scholarly journals What is the taxonomic identity of Minnesota wolves?

2010 ◽  
Vol 88 (2) ◽  
pp. 129-138 ◽  
Author(s):  
L. D. Mech

The taxonomic identity of the historical and current wolf ( Canis lupus L., 1758 or Canis lycaon Schreber, 1775 or their hybrids) population in Minnesota (MN) and the Great Lakes region has been, and continues to be, controversial. So too does its legal status under the U.S. Endangered Species Act. This review summarizes the morphological and genetic information about that population and concludes that historically the MN population consisted of a gray wolf (C. lupus) in the west and an eastern type ( Canis lupus lycaon or C. lycaon) in the east with intergrades or hybrids between the two in most of the state. After extirpation in much of its original MN range, the now-recovered population was infused with gray wolves from Ontario but still consists of hybrid lycaon × gray wolves, probably with higher content gray wolves in the west and higher content lycaon in the east but with most wolves morphologically appearing to be gray wolves. Because the current Wisconsin and Michigan wolf population was derived from MN wolves, they would be primarily hybrids as well. Future research should seek to relate genetic data with morphological measurements in MN wolves. In addition, attempts to breed coyotes ( Canis latrans Say, 1823) with gray wolves in captivity would shed considerable light on the controversy over the origin and taxonomic identity of the newly proposed C. lycaon.

2020 ◽  
Vol 134 (1) ◽  
pp. 36-41
Author(s):  
Richard P. Thiel

North American Canis genetics research varies in interpreting the Pre-Columbian distribution of Coyotes (Canis latrans). Many studies have relied on generalized species-distribution maps and a few actually cite earlier genetics works as secondary sources. I use archaeological, paleontological, and settlement era documents to demonstrate that Coyotes were present in portions of Minnesota, Wisconsin, and Illinois thousands of years prior to European arrival. This review provides important clarification of historical Coyote distribution in the region and may have implications on the various interpretations of introgressed Coyote haplotypes present in Gray Wolves (Canis lupus) throughout the Great Lakes region.


2008 ◽  
Vol 5 (1) ◽  
pp. 101-104 ◽  
Author(s):  
Tyler Wheeldon ◽  
Bradley N White

The genetic status of wolves in the western Great Lakes region has received increased attention following the decision to remove them from protection under the US Endangered Species Act. A recent study of mitochondrial DNA has suggested that the recovered wolf population is not genetically representative of the historic population. We present microsatellite genotype data on three historic samples and compare them with extant populations, and interpret published genetic data to show that the pre-recovery population was admixed over a century ago by eastern wolf ( Canis lycaon ) and grey wolf ( Canis lupus ) hybridization. The DNA profiles of the historic samples are similar to those of extant animals in the region, suggesting that the current Great Lakes wolves are representative of the historic population.


2007 ◽  
Vol 85 (2) ◽  
pp. 295-300 ◽  
Author(s):  
V.E. Sidorovich ◽  
V.P. Stolyarov ◽  
N.N. Vorobei ◽  
N.V. Ivanova ◽  
B. Jędrzejewska

Gray wolf ( Canis lupus L., 1758) population fluctuations in northern Belarus (Vitebsk region) between 1990 and 2003 were significantly affected by hunting pressure by humans. Mean litter size was inversely density dependent and varied from 4.8 to 7.7 pups (range 2–10). The increase in litter size with declining density of wolf population concerned only female pups, whereas the number of male pups in a litter was not related to population density. The sex ratio of pups varied significantly: the proportion of females reached 70% in a low-density wolf population and declined to 40%–50% in a high-density population. The age structure also varied. In years following heavy hunting pressure, 55% of individuals shot were juveniles <1 year old (with a strong predominance of females that constituted 69% of juveniles shot), and only 11% of wolves were older than 4 years. The mean age of all wolves shot was 1.5 years. In years following low hunting pressure, 34% of animals shot were juveniles and 20% exceeded 4 years. The mean age was 2.8 years. A female-biased sex ratio of wolf pups conforms to Hiraiwa-Hasegawa’s hypothesis of the advantaged daughter, proposed for species in which mothers are able to influence the reproductive success of their daughters through transmission of rank.


2018 ◽  
Vol 96 (7) ◽  
pp. 760-768 ◽  
Author(s):  
J.A. Dellinger ◽  
C.R. Shores ◽  
M. Marsh ◽  
M.R. Heithaus ◽  
W.J. Ripple ◽  
...  

There is growing recognition that humans may mediate the strength and nature of the ecological effects of large predators. We took advantage of ongoing gray wolf (Canis lupus Linnaeus, 1758) recolonization in Washington, USA, to contrast adult survival rates and sources of mortality for mule deer (Odocoileus hemionus (Rafinesque, 1817)) and white-tailed deer (Odocoileus virginianus (Zimmermann, 1780)) in areas with and without wolf packs in a managed landscape dominated by multiple human uses. We tested the hypothesis that the addition of wolves to the existing predator guild would augment predator-induced mortality rates for both ungulates. Source of mortality data from adult mule deer and white-tailed deer, respectively, revealed that wolf-related mortality was low compared with that inflicted by other predators or humans. Predator-caused mortality was largely confined to winter. There was little effect of wolf presence on adult deer mortality rates, and there was no difference in mortality between the two deer species relative to wolf-free or wolf-occupied sites. Although this study occurred early in wolf recovery in Washington, our results differ from those demonstrated for gray wolves in protected areas. Thus, we encourage further investigation of effects of direct predation by recolonizing large carnivores on prey in human-dominated landscapes.


2013 ◽  
Vol 126 (3) ◽  
pp. 238 ◽  
Author(s):  
Shannon Barber-Meyer

Whereas dental injuries and abnormalities have been documented in Gray Wolves (Canis lupus), severe maxillary necrosis has not previously been implicated in a Gray Wolf fatality. Here I report maxillary osteomyelitis in a wild Gray Wolf from northeastern Minnesota of such severity that I hypothesize it ultimately led to death by starvation.


2021 ◽  
Author(s):  
Jun Gojobori ◽  
Nami Arakawa ◽  
Xiaokaiti Xiayire ◽  
Yuki Matsumoto ◽  
Shuichi Matsumura ◽  
...  

The Japanese wolf (Canis lupus hodophilax Temminck, 1839) was a subspecies of the gray wolf that inhabited the Japanese Archipelago and became extinct 100-120 years ago. In this study, we determined the whole genomes of nine Japanese wolves from the 19th- early 20th centuries and 11 Japanese dogs and analyzed them along with both modern and ancient wolves and dogs. Genomic analyses indicate that the Japanese wolf was a unique subspecies of the gray wolf that was genetically distinct from both modern and ancient gray wolves, lacking gene flow with other gray wolves. A Phylogenetic tree that minimizes the effects of introgression shows that Japanese wolves are closest to the dog monophyletic group among the gray wolves. Moreover, Japanese wolves show significant genetic affinities with East Eurasian dogs. We estimated the level of introgression from the ancestor of the Japanese wolves to the ancestor of East Eurasian dogs that had occurred in the transitional period from the Pleistocene to the Holocene, at an early stage after divergence from West Eurasian dog lineages. Because of this introgression, Japanese wolf ancestry has been inherited by many dogs through admixture between East Eurasian dog lineages. As a result of this heredity, up to 5.5% of modern dog genomes throughout East Eurasia are derived from Japanese wolf ancestry.


2018 ◽  
Vol 14 (1) ◽  
pp. 20170613 ◽  
Author(s):  
Susumu Tomiya ◽  
Julie A. Meachen

Recent advances in genomics and palaeontology have begun to unravel the complex evolutionary history of the gray wolf, Canis lupus . Still, much of their phenotypic variation across time and space remains to be documented. We examined the limb morphology of the fossil and modern North American gray wolves from the late Quaternary (< ca 70 ka) to better understand their postcranial diversity through time. We found that the late-Pleistocene gray wolves were characterized by short-leggedness on both sides of the Cordilleran–Laurentide ice sheets, and that this trait survived well into the Holocene despite the collapse of Pleistocene megafauna and disappearance of the ‘Beringian wolf' from Alaska. By contrast, extant populations in the Midwestern USA and northwestern North America are distinguished by their elongate limbs with long distal segments, which appear to have evolved during the Holocene possibly in response to a new level or type of prey depletion. One of the consequences of recent extirpation of the Plains ( Canis lupus nubilus ) and Mexican wolves ( C. l. baileyi ) from much of the USA is an unprecedented loss of postcranial diversity through removal of short-legged forms. Conservation of these wolves is thus critical to restoration of the ecophenotypic diversity and evolutionary potential of gray wolves in North America.


2010 ◽  
Vol 124 (3) ◽  
pp. 215 ◽  
Author(s):  
L. David Mech ◽  
H. Dean Cluff

Dominance is one of the most pervasive and important behaviors among wolves in a pack, yet its significance in free-ranging packs has been little studied. Insights into a behavior can often be gained by examining unusual examples of it. In the High Arctic near Eureka, Nunavut, Canada, we videotaped and described an unusually prolonged and intensive behavioral bout between an adult male Gray Wolf (Canis lupus) and a male member of his pack, thought to be a maturing son. With tail raised, the adult approached a male pack mate about 50 m from us and pinned and straddled this packmate repeatedly over 6.5 minutes, longer than we had ever seen in over 50 years of studying wolves. We interpreted this behavior as an extreme example of an adult wolf harassing a maturing offspring, perhaps in prelude to the offspring's dispersal.


1991 ◽  
Vol 69 (5) ◽  
pp. 1183-1188 ◽  
Author(s):  
Phyllis K. Kennedy ◽  
Michael L. Kennedy ◽  
Peter L. Clarkson ◽  
Ilme S. Liepins

The genetic variability of gray wolves (Canis lupus) from northwestern Canada was assessed through starch-gel electrophoresis. Of 27 protein systems examined, 25, representing 37 presumptive loci, were consistently scorable; 7 proteins (5 were consistently scorable) exhibited polymorphism. The level of heterozygosity (3.0%) was medial relative to values reported for natural populations of Carnivora and high relative to values reported for natural populations of canids. An overall pattern of few deviations from Hardy–Weinberg expectations and some spatial heterogeneity was observed. Wolves associated with different caribou herds exhibited a low level of differentiation (FST = 0.029). The pattern of variability supports the view of a large panmictic population resulting from extensive movements of individuals and packs and from natural and human impacts on pack structure and formation.


2005 ◽  
Vol 83 (2) ◽  
pp. 312-323 ◽  
Author(s):  
Juan Carlos Blanco ◽  
Yolanda Cortés ◽  
Emilio Virgós

We examined the effect of two kinds of barriers on an expanding gray wolf, Canis lupus L., 1758, population in an agricultural habitat in north-central Spain. The barriers were (i) a four-lane fenced highway along a flat area without wildlife-crossing facilities, and (ii) the River Duero Artery (RDA), comprising the river itself (50–100 m wide) and several small infrastructures along it. From March 1997 to October 2001, all 4 radio-collared wolves living <15 km from the highway (1 adult territorial male, 1 territorial breeder female, 1 dispersing male, and 1 female in 3 periods of her life (territorial immature, disperser, and territorial breeder) crossed it on between 4% and 33% of 45–163 monitoring days via vehicle bridges. Moreover, 4 more highways that we monitored in areas without radio-collared wolves have not delayed expansion of the increasing wolf population, suggesting that these highways are not an important barrier for wolves in our study area. In contrast, only 3 of 8 wolves radio-collared <5 km from the RDA were detected crossing it, and 2 of those 3 started to cross it only after severe habitat disturbance; in addition, the RDA seems to have delayed wolf expansion for some 15 years, which suggests that it is a semipermeable barrier for wolves. We discuss the likely consequences of the RDA on the recovery of the Iberian wolf population.


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