with environmentalpreservation.10.Conclusion:Summarize the main points of your essay and emphasize the importance of addressing population issues responsibly.Suggest that a collaborative approach involving governments,communities,and individuals is necessary to ensure a sustainable future.Remember to support your arguments with relevant data and examples,and to maintain a clear and logical flow throughout your essay.。

第7单元A课文翻译 研究生英语

第7单元A课文翻译 研究生英语

参考译文伴生物种1. 伴生物种是指不被计算在上岸渔获量中的,但是受到捕捞影响的物种。

跨界鱼类种群,高度洄游鱼类和公海鱼类种群因受到如下因素的影响而影响其他物种:(1)丢弃,(2)未被捕捞上来的生物与渔具发生身体接触,(3)间接过程。

2. 渔业通过很多种机制来影响伴生物种,丢弃是目前人类获取知识最多的一种,尽管人类所知有限。

关于丢弃的全球最新信息是一份粮农组织的报告。

该报告估计全球海洋渔业的丢弃率约为百分之八,丢弃率会根据不同的国家,齿轮类型,目标物种和统计区发生改变。

3. 虾类拖网作业的平均丢弃率最高,为百分之六是二点三。

不同渔业的丢弃率差别很大,在零到百分之九十六之间变化。

尽管有一些跨界的或其他公海中的虾类种群的捕捞,大多数虾类拖网作业仍然限于对专属经济区中虾类种群的捕捞。

专属经济区中虾类的捕捞目标很有可能是生活在较深水域或冷水水域的物种。

冷/深水水域捕虾业的总丢弃率是百分之三十九,但在使用副渔获减少装置(BRDs)后(比如在格林兰岛),丢弃率相对较低,在百分之五左右。

混获的有各种长须鲸和无脊椎动物物种,也包括其他渔业中目标物种的幼鱼。

对于虾类拖网作业中丢弃的长须鲸物种(尤其是比目鱼)的关注促使一些渔业强制使用副渔获减少装置(BRDs)。

4. 延绳钓捕捞高洄游鱼种(主要是金枪鱼和类金枪鱼属物种)具有仅次于虾类拖网作业的丢弃率(平均丢弃率为百分之二十八,并且在零百分之四十范围内浮动)。

延绳钓中最常见的丢弃物种是蓝鲨。

其他鲨鱼,受到鲨鱼和海洋哺乳动物损害的目标物种,扁舵鲣,鲔,印度洋国王鲭鱼,和土魠鱼也在被捕获后丢弃。

5. 跨界鱼类种群和公海鱼类种群主要采用底层拖网捕捞。

目标为底栖鱼类的拖网渔船丢弃率百分之九点六(所有渔业)。

没有根据来判断跨界鱼类种群和公海鱼类种群的丢弃率与专属经济区鱼类种群的丢弃率孰高孰低。

专属经济区鱼类种群的捕捞量在总捕捞量中所占的比例如此之高以至于研究者估计目标为底栖鱼类的底层拖网捕捞所导致的1,700,000吨丢弃物大多来源于专属经济区渔业。

随着人越来越多我们要去别的星球住英语作文

随着人越来越多我们要去别的星球住英语作文As the population of Earth continues to explode, the question of whether we should seek new habitats on other planets becomes increasingly urgent. With finite resources and limited space, the Earth's ability to sustain humanlife is being stretched to its limits. In this essay, we will explore the reasons why interstellar migration may become necessary, the challenges we face in achieving it, and the potential benefits it could bring to humanity.Firstly, the population growth on Earth is exponential, with the global population expected to reach over 9 billion by 2050. This rapid growth is putting immense pressure on the planet's natural resources, leading to issues such as climate change, water scarcity, and food insecurity. As these problems worsen, the viability of sustaining human life on Earth becomes increasingly questionable.Secondly, the search for alternative habitats is motivated by the desire for human survival and progress. As a species, we have always been explorers and pioneers, pushing the boundaries of what is possible. Interstellarmigration would be a巨大leap forward in our evolutionary journey, allowing us to expand our horizons and potentially discover new sources of energy, minerals, and even life itself.However, the challenges of interstellar migration are numerous and daunting. The technology required to travel to other planets is still in its infancy, and the costs are astronomical. Additionally, the physical and psychological toll on astronauts during such long journeys is a major concern. Furthermore, the political and ethicalimplications of colonizing other planets are complex and controversial.Despite these challenges, the potential benefits of interstellar migration are immense. It could provide a new home for humanity, relieving the pressure on Earth's resources and environment. It could also lead to new scientific discoveries and technological advancements,推动人类文明的进步和发展。

GRE真题: 9月21日杭州GRE机经回忆

GRE真题: 9月21日杭州GRE机经回忆一个三空题是说科学家门认为科学的演进过程是(不断变化的)有些人认为是(gradually)的变化--同位语解释缓慢的更新,调整适应;但是有些比较抽象的学科是(revolutionary)的变化。

一个双选题:尽管环境学家不喜欢核武器认为是不好的,但是核武器(选正向词),可以消除全球变暖一个逻辑题说seal的灭绝是病毒和细菌的同时作用,但是因为发现很多细菌在seal生活的水里,所以科学家认为是细菌引起Seal的灭绝,since----选病毒对seal小宝宝有影响,而seal死的都是成年人。

一篇短阅读---说女性文章总是被人忽视,因为男性的文章是具体的专一的,但是女性的文章是多元化的,考点----女性的文章受她们行动范围的限制--仅局限于村里,但是他们会记载多种人的思维想法行为进行比较,所以是diversity--这是一个优点。

题目记得有个是说引用一个人说的diversity是为了说明什么--选diversity是高级作家应该有的特点。

长阅读关于历史的美国南方贵族loyalist还是dissent的变化---主要讲的是科学家们研究方面的转化。

不太记得了嘿嘿还有篇阅读说19世纪的人喜欢看didactic说教性的文章,但是在20世纪这些文章就不流行了,因为20世纪喜欢小说崇尚创新。

填空还有一道是说--因为人们对特立独行的限制,现在的特别的人不是(excess),反而是defiency,很少很少。

还有一个是说一个研究者整个是个悲剧,他的研究一开始的时候是intellect和spare的后来就变得死板和(prolix, 还有一个也是说话多的词不记得了)。

反正这题就是spare和要选的空是相反的意思。

还记得一题不太会说一个老奶奶是个(numinous)人,她总是觉得小时候住的房子在脑海里haunted。

我选的是numinous神经兮兮的意思吧。

9.21杭州教育大厦issue是Claim: The best test of an argument is its ability to convince someone with anopposing viewpoint.Reason: Only by being forced to defend an idea against the doubts and contrastingviews of others does one really discover the value of that idea.argument是Humans arrived in the Kaliko Islands about 7,000 years ago, and within 3,000 years most of the large mammal species that had lived in the forests of the Kaliko Islands had become extinct. Yet humans cannot have been a factor in the species’ extinctions, because there is no evidence that the humans had any significant contact with the mammals. Further, archaeologists have discovered numerous sites where the bones of fish had been discarded, but they found no such areas containing the bones of large mammals, so the humans cannot have hunted the mammals. Therefore, some climate change or other environmental factor must have caused the species’ exti nctions.加试是Q,感觉数学不太难,但是有一道几何题做错了,是比较两个三角形的面积大小,要注意两个三角形的高是一样的。

动物种群的趋势英语作文

动物种群的趋势英语作文Title: The Evolutionary Trend of Animal PopulationsAnimal populations are constantly evolving, adapting to their environments in a dynamic dance of survival and reproduction. The trend of these populations is influenced by a range of factors, including natural resources, predators, competitors, and changes in the ecological niche. Over time, these changes can lead to either a growth or decline in population numbers, ultimately shaping the future of species.One significant trend observed in animal populations is the impact of human activity. As human populations expand and urbanization increases, natural habitats are often destroyed or fragmented, leading to a decrease in population size and genetic diversity. Additionally, pollution and climate change can have devastating effects on animal populations, causing widespread mortality and affecting reproductive success.On the other hand, some animal populations have shown resilience in the face of these challenges. Species that are able to adapt quickly to environmental changes, such as those with high genetic diversity, may thrive even in the face of significant anthropogenic pressure. Furthermore, conservation efforts and protected areas can provide a safe haven for these animals, allowing their populations to recover and even expand.In conclusion, the trend of animal populations is a complex interplay of natural and anthropogenic factors. Understanding these trends is crucial for conserving biodiversity and ensuring the long-term survival of species. As we continue to study and monitor animal populations, we gain a deeper understanding of the intricate web of life and the critical role we play in shaping its future.翻译:动物种群的演变趋势动物种群在不断演变,以适应其生存和繁殖的环境。

英语作文:人口增长对野生动物的影响

英语作文:人口增长对野生动物的影响Essay 1: The Impact of Population Growth on WildlifeAs human population continues to rise, the impact on wildlife becomes increasingly significant. The expanding human settlements encroach upon wildlife habitats, resulting in habitat loss, fragmentation, and degradation. This has detrimental consequences for various wildlife species.Habitat loss is one of the most immediate and devastating effects of population growth on wildlife. As more land is required for infrastructure development, agriculture, and housing, natural habitats are destroyed or modified. This loss of habitat disrupts the delicate balance between species, making it difficult for wildlife to find suitable shelter, food, and breeding grounds.Another consequence of population growth is habitat fragmentation. Large areas of natural habitat are divided into smaller patches, isolated by roads, agricultural fields, and human settlements. This fragmentation disrupts animal movement, making it harder for them to find mates, forage for food, and escape from predators. It also increases the risk of inbreeding and reduces genetic diversity, making wildlife populations more susceptible to diseases and other threats.Additionally, population growth leads to habitat degradation. Increased human activities such as pollution, deforestation, and poaching further deteriorate the quality of wildlife habitats. Pollution from industrial and urban areas contaminates water sources, making it difficult for aquatic wildlife to survive.Deforestation for agricultural purposes removes essential tree cover, exposing wildlife to extreme weather conditions and reducing their food sources.Furthermore, the increasing demand for natural resources driven by population growth puts immense pressure on wildlife. Over-hunting and poaching for bushmeat, fur, and other products drive many species to the brink of extinction. Rapid urbanization and industrialization also contribute to increased pollution and climate change, which further threaten wildlife populations.In conclusion, the rapid growth of the human population has had a significant impact on wildlife. Habitat loss, fragmentation, degradation, and increased pressure on natural resources are some of the consequences. It is crucial for societies to recognize the importance of protecting wildlife and implementing conservation strategies to ensure the survival of these magnificent creatures for future generations.Essay 2: Mitigating the Impact of Population Growth on WildlifeWith the global population continuing to grow, it is crucial to consider the impact on wildlife and take steps to mitigate any negative effects. While population growth can pose challenges for wildlife, there are potential solutions that can help protect and preserve their habitats and ecosystems.One approach is the establishment of protected areas and wildlife sanctuaries. By designating specific areas as protected, governments and conservation organizations can ensure thatwildlife habitats remain intact, minimizing the risk of habitat loss and fragmentation. These protected areas can also play a vital role in promoting breeding and conservation efforts to restore wildlife populations.Another strategy is to promote sustainable development practices. Rather than expanding into natural habitats, urban planning should focus on promoting compact and sustainable cities. This reduces the need for extensive land use and preserves wildlife habitats. Additionally, sustainable farming practices can minimize the impact of agriculture on wildlife by reducing the use of pesticides, preserving natural vegetation, and implementing wildlife-friendly practices.Education and awareness play a crucial role in mitigating the impact of population growth on wildlife. By raising awareness about the importance of conservation and the need to protect wildlife habitats, individuals can make more informed choices. Education programs can help people understand the consequences of their actions and encourage them to adopt sustainable practices in their daily lives.Furthermore, stricter laws and regulations need to be implemented and enforced to curb illegal wildlife trade and poaching. Governments should collaborate with international organizations to combat wildlife trafficking networks and increase penalties for those caught engaging in illegal activities. By decreasing the demand for products derived from wildlife, populations can be better protected from exploitation.In conclusion, while population growth poses challenges for wildlife, there are practical solutions to mitigate its impact. Establishing protected areas, promoting sustainable development practices, raising awareness, and enforcing stricter laws can all contribute to ensuring the preservation and survival of wildlife for future generations.Essay 3: Balancing Population Growth and Wildlife ConservationManaging population growth while ensuring the conservation of wildlife is a delicate balance that must be achieved for the well-being of both human society and the natural world. While population growth can have harmful effects on wildlife, it is essential to approach the issue holistically, considering sustainable practices that promote coexistence between humans and wildlife.One approach is to support family planning and reproductive health services. By providing access to contraception and empowering individuals and communities with the knowledge of reproductive health, population growth can be slowed or stabilized. This, in turn, reduces the demand for expanding human settlements into wildlife habitats.Another strategy is promoting sustainable land use practices. By encouraging responsible land management, such as reforestation, sustainable agriculture, and controlled development, we can protect wildlife habitats while still meeting the needs of the growing population. Restoring degraded habitats and creating wildlife corridors can also facilitate the movement of animals between fragmented areas, enhancing their chances of survival.Increasing public awareness and engagement is vital in achieving the balance between population growth and wildlife conservation. Educating individuals about the importance of wildlife and biodiversity, the impact of human activities, and the need for sustainable practices can foster a sense of responsibility towards coexistence with wildlife. Encouraging citizen science initiatives and promoting ecotourism can also create economic incentives for preserving wildlife habitats.Moreover, international cooperation is crucial. Global challenges such as climate change, habitat loss, and wildlife trafficking require collaborative efforts between nations. By sharing knowledge, resources, and best practices, countries can develop comprehensive strategies and policies that prioritize both human and wildlife well-being.In conclusion, achieving a balance between population growth and wildlife conservation is essential for the sustainable future of our planet. By supporting family planning, promoting sustainable land use practices, increasing public awareness, and fostering international cooperation, we can create a harmonious coexistence between humans and wildlife, ensuring their survival and fostering a healthier and more sustainable planet.。

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a r X i v :a s t r o -p h /0501204v 1 12 J a n 2005Mon.Not.R.Astron.Soc.000,1–17(2005)Printed 5February 2008(MN L A T E X style file v2.2)Evolutionary Stellar Population Synthesis at High SpectralResolution:Optical WavelengthsR.M.Gonz´a lez Delgado 1⋆,M.Cervi˜n o 1,L.P.Martins 2,C.Leitherer 2,P.H.Hauschildt 31Instituto de Astrof´ısica de Andaluc´ıa (CSIC),Apdo.3004,18080Granada,Spain2SpaceTelescope Science Institute,3700San Martin Drive,Baltimore,MD 212183Hamburger Sternwarte,Gojenbergsweg 112,21029Hamburg,GermanyAccepted 2004November.Received 2004May;in original form 2004MayABSTRACTWe present the single stellar population (SSP)synthesis results of our new syn-thetic stellar atmosphere models library with a spectral sampling of 0.3˚A ,coveringthe wavelength range from 3000˚A to 7000˚A for a wide range of metallicities (twicesolar,solar,half solar and 1/10solar).The stellar library is composed of 1650spec-tra computed with the latest improvements in stellar atmospheres.In particular,it incorporates non-LTE line-blanketed models for hot (T eff 27500K),and LTE line-blanketed models (Phoenix)for cool (3000 T eff 4500K)stars.Because of the high spectral resolution of this library,evolutionary synthesis models can be used to predict the strength of numerous weak absorption lines and the evolution of the profiles of the strongest lines over a wide range of ages.The SSP results have been calculated for ages 1Myr to 17Gyr using the stellar evolutionary tracks provided by the Geneva and Padova groups.For young stellar populations,our results have a very detailed coverage of high-temperature stars with similar results for the Padova and Geneva isochrones.For intermediate and old stellar populations,our results,once degraded to a lower resolution,are similar to the ones obtained by other groups (limitations imposed by the stellar evolutionary physics notwidthstanding).The limitations and advantages of our models for the analysis of integrated populations are described.The full set of the stellar library and the evolutionary models are available for retrieval at the websites http://www.iaa.csic.es/∼rosa and http://www.iaa.csic.es/∼mcs/Sed@,or on request from the first two authors.Key words:galaxies:evolution –galaxies:stellar content –stars:evolution.1INTRODUCTIONEvolutionary synthesis,introduced by Tinsley (1968),is a powerful tool for interpreting the integrated light of a stellar population.This technique makes a prediction for the properties of a stellar population taking as a free pa-rameter the star formation rate,the initial mass func-tion (IMF)and the metallicity.During the past decade,evolutionary synthesis models have been developed and improved significantly,using the newest and more ad-vanced stellar evolutionary tracks and stellar libraries (e.g.Cervi˜n o &Mas-Hesse 1994;Fioc &Rocca-Volmerange 1997;Leitherer et al.1999;Vazdekis 1999;Buzzoni 2002a;Schulz et al.2002;Bruzual &Charlot 2003).In addition,⋆E-mail:rosa@iaa.es (RGD);mcs@iaa.es (MC);mar-tins@ (LPM);leitherer@ (CL);yeti@hs.uni-hamburg.de (PH)they have been extended to new wavelength domains (e.g.Cervi˜n o et al.2000;Cervi˜n o,Mas-Hesse,&Kunth 2002,for γand X-rays respectively).However,it is also well known that the power of this technique is very dependent on the reliability of the stellar models and libraries used as ingredients (Leitherer,Fritze-v.Alvensleben,&Huchra 1996,and references therein),as well as on the size of the system to which the models are ap-plied (Cervi˜n o,Luridiana,&Castander 2000;Bruzual 2002;Cervi˜n o et al.2001,2002;Cervi˜n o &Luridiana 2004;Gilfanov,Grimm,&Sunyaev 2004).One important ques-tion related to this technique is whether it is actually up to the challenge of interpreting multi-wavelength data to infer the properties of stellar populations of very different ages and metallicities (e.g.Origlia et al.1999;Massey &Olsen 2003).In recent years,numerous observational surveys have been undertaken to measure the redshift evolution of the2R.M.Gonz´a lez Delgado et al.stellar properties of distant galaxies,with the goal of under-standing the formation and evolution of galaxies.Spectral observations of intermediate and high redshift galaxies have shown a large variety of stellar populations.The integrated light of these galaxies has been analyzed with evolution-ary synthesis models to derive ages,masses and metallici-ties.At ultraviolet(UV)wavelengths,many of these galaxies show the footprints of recent bursts of star formation.They are classified as star forming galaxies(Steidel et al.1996). The UV spectra of these galaxies,which are very similar to local starbursts,are dominated by resonance lines formed in the interstellar medium and/or in the winds of massive stars(Pettini et al.2000).Observations at rest-frame optical wavelengths of these high redshift galaxies(z 2)are scarce due to the lack of non-cryogenic near-infrared(NIR)multi-object spectrographs in very large telescopes.Hαnebular emission has been detected in a few of these galaxies.How-ever,as in nearby star forming galaxies(Brinchmann et al. 2004),the higher order Balmer lines appear in absorption,or in emission with strong absorption wings.Thus,to estimate the star formation rate in these galaxies requires a carefulfit of the stellar continuum and subtraction of the absorption component of the Balmer lines.Evolutionary synthesis mod-els at intermediate or at high spectral resolution are needed to perform thisfit.With this motivation,Gonz´a lez Delgado,Leitherer,& Heckman(1999,hereafter GLH99)built synthetic spectra of H Balmer and He absorption lines of starbursts and post-starburst galaxies,using as input to the evolutionary code Starburst99(Leitherer et al.1999)a stellar library of syn-thetic spectra,with a sampling of0.3˚A,effective tempera-ture from50000to4000K,and gravity in the range0.0 log g 5.0at solar metallicity(Gonz´a lez Delgado&Leitherer 1999,hereafter GL99).The line profiles were computed us-ing a set of programs developed by Hubeny and collabora-tors(Hubeny1988;Hubeny,Lanz,&Jeffery1995).Due to computational restrictions,we only computed small spectral ranges around the most important Balmer and He i lines.Many beautiful data sets on starbursts and galaxies with active galactic nuclei(AGN)have been obtained at intermediate spectral resolution in the last few years to date the stellar popula-tion(Gonz´a lez Delgado,Heckman,&Leitherer2001; Cid Fernandes et al.2001;Aretxaga et al.2001; Kauffmann et al.2003a,b,c;Cid Fernandes et al.2004; Gonz´a lez Delgado et al.2004;Tadhunter et al.2004). These results have motivated us to build a much improved stellar library,both in the mapping of the(T eff,log g) plane and in the complete coverage of the optical spectral range at high spectral resolution.With this new library it is possible to predict the spectral evolution not only of young starbursts but also the properties of old stellar systems.Intermediate or high spectral resolution mod-els are also required to constrain the stellar population in ellipticals,and to break the age-metallicity degener-acy(Vazdekis&Arimoto1999).With this motivation, Bruzual&Charlot(2003)presented models,computed with their code galaxev,at intermediate resolution(3˚A)covering a large range in ages(0.1Myr to20Ga), and wavelengths(3200–9500˚A)for several metallicities. galaxev models are in some aspects similar to thosepresented in this paper,but they have much lower spectral resolution,different coverage of the(T eff,log g)plane and, most importantly,they use empirical stellar spectra.A comparison of the two sets of models is presented Section5.This paper is organized as follows.In Section2,we briefly discuss the stellar library.A more detailed descrip-tion is given by Martins et al.(2004).Section3describes the main stellar ingredients,the assumptions,and the computa-tional techniques of the synthesis models.Section4presents the results and a discussion of the spectral evolution of stel-lar populations,at several metallicities,which evolve accord-ing to the Geneva or Padova isochrones.The models are compared with previous work in Section5,and with obser-vations of star clusters in the Large and Small Magellanic Clouds in Section6.We discuss the limitation of the models in the red supergiant phase in Section7.The summary and conclusions are in Section8.2STELLAR LIBRARYThis stellar library is an extension of the library built by GL99.Here,we present a brief description.A full discussion is given in Martins et al.(2004).The grid includes the synthetic stellar spectra from3000 to7000˚A with afinal spectral sampling of0.3˚A.The spectra span a range of effective temperature from3000to55000K, with variable steps from500to2500K,and a surface gravity log g=−0.5to5.5with dex steps of0.25and0.5.For each temperature,the minimum gravity is set by the Eddington limit.The library covers several metallicities:twice solar,so-lar,half and1/10solar.We assume solar abundance ratios for all the elements,and a helium abundance of He/H=0.1 by number.In addition to the spectral and metallicity cov-erage,this new library presents the following improvements with respect to GL99:(i)Hot stars.Line-blanketed,non-LTE,plane-parallel, hydrostatic atmospheres are used to compute the stellar spectra of O-type stars.The spectra are from the grid of Lanz&Hubeny(2003)1.This grid has12effective temper-atures,27500 T eff 55000K,with2500K steps,and eight values of the surface gravity,3.0 log g 4.75,with0.25 dex steps.These models assume a microturbulence velocity of10km s−1.(ii)Cool stars.Line-blanketed,LTE,spherical at-mospheres are computed with the PHOENIX code (Hauschildt&Baron1999;Allard et al.2001)for stars with 3000 T eff 4500K,with steps of500K.The grid covers 13values of surface gravity,−0.5 log g 5.5,with0.5dex steps.The models assume a mass of1M⊙,a mixing-length equal to2.0,and a microturbulence velocity of2km s−1. (iii)Intermediate temperature stars.As in GL99,the syn-thetic spectra for stars with8000 T eff 27000K are ob-tained with Kurucz LTE atmospheres2(Kurucz1993)and the program SYNSPEC3(Hubeny,Lanz,&Jeffery1995), except that for stars with4750 T eff 7750K,we 1Available at 2Available at /3Available at Evolutionary Stellar Population Synthesis at High Spectral Resolution:Optical wavelengths3use the program SPECTRUM4(Gray&Corbally1994), together with Kurucz atmospheres.Differences found be-tween the metallic line strengths and molecular bands using SPECTRUM and SYNSPEC are discussed in Martins et al. (2004).In all the cases,the maximum distance between two neighboring frequency points for evaluating the spectrum is 0.01˚A.However,the spectra are degraded to have afinal resolution of0.3˚A by performing a rotational and instru-mental convolution for each spectrum.The library contains415,409,416and411spectra forZ=0.002,0.010,0.020(solar)and0.040,respectively.The typical grid coverage is illustrated in Figure1.Isochrones obtained with the evolutionary tracks from the Geneva and Padova groups(cf.Section3)have been over-plotted.Thefigure illustrates that this library constitutes a homogeneous set of stellar spectra covering a dense grid of fundamental parameters,including a significant number of models that reduce the problems of the close model assignation,assumedin most synthesis codes(see,however,Jamet et al.2004,for a different approach).This library also presents some improvements with respect to STELIB5(Le Borgne et al. 2003),the stellar library used by galaxev;in particular,it includes models with T eff 25000K,and T eff 4000K and log g 1.0,which allow the prediction of the spec-tral evolution of the stellar populations of both very young starbursts and old systems.Furthermore,the high spectral resolution of the library allows us to predict the evolution of the He i and He ii lines,and to estimate the absorption cor-rection to the nebular He emission lines.This correction is very important for an accurate determination of primordial He abundance using nebular emission lines of star forming galaxies.The full set of the stellar library is available for retrievalat the website(http://www.iaa.csic.es/∼rosa)or on request from the authors.3DESCRIPTION OF THE INPUTSThe library has been implemented in Starburst99and Sed@6.There are no significant differences between the re-sults obtained with the two codes when models with the same ingredients(evolutionary tracks,IMF,....)are com-pared.Here,we describe only the assumptions and prescrip-tions related to Sed@models.There is,however,a principal difference in the way the two codes.Starburst99computes the isochrones from the im-plemented evolutionary tracks and obtains the results from4Available at/dept/physics/spectrum/spectrum.html 5Available at http://webast.ast.obs-mip.fr/stelib/6Sed@is a synthesis code included in the Legacy Tool projectof the Violent Star Formation European Network.The code is written in ANSI C under GNU Public License and,currently,is coordinated by M.Cervi˜n o;the code and their results must be referred to solely by its documentation,Sed@Reference Man-ual(in preparation),its web address and the citations in the headers of the resultingfiles.More information can be found at http://www.iaa.csic.es/∼mcs/Sed@the implemented atmosphere library.In contrast,Sed@cur-rently does not compute isochrones,but takes them from the literature if they are in the appropriate format.3.1Stellar initial mass function(IMF)and starformation lawThe results presented here assume a power law IMF,Φ(m)= Cmα,where the constant C is determined by the total gas mass converted into stars.The slopeα=−2.35is that de-rived by Salpeter(1955).The low-mass and high-mass cut-offs have been chosen as M low=0.1M⊙and M up=120M⊙, respectively(see Girardi&Bica1993,for a detailed discus-sion about the more appropriate choice of the lower mass limit).The IMF is binned into a grid of the initial masses determined by the particular isochrone,and all the stars be-longing to the same mass bin are assumed to have exactly the same properties.The synthesis is done directly by adding the different contributions from the stars to all the synthe-sised wavelengths.Here,we explore only instantaneous burst models,normalized to1M⊙.3.2Stellar evolution and isochrone integration The models have been computed using the isochrone tech-nique to produce a smooth spectral evolution.This tech-nique was introduced by Charlot&Bruzual(1991)to avoid abrupt changes of the properties of the stellar popula-tions associated with changes in the evolutionary stages of the stars when the mass resolution of the stellar tracks is inadequate.The isochrone synthesis technique is differ-ent from the one used by Tinsley&Gunn(1976),takes into account the lifetime of the stars in each evolutionary phases considered,imposing that the number of stars in a given phase of the stellar evolution must be proportional to the life time of such phase of an individual star.Such a condition,the so called Fuel Consumption Theorem,FCT (Renzini&Buzzoni1986;Buzzoni1989),is specially rele-vant for the faster phases of the stellar evolution.Although both methods should be equivalent,the results depend on the method used(see Buzzoni1995,2002b,for an extensive discussion).In this work,two different sets of stellar isochrones are used.Thefirst one is the set of isochrones from the Padova group by Bertelli et al.(1994)and Girardi et al.(2000)pre-sented in Girardi et al.(2002)7,with metallicities Z=0.019 (solar),0.008and0.004(hereafter Padova isochrones).The initial mass resolution of the used Padova isochrones is suf-ficient to assure a correct integration of the isochrone-IMF product.These models follow the evolution from the zero-age main sequence to the early asymptotic giant branch (AGB)and to thefirst thermal pulse,or to the carbon ignition depending on the initial mass.They cover an age range from4Myr to17Ga in a set of74isochrones with a0.06log time sampling.An additional set at Z=0.030 and0.002is also available on the Padova web server but it comprises a smaller range of ages(0.063to15.8Gyr). We note that there are different sets of isochrones released by the Padova group,in particular,the isochrones from 7The full set is available at http://pleiadi.pd.astro.it/4R.M.Gonz´a lez Delgado etal.Figure1.HR diagram:Points represent the stellar library grid.Lines are isochrones of stellar populations that evolve following the Geneva(left)and the Padova(right)evolutionary tracks at metallicities Z=0.040and Z=0.008,respectively.The isochrone ages are from 1Myr to10Gyr for the Geneva and4Myr to17Gyr for the Padova models.Marigo&Girardi(2001)fulfill the FCT requirements,un-fortunately such isochrones do not cover the early ages of theevolution of stellar clusters.In this work we only present theresults for the quoted Bertelli et al.(1994)and Girardi et al.(2000)set of isochrones.Our second set has been computed from the list ofnon-rotating tracks of the Geneva group(Schaller et al.1992;Schaerer et al.1993a,b;Charbonnel et al.1993),in-cluding standardmass-loss rates computed atfive metallici-ties:Z=0.040,0.020(solar),0.008,0.004and0.0018.Thesetracks include all the phases of the stellar evolution fromthe zero-age main sequence to the end of the giant branchor the carbon ignition.The Geneva isochrones are calcu-lated by means of a parabolic interpolation between thetracks(log M,log t k)in the HR diagram on a variable massgrid as prescribed in Cervi˜n o et al.(2001).This prescriptionis also used for the isochrone computations in Starburst99.The isochrones were generated at specific ages with a vari-able time step:∆t=1Myr for1-10Myr,∆t=5Myrfor10-100Myr,∆t=100Myr for100Myr to1Gyr,and∆t=1Gyr for1-10Gyr.Unfortunately this computationof the isochrones did not assure the FCT requirements(butit is partially implicit in the use of the parabolic interpo-lations),neither did it include the evolution of stars in thehorizontal branch or later phases,which are quite relevantfor the resulting spectrum at ages older than1Gyr9.We re-fer to Lan¸c on et al.(2001)and V´a zquez&Leitherer(2004)for other details about the completeness of the evolutionaryphases and their relevance in the isochrones.Since we are working with SSPs,we do not need totreat chemical evolution self-consistently in the evolutionary8Note that the default in Starburst99are the”enhanced”,notthe”standard”mass-loss rate.9The Geneva group also produces evolutionary tracks from thebegining of the horizontal branch to thefirst thermal pulse in theAGB phase(Charbonnel et al.1996).However,these evolution-ary phases have not been included due to the variations of thenumber of equivalent evolutionary points depending on the initialstellar mass.tracks.Therefore each star generation has the same metal-licity during the evolution.On the other hand,the chemicalevolution in the atmosphere of the individual stars has notbeen considered in the isochrone-atmosphere model assigna-tion.Because the isochrone metallicities do not coincide to-tally with the stellar atmospheres metallicities,we computethe models combining the isochrones and atmospheres asfollow:isochrones at Z=0.040and0.030with the twice so-lar atmospheres;isochrones at Z=0.020and0.019with thesolar atmospheres;isochrones at Z=0.008and0.004withthe half solar atmospheres;and isochrones at Z=0.001withthe1/10solar atmospheres.4RESULTSWe are presenting the model predictions for the spectralevolution of single stellar populations.First,we describe thespectral energy distribution in the3000–7000˚A range.Then,we present the spectral evolution of the hydrogen and heliumlines(section4.2)and of the metallic lines(section4.3).Theeffect of metallicity on the spectra is illustrated,and themodels are discussed for two different isochrone sets(Genevaand Padova).4.1Spectral evolutionFigure2shows the spectral evolution of a single stellar pop-ulation with solar metallicity at seven different ages of4Myr,10Myr,50Myr,200Myr,1Gyr,3Gyr,and10Gyr.Thefirst effect to notice is the decrease with time of thestellar population luminosity,due to the most massive starsdying off.The second effect is the change in the shape ofthe continuum with time,up to a few Gyr;this is a conse-quence of the large variation of the effective temperature ofmassive and intermediate mass stars during their evolution.However,after3Gyr,the shape of the optical continuumis almost constant because low mass stars evolve within asmall range of effective temperature.This results from theEvolutionary Stellar Population Synthesis at High Spectral Resolution:Optical wavelengths5 strong concentration of the isochrones at ages older than3-4Gyr(see Figure1).Additionally,Figure2illustrates thestrong time evolution of the Balmer and the4000˚A breaks. The evolution of the strength of the Balmer lines is also striking.They have a maximum around400Myr,when A stars dominate the optical continuum.Figure2also shows that Geneva and Padova models have similar overall spectral characteristics;however,several detailed differences are clearly visible in thisfigure.First,the spectra obtained with the Padova models are always more luminous than the corresponding Geneva spectra.Second, the continuum shapes diverge in several stages of the evo-lution.For example,at older ages( 2Gyr),the Padova spectra are systematically redder than Geneva’s due to the inclusion of more evolved phases after the tip of the red giant branch,and the absence of low-mass stars10.These phases and low-mass stellar tracks are not included in the Geneva isochrones.However,at younger ages( 100Myr), there is no systematic change of the shape of the contin-uum,with the Padova spectra bluer or redder than Geneva depending on the given age.These differences result directly from the isochrones(Figure3).For example,at50Myr,the main sequence turnoffin the Padova isochrones is bluer than in Geneva,and the coolest stars in the Geneva tracks have lower T effthan in the Padova models;these differences make the Padova spectrum bluer than the Geneva spectrum at50 Myr.A significant difference between both sets of models is at RSG ages,i.e.,10Myr at solar metallicity.At this age, the Geneva spectrum is steeper and shows stronger metallic bands at red wavelengths(λ 5500˚A)than the Padova spectrum.These differences are produced by a larger contri-bution of cool and low gravity stars(Teff∼4000K,and log g∼0)to the total luminosity in the Geneva with respect to the Padova models(Figure3).The metallicity effect on the spectral evolution is shown in Figure4.We plot the spectra of a1Gyr stellar popula-tion at four different metallicities.The effect is appreciated in the slope of the continuum and in the strength of the lines.At this age,lower metallicity spectra are bluer,have stronger Balmer lines,and weaker metallic lines(Figure4a). These changes are produced by the shift of the isochrones to higher temperatures with decreasing metallicity,which is a consequence of stars being brighter and hotter at lower metallicity.The effect of metallicity is also evident in spec-tra at older ages(>few Gyr),where the continuum shape is similar in all the models,but there is a strengthening of the metallic lines from the most metal-poor to the most metal-rich stellar populations(Figure4b).4.2Helium linesThe high spectral resolution of our stellar library allows the prediction of the strength of many weak helium absorption lines that form in the optical continuum of young stellar populations.In Figure5,we have labeled some of the most relevant He i and He ii lines in the spectrum of a7Myr stellar10Note that the Geneva tracks are truncated at0.8M⊙while the Padova isochrones include stars with mass M 0.2M⊙.According with V´a zquez&Leitherer(2004),the differences between Padova and Geneva models are mainly due to thistruncation.Figure5.Spectrum predicted for a7Myr instantaneous burst at Z=0.001.Hydrogen and helium lines in the3650–5000˚A interval are indicated.population at Z=0.001.They are:He iλ3819,λ4026,λ4387,λ4471,λ4922,andλ5876;and He iiλ4200,λ4541,λ4686 andλ5412.He ii lines are detected only during thefirst few years of the evolution;their equivalent widths decreasing with time from values of about0.5˚A.He i lines are more prominent and are detected during thefirst100Myr of evo-lution,when the optical continuum is dominated by B stars. Some of these He i lines have been calculated previously by us(GLH99).We measured the equivalent widths of three of these lines(He iλ4026,λ4471andλ5876)in windows of9-14˚A, integrating theflux from the pseudo-continuum obtained by afirst-order polynomialfit to the continuum windows de-fined in Table1.Figure6shows the equivalent widths of these lines for a stellar population at solar metallicity.He i λ4026is one of the stronger lines,while He iλ5876is much weaker.The He i lines present a maximum value between20 Myr and50Myr when the stellar population is dominated by B stars.He i lines do not form after100Myr,the lifetime of B stars.The equivalent width has also a maximum be-tween7-15Myr due to the presence of post-main sequence stars with T eff 8000K(see Figure7in GLH99).Note,however,that these predictions for hot stars are estimated using static stellar atmosphere models (Lanz&Hubeny2003).They do not account for wind ef-fects,which are important in very massive and evolved O stars.The lines most affected by winds are Hαand He ii λ4686.The wind effects are less important in the Balmer and He i lines in the blue spectral range,and at low metal-licity(Walborn et al.1995).The main effect of the metallicity on the He i lines re-sults from the effect of the metallicity on the temperature of the turnoff,with metal-poor stellar populations having a higher turnofftemperature.The equivalent width of He i lines is a function of T effand gravity,with a maximum at 20000K and log g=5.0(GL99).Thus,the variation of EW(He i)with metallicity depends on the variation of the turnofftemperature of the stellar population with metallic-ity.4.3Hydrogen linesFigure7shows the synthetic profiles of the Balmer lines(Hα, Hβ,Hγ,Hδ,Hǫ,H8,H9,H10,...,to the Balmer limit)for6R.M.Gonz´a lez Delgado et al.Figure2.Spectral evolution for a single stellar population model at solar metallicity following the Geneva(left)evolutionary tracks with standard mass loss,and the Padova(right)tracks.Ages from top to bottom are4Myr,10Myr,50Myr,200Myr,1Gyr,3Gyr, and10Gyr.Table1.Hydrogen and helium lines and continuum windowsHδ4092–4112;4087–4117;4070–41304012–40204158–4169Hγ4330–4350;4325–4355;4310–43704262–42704445–4453Hβ4852–4872;4847–4877;4832–48924770–47824942–4954Hα6553–6573;6548–65786506–65146612-6620He iλ40264020–40314012–40204158–4169He iλ44714464–44784665–46754464–4478He iλ58765871–58805835–58455904–5912Evolutionary Stellar Population Synthesis at High Spectral Resolution:Optical wavelengths7 Figure3.Upper panel:Comparison of the isochrones obtained with the Padova(black line)and Geneva(red dotted line)tracks for solar metallicity and ages of50Myr,200Myr and2Gyr.Lower panel:Comparison of the Geneva(left)and Padova(right)isochrones at10Myr weighted by the number of stars in each luminosity bin.Note that the relative contribution to the total luminosity of stars with T ef f=4000K is significantly larger in the Geneva than in the Padovamodels.Figure4.Spectra predicted for a single stellar population at different ages for different metallicities(as labeled),obtained with the Geneva(left)and Padova(right)isochrones.million years,the EW is almost constant at∼3˚A.Then,theequivalent width increases with time until400Myr,whenstars of10000–9000K dominate the optical continuum.Thetime evolution of Hαis smoother,changing from3to6˚A.Note that the evolution of the strength of these lines is verysimilar in the Geneva and Padova spectra if the stellar pop-ulation is younger than1Gyr.However,Padova models willpredict younger ages than the Geneva models in old stellarpopulations.We have not plotted the equivalent widths of the high-order Balmer series.They have a similar behavior as HβandHγ,with values that range from2-3to10˚A(GLH99).Theselines are very useful for constraining the stellar ages in thenuclei of galaxies with an important contribution from nebu-lar emission(e.g.Gonz´a lez Delgado,Heckman,&Leitherer。

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