1. Introduction
Yaks (
Bos grunniens) represent the cornerstone of livestock husbandry in Ganzi Prefecture, Sichuan Province, and are an endemic species of the Qinghai–Tibetan Plateau that has long adapted to extreme environments, serving as indispensable resources for local production and livelihoods [
1,
2]. Renowned for their remarkable physiological resilience, yaks thrive in harsh environments characterized by hypoxia, low temperatures, and intense ultraviolet radiation. However, this adaptation is critically dependent on the internal homeostasis of various essential mineral elements. Deficiencies in these elements impair physiological function and productivity, compromising the efficient development of the regional economy [
3]. Ensuring adequate intake of essential nutrients remains challenging due to the extensive grazing-based livestock systems predominant in the Ganzi region [
4,
5]. Furthermore, seasonal fluctuations in forage availability and regional soil mineral compositions contribute to inconsistent patterns of nutritional deficiency across different pastoral zones. Accurate nutritional assessment necessitates localized sampling and targeted analyses to inform region-specific supplementation strategies. To date, limited studies have systematically evaluated mineral element status in yak calves across varying altitude gradients, and investigations exploring mineral element levels and their interrelationships within the soil–forage–livestock ecosystem in Ganzi Prefecture remain scarce. This study addresses these gaps by providing foundational data to guide targeted nutritional interventions.
Serum analysis is commonly employed to assess mineral status in livestock, as it reflects the current physiological state and enables dynamic monitoring of nutritional or disease responses. Although less frequently utilized, hair analysis offers complementary value by reflecting long-term mineral deposition and metabolic trends [
6]. Hair is easily collected, remains stable during storage, and is suitable for retrospective mineral evaluation. Certain elements, such as zinc and selenium, accumulate at higher concentrations in hair, rendering changes more readily detectable [
7]. Furthermore, studies have demonstrated correlations between mineral levels in hair and serum concentrations of specific elements. Therefore, the combined application of serum and hair analyses provides a more comprehensive assessment of both short-term dynamics and long-term mineral status, particularly within the context of environmental influences such as altitude gradients [
8].
The maintenance of mineral homeostasis, encompassing both macroelements and trace elements, is essential for the health and productivity of livestock [
9]. Soil pH is a core factor influencing forage mineral element bioavailability. For instance, under the specific soil conditions of alpine meadows on the Qinghai–Tibetan Plateau, soil pH may be associated with carbon cycling and nutrient mineralization processes [
10]. Studies have demonstrated that soil pH becomes a key driving factor affecting nutrient release during the later stages of litter decomposition. In alpine meadows, compared with moist soils (e.g., riparian zones), the entire plant community on sunny slopes exhibits the highest forage value [
11]. Studies have demonstrated that the concentrations of macroelements and trace elements in forage directly influence mineral element concentrations in yak serum [
12]. Mineral deficiencies in forage exert profound effects on yak health through the food chain. In the Tianjun region of Qinghai, elevated molybdenum content in forage led to an imbalanced molybdenum-to-copper ratio, inducing secondary copper deficiency in yaks, which manifested as emaciation, unsteady gait, and “swayback” symptoms [
13]. Similarly, insufficient phosphorus content in forage caused “stiff limb disease” in yaks, characterized by emaciation, lameness, and rigid gait [
14]. Numerous studies have confirmed that mineral element concentrations in soil, forage, and livestock exhibit significant regional variations attributable to geological and environmental heterogeneity. Moreover, these elements demonstrate varying degrees of correlation among the three compartments [
15]. The contents and distribution of mineral elements in soils are primarily dependent on the parent materials of naturally developed soils, as well as on vegetation growth and environmental pollution [
16,
17]. In contrast, mineral element concentrations in forage are closely associated with plant species/cultivar, growth and physiological stages, and seasonal and climatic conditions [
18].
This study aimed to investigate the mineral element status of healthy yak calves in Ganzi Prefecture, as well as the mineral element contents in grazing soil and forage. By analyzing eleven key mineral elements in yak hair, serum, soil, and forage samples, this research elucidated deficiency patterns and spatial distribution characteristics along different altitude gradients, and explored the mineral element levels and their interrelationships within the “soil–forage–animal” ecosystem. The findings provide a scientific basis for guiding targeted mineral supplementation and ecological management strategies, thereby supporting yak health and promoting sustainable development of animal husbandry in high-altitude pastoral areas.
4. Discussion
This study investigated mineral element deficiencies in four types of samples (hair, serum, forage, and soil) across seven regions. Deficiencies were more prevalent in hair and serum, involving Na, Mg, S, Cu, Co, and Se. These findings emphasize the importance of developing targeted mineral supplementation strategies for localized deficiencies to safeguard the health and development of yak calves.
Manganese is closely associated with bone formation and reproductive performance in yaks [
3]. Manganese deficiency directly impairs the resistance of yaks to pathogens, leading to issues such as diarrhea [
25]. Mn content in hair was negatively correlated with altitude (r = −0.89,
p < 0.05), with Mn deficiency being more prevalent at higher altitudes. This may be attributed to the fact that higher altitudes are generally characterized by lower temperatures, which weaken soil microbial activity and slow organic matter decomposition, thereby potentially reducing the release of bioavailable manganese (Mn) in the soil and consequently decreasing Mn uptake and accumulation by forage plants. Soil Mn is directly transferred to forage, and as the primary dietary source for yaks, forage Mn content represents the principal determinant of animal Mn intake [
12,
26]. Therefore, Mn deficiency is essentially absent in lower-altitude regions, whereas Shiqu, as a high-altitude area, exhibits a deficiency that warrants appropriate Mn supplementation.
Sodium is an essential electrolyte involved in numerous physiological functions, including fluid balance and cellular activities. Sodium deficiency can lead to lethargy, anorexia, poor coat condition, and severe neurological symptoms in advanced cases [
27]. Our results indicated varying degrees of Na deficiency in hair samples from Jiulong, Seda, Luhuo, and Yajiang, with deficiency rates of 48.1%, 37.5%, 11.7%, and 2%, respectively. The results suggest that the trace element sodium has been chronically deficient in yaks from these four regions. However, serum Na levels in all six regions remained within reference ranges, possibly attributable to recent dietary adjustments. Under natural conditions, soil sodium is released through weathering and leaching processes and subsequently absorbed by plant roots. When soil Na concentrations are elevated, plants tend to accumulate more sodium, which is then ingested by yaks and ultimately reflected in hair. This typical “soil–plant–animal” transfer chain constitutes the fundamental mechanism underlying the positive correlation between soil and hair Na concentrations [
28,
29]. However, the Na deficiency observed in yak hair from Seda County suggests low soil Na levels in this region, likely attributable to intense soil weathering and strong leaching that result in substantial Na loss, thereby reducing plant-available Na [
30].
Calcium (Ca) is one of the most abundant mineral elements in animals, with essential functions in bone and tooth formation, muscle contraction, nerve impulse conduction, and blood coagulation. Hypocalcemia can lead to decreased excitability of systemic muscles, directly increasing the risk of diseases such as ruminal tympany (bloat) and abomasal displacement in cattle [
31]. The serum calcium concentrations in yaks from all five regions in Ganzi Prefecture exceeded the normal reference range. We attribute this observation to the following factors. First, August coincides with the peak growing season of alpine forage, during which the herbage is rich in calcium and yaks exhibit high feed intake. Second, intense solar radiation at high altitudes reaches its annual peak during this period, stimulating substantial cutaneous synthesis of vitamin D in yaks, which markedly enhances the intestinal absorption of calcium from the forage. Consequently, the combined effects of high dietary calcium availability and vitamin D-mediated efficient absorption result in serum calcium levels that exceed the normal physiological average.
Magnesium serves as a cofactor for many enzymes involved in various physiological and biochemical reactions, playing critical roles in cardiovascular protection and skeletal health. Mg deficiency in cattle can cause restlessness, tremors, frothing, and convulsions, compromising animal welfare [
32]. Our findings revealed that Mg content in hair was deficient only in Shiqu, with a remarkably high deficiency rate of 67.0%. In contrast, serum analysis demonstrated varying degrees of Mg deficiency in Luhuo, Shiqu, Ganzi, and Yajiang, with deficiency rates of 39.3%, 32.9%, 9.8%, and 5.0%, respectively. Both hair and serum samples from Shiqu County showed magnesium deficiency, indicating that yaks in this region experience magnesium depletion both chronically and acutely; therefore, moderate magnesium supplementation is recommended. In contrast, the serum magnesium deficiency observed in the other three regions may be attributed to summer conditions, where a marked increase in the temperature-humidity index directly causes a sharp decline in serum magnesium levels in animals [
33]. Furthermore, studies have shown that even when pre-grazing serum magnesium levels appear adequate, exposure to summer pastures or stressful environmental changes (e.g., herd relocation, high temperatures in enclosures) can lead to a rapid decrease in serum magnesium concentration within a short period [
34].
Sulfur constitutes an essential component of sulfur-containing amino acids, participating in protein structure, coenzyme and vitamin synthesis, and connective tissue formation [
35]. Yaks obtain sulfur primarily through forage consumption, and this sulfur is utilized for the synthesis of sulfur-containing amino acids in vivo, which are subsequently transported to hair follicles to support hair growth [
36,
37]. An increase in forage sulfur content directly elevates the available sulfur reserves in yaks, ultimately resulting in a concomitant increase in hair sulfur levels [
38]. The absence of sulfur deficiency in yak hair samples from the Ganzi region (
Table 2) indirectly indicates that forage sulfur content in this region is abundant. However, the sulfur deficiency observed in serum samples from the Ganzi region (
Table 4) may be attributed to excessive intake of or exposure to metal ions (e.g., via feed or the environment); sulfur may bind extensively with metal ions such as silver and copper, forming insoluble sulfide deposits in hair or other tissues, thereby reducing circulating free sulfur and resulting in decreased serum sulfur levels [
39]. In the Jiulong region, sulfur exhibited a positive correlation between soil and serum. This can be explained by the fact that forage plants absorb sulfur from the soil and convert it into sulfur-containing amino acids. During summer, when forage growth is vigorous, yaks consume substantial quantities of herbage, and serum sulfur levels would be expected to rise following digestion and absorption [
40]. However, the slightly subnormal serum sulfur levels observed in the Jiulong region may be attributed to excessive intake of or exposure to metal ions (e.g., via feed or the environment), a situation similar to that observed in the Ganzi region.
Copper functions as a critical component of the active centers of numerous enzymes, extensively participating in energy metabolism, antioxidant functions, and elastin and collagen production. Cu deficiency predisposes cattle to cardiovascular diseases, compromised immune responses, growth retardation and diarrhea in calves, reduced fertility and sperm quality in bulls, and impaired steroid hormone synthesis in ovarian granulosa cells [
41]. Our results demonstrated that hair Cu contents were normal across all six regions, whereas serum Cu deficiency occurred to varying degrees in all six regions. Serum copper primarily reflects recent (hours to days) dietary copper intake and the dynamic equilibrium of systemic copper metabolism, whereas hair copper represents long-term copper accumulation over weeks to months [
42]. The copper deficiency observed in serum from five regions (excluding Jiulong) may be attributable to antagonistic effects caused by high molybdenum or iron contents in soil and forage, resulting in relatively low bioavailability of copper in yak milk or dietary rations [
13,
43]. As a terminal tissue, hair exhibits slower copper deposition kinetics and possesses inherent buffering capacity; consequently, short-term insufficient copper intake may not yet significantly alter the total copper accumulation in hair, thereby leading to apparently normal hair copper levels.
Cobalt serves as the core element of vitamin B12, participating in erythrocyte maturation and thereby influencing hematopoietic function. It is also involved in energy metabolism and protein synthesis [
44]. Co deficiency can result in anorexia, rough and dull hair coat, anemia, developmental retardation, and emaciation [
45]. In our study, varying degrees of Co deficiency were detected in hair samples from all six regions, whereas serum Co contents in all six regions exceeded reference values. Cobalt exhibits a significant biological transmission relationship among soil, forage, and animal blood [
46]. Previous studies have demonstrated that lower pH values (acidic conditions) increase the solubility and bioavailability of metal ions such as cobalt, facilitating their absorption by forage roots, whereas higher pH values (alkaline conditions) promote metal ion precipitation or adsorption, thereby reducing their availability [
47]. During summer, when forage is abundant, forage serves as the primary dietary source of cobalt for ruminants. Following consumption by yaks, cobalt is utilized by rumen microorganisms for vitamin B
12 synthesis, directly confirming the biological transmission efficiency of cobalt through the food chain [
48,
49]. The positive correlation between serum and forage cobalt concentrations in the Shiqu region, together with the absence of serum cobalt deficiency in the Jiulong region, provides corroborating evidence for this biological transmission pathway. Additionally, the subnormal cobalt levels detected in yak hair from Shiqu and Jiulong may be attributed to the cumulative effect of sustained low cobalt nutritional status over the preceding months, particularly during the winter and spring seasons.
The primary physiological function of selenium involves serving as the core component of glutathione peroxidase (GPX), catalyzing the decomposition of peroxides and synergistically acting with vitamin E as antioxidants, playing crucial roles in protecting cellular structures and protein synthesis [
50]. Previous studies have indicated that Se deficiency primarily affects normal growth and development in calves, impedes fat and vitamin E metabolism and utilization, and predominantly causes necrosis of cardiac and skeletal muscle, with affected muscle regions losing their original color and presenting pallor (white muscle disease) [
51]. Forage plants primarily absorb selenium from the soil through their roots, mainly in the forms of selenate and selenite. Selenate is an inorganic form of selenium with relatively low bioavailability [
52]. Conversely, forage plants can convert selenium into organic forms through their own metabolic pathways, which represents the primary absorption mechanism in animals [
53]. During summer, when forage supply is abundant, yaks may maintain metabolic homeostasis by enhancing selenium excretion (e.g., via feces and urine) or transferring selenium into milk (in lactating cows), thereby preventing a significant increase in serum selenium and preserving steady-state levels [
54]. Additionally, another possible explanation is that previous studies have demonstrated that under alkaline and oxidizing soil conditions, selenium exists predominantly in the form of selenate, which is readily absorbed by plants. The soil characteristics in the Yajiang region may result in relatively low selenium bioavailability; although total selenium content may not be deficient, a greater proportion of selenium within plants exists as inorganic forms with lower bioavailability [
55]. This may account for the significant negative correlation between forage and serum selenium observed in the Yajiang region. Previous studies have demonstrated that soil selenium content is a critical determinant of forage selenium nutritional status, and total soil selenium content is typically significantly positively correlated with forage selenium levels, which is consistent with the correlation analysis results between soil and forage selenium in Seda [
52,
56]. However, the observed selenium deficiency in yak hair and serum in the Seda region may be attributable to the influence of soil pH and other factors on forage selenium speciation; a greater proportion of selenium within the forage may exist as inorganic forms, resulting in insufficient bioavailability for the animals [
55].
Zinc is an essential cofactor for numerous enzymes and participates in the synthesis, storage, and release of insulin, growth hormone, and other biomolecules, playing a critical role in bone development, tissue regeneration, and repair processes [
57,
58,
59]. Zinc deficiency can lead to multiple disorders, including growth retardation, compromised immunity, and cardiovascular diseases [
60,
61]. We found no evidence of zinc (Zn) deficiency in yak hair or serum samples from Ganzi Prefecture. However, soil Zn exhibited a significant negative correlation with altitude, decreasing with increasing elevation. This pattern may be explained by the fact that trace element concentrations in remote high-altitude areas are typically low, primarily originating from atmospheric deposition rather than local primary release. Soil Zn content at high elevations reflects the combined effects of natural weathering processes and minor contributions from long-distance atmospheric transport, while lacking localized anthropogenic enrichment sources [
62]. Furthermore, microbial community structure in high-altitude regions is significantly influenced by elevation; changes in soil microbial activity and composition may affect Zn speciation transformation and bioavailability [
63]. In Luhuo region, zinc content in animals is regulated by multiple physiological processes [
64]. When forage zinc levels increase, animals may activate homeostatic regulatory mechanisms, such as enhancing excretion or reducing absorption efficiency, to maintain internal environmental stability. This may lead to increased zinc excretion in feces, thereby making tissue zinc concentrations relatively stable or even decreased [
65].
This study has several limitations. First, the relatively small sample size (42 animals) and the restricted geographical scope (six regions within Ganzi Prefecture) may limit the generalizability of our findings. Second, hair and blood samples from yaks were collected during a single sampling campaign within one year, potentially compromising temporal representativeness. Third, the number and spatial coverage of soil and forage sampling sites were limited. Future research should address these gaps by expanding the sample size, conducting multi-time-point or multi-year sampling, and increasing both the number and spatial extent of soil and forage sampling sites.