Rodents As a Food Source
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Fraud in Animal Origin Food Products: Advances in Emerging Spectroscopic Detection Methods Over the Past Five Years
foods Review Fraud in Animal Origin Food Products: Advances in Emerging Spectroscopic Detection Methods over the Past Five Years Abdo Hassoun 1,* , Ingrid Måge 1 , Walter F. Schmidt 2, Havva Tümay Temiz 3, Li Li 4, Hae-Yeong Kim 5 , Heidi Nilsen 1, Alessandra Biancolillo 6 , Abderrahmane Aït-Kaddour 7 , Marek Sikorski 8 , Ewa Sikorska 9 , Silvia Grassi 10 and Daniel Cozzolino 11 1 Nofima AS, Norwegian Institute of Food, Fisheries, and Aquaculture Research, Muninbakken 9-13, 9291 Tromsø, Norway; ingrid.mage@Nofima.no (I.M.); heidi.nilsen@nofima.no (H.N.) 2 United States Department of Agriculture, Agricultural Research Service, 10300 Baltimore Avenue, Beltsville, MD 20705-2325, USA; [email protected] 3 Department of Food Engineering, Bingol University, 12000 Bingol, Turkey; [email protected] 4 Key Laboratory of Mariculture, Ministry of Education, Ocean University of China, Qingdao 266003, China; [email protected] 5 Department of Food Science and Biotechnology, Kyung Hee University, Yongin 17104, Korea; [email protected] 6 Department of Physical and Chemical Sciences, University of L’Aquila, 67100 Via Vetoio, Coppito, L’Aquila, Italy; [email protected] 7 Université Clermont-Auvergne, INRAE, VetAgro Sup, UMR F, 63370 Lempdes, France; [email protected] 8 Faculty of Chemistry, Adam Mickiewicz University in Poznan, Uniwersytetu Poznanskiego 8, 61-614 Poznan, Poland; [email protected] 9 Institute of Quality Science, Pozna´nUniversity of Economics and Business, al. Niepodległo´sci10, 61-875 Pozna´n,Poland; -
Mammals of the California Desert
MAMMALS OF THE CALIFORNIA DESERT William F. Laudenslayer, Jr. Karen Boyer Buckingham Theodore A. Rado INTRODUCTION I ,+! The desert lands of southern California (Figure 1) support a rich variety of wildlife, of which mammals comprise an important element. Of the 19 living orders of mammals known in the world i- *- loday, nine are represented in the California desert15. Ninety-seven mammal species are known to t ':i he in this area. The southwestern United States has a larger number of mammal subspecies than my other continental area of comparable size (Hall 1981). This high degree of subspeciation, which f I;, ; leads to the development of new species, seems to be due to the great variation in topography, , , elevation, temperature, soils, and isolation caused by natural barriers. The order Rodentia may be k., 2:' , considered the most successful of the mammalian taxa in the desert; it is represented by 48 species Lc - occupying a wide variety of habitats. Bats comprise the second largest contingent of species. Of the 97 mammal species, 48 are found throughout the desert; the remaining 49 occur peripherally, with many restricted to the bordering mountain ranges or the Colorado River Valley. Four of the 97 I ?$ are non-native, having been introduced into the California desert. These are the Virginia opossum, ' >% Rocky Mountain mule deer, horse, and burro. Table 1 lists the desert mammals and their range 1 ;>?-axurrence as well as their current status of endangerment as determined by the U.S. fish and $' Wildlife Service (USWS 1989, 1990) and the California Department of Fish and Game (Calif. -
The South American Plains Vizcacha, Lagostomus Maximus, As a Valuable Animal Model for Reproductive Studies
Central JSM Anatomy & Physiology Bringing Excellence in Open Access Editorial *Corresponding author Verónica Berta Dorfman, Centro de Estudios Biomédicos, Biotecnológicos, Ambientales y The South American Plains Diagnóstico (CEBBAD), Universidad Maimónides, Hidalgo 775 6to piso, C1405BCK, Ciudad Autónoma Vizcacha, Lagostomus maximus, de Buenos Aires, Argentina, Tel: 54 11 49051100; Email: Submitted: 08 October 2016 as a Valuable Animal Model for Accepted: 11 October 2016 Published: 12 October 2016 Copyright Reproductive Studies © 2016 Dorfman et al. Verónica Berta Dorfman1,2*, Pablo Ignacio Felipe Inserra1,2, OPEN ACCESS Noelia Paola Leopardo1,2, Julia Halperin1,2, and Alfredo Daniel Vitullo1,2 1Centro de Estudios Biomédicos, Biotecnológicos, Ambientales y Diagnóstico, Universidad Maimónides, Argentina 2Consejo Nacional de Investigaciones Científicas y Técnicas, Argentina INTRODUCTION anti-apoptotic BCL-2 over the pro-apoptotic BAX protein which leads to a down-regulation of apoptotic pathways and promotes The vast majority of our understanding of the mammalian a continuous oocyte production [6,7]. Moreover, the inversion reproductive biology comes from investigations mainly in the BAX/BCL-2 balance is expressed in embryonic ovaries performed in mice, rats and humans. However, evidence throughout development, pinpointing this physiological aspect gathered from non-conventional laboratory models, farm and as a constitutive feature of the vizcacha´s ovary, which precludes wild animals strongly suggests that reproductive mechanisms show a plethora of different strategies among species. For massive intra-ovarian germ cell elimination. Massive intra- instance, studies developed in unconventional rodents such ovarian germ cell elimination through apoptosis during fetal life as guinea pigs and hamsters, that share with humans some accounts for 66 to 85% loss at birth as recorded for human, mouse endocrine and reproductive characters, have contributed to a and rat [8]. -
Pleistocene Mammals and Paleoecology of the Western Amazon
PLEISTOCENE MAMMALS AND PALEOECOLOGY OF THE WESTERN AMAZON By ALCEU RANCY A DISSERTATION PRESENTED TO THE GRADUATE SCHOOL OF THE UNIVERSITY OF FLORIDA IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY UNIVERSITY OF FLORIDA 1991 . To Cleusa, Bianca, Tiago, Thomas, and Nono Saul (Pistolin de Oro) . ACKNOWLEDGMENTS This work received strong support from John Eisenberg (chairman) and David Webb, both naturalists, humanists, and educators. Both were of special value, contributing more than the normal duties as members of my committee. Bruce MacFadden provided valuable insights at several periods of uncertainty. Ronald Labisky and Kent Redford also provided support and encouragement. My field work in the western Amazon was supported by several grants from the Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq) , and the Universidade Federal do Acre (UFAC) , Brazil. I also benefitted from grants awarded to Ken Campbell and Carl Frailey from the National Science Foundation (NSF) I thank Daryl Paul Domning, Jean Bocquentin Villanueva, Jonas Pereira de Souza Filho, Ken Campbell, Jose Carlos Rodrigues dos Santos, David Webb, Jorge Ferigolo, Carl Frailey, Ernesto Lavina, Michael Stokes, Marcondes Costa, and Ricardo Negri for sharing with me fruitful and adventurous field trips along the Amazonian rivers. The CNPq and the Universidade Federal do Acre, supported my visit to the. following institutions (and colleagues) to examine their vertebrate collections: iii . ; ; Universidade do Amazonas, Manaus -
Hystrix Africaeaustralis)
Reproduction in captive female Cape porcupines (Hystrix africaeaustralis) R. J. van Aarde Mammal Research Institute, University ofPretoria, Pretoria 0002, South Africa Summary. Captive females attained sexual maturity at an age of 9\p=n-\16months and con- ceived for the first time when 10\p=n-\25months old. Adult females were polyoestrous but did not cycle while lactating or when isolated from males. The length of the cycle varied from 17 to 42 days (mean \m=+-\s.d. 31\m=.\2\m=+-\6\m=.\5days; n = 43) and females experienced 3\p=n-\7 sterile cycles before conceiving. Pregnancy lasted for 93\p=n-\94days (93\m=.\5\m=+-\0\m=.\6days; N = 4) and litter intervals varied from 296 to 500 days (385 \m=+-\60\m=.\4;n = 10). Litter size varied from 1 to 3 (1\m=.\5\m=+-\0\m=.\66;n = 165) and the well-developed precocial young weighed 300\p=n-\400g (351 \m=+-\47\m=.\4g; n= 19) at birth. Captive females reproduced throughout the year with most litters (78\m=.\7%;n = 165) being produced between August and March. Introduction Cape porcupines (Hystrix africaeaustralis) inhabit tropical forests, woodlands, grassland savannas, semi-arid and arid environments throughout southern Africa. Despite this widespread distribution little attention has been given to these nocturnal, Old World hystricomorph rodents, which shelter and breed in subterranean burrows, rock crevices and caves. Some information on reproduction in female porcupines has been published on the crested porcupine (H. cristata) (Weir, 1967), the Himalayan porcupine (H. hodgsoni) (Gosling, 1980) and the Indian porcupine (H. -
The Beaver's Phylogenetic Lineage Illuminated by Retroposon Reads
www.nature.com/scientificreports OPEN The Beaver’s Phylogenetic Lineage Illuminated by Retroposon Reads Liliya Doronina1,*, Andreas Matzke1,*, Gennady Churakov1,2, Monika Stoll3, Andreas Huge3 & Jürgen Schmitz1 Received: 13 October 2016 Solving problematic phylogenetic relationships often requires high quality genome data. However, Accepted: 25 January 2017 for many organisms such data are still not available. Among rodents, the phylogenetic position of the Published: 03 March 2017 beaver has always attracted special interest. The arrangement of the beaver’s masseter (jaw-closer) muscle once suggested a strong affinity to some sciurid rodents (e.g., squirrels), placing them in the Sciuromorpha suborder. Modern molecular data, however, suggested a closer relationship of beaver to the representatives of the mouse-related clade, but significant data from virtually homoplasy- free markers (for example retroposon insertions) for the exact position of the beaver have not been available. We derived a gross genome assembly from deposited genomic Illumina paired-end reads and extracted thousands of potential phylogenetically informative retroposon markers using the new bioinformatics coordinate extractor fastCOEX, enabling us to evaluate different hypotheses for the phylogenetic position of the beaver. Comparative results provided significant support for a clear relationship between beavers (Castoridae) and kangaroo rat-related species (Geomyoidea) (p < 0.0015, six markers, no conflicting data) within a significantly supported mouse-related clade (including Myodonta, Anomaluromorpha, and Castorimorpha) (p < 0.0015, six markers, no conflicting data). Most of an organism’s phylogenetic history is fossilized in their heritable genomic material. Using data from genome sequencing projects, particularly informative regions of this material can be extracted in sufficient num- bers to resolve the deepest history of speciation. -
Activity Pattern of Medium and Large Sized Mammals and Density Estimates of Cuniculus Paca (Rodentia: Cuniculidae) in the Brazilian Pampa C
Brazilian Journal of Biology http://dx.doi.org/10.1590/1519-6984.174403 ISSN 1519-6984 (Print) Original Article ISSN 1678-4375 (Online) Activity pattern of medium and large sized mammals and density estimates of Cuniculus paca (Rodentia: Cuniculidae) in the Brazilian Pampa C. Leuchtenbergera*, Ê. S. de Oliveirab, L. P. Cariolattoc and C. B. Kasperb aInstituto Federal Farroupilha – IFFAR, Coordenação de Ciências Biológicas, Rua Erechim, nº 860, Campus Panambi, CEP 98280-000, Panambi, RS, Brazil bUniversidade Federal do Pampa – UNIPAMPA, Laboratório de Biologia de Mamíferos e Aves – LABIMAVE, Av. Antônio Trilha, nº 1847, CEP 97300-000, São Gabriel, RS, Brazil cInstituto Federal Farroupilha – IFFAR, RS-377, Km 27, Campus Alegrete, Passo Novo, CEP 97555-000, Alegrete, RS, Brazil *e-mail: [email protected] Received: January 13, 2017 – Accepted: June 26, 2017 – Distributed: November 30, 2018 (With 2 figures) Abstract Between July 2014 and April 2015, we conducted weekly inventories of the circadian activity patterns of mammals in Passo Novo locality, municipality of Alegrete, southern Brazil. The vegetation is comprised by a grassy-woody steppe (grassland). We used two camera traps alternately located on one of four 1 km transects, each separated by 1 km. We classified the activity pattern of species by the percentage of photographic records taken in each daily period. We identify Cuniculus paca individuals by differences in the patterns of flank spots. We then estimate the density 1) considering the area of riparian forest present in the sampling area, and 2) through capture/recapture analysis. Cuniculus paca, Conepatus chinga and Hydrochoerus hydrochaeris were nocturnal, Cerdocyon thous had a crepuscular/nocturnal pattern, while Mazama gouazoubira was cathemeral. -
Complement Fixation Tests for Murine Typhus
ice under glass seal. The animals' brains were Complement Fixation Tests removed for tissue infectivity tests and were also stored on dry ice. Tests of the tissues of For Murine Typhus serologically reactive animals and pools of their fleas aided in evaluating the significance of low On Small Mammals titers. Blood samples were obtained by cardiac By RUTH KEATON, B.S. puncture soon after capture of the animals. BILLIE JO NASH, B.A. Serums were separated aseptically and were J. N. MURPHY, JR., M.A., M.S.P.H. kept at ice-box temperature until examination. J. V. IRONS, Sc.D. Serums were inactivated 30 minutes immedi- ately before testing at 56° C. Each serum was subjected to a quantitative complement tT HE IMPORTANCE of commensal rats fixation test employing endemic typhus rick- and their fleas in the epidemiology of en- ettsiae. A slight modification of the pro- demic typhus was well establislhed in 1931 (1,2). cedure described by Brigham and Bensgton Following Dyer's report (3) on the experi- (11) was used. The result was recorded as mental infection of the woodchuck, meadow reactive when a 3 + or greater reaction was ob- mouse, and whitefooted mouse with endemic tained with satisfactory controls at a 1: 20 or tvphus, Brigham (4, 5) indicated that many greater dilution of serum. species of rodents and other mammals were ap- When a serum was reactive, the correspond- parently susceptible to endemic typhus. Spar- ing brain suspension was emulsified and inocu- row (6) recovered a strain of endemic typhus lated individually into hamsters for evidence of rickettsiae in the house mouse (.Mus musodus), typhus. -
The Use of Species-Specific Primer Targeting on D-Loop Mitochondrial
Journal of Advanced Veterinary and Animal Research ISSN 2311-7710 (Electronic) http://doi.org/10.5455/javar.2018.e275 September 2018 A periodical of the Network for the Veterinarians of Bangladesh (BDvetNET) Vol 5 No 3, Pages 361-368. Short Communication The use of species-specific primer targeting on D-loop mitochondrial for identification of wild boar meat in meatball formulation Rien Larasati Arini1, Dwiky Ramadhani1, Ni wayan Pebriyanti1, Sismindari 2 and Abdul Rohman 2,# • Received: June 4, 2018 • Revised: July 18, 2018 • Accepted: July 21, 2018 • Published Online: August 6, 2018 AFFILIATIONS ABSTRACT 1Faculty of Pharmacy, Gadjah Mada Objective: The study was intended to design the new specific primer targeting on University, Sekip Utara, Yogyakarta mitochondrial D-Loop gene (D-Loop 443 primer) combined with a real-time 55281, Indonesia. polymerase chain reaction (PCR) for the analysis of wild boar meat (WBM) in food products of meatball. 2Departement of Pharmaceutical Materials and methods: The primer was designed and subjected to primer-basic Chemistry, Gadjah Mada University, local alignment search tool using National Center for Biotechnology Information Sekip Utara, Yogyakarta 55281, software. Validation of real-time PCR using designed primer was performed by Indonesia. evaluation of several performance characteristics which included specificity, sensitivity, repeatability, linearity, and efficiency. Results: The results showed that the D-loop primer could be attached at 60.7°C and no amplification was detected against other species confirming the specificity of the primers. The limits of detection were found to be 4.68 ng and 2.34 ng using DNA extracted from WBM and that extracted from wild boar in meatball product. -
Red-Rumped Agouti)
UWI The Online Guide to the Animals of Trinidad and Tobago Behaviour Dasyprocta leporina (Red-rumped Agouti) Family: Dasyproctidae (Agoutis) Order: Rodentia (Rodents) Class: Mammalia (Mammals) Fig. 1. Red-rumped agouti, Dasyprocta leporina. [http://upload.wikimedia.org/wikipedia/commons/3/3b/Dasyprocta.leporina-03-ZOO.Dvur.Kralove.jpg, downloaded 12 November 2012] TRAITS. Formerly Dasyprocta aguti, and also known as the Brazilian agouti and as “Cutia” in Brazil and “Acure” in Venezuela. The average Dasyprocta leporina weighs approximately between 3 kg and 6 kg with a body length of about 49-64 cm. They are medium sized caviomorph rodents (Wilson and Reeder, 2005) with brown fur consisting of darker spots of brown covering their upper body and a white stripe running down the centre of their underside (Eisenberg, 1989). Show sexual dimorphism as the males are usually smaller in size than the females but have a similar appearance (Wilson and Reeder, 2005). Locomotion is quadrupedal. Forefeet have four toes while hind feet (usually longer than forefeet) have 3. Small round ears with short hairless tail not more than 6 cm in length (Dubost 1998). UWI The Online Guide to the Animals of Trinidad and Tobago Behaviour ECOLOGY. Dasyprocta leporina is found in the tropical forests of Trinidad and conserved in the Central Range Wildlife Sanctuary at the headwaters of the Tempuna and Talparo watersheds in central Trinidad (Bacon and Ffrench 1972). They are South American natives and are distributed widely in Venezuela, French Guiana and Amazon forests of Brazil (Asquith et al. 1999; Dubost 1998). Has widespread distribution in the Neotropics (Eisenberg 1989; Emmons and Feer 1997). -
Using Allele-Specific
NOTES AND COMMENTS Rapid identification of capybara (Hydrochaeris hydrochaeris) using allele-specific PCR Henrique-Silva, F.*, Cervini, M., Rios, WM., Lusa, AL., Lopes, A., Gonçalves, D., Fonseca, D., Franzin, F., Damalio, J., Scaramuzzi, K., Camilo, R., Ferrarezi, T., Liberato, M., Mortari, N. and Matheucci Jr., E. Departamento de Genética e Evolução, Universidade Federal de São Carlos – UFSCar, Rod. Washington Luiz, Km 235, CEP 13565-905, São Carlos, SP, Brazil *e-mail: [email protected] Received August 11, 2005 – Accepted February 10, 2006 – Distributed February 28, 2007 (With 1 figure) The capybara is the largest rodent in the world and is ments of frozen meat using treatment with proteinase K, widely distributed throughout Central and South America as described in (Sambrook et al., 1989). Basically, the (Paula et al., 1999). It is an animal of economic interest meat fragments were incubated in 400 µL buffer (10 mM due to the pleasant flavor of its meat and higher protein Tris-HCl, pH:7.8; 5 mM EDTA; 0.5% SDS) containing content in comparison to beef and pork meat. The hide, 400 µg of. proteinase K at 65 °C for 2 hours. After that, hair and fat also have economic advantages. Thus, as an the solution was treated with an equal volume of phenol- animal with such high economic potential, it is the target chloroform, and the DNA was purified from the aqueous of hunters, even though hunting capybara is prohibited phase by ethanol precipitation. Approximately 50 ng of by law in Brazil (Fauna Law, number 9.605/98). the DNA was used in amplification reactions containing Due to their similarities, capybara meat is easily 20 mM Tris.HCl pH 8.4; 50 mM KCl; 1.5 mM MgCl2, confused with pork. -
Overkill, Glacial History, and the Extinction of North America's Ice Age Megafauna
PERSPECTIVE Overkill, glacial history, and the extinction of North America’s Ice Age megafauna PERSPECTIVE David J. Meltzera,1 Edited by Richard G. Klein, Stanford University, Stanford, CA, and approved September 23, 2020 (received for review July 21, 2020) The end of the Pleistocene in North America saw the extinction of 38 genera of mostly large mammals. As their disappearance seemingly coincided with the arrival of people in the Americas, their extinction is often attributed to human overkill, notwithstanding a dearth of archaeological evidence of human predation. Moreover, this period saw the extinction of other species, along with significant changes in many surviving taxa, suggesting a broader cause, notably, the ecological upheaval that occurred as Earth shifted from a glacial to an interglacial climate. But, overkill advocates ask, if extinctions were due to climate changes, why did these large mammals survive previous glacial−interglacial transitions, only to vanish at the one when human hunters were present? This question rests on two assumptions: that pre- vious glacial−interglacial transitions were similar to the end of the Pleistocene, and that the large mammal genera survived unchanged over multiple such cycles. Neither is demonstrably correct. Resolving the cause of large mammal extinctions requires greater knowledge of individual species’ histories and their adaptive tolerances, a fuller understanding of how past climatic and ecological changes impacted those animals and their biotic communities, and what changes occurred at the Pleistocene−Holocene boundary that might have led to those genera going extinct at that time. Then we will be able to ascertain whether the sole ecologically significant difference between previous glacial−interglacial transitions and the very last one was a human presence.