Evolution Before Darwin: the Musings of Constantine Rafinesque
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"National List of Vascular Plant Species That Occur in Wetlands: 1996 National Summary."
Intro 1996 National List of Vascular Plant Species That Occur in Wetlands The Fish and Wildlife Service has prepared a National List of Vascular Plant Species That Occur in Wetlands: 1996 National Summary (1996 National List). The 1996 National List is a draft revision of the National List of Plant Species That Occur in Wetlands: 1988 National Summary (Reed 1988) (1988 National List). The 1996 National List is provided to encourage additional public review and comments on the draft regional wetland indicator assignments. The 1996 National List reflects a significant amount of new information that has become available since 1988 on the wetland affinity of vascular plants. This new information has resulted from the extensive use of the 1988 National List in the field by individuals involved in wetland and other resource inventories, wetland identification and delineation, and wetland research. Interim Regional Interagency Review Panel (Regional Panel) changes in indicator status as well as additions and deletions to the 1988 National List were documented in Regional supplements. The National List was originally developed as an appendix to the Classification of Wetlands and Deepwater Habitats of the United States (Cowardin et al.1979) to aid in the consistent application of this classification system for wetlands in the field.. The 1996 National List also was developed to aid in determining the presence of hydrophytic vegetation in the Clean Water Act Section 404 wetland regulatory program and in the implementation of the swampbuster provisions of the Food Security Act. While not required by law or regulation, the Fish and Wildlife Service is making the 1996 National List available for review and comment. -
Outline of Angiosperm Phylogeny
Outline of angiosperm phylogeny: orders, families, and representative genera with emphasis on Oregon native plants Priscilla Spears December 2013 The following listing gives an introduction to the phylogenetic classification of the flowering plants that has emerged in recent decades, and which is based on nucleic acid sequences as well as morphological and developmental data. This listing emphasizes temperate families of the Northern Hemisphere and is meant as an overview with examples of Oregon native plants. It includes many exotic genera that are grown in Oregon as ornamentals plus other plants of interest worldwide. The genera that are Oregon natives are printed in a blue font. Genera that are exotics are shown in black, however genera in blue may also contain non-native species. Names separated by a slash are alternatives or else the nomenclature is in flux. When several genera have the same common name, the names are separated by commas. The order of the family names is from the linear listing of families in the APG III report. For further information, see the references on the last page. Basal Angiosperms (ANITA grade) Amborellales Amborellaceae, sole family, the earliest branch of flowering plants, a shrub native to New Caledonia – Amborella Nymphaeales Hydatellaceae – aquatics from Australasia, previously classified as a grass Cabombaceae (water shield – Brasenia, fanwort – Cabomba) Nymphaeaceae (water lilies – Nymphaea; pond lilies – Nuphar) Austrobaileyales Schisandraceae (wild sarsaparilla, star vine – Schisandra; Japanese -
Wildflower Talk
Wildflower Talk These are a series of short articles written by Kristen Currin of Humble Roots Native Plant Nursery in Mosier, Oregon, featuring plants from around the Columbia Gorge. Each of these articles appeared in an issue of the Wasco County Soil and Water Conservation District’s newsletter, GROUNDWORK. I hope you enjoy them. All photos are courtesy of Kristen Currin. Please ask permission before using. www.humblerootsnursery.com Nothing in this document is to be construed as medical advice. A licensed herbalist should be consulted for proper identification and preparation before eating those plants designated as edible. Humble Roots Nursery nor the Conservation District are liable for improper consumption of plants listed in this document. INDEX Arnica, Heart-Leaf Glacier Lily Phlox, Cushion Bachelor Buttons Goldenrod Pineapple Weed Balsamroot Grass Widow Prairie Stars Bitterroot Indian Hemp Rabbitbrush (sp) Buckwheat, Arrowleaf Juniper Rabbitbrush, Gray Buckwheat, Snow Larkspur, Upland Rose, Wild California Poppy Kinnickinick Saxifrage Cattail Mariposa Lily Serviceberry Ceanothus Milkweed, Showy Shooting Star, Poet’s Chocolate Lily Miner’s Lettuce Sumac, Smooth Columbia Coreopsis Mugwort, Western Wapato Currant, Golden Native Shrubs Washington Lily Dutchman’s Breeches Nettle, Stinging Western Bunchberry Desert Parsley, Columbia Oceanspray Yellow Bee Plant Desert Parsley, Gray’s Oregon Grape Yellow Bells Elderberry, Blue Pearly Everlasting Yellow Star Thistle Gairdners Yampah Phantom Orchid 1 TOP Page Heart-leaf Arnica Arnica cordifolia Look for arnica's yellow flowers in spring. Arnica is an important native medicinal plant used topically to soothe sore muscles and sprains. A woodland plant and a good choice for the shady xeric garden. Bachelor Buttons, Cornflower Centaurea cyanus Many may think this beautiful blue flower is a native plant due to the fact that it dominates many of our meadows and is commonly sold in wildflower seed mixes. -
Introduction to Macroevolution
Spring, 2012 Phylogenetics 200A Modes of Macroevolution Macroevolution is used to refer to any evolutionary change at or above the level of species. Darwin illustrated the combined action of descent with modification, the principle of divergence, and extinction in the only figure in On the Origin of Species (Fig. 1), showing the link between microevolution and macroevolution. The New Synthesis sought to distance itself from the ‘origin of species’ (= macroevolution) and concentrated instead on microevolution - variation within populations and reproductive isolation. “Darwin’s principle of divergence derives from what he thought to be one of the most potent components of the struggle for existence. He argued that the strongest interactions would be among individuals within a population or among closely related populations or species, because these organisms have the most similar requirements. Darwin’s principle of divergence predicts that the individuals, populations or species most likely to succeed in the struggle are those that differ most from their close relatives in the way they achieve their needs for survival and reproduction.” (Reznick & Ricklefs 2009. Nature 457) Macroevolution also fell into disfavor with its invocation for hopeful monsters in development as well as its implication in some Neo-Lamarckian theories. Interest in macroevolution revived by several paleontologists including Steven Stanley, Stephen Jay Gould and Niles Eldredge, the latter two in the context of punctuated equilibrium. They proposed that what happens in evolution beyond the species level is due to processes that operate beyond the level of populations – including species selection. Niles Eldredge, in particular, has written extensively on the macroevolutionary hierarchy. -
Microevolution and the Genetics of Populations Microevolution Refers to Varieties Within a Given Type
Chapter 8: Evolution Lesson 8.3: Microevolution and the Genetics of Populations Microevolution refers to varieties within a given type. Change happens within a group, but the descendant is clearly of the same type as the ancestor. This might better be called variation, or adaptation, but the changes are "horizontal" in effect, not "vertical." Such changes might be accomplished by "natural selection," in which a trait within the present variety is selected as the best for a given set of conditions, or accomplished by "artificial selection," such as when dog breeders produce a new breed of dog. Lesson Objectives ● Distinguish what is microevolution and how it affects changes in populations. ● Define gene pool, and explain how to calculate allele frequencies. ● State the Hardy-Weinberg theorem ● Identify the five forces of evolution. Vocabulary ● adaptive radiation ● gene pool ● migration ● allele frequency ● genetic drift ● mutation ● artificial selection ● Hardy-Weinberg theorem ● natural selection ● directional selection ● macroevolution ● population genetics ● disruptive selection ● microevolution ● stabilizing selection ● gene flow Introduction Darwin knew that heritable variations are needed for evolution to occur. However, he knew nothing about Mendel’s laws of genetics. Mendel’s laws were rediscovered in the early 1900s. Only then could scientists fully understand the process of evolution. Microevolution is how individual traits within a population change over time. In order for a population to change, some things must be assumed to be true. In other words, there must be some sort of process happening that causes microevolution. The five ways alleles within a population change over time are natural selection, migration (gene flow), mating, mutations, or genetic drift. -
Selected Wildflowers of the Modoc National Forest Selected Wildflowers of the Modoc National Forest
United States Department of Agriculture Selected Wildflowers Forest Service of the Modoc National Forest An introduction to the flora of the Modoc Plateau U.S. Forest Service, Pacific Southwest Region i Cover image: Spotted Mission-Bells (Fritillaria atropurpurea) ii Selected Wildflowers of the Modoc National Forest Selected Wildflowers of the Modoc National Forest Modoc National Forest, Pacific Southwest Region U.S. Forest Service, Pacific Southwest Region iii Introduction Dear Visitor, e in the Modoc National Forest Botany program thank you for your interest in Wour local flora. This booklet was prepared with funds from the Forest Service Celebrating Wildflowers program, whose goals are to serve our nation by introducing the American public to the aesthetic, recreational, biological, ecological, medicinal, and economic values of our native botanical resources. By becoming more thoroughly acquainted with local plants and their multiple values, we hope to consequently in- crease awareness and understanding of the Forest Service’s management undertakings regarding plants, including our rare plant conservation programs, invasive plant man- agement programs, native plant materials programs, and botanical research initiatives. This booklet is a trial booklet whose purpose, as part of the Celebrating Wildflowers program (as above explained), is to increase awareness of local plants. The Modoc NF Botany program earnestly welcomes your feedback; whether you found the book help- ful or not, if there were too many plants represented or too few, if the information was useful to you or if there is more useful information that could be added, or any other comments or concerns. Thank you. Forest J. R. Gauna Asst. -
Patterns and Power of Phenotypic Selection in Nature
Articles Patterns and Power of Phenotypic Selection in Nature JOEL G. KINGSOLVER AND DAVID W. PFENNIG Phenotypic selection occurs when individuals with certain characteristics produce more surviving offspring than individuals with other characteristics. Although selection is regarded as the chief engine of evolutionary change, scientists have only recently begun to measure its action in the wild. These studies raise numerous questions: How strong is selection, and do different types of traits experience different patterns of selection? Is selection on traits that affect mating success as strong as selection on traits that affect survival? Does selection tend to favor larger body size, and, if so, what are its consequences? We explore these questions and discuss the pitfalls and future prospects of measuring selection in natural populations. Keywords: adaptive landscape, Cope’s rule, natural selection, rapid evolution, sexual selection henotypic selection occurs when individuals with selection on traits that affect survival stronger than on those Pdifferent characteristics (i.e., different phenotypes) that affect only mating success? In this article, we explore these differ in their survival, fecundity, or mating success. The idea and other questions about the patterns and power of phe- of phenotypic selection traces back to Darwin and Wallace notypic selection in nature. (1858), and selection is widely accepted as the primary cause of adaptive evolution within natural populations.Yet Darwin What is selection, and how does it work? never attempted to measure selection in nature, and in the Selection is the nonrandom differential survival or repro- century following the publication of On the Origin of Species duction of phenotypically different individuals. -
Bristlecone Chapter of the California Native Plant Society
Dedicated to the Preservation of California Native Flora The California Native Plant Society Bristlecone Chapter Newsletter Volume 40, No. 3 May–June 2019 President’s Message, May 2019 May General Meeting and Potluck Wednesday, May 22nd, 6:00 p.m. potluck, I went for a walk in the Tungsten Hills today and I 7:00–8:00 p.m. presentations was thinking about how I like to hike. The first time I U.S. Forest Service Supervisor’s Office, hiked this trail, I had to go explore every little side 351 Pacu Lane, Bishop road that branched off the trail I had discovered to every piece of mining artifact that I came across. Now Three recipients of the CNPS Bristlecone Chapter I have hiked this nice little loop a few times and I DeDecker Grants will present the findings of their don’t need to go to every hole in the ground or rusty botanical explorations and research of eastern piece of metal, I am satisfied that I already know California. Please join us for a potluck beginning at where those explorations will lead. The joy of this 6pm and presentations at 7pm with desserts. Bring a trail now is seeing how the plants change with the dish to share if you can. seasons. Today, the slopes were predominantly Speakers: yellow with scale bud, desert dandelion, and fiddleneck; the white layia and purple chia accented Sophia Winitsky, the slopes. It was interesting to see that at lower Rancho Santa Ana Botanic Garden elevations the dandelions were the dominate flower, A Flora of Adobe Valley, Mono County but as I moved up the slope, they were replaced by Trevor Carter, UN Reno scale bud. -
Riverside State Park
Provisonal Report Rare Plant and Vegetation Survey of Riverside State Park Pacific Biodiversity Institute 2 Provisonal Report Rare Plant and Vegetation Survey of Riverside State Park Peter H. Morrison [email protected] George Wooten [email protected] Juliet Rhodes [email protected] Robin O’Quinn, Ph.D. [email protected] Hans M. Smith IV [email protected] January 2009 Pacific Biodiversity Institute P.O. Box 298 Winthrop, Washington 98862 509-996-2490 Recommended Citation Morrison, P.H., G. Wooten, J. Rhodes, R. O’Quinn and H.M. Smith IV, 2008. Provisional Report: Rare Plant and Vegetation Survey of Riverside State Park. Pacific Biodiversity Institute, Winthrop, Washington. 433 p. Acknowledgements Diana Hackenburg and Alexis Monetta assisted with entering and checking the data we collected into databases. The photographs in this report were taken by Peter Morrison, Robin O’Quinn, Geroge Wooten, and Diana Hackenburg. Project Funding This project was funded by the Washington State Parks and Recreation Commission. 3 Executive Summary Pacific Biodiversity Institute (PBI) conducted a rare plant and vegetation survey of Riverside State Park (RSP) for the Washington State Parks and Recreation Commission (WSPRC). RSP is located in Spokane County, Washington. A large portion of the park is located within the City of Spokane. RSP extends along both sides of the Spokane River and includes upland areas on the basalt plateau above the river terraces. The park also includes the lower portion of the Little Spokane River and adjacent uplands. The park contains numerous trails, campgrounds and other recreational facilities. The park receives a tremendous amount of recreational use from the nearby population. -
Tempo and Mode in the Macroevolutionary Reconstruction of Darwinism STEPHEN JAY GOULD Museum of Comparative Zoology, Harvard University, Cambridge, MA 02138
Proc. Nadl. Acad. Sci. USA Vol. 91, pp. 6764-6771, July 1994 Colloquium Paper This paper was presented at a coloquium ented "Tempo and Mode in Evolution" organized by Walter M. Fitch and Francisco J. Ayala, held January 27-29, 1994, by the National Academy of Sciences, in Irvine, CA. Tempo and mode in the macroevolutionary reconstruction of Darwinism STEPHEN JAY GOULD Museum of Comparative Zoology, Harvard University, Cambridge, MA 02138 ABSTRACT Among the several central nings of Dar- But conceptual complexity is not reducible to a formula or winism, his version ofLyellian uniformitranism-the extrap- epigram (as we taxonomists of life's diversity should know olationist commitment to viewing causes ofsmall-scale, observ- better than most). Too much ink has been wasted in vain able change in modern populations as the complete source, by attempts to define the essence ofDarwin's ideas, or Darwin- smooth extension through geological time, of all magnitudes ism itself. Mayr (1) has correctly emphasized that many and sequences in evolution-has most contributed to the causal different, if related, Darwinisms exist, both in the thought of hegemony of microevolutlon and the assumption that paleon- the eponym himself, and in the subsequent history of evo- tology can document the contingent history of life but cannot lutionary biology-ranging from natural selection, to genea- act as a domain of novel evolutionary theory. G. G. Simpson logical connection of all living beings, to gradualism of tried to combat this view of paleontology as theoretically inert change. in his classic work, Tempo and Mode in Evolution (1944), with It would therefore be fatuous to claim that any one legit- a brilliant argument that the two subjects of his tide fall into a imate "essence" can be more basic or important than an- unue paleontological domain and that modes (processes and other. -
Garden of the Month APRIL the NATIVE PLANT GARDEN Spring Comes Early to the Native Plant Garden
Garden of the Month APRIL THE NATIVE PLANT GARDEN Spring comes early to the Native Plant garden. With our Mediterranean climate of wet winters and dry summers, most of our native flowers bloom in spring and are dormant by July. The blossoms of June plum (Oemleria cerasiformis) (1), gummy gooseberry (Ribes lobbii)(2) and satin flower (Olsynium douglasii)(3) have been and gone. Now the second wave of bloom is underway, with fawn lilies (Erythronium oregonum, E. revolutum)(4), camas (Camassia quamash, C. leichtlinii)(5), chocolate lilies (Fritillaria affinis)(6), sea blush (Plectritis congesta)(7),, shooting star (Dodecatheon hendersonii)(8), skunk cabbage (Lysichiton americanum)(9) and red-flowering currant (Ribes sanguinium) (10) in flower. Trillium (Trillium ovatum)(11) and coast penstemon (Penstemon serrulatus)(12) will soon emerge. 1 2 3 4 5 6 7 8 9 10 11 12 THE GARRY OAK MEADOW FLOWER GARDEN You are welcome to visit the Garry Oak Meadow Flower Garden, located down the hill above the lake, framed by the large Douglas Fir trees and the great lawn. This ethnobotanical garden is a loop of the larger W̱ SÁNEĆ Ethnobotanical Trail, you could follow the trail signs or just wander past the round Gathering Place to find it. All the plants species in this garden are native to this area and represent the Garry oak ecosystem. Most of them have medicinal, food or technological values. CONTINUED OVERLEAF The Gardens at HCP, 505 Quayle Road, Saanich, V9E 2 J7 | Tel: 250 479 6162 | www.hcp.ca Garden of the Month THE GARRY OAK MEADOW FLOWER GARDEN (CONTINUED) Just as we pass the Spring Equinox and the Spring season begins, the Garry oak Meadow Flower Garden wakes up. -
Population Genetics of the Narrow Endemic Hladnikia Pastinacifolia Rchb
ACTA BIOLOGICA CRACOVIENSIA Series Botanica 54/1: 84–96, 2012 DOI: 10.2478/v10182-012-0009-8 POPULATION GENETICS OF THE NARROW ENDEMIC HLADNIKIA PASTINACIFOLIA RCHB. (APIACEAE) INDICATES SURVIVAL IN SITU DURING THE PLEISTOCENE NINA ŠAJNA1*, TATJANA KAVAR2, JELKA ŠUŠTAR-VOZLIÈ2, and MITJA KALIGARIÈ1 1University of Maribor, Biology Department, Faculty of Natural Sciences and Mathematics, Koroška c. 160, SI – 2000 Maribor, Slovenia 2Agricultural Institute of Slovenia, Field Crop and Seed Production Department, Hacquetova 17, SI-1000 Ljubljana, Slovenia Received July 15, 2011; revision accepted April 6, 2012 Hladnikia pastinacifolia Rchb., a narrow endemic, has an extremely restricted distribution in Trnovski gozd (Slovenia), despite the presence of many sites with suitable habitats. We compared the morphological traits of plants from different populations and habitats. The overall pattern showed that the smallest plants, with low fruit number, are found on Èaven (locus classicus or type locality); the largest individuals, with high fruit number, grow in the Golobnica gorge. As judged by plant size and seed set, the optimal habitats are screes. We used RAPD mark- ers to estimate genetic variation between and within populations, as well as between and within the northern and the southern parts of the distribution area. Hladnikia showed only a low level of RAPD variability. AMOVA parti- tioned the majority of genetic diversity within selected populations. The low genetic differentiation between popu- lations and their genetic depauperation indicates survival in situ, since the Trnovski gozd plateau most likely was a nunatak region in the southern Prealps during Pleistocene glaciations. Later range expansion of extant popula- tions was limited by poor seed dispersal.