Next Article in Journal
Down-Regulation of Photosynthetic Electron Transport and Decline in CO2 Assimilation under Low Frequencies of Pulsed Lights
Next Article in Special Issue
Comparative Effect of Inoculation of Phosphorus-Solubilizing Bacteria and Phosphorus as Sustainable Fertilizer on Yield and Quality of Mung Bean (Vigna radiata L.)
Previous Article in Journal
Effects of Dipsacus asperoides and Phlomis umbrosa Extracts in a Rat Model of Osteoarthritis
Previous Article in Special Issue
Source–Sink Manipulation Affects Accumulation of Zinc and Other Nutrient Elements in Wheat Grains
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Characterizing Biomass Yield and Nutritional Value of Selected Indigenous Range Species from Arid Tunisia

1
International Center for Agricultural Research in the Dry Areas (ICARDA), Tunis 1004, Tunisia
2
Department of Animal and Rangeland Science, Oregon State University, Corvallis, OR 97331, USA
3
International Center for Agricultural Research in the Dry Areas (ICARDA), Amman 11185, Jordan
*
Author to whom correspondence should be addressed.
Plants 2021, 10(10), 2031; https://doi.org/10.3390/plants10102031
Submission received: 17 August 2021 / Revised: 19 September 2021 / Accepted: 22 September 2021 / Published: 27 September 2021
(This article belongs to the Special Issue Mineral Nutrition and Plant Responses to Environmental Changes)

Abstract

:
Rangelands of Tunisia show a great indigenous species diversity with considerable potential as forage for livestock. However, information on their fodder yield and quality is scanty and restricted to few species. The objective of the study was to evaluate the nutritive values of selected key perennial species based on their biomass yield, chemical composition, in vitro organic matter digestibility (IVOMD), and mineral composition. The species evaluated included four grass species (Stipa lagascae Roem. and Schult., Stipa tenacissima L., Stipagrostis plumosa (L.) Munro ex T. Anderson, and Stipagrostis pungens (Desf.) de Winter.) and eight shrub species (Anthyllis henoniana Coss. ex Batt., Argyrolobium uniflorum (Deene.) Jaub. and Spach., Echiochilon fruticosum Desf., Gymnocarpos decander Forssk., Helianthemum kahiricum Delile., Helianthemum lippii (L.) Dum. Cours., Plantago albicans L. and Rhanterium suaveolens Desf.). Results showed that shrub species contained higher concentrations of the crude protein (CP), acid detergent lignin (ADL), but lower neutral detergent fiber (aNDFom) and acid detergent fiber (ADFom) concentrations than grasses. The greatest concentration of CP was 135 g/kg DM for R. suaveolens. The greatest aNDFom concentration was found within the grasses with maximum of 744.5 g/kg DM in S. plumosa. The shrub species E. fruticosum, A. uniflorum, P. albicans, G. decander, R. suaveolens, and A. henoniana had the highest IVOMD with over 500 g/kg DM and have the potential to supply energy to livestock. Overall, the moderate to high protein, low fiber, and high in vitro digestibility measured for shrubs, suggest they have high nutritional values and can be used to enhance local livestock production.

1. Introduction

Rangelands cover about 27% of the world’s land surface area and comprise 70% of the world’s agricultural land area [1]. In Tunisia, rangelands comprise nearly one-quarter of the entire land cover, totaling about 5.5 million hectares, 87% of which consist of arid to semi-arid conditions [2]. The rangelands of Tunisia show a great diversity of species composition [3] and ultimately play a key role in domestic livestock feeding as a fundamental component of animal diets during grazing periods [4]. Range animal productivity depends on palatability, availability, and forage nutritive value [5]. Thus, sustainable use of these rangelands is an important element of successful livestock production.
Unfortunately, rangelands in Tunisia are facing a myriad of problems, in particular, overgrazing and droughts. Heavy grazing of natural rangelands results in a decline of species richness of highly palatable plant species [6] and destruction of native forage plants, which are then replaced either by annuals that have little forage value or by unpalatable and toxic species [7,8]. For instance, Astragalus armatus Willd., a long-spined species, and Thymelaea hirsuta (L.) Endl., a toxic and highly fibrous species are widespread in southern Tunisian rangelands that have been subject to heavy grazing [9]. The protection of rangelands to exclude livestock grazing is widely considered to be a simple and effective practice for restoring the vegetation structure in degraded arid rangelands and has been found to increase the number of palatable plant species, such as Echiochilon fruticosum Desf., Helianthemum lippii (L.) Dum. Cours., Stipa lagascae Roem. and Schult. and Stipagrostis plumosa (L.) Munro ex T. Anderson [2,10].
In Tunisia’s southeastern rangelands, protection has increased the proportion of palatable species to more than 50%, much higher than in overgrazed areas [11]. Livestock feed resources in the southern region of Tunisia include natural rangelands, crop residue and agro-industrial by-products, of which the first contribute the largest share. Despite the significant degradation of these rangelands as a result of overgrazing and climate change, they remain the predominant and most cost-effective natural source of nutrients for ruminants [12,13].
The arid areas of Tunisia, including desert rangelands, are mainly constrained by dry season feed shortages, with the lack of protein, minerals and energy being the most limiting. The fodder resources of natural rangelands are very low in total nitrogen (N) and crude protein (CP), ranging between 5–25%, as well as low digestibility potential and low mineral concentration [14]. While natural rangelands can provide sufficient feed during the rainy season, seasons of drought are normally accompanied by persistent feed shortages and a rapid decrease in palatable species with high nutritive value, thereby constraining sustainable animal production.
During the dry season, the CP concentration of mature grasses, for example, declines to 1–2% in tropical grasslands compared to wet seasons [15]. In Tunisia’s arid zones, the production of Chamaephyte shrubs, such as Anthyllis henoniana Coss. ex Batt., Argyrolobium uniflorum (Deene.) Jaub. and Spach., E. fruticosum, Gymnocarpos decander Forssk., Helianthemum kahiricum Delile., H. lippii, and Rhanterium suaveolens Desf. represent a significant amount of annual production. The variability of annual production is 60–80% or 50–90%, expressed as a percentage of total annual dry matter (DM) production [16,17].
Rangeland degradation based on qualitative and quantitative estimates has, in some situations, led to desertification and facilitated the introduction of non-indigenous species for rangeland restoration in Tunisia [18]. Awareness of the phylogenetic heritage of pastoral plant species has thus received increasing attention over the years, leading to the collection of major plant species from their native habitats and storing the seeds in gene banks to establish a reference collection for Tunisia’s arid and desert area indigenous species [19]. However, there is limited information about the nutritional value of these indigenous species. Since the nutritional status of available forage has a direct effect on livestock production [20], range managers must understand the nutritional dynamics of forages for the purpose of adopting strategies to maintain adequate animal growth and reproduction [21].
An evaluation of the nutritional content of forage species is generally made by measuring the content of nutrients [22]. Frequently used indicators of forage nutritive value are crude protein (CP), metabolizable energy (ME), neutral detergent fiber (aNDFom), and acid detergent fiber (ADFom) [23,24,25]. Although forage species in natural rangelands generally provide nutrients at a lower cost than concentrate feeds, they are inherently variable in their nutritive value [26]. Factors such as the forage species, degree of plant maturity, soil type and local climate all influence a plant’s nutritional value [20]. In addition, the chemical composition of forage is an important palatability factor influencing yield quantity and quality [27]. The objective of this study was to characterize and assess the extent of variation in fodder biomass and quality among key rangeland species grown in dryland environments in southern Tunisia. These findings will contribute to enhanced livestock production by supporting decisions that optimize both forage yield and nutritive value.

2. Results

2.1. Plant Growth and Yield Attributes

This Plant height, width, and vegetation cover varied (p < 0.05) by species (Figure 1). Plant height, width, and vegetation cover were highest in the grass species Stipagrostis Pungens (Desf.) de Winter. (height: 136 cm, width: 221 cm, vegetation cover 23.9%). A. uniflorum had the lowest height of 14 cm. The shrub species Plantago Albicans L. had the least plant width (14 cm). The vegetation cover of shrub species P. albicans and H. lippii was the lowest (~14%) among all the studied species (Figure 1).
Biomass yield varied (p < 0.05) among species (Figure 2). Fodder biomass ranged from 221 g DM plant−1 in S. pungens to 7 g DM plant−1 in P. albicans with an average of 56.9 g DM plant−1. The fodder biomass of Stipa tenacissima L. and R. suaveolens was relatively greater than the average (Figure 2).
Fodder biomass was correlated with plant height (r = +83, p < 0.0001), plant length (r = +0.93, p < 0.001), and plant vegetation cover (r = +91, p < 0.0001; Figure 3).

2.2. Chemical Composition

The chemical composition of the twelve species is shown in Figure 4. When compared with Stipa species, the foliage of R. suaveolens, H. lippii, and E. fruticosum species tends to be more nutritious. Considerable variation in CP concentration was observed among the species studied and ranged from 49.8 g/kg DM (S. tenacissima) to 13.5% (R. suaveolens). The greatest ADFom and aNDFom concentrations were found within species of the Poaceae family. S. tenacissima and S. pungens recorded the greatest ADFom and aNDFom (538.4; 744.5 g/kg DM), respectively. G. decander had the least aNDFom concentration (396.5 g/kg DM), and H. lippii had the least ADFom concentration (329.9 g/kg DM). Acid detergent lignin (ADL) concentration ranged between 102.4 and 50.9 g/kg DM. H. kahiricum had the greatest ADL concentration (102.4 g/kg DM), while low ADL concentration was recorded in species of the Poaceae family; “S. lagascae” (Figure 4).
The metabolizable energy concentration varied between 5.5 and 7.7 MJ kg DM−1 with the highest value for A. uniflorum and E. fruticosum and the lowest for H. kahiricum (Figure 5). The IVOMD of E. fruticosum and A. uniflorum was the highest (579 and 573 g kg−1, respectively) and lowest in H. kahiricum (425 g kg DM) with significant differences between species. The means of IVOMD and metabolizable energy (ME) followed a similar trend. Relative feed values (RFV) varied (p < 0.05) among species was lowest in S. tenacissima (53) and highest in G. decander (132). Among all species studied, Stipa recorded the lowest values for RFV, ranging from 53–62 (Figure 5).
There were positive and significant correlations between the IVOMD and ME (r = +0.82), and REF (r = +0.70) (Figure 6). A high negative and significant correlation was recorded between aNDFom concentration and RFV (r = −0.95). Crude protein concentrations showed a negative correlation with ADF (r = −0.82) and aNDFom (r = −0.78). Crude protein had a strong correlation with RFV (r = +0.79) and acceptability index (r = +0.71) (Figure 6).

2.3. Mineral Composition

Mineral concentration also varied (p < 0.05) among the sampled species (Table 1). G. decander was exceptionally high in Ca and Mg concentration (47.95 and 7.75 g/kg, respectively) and H. lippii contained the greatest concentration of Mn (716.2 g/kg DM). Stipa species showed lower levels of Ca, Mg and Mn than the other species. The Fe concentrating ranged from (mg/kg), the greatest value was in P. albicans and the least was in S. lagascae. The highest mean Cu concentrate was observed in P. albicans species with 107.8 g/kg DM, with a statistically significant difference (p < 0.05) from the other plant species except for E. fruticosum. The Zn ranged from 11.15 to 30.05 mg/kg DM and was lowest in G. decander and greatest in S. pungens. Na concentration varied greatly from 2.38 in A. uniflorum to more than 2.5 mg/kg in R. suaveolens.

2.4. Classification of Species

Clusters were formed using Ward’s hierarchical clustering method and combined at each step by the method of average linkage. The data were divided into three clusters using the 21 variables measured in each species. The average CP, IVOMD, RFV, and palatability index for Cluster 1 were 42%, 8%, 4%, 8% and 50%, respectively, and greater than Cluster 3. The average species fodder biomass, height and length of Cluster 3 were more than 2.5 times that of Cluster 2. The amounts of Zn, Cu, Mn, and Na in Cluster 2 were significantly greater than in Cluster 3. In contrast, the average species fodder biomass, vegetation cover, and cell wall concentrations (ADFom and aNDFom) for Cluster 3 were significantly greater than that of Clusters 1 and 2 (Figure 7).

3. Discussion

The arid rangelands of southern Tunisia are dominated by perennial shrubs and grasses that serve as the major source of feed for livestock. A sound knowledge of the nutritional value of these species can be used to determine forage requirements, rangeland carrying capacity and suitable grazing time to optimize animal production while ensuring long-term vegetative cover [28,29,30,31]. The chemical analysis of range forage plants is used to measure nutritional value and mineral concentration [32]. Shrubs contained significantly greater CP than grasses, consistent with Hussain and Durrani [33], Mahmoud et al. [34], and Julian et al. [35]. Rhanterium suaveolens, A. uniflorum, and E. fruticosum shrubs showed high CP concentrations, while CP was lower in grasses (Stipa species). Compared to the other species studied and despite its low preference by grazing animals, R. suaveolens is a keystone species critical to rangeland structure and functioning and has important forage value [36]. The differences in CP concentration between forages may be attributed to the inherent characteristics of each species’ ability to withdraw nutrients from the soil and store them in their tissues [31,37,38]. Another reason the CP concentrations differ between species may result from differences in the accumulation of nitrogen in these forage plants during different growth periods [39]. Apart from grasses, the concentrations of CP in all other species were above 88 g/kg DM and ranged between 88–135 g/kg DM which can be classified as medium in terms of meeting sheep nutrition requirements [40].
The neutral detergent fiber (aNDFom) and the acid detergent fiber (ADFom) of grass species were higher than in other forages, which agrees with findings reported by several authors [33,41,42,43,44,45]. This is due to the fact that grasses have more stems and higher stem to leaf ratios, which results in greater concentrations of fibrous tissues compared to other forage types [31]. Generally, higher fiber concentrations result in low nutritional feed value for animals [26]. Therefore, these grass species may offer poor-quality forage compared to other species.
The higher aNDFom values within grasses were relatively close to the results reported by Megersa et al. [46], Muhakka et al. [47], and da Silva Pause et al. [48] who assessed different species of grasses in various regions. Results revealed that the mean ADFom concentration present in grasses was 460 g/kg DM, which was greater than the reported values of 326 g/kg DM and 384 g/kg DM by Katongole et al. [49] and Mosisa et al. [50]. This might be attributed to the different stages of maturity of plants at sampling [51]. Among grass species, both S. lagascae and S. plumosa appeared to have a higher palatability index and a higher nutritive value compared to other species. Both species are shorter and show lower ADFom concentrations than the other Stipa species. Holechek et al. [52] reported that tall grasses in general contain lower levels of nutrients than do short grasses. Unlike the aNDFom and ADFom concentrations, the ADL values tended to be greater in shrubs than grasses. These findings are in line with those of Hussain and Durrani [33] who observed higher lignin concentrations in shrubs than grasses.
Forage species with a high in vitro organic matter digestibility (IVOMD) are likely to have high nutritional value [53]. Both IVOMD and metabolizable energy (ME) are important to enhance animal performance and should be considered when preparing any feed ration. The IVOMD and ME showed a higher trend for the shrubs group compared to grasses. All studied forage species except Stipa and Helianthemum showed values of IVOMD above 500 g/kg DM, which is considered a good indicator that forage species have an adequate energy supply for animals [54,55]. The higher IVOMD values obtained in shrubs are within the range of 500–620 g/kg DM reported [56,57].
The ME results showed the same trend as the IVOMD. The highest ME concentration estimated for shrubs is comparable to other types of shrubs [58,59,60]. The ME depends mainly on IVOMD, which is indicated by the high positive correlation (r = +0.82) in line with Evitayani et al., [54]. The dry matter intake (DMI) is a primary factor contributing to feed efficiency and animal performance and it can be affected by the forage quality [61]. Grasses showed lower amounts of DMI and RFV compared to shrubs. This might be related to a higher aNDFom concentration that affects how much feed an animal can take in [62]. Our results confirm this finding as there was a high negative correlation between RFV and aNDFom (r = −0.95).
Minerals are essential for livestock reproductive physiology and performance due to their role in maintenance, metabolism, and growth [63,64]. In this study, mineral concentrations varied among the sampled species and the results agree with Dambe et al. [65]. The plant mineral content varies depending on species, stage of growth and environmental factors [66]. Grasses (Stipa spp.) had the lowest mineral concentrations. However, all other species showed Ca, Mg, Fe, Na, Mn and Cu concentration values higher than the maintenance requirements for sheep as found by Zervas [67]. Plant functional groups (grasses and shrubs) show differential mechanisms of nutrient uptake due to their contrasting root distributions, which may contribute to species coexistence [68]. On the other hand, the Zn concentration of all species was lower than the amount needed for small ruminant maintenance [69].
Our results identified three clusters. These clusters suggest that yield (shrub fodder biomass, height, and length) and fodder quality parameters could be used to identify promising forage species for rangeland rehabilitation programs. The higher fodder yield, CP, IVOMD, RFV coupled with lower values of fiber in Cluster 1 suggest that the species in this cluster could be a good option for livestock feed, especially since all the three species have a high preference index.

4. Materials and Methods

4.1. Study Area

The study area is located in the arid rangelands of Chenenni in the Governorate of Tataouine, Southern Tunisia (32°54′38.0″ N 10°15′40.2″ E, Figure 8). The climate is arid Mediterranean with a mild rainy season concentrated during autumn and spring (the growth season is from September to April) and a dry, rain-free summer lasting about four months from May to August. The landscape is dominated by villafranchian limestone crust forming undulating hills. The soil is regosol, with friable caliches at depths of 10–25 cm and gypsum outcrops.

4.2. Species Collection

Four grasses and eight shrub species of the most common plant species for grazing animals in the Chenenni rangelands were evaluated. Sampling collection was carried out at the flowering stage of growth during the spring of 2018. Of the 12 perennials species collected, seven were Chamaephyte and five were Hemicryptophyte. Only one of the grass species was classified as a low-acceptability species and nine as very- to high-acceptability species (Table 2).

4.2.1. Anthyllis henoniana Coss. ex Batt.

Perennial, silky, hairy shrub species 30 to 60 cm tall belongs to the Fabaceae family. This species comes into vegetative activity after the first autumn rains. It blooms from late winter and fruiting begins in April. A. henoniana is a deep-rooted legume with the top fine roots found at a depth of 8 cm. Anthyllis takes up newly available water more rapidly than other species despite having fewer surficial roots. In areas of very low or irregular rainfall, the morphology and anatomy of A. henoniana have evolved to favor the interception and absorption of dew or rain directly by the shoots rather than via soil. The plant is abundant in the desert steppes mainly on calcareous and gypsum soils. It has a low presence in the arid zones but is especially common in the Saharan zones. From an edaphic point of view, steppes A. henoniana occupy stony and gravelly plains (Regs) that are shallow and overlain by a sandy loam, skeletal soil or by sand (sailing wind or barkanes). The plant is very palatable and is an appropriate species for the rehabilitation of degraded areas [71] and shows potential for rangeland protection against wind erosion and improvement of rangeland value [72].

4.2.2. Argyrolobium uniflorum (Deene.) Jaub. and Spach

Perennial dwarf shrub with arcuate-ascending and densely appressed hairy stems. The plant has spreading leaves and a subterete petiole. The flowers are single, small, and have opposite leaves on short peduncles with two small, herbaceous and linear bracteoles near the middle. The legume is shortly pedunculated, densely villous-silky, torulose, dehiscent, with a persistent calyx toward the base. It produces five to seven olive-green seeds. A. uniflorum lives on various substrates such as limestone and sandy soils. The species lives on the upper horizon of the thermo Mediterranean belt with a semi-arid rain climate on greatly degraded soils. A. uniflorum is a pastoral and forage legume widely distributed in arid and semi-arid regions of Tunisia and is highly palatable and preferentially consumed by grazing animals. This plant plays an important role in the maintenance of soil fertility, soil coverage and dune stability.

4.2.3. Echiochilon fruticosum Desf.

Small perennial shrub (10–50 cm) belongs to the Boraginaceae family. Many branches sprout from a hairy base, with the grey bark splitting to give way to reddish-brown bark. The shrub is recognizable by its sessile, pointed, thick, elongated and narrow leaves. The flowers are zygomorphic with five blue petals. E. fruticosum is the only species in the genus Echiochilon found in Tunisia. The shrub is endemic to Saharan Africa and is particularly abundant in deserts and dry rangelands on sandy ground and riverbeds of the northeast coastal areas, the center and the south and extreme south of the country. It is highly resistant to both grazing and pedo-climatic conditions. This Chamaephytic species is also among the native and keystone species historically predominant on Tunisia’s arid rangelands but currently threatened by extinction. E. fruticosum is known to have good nutritive value, high palatability, and is frequently foraged by small herds of sheep and goats.

4.2.4. Gymnocarpos decander Forssk.

It is a member of the Caryophyllaceae family. A perennial undershrub 30–50 cm tall, G. decander is erect, suffrutescent and highly branched. The stems and branches are rough, ash grey, entangled and knotted at the nodes. The leaves are 8 to 16 mm long, 2 mm wide, obtuse, entire, mucronate and glabrous. Its flowers are sessile, pentamerous and yellowish-green and produce a one-seeded, membranous, indehiscent utricle fruit that is enclosed by persistent sepals. The seed is somewhat oblong, compressed, and dark brown with a radicle superior. Gymnocarpos decander, a desert plant, ideally grows among rocks and stony ridges without sand. Locally, the species is used as fuel wood and feed for grazing and therefore has economic value [73]. Because the young branches are eaten by camels and goats, plants rarely attain full growth. Gymnocarpos decander are palatable shrubs and are usually heavily grazed [74].

4.2.5. Helianthemum kahiricum Delile

Perennial herb 15 cm tall that belongs to the Cistaceae family. It is widely distributed in the Mediterranean basin [75]. Covered by glandular hairs, the leaves are whorled, and the sessile flowers have five sepals, five yellow petals [76], numerous stamens and three to five carpels defining a unilocular ovary. The fruit is a hairy capsule. Helianthemum kahiricum has important pastoral, ecological, economic, and medicinal uses [77,78]. The soil habitat of this species is characterized by a moderately coarse texture, sandy loam, good water retention capacity, low organic matter concentration, basic pH and low calcium carbonate concentration. Helianthemum kahiricum has great potential as a forage species and is palatable to sheep, goats, and camels.

4.2.6. Helianthemum lippii (L.) Dum. Cours.

An endemic perennial dwarf shrub belongs to the Cistaceae family. It is found in sandy regions of arid and semi-arid areas in the Mediterranean. A much-branched shrub that grows up to 60 cm tall, the branches are rigid, usually sharply tipped (in dry conditions) and whitish in appearance. Leaf length and width vary according to season (5 to 15 mm × 1 to 5 mm). The flowers are small and sessile with yellowish petals that are equal to or slightly exceed the sepals. Helianthemum lippii is related to desert truffles and establishes mycorrhizal symbiosis with them [79,80] and is therefore of important ecological value. Helianthemum lippii is one species of the genus Helianthemum that, according to several studies, exhibits anti-inflammatory and analgesic properties [81,82,83].

4.2.7. Plantago albicans L.

Perennial plant belongs to the Plantaginaceae family, with a rosette hemicryptophyte form. It is recognizable by its silky, hairy aspect and lanceolate leaves with wavy margins. Its rhizomatous basis bears suckers that ensure plant survival in dry years and enables active vegetative multiplication during the growing season. The plant grows in wastelands, slopes, and stony rangelands on dry and sun-exposed soils. It colonizes open, arid parts of the Mediterranean region and runs southward in North Africa as far as sub-desertic environments. It may also occur on deep, sandy soil on surfaces of leveled silt with sharply dipping strata. Plantago albicans has high feed value and is collected for its various medicinal and economic uses. For instance, Plantago species have been found to possess antioxidant, antiviral, hepatoprotective, immunomodulatory, anti-inflammatory, antidiabetic, and anticancer properties [84,85,86].

4.2.8. Rhanterium suaveolens Desf.

Perennial shrub 40 to 60 cm tall belongs to the Asteraceae family. Highly branched, the plant is also recognizable by the presence of its whitish hairs and leaves that are sessile, alternate, small, toothed, and inflorescence in capitules with ligulated, tubular yellow flowers. Endemic to the Sahara, this species is frequent in the northern region of the desert where it colonizes stabilized accumulations of sand. Rhanterium suaveolens dominates the shrub-steppe on sandy plains that are characterized by deep sierozem. In the period between 1975 and 2000 and despite its low palatability, the presence of R. suaveolens pastures on sandy soils decreased either as a result of cultivation, in particular through soil truncation, or because of overgrazing. Rhanterium suaveolens shrub-steppes play an important ecological role in the areas they inhabit. Its low palatability allows the plant to grow better, thus improving vegetation cover and fixing soil, which protects rangelands against desertification.

4.2.9. Stipa lagascae R. and Sch

Perennial bunchgrass, hemicryptophyte and psammophile grass culm of 30–60 cm long. It belongs to the Poaceae family and is widely distributed throughout the Mediterranean region [87]. The flowering plant grows from the beginning of April until June [88]. It is a grazing-tolerant species but is also threatened with extinction through overgrazing [89]. It is well adapted to dry environmental conditions and can maintain growth activity during severe water deficits [90]. Stipa lagascae grows in sandy soils and is highly palatable for livestock. It is the most promising native grass species for land rehabilitation in arid regions [72,89,91].

4.2.10. Stipa tenacissima L.

Perennial and rhizomatous tussock grass belongs to the Poaceae family. It has a shallow root system reaching a maximum depth of 0.5 m. Its fiber-rich leaves can reach 1 m in length. The tufts of S. tenacissima are circular and homogeneous when young but become empty at the center as they age and begin to die. The leaves are thin, ribbon-like, smooth, shiny and solid and are covered at the base with a hairy sheath. Esparto leaves mature in the fourth to eleventh month after budding, depending on location and climate conditions. The species is native to North Africa and is widely distributed in arid and semi-arid ecosystems of the south and western Mediterranean basin. It is a suitable species for the reclamation and rehabilitation of degraded soils as it can grow in nutrient-deficient soils, and forms a dense clump that can trap sediments and seeds and provides shelter for other species to grow. Stipa tenacissima is highly palatable. It is also the only raw material for making paper in Algeria, Morocco, and Tunisia and produces a fiber called esparto which is used to make cords, baskets, and espadrilles.

4.2.11. Stipagrostis plumosa (L.) Munro ex T. Anderson

Densely caespitose, perennial desert grass belongs to the Poaceae family. It grows in dense tufts and the culms, which are erect or geniculately ascending, grow to 15 cm to 30 cm long. The lowest sheaths and internodes are covered with a thick, flocculent, and fugacious wool. The leaf blades, which are filiform, rolled, smooth, pungent, and curved, are 4 cm to 12 cm long and sometimes form a semi-circle or complete circle. The grass grows in sandy, stony, and slightly saline soils and is found in areas where the sand is stable, and also in deflation sites where it survives even when the roots and rhizosheaths are exposed. The relatively dense horizontal structure of S. plumosa prevents sand accumulation within the tuft. A vertical cross section through the plant has the shape of an inverted pyramid, which may act as a windbreak [92]. Stipagrostis plumosa is an important rangeland grass in the steppes of deserts and semi-desert regions and has high nutritive value and palatability to livestock.

4.2.12. Stipagrostis pungens (Desf.) de Winter

Perennial grass belongs to the Poaceae family. It grows on dunes and sandy wadis. Although considered psammophyte, the species tolerates the presence of gypsum in quicksand-covered substrates. This species is much appreciated by dromedaries and to a lesser degree by small ruminants.

4.3. Sampling Procedure

Four For the twelve species, three plants per species with the same approximate size during the full bloom stage of the plant’s growth cycle in the spring of 2018 were selected and measured for length, width, and height. Plant cover was estimated using the supervised method in VegMeasure software (Corvallis, OR, USA). Straight-down images were taken using a Nikon Coolpix 130 digital camera (Nikon, Tokyo, Japan) with 28–140 mm zoom lens mounted to a Bogen Manfrotto 676B Monopod (Manfrotto, Cassola, Italy). Photos were taken from 1.35 m above the ground for individual plants. The dimensions of each JPG image were 4608 × 3456 pixels. A supervised classification of plant vegetative cover and soil surface was set up for images and then processed using VegMeasure software to generate processed images and summary Excel files that expressed the values (%) of the vegetative cover and soil surface in each picture [93].
Afterward, three plants of each species were sampled and pruned to one-third of the plant height above ground and separated into grazable materials (leaves plus stems less than 10 mm in diameter) and woody parts. The grazable materials were oven-dried at 60 °C for 48 h to determine dry matter concentrations for each plant.

4.4. Proximate Analysis

Plant samples were ground in a Thomas Model 4 Wiley mill and passed through a 1 mm sieve prior to analyses. Ash concentration was determined by burning the samples at 550 °C, and CP was determined using the Kjeldahl method. The aNDFom, ADFom, and acid detergent lignin (ADL) concentrations were determined by the sodium sulphite and alpha amylase procedure [94] and expressed exclusive of residual ash.
In vitro organic matter digestibility (IVOMD) was determined in the laboratory using the two-step procedure described by Tilley and Terry [95].
Metabolizable energy (ME) was estimated using the Menke et al. [96] equation:
ME (MJ/kg DM) = 2.2 + 0.136 G24 + 0.057 CP
where: CP = crude Protein, G24 = gas production value (mL/200 mg) at 24 h.
Relative feed value (RFV) is an index used to estimate the quality of forages compared with reference feeds, i.e., alfalfa at full bloom, which is equal to 100 [97,98]. In addition to forage crops, this index has been used to estimate the quality of various and rangelands species [99,100,101]. The RFV was calculated according to Stalling [102] using the following equation:
RFV = (DMD × DMI)/1.29
where: DMD = dry matter digestibility, DMI = dry matter intake, 1.29 = the expected digestible dry matter intake as % of body weight; DMI = 120/(% aNDFom)
DMD was estimated using the formula developed by Oddy et al. [103]:
DMD% = 83.58 − 0.824 ADFom% + 2.626 N%
Iron (Fe), zinc (Zn), copper (Cu), manganese (Mn), sodium (Na), calcium (Ca), and magnesium (Mg) concentrations were determined by PinAAcle 900TAtomic Absorption Spectrometer (AAS).

4.5. Statistical Analysis

An analysis of variance was performed using the general linear model procedure of SAS (1990, SAS Institute Inc., Cary, NC, USA) to determine the differences between the nutritive values and the productive parameters. The following equation was used:
Yit = μ + τi + εit
where: Yit = biomass yield or nutritional variable; μ = biomass yield or nutritional variable; τi = the effect of the rangeland’s species on the response, εit = residual error.
A univariate correlation was used to establish relationships between variables. Average values for plant height, vegetation cover, and species mineral content for each species were subjected to cluster analysis, using the Ward method to group the species into clusters. Cluster analysis and correlation were performed using SAS JMP Statistical Discovery Pro 2020 (SAS Institute Inc., Cary, NC, USA). Duncan’s Multiple Range Test was used to separate means when p ≤ 0.05.

5. Conclusions

In the arid rangelands of southern Tunisia, the production of Chamaephytes and hemicryptophytes is mainly represented by the Poaceae family, which are the dominant contributors to fodder production for livestock. The nutritive values vary widely among species but appear quite promising in energy and mineral elements for animal feeding. The moderate to high CP and low fiber concentrations along with high IVOMD found in E. fruticosum, A. uniflorum, P. albicans, G. decander, R. suaveolens, and A. henoniana suggest that these shrub species have a higher nutritive value than the highly fibrous, low IVOMD grass species S. lagascae, S. tenacissima, S. plumosa, and S. pungens. The concentration of all minerals except zinc among these shrub species was higher, suggesting that these plants are best for rangeland forages and for maintaining and enhancing livestock productivity. Therefore, it is recommended to reduce human disturbances through overgrazing or cultivation encroachment to preserve these plant communities in their natural habitats. To ensure that plant biodiversity is maintained, it will be necessary to enforce policies that ban cultivation in these fragile ecosystems and promote sustainable grazing management.

Author Contributions

Conceptualization, M.L., M.G. and S.H.; methodology, M.L., M.G. and S.H.; formal analysis, S.H. and M.L.; investigation, M.L., M.G. and S.H.; writing—original draft preparation, M.G. and S.H.; writing—review and editing, M.L., M.G., S.H. and M.A.B.A.; supervision, M.L., project administration, M.L., funding acquisition, M.L. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the CGIAR Research Program on Livestock, agreement number 200172, and the APC was also funded by the same source of funding.

Data Availability Statement

All data are available upon request.

Acknowledgments

This work was supported by the International Center for Agricultural Research in the Dry Areas (ICARDA) and the CGIAR Research Program on Livestock (CRP Livestock), led by the International Livestock Research Institute (ILRI). The authors would like to extend their thanks to José Carlos Batista Dubeux Jr. (University of Florida, USA) for his constructive comments.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. FAO. Are Grasslands under Threat? Brief Analysis of FAO Statistical Data on Pasture and Fodder Crops. 2008. Available online: http://www.fao.org/uploads/media/grass_stats_1.pdf (accessed on 29 July 2021).
  2. Gamoun, M.; Ouled Belgacem, A.; Louhaichi, M. Diversity of desert rangelands of Tunisia. Plant Divers. 2018, 40, 217–225. [Google Scholar] [CrossRef]
  3. Gamoun, M.; Louhaichi, M. Botanical composition and species diversity of arid and desert rangelands in Tataouine, Tunisia. Land 2021, 10, 313. [Google Scholar] [CrossRef]
  4. Gamoun, M. Management and resilience of Saharan rangelands: South Tunisia. Fourrages 2013, 216, 321–328. [Google Scholar]
  5. Abdullah, M.; Rafay, M.; Hussain, T.; Ahmad, H.; Tahir, U.; Rasheed, F.; Ruby, T.; Khalil, S. Nutritive potential and palatability preference of browse foliage by livestock in arid rangelands of Cholistan desert (Pakistan). Anim. Plant Sci. 2017, 27, 1656–1664. [Google Scholar]
  6. Louhaichi, M.; Salkini, A.K.; Petersen, S.L. Effect of small ruminant grazing on the plant community characteristics of semi-arid Mediterranean ecosystems. Int. J. Agric. Biol. 2009, 11, 681–689. [Google Scholar]
  7. Gondard, H.; Jauffret, S.; Aronson, J.; Lavorel, S. Plant functional types: A promising tool for management and restoration of degraded lands. Appl. Veg. Sci. 2003, 6, 223–234. [Google Scholar] [CrossRef]
  8. Ouled Belgacem, A.; Louhaichi, M. The vulnerability of native rangeland plant species to global climate change in the West Asia and North African regions. Clim. Change 2013, 119, 451–463. [Google Scholar] [CrossRef] [Green Version]
  9. Jauffret, S.; Lavorel, S. Are plant functional types relevant to describe degradation in arid, southern Tunisian steppes? J. Veg. Sci. 2003, 14, 399–408. [Google Scholar] [CrossRef]
  10. Ouled Belgacem, A.; Tarhouni, M.; Louhaichi, M. Effect of protection on plant dynamics in the Mediterranean arid zone of southern Tunisia: The case of Bou Hedma national park. Land Degrad. Dev. 2013, 24, 57–62. [Google Scholar] [CrossRef]
  11. Gamoun, M. Grazing intensity effects on the vegetation in desert rangelands of Southern Tunisia. J. Arid Land 2014, 6, 324–333. [Google Scholar] [CrossRef] [Green Version]
  12. Ouled Belgacem, A.; Ben Salem, F.; Gamoun, M.; Chibani, R.; Louhaichi, M. Revival of traditional best practices for rangeland restoration under climate change in the dry areas: A case study from Southern Tunisia. Int. J. Clim. Chang. Strateg. Manag. 2019, 11, 643–659. [Google Scholar] [CrossRef]
  13. Tarhouni, M.; Ben Hmida, W.; Ouled Belgacem, A.; Louhaichi, M.; Neffati, M. Is long-term protection useful for the regeneration of disturbed plant communities in dry areas? Afr. J. Ecol. 2017, 55, 509–517. [Google Scholar] [CrossRef]
  14. Le Houérou, H.N. Browse in Africa: The current state of knowledge. In Proceedings of the International Symposium on Browse in Africa, Addis Ababa, Etiopia, 8–12 April 1980; International Livestock Center for Africa: Addis Ababa, Ethiopia, 1980. [Google Scholar]
  15. Crowder, L.V.; Cheddah, H.R. Tropical Grassland Husbandry; Longman Inc: New York, NY, USA, 1982. [Google Scholar]
  16. Le Houérou, H.N.; Haywood, M.; Claudin, J. Etude Phytoécologique du Hodna; AGS: DP/ALG/66/509; FAO: Rome, Italy, 1974. [Google Scholar]
  17. Floret, C.; Pontanier, R. Aridité climatique, aridité édaphique. Actual. Bot. 1984, 131, 265–275. [Google Scholar] [CrossRef] [Green Version]
  18. Zaafouri, M.S. Contraintes du Milieu et Réponses de Quelques Espèces Arbustives Exotiques Introduites en Tunisie Présaharienne. Ph.D. Thesis, Aix-Marseille University, Marseille, France, 1993. [Google Scholar]
  19. Neffati, M.; Akrimi, N. Gene Bank of spontaneous plants of the desert and arid zones of Tunisia. Plant Genet. Resour. Newsl. 1996, 108, 26–32. [Google Scholar]
  20. Schut, A.G.T.; Gherardi, S.G.; Wood, D.A. Empirical models to quantify the nutritive characteristics of annual pastures in south-west Western Australia. Crop Pasture Sci. 2010, 61, 32–43. [Google Scholar] [CrossRef]
  21. Gwelo, F.A. Farmers’ Perceptions of Livestock Feeding and Rangeland Management; Dynamics of Soil, Forage and Cattle Blood Serum Mineral Levels in Two Communal Areas in the Eastern Cape, South Africa. Ph.D. Thesis, University of Fort Hare, Alice, South Africa, 2013. [Google Scholar]
  22. Singh, S.; Bhat, B.V.; Shukla, G.P.; Singh, K.; Gehrana, D. Variation in carbohydrate and protein fractions, energy, digestibility and mineral concentrations in stover of sorghum cultivars. Trop. Grassl. Forrajes Trop. 2018, 6, 42–52. [Google Scholar] [CrossRef] [Green Version]
  23. Dehghani Bidgoli, R. Forage quality of Calligonum comosum in three phenological growth stages (Case study: Kashan rangelands, Iran). J. Rangel. Sci. 2018, 8, 309–314. [Google Scholar]
  24. Zhao, G.Q.; Wei, S.N.; Li, Y.F.; Jeong, E.C.; Kim, H.J.; Kim, J.G. Comparison of forage quality, productivity and β-carotene content according to maturity of forage rye (Secale cereale L.). J. Kor. Grassl. Forage. Sci. 2020, 40, 123–130. [Google Scholar] [CrossRef]
  25. Arrekhi, A.; Gharmakher, H.N.G.; Bachinger, J.; Bloch, R.; Hufnagel, J. Forage Quality of Salsola turcomanica (Litv) in Semi-arid region of Gomishan, Golestan Province, Iran. J. Rangel. Sci. 2021, 11, 74–86. [Google Scholar]
  26. Lee, M.A. A global comparison of the nutritive values of forage plants grown in contrasting environments. J. Plant Res. 2018, 131, 641–654. [Google Scholar] [CrossRef]
  27. Martiniello, P.; Teixeira da Silva, J.A. Physiological and bioagronomical aspects involved in growth and yield components of cultivated forage species in Mediterranean environments: A review. Eur. J. Plant Sci. Biotechnol. 2011, 5, 64–98. [Google Scholar]
  28. Newman, Y.C.; Lambert, B.; Muir, J.P. Defining forage quality. EDIS Publication SS-AGR-322; Agronomy Department, UF/IFAS Extension Service: Gainesville, FL, USA, 2009; Available online: http://publications.tamu.edu/FORAGE/PUB_forage_Defining%20Forage%20Quality.pdf (accessed on 29 July 2021).
  29. Asaadi, A.M.; Dadkhah, A.R. The study of forage quality of Haloxylon aphyllum and Eurotia ceratoides in different phenological stages. Res. J. Biol. Sci. 2010, 5, 470–475. [Google Scholar] [CrossRef]
  30. Waldron, B.L.; Greenhalgh, L.K.; ZoBell, D.R.; Olson, K.C.; Davenport, B.W.; Palmer, M.D. Forage kochia (Kochia prostrata) increases nutritional value, carrying capacity, and livestock performance on semiarid rangelands. Forage Grazinglands 2011, 9, 1–6. [Google Scholar] [CrossRef]
  31. Amiri, F.; Shari, A.R.M. Comparison of nutritive values of grasses and legume species using forage quality index. Songklanakarin J. Sci. Technol. 2012, 34, 577–586. [Google Scholar]
  32. Olowu, O.O.; Yaman Firincioğlu, S. Feed Evaluation methods: Performance, economy and environment. Eurasian J. Agric. Res. 2019, 3, 48–57. [Google Scholar]
  33. Hussain, F.; Durrani, M.J. Nutritional evaluation of some forage plants from Harboi rangeland, Kalat, Pakistan. Pak. J. Bot. 2009, 41, 1137–1154. [Google Scholar]
  34. Mahmoud, A.E.; Abbas, M.S.; Cieslak, A.; Szumacher-Strabel, M. Evaluation of chemical composition and in vitro dry and organic matter digestibility of some forage plant species derived from Egyptian rangelands. J. Anim. Plant Sci. 2017, 27, 1573–1581. [Google Scholar]
  35. Julian, A.A.M.; Scasta, J.D.; Stam, B.R.; Sebade, B.M.; Page, C.M.; Springer, B.E.; Renner, W.T.; Cunningham-Hollinger, H.; Stewart, W.C. Mineral element concentrations of common grass and shrub species on sheep winter range in Wyoming: Insights for mineral supplementation strategies. Transl. Anim. Sci. 2020, 4 (Suppl. 1), S11–S16. [Google Scholar] [CrossRef] [PubMed]
  36. Louhaichi, M.; Gamoun, M. Rhanterium suaveolens Desf: A Keystone Species Critical to Rangeland Structure and Functioning. Managing Rangelands: Promoting Native Shrub Species. 2018. Available online: https://hdl.handle.net/20.500.11766/8494 (accessed on 29 July 2021).
  37. Cook, C.W.; Stubbendieck, J. Range Research: Basic Problems and Techniques; Society for Range Management: Denver, CO, USA, 1986; p. 317. [Google Scholar]
  38. Njidda, A.A. Chemical composition, fibre fraction and anti-nutritional substances of semi-arid browse forages of North-Eastern Nigeria. Nig. J. Basic Appl. Sci. 2010, 18, 181–188. [Google Scholar] [CrossRef] [Green Version]
  39. Salem, A.Z.M.; Salem, M.Z.M.; El-Adawy, M.M.; Robinson, P.H. Nutritive evaluations of some browse tree foliages during the dry season: Secondary compounds, feed intake and in vivo digestibility in sheep and goats. Anim. Feed Sci. 2006, 127, 251–267. [Google Scholar] [CrossRef]
  40. Salah, N.; Sauvant, D.; Archimède, H. Nutritional requirements of sheep, goats and cattle in warm climates: A meta-analysis. Animal 2014, 8, 1439–1447. [Google Scholar] [CrossRef]
  41. Tufarelli, V.; Cazzato, E.; Ficco, A.; Laudadio, V. Assessing nutritional value and in vitro digestibility of Mediterranean pasture species using yak (Bos grunniens) faeces as alternative microbial inoculum in a Daisy incubator. J. Food Agric. Environ. 2010, 8, 477–481. [Google Scholar]
  42. Boufennara, S.; Lopez, S.; Bousseboua, H.; Rodríguez, R.B.; Bouazza, L. Chemical composition and digestibility of some browse plant species collected from Algerian arid rangelands. Span. J. Agric. Res. 2012, 1, 88–98. [Google Scholar] [CrossRef] [Green Version]
  43. Foroughbakhch, R.; Hernandez-Pinero, J.L.; Carrillo-Parra, A. Nutrient profile, floristic compositions and preference index of shrubs and herbs consumed by goats in semiarid region of Northeastern Mexico. J. Anim. Vet. Adv. 2012, 11, 1299–1305. [Google Scholar] [CrossRef] [Green Version]
  44. Bidgoli, R.D.; Ranjbarfordoei, A. Vegetation types and rangeland species nutritional values and forage quality indicators at various phonological stages. Int. J. Plant Physiol. Biochem. 2013, 5, 16–24. [Google Scholar]
  45. Elgersma, A.; Søegaard, K. Changes in nutritive value and herbage yield during extended growth intervals in grass–legume mixtures: Effects of species, maturity at harvest, and relationships between productivity. Grass Forage Sci. 2016, 73, 78–93. [Google Scholar] [CrossRef]
  46. Megersa, E.; Mengistu, A.; Asebe, G. Nutritional characterization of selected fodder species in Abol and Lare districts of Gambella region, Ethiopia. J. Nutr. Food Sci. 2017, 7, 1000581. [Google Scholar] [CrossRef]
  47. Muhakka, M.M.; Suwignyo, R.A.; Budianta, D. Nutritional values of swamp grasses as feed for Pampangan Buffaloes in South Sumatra, Indonesia. Biodiversitas 2020, 21, 956–967. [Google Scholar] [CrossRef]
  48. da Silva Pause, A.G.; de Souza França, A.F.; Okada, E.S.M.; Gandra, J.R.; Dupas, E.; de Oliveira, E.R.; Ferreira, J.L.; Marques, O.F.C. Nutritional value of Mombasa grass submitted to different grazing heights and nitrogen fertilization. Braz. J. Anim. Environ. Res. 2021, 4, 860–874. [Google Scholar] [CrossRef]
  49. Katongole, C.B.; Lumu, R.; Lindberg, J.E. Comparative chemical composition and rumen degradation of common reed and elephant grass in urban/peri-urban dairying systems in Uganda. Agroecol. Sustain. Food Syst. 2021, 45, 892–906. [Google Scholar] [CrossRef]
  50. Mosisa, A.; Nurfeta, A.; Bezabih, M.; Tolera, A.; Mengistu, S.; Yigrem, S.; Hassen, A. Assessment of botanical composition, biomass yield, nutritional quality and methane production of forages in selected grasslands, southern highlands of Ethiopia. Sci. Afr. 2021, 12, e00726. [Google Scholar] [CrossRef]
  51. Chakravarthi, M.K.; Reddy, Y.R.; Rao, K.S.; Ravi, A.; Punyakumari, B.; Ekambaram, B. A study on nutritive value and chemical composition of sorghum fodder. Int. J. Sci. Environ. Technol. 2017, 6, 104–109. [Google Scholar]
  52. Holechek, J.L.; Pieper, R.D.; Herbel, C.H. Range Management Principles and Practices; Prentice Hall: Englewood Cliff, NJ, USA, 2001. [Google Scholar]
  53. Bezabih, M.; Pellikaan, W.F.; Tolera, A.; Khan, N.A.; Hendriks, W.H. Chemical composition and in vitro total gas and methane production of forage species from the Mid Rift Valley grasslands of Ethiopia. Grass Forage Sci. 2014, 69, 635–643. [Google Scholar] [CrossRef]
  54. Evitayani, L.; Warly, L.; Fariani, A.; Ichinohe, T.; Abdulrazak, S.A.; Hayashida, M.; Fujihara, T. Study on nutritive value of tropical forages in North Sumatra, Indonesia. Anim. Sci. J. 2005, 76, 461–468. [Google Scholar] [CrossRef]
  55. Andualem, D.; Negesse, T.; Tolera, A. Chemical composition, in vitro organic matter digestibility and kinetics of rumen dry matter degradability of morphological fractions of stinging nettle (Urticasimensis). Adv. Biol. Res. 2016, 10, 183–190. [Google Scholar] [CrossRef]
  56. Rahim, I.; Sultan, J.I.; Sharif, M.; Bilal, M.Q. Chemical composition, mineral profile, palatability and in vitro digestibility of shrubs. J. Anim. Plant. Sci. 2013, 23, 45–49. [Google Scholar]
  57. Castro, M.; Teixeira, A.; Fernández-Núñez, E. The nutritive value of different Mediterranean browse species used as animal feeds under oak silvopastoral systems in Northern Portugal. Agrofor. Syst. 2021, 95, 269–278. [Google Scholar] [CrossRef]
  58. Flores, M.P.; Robles Cruz, A.B.; Rodríguez, R.; Ventura, M.R.; Caravaca, F.P. Effect of season on chemical composition and in vitro digestibility of six native forage shrubs species grazed by goats in protected areas in Canary Islands, Spain. Int. J. Agric. Biol. 2020, 23, 49–53. [Google Scholar] [CrossRef]
  59. Akbag, H.I. Potential nutritive value of Anagyris foetida shrub for goats. Agrofor. Syst. 2021, 95, 191–200. [Google Scholar] [CrossRef]
  60. Chebli, Y.; El Otmani, S.; Chentouf, M.; Hornick, J.L.; Cabaraux, J.F. Temporal variations in chemical composition, in vitro digestibility, and metabolizable energy of plant species browsed by goats in southern mediterranean forest rangeland. Animals 2021, 11, 1441. [Google Scholar] [CrossRef] [PubMed]
  61. Hutjens, M.F. Revisiting feed efficiency and its economic impact. In Proceedings of the Four-State Dairy Nutrition and Management Conference, Midwest Plan Service, Iowa State University, Ames, IA, USA, 6 June 2005; pp. 177–182. [Google Scholar]
  62. Decruyenaere, V.; Buldgen, A.; Stilmant, D. Factors affecting intake by grazing ruminants and related quantification methods: A review. Biotechnol. Agron. Soc. Environ. 2009, 13, 559–573. [Google Scholar]
  63. Balamurugan, B.; Ramamoorthy, M.; Mandal, R.S.K.; Keerthana, J.; Gopalakrishnan, G.; Kavya, K.; Katiyar, R. Mineral an important nutrient for efficient reproductive health in dairy cattle. Int. J. Environ. Sci. Technol. 2017, 6, 694–701. [Google Scholar]
  64. Hadiya, K.K.; Derashri, H.J.; Devalia, B.R.; Jani, R.G. Effect of supplementation of minerals and enzymes on service period and postpartum plasma minerals profile in crossbred cows. Vet. World. 2010, 3, 173–176. [Google Scholar]
  65. Dambe, L.M.; Mogotsi, K.; Odubeng, M.; Kgosikoma, O.E. Nutritive value of some important indigenous livestock browse species in semi-arid mixed Mopane bushveld, Botswana. Livest. Res. Rural. Dev. 2015, 27, 1–10. [Google Scholar]
  66. Suttle, N.F. Mineral Nutrition of Livestock; CABI Publishing: Wallingford, UK, 2010. [Google Scholar]
  67. Zervas, G. Feeding of Ruminants; Stamoulis Publications: Athens, Greece, 2013. (In Greek) [Google Scholar]
  68. Mata-González, R.; Hovland, M.; Abdallah, M.A.B.; Martin, D.W.; Noller, J.S. Nutrient uptake and gas exchange of Great Basin plants provide insight into drought adaptations and coexistence. Plant Ecol. 2021, 14, 854–869. [Google Scholar] [CrossRef]
  69. National Research Council (NRC). Nutrient Requirements of Small Ruminants; National Academic Press: Washington, DC, USA, 2007; pp. 271–280. [Google Scholar]
  70. DGF-Direction Générale des Forêts de Tunis. Résultats du Deuxième Inventaire Forestier et Pastoralnational, Inventaire des Forêts par Télédétection (IFPN); Direction Générale des Forêts de Tunis: Tunis, Tunisia, 2010; p. 195. [Google Scholar]
  71. Derbel, S.; Chaieb, M. Growth establishment and phenology of four woody Saharan species. Afr. J. Ecol. 2013, 51, 307–318. [Google Scholar] [CrossRef]
  72. Aronson, J.; Floret, C.; Le Floc’h, E.; Ovalle, C.; Pontanier, R. Restoration and rehabilitation of degraded ecosystems in arid and semi-arid lands. II. Case studies from Southern Tunisia, Central Chile and Northern Cameroon. Restor. Ecol. 1993, 1, 168–187. [Google Scholar] [CrossRef]
  73. Le Houérou, H.N. The nature and causes of desertization. In Desertification; Glantz, M., Ed.; Westview Press: Boulder, CO, USA, 1977; pp. 16–38. [Google Scholar]
  74. Heneidy, S.Z. A Study of the Nutrient Content and Nutritive Values of Range of Plants at Omayed, Egypt. Master’s Thesis, Alexandria University, Alexandria, Egypt, 1986. [Google Scholar]
  75. Raynaud, C. Atlanthemum Raynaud, un nouveau genre pour la famille des Cistaceae. An. Jard. Bot. Madr. 1987, 44, 309–317. [Google Scholar]
  76. Ozenda, P. Flore et Végétation du Sahara, 3rd ed.; CNRS: Paris, France, 1977. [Google Scholar]
  77. Hsia, C.N.; Korban, S. Effect of growth regulators, dark treatment and light intensity on shoot organogenesis from leaf tissues of evergreen azalea. J. Hortic. Sci. Biotechnol. 1998, 73, 53–60. [Google Scholar] [CrossRef]
  78. Radice, S.; Caso, O.H. In vitro organogenesis in leaves of azaleas ‘Petrick’ and ‘Rex’. Sci. Hortic. 1990, 41, 343–347. [Google Scholar] [CrossRef]
  79. Le Floc’h, E. Contribution à une Étude Ethnobotanique de la Flore Tunisienne; Imprimerie Officielle de la République Tunisienne: Tunis, Tunisia, 1983. [Google Scholar]
  80. Slama, A.; Fortas, Z.; Boudabous, A.; Neffati, M. Cultivation of an edible desert truffle (Terfezia boudieri Chatin). Afr. J. Microbiol. Res. 2010, 4, 2350–2356. [Google Scholar]
  81. Ermeli, N.B.; Alsabri, S.G.; Bensaber, S.M.; Mohamed, S.B.; Zetrini, A.A.; Aburas, K.M.; Fitouri, S.R.; Jaeda, M.I.; Mrema, I.A.; Hermann, A.; et al. Screening of analgesic and anti-inflammatory activities for two Libyan medicinal plants: Helianthemum lippii and Launaea residifolia. J. Chem. Pharm. Res. 2012, 4, 4201–4205. [Google Scholar]
  82. Alsabri, S.G.; Rmeli, N.B.; Zetrini, A.A.; Mohamed, S.B.; Meshri, M.I.; Aburas, K.M.; Bensaber, S.M.; Mrema, I.A.; Mosbah, A.A.; Allahresh, K.A.; et al. Phytochemical, anti-oxidant, anti-microbial, anti-inflammatory and anti-ulcer properties of Helianthemum lippii. J. Pharmacogn. Phytochem. 2013, 2, 86–96. [Google Scholar]
  83. Heneidy, S.Z.; Halmy, M.W.A.; Bidak, L.M. The ethnobotanical importance and conservation value of native plants in eastern Arabian Peninsula. Feddes Repert 2017, 128, 105–128. [Google Scholar] [CrossRef]
  84. Kartini, S.P.; Thongpraditchote, S.; Siripong, P.; Vallisuta, O. Effects of Plantago major extracts and its chemical compounds on proliferation of cancer cells and cytokines production of lipopolysaccharide-activated THP-1 macrophages. Pharmacogn. Mag. 2017, 13, 393–399. [Google Scholar] [CrossRef] [Green Version]
  85. Eldesoky, A.H.; Abdel-Rahman, R.F.; Ahmed, O.K.; Soliman, G.A.; Saeedan, A.S.; Elzorba, H.Y.; Elansary, A.A.; Hattori, M. Antioxidant and hepatoprotective potential of Plantago major growing in Egypt and its major phenylethanoid glycoside, acteoside. J. Food Biochem. 2018, 42, e12567. [Google Scholar] [CrossRef]
  86. Farcaș, A.D.; Moț, A.C.; Pârvu, A.E.; Toma, V.A.; Popa, M.A.; Mihai, M.C.; Sevastre, B.; Roman, L.; Vlase, L.; Pârvu, M. In vivo pharmacological and anti-inflammatory evaluation of Xerophyte Plantago sempervirens crantz. Oxid. Med. Cell. Longev. 2019, 2019, 13. [Google Scholar] [CrossRef]
  87. Scholz, H. Stipa tunetana, eine neue Artaus Tunesien, und das St. lagascae Aggregat (Gramineae). Willdenowia 1991, 26, 225–228. [Google Scholar] [CrossRef] [Green Version]
  88. Neffati, M. Caractérisation Morpho-Biologique de Quelques Espèces Végétales Nord Africaines: Implication Pour L’amélioration Pastorale. Ph.D. Thesis, University of Gent, Gent, Belgium, 1994. [Google Scholar]
  89. Le Floc’h, E.; Neffati, M.; Chaieb, M.; Floret, C.; Pontanier, R. Rehabilitation experiment at Menzel Habib, Southern Tunisia. Arid Soil Res. Rehabil. 1999, 13, 357–368. [Google Scholar] [CrossRef]
  90. Boughalleb, F.; Abdellaoui, R.; Hadded, Z.; Neffati, M. Anatomical adaptations of the desert species Stipa lagascae against drought stress. Biologia 2015, 70, 1042–1052. [Google Scholar] [CrossRef]
  91. Ouled Belgacem, A.; Neffati, M.; Papanastasis, V.P.; Chaieb, M. Effects of seed age and seeding depth on growth of Stipa lagascae R. & Sch. seedlings. J. Arid Environ. 2006, 65, 682–687. [Google Scholar] [CrossRef]
  92. Danin, A. Plants of desert dunes. In Cloudsley—Adaptations of Organisms to the Desert; Thompson, J.L., Ed.; Springer: Berlin/Heidelberg, Germany, 1996. [Google Scholar]
  93. Louhaichi, M.; Hassan, S.; Clifton, K.; Johnson, D.E. A reliable and non-destructive method for estimating forage shrub cover and biomass in arid environments using digital vegetation charting technique. Agrofor. Syst. 2018, 92, 1341–1352. [Google Scholar] [CrossRef] [Green Version]
  94. Van Soest, P.J.; Robertson, J.B.; Lewis, B.A. Methods for dietary fiber, neutral detergent fiber, and non-starch polysaccharides in relation to animal nutrition. J. Dairy Sci. 1991, 74, 3583–3597. [Google Scholar] [CrossRef]
  95. Tilley, J.M.A.; Terry, R.A. A two-stage technique for the in vitro digestion of forage crops. Grass Forage Sci. 1963, 18, 104–111. [Google Scholar] [CrossRef]
  96. Menke, K.H.; Raab, L.; Salewski, A.; Steingass, H.; Fritz, D.; Schneider, W. The estimation of the digestibility and metabolizable energy content of ruminant feeding stuffs from the gas production when they are incubated with rumen liquor in vitro. J. Agric. Sci. 1979, 93, 217–222. [Google Scholar] [CrossRef] [Green Version]
  97. Rivera, J.D.; Parish, J.A. Interpreting Forage and Feed Analysis Reports. Extension Service of Mississippi State University, Cooperating with U.S. 2010. Available online: https://extension.msstate.edu/sites/default/files/publications/publications/p2620.pdf (accessed on 29 July 2021).
  98. Undersander, D.; Moore, J.E.; Schneider, N. Relative forage quality. Focus Forag. 2002, 4, 1–2. [Google Scholar] [CrossRef]
  99. Geng, Y.; Ranjitkar, S.; Yanet, Q. Nutrient value of wild fodder species and the implications for improving the diet of mithun (Bos frontalis) in Dulongjiang area, Yunnan Province. China Plant Divers. 2020, 42, 455–463. [Google Scholar] [CrossRef]
  100. Esbati, M.; Farzadmehr, J.; Foroughi, A.; Rahdari, M.R.; Rodrigo-Comino, J. Assessment of the nutritional value of Gundelia tournefortii during its growth stages as a key element in the Senowbar rangeland ecosystem, Northeast of Iran. Int. J. Environ. Sci. Technol. 2021, 18, 1731–1738. [Google Scholar] [CrossRef]
  101. Habte, M.; Eshetu, M.; Andualem, D.; Maryo, M.; Legesse, A. The inventory of camel feed resource and the evaluation of its chemical composition in south-east rangelands of Ethiopia. Vet. Med. Sci. 2021, 7, 1172–1184. [Google Scholar] [CrossRef]
  102. Stalling, C.C. Test Available for Measuring Forage Quality. Virginia Cooperative Extension Dairy Guideline 404–424. 2005. Available online: https://vtechworks.lib.vt.edu/handle/10919/48380 (accessed on 29 July 2021).
  103. Oddy, V.H.; Robards, G.E.; Low, S.G. Prediction of in vivo dry matter digestibility from the fiber nitrogen content of a feed. In Feed Information and Animal Production; Robards, G.E., Packham, R.G., Eds.; Commonwealth Agricultural Bureaux: Farnham Royal, UK, 1983; pp. 395–398. [Google Scholar]
Figure 1. Plant height (cm), width (cm), and vegetation cover (%) of twelve native perennial species from arid rangelands of southern Tunisia. Values are the means ± standard error (SE) from 3 replicates (means ± SE).
Figure 1. Plant height (cm), width (cm), and vegetation cover (%) of twelve native perennial species from arid rangelands of southern Tunisia. Values are the means ± standard error (SE) from 3 replicates (means ± SE).
Plants 10 02031 g001
Figure 2. Biomass (g DM plant−1) of twelve native perennial species from arid rangelands of southern Tunisia. Values are the means ± standard error (SE) from 3 replicates (means ± SE).
Figure 2. Biomass (g DM plant−1) of twelve native perennial species from arid rangelands of southern Tunisia. Values are the means ± standard error (SE) from 3 replicates (means ± SE).
Plants 10 02031 g002
Figure 3. Correlation coefficients between yield attributes of twelve native perennial species from arid rangelands of southern Tunisia.
Figure 3. Correlation coefficients between yield attributes of twelve native perennial species from arid rangelands of southern Tunisia.
Plants 10 02031 g003
Figure 4. The chemical composition crude protein (CP; g/kg DM), acid detergent fiber (ADFom; g/kg DM), neutral detergent fiber (aNDFom; g/kg DM) and acid detergent lignin (ADL; g/kg DM) of twelve native perennial species from arid rangelands of southern Tunisia. Values are the means ± standard error (SE) from 3 replicates (means ± SE).
Figure 4. The chemical composition crude protein (CP; g/kg DM), acid detergent fiber (ADFom; g/kg DM), neutral detergent fiber (aNDFom; g/kg DM) and acid detergent lignin (ADL; g/kg DM) of twelve native perennial species from arid rangelands of southern Tunisia. Values are the means ± standard error (SE) from 3 replicates (means ± SE).
Plants 10 02031 g004
Figure 5. In vitro organic matter digestibility (IVOMD; g/kg DM), metabolizable energy (ME; MJ/kg) and relative feed value (RFV) of twelve native perennial species from arid rangelands of southern Tunisia. Values are the means ± standard error (SE) from 3 replicates (means ± SE).
Figure 5. In vitro organic matter digestibility (IVOMD; g/kg DM), metabolizable energy (ME; MJ/kg) and relative feed value (RFV) of twelve native perennial species from arid rangelands of southern Tunisia. Values are the means ± standard error (SE) from 3 replicates (means ± SE).
Plants 10 02031 g005
Figure 6. Correlation coefficients between quality attributes (CP; g/kg DM), acid detergent fiber (ADFom; g/kg DM), neutral detergent fiber (aNDFom; g/kg DM), acid detergent lignin (ADL; g/kg DM), in vitro organic matter digestibility (IVOMD; g/kg DM), metabolizable energy (ME; MJ/kg) and relative feed value (RFV), acceptability index (AI) of twelve native perennial species from arid rangelands of southern Tunisia.
Figure 6. Correlation coefficients between quality attributes (CP; g/kg DM), acid detergent fiber (ADFom; g/kg DM), neutral detergent fiber (aNDFom; g/kg DM), acid detergent lignin (ADL; g/kg DM), in vitro organic matter digestibility (IVOMD; g/kg DM), metabolizable energy (ME; MJ/kg) and relative feed value (RFV), acceptability index (AI) of twelve native perennial species from arid rangelands of southern Tunisia.
Plants 10 02031 g006
Figure 7. Dendrogram for twelve native perennial species from arid rangelands of southern Tunisia by average linkage method based on forage biomass yield, plant measurements and determinants of forage quality. Different colors represent different clusters (red: Cluster 1 color, green: Cluster 2: color, blue: Cluster 3).
Figure 7. Dendrogram for twelve native perennial species from arid rangelands of southern Tunisia by average linkage method based on forage biomass yield, plant measurements and determinants of forage quality. Different colors represent different clusters (red: Cluster 1 color, green: Cluster 2: color, blue: Cluster 3).
Plants 10 02031 g007
Figure 8. Map of Tunisia (based on land cover type [70]) showing the study site in Chenenni in the Governorate of Tataouine, Southern Tunisia.
Figure 8. Map of Tunisia (based on land cover type [70]) showing the study site in Chenenni in the Governorate of Tataouine, Southern Tunisia.
Plants 10 02031 g008
Table 1. Mineral concentration (Values are the means ± standard error (SE)). of native species on arid rangelands of southern Tunisia.
Table 1. Mineral concentration (Values are the means ± standard error (SE)). of native species on arid rangelands of southern Tunisia.
SpeciesFe (mg/kg DM)Zn (mg/kg DM)Cu (mg/kg DM)Mn (mg/kg DM)Na (g/kg DM)Ca (g/kg DM)Mg (g/kg DM)
A. henoniana1690.3 ± 2.76 b15 ± 0.03 h5 ± 0.05 j31 ± 0.06 h0.6 ± 0.01 g25.8 ± 0.13 d3.1 ± 0.06 cd
A. uniflorum1580.7 ± 2.12 c17.6 ± 0.03 e9.6 ± 0.03 c47.7 ± 0.12 d0.2 ± 0.01 k21.3 ± 0.25 e2.7 ± 0.35 de
E. fruticosum543.7 ± 2.1 j15.7 ± 0.02 f10.2 ± 0.01 b70.9 ± 0.02 b1.2 ± 0.02 c26.4 ± 0.16 c1.9 ± 0.06 f
G. decander1129.1 ± 2.08 f11.2 ± 0.02 k5.7 ± 0.02 h33.6 ± 0.03 e1.6 ± 0.01 b48 ± 0.06 a7.8 ± 0.18 a
H. kahiricum1500.9 ± 2.6 d15.3 ± 0.02 g7.2 ± 0.03 f33 ± 0.05 g0.6 ± 0.02 f19.8 ± 0.16 f2.7 ± 0.12 cde
H. lippii1277.1 ± 2.54 e27.3 ± 0.03 b7.7 ± 0.02 e71.6 ± 0.02 a0.5 ± 0.01 h20 ± 0.09 f3.1 ± 0.06 c
P. albicans2106.4 ± 0.03 a21.5 ± 0.03 c10.8 ± 0.03 a54.8 ± 0.02 c0.8 ± 0.02 d28.6 ± 0.14 b4.3 ± 0.15 b
R. suaveolens819.9 ± 1.06 g21.3 ± 0.02 d8.9 ± 0.12 d33.3 ± 0.14 f2.5 ± 0.01 a13.6 ± 0.2 g2.5 ± 0.03 e
S. lagascae387 ± 1.15 l12.6 ± 0.02 j3 ± 0.02 k23 ± 0.03 i0.5 ± 0.01 h4.4 ± 0.25 j0.8 ± 0.03 g
S. tenacissima619.9 ± 2.06 h21.5 ± 0.02 c2.8 ± 0.01 l20.6 ± 0.01 j0.7 ± 0.01 e5.5 ± 0.15 i1 ± 0.08 g
S. plumosa604.1 ± 2.1 i,**14.3 ± 0.03 i5.8 ± 0.01 g18.7 ± 0.02 k0.3 ± 0.01 i6.9 ± 0.03 h1.1 ± 0.06 g
S. pungens537.9 ± 2.1 k30.1 ± 0.05 a5.4 ± 0.02 i17.8 ± 0.12 l0.3 ± 0.01 j6.9 ± 0.06 h1.1 ± 0.09 g
Mean 1066.4118.66.838.00.8118.92.7
df11111111111111
F value1438314608451888385841426755182
** Means in a column with different letter(s) differ (p < 0.0001).
Table 2. Family, life form, and livestock acceptability index of studied species of southern Tunisia. 0: refusal or toxic; 1: occasionally palatable; 2: few palatable; 3: palatable; 4: very palatable; 5: extremely palatable.
Table 2. Family, life form, and livestock acceptability index of studied species of southern Tunisia. 0: refusal or toxic; 1: occasionally palatable; 2: few palatable; 3: palatable; 4: very palatable; 5: extremely palatable.
SpeciesFamilyLife FormAcceptability Index
Anthyllis henoniana Coss. ex Batt.FabaceaeChamaephyte4
Argyrolobium uniflorum (Deene.) Jaub. and Spach.FabaceaeChamaephyte5
Echiochilon fruticosum Desf.BoraginaceaeChamaephyte5
Gymnocarpos decander Forssk.CaryophyllaceaeChamaephyte5
Helianthemum kahiricum Delile.CistaceaeChamaephyte4
Helianthemum lippii (L.) Dum. Cours.CistaceaeChamaephyte5
Plantago albicans L.PlantaginaceaeHemicryptophyte5
Rhanterium suaveolens Desf.AsteraceaeChamaephyte2
Stipa lagascae Roem. and Schult.PoaceaeHemicryptophyte4
Stipa tenacissima L.PoaceaeHemicryptophyte1
Stipagrostis plumosa (L.) Munro ex T. AndersonPoaceaeHemicryptophyte4
Stipagrostis pungens (Desf.) de Winter.PoaceaeHemicryptophyte3
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Louhaichi, M.; Gamoun, M.; Hassan, S.; Abdallah, M.A.B. Characterizing Biomass Yield and Nutritional Value of Selected Indigenous Range Species from Arid Tunisia. Plants 2021, 10, 2031. https://doi.org/10.3390/plants10102031

AMA Style

Louhaichi M, Gamoun M, Hassan S, Abdallah MAB. Characterizing Biomass Yield and Nutritional Value of Selected Indigenous Range Species from Arid Tunisia. Plants. 2021; 10(10):2031. https://doi.org/10.3390/plants10102031

Chicago/Turabian Style

Louhaichi, Mounir, Mouldi Gamoun, Sawsan Hassan, and Mohamed A. B. Abdallah. 2021. "Characterizing Biomass Yield and Nutritional Value of Selected Indigenous Range Species from Arid Tunisia" Plants 10, no. 10: 2031. https://doi.org/10.3390/plants10102031

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop