A Field Guide to the Animals of Vernal Pools
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Fig. Ap. 2.1. Denton Tending His Fairy Shrimp Collection
Fig. Ap. 2.1. Denton tending his fairy shrimp collection. 176 Appendix 1 Hatching and Rearing Back in the bowels of this book we noted that However, salts may leach from soils to ultimately if one takes dry soil samples from a pool basin, make the water salty, a situation which commonly preferably at its deepest point, one can then "just turns off hatching. Tap water is usually unsatis- add water and stir". In a day or two nauplii ap- factory, either because it has high TDS, or because pear if their cysts are present. O.K., so they won't it contains chlorine or chloramine, disinfectants always appear, but you get the idea. which may inhibit hatching or kill emerging If your desire is to hatch and rear fairy nauplii. shrimps the hi-tech way, you should get some As you have read time and again in Chapter 5, guidance from Brendonck et al. (1990) and temperature is an important environmental cue for Maeda-Martinez et al. (1995c). If you merely coaxing larvae from their dormant state. You can want to see what an anostracan is like, buy some guess what temperatures might need to be ap- Artemia cysts at the local aquarium shop and fol- proximated given the sample's origin. Try incu- low directions on the container. Should you wish bation at about 3-5°C if it came from the moun- to find out what's in your favorite pool, or gather tains or high desert. If from California grass- together sufficient animals for a study of behavior lands, 10° is a good level at which to start. -
Phylogenetic Analysis of Anostracans (Branchiopoda: Anostraca) Inferred from Nuclear 18S Ribosomal DNA (18S Rdna) Sequences
MOLECULAR PHYLOGENETICS AND EVOLUTION Molecular Phylogenetics and Evolution 25 (2002) 535–544 www.academicpress.com Phylogenetic analysis of anostracans (Branchiopoda: Anostraca) inferred from nuclear 18S ribosomal DNA (18S rDNA) sequences Peter H.H. Weekers,a,* Gopal Murugan,a,1 Jacques R. Vanfleteren,a Denton Belk,b and Henri J. Dumonta a Department of Biology, Ghent University, Ledeganckstraat 35, B-9000 Ghent, Belgium b Biology Department, Our Lady of the Lake University of San Antonio, San Antonio, TX 78207, USA Received 20 February 2001; received in revised form 18 June 2002 Abstract The nuclear small subunit ribosomal DNA (18S rDNA) of 27 anostracans (Branchiopoda: Anostraca) belonging to 14 genera and eight out of nine traditionally recognized families has been sequenced and used for phylogenetic analysis. The 18S rDNA phylogeny shows that the anostracans are monophyletic. The taxa under examination form two clades of subordinal level and eight clades of family level. Two families the Polyartemiidae and Linderiellidae are suppressed and merged with the Chirocephalidae, of which together they form a subfamily. In contrast, the Parartemiinae are removed from the Branchipodidae, raised to family level (Parartemiidae) and cluster as a sister group to the Artemiidae in a clade defined here as the Artemiina (new suborder). A number of morphological traits support this new suborder. The Branchipodidae are separated into two families, the Branchipodidae and Ta- nymastigidae (new family). The relationship between Dendrocephalus and Thamnocephalus requires further study and needs the addition of Branchinella sequences to decide whether the Thamnocephalidae are monophyletic. Surprisingly, Polyartemiella hazeni and Polyartemia forcipata (‘‘Family’’ Polyartemiidae), with 17 and 19 thoracic segments and pairs of trunk limb as opposed to all other anostracans with only 11 pairs, do not cluster but are separated by Linderiella santarosae (‘‘Family’’ Linderiellidae), which has 11 pairs of trunk limbs. -
Helminth Communities in the Northern Spring Peeper, Pseudacris C. Crucifer Wied, and the Wood Frog, Rana Sylvatica Le Conte, from Southeastern Wisconsin
J. Helminthol. Soc. Wash. 63(2), 1996, pp. 211-214 Helminth Communities in the Northern Spring Peeper, Pseudacris c. crucifer Wied, and the Wood Frog, Rana sylvatica Le Conte, from Southeastern Wisconsin H. RANDALL YODER AND JAMES R. COGGINS Department of Biological Sciences, University of Wisconsin-Milwaukee, Milwaukee, Wisconsin 53201 ABSTRACT: Fifteen spring peepers and 20 wood frogs were collected in April 1993 from 2 temporary ponds in southeastern Wisconsin. Five species of adult and larval nematodes, 4 species of adult and larval trematodes, and 1 larval cestode infected wood frogs. Spring peepers harbored 1 adult and 1 larval nematode species as well as 1 adult and 5 larval trematode species. Sixteen of 20 (80%) wood frogs were infected with helminths. Mean species richness and mean helminth abundance were 2.15 and 4.90, respectively. Eight of 15 (53%) spring peepers were infected. Only 1 individual was infected by more than 1 helminth species and only 1 parasite species infected more than 1 spring peeper. Low prevalence and intensities of helminths as well as low diversity within infracommunities suggest depauperate, isolationist helminth communities in these 2 populations of anurans. This work represents new records for 5 helminth species in Wisconsin wood frogs and 3 helminth species in Wisconsin spring peepers. KEY WORDS: Rana sylvatica, Pseudacris crucifer, Oswaldocruzia pipiens, Cosmocercoides dukae, Rhabdias ranae, Glypthelmins pennsylvaniensis, Hematoloechus varioplexus, Fibricola texensis, Alaria mustelae, diplo- stomula, mesocercaria, Wisconsin. Rana sylvatica Le Conte is found from New and wet weight (g) were recorded. The external surfaces Brunswick to eastern Manitoba and south to as well as the mouth and eustachian tubes, the internal organs, including the brain, and the musculature of the Georgia and eastern Texas (Vogt, 1981). -
Species Dossier: Hagenella Clathrata
Species dossier: Hagenella clathrata Window winged sedge July 2011 Mating adult pair Hagenella clathata Contact details Ian Wallace, Curator of Conchology & Aquatic Biology World Museum William Brown Street, Liverpool, L3 8EN Tel: 0151 478 4385 Email: [email protected] Species dossier: Hagenella clathrata Contents Introduction ................................................................................... 3 Summary....................................................................................... 3 Ecology ......................................................................................... 3 History in Britain ............................................................................ 6 European distribution .................................................................... 9 Recent Survey Work ..................................................................... 9 Survey methods ............................................................................ 9 Identification.................................................................................. 9 Threats........................................................................................ 10 Action plan for the Window Winged Sedge ( Hagenella clathrata ) 11 List of references......................................................................... 12 Appendix 2 Records of ( Hagenella clathrata ) from the UK ......... 15 Cover image © Matthew Wallace (2009) Hagenella clathrata (Kolenati, 1848) Window winged sedge (Trichoptera: Phryganeidae) Genus -
Blue–Spotted Salamander Ambystoma Laterale Status: Wisconsin – Common Minnesota – Common Iowa – Endangered
Species Descriptions Blue–spotted Salamander Ambystoma laterale Status: Wisconsin – Common Minnesota – Common Iowa – Endangered 1 cm Size at hatching, 8 – 10 mm total length; at metamorphosis, ~ 34 mm snout–vent length The Blue-spotted Salamander is one of four mole salamanders in our region. Other mole salamanders include the Spotted, Small-mouthed, and Tiger Salamanders. As adults, mole salamanders live under cover objects such as rotting logs or in burrows in the forest floor (Parmelee 1993). In early spring (March and April), adults migrate to temporary ponds to breed. Larvae develop during spring and summer and usually metamorphose in the fall. The Blue-spotted Salamander is a woodland species of northern North America. The eggs are laid in small clumps (7–40 eggs) attached to vegetation or debris at the bottom of ponds. The larvae are similar to Spotted Salamanders but are more darkly colored with the fins mottled with black, and dark blotches on the dorsum. Blue-spotted Salamanders metamorphose at about the same size as Spotted Salamanders but are darker, sometimes with flecks of blue. 14 15 Spotted Salamander Ambystoma maculatum Status: Wisconsin – Locally abundant Minnesota – Status to be determined 1 cm Size at hatching, 12 – 17 mm; at metamorphosis, 49 – 60 mm total length The Spotted Salamander is present only in the northeastern part of our range (where it is sympatric with up to two other mole salamanders). Females deposit eggs in a firm oval mass (60–100 mm in diameter) attached to vegetation near the surface of the water. The eggs (1–250 per mass) are black, but the egg mass may be clear or milky, with a greenish hue because of symbiotic algae. -
Spotted Salamander (Ambystoma Maculafum)
Spotted Salamander (Ambystoma maculafum) RANGE: Nova Scotia and the Gaspe Peninsula to s. On- BREEDINGPERIOD: March to mid-April. Mass breeding tario, s. through Wisconsin, s. Illinois excluding prairie migrations occur in this species: individuals enter and regions, toe. Kansas andTexas, and through the Eastern leave breeding ponds using the same track each year, United States, except Florida, the Delmarva Peninsula, and exhibit fidelity to breeding ponds (Shoop 1956, and s. New Jersey. 1974). Individuals may not breed in consecutive years (Husting 1965). Breeding migrations occur during RELATIVE ABUNDANCEIN NEW ENGLAND:Common steady evening rainstorms. though populations declining, probably due to acid pre- cipitation. EGG DEPOSITION:1 to 6 days after first appearance of adults at ponds (Bishop 1941 : 114). HABITAT:Fossorial; found in moist woods, steambanks, beneath stones, logs, boards. Prefers deciduous or NO. EGGS/MASS:100 to 200 eggs, average of 125, laid in mixed woods on rocky hillsides and shallow woodland large masses of jelly, sometimes milky, attached to stems ponds or marshy pools that hold water through the sum- about 15 cm (6 inches) under water. Each female lays 1 to mer for breeding. Usually does not inhabit ponds con- 10 masses (average of 2 to 3) of eggs (Wright and Allen taining fish (Anderson 1967a). Terrestrial hibernator. In 1909).Woodward (1982)reported that females breeding summer often wanders far from water source. Found in in permanent ponds produced smaller, more numerous low oak-hickory forests with creeks and nearby swamps eggs than females using temporary ponds. in Illinois (Cagle 1942, cited in Smith 1961 :30). -
The Natural History, Distribution, and Phenotypic Variation of Cave-Dwelling Spring Salamanders, Gyrinophilus Spp
Marshall University Marshall Digital Scholar Theses, Dissertations and Capstones 2005 The aN tural History, Distribution, and Phenotypic Variation of Cave-dwelling Spring Salamanders, Gyrinophilus spp. Cope (Plethodontidae), in West Virginia Michael Steven Osbourn Follow this and additional works at: http://mds.marshall.edu/etd Part of the Aquaculture and Fisheries Commons, and the Ecology and Evolutionary Biology Commons Recommended Citation Osbourn, Michael Steven, "The aN tural History, Distribution, and Phenotypic Variation of Cave-dwelling Spring Salamanders, Gyrinophilus spp. Cope (Plethodontidae), in West Virginia" (2005). Theses, Dissertations and Capstones. Paper 735. This Thesis is brought to you for free and open access by Marshall Digital Scholar. It has been accepted for inclusion in Theses, Dissertations and Capstones by an authorized administrator of Marshall Digital Scholar. For more information, please contact [email protected]. The Natural History, Distribution, and Phenotypic Variation of Cave-dwelling Spring Salamanders, Gyrinophilus spp. Cope (Plethodontidae), in West Virginia. Thesis submitted to The Graduate College of Marshall University In partial fulfillment of the Requirements for the degree of Master of Science Biological Sciences By Michael Steven Osbourn Thomas K. Pauley, Committee Chairperson Daniel K. Evans, PhD Thomas G. Jones, PhD Marshall University May 2005 Abstract The Natural History, Distribution, and Phenotypic Variation of Cave-dwelling Spring Salamanders, Gyrinophilus spp. Cope (Plethodontidae), in West Virginia. Michael S. Osbourn There are over 4000 documented caves in West Virginia, potentially providing refuge and habitat for a diversity of amphibians and reptiles. Spring Salamanders, Gyrinophilus porphyriticus, are among the most frequently encountered amphibians in caves. Surveys of 25 caves provided expanded distribution records and insight into ecology and diet of G. -
Heterotrophic Carbon Fixation in a Salamander-Alga Symbiosis
bioRxiv preprint doi: https://doi.org/10.1101/2020.02.14.948299; this version posted February 18, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. Heterotrophic Carbon Fixation in a Salamander-Alga Symbiosis. John A. Burns1,2, Ryan Kerney3, Solange Duhamel1,4 1Lamont-Doherty Earth Observatory of Columbia University, Division of Biology and Paleo Environment, Palisades, NY 2Bigelow Laboratory for Ocean Sciences, East Boothbay, ME 3Gettysburg College, Biology, Gettysburg, PA 4University of Arizona, Department of Molecular and Cellular Biology, Tucson, AZ Abstract The unique symbiosis between a vertebrate salamander, Ambystoma maculatum, and unicellular green alga, Oophila amblystomatis, involves multiple modes of interaction. These include an ectosymbiotic interaction where the alga colonizes the egg capsule, and an intracellular interaction where the alga enters tissues and cells of the salamander. One common interaction in mutualist photosymbioses is the transfer of photosynthate from the algal symbiont to the host animal. In the A. maculatum-O. amblystomatis interaction, there is conflicting evidence regarding whether the algae in the egg capsule transfer chemical energy captured during photosynthesis to the developing salamander embryo. In experiments where we took care to separate the carbon fixation contributions of the salamander embryo and algal symbionts, we show that inorganic carbon fixed by A. maculatum embryos reaches 2% of the inorganic carbon fixed by O. amblystomatis algae within an egg capsule after 2 hours in the light. -
Vernal Pool Fairy Shrimp (Branchinecta Lynchi)
Invertebrates Vernal Pool Fairy Shrimp (Branchinecta lynchi) Vernal Pool Fairy Shrimp (Brachinecta lynchi) Status State: Meets the requirements as a “rare, threatened, or endangered species” under CEQA Federal: Threatened Critical Habitat: Designated 2006 (USFWS 2006) Population Trend Global: Declining due to habitat loss and fragmentation (Eriksen and Belk 1999) State: As above Within Inventory Area: Unknown Data Characterization The location database for the vernal pool fairy shrimp (Brachinecta lynchi) within the inventory area includes 6 records from 1993, 1997, and 1999. The majority of locations are vernal pools within non-native grassland. Other natural and artificial habitats have a high probability of being occupied by additional populations of the vernal pool fairy shrimp throughout the grassland habitats within the ECCC HCP/NCCP inventory area. Beyond the original description (Eng et al. 1990), a scanning electron micrograph of the cyst (resting egg) (Hill and Shepard 1997), and some generalized natural history data (Helm 1997), no peer-reviewed technical literature has been published concerning the vernal pool fairy shrimp. Eriksen and Belk (1999) presented a brief discussion of the vernal pool fairy shrimp and provided a distribution map. Range The vernal pool fairy shrimp is found from Jackson County near Medford, Oregon, throughout the Central Valley, and west to the central Coast Ranges. Isolated southern populations occur on the Santa Rosa Plateau and near Rancho California in Riverside County (Eng et al.1990, Eriksen -
Meramec River Watershed Demonstration Project
MERAMEC RIVER WATERSHED DEMONSTRATION PROJECT Funded by: U.S. Environmental Protection Agency prepared by: Todd J. Blanc Fisheries Biologist Missouri Department of Conservation Sullivan, Missouri and Mark Caldwell and Michelle Hawks Fisheries GIS Specialist and GIS Analyst Missouri Department of Conservation Columbia, Missouri November 1998 Contributors include: Andrew Austin, Ronald Burke, George Kromrey, Kevin Meneau, Michael Smith, John Stanovick, Richard Wehnes Reviewers and other contributors include: Sue Bruenderman, Kenda Flores, Marlyn Miller, Robert Pulliam, Lynn Schrader, William Turner, Kevin Richards, Matt Winston For additional information contact East Central Regional Fisheries Staff P.O. Box 248 Sullivan, MO 63080 EXECUTIVE SUMMARY Project Overview The overall purpose of the Meramec River Watershed Demonstration Project is to bring together relevant information about the Meramec River basin and evaluate the status of the stream, watershed, and wetland resource base. The project has three primary objectives, which have been met. The objectives are: 1) Prepare an inventory of the Meramec River basin to provide background information about past and present conditions. 2) Facilitate the reduction of riparian wetland losses through identification of priority areas for protection and management. 3) Identify potential partners and programs to assist citizens in selecting approaches to the management of the Meramec River system. These objectives are dealt with in the following sections titled Inventory, Geographic Information Systems (GIS) Analyses, and Action Plan. Inventory The Meramec River basin is located in east central Missouri in Crawford, Dent, Franklin, Iron, Jefferson, Phelps, Reynolds, St. Louis, Texas, and Washington counties. Found in the northeast corner of the Ozark Highlands, the Meramec River and its tributaries drain 2,149 square miles. -
Publications of Glenn B
Publications: Glenn B. Wiggins, Curator Emeritus, Entomology 2010 Wiggins, G.B. “No small matters. Introducing Biological Notes on an Old Farm: Exploring Common Things in the Kingdoms of Life.” ROM Magazine, 42(2): 29- 31. * 2009 Wiggins, G.B. Biological Notes on an Old Farm: Exploring Common Things in the Kingdoms of Life. Royal Ontario Museum, Toronto. 2008 Wiggins, G.B. and D.C. Currie. “Trichoptera Families.” In An Introduction to the Aquatic Insects of North America, edited by R.W. Merritt, K.W. Cummins, and M.B. Berg. Kendall/Hunt, Dubuque, Iowa (4th edition, revised). 2007 Wiggins, G.B. “Architects under water.” American Entomologist, 53(2): 78-85. 2005b Wiggins, G.B. “Review: Vernal pools, natural history and conservation by Elizabeth A. Colburn.” Journal of the North American Benthological Society, 24(4): 1009-1013. 2005a Vineyard, R.N., G.B. Wiggins, H.E. Frania, and P.W. Schefter. “The caddisfly genus Neophylax (Trichoptera: Uenoidae).” Royal Ontario Museum Contributions in Science, 2: 1-141. * 2004b Wiggins, G.B. Caddisflies: The Underwater Architects. University of Toronto Press. 2004a Wiggins, G.B. “Caddisflies: glimpses into evolutionary history.” Rotunda, 38(2): 32-39. 2002 Wiggins, G.B. “Biogeography of amphipolar caddisflies in the subfamily Dicosmoecinae (Trichoptera, Limnephilidae).” Mitteilungen aus dem Museum für Naturkunde in Berlin, Deutsche Entomologische Zeitschrift, 49(2002) 2: 227- 259. 2001 Wiggins, G.B. “Construction behavior for new pupal cases by case-making caddis larvae: Further comment. (Trichoptera: Integripalpia).” Braueria, 28: 7-9. 1999b Gall, W.K. and G.B. Wiggins. “Evidence bearing on a sister-group relationship between the families Phryganeidae and Plectrotarsidae (Trichoptera).” Proceedings of the Ninth International Symposium on Trichoptera, Chiang Mai, Thailand, 1998, edited by H. -
NOTES on WATER BUGS from SOUTH EAST ASIA and AUSTRALIA (Heteroptera: Nepomorpha & Gerromorpha)
F. M. BUZZETTI, N. NIESER & J. DAMGAARD: Notes on water bugs ... 31 FILIPPO MARIA BUZZETTI, NICO NIESER & JAKOB DAMGAARD NOTES ON WATER BUGS FROM SOUTH EAST ASIA AND AUSTRALIA (Heteroptera: Nepomorpha & Gerromorpha) ABSTRACT - BUZZETTI F.M., NIESER N. & DAMGAARD J., 2006 - Notes on water bugs from South East Asia and Australia (Heteroptera: Nepomorpha & Gerromorpha). Atti Acc. Rov. Agiati, a. 256, 2006, ser. VIII, vol. VI, B: 31-45. Faunistical data on some Nepomorpha and Gerromorpha from South East Asia and Australia are given. Hydrometra greeni Kirk., Limnogonus (Limnogonoides) pecto- ralis Mayr and Halobates sp. are reported as new records for Myanmar. KEY WORDS - Faunistics. RIASSUNTO - BUZZETTI F.M., NIESER N. & DAMGAARD J., 2006 - Su alcuni Emitteri acquatici del Sud Est Asiatico e dellAustralia (Heteroptera: Nepomorpha & Gerro- morpha). Si riportano alcuni dati faunistici relativi a Nepomorfi e Gerromorfi dal Sud Est Asiatico e dallAustralia. Hydrometra greeni Kirk., Limnogonus (Limnogonoides) pecto- ralis Mayr e Halobates sp. sono per la prima volta citati per il Myanmar. PAROLE CHIAVE - Faunistica. INTRODUCTION In this publication the Nepomorpha and Gerromorpha from South East Asia and Australia presently in the F. M. B. private collection are reported. Some specimens transferred to the Nieser collection are indi- cated NCTN. Other data from the collection of the Zoological Muse- um of Copenhagen University are indicated as ZMUC. Some synony- my is abbraviated but can be found in the publications cited under the various species. When given, measurements are in mm. The collecting localities from Myanmar are shown in Map 1. 32 Atti Acc. Rov. Agiati, a. 256, 2006, ser.