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Biostratigraphy and Paleoecology of Continental Tertiary Vertebrate Faunas in the Lower Rhine Embayment (NW-Germany)
Netherlands Journal of Geosciences / Geologie en Mijnbouw 81 (2): 177-183 (2002) Biostratigraphy and paleoecology of continental Tertiary vertebrate faunas in the Lower Rhine Embayment (NW-Germany) Th. Mors Naturhistoriska Riksmuseet/Swedish Museum of Natural History, Department of Palaeozoology, P.O. Box 50007, SE-104 05 Stockholm, Sweden; e-mail: [email protected] Manuscript received: October 2000; accepted: January 2002 ^ Abstract This paper discusses the faunal content, the mammal biostratigraphy, and the environmental ecology of three important con tinental Tertiary vertebrate faunas from the Lower Rhine Embayment. The sites investigated are Rott (MP 30, Late Oligocene), Hambach 6C (MN 5, Middle Miocene), Frechen and Hambach 11 (both MN 16, Late Pliocene). Comparative analysis of the entire faunas shows the assemblages to exhibit many conformities in their general composition, presumably re sulting from their preference for wet lowlands. It appears that very similar environmental conditions for vertebrates reoc- curred during at least 20 Ma although the sites are located in a tectonically active region with high subsidence rates. Differ ences in the faunal composition are partly due to local differences in the depositional environment of the sites: lake deposits at the margin of the embayment (Rott), coal swamp and estuarine conditions in the centre of the embayment (Hambach 6C), and flood plain environments with small rivulets (Frechen and Hambach 1 l).The composition of the faunal assemblages (di versity and taxonomy) also documents faunal turnovers with extinctions and immigrations (Oligocene/Miocene and post- Middle Miocene), as a result of changing climate conditions. Additional vertebrate faunal data were retrieved from two new assemblages collected from younger strata at the Hambach mine (Hambach 11C and 14). -
Evidence of Hidden Diversity and Taxonomic Conflicts in Five Stream Fishes from the Eastern Zimbabwe Highlands Freshwater Ecoregion
A peer-reviewed open-access journal ZooKeys 768: 69–95Evidence (2018) of hidden diversity and taxonomic conflicts in five stream fishes... 69 doi: 10.3897/zookeys.768.21944 RESEARCH ARTICLE http://zookeys.pensoft.net Launched to accelerate biodiversity research Evidence of hidden diversity and taxonomic conflicts in five stream fishes from the Eastern Zimbabwe Highlands freshwater ecoregion Albert Chakona1,2, Wilbert T. Kadye2, Taurai Bere3, Daniel N. Mazungula1,2, Emmanuel Vreven4,5 1 South African Institute for Aquatic Biodiversity, Private Bag 1015, Grahamstown, South Africa, 6140 2 Department of Ichthyology and Fisheries Science, Rhodes University, P.O. Box 94, Grahamstown, South Africa, 6140 3 School of Wildlife, Ecology and Conservation, Chinhoyi University of Technology, P. Bag 7724, Chinhoyi, Zimbabwe 4 Royal Museum for Central Africa, Section of Vertebrates, Ichthyology, Leuvensesteenweg 13, 3080, Tervuren, Belgium 5 KU Leuven, Department of Biology, Laboratory of Biodiversity and Evolutio- nary Genomics, Deberiotstraat 32, 3000 Leuven, Belgium Corresponding author: Albert Chakona ([email protected]) Academic editor: N. Bogutskaya | Received 30 October 2018 | Accepted 25 April 2018 | Published 19 June 2018 http://zoobank.org/9621930C-8C43-40D0-8554-684035E99FAA Citation: Chakona A, Kadye WT, Bere T, Mazungula DN, Vreven E (2018) Evidence of hidden diversity and taxonomic conflicts in five stream fishes from the Eastern Zimbabwe Highlands freshwater ecoregion. ZooKeys 768: 69–95. https://doi.org/10.3897/zookeys.768.21944 Abstract -
Fish, Various Invertebrates
Zambezi Basin Wetlands Volume II : Chapters 7 - 11 - Contents i Back to links page CONTENTS VOLUME II Technical Reviews Page CHAPTER 7 : FRESHWATER FISHES .............................. 393 7.1 Introduction .................................................................... 393 7.2 The origin and zoogeography of Zambezian fishes ....... 393 7.3 Ichthyological regions of the Zambezi .......................... 404 7.4 Threats to biodiversity ................................................... 416 7.5 Wetlands of special interest .......................................... 432 7.6 Conservation and future directions ............................... 440 7.7 References ..................................................................... 443 TABLE 7.2: The fishes of the Zambezi River system .............. 449 APPENDIX 7.1 : Zambezi Delta Survey .................................. 461 CHAPTER 8 : FRESHWATER MOLLUSCS ................... 487 8.1 Introduction ................................................................. 487 8.2 Literature review ......................................................... 488 8.3 The Zambezi River basin ............................................ 489 8.4 The Molluscan fauna .................................................. 491 8.5 Biogeography ............................................................... 508 8.6 Biomphalaria, Bulinis and Schistosomiasis ................ 515 8.7 Conservation ................................................................ 516 8.8 Further investigations ................................................. -
Phylogeny and Classification of the Melastomataceae and Memecylaceae
Nord. J. Bot. - Section of tropical taxonomy Phylogeny and classification of the Melastomataceae and Memecy laceae Susanne S. Renner Renner, S. S. 1993. Phylogeny and classification of the Melastomataceae and Memecy- laceae. - Nord. J. Bot. 13: 519-540. Copenhagen. ISSN 0107-055X. A systematic analysis of the Melastomataceae, a pantropical family of about 4200- 4500 species in c. 166 genera, and their traditional allies, the Memecylaceae, with c. 430 species in six genera, suggests a phylogeny in which there are two major lineages in the Melastomataceae and a clearly distinct Memecylaceae. Melastomataceae have close affinities with Crypteroniaceae and Lythraceae, while Memecylaceae seem closer to Myrtaceae, all of which were considered as possible outgroups, but sister group relationships in this plexus could not be resolved. Based on an analysis of all morph- ological and anatomical characters useful for higher level grouping in the Melastoma- taceae and Memecylaceae a cladistic analysis of the evolutionary relationships of the tribes of the Melastomataceae was performed, employing part of the ingroup as outgroup. Using 7 of the 21 characters scored for all genera, the maximum parsimony program PAUP in an exhaustive search found four 8-step trees with a consistency index of 0.86. Because of the limited number of characters used and the uncertain monophyly of some of the tribes, however, all presented phylogenetic hypotheses are weak. A synapomorphy of the Memecylaceae is the presence of a dorsal terpenoid-producing connective gland, a synapomorphy of the Melastomataceae is the perfectly acrodro- mous leaf venation. Within the Melastomataceae, a basal monophyletic group consists of the Kibessioideae (Prernandra) characterized by fiber tracheids, radially and axially included phloem, and median-parietal placentation (placentas along the mid-veins of the locule walls). -
Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- ERICACEAE
Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- ERICACEAE ERICACEAE (Heath Family) A family of about 107 genera and 3400 species, primarily shrubs, small trees, and subshrubs, nearly cosmopolitan. The Ericaceae is very important in our area, with a great diversity of genera and species, many of them rather narrowly endemic. Our area is one of the north temperate centers of diversity for the Ericaceae. Along with Quercus and Pinus, various members of this family are dominant in much of our landscape. References: Kron et al. (2002); Wood (1961); Judd & Kron (1993); Kron & Chase (1993); Luteyn et al. (1996)=L; Dorr & Barrie (1993); Cullings & Hileman (1997). Main Key, for use with flowering or fruiting material 1 Plant an herb, subshrub, or sprawling shrub, not clonal by underground rhizomes (except Gaultheria procumbens and Epigaea repens), rarely more than 3 dm tall; plants mycotrophic or hemi-mycotrophic (except Epigaea, Gaultheria, and Arctostaphylos). 2 Plants without chlorophyll (fully mycotrophic); stems fleshy; leaves represented by bract-like scales, white or variously colored, but not green; pollen grains single; [subfamily Monotropoideae; section Monotropeae]. 3 Petals united; fruit nodding, a berry; flower and fruit several per stem . Monotropsis 3 Petals separate; fruit erect, a capsule; flower and fruit 1-several per stem. 4 Flowers few to many, racemose; stem pubescent, at least in the inflorescence; plant yellow, orange, or red when fresh, aging or drying dark brown ...............................................Hypopitys 4 Flower solitary; stem glabrous; plant white (rarely pink) when fresh, aging or drying black . Monotropa 2 Plants with chlorophyll (hemi-mycotrophic or autotrophic); stems woody; leaves present and well-developed, green; pollen grains in tetrads (single in Orthilia). -
Appendix 2: Plant Lists
Appendix 2: Plant Lists Master List and Section Lists Mahlon Dickerson Reservation Botanical Survey and Stewardship Assessment Wild Ridge Plants, LLC 2015 2015 MASTER PLANT LIST MAHLON DICKERSON RESERVATION SCIENTIFIC NAME NATIVENESS S-RANK CC PLANT HABIT # OF SECTIONS Acalypha rhomboidea Native 1 Forb 9 Acer palmatum Invasive 0 Tree 1 Acer pensylvanicum Native 7 Tree 2 Acer platanoides Invasive 0 Tree 4 Acer rubrum Native 3 Tree 27 Acer saccharum Native 5 Tree 24 Achillea millefolium Native 0 Forb 18 Acorus calamus Alien 0 Forb 1 Actaea pachypoda Native 5 Forb 10 Adiantum pedatum Native 7 Fern 7 Ageratina altissima v. altissima Native 3 Forb 23 Agrimonia gryposepala Native 4 Forb 4 Agrostis canina Alien 0 Graminoid 2 Agrostis gigantea Alien 0 Graminoid 8 Agrostis hyemalis Native 2 Graminoid 3 Agrostis perennans Native 5 Graminoid 18 Agrostis stolonifera Invasive 0 Graminoid 3 Ailanthus altissima Invasive 0 Tree 8 Ajuga reptans Invasive 0 Forb 3 Alisma subcordatum Native 3 Forb 3 Alliaria petiolata Invasive 0 Forb 17 Allium tricoccum Native 8 Forb 3 Allium vineale Alien 0 Forb 2 Alnus incana ssp rugosa Native 6 Shrub 5 Alnus serrulata Native 4 Shrub 3 Ambrosia artemisiifolia Native 0 Forb 14 Amelanchier arborea Native 7 Tree 26 Amphicarpaea bracteata Native 4 Vine, herbaceous 18 2015 MASTER PLANT LIST MAHLON DICKERSON RESERVATION SCIENTIFIC NAME NATIVENESS S-RANK CC PLANT HABIT # OF SECTIONS Anagallis arvensis Alien 0 Forb 4 Anaphalis margaritacea Native 2 Forb 3 Andropogon gerardii Native 4 Graminoid 1 Andropogon virginicus Native 2 Graminoid 1 Anemone americana Native 9 Forb 6 Anemone quinquefolia Native 7 Forb 13 Anemone virginiana Native 4 Forb 5 Antennaria neglecta Native 2 Forb 2 Antennaria neodioica ssp. -
BREAK-OUT SESSIONS at a GLANCE THURSDAY, 24 JULY, Afternoon Sessions
2008 Joint Meeting (JMIH), Montreal, Canada BREAK-OUT SESSIONS AT A GLANCE THURSDAY, 24 JULY, Afternoon Sessions ROOM Salon Drummond West & Center Salons A&B Salons 6&7 SESSION/ Fish Ecology I Herp Behavior Fish Morphology & Histology I SYMPOSIUM MODERATOR J Knouft M Whiting M Dean 1:30 PM M Whiting M Dean Can She-male Flat Lizards (Platysaurus broadleyi) use Micro-mechanics and material properties of the Multiple Signals to Deceive Male Rivals? tessellated skeleton of cartilaginous fishes 1:45 PM J Webb M Paulissen K Conway - GDM The interopercular-preopercular articulation: a novel Is prey detection mediated by the widened lateral line Variation In Spatial Learning Within And Between Two feature suggesting a close relationship between canal system in the Lake Malawi cichlid, Aulonocara Species Of North American Skinks Psilorhynchus and labeonin cyprinids (Ostariophysi: hansbaenchi? Cypriniformes) 2:00 PM I Dolinsek M Venesky D Adriaens Homing And Straying Following Experimental Effects of Batrachochytrium dendrobatidis infections on Biting for Blood: A Novel Jaw Mechanism in Translocation Of PIT Tagged Fishes larval foraging performance Haematophagous Candirú Catfish (Vandellia sp.) 2:15 PM Z Benzaken K Summers J Bagley - GDM Taxonomy, population genetics, and body shape The tale of the two shoals: How individual experience A Key Ecological Trait Drives the Evolution of Monogamy variation of Alabama spotted bass Micropterus influences shoal behaviour in a Peruvian Poison Frog punctulatus henshalli 2:30 PM M Pyron K Parris L Chapman -
New Species of Congoglanis (Siluriformes: Amphiliidae) from the Southern Congo River Basin
New Species of Congoglanis (Siluriformes: Amphiliidae) from the Southern Congo River Basin Richard P. Vari1, Carl J. Ferraris, Jr.2, and Paul H. Skelton3 Copeia 2012, No. 4, 626–630 New Species of Congoglanis (Siluriformes: Amphiliidae) from the Southern Congo River Basin Richard P. Vari1, Carl J. Ferraris, Jr.2, and Paul H. Skelton3 A new species of catfish of the subfamily Doumeinae, of the African family Amphiliidae, was discovered from the Kasai River system in northeastern Angola and given the name Congoglanis howesi. The new species exhibits a combination of proportional body measurements that readily distinguishes it from all congeners. This brings to four the number of species of Congoglanis, all of which are endemic to the Congo River basin. ECENT analyses of catfishes of the subfamily Congoglanis howesi, new species Doumeinae of the African family Amphiliidae Figures 1, 2; Table 1 R documented that the species-level diversity and Doumea alula, Poll, 1967:265, fig. 126 [in part, samples from morphological variation of some components of the Angola, Luachimo River, Luachimo rapids; habitat infor- subfamily were dramatically higher than previously mation; indigenous names]. suspected (Ferraris et al., 2010, 2011). One noteworthy discovery was that what had been thought to be Doumea Holotype.—MRAC 162332, 81 mm SL, Angola, Lunda Norte, alula not only encompassed three species, but also that Kasai River basin, Luachimo River, Luachimo rapids, 7u219S, they all lacked some characters considered diagnostic of 20u509E, in residual pools downstream of dam, A. de Barros the Doumeinae. Ferraris et al. (2011) assigned those Machado, E. Luna de Carvalho, and local fishers, 10 Congoglanis species to a new genus, , which they hypoth- February 1957. -
MARITIME DECIDUOUS FOREST Concept
MARITIME DECIDUOUS FOREST Concept: Maritime Deciduous Forests are barrier island upland forests dominated or codominated by deciduous hardwood trees, especially Quercus falcata, Fagus grandifolia, and Quercus nigra along with Pinus taeda. This community needs more shelter from salt spray than Maritime Evergreen Forest but has distinctive species combinations not found in mainland forests. Distinguishing Features: Maritime Deciduous Forest is readily distinguished from all other barrier island upland forests by the dominance or codominance of deciduous hardwoods. Maritime Swamp Forest differs its dominance by wetland tree species. In the few cases of forests dominated by species that could belong to either, such as Acer rubrum or Liquidambar styraciflua, the lower strata should distinguish upland and wetland communities. Maritime Deciduous Forests may resemble some Mesic Mixed Hardwood Forest (Coastal Plain Subtype) communities of the mainland, but the former have lower species richness while at the same time, having species suggestive of a greater range of moisture tolerance. In addition, maritime species such as Quercus hemisphaerica and Quercus virginiana are often present in Maritime Deciduous Forest. Synonyms: Quercus falcata - Pinus taeda - (Fagus grandifolia, Quercus nigra) / Persea palustris Maritime Forest (CEGL007540). Ecological Systems: Northern Atlantic Coastal Plain Maritime Forest (CES203.302). Sites: Maritime Deciduous Forests occur only on the more sheltered parts of unusually wide stable barrier islands. They are farther from the ocean and have more shelter from salt spray than even most Maritime Evergreen Forest occurrences. Soils: Most areas are mapped as Fripp (Typic Quartzipsamment). A few parts are mapped as Ousley (Aquic Quartzipsamment) and Duckston (Typic Psammaquent). Hydrology: Hydrology is typical of the theme as a whole, ranging from apparently xeric to mesic. -
18 Special Habitats and Special Adaptations 395
THE DIVERSITY OF FISHES Dedications: To our parents, for their encouragement of our nascent interest in things biological; To our wives – Judy, Sara, Janice, and RuthEllen – for their patience and understanding during the production of this volume; And to students and lovers of fishes for their efforts toward preserving biodiversity for future generations. Front cover photo: A Leafy Sea Dragon, Phycodurus eques, South Australia. Well camouflaged in their natural, heavily vegetated habitat, Leafy Sea Dragons are closely related to seahorses (Gasterosteiformes: Syngnathidae). “Leafies” are protected by Australian and international law because of their limited distribution, rarity, and popularity in the aquarium trade. Legal collection is highly regulated, limited to one “pregnant” male per year. See Chapters 15, 21, and 26. Photo by D. Hall, www.seaphotos.com. Back cover photos (from top to bottom): A school of Blackfin Barracuda, Sphyraena qenie (Perciformes, Sphyraenidae). Most of the 21 species of barracuda occur in schools, highlighting the observation that predatory as well as prey fishes form aggregations (Chapters 19, 20, 22). Blackfins grow to about 1 m length, display the silvery coloration typical of water column dwellers, and are frequently encountered by divers around Indo-Pacific reefs. Barracudas are fast-start predators (Chapter 8), and the pan-tropical Great Barracuda, Sphyraena barracuda, frequently causes ciguatera fish poisoning among humans (Chapter 25). Longhorn Cowfish, Lactoria cornuta (Tetraodontiformes: Ostraciidae), Papua New Guinea. Slow moving and seemingly awkwardly shaped, the pattern of flattened, curved, and angular trunk areas made possible by the rigid dermal covering provides remarkable lift and stability (Chapter 8). A Silvertip Shark, Carcharhinus albimarginatus (Carcharhiniformes: Carcharhinidae), with a Sharksucker (Echeneis naucrates, Perciformes: Echeneidae) attached. -
Addendum to the Guide to the Natural Communities of the Delaware Estuary
ADDENDUM TO THE UIDE TO THE ATURAL OMMUNITIES G N C OF THE DELAWARE ESTUARY SEPTEMBER0 2009 Citation: Largay, E. and L. Sneddon. 2009. Addendum to the Guide to the Ecological Systems and Vegetation Communities of the Delaware Estuary. NatureServe. Arlington, Virginia. Partnership for the Delaware Estuary, Report #09-XX. 112 pp. PDE Report No. 09-XX Copyright © 2009 NatureServe COVER PHOTOS Top L: Overwash Dunes, photo from Delaware Natural Heritage Program Top R: Coastal Plain Muck Pondshore, photo by Kathleen Strakosch Walz, New Jersey Natural Heritage Program Bottom L: Dry Oak Hickory Forest, photo by Tony Davis, Pennsylvania Natural Heritage Program Bottom R: Inland Dune and Ridge Forest/Woodland, Kathleen Strakosch Walz, New Jersey Natural Heritage Program ADDENDUM TO THE GUIDE TO THE NATURAL COMMUNITIES OF THE DELAWARE ESTUARY Ery Largay Lesley Sneddon September 2009 Acknowledgements: This work was made possible through funding from the Delaware Estuary Program (EPA 320 Funding). Kristin Snow and Mary Russo from NatureServe provided essential data management services to develop this report and report format. Robert Coxe and Bill McAvoy from the Delaware Natural Heritage Program, Kathleen Strakosch Walz from the New Jersey Natural Heritage Program, Tony Davis from the Pennsylvania Natural Heritage Program, Linda Kelly and Karl Anderson, independent botanists, provided ecological expertise, energy and insight. Mark Anderson and Charles Ferree from The Nature Conservancy developed ecological systems maps to accompany this work. Danielle Kreeger, Laura Whalen, and Martha-Maxwell Doyle from the Partnership for the Delaware Estuary provided support and guidance throughout this project. We thank everyone who helped us with this effort. -
Aplodontid, Sciurid, Castorid, Zapodid and Geomyoid Rodents of the Rodent Hill Locality, Cypress Hills Formation, Southwest Saskatchewan
APLODONTID, SCIURID, CASTORID, ZAPODID AND GEOMYOID RODENTS OF THE RODENT HILL LOCALITY, CYPRESS HILLS FORMATION, SOUTHWEST SASKATCHEWAN A Thesis Submitted to the College of Graduate Studies and Research in Partial Fulfillment of the Requirements for the Degree of Master of Science in the Department of Geological Sciences University of Saskatchewan Saskatoon By Sean D. Bell © Copyright Sean D. Bell, December 2004. All rights reserved. PERMISSION TO USE In presenting this thesis in partial fulfilment of the requirements for a Master’s degree from the University of Saskatchewan, I agree that the libraries of the University of Saskatchewan may make it freely available for inspection. I further agree that permission for copying of this thesis in any manner, in whole or in part, for scholarly purposes may be granted by the professors who supervised my thesis work or, in their absence, by the Head of the Department of Geological Sciences or the Dean of the College of Graduate Studies and Research. It is understood that any copying or publication or use of this thesis or parts thereof for financial gain shall not be allowed without my written permission. It is also understood that due recognition shall be given to me and to the University of Saskatchewan in any scholarly use which may be made of any material in my thesis. Requests for permission to copy or to make other use of material in this thesis in whole or part should be addressed to: Head of the Department of Geological Sciences 114 Science Place University of Saskatchewan Saskatoon, Saskatchewan S7N 5E2 i ABSTRACT The Rodent Hill Locality is a fossil-bearing site that is part of the Cypress Hills Formation, and is located roughly 15 km northwest of the town of Eastend, Saskatchewan.