Search

This experiment was conducted to evaluate different microalgae species as protein supplements in the nutrition of lactating dairy cows in comparison to soya bean meal. Four multiparous lactating Finnish Ayrshire cows (112 days in milk) were used in a balanced 4 × 4 Latin square study. Cows were fed separately fixed amount of cereal-sugar beet pulp based concentrate (12.5 kg/d) and grass silage ad libitum. Experimental treatments consisted of four isonitrogenous protein supplements: soya bean meal (SOY), Spirulina platensis (SPI), Chlorella vulgaris (CHL) and a mixture of C. vulgaris and Nannochloropsis gaditana (1:1 on dry matter (DM) basis; CHL-NAN). The substitution of soya bean meal by microalgae did not affect the quantity of total DM intake (DMI), but changed the composition of DMI by decreasing the concentrate:forage ratio of the diet (P=0.054) owing to the poorer palatability of microalgae. Intake of methionine was increased (P

Ruminant-based food production faces currently multiple challenges such as environmental emissions, climate change and accelerating food-feed-fuel competition for arable land. Therefore, more sustainable feed production is needed together with the exploitation of novel resources. In addition to numerous food industry (milling, sugar, starch, alcohol or plant oil) side streams already in use, new ones such as vegetable and fruit residues are explored, but their conservation is challenging and production often seasonal. In the temperate zones, lipid-rich camelina (Camelina sativa) expeller as an example of oilseed by-products has potential to enrich ruminant milk and meat fat with bioactive trans-11 18:1 and cis-9,trans-11 18:2 fatty acids and mitigate methane emissions. Regardless of the lower methionine content of alternative grain legume protein relative to soya bean meal (Glycine max), the lactation performance or the growth of ruminants fed faba beans (Vicia faba), peas (Pisum sativum) and lupins (Lupinus sp.) are comparable. Wood is the most abundant carbohydrate worldwide, but agroforestry approaches in ruminant nutrition are not common in the temperate areas. Untreated wood is poorly utilised by ruminants because of linkages between cellulose and lignin, but the utilisability can be improved by various processing methods. In the tropics, the leaves of fodder trees and shrubs (e.g. cassava (Manihot esculenta), Leucaena sp., Flemingia sp.) are good protein supplements for ruminants. A food-feed production system integrates the leaves and the by-products of on-farm food production to grass production in ruminant feeding. It can improve animal performance sustainably at smallholder farms. For larger-scale animal production, detoxified jatropha (Jatropha sp.) meal is a noteworthy alternative protein source. Globally, the advantages of single-cell protein (bacteria, yeast, fungi, microalgae) and aquatic biomass (seaweed, duckweed) over land crops are the independence of production from arable land and weather. The chemical composition of these feeds varies widely depending on the species and growth conditions. Microalgae have shown good potential both as lipid (e.g. Schizochytrium sp.) and protein supplements (e.g. Spirulina platensis) for ruminants. To conclude, various novel or underexploited feeds have potential to replace or supplement the traditional crops in ruminant rations. In the short-term, N-fixing grain legumes, oilseeds such as camelina and increased use of food and/or fuel industry by-products have the greatest potential to replace or supplement the traditional crops especially in the temperate zones. In the long-term, microalgae and duckweed of high-yield potential as well as wood industry by-products may become economically competitive feed options worldwide.

Two experiments were conducted to evaluate microalgae as a protein supplement in the nutrition of lactating dairy cows in relation to unsupplemented and rapeseed meal supplemented diets. In both experiments multiparous Finnish Ayrshire cows were fed separately fixed amount of cereal-sugar beet pulp based concentrate (11 kg/d in Exp. 1 and 12 kg/d in Exp. 2), and grass silage ad libitum. In Exp. 1, six cows (212 days in milk; DIM) were used in a replicated 3 × 3 Latin square. Diets were supplemented isonitrogenously with rapeseed meal (pelleted rapeseed supplement, RSS), mixture of Spirulina platensis and Chlorella vulgaris microalgae (1:1 on dry matter (DM) basis; ALG) or a mixture of RSS and ALG (1:1 on crude protein (CP) basis; RSS-ALG). In Exp. 2, four intact cows and four rumen cannulated cows (190 DIM) were used in a replicated 4 × 4 Latin square. Treatments consisted of basal diet without protein supplement (NEG) or supplemented similarly as in Exp. 1 with the exception of RSS-ALG and ALG containing only S. platensis. Protein supplementation increased fibre and N digestibility but did not affect dry matter intake (DMI) or milk yield. The substitution of rapeseed by microalgae did not affect total DMI or milk yield in neither of the experiments, but changed the quality of DMI in Exp.2 by linearly decreasing concentrate:forage ratio of the diet due to poorer palatability of microalgae. The efficiency of N utilisation (NUE) in milk production varied from moderate (Exp. 1) to high (Exp. 2), and in Exp. 2 was decreased by both protein supplementation and microalgae inclusion in the diet. Protein supplementation or microalgae inclusion in the diet did not affect ruminal pH or major volatile fatty acids in Exp. 2, but both increased ruminal NH3-N concentration. There was likely a shortage of N for rumen microbes on NEG in Exp. 2 as indicated by low milk urea N and increased microbial N flow on protein supplemented diets. In both experiments, only minor differences were observed in plasma metabolites when microalgae substituted rapeseed. Even though arterial histidine concentrations were high, arterial histidine and carnosine concentrations (Exp. 1 and 2) and milk protein yields (Exp. 2) decreased by microalgae inclusion suggesting that histidine supply may become suboptimal on microalgae supplemented diets. Experiments demonstrated the suitability of microalgae as protein supplement for dairy cows, however, the protein value of microalgae is likely slightly lower than that of rapeseed meal. Two experiments were conducted to evaluate microalgae as a protein supplement in the nutrition of lactating dairy cows in relation to unsupplemented and rapeseed meal supplemented diets. In both experiments multiparous Finnish Ayrshire cows were fed separately fixed amount of cereal-sugar beet pulp based concentrate (11 kg/d in Exp. 1 and 12 kg/d in Exp. 2), and grass silage ad libitum. In Exp. 1, six cows (212 days in milk; DIM) were used in a replicated 3 × 3 Latin square. Diets were supplemented isonitrogenously with rapeseed meal (pelleted rapeseed supplement, RSS), mixture of Spirulina platensis and Chlorella vulgaris microalgae (1:1 on dry matter (DM) basis; ALG) or a mixture of RSS and ALG (1:1 on crude protein (CP) basis; RSS-ALG). In Exp. 2, four intact cows and four rumen cannulated cows (190 DIM) were used in a replicated 4 × 4 Latin square. Treatments consisted of basal diet without protein supplement (NEG) or supplemented similarly as in Exp. 1 with the exception of RSS-ALG and ALG containing only S. platensis. Protein supplementation increased fibre and N digestibility but did not affect dry matter intake (DMI) or milk yield. The substitution of rapeseed by microalgae did not affect total DMI or milk yield in neither of the experiments, but changed the quality of DMI in Exp.2 by linearly decreasing concentrate:forage ratio of the diet due to poorer palatability of microalgae. The efficiency of N utilisation (NUE) in milk production varied from moderate (Exp. 1) to high (Exp. 2), and in Exp. 2 was decreased by both protein supplementation and microalgae inclusion in the diet. Protein supplementation or microalgae inclusion in the diet did not affect ruminal pH or major volatile fatty acids in Exp. 2, but both increased ruminal NH3-N concentration. There was likely a shortage of N for rumen microbes on NEG in Exp. 2 as indicated by low milk urea N and increased microbial N flow on protein supplemented diets. In both experiments, only minor differences were observed in plasma metabolites when microalgae substituted rapeseed. Even though arterial histidine concentrations were high, arterial histidine and carnosine concentrations (Exp. 1 and 2) and milk protein yields (Exp. 2) decreased by microalgae inclusion suggesting that histidine supply may become suboptimal on microalgae supplemented diets. Experiments demonstrated the suitability of microalgae as protein supplement for dairy cows, however, the protein value of microalgae is likely slightly lower than that of rapeseed meal.