Ultrastructure and Nanomorphology of the American Mink (Mustela vison) Kidney.

The ultrastructure of the nephron subcellular organelles was studied in healthy mink kidneys. The data obtained were compared with the results of transmission electron microscopy. The renal cell nanomorphology proved to be similar when electronograms and the atomic force microscopy images were analyzed. The methods used enabled us to visualize the glomerular capillary endotheliocytes with cytolemma pits in the area of fenestrae that provide blood filtration; in the proximal nephron part, on the apical pole of the epithelial cells, brush-border soft microvilli were observed. The microvilli were characterized by a well-organized structure along their entire length and the membrane integrity. The data obtained show morphological parameters of the healthy mink organ and can be helpful in diagnosing of nephropathology.

Comparative morphology of the lingual papillae and their connective tissue cores in the tongue of the American mink, Neovison vison.

We observed the morphology of the lingual papillae (filiform, conical, fungiform, and vallate papillae, and lateral organ) and their connective tissue cores (CTCs) in the American mink (Neovison vison) using light and scanning electron microscopy. Filiform papillae were distributed on the apex linguae and rostral regions of the corpus linguae. Conical papillae were distributed over the caudal region and absent in the radix linguae. Numerous ridges were present in the radix linguae. Four to six vallate papillae were situated at the border between the corpus and radix linguae. Instead of foliate papillae, a pair of lateral organs was situated on the caudal edge of the corpus. The epithelial surface of each filiform papilla consisted of a single main process and 10-12 accessory processes. Notably, filiform papillae in the apex linguae exhibited morphological variation, and some were dome-like and lacked processes. In contrast, filiform papillae on the rostral part were not variable, were extended to a sharp tip, were associated with an eosinophilic stratum corneum, and lacked nuclei. The CTCs of the filiform papillae consisted of a main core and slender accessory cores surrounding a concavity. Those in the apex linguae were similar in appearance and consisted of main and adjacent accessory cores. The fungiform papillae had a dome-like epithelial surface and their CTCs were columnar, with upper concavities and flanges. The simplified lingual morphology of the American mink, particularly in the filiform papillae in the apex linguae, may be influenced by its diet and semiaquatic lifestyle.

[Odontologic anomaly in the American mink Neovison vison (Carnivora, Mustelidae) and possible reasons for its appearance].

The paper describes the phenomenon of substitution of the reduced M2 with a tooth of a complex structure in the American mink Neovison vison Schreber. The anomaly is observed on three skulls out of the 574 examined (0.52%) and is characterized by a clear localization, identical structure, and symmetrical manifestation. Atypical molars have two roots, equally well-developed paraconid, eokonid, hypoconid, and a less pronounced metaconid. Some possible hypotheses for the anomaly that are considered include disruption in the development of the dental germ, mutation, and phenotypic expression of genes that are characteristic of plesiomorphic species of mustelids. The substantiated viewpoint is that the cause of this phenomenon may be the "awakening of dormant genes" as a result of destabilizing selection and hybrid dysgenesis in the area of contact of farm and feral American minks.

Genome analysis of American minks reveals link of mutations in Ras-related protein-38 gene to Moyle brown coat phenotype.

Over 35 fur colours have been described in American mink (Neovison vison), only six of which have been previously linked to specific genes. Moyle fur colour belongs to a wide group of brownish colours that are highly similar to each other, which complicates selection and breeding procedures. We performed whole genome sequencing for two American minks with Moyle (m/m) and Violet (a/a m/m /p/p) phenotypes. We identified two frame-shift mutations in the gene encoding Ras-related protein-38 (RAB38), which regulates the trafficking of tyrosinase-containing vesicles to maturing melanosomes. The results highlight the role of RAB38 in the biogenesis of melanosomes and melanin and the genetic mechanism contributing to hair colour variety and intensity. These data are also useful for tracking economically valuable fur traits in mink breeding programmes.

The number of neurons in specific amygdala regions is associated with boldness in mink: a study in animal personality.

Conspecifics vary consistently in their behavioural responses towards environment stimuli such as exposure to novel objects; ethologists often refer to this variability as animal personality. The neurological mechanisms underlying animal personality traits remain largely unknown, but linking the individual variation in emotional expression to brain structural and neurochemical factors is attracting renewed interest. While considerable research has focused on hormonal and neurotransmitter effects on behavioural responses, less is known about how individual variation in the number of specific neuron populations contributes to individual variation in behaviour. The basolateral amygdala (BLA) and the central nuclei of the amygdala (CeA) mediate emotional processing by regulating behavioural responses of animals in a potentially threatening situation. As such, these structures are good candidates for evaluating the relationship between neuronal populations and behavioural traits. We now show that individual American mink (Neovison vison) reacting more boldly towards novelty have more neurons in the BLA than do their more timid conspecifics, suggesting that a developmental pattern of the number of amygdala neurons can influence behavioural traits of an adult animal. Furthermore, post hoc correlations revealed that individuals performing with higher arousal, as reflected by their frequency of startle behaviour, have more CeA neurons. Our results support a direct link between the number of neurons in amygdala regions and aspects of animal personality.

Serial homology and the evolution of mammalian limb covariation structure.

The tetrapod forelimb and hindlimb are serially homologous structures that share a broad range of developmental pathways responsible for their patterning and outgrowth. Covariation between limbs, which can introduce constraints on the production of variation, is related to the duplication of these developmental factors. Despite this constraint, there is remarkable diversity in limb morphology, with a variety of functional relationships between and within forelimb and hindlimb elements. Here we assess a hierarchical model of limb covariation structure based on shared developmental factors. We also test whether selection for morphologically divergent forelimbs or hindlimbs is associated with reduced covariation between limbs. Our sample includes primates, murines, a carnivoran, and a chiropteran that exhibit varying degrees of forelimb and hindlimb specialization, limb size divergence, and/or phylogenetic relatedness. We analyze the pattern and significance of between-limb morphological covariation with linear distance data collected using standard morphometric techniques and analyzed by matrix correlations, eigenanalysis, and partial correlations. Results support a common limb covariation structure across these taxa and reduced covariation between limbs in nonquadruped species. This result indicates that diversity in limb morphology has evolved without signficant modifications to a common covariation structure but that the higher degree of functional limb divergence in bats and, to some extent, gibbons is associated with weaker integration between limbs. This result supports the hypothesis that limb divergence, particularly selection for increased functional specialization, involves the reduction of developmental factors common to both limbs, thereby reducing covariation.

Effect of pre-fixation delay and freezing on mink testicular endpoints for environmental research.

There is growing interest in using wild animals to monitor the real-life cocktail effect of environmental chemicals on male reproduction. However, practical difficulties, such as long distances to the laboratory, generally prolong the time between euthanisation and specimen handling. For instance, tissue fixation is often performed on frozen material or on material where deterioration has started, which may affect tissue morphology. This study examined the effect of pre-fixation delay and freezing on mink testicular endpoints in order to determine robust endpoints in suboptimally handled specimens. Sexually mature farmed mink (n=30) selected at culling were divided into six groups and subjected to different time intervals between euthanisation and fixation or freezing: 0 hours (fixed immediately post mortem), 6 hours, 18 hours, 30 hours, 42 hours, or frozen 6 hours post mortem and thawed overnight. Unaffected endpoints when pre-fixation storage was extended to 30 hours included: area and diameter of the seminiferous tubules, length and weight of the testes, and acrosomes marked with Gata-4. Epithelial height, Sertoli cells marked with Gata-4 and cell morphology were affected endpoints after 6 hours of storage. Freezing the tissue prior to fixation severely altered cell morphology and reduced testicular weight, tubular diameter and area. Morphological changes seen after 6 hours included shredded germ cells and excess cytoplasm in seminiferous tubular lumen, chromatin rearrangements and increased germ cell death. Extended delay before fixation and freezing affected many endpoints in the mink testicular tissue. Some of these endpoints may mimic chemically induced effects, which is important to consider when evaluating specimens from wild animals for environmental toxicity.

Anatomy of the retina of the mink (Mustela vison).

The retina of the normal pigmented mink has been studied by light and electron microscopy. This retina resembles the typical vertebrate retinia in its patterns of lamination and synaptic interconnectivity. Rod and cone outer segments and receptor spherule and pedicle endings are found. At least two different types of horizontal cell processes are seen with the electron microscope, suggestive of rabbit A and B types. Ribbon and conventional synapses are found in both plexiform layers; conventional synapses are also present in the inner nuclear layer. Quantitative studies of the inner plexiform layer revealed amacrine:bipolar synapse ratios (3.3:1) similar to those of the cat and monkey. Other quantitative parameters also resembled those previously reported for species with retinas that predominantly contain concentric-type receptive fields.

Abnormal retino-geniculate and geniculo-cortical pathways in several genetically distinct color phases of the mink (Mustela vison).

Several genetically distinct color phases of mink, which all show an abnormal reduction of pigment in the retinal pigment epithelium and which also show abnormalities of the retinofugal pathways, have been studied. Autoradiographic methods have been used to demonstrate the retino-geniculate pathways, and retrograde degeneration or the retrograde transport of horseradish peroxidase has been used for the geniculo-cortical pathways. The retino-geniculate abnormality is mild in some of the color phases and extremely severe in others, but within any one color phase the variability is relatively low. Although the severity of the abnormality varies between color phases, a rather specific pattern of abnormal geniculate innervation is recognizable for mink in general and this is distinct from that found in Siamese cats. In the abnormal mink the size of geniculate lamina A1 is reduced and there is an abnormal crossed input going to the intermediate sectors of this reduced layer. Layer C1 also receives an abnormal crossed input, but this is more variable than that going to A1 and there appears to be little correspondence, retinotopically, between the normal inputs to layers A1 and C1. In some of the abnormal mink there are interruptions within the cytoarchitectionically definable layer A1, and opposite these gaps reduplications of layer A are commonly seen, as though there is an intrinsic geniculate mechanism for generating the characteristic multilaminar geniculate structure. However, there are also numerous examples of fusions between layers receiving afferents from the same eye, and these demonstrate that the development of geniculate lamination must also be under the influence of the retinal inputs. The geniculo-cortical pathway shows a normal topography in most of the mink. Abnormal geniculo-cortical projections, comparable to the "Boston" pattern of Siamese cats are extremely rare, and their occurrence could not be correlated with the severity of the retino-geniculate abnormality or with the laminar pattern in the lateral geniculate nucleus. We suggest that the development of one or the other pattern of geniculo-cortical projection may depend upon the relative timing of the two mechanisms that produce the geniculate lamination.

Anatomical organization of the visual system of the mink, Mustela vison.

The organization of the retinogeniculocortical visual system of the mink was studied by anterograde and retrograde tracer techniques, by physiological mapping, and by direct recordings from axonal terminals after injection of kainic acid. In the lateral geniculate nucleus, retinogeniculate afferents are segregated according to eye of origin between the two principal layers, A and A1. Within each of these layers there is a further parcellation according to functional type: on-center afferents terminate in the anterior leaflets of A and A1, and off-center afferents in the posterior leaflets. This separation is preserved in area 17: geniculocortical afferents terminate in ocular dominance patches in layer IV, and these patches coexist with an alternating, partially overlapping set of patches for on-center and off-center inputs that we have demonstrated previously (McConnell and LeVay: Proc. Natl. Acad. Sci. USA 81:1590-1593, '84). In both the lateral geniculate nucleus and in area 17, the contralateral eye predominates to a much greater extent than in the cat. Visual cortical areas corresponding to the cat's areas 17, 18, and 19 can be identified in the mink, but they are shifted posterolaterally in the hemisphere, and they show less emphasis on the representation of central retina. Mapping studies also revealed the existence of a fourth visual area in the splenial sulcus (area SV) adjacent to the representation of the far periphery in area 17. This area differs from the corresponding region in the cat in that it receives direct projections from the lateral geniculate nucleus and from areas 17 and 18. The lateral geniculate nucleus projects to each of the four cortical areas that were mapped. The bulk of the projection to area 17 is derived from the principal layers, A and A1, while most cells projecting to areas 18 and SV are found in the C-layer complex. The recurrent projection from area 17 to the lateral geniculate nucleus arises from pyramidal neurons in layer VI, and terminates through all layers of the lateral geniculate nucleus, but most densely in the interlaminar zones. Areas 18 and SV project predominantly to the C layers. Areas 17, 18, and SV are reciprocally connected with the claustrum and the LP-pulvinar complex, and project to the superior colliculus. All four visual cortical areas are mutually interconnected; these associational projections arise from both the supragranular and infragranular layers.

Vascular interrelationships of near-term mink placenta: light microscopy combined with scanning electron microscopy of corrosion casts.

The microvasculature of the near-term zonary placenta of the mink has been studied using light microscopy and scanning electron microscopy of corrosion casts, prepared from maternal and fetal vessel systems, respectively. The zonary area, most important for placental exchange, includes a characteristic labyrinth. The labyrinth is composed of lobules oriented in a maternal-fetal direction. One maternal stem artery serves as the central axis of a lobule, and about six pairs of fetal stem arteries and stem veins of the chorionic primary villi mark the periphery of the lobule. Viewed from the fetal side of the labyrinth, this lobular structure presents a roughly hexagonal pattern, with the central maternal stem artery and radially oriented arteriolar branches giving the lobule the shape of a star. These arterioles frequently form bridges to neighboring lobular systems; however, the majority continue into the feto-maternally oriented three-dimensional network of maternal capillary sinusoids, which converge on the outlets of the maternal stem veins on the maternal side of the labyrinth. Maternal main crypts are delimited by the rays of the star-shaped lobules containing chorionic primary villi. The latter penetrate into maternal crypts from the fetal side, and are characterized by their axial arterial and venous stem vessels. Fetal secondary villi are arranged at different levels from these stem vessels. The secondary villi are characterized by arterioles and venules branching in pairs from the stem vessels and supply the tributary capillary complexes of terminal villi. The lobular structure of the placental labyrinth provides a three-dimensional framework of vessels where maternal capillary sinusoids and fetal capillaries meet in a one-way cross-current arrangement. The blood flow conditions and the peculiarities of the mink placenta interhemal membrane are compared to those of other carnivores and discussed with respect to the efficiency of the endotheliochorial placenta.

Freeze-fracture study of cell junctions in the epididymis and vas deferens of a seasonal breeder: the mink (Mustela vison).

The present study used the freeze-fracture technique and vascular infusion of horseradish peroxidase (HRP) as a junction permeability tracer, visible in thin sections, to investigate potential seasonal variations in the mink epididymis and vas deferens cell junctions. The junctions were studied in kits during the neonatal period, during and after puberty, and during adulthood monthly throughout the annual reproductive cycle. Results showed the existence, at the time of birth, of a junctional complex joining ductal cells that reached the lumen of the epididymis and vas deferens. The lumenal impermeable segment of the junctional complex was characterized by the presence of an occluding zonule made up of continuous tight junctional ridges extending around the perimeter of the cell. The basal permeable segment of the junctional complex contained mainly discontinuous ridges with frequent forming gap and tight junctions next to adhering junctions. Receding annular junctions were present in the apical and lateral cytoplasm of principal and clear cells. The membrane domain apical to the occluding zonule bore 30-35 nm exo/endocytosis blebs and 40-60 crenations associated with deforming tight and gap junctions made up of randomly scattered particles. Patterns of junctional strands varied greatly from one principal and/or clear cell to another. However, cell junctions did not significantly vary from the neonatal period to adulthood nor from breeding to testicular regression. Anatomical subdivisions of the epididymis with fewer junctional strands per zonule and high diversity in their patterns exhibit no permeability differences to HRP when compared with subdivisions containing more numerous strands. The junctions were impermeable during the neonatal period and throughout the annual reproductive cycle. The following conclusions were reached: 1) a competent occluding zonule developed in the mink epididymis and vas deferens before it did in the testis; 2) the number of strands and the diversity of patterns did not correlate with permeability differences; 3) after the development of a lumen in the testicular excurrent duct, neither receding cellular changes caused by testicular regression nor seasonal passage of a bolus of sperm through the duct modified the occluding zonules; and 4) in the testicular excurrent duct, junction modulation (i.e., formation and deformation) paralleled that in the testis and followed the direction of the synthesis-transport-secretion process.

The form and function of retractile claws in the Felidae and other representative carnivorans.

Recent behavioral studies have shown the primary organ of prehension used in capturing prey to be the claw equipped forelimbs. In light of its functional importance, the claw retractile mechanism for 15 felid species is described and its function studied . The anatomy of the claw retractile mechanism for felids is then compared to that of other carnivorans. For felids,claw retraction is mechanically possible due to the unique shape of the middle and distal phalanges. Claw retraction, however, is a function of the dorsal elastic ligaments and not of the forearm extensor muscles. The resistance provided by these ligaments allows for flexion of the wrist and digital joints without claw protrusion. Moreover, co-contraction of both forearm flexor and extensor muscles is necessary to produce claw protrusion. The functional anatomy of claw retraction for felids differs considerably from that of most other carnivorans. However, the claw retractile mechanism for some advanced viverrids is structurally similar to that of the felids. For these viverrids prey seizing, as in the felids, has become a function of the forelimbs. For the other families of carnivorans, the jaws and not the forelimbs are used as the primary organ of prehension and the anatomy of the claw retractile mechanism reflects functional demands placed on it other than grasping and holding prey.

Cranial variation in British mustelids.

Nineteen measurements were made on 136 skulls belonging to seven mustelid species: Meles meles (Eurasian badger), Mustela nivalis, (weasel), Mustela erminea (stoat), Mustela putorius (polecat), Lutra lutra (otter), Mustela furo (ferret), and Mustela vison (American mink), and polecat-ferret hybrids. To investigate shape, size-related effects were eliminated by dividing all measurements by their geometric means. Canonical variate analysis was used to reveal major interspecies distinctions. Excluding the ferrets and polecat-ferrets from the analysis, only 3.2% of the skulls misclassified (one mink, one weasel, and two stoats). Three groups separated on the first canonical axis: 1) badgers, 2) polecats, mink, and otters, and 3) stoats and weasels. The important variables were width of zygomatic arch and height of sagittal crest opposed to the postorbital distance, condylobasal length, and basilar length. Otters separated out on the second canonical axis; the most important variables were postorbital breadth and width of the postorbital constriction opposed to the basioccipital width. There was reasonable separation of polecats from mink on a combination of the second and third canonical axes. On the latter the most important variables were postorbital breadth opposed to postorbital distance. Addition of the ferret data showed that they lay closest to, and overlapped with, the polecats. The stoat and weasel data alone gave complete separation, with height of sagittal crest and width of zygomatic arch opposed to basioccipital width. However, using size-in data the best separation was the relationship between postorbital breadth and either basioccipital width or postorbital distance. Sexual dimorphism was demonstrated in the skulls of badgers but was shown to be relatively insignificant when compared to the interspecific differences.

Uhl's anomaly in the mink. Partial absence of the right atrial and ventricular myocardium.

Congenital marked hypoplasia of the right atrial and ventricular myocardium (Uhl's anomaly), without other cardiac anomalies, was observed at autopsy in a mink. The animal died unexpectedly without previous symptoms at the age of 2 years, suggesting that the cause of sudden death was acute congestive heart failure. This cause demonstrates that this malformation can occur in species other than man. Embryologically, this anomaly might be due to myocardial injury to the right cardiogenic fold at a relatively early stage of embryogenesis.

Presence of mammosomatotropic (MS) cells in mink (Mustela vison) adenohypophysis.

This study was undertaken to investigate the presence of mammosomatotrophs (MS) cells in the suckling mink. Using the double immunolabeling procedure, with colloidal gold as label, we demonstrated the existence of MS cells in these animals. Only one type of MS cells has been observed. These cells showed a great morphological similarity to classic prolactin (PRL) cells. MS cells of suckling mink were pleomorphic in appearance with many processes, their nuclei were irregular and their Golgi apparatus and endoplasmic reticulum were poorly developed. Their secretory granules were small (about 144 nm in mean diameter) and round. Two types of secretory granules have been found: monohormonal including PRL (the more frequent) and growth hormone (GH) (very scanty) granules, and bihormonal granules distributed between the former. We propose that MS cells of the mink, like other species, could represent an intermediate cell type in the transformation process of GH cells into PRL cells.

Comparative anatomy of the vomeronasal cartilage in mammals: mink, cat, dog, pig, cow and horse.

The vomeronasal cartilages of mink, cat, dog, pig, cow and horse were studied by dissection, microdissection and by means of series of transverse sections. In all the species studied the cartilage is of hyaline type and the medial sheet is well-defined and perfectly moulded to the adjacent bone. However, interspecies differences are apparent in the manner in which the medial sheet associates and eventually fuses with the cartilage of the incisive duct; the morphology of the horse vomeronasal cartilage is particularly distinctive in this respect. The lateral sheet of the vomeronasal cartilage, although always present, has a different arrangement in each species studied. Similarly, the gaps in the lateral sheet (corresponding to the opening of the vomeronasal organ) differ among the species studied in form, location and number.

Ultrastructure of the pineal gland of the mink (Mustela vison).

The pineal gland of the mink (Mustela vison) was examined, using light and electron microscopy. Its cellular structure was compared with that of the pineal gland in other mammalian species, including that of a close taxonomic relative, the ferret. The pineal gland of the mink was composed to pinealocytes and neuroglial cells, as well as numerous neuron cell processes and nerve endings, which provide extensive neural input to the pineal gland. A high degree of vascularity, extent of neural innervation, pinealocyte organelles, and presence of extensive pinealocyte processes with secretory granules indicate an active secretory function. This secretory function is postulated to be associated with the onset of the yearly reproductive cycle in the mink.

Mink.

This chapter presents the basic biology and husbandry of mink as they have been used in commercial production units. Clinical laboratory data are summarized. Veterinary care is divided into viral and bacterial diseases along with several noninfectious disease sections.