Floristic composition and nutritional value of fallow land
The floristic analysis of grazed areas revealed a plant diversity composed mainly of
Melilotus infesta, Daucus carota, Medicagopolymorpha, Vicia sativa, Sonchusoleraceus, Erodium moschatum, Erodium malacoides, Brassica rapa, Raphanus raphanistrum, Calendula arvensis, Bromus hordeaceus, Anacyclus clavatus, Emex spinosa, Bromusmadritensis and other spontaneous species characteristic of Mediterranean fallow land.
The nutritional value of grazed grass varies according to the month of sampling (Table 1). A progressive increase in productivity was observed from February (1.51 TDM/ha) to April (2.67 TDM/ha), accompanied by a decrease in the leaf/stem ratio.
Dry matter increased gradually (from 16.66% to 29.77%), while total nitrogen decreased (from 28.53% to 14.58%). A similar trend was observed for organic matter digestibility, which decreased sharply between February and April (from 80.76% to 32.99%).
The energy values (NEL and NEg) have decreased slightly over time, indicating a progressive degradation of the nutritional quality of the forage.
Nutritional value of concentrates and straw
Concentrates have higher protein and energy content than cereal straw (Table 2). Concentrates (milk feed, fattening feed, corn, wheat bran, barley) have protein contents ranging from 7.37% to 18.26%, while straw has much lower values (1.88-4.60%).
Fiber content is low in concentrates (2.37-7.8%) and very high in straw (75-87.4%), confirming its role as a roughage with low energy value.
Starch is particularly high in corn (67.44%), making it a major energy source. These results confirm the clear difference in composition between the two types of feed.
Physicochemical quality of milk
Samples were obtained from raw milk of healthy ewes with healthy-looking udders and no signs of redness, heat, or edema for each day of sampling. The milk samples were bright white with no unusual odor.
The physicochemical characteristics of the milk are shown in Fig 1. The pH of the milk remained stable in both farms, ranging from 6.61 to 6.75, with no significant difference. The acidity of the milk ranged from 19.67°D to 24°D, with slightly higher values in the concentrate-fed system.
Fat and protein content were significantly higher in the farm receiving a concentrate and straw-based ration compared to the pasture-only system. The milk dry matter content is also higher in farm 1 (15.88 to 19.44 g/L) than in farm 2 (13.82 to 17.04 g/L). The mineral content follows the same trend, with slightly higher values in the intensive system.
Effect of diet on milk quality
Statistical analysis (Table 3) shows that diet has no significant effect on pH (p>0.05). However, highly significant differences (p<0.0001) are observed for acidity, fat content, protein content, dry matter and mineral content. Ewes fed a concentrated ration produce milk richer in fat and protein than those raised on pasture.
The results obtained show that the nutritional quality of the pasture varies significantly over the study period, with a progressive increase in dry matter and crude fiber, associated with a decrease in total nitrogen and digestibility. This evolution is mainly explained by the maturity stage of the plant species, where the transition from the vegetative to the senescent stage leads to increased tissue lignification and a decrease in the protein value of the forage. This result is consistent with the observations of
Demarquilly (1987), who reported an increase in fiber with plant age. According to
Boudechiche et al. (2010), the mineral content decreases with age. According to
Demarquilly and Andrieu (1988), leaves contain more ash than stems and this concentration tends to decrease with the progression of development and the age of the plant. Compared to
Salhi (2013) study on grass, the protein concentration is low.
This decline in forage quality has direct repercussions on milk composition, particularly protein and fat content. Indeed, the data from this study show superior physicochemical values in milk from the system receiving concentrates compared to the system based solely on grazing. This difference can be attributed to the higher energy and nitrogen density of the supplemented rations, which promotes greater udder synthesis.
The role of diet in modulating milk composition has been widely demonstrated.
Bocquier and Caja (2001) showed that the energy level of the ration directly influences milk fat content. In our study, the higher fat values in the concentrate system confirm this relationship. Furthermore, the decrease in protein content observed in the pasture system may be linked to the decline in forage nitrogen content over time.
The acidity and pH of the milk remained relatively stable between the two systems, indicating that the sanitary and hygienic conditions of milking were generally well controlled. These results are consistent with the values reported for ewe’s milk under similar conditions (
Mathieu, 1998;
Benlahcen et al., 2013).
The dry matter and mineral content of milk follow the same trend as the protein and lipid components, with higher values in the intensive system. This suggests better nutrient availability in the supplemented ration, allowing for more efficient synthesis of milk constituents. This finding is consistent with
Gonzalo (2005), who emphasizes the importance of nutritional supplementation in influencing the variation of milk dry matter.
The results concerning the pH of ewe’s milk fall within the ranges generally reported in recent literature (6.4–6.8), confirming the buffering effect exerted by phosphate, citrate and protein systems, particularly caseins. Recent studies show that this parameter remains relatively stable but can be influenced by diet and stage of lactation
(Claeys et al., 2021; Park, 2021). The slight alkalinity observed in some samples could be related to a diet rich in green forage or to physiological variations in the animals.
The higher titratable acidity of sheep’s milk compared to other species is consistent with its high dry matter and protein content. Recent studies confirm that sheep’s milk has a higher acidity due to its high concentration of caseins and minerals
(Pulina et al., 2022). This characteristic gives sheep’s milk better technological suitability, particularly for cheesemaking.
The observed fat content, close to or above 7%, is consistent with values reported in several recent studies. It is well established that the fat content is strongly influenced by diet, particularly the proportion of fiber and fatty acids in the ration
(Nudda et al., 2020). Furthermore, the stage of lactation plays a crucial role, with a progressive increase in fat content towards the end of lactation, a phenomenon confirmed by numerous contemporary studies
(Pulina et al., 2022; Lankri et al., 2024).
Regarding protein, the high values recorded in this study exceed those generally reported, which could be attributed to genetic, nutritional, or environmental factors. Recent research highlights that the protein composition of sheep milk is particularly sensitive to feed quality and rearing conditions (
Park, 2021;
Claeys et al., 2021). The high protein content of sheep milk is a major asset for its nutritional and technological qualities.
The observed total solids and ash content confirm the high nutritional density of sheep milk. Recent studies indicate that these parameters are generally higher than in cow and goat milk, due to the greater concentration of nutrients
(Pulina et al., 2022). However, the variations observed between farms can be explained by differences in farming practices, particularly the type of feed and climatic conditions.
Furthermore, the impact of nutritional supplements, particularly lipid intake, on milk composition has been widely demonstrated. Enriching the ration with fatty acids significantly alters the milk lipid profile, increasing the proportion of unsaturated fatty acids
(Nudda et al., 2020). This phenomenon is of significant nutritional interest for human health.
It is also important to note that the differences observed between the two systems cannot be attributed solely to diet. The stage of lactation constitutes an additional factor influencing milk composition, particularly the variation in butterfat and protein levels over time. Several factors, including breed, season, stage of lactation and litter size, significantly influence the milk quality of goats
(Singh et al., 2026). The incorporation of feed additives in dairy animal nutrition plays an important role in improving milk production and overall performance
(Ahmed et al., 2022). Furthermore, reducing the proportion of barley grain in ewe diets during the third stage of lactation did not adversely affect milk yield or its composition, representing an economically beneficial strategy through reduced feeding costs. In addition, supplementation with yeast in low-barley, high-fiber diets improved energy utilization efficiency, thereby enhancing the nutritional value of the ration
(Almallah et al., 2021).
Finally, although the literature confirms the importance of diet in milk composition
(Nudda et al., 2021), the results of this study highlight that systems based solely on grazing exhibit greater variability, linked to the seasonal fluctuation in the availability and quality of forage resources.