Why are American mink sexually dimorphic? A role for niche separation

American mink are highly sexually dimorphic, with males being up to twice the size of females. Sexual dimorphism may arise for several reasons, including intra- or inter-sexual selection, inter-sexual competition, or divergent reproductive roles. Whether or not dimorphism arises from competition, a degree of niche separation is expected in dimorphic species. Sexual divergence in feeding niche has been reported for many species, including mink. This is likely to be manifested in a greater degree of dimorphism in those structures, such as teeth, that are used for the acquisition of prey. We tested the hypothesis that teeth and other trophic structures of male mink would be significantly larger than those of females, after controlling for underlying skeletal size differences. Canine and carnassial teeth, and several skull dimensions, were larger than predicted in males. There is good evidence that sexual dimorphism in mink trophic apparati is greater than predicted from allometry. We examined the development of dimorphism in various features with age and found that it was not consistent. Several trophic features were dimorphic amongst juveniles, and the degree of dimorphism remained relatively constant with age. Dimorphism in canines, and in relative body mass, was less apparent amongst juveniles and increased with increasing age. We discuss our results in the light of contemporary theories on the evolution and maintenance of sexual size dimorphism and argue that niche separation as a result of dimorphism in trophic features, while probably not the driving force behind sexual size dimorphism, may play a role in its maintenance.     

老年心功能不全患者mink S38G多态性与房颤的相关性

探讨老年慢性心功能不全患者中,心肌细胞Iks通道β亚单位基因mink-S38G多态性与心房颤动（atrial fibrillation, AF）发生的相关性.收集慢性心功能不全患者共127例,其中房颤组63例,窦律组64例.采用聚合酶链反应限制性片段长度多态性（restriction fragment length polymorphism, PCR—RFLP）检测房颤组和窦律组的mink基因S38G多态性位点的基因型.房颤组与窦律组之间minkS38G的3种基因型频率为SS(9.52% vs 23.44%),SG(41.27% vs 50.00%),GG(49.21% vs 26.56%).在房颤组中,GG基因型的频率明显高于窦律组,两组间基因型存在明显差异, P=0.013;多因素Logistic回归提示,minkS38G多态性与房颤的发生有明显相关（P=0.010）.因此,在老年慢性心功能不全患者中,mink基因S38G多态性与房颤的发生有关,具有GG基因型的患者其发生房颤的风险较高     

The mink gene for the λ light immunoglobulin chain: Characterization of cDNA and chromosomal localization

A cDNA library from mink spleen was constructed by use of the phage gt11. The library was screened using polyvalent serum raised against the mink immunoglobulin chain. As a result, several clones expressing mink immunoglobulin light chains were identified. Sequencing of one of the clones with an 803 bp insert was performed. The insert comprised nearly the entire coding region for the mature light immunoglobulin gene with the exception of the leader polypeptide and several amino acids of the RF1 region of the V segment. Compared with the rabbit, mouse and human light immunoglobulin genes, the homology of the cloned sequence was found to be highest relative to the rabbit gene. With the cloned mink cDNA containing the C-region only as a probe, the DNAs from mink-Chinese hamster hybrid clones were studied. The results of segregation analysis of this mink cDNA sequence and mink chromosomes in the mink-Chinese hamster clone panel allowed us to assign the gene for the light immunoglobulin constant polypeptide (IGLC) to mink Chromosome (Chr) 4.     

Localization of the α2-macroglobulin gene and Lpm gene family on mink chromosome 9

Summary Using cloned cDNA for human ₂-macroglobulin (A2M) as a probe, mink-Chinese hamster hybrid cells were analysed. The results allowed us to assign a gene for A2M to mink chromosome 9. Breeding tests demonstrated that the Lpm-locus coding for other related -macroglobulin protein and the gene for peptidase B (PEPB) are linked 11±3 cm apart. The PEPB gene is located on mink chromosome 9, and hence, the Lpw-locus is on the same mink chromosome. The relationship of the genetic systems controlling the isotypically different -macroglobulins in mink serum are discussed.     

Energy intake and milk production in mink (MUSTELA vison)‐effect of litter size

Energy intake and milk production were measured in 12 mink dams raising litters of 3, 6 and 9 kits one to four weeks post partum by means of balance experiments and measurements of milk intake of the kits by the water isotope dilution technique. The dams were fed ad libitum on a conventional wet mink diet (DM: 323 g/kg; CP: 173 g/kg; ME: 4.4 MJ/kg). Milk samples collected from dams with corresponding litter sizes and lactation weeks, and body composition of kits nursed by these dams, were analysed for content of DM, ash, N and fat. The ME and drinking water consumption were higher in dams nursing 9 kits than in dams nursing 3 kits. The N and water balances as well as the live weight of dams were not affected by litter size. Daily milk production was higher in dams nursing 9 kits than in dams nursing 3 kits. The DM, N and fat content of the milk increased during lactation, but were not affected by litter size. Individual kit live weight was higher in litters of 3 than in litters of 6 and 9 kits four weeks post partum. The DM and fat content of the kits were lowest in kits from litters of 9 kits, whereas these kits had the highest protein content. Daily ME for maintenance of kits and the efficiency of utilisation of ME in milk for body gain were estimated to 356 kJ/kg^0.75, k_p ≈0.53 and k_f ≈0.71, respectively. In conclusion, daily milk production increased with increasing litter size, but not in proportion to the number of kits, indicating that milk production limits the growth rate of the young. In the fourth week of lactation, milk production was not different between dams nursing 6 or 9 kits, indicating a maximum capacity.     

Do alien North American mink compete for resources with native South American river otter in Argentinean Patagonia?

American mink Mustela vison , originally bred in fur farms, have become established in areas occupied by native endangered Southern river otter Lontra provocax , in Patagonia. In accordance with European experience, this biological invasion in South America raises questions about the interaction between invasive mink and native otter, from the viewpoints of both community assembly and conservation. We set out (1) to find which aspects of habitat structure were related to the distribution of signs of both this invasive species and Southern river otter Lontra provocax , in Argentinean Patagonia and their most common prey and (2) to test general predictions of niche partitioning between these two species. Based on surveys of 447 of 600 m transects for otter and mink scats/footprints along the waterside of lakes and rivers in the Andean Patagonian region, we compared diet composition (from scat analysis) and micro-habitat preferences (from field signs) of the two species. Otters were more specialist than mink in habitat use and diet. Mink used different habitats in other river basins where otters were absent. Where they occurred together in the basin of the Limay River, the distributions of their signs were similar, and mink diet was more similar to that of otters. There was no detectable difference in otter diet before and after mink arrival in the Limay basin. Contrary to the prediction of niche partitioning, and to the findings of European studies, resource use by mink was more similar to that of otters where the species occurred sympatrically than where they were allopatric.     

Immunogenetic study on the polymorphism of serum α2-lipoprotein in mink. III. Ld1 allotype of low-density lipoprotein

Mink Ld1 antigen of serum low-density lipoprotein was demonstrated by alloantibodies. No genetic relation was found between Ld1 and the Lpm system of very-high-density lipoprotein. The existence of an autosomal dominant gene, coding for the new alloantigenic marker, is postulated on the basis of mink breeding data.     

Immunogenetic study on the polymorphism of serum α2-lipoproteins in mink. I. Identification and genetic control of five Lpm allotypes

Five allotypes, Lpm 1, Lpm 2, Lpm 3, Lpm 4, and Lpm 5, were detected by isoimmunization in mink sera. Immunoelectrophoresis, preparative ultracentrifugation, and histochemical tests for lipids and esterase permitted reference of these alloantigenic markers to a very high density ₂-lipoprotein. Based on population analysis and breeding tests, five genetic units are postulated: Lpm ¹, Lpm⁴, Lpm^3,4, Lpm^1,2, and Lpm ^2,4,5. These units determine the polymorphism of the Lpm system and behave as Mendelian alleles.     

Relative abundance of culled and not culled American mink populations in northeast Spain and their potential distribution: are culling campaigns effective?

The effectiveness of culling campaigns to eradicate or limit populations of the alien, invasive American mink in Catalonia was studied by comparing the annual relative abundance of culled versus non-culled populations. We selected three populations that were culled under government campaigns and a fourth that served as a control and hence was left undisturbed (not culled). The study took place between 2002 and 2006 and annual relative abundances were estimated from trapping with bankside traps. The abundance of all four populations remained relatively stable throughout the study period. However, the annual relative abundance of the culled populations was lower than that of the non-culled population, which indicates that culling may have lowered the densities of mink, although eradication was not achieved. We also determined the potential distribution of the American mink in Catalonia by means of a habitat suitability model. The final aim was to assist in planning this species’ management. Almost all watercourses in Catalonia were identified as suitable for the American mink, with preferred areas located in the northeast. We recommend that the government and administrations promote culling campaigns focused on limiting the spread of the American mink as eradication is likely to be difficult to be achieved under the current situation. Target areas should be located on the edges of the American mink’s range and should be prioritized to limit the spread of this species to areas in which there are endangered native species.     

Immunogenetic study on the polymorphism of serum α2-lipoproteins in mink. IV. Diallelism at the Ld locus of low-density lipoprotein

Antibodies against a new allotype, Ld2, of mink low-density lipoprotein (LDL) were obtained by alloimmunization with a preparation of this lipoprotein. The two known allotypes of LDL, designated Ld1 and Ld2, are coded for by codominant alleles of the autosomal Ld locus. This locus is probably involved in the genetic control of the whole serum pool of LDL molecules. In Ld1/Ld2 heterozygotes, LDL is represented by two homozygous types of molecules, Ld1 and Ld2; it has no hybrid molecules bearing both allotypic specificities together. The results suggest that the Ld locus has, presumably, only two alleles in the mink populations studies. Mink LDL having allotypes Ld1 and Ld2 was found to be homologous to human and pig LDLs. Antigenic specificity of Ld1 allotype was established in the sera of a wide phylogenetic range of mammals and in the human LDL. The parallelism between the phylogenetic antiquity of the Ld1 gene and its high frequency in mink and other species may be attributed to the selective value of this gene, which has been retained unaltered during macroevolution.     

A synergistic trio of invasive mammals? Facilitative interactions among beavers,muskrats, and mink at the southern end of the Americas

With ecosystems increasingly having co-occurring invasive species, it is becoming more important to understand invasive species interactions. At the southern end of the Americas, American beavers (Castor canadensis), muskrats (Ondatra zibethicus), and American mink (Neovison vison), were independently introduced. We used generalized linear models to investigate how muskrat presence related to beaver-modified habitats on Navarino Island, Chile. We also investigated the trophic interactions of the mink with muskrats and beavers by studying mink diet. Additionally, we proposed a conceptual species interaction framework involving these invasive species on the new terrestrial community. Our results indicated a positive association between muskrat presence and beaver-modified habitats. Model average coefficients indicated that muskrats preferred beaver-modified freshwater ecosystems, compared to not dammed naturally flowing streams. In addition, mammals and fish represented the main prey items for mink. Although fish were mink’s dominant prey in marine coastal habitats, muskrats represented >50 % of the biomass of mink diet in inland environments. We propose that beavers affect river flow and native vegetation, changing forests into wetlands with abundant grasses and rush vegetation. Thus, beavers facilitate the existence of muskrats, which in turn sustain inland mink populations. The latter have major impacts on the native biota, especially on native birds and small rodents. The facilitative interactions among beavers, muskrats, and mink that we explored in this study, together with other non-native species, suggest that an invasive meltdown process may exist; however further research is needed to confirm this hypothesis. Finally, we propose a community-level management to conserve the biological integrity of native ecosystems.     

Assessing the control/eradication of an invasive species,the American mink,based on field data; how much would it cost?

Biological invasions are an important cause of biodiversity loss, American mink being one of the worst invasive species in Europe. We performed a 13-week control program of the species in the Butron river system (Northern Spain), where a natural population of the European mink is found. Three population estimates were considered: an absolute minimum, an intermediate scenario and a pessimistic one (n = 35, 49 and 70 animals, respectively). After 2,242 cage trap-nights, trapping success varied from 44 to 89% of these estimates. In addition, we evaluated the costs of eradicating the estimated populations; costs ranged between 652.5 and 2,970 € per mink, and would rise up to 83,462 € for the intermediate estimate under an exponential function linking captures and costs, or ca. 172.500 € to capture the highest estimate under a log-function. The implications of these numbers for the design and implementation of future control projects are discussed.     

Mustela or Vison? Evidence for the taxonomic status of the American mink and a distinct biogeographic radiation of American weasels

The American mink’s relationship to the weasels in Mustela has been uncertain. Karyological, morphological, and phylogenetic comparisons to Eurasian Mustela support placing the mink outside the genus as Neovison vison. However, genetic comparisons that incorporate other endemic American Mustela suggest the interpretation of N. vison’s position to Mustela has been handicapped by biased geographic sampling. Here, we analyzed mitochondrial cytochrome-b from all weasels endemic to the Americas, including two poorly known South American species (M. felipei, M. africana), weasels native to North America (M. vison, M. frenata, M. nigripes), Mustela migrant to North America (M. erminea, M. nivalis), palearctic Mustela, and other American members of Mustelidae. Bayesian and likelihood inference methods were used to construct a phylogeny of Mustela, and relaxed Bayesian phylogenetic techniques estimated ages of divergence within the genus using priors calibrated by fossil ages. Our analyses show that the American mink and the smaller Mustela endemic to the Americas represent a distinct phylogenetic heritage apart from their Eurasian cousins, and biogeographic barriers like the Bering and Panamanian land bridges have influenced the evolutionary history of Mustela in the Americas.     

Radio tagging American mink (<Emphasis Type="Italic">Mustela vison</Emphasis>)—experience with collar and intraperitoneal-implanted transmitters

American minks (Mustela vison) are difficult to radio tag because of their similar head and neck circumference as well as their semi-aquatic and frequently subterranean behaviour patterns. During a radio-telemetry study of American mink, we compared collar transmitters and intraperitoneal-implanted transmitters with reference to animal welfare and practicability in the field. Between October 2003 and March 2004, we fitted eight minks with collar transmitters. Six showed serious neck injuries caused by carrying the radio collars. From April 2004 to June 2005, radio transmitters were surgically implanted in the peritoneal cavity of 14 minks by veterinarians. After surgery, the observation of mink in a quarantine cage for 72 h appeared adequate to ensure that they do not attack the sutures. During quarantine, minks were calm and took the offered food (fresh carp). The replacement of five failed implanted transmitters after 2–10 months revealed that the transmitters were floating freely in the peritoneal cavity, and no local reactions were observed. Except for one male, intraperitoneal implants do not appear to affect short-term survival or reproductive potential of minks. For long-term telemetry studies, we recommend implanted transmitters instead of external radio collars to radio tag American minks.     

Chromosome localization of the genes for ENO1, HK1, ADK,ACP2, MPI,ITPA, ACON1 and α-GAL in the American mink (Mustela vison)

Summary Twenty-eight American mink × Chinese hamster somatic cell hybrids were analysed for the expression of mink enzymes and the segregation of mink chromosomes. The results demonstrated that the gene for enolase-1 is located on the long arm of mink chromosome 2, and those for hexokinase-1 and adenosine kinase, on its short arm. Segregation analysis of mink chromosomes and mink acid phosphatase-2, mannose phosphate isomerase, inosine triphosphatase and aconitase-1 provided data allowing us to assign the genes for these markers to mink chromosomes 7, 10, 11 and 12, respectively. The expression of mink -galactosidase was highly coincidental with mink × chromosome as well as with its markers: hypoxanthine-phosphoribosyltransferase, glucose-6-phosphate dehydrogenase and phosphoglycerate kinase-1. This result confirms the assignment of the gene for -galactosidase to the mink × chromosome.     

MHC class II variation in the endangered European mink <Emphasis Type="Italic">Mustela lutreola</Emphasis> (L. 1761)—consequences for species conservation

The polymorphic major histocompatibility complex (MHC) has gained a specific relevance in pathogen resistance and mate choice. Particularly the antigen-binding site (ABS), encoded by exon 2 of the DRB class II gene, exhibits numerous alleles and extensive sequence variations between alleles. A lack of MHC variability has attributed to instances such as bottleneck effects or relaxed selection pressure and has a certain impact on the long-term viability of the species concerned. As a result of seriously decreased population density during the last century, the current population of the endangered European mink (Mustela lutreola, L. 1761) has suffered from geographic isolation. In this study, we amplified a partial sequence of the MHC class II DRB exon 2 (229 bp), assessed the degree of genetic variation and compared the variability with those of other Mustelidae. As a result, nine alleles were detected in 20 investigated individuals, which differ from each other by four to 25 nucleotide substitutions (two to 11 amino acid substitutions). Whilst an equal ratio for synonymous and non-synonymous substitutions was found inside the ABS, synonymous substitutions were significantly higher than non-synonymous substitutions in the non-ABS region. Results might indicate that no positive selection exists within the ex situ population of M. lutreola, at least in the analysed fragment. In addition, phylogenetic analyses support the trans-species model of evolution. Becker and Nieberg have contributed equally to this work.     

Immunogenetic study on the polymorphism of serum α2-lipoproteins in mink. II. Identification of allotypes Lpm-7 and Lpm-8 and genetic control of seven markers of the Lpm system

By means of alloimmunization of mink, two new antigens, Lpm-7 and Lpm-8, were detected in their sera. Lpm-7 and Lpm-8 allospecificities were referred to a very high density ₂-lipoprotein (Lpm) by the following criteria: histochemical tests, immunoelectrophoresis, preparative ultracentrifugation, and coalescence of alloprecipitates with heteroprecipitates in double diffusion tests. Genetic analysis indicated that Lpm-7 and Lpm-8, together with the earlier described Lpm-1, Lpm-2, Lpm-3, Lpm-4, and Lpm-5, share a common immunogenetic system. Polymorphism for the seven markers is conditioned by the genetic units Lpm ⁸, Lpm ⁴, Lpm ^{4, 8}, Lpm ^{4, 7}, Lpm ^{3, 4, 8}, Lpm ^{1, 8}, Lpm ^{1, 2, 7}, and Lpm ^{2, 4, 5, 7}, which behave as alleles. Of these units, the latter six are probably haploid sets of closely linked genes.