A Framework for Community and Ecosystem Genetics: from Genes to Ecosystems
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Energy Economics in Ecosystems By: J
Energy Economics in Ecosystems By: J. Michael Beman (School of Natural Sciences, University of California at Merced) © 2010 Nature Education Citation: Beman, J. (2010) Energy Economics in Ecosystems. Nature Education Knowledge 3(10):13 What powers life? In most ecosystems, sunlight is absorbed and converted into usable forms of energy via photosynthesis. These usable forms of energy are carbonbased. The laws of physics describe the interactions between energy and mass: the energy in a closed system is conserved, and matter can neither be created nor destroyed. Modern physics has shown that reality is more 2 complex at very large and very small scales (e.g., Einstein’s famous equation, E = mc demonstrated that mass can be converted to energy in the sun or nuclear reactors), but in the context of Earth’s ecosystems, energy is conserved and matter can neither be created nor destroyed. This seemingly simplistic statement has profound consequences when we study how ecosystems function. In particular, the energy present within an ecosystem is collected and shared by organisms in many different ways; this "sharing" takes place through ecological interactions, such as predatorprey dynamics and symbioses. When we move to the ecosystem level, however, we consider interactions among organisms, populations, communities, and their physical and chemical environment. These interactions have an important bearing on the structure of organisms, ecosystems, and, over geologic time, the planet itself. A primary example of this involves the energy currency in ecosystems, which is carbon. The amount and form of carbon present in different ecosystem pools — such as plants, animals, air, soil, and water — is controlled by organisms, and ultimately affects their ecological success. -
Meta-Ecosystems: a Theoretical Framework for a Spatial Ecosystem Ecology
Ecology Letters, (2003) 6: 673–679 doi: 10.1046/j.1461-0248.2003.00483.x IDEAS AND PERSPECTIVES Meta-ecosystems: a theoretical framework for a spatial ecosystem ecology Abstract Michel Loreau1*, Nicolas This contribution proposes the meta-ecosystem concept as a natural extension of the Mouquet2,4 and Robert D. Holt3 metapopulation and metacommunity concepts. A meta-ecosystem is defined as a set of 1Laboratoire d’Ecologie, UMR ecosystems connected by spatial flows of energy, materials and organisms across 7625, Ecole Normale Supe´rieure, ecosystem boundaries. This concept provides a powerful theoretical tool to understand 46 rue d’Ulm, F–75230 Paris the emergent properties that arise from spatial coupling of local ecosystems, such as Cedex 05, France global source–sink constraints, diversity–productivity patterns, stabilization of ecosystem 2Department of Biological processes and indirect interactions at landscape or regional scales. The meta-ecosystem Science and School of perspective thereby has the potential to integrate the perspectives of community and Computational Science and Information Technology, Florida landscape ecology, to provide novel fundamental insights into the dynamics and State University, Tallahassee, FL functioning of ecosystems from local to global scales, and to increase our ability to 32306-1100, USA predict the consequences of land-use changes on biodiversity and the provision of 3Department of Zoology, ecosystem services to human societies. University of Florida, 111 Bartram Hall, Gainesville, FL Keywords 32611-8525, -
Insects That Feed on Trees and Shrubs
INSECTS THAT FEED ON COLORADO TREES AND SHRUBS1 Whitney Cranshaw David Leatherman Boris Kondratieff Bulletin 506A TABLE OF CONTENTS DEFOLIATORS .................................................... 8 Leaf Feeding Caterpillars .............................................. 8 Cecropia Moth ................................................ 8 Polyphemus Moth ............................................. 9 Nevada Buck Moth ............................................. 9 Pandora Moth ............................................... 10 Io Moth .................................................... 10 Fall Webworm ............................................... 11 Tiger Moth ................................................. 12 American Dagger Moth ......................................... 13 Redhumped Caterpillar ......................................... 13 Achemon Sphinx ............................................. 14 Table 1. Common sphinx moths of Colorado .......................... 14 Douglas-fir Tussock Moth ....................................... 15 1. Whitney Cranshaw, Colorado State University Cooperative Extension etnomologist and associate professor, entomology; David Leatherman, entomologist, Colorado State Forest Service; Boris Kondratieff, associate professor, entomology. 8/93. ©Colorado State University Cooperative Extension. 1994. For more information, contact your county Cooperative Extension office. Issued in furtherance of Cooperative Extension work, Acts of May 8 and June 30, 1914, in cooperation with the U.S. Department of Agriculture, -
Biogeography: an Ecosystems Approach (Geography 338)
WELCOME TO GEOGRAPHY/BOTANY 338: ENVIRONMENTAL BIOGEOGRAPHY Fall 2018 Schedule: Monday & Wednesday 2:30-3:45 pm, Humanities 1641 Credits: 3 Instructor: Professor Ken Keefover-Ring Email: [email protected] Office: Science Hall 115C Office Hours: Tuesday 3:00-4:00 pm & Wednesday 12:00-1:00 pm or by appointment Note: This course fulfills the Biological Science breadth requirement. COURSE DESCRIPTION: This course takes an ecosystems approach to understand how physical -- climate, geologic history, soils -- and biological -- physiology, evolution, extinction, dispersal, competition, predation -- factors interact to affect the past, present and future distribution of terrestrial biomes and all levels of biodiversity: ecosystems, species and genes. A particular focus will be placed on the role of disturbance and to recent human-driven climatic and land-cover changes and biological invasions on differences in historical and current distributions of global biodiversity. COURSE GOALS: • To learn patterns and mechanisms of local to global gene, species, ecosystem and biome distributions • To learn how past, current and future environmental change affect biogeography • To learn how humans affect geographic patterns of biodiversity • To learn how to apply concepts from biogeography to current environmental problems • To learn how to read and interpret the primary literature, that is, scientific articles in peer- reviewed journals. COURSE POLICY: I expect you to attend all lectures and come prepared to participate in discussion. I will take attendance. Please let me know if you need to miss three or more lectures. Please respect your fellow students, professor, and guest speakers and turn off the ringers on your cell phones and refrain from texting during class time. -
Plant Species Traits Are the Predominant Control on Litter Decomposition Rates Within Biomes Worldwide
Ecology Letters, (2008) 11: 1065–1071 doi: 10.1111/j.1461-0248.2008.01219.x LETTER Plant species traits are the predominant control on litter decomposition rates within biomes worldwide Abstract William K. Cornwell,1* Johannes Worldwide decomposition rates depend both on climate and the legacy of plant functional H. C. Cornelissen,1 Kathryn traits as litter quality. To quantify the degree to which functional differentiation among Amatangelo,2 Ellen Dorrepaal,1 species affects their litter decomposition rates, we brought together leaf trait and litter mass 3 4 Valerie T. Eviner, Oscar Godoy, loss data for 818 species from 66 decomposition experiments on six continents. We show Sarah E. Hobbie,5 Bart Hoorens,1 6,7 that: (i) the magnitude of species-driven differences is much larger than previously thought Hiroko Kurokawa, Natalia and greater than climate-driven variation; (ii) the decomposability of a speciesÕ litter is Pe´ rez-Harguindeguy,8 Helen M. consistently correlated with that speciesÕ ecological strategy within different ecosystems Quested,9 Louis S. Santiago,10 David A. Wardle,11,12 Ian J. globally, representing a new connection between whole plant carbon strategy and Wright,13 Rien Aerts,1 Steven D. biogeochemical cycling. This connection between plant strategies and decomposability is Allison,14 Peter van Bodegom,1 crucial for both understanding vegetation–soil feedbacks, and for improving forecasts of Victor Brovkin,15 Alex Chatain,16 the global carbon cycle. Terry V. Callaghan,17,18 Sandra Dı´az,7 Eric Garnier,19 Diego E. Keywords Gurvich,8 Elena Kazakou,19 Julia Carbon cycling, decomposition, leaf economic spectrum, leaf traits, meta-analysis. -
A General Model of Litter Decomposition in the Northern Chihuahuan Desert
Ecological Modelling, 56 (1991) 197-219 197 Elsevier Science Publishers B.V., Amsterdam A general model of litter decomposition in the northern Chihuahuan Desert Daryl L. Moorhead Ecology Program, Department of Biological Sciences, Texas Tech University, Lubbock, TX 79409-3131, USA James F. Reynolds Systems Ecology Research Group, College of Sciences, San Diego State University, San Diego, CA 92182-0401, USA (Accepted 13 November 1990) ABSTRACT Moorhead, D.L. and Reynolds, J.F., 1991. A general model of litter decomposition in the northern Chihuahuan Desert. Ecol. Modelling, 56: 197-219. Numerous empirical studies have described the pathways of mass, C and N flows during decomposition, but there remains a paucity of data on underlying mechanisms in arid ecosystems. In the northern Chihuahuan Desert, termites remove large quantities of litter and act as carbon and nitrogen sinks, contributing to low soil fertility. In their absence, decomposition at the soil surface is primarily driven by abiotic weathering, but studies suggest buried litter decay occurs through microbiological activities. We develop a general, synthetic model to examine the interactions between buried litter, decomposer microorgan- isms, and C and N pools in this ecosystem. Our goal is to explore the mechanisms underlying observed patterns of decomposition in arid systems using a modeling approach that balances simplicity with enough detail to suggest the reasons for system behavior. To this end, we utilize elements of existing models, interfacing microbial physiology and population dynamics with empirical observations of C and N pool dynamics, litter mass loss and changing C:N ratios. Good agreement was achieved between simulated and observed patterns of mass loss and nitrogen concentrations once a time lag describing the microbial colonization of litter was included. -
19 | Population and Community Ecology 515
CHAPTER 19 | POPULATION AND COMMUNITY ECOLOGY 515 19 | POPULATION AND COMMUNITY ECOLOGY Figure 19.1 Asian carp jump out of the water in response to electrofishing. The Asian carp in the inset photograph were harvested from the Little Calumet River in Illinois in May, 2010, using rotenone, a toxin often used as an insecticide, in an effort to learn more about the population of the species. (credit main image: modification of work by USGS; credit inset: modification of work by Lt. David French, USCG) Chapter Outline 19.1: Population Demographics and Dynamics 19.2: Population Growth and Regulation 19.3: The Human Population 19.4: Community Ecology Introduction Imagine sailing down a river in a small motorboat on a weekend afternoon; the water is smooth, and you are enjoying the sunshine and cool breeze when suddenly you are hit in the head by a 20-pound silver carp. This is a risk now on many rivers and canal systems in Illinois and Missouri because of the presence of Asian carp. This fish—actually a group of species including the silver, black, grass, and big head carp—has been farmed and eaten in China for over 1,000 years. It is one of the most important aquaculture food resources worldwide. In the United States, however, Asian carp is considered a dangerous invasive species that disrupts ecological community structure to the point of threatening native species. The effects of invasive species (such as the Asian carp, kudzu vine, predatory snakehead fish, and zebra mussel) are just one aspect of what ecologists study to understand how populations interact within ecological communities, and what impact natural and human-induced disturbances have on the characteristics of communities. -
Distribution, Host Plants and Natural Enemies of Sugar Beet Root Aphid (Pemphigus Fuscicornis) in Slovakia*
Zbornik Matice srpske za prirodne nauke / Proc. Nat. Sci, Matica Srpska Novi Sad, ¥ 110, 221—226, 2006 UDC 633.63:632.752(437.6-14)“2003/2004" Peter Tóth, Ján I. Tancik, Monika Tóthová, Vladimír Paåuta Slovak Agricultural University, A. Hlinku 2 949 76 Nitra, Slovak Republic DISTRIBUTION, HOST PLANTS AND NATURAL ENEMIES OF SUGAR BEET ROOT APHID (PEMPHIGUS FUSCICORNIS) IN SLOVAKIA* ABSTRACT: During 2003—2004, field surveys were realized to observe the distribu- tion of sugar beet aphid, Pemphigus fuscicornis (K o c h) (Sternorrhyncha: Pemphigidae)in southwestern Slovakia. The research was carried out at 60 different localities with altitudes 112—220 m a. s. l. Sugar beet root aphid was recorded at 30 localities. The aphid was re- corded in Slovakia for the first time, but its occurrence was predicted and symptoms and harmfulness overlooked by now. The presence of P. fuscicornis was investigated on roots of various plants from Chenopodiaceae. The most important host plants were various speci- es of lambsquarters (above all Chenopodium album). Furthermore sugar beet (Beta vulgaris provar. altissima), red beet (B. vulgaris provar. conditiva) and oraches (Atriplex spp.) act as host plants. Infestation of sugar beet by P. fuscicornis never exceeded 5% at single locality in Slovakia. Dry and warm weather create presumptions for strong harmfulness. In Slo- vakia, Chenopodium album is a very important indicator of sugar beet aphid presence allowing evaluation of control requirements. During the study, the larvae of Thaumatomyia glabra (Diptera: Chloropidae) were detected as important natural enemies of sugar beet ap- hid. The species occurred at each location evaluated. -
Modeling Foundation Species in Food Webs 1,3, 2 1 BENJAMIN BAISER, NATHANIEL WHITAKER, and AARON M
Modeling foundation species in food webs 1,3, 2 1 BENJAMIN BAISER, NATHANIEL WHITAKER, AND AARON M. ELLISON 1Harvard University, Harvard Forest, 324 N. Main Street, Petersham, Massachusetts 01366 USA 2Department of Mathematics and Statistics, University of Massachusetts at Amherst, 1424 Lederle Graduate Research Center, Amherst, Massachusetts 01003-9305 USA Citation: Baiser, B., N. Whitaker, and A. M. Ellison. 2013. Modeling foundation species in food webs. Ecosphere 4(12):146. http://dx.doi.org/10.1890/ES13-00265.1 Abstract. Foundation species are basal species that play an important role in determining community composition by physically structuring ecosystems and modulating ecosystem processes. Foundation species largely operate via non-trophic interactions, presenting a challenge to incorporating them into food web models. Here, we used non-linear, bioenergetic predator-prey models to explore the role of foundation species and their non-trophic effects. We explored four types of models in which the foundation species reduced the metabolic rates of species in a specific trophic position. We examined the outcomes of each of these models for six metabolic rate ‘‘treatments’’ in which the foundation species altered the metabolic rates of associated species by one-tenth to ten times their allometric baseline metabolic rates. For each model simulation, we looked at how foundation species influenced food web structure during community assembly and the subsequent change in food web structure when the foundation species was removed. When a foundation species lowered the metabolic rate of only basal species, the resultant webs were complex, species-rich, and robust to foundation species removals. On the other hand, when a foundation species lowered the metabolic rate of only consumer species, all species, or no species, the resultant webs were species-poor and the subsequent removal of the foundation species resulted in the further loss of species and complexity. -
AP Bio Summer Assignment 2018 Mrs. Oswald Welcome to AP Biology! I Look Forward to a Great Year. Due to the Large Volume Of
AP Bio Summer Assignment 2018 Mrs. Oswald Welcome to AP Biology! I look forward to a great year. Due to the large volume of content we have to cover, your summer assignment will be to read the Ecology Unit--Chapters 52-56 in Campbell Biology, 11th Edition --and complete the following. Support each of the following main ideas in 4-6 sentences . Use many of the provided chapter terms in your answer, but do not feel that you need to use them all. Please highlight the terms that you choose to use in your responses. Your answers should be typed in Google docs using Times New Roman, 12-pt font, double- spaced, and will be Google-checked for original wording upon submission. Please share them with me at [email protected] by the first day of school. You should have approximately 8-10 pages of typed summary by the end of the summer. Please see the example and video references at the end of this document. We will start the school year with a short ecology review followed by an ecology assessment before beginning a new unit. Chapter 52: An Introduction to Ecology and the Biosphere ● Main Ideas ○ Earth’s climate varies by latitude and season and is changing rapidly. ○ The structure and distribution of terrestrial biomes are controlled by climate and disturbance. ○ Aquatic biomes are diverse and dynamic systems that cover most of Earth. ○ Interactions between organisms and the environment limit the distribution of species. ● Chapter Terms o climate, microclimate, macroclimate, tropics, abiotic, biotic, biome, climograph, ecotone, canopy, -
The Biology of Pemphigus Spyrothecae Galls On
THE BIOLOGY OF PEMPHIGUS SPYROTHECAE GALLS ON POPLAR LEAVES KARIN L. ALTON B.Sc. Thesis submitted to the University of Nottingham for the Degree of Doctor of Philosophy Department of Biological Sciences University of Nottingham Nottingham NG7 2RD November 1999 CONTENTS ABSTRACT 1 Chapter 1: INTRODUCTION 1.1 Habitat selection 2 1.2 Models of habitat selection 3 1.3 Applying theory to real situations: galling aphids as a model system 12 1.4 Biology of aphid galls 15 1.5 Biology of Pemphigus spyrothecae Pass. (1860) 19 1.6 Site description 23 1.7 Study objectives 24 Chapter 2: INTER-PLANT VARIATION AND THE EFFECTS ON APHID POPULATION DYNAMICS 2.1 Introduction 31 2.2 Methods 33 2.3 Results 35 2.4 Discussion 38 Chapter 3: WITHIN-PLANT HETEROGENEITY AND THE EFFECTS ON APHID POPULATION DYNAMICS 3. 1 Introduction 55 3.2 Methods 57 3.3 Results 61 3.4 Discussion 63 Chapter4: APHID EMERGENCE AT BUDBURST 4.1 Introduction 95 4.2 Methods 98 4.3 Results 102 4.4 Discussion 108 Chapter 5: THE PHENOLOGICAL BACKGROUND TO APHID NUMBERS IN THE GALL 5.1 Introduction 149 5.2 Methods 151 5.3 Results 153 5.4 Discussion 156 Chapter 6: THE EFFECTS OF MULTIPLY GALLED PETIOLES ON APHID FITNESS 6.1 Introduction 183 6.2 Methods 185 6.3 Results 187 6.4 Discussion 189 Chapter 7: DO PREDATORS AFFECT APHID GALL DISTRIBUTION AND MORTALITY? 7.1 Introduction 213 7.2 Methods 215 7.3 Results 217 7.4 Discussion 219 Chapter 8: DISCUSSION 235 REFERENCES 240 ACKNOWLEDGEMENTS 259 1 ABSTRACT The gall forming aphid Pemphigus spyrothecae is a plant parasite that colonises the leaf petiole of the black poplar Populus nigra and its hybrids and varieties. -
Gall-Inducing Aphids (Hemiptera: Aphidoidea: Eriosomatinae) Associated with Salicaceae and Ulmaceae in Razavi Khorasan Province, with New Records for Fauna of Iran
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Repository of the Academy's Library Acta Phytopathologica et Entomologica Hungarica 54 (1), pp. 113–126 (2019) DOI: 10.1556/038.54.2019.010 Gall-inducing Aphids (Hemiptera: Aphidoidea: Eriosomatinae) Associated with Salicaceae and Ulmaceae in Razavi Khorasan Province, with New Records for Fauna of Iran A. NAJMI1, H. S. NAMAGHI1*, S. BARJADZE2 and L. FEKRAT1 1Department of Plant Protection, Faculty of Agriculture, Ferdowsi University of Mashhad, Mashhad, Iran 2Institute of Zoology, Ilia State University, Tbilisi, Georgia (Received: 11 November 2018; accepted: 16 November 2018) A survey of gall-inducing aphids on elm and poplar trees was carried out during 2017 in Razavi Kho- rasan province, NE Iran. As a result, 15 species of gall-inducing aphids from 5 genera, all belonging to the subfamily Eriosomatinae, were recorded on 6 host plant species. The collected species included the genera Eriosoma, Kaltenbachiella, Pemphigus, Tetraneura and Thecabius. Pemphigus passeki Börner (Hemiptera: Aphididae) and Pemphigus populinigrae (Schrank) (Hemiptera: Aphididae) on Populus nigra var. italica (Sal- icaceae) were new records for the Iranian aphid fauna. Both new recorded species belong to the tribe Pem- phigini, subfamily Eriosomatinae. Among the identified species, 8 aphid species were new records for Razavi Khorasan province. Keywords: Aphid, elm, poplar, fauna, gall-inducing aphid. Many insect groups, around 13,000 species, are known as plant gall makers (Nyman and Julkunen-Tiitto, 2000; Suzuki et al., 2009). Among them, Aphidoidea is a very large superfamily in the hemipteran suborder Sternorrhyncha with about 5000 known species (Blackman and Eastop, 2000; Ge et al., 2016).