Glacier National Park Winter Ecology Lessons
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Do Not Disturb Hibernating Bats Or Nursery Colonies Debbie C
Part 2-Conservation, Management, Ethics: Buecher-Do Not Disturb Bats 43 Section A-Identifying and Protecting Cave Resources Do Not Disturb Hibernating Bats or Nursery Colonies Debbie C. Buecher In the United States, caving has increased in popularity during the last three decades. Unfortunately, human visitation in caves, even by the most conscientious cavers, gradually leaves negative impacts. Because we love our caves there is increasing awareness among the caving community toward performing ongoing restoration or building secure gates to maintain the integrity of caves we visit. However, we must consider the negative implications that our restoration efforts may have on the cave organisms adapted to this unique environment. Roosting Sites and Nursery Colonies Bats are extremely intolerant of human intrusion into their roosting sites (Mann and others 2002, Tuttle 1979) and roost disturbance over time can negatively impact population size (Mohr 1972). (See bat sensitivity, page 40.) Some people mistakenly believe that bats can use any cave or portion of a cave as their daily roosting area. Unfortunately this is not the case (Kunz 1982). Bats choose sites because ofa constrained range of tolerant temperature and humidity requirements-conditions that help insure their survival (McNab 1982). There are two extremely critical times in a bat's life when the roosting site is particularly important, during reproduction and during hibernation (Twente 1955). The location where female bats give birth and rear their young is called a maternity roost. For most temperate bat species that use caves, mating occurs in the fall, the bats then hibernatc until late spring, Figure t. -
Cold-Hearted Bats: Uncoupling of Heart Rate and Metabolism During Torpor at Sub-Zero Temperatures Shannon E
© 2018. Published by The Company of Biologists Ltd | Journal of Experimental Biology (2018) 221, jeb170894. doi:10.1242/jeb.170894 RESEARCH ARTICLE Cold-hearted bats: uncoupling of heart rate and metabolism during torpor at sub-zero temperatures Shannon E. Currie1,2,*, Clare Stawski1,3 and Fritz Geiser1 ABSTRACT Depending on ambient conditions, animals will thermoconform Many hibernating animals thermoregulate during torpor and defend down to this Tb/Ta (Heller, 1979; Geiser, 2011). However, when Ta falls below Tcrit, animals can either rewarm entirely to a their body temperature (Tb) near 0°C by an increase in metabolic rate. normothermic Tb or remain torpid and increase metabolic heat Above a critical temperature (Tcrit), animals usually thermoconform. production to thermoregulate and defend minimum Tb. We investigated the physiological responses above and below Tcrit for a small tree-dwelling bat (Chalinolobus gouldii, ∼14 g) that is often Details regarding thermoregulation during torpor at sub-zero exposed to sub-zero temperatures during winter. Through temperatures are scant and restricted to medium-sized northern mammals such as ground squirrels (Geiser and Kenagy, 1988; Buck simultaneous measurement of heart rate (fH) and oxygen ̇ and Barnes, 2000; Richter et al., 2015). However, small hibernators, consumption (VO2), we show that the relationship between oxygen transport and cardiac function is substantially altered in such as temperate insectivorous bats, often use torpor year round thermoregulating torpid bats between 1 and −2°C, compared with (Eisentraut, 1956; Davis and Reite, 1967; Masing and Lutsar, 2007; Wojciechowski et al., 2007). Thermoregulation during torpor, while thermoconforming torpid bats at mild ambient temperatures (Ta 5–20° still conserving substantial amounts of energy, can be expensive C). -
Our Legacy of Caring, Scholarship, and Scientific Discovery
Our Legacy of Caring, Scholarship, and Scientific Discovery Duke Lemur Center EST. 1966, DUKE UNIVERSITY The Duke Lemur Center An extraordinary place exists in the heart of Duke Forest: an 80-acre campus of buildings and forested animal enclosures bustling with students, scientists, and visitors from around the world. They are drawn to this place to see, learn about, and explore the animals that call this place home: a colony of more than 200 of the most endangered mammals on Earth—lemurs. A world leader in the study, care, and protection of lemurs, the Duke Lemur Center (DLC) was established in 1966 on the campus of Duke University in Durham, NC. For over 50 years, the DLC has brought together scientists, conservation biologists, and educators to understand and protect these extraordinary primates and make new and exciting discoveries through interdisciplinary non-invasive research. The DLC works tirelessly not just in Durham but also in in Madagascar, the only place on Earth where lemurs exist in the wild. We’re proud to work with the organizations and people of Madagascar to create opportunities for positive change, and to play a leading role in preventing the island’s legendary population of endemic and endangered national treasures from being lost forever. “To look at the Duke Lemur Center today, you would never know it was once an unknown part of the Duke University campus. Today it’s a thriving hub of learning where Duke students and alumni, scientists, and animal lovers of all ages from around the world explore the importance of lemurs, scientific discovery, and conservation. -
Insects by Cindy Grigg
Insects By Cindy Grigg 1 Like you, insects are alive. Both people and insects are animals. Insects are different from most other animals. Let's read to find out how they are different. 2 Insects are invertebrate animals. That means they have no backbone. Insects are the largest group of animals on Earth. In fact, about half of all animals that scientists know are insects! 3 Insects have three main body parts. They are the head, the thorax, and the abdomen. They have six legs. Many adult insects also have wings. The wings and legs are attached to the thorax. 4 Some invertebrate animals look like insects, but they are not. Spiders and scorpions, for example, are commonly confused with insects. Spiders and scorpions are not insects because they have eight legs, not six. They also have only two body segments instead of three. 5 Most insects lay eggs. Some young insects look like their parents. Other young insects, such as caterpillars, look very different from their parents. 6 All the stages in the life of an animal make up the animal's life cycle. Butterflies have a four-stage life cycle. Butterflies often lay eggs on leaves the insects can eat after they hatch. The egg is the first stage of the butterfly's life cycle. 7 When the egg hatches, a larva comes out of the egg. We often call the larva a caterpillar. This is the second stage. The caterpillar looks very different from the adult butterfly. The larva eats the leaves and grows very quickly. 8 After the larva grows big enough, it makes a hard covering for itself. -
Thrips Page 1
Insect Order Identification Home Thysanoptera–Thrips Page 1 Life Cycle--Intermediate metamorphosis (between complete and simple). Winged adults mate and lay eggs. Larvae (nymphs) look similar to adults in form and shape but lack both wings and wingbuds. Larvae eat, molt, and grow larger until entering a non-feeding larval stage (pupa) in which wings form and a color change may occur but the form remains essentially the same. Some species have one or more non-feeding pre-pupal stages. The emerging winged adult looks similar to the larva. Adults--Minuscule insects (usually 1/16 inch or less). Magnification may be needed to see them. Adults are usually dark-colored, yellow to black. Shape elongated and slender. Two pairs of wings are long and narrow and held over the body. Edges of both forewings and hindwings are fringed or feathery. (Click images to enlarge.) Black dots are Feathery-edged wings Wings tube-tailed thrips long & narrow Brown dots are mixture of adults, larvae & damage One of the black dots above Feathery-edged One of the wings brown dots above Insect Order Identification Home Thysanoptera–Thrips Page 2 Eggs--Some female thrips lay their eggs in tiny slits cut into the surface of leaves, fruits, flowers, and stems. Indoors, the eggs can be laid any time of year and hatch within a few days in warm, indoor conditions. In some species the fertilized eggs are all parthenogenic females (able to reproduce without sex) and the unfertilized are males. (Click images to enlarge.) Thrips eggs Close-up of eggs Larvae (Nymphs)--Look similar to adults but entirely wingless and usually pale-colored, white to cream or pale green. -
Reproductionreview
REPRODUCTIONREVIEW Focus on Implantation Embryonic diapause and its regulation Flavia L Lopes, Joe¨lle A Desmarais and Bruce D Murphy Centre de Recherche en Reproduction Animale, Faculte´ de Me´decine Ve´te´rinaire, Universite´ de Montre´al, 3200 rue Sicotte, St-Hyacinthe, Quebec, Canada J2S7C6 Correspondence should be addressed to B D Murphy; Email: [email protected] Abstract Embryonic diapause, a condition of temporary suspension of development of the mammalian embryo, occurs due to suppres- sion of cell proliferation at the blastocyst stage. It is an evolutionary strategy to ensure the survival of neonates. Obligate dia- pause occurs in every gestation of some species, while facultative diapause ensues in others, associated with metabolic stress, usually lactation. The onset, maintenance and escape from diapause are regulated by cascades of environmental, hypophyseal, ovarian and uterine mechanisms that vary among species and between the obligate and facultative condition. In the best- known models, the rodents, the uterine environment maintains the embryo in diapause, while estrogens, in combination with growth factors, reinitiate development. Mitotic arrest in the mammalian embryo occurs at the G0 or G1 phase of the cell cycle, and may be due to expression of a specific cell cycle inhibitor. Regulation of proliferation in non- mammalian models of diapause provide clues to orthologous genes whose expression may regulate the reprise of proliferation in the mammalian context. Reproduction (2004) 128 669–678 Introduction recently been discussed in depth (Dey et al. 2004). In this presentation we address the characteristics of the embryo Embryonic diapause, also known as discontinuous devel- in diapause and focus on the mechanisms of regulation of opment or, in mammals, delayed implantation, is among this phenomenon, including the environmental and meta- the evolutionary strategies that ensure successful repro- bolic stimuli that induce and terminate this condition, the duction. -
Colorado Potato Beetle.Pub
CORNELL COOPERATIVE EXTENSION OF ONEIDA COUNTY 121 Second Street Oriskany, NY 13424-9799 (315) 736-3394 or (315) 337-2531 FAX: (315) 736-2580 Colorado Potato Beetle Leptinotarsa decemlineata Description: The Colorado potato beetle was first described in 1824 from the upper Missouri River Valley where it fed on a weed called buffalo bur or sand bur, but when early settlers first began to plant potatoes, the beetles discovered the new food plant and liked it. Adult Colorado Potato Beetle Colorado Potato Beetle larva Injury: Larvae and adults feed on the foliage of potato, eggplant, tomatoes and peppers. They may reach large numbers and eat all the foliage from the plant as well as spoil the fruit by eating into it. They are especially de- structive to small plantings. Life History: Adult beetles come out of winter hibernation in mid-May on Long Island and a week or ten days later in central New York just before the early-planted potatoes are up. Clusters of 20 or more eggs are laid on the underside of the leaves soon after the beetles emerge. The eggs hatch in seven to ten days. The larvae feed on the foliage, grow rapidly and complete their development in 18 to 21 days. The full-grown larva burrows into the ground and changes to the pupa or resting stage. After seven to ten days, the adult beetle emerges from the pupa, crawls up out of the ground, and after a short period of waiting, lays eggs for the second generation. Management: In the past several years, the Colorado potato beetle has become increasingly difficult to control because it has developed resistance to many commonly used chemical insecticides. -
Introduction to Pregnancy in Waiting: Embryonic Diapause in Mammals Proceedings of the Third International Symposium on Embryonic Diapause
Proceedings of III International Symposium on Embryonic Diapause DOI: 10.1530/biosciprocs.10.001 Introduction to Pregnancy in Waiting: Embryonic Diapause in Mammals Proceedings of the Third International Symposium on Embryonic Diapause BD Murphy1, K Jewgenow2, MB Renfree3, SE Ulbrich4 1Centre de recherche en reproduction et fertilité, Université de Montréal, Canada 2Leibniz-Institute for Zoo and Wildlife Research, Berlin, Germany 3School of BioSciences, University of Melbourne, Australia 4Institute of Agricultural Sciences, ETH Zurich, Switzerland The capacity of the mammalian embryo to arrest development during early gestation is a topic that has fascinated biologists for over 150 years. The first known observation of this phenomenon was in a ruminant, the roe deer (Capreolus capreolus) in 1854, later confirmed in a number of studies in the last century [1]. The phenomenon, now known as embryonic diapause, was then found to be present in a wide range of species and across multiple taxa. Since that time, its biological mystery has attracted studies by scientists from around the globe. The First International Symposium on the topic of embryonic diapause in mammals was held in 1963 at Rice University, Houston, Texas. It resulted in a proceedings volume entitled “Delayed Implantation”, edited by A.C. Enders [2]. The symposium was distinguished by the novel recognition of that era that a wide range of species had been identified with embryonic diapause, including rodents, marsupials and carnivores. The emerging technology of the time, particularly structural approaches, permitted new understanding of the events of diapause and embryo reactivation. The newest methods provided key data on the temporal window of implantation in rodents, introduced new physiological approaches, and illustrated some of the first transmission electron microscope investigations of the blastocyst. -
Embryonic Diapause in Mammals and Dormancy in Embryonic Stem Cells with the European Roe Deer As Experimental Model
CSIRO PUBLISHING Reproduction, Fertility and Development, 2021, 33, 76–81 https://doi.org/10.1071/RD20256 Embryonic diapause in mammals and dormancy in embryonic stem cells with the European roe deer as experimental model Vera A. van der WeijdenA,*, Anna B. Ru¨eggA,*, Sandra M. Bernal-UlloaA and Susanne E. UlbrichA,B AETH Zurich, Animal Physiology, Institute of Agricultural Sciences, Universitaetstrasse 2, 8092 Zurich, Switzerland. BCorresponding author. Email: [email protected] Abstract. In species displaying embryonic diapause, the developmental pace of the embryo is either temporarily and reversibly halted or largely reduced. Only limited knowledge on its regulation and the inhibition of cell proliferation extending pluripotency is available. In contrast with embryos from other diapausing species that reversibly halt during diapause, embryos of the roe deer Capreolus capreolus slowly proliferate over a period of 4–5 months to reach a diameter of approximately 4 mm before elongation. The diapausing roe deer embryos present an interesting model species for research on preimplantation developmental progression. Based on our and other research, we summarise the available knowledge and indicate that the use of embryonic stem cells (ESCs) would help to increase our understanding of embryonic diapause. We report on known molecular mechanisms regulating embryonic diapause, as well as cellular dormancy of pluripotent cells. Further, we address the promising application of ESCs to study embryonic diapause, and highlight the current knowledge on the cellular microenvironment regulating embryonic diapause and cellular dormancy. Keywords: dormancy, embryonic diapause, embryonic stem cells, European roe deer Capreolus capreolus. Published online 8 January 2021 Embryonic diapause conditions. The roe deer is the only known ungulate exhibiting The time between fertilisation and embryo implantation varies embryonic diapause. -
Energetics of Metamorphosis in Drosophila Melanogaster ⇑ Allison B
Journal of Insect Physiology 57 (2011) 1437–1445 Contents lists available at ScienceDirect Journal of Insect Physiology journal homepage: www.elsevier.com/locate/jinsphys Energetics of metamorphosis in Drosophila melanogaster ⇑ Allison B. Merkey, Carrie K. Wong 1, Deborah K. Hoshizaki 2, Allen G. Gibbs School of Life Sciences, 4505 S. Maryland Pkwy., University of Nevada, Las Vegas, Nevada 89154, USA article info abstract Article history: We measured the energetic cost of metamorphosis in the fruitfly, Drosophila melanogaster. Metabolic Received 26 May 2011 rates decreased rapidly in the first 24 h and remained low until shortly before eclosion, when the rates Received in revised form 18 July 2011 increased rapidly, thus creating a U-shaped metabolic curve. The primary fuel used during metamorpho- Accepted 19 July 2011 sis was lipid, which accounted for >80% of total metabolism. The total energy consumed during metamor- Available online 24 July 2011 phosis was lowest at 25 °C, compared to 18 and 29 °C, due to differences in metabolic rates and the length of pupal development. Temperature differentially affected metabolic rates during different stages of Keywords: metamorphosis. Prepupal and late pupal stages exhibited typical increases in metabolic rate at high tem- Drosophila peratures, whereas metabolic rates were independent of temperature during the first 2/3 of pupal devel- Energetics Lipid opment. Metabolic rate We tested two hypotheses for the underlying cause of the U-shaped metabolic curve. The first hypoth- Metamorphosis esis was that pupae become oxygen restricted as a result of remodeling of the larval tracheal system. We tested this hypothesis by exposing pupae to hypoxic and hyperoxic atmospheres, and by measuring lactic acid production during normoxic development. -
WILDLIFE in WINTER Do You Know What Different Animals Do During the Winter?
WILDLIFE IN WINTER Do you know what different animals do during the winter? Animals have different strategies for surviving the winter. The most common strategies are hibernation, brumation, diapause, torpor, migration and adaptation. Hibernation Torpor Hibernation occurs when an animal enters a deep sleep Torpor is a state that some animals for the entire winter. Animals that hibernate eat extra food enter during the winter. Similar to during the fall to store up fat before winter begins. When it’s hibernation, the animal lowers its body time to hibernate, the animal drops its body temperature temperature and slows its breathing and by 20 °C or more and slows its heart rate and breathing in heart rate. However, animals that use torpor order to use less energy. during the winter may wake up occasionally or regularly to hunt, eat and defecate. Some animals Brumation are also able to go in and out of torpor regularly, like Brumation is a state of inactivity that cold-blooded creatures when it gets very cold at night. enter during winter. Think of this as hibernation for reptiles and amphibians. During extended cold periods, their bodies Migration produce high levels of sugar and slow or shutdown their Migration is the act of moving from one place to another. internal processes. Some animals can even freeze! Some creatures migrate to a warmer location when the weather gets too cold. They may travel alone or in large Diapause groups to areas where food is plentiful. Diapause occurs when insects pause their development to prepare for winter. Some insects stop all body processes and Adaptation sometimes freeze until the weather warms up in the spring, Adaptation to winter weather can take many different forms. -
Telemetry Experiments with a Hibernating Black Bear
Paper 37 Telemetry Experiments with a Hibernating Black Bear JOHN J. CRAIGHEAD Montana Cooperative Wildlife Research Unit, University of Montana, Missoula, Montana 59801 J. R. VARNEY Aeronutronic Ford Corporation, 3939 Fabian Way, Palo Alta, California 9430 F. C. CRAIGHEAD,JR. Environmental Research Institute, Moose, Wyoming 83012 J. S. SUMNER Montana Cooperative Wildlife Research Unit, University of Montana, Missoula, Montana 59801 INTRODUCTION During the winter of 1966-67 the body temperature of a male black bear (Ursus americanus) was telemetered in winter sleep under natural denning conditions (Craighead et al. 1971). To improve equipment and techniques for studying the physiology and behavior of bears under natural conditions, a captive black bear was used to continue the investigations during the winter of 1971-72. This paper describes the experiments and the results. Other investigators (Essler and Folk 1961; Folk et al. 1965, 1968, 1972; Hedge et al. 1965) have studied the physiology and hibernation behavior of captive bears under simulated natural conditions. Our own long-range objectives are to develop the means of obtaining ecological, behavioral and physiological data from unrestrained hibernating animals in the wild through the use of recent electronic and technological advances, including earth-orbiting satel- lites (Craighead et al. 1971). The specific objectives of the work described here were to develop and test telemetry equipment suitable for monitoring a typical physiological parameter (body temperature) by satellite; to refine immobilizing and handling techniques; to visually observe a bear throughout the hibernation period and correlate its behavior with body and den temperatures; and to outline surgical techniques for implanting telemetry transmitters in the body of a wild black bear.