A mathematical model of the aerobic deterioration of silage

A mathematical model of the aerobic deterioration of silage is described that includes the physical processes of gas and heat Rows, as well as an established model of microbial growth and the associated chemical changes. Yeasts and acetic acid bacteria are included in the growth model. The version of the model described relates to a cylinder of silage subject to forced aeration, a common experimental configuration. The model was very sensitive to variations in insulation thickness and yeast growth rate, and to initial pH, especially when maize was the forage. Great care is needed when selecting input data for use in the model to be sure that the physical and chemical properties are accurate. The model solution was sensitive to grid size, but with 361 cells, the maximum grid resolution that could be used on a 486 series PC, solutions were achieved with an acceptably small loss of accuracy. The model predicted the results of an experiment on silage deterioration quite accurately. However, the model also predicted that considerable spatial gradients of parameters, such as temperature, pH, and lactic acid, would occur. This indicates the need for care when taking samples or making temperature measurements in deterioration experiments. The model is potentially a useful tool in predicting the optimal time and position to take samples for analysis in a time-course experiment.     

A mathematical model of the aerobic deterioration of big-hale silage and its implications for the growth of Listeria monocytogenes

Aerobically spoiled silage has often been shown to harbour dangerously high levels of Listeria monocytogenes. This paper investigates the dynamics of aerobic deterioration in a silage bale as it occurs close to a site of damage to the cover. The underlying aim was to enable prediction of the extent of the silage that may become suitable for Listeria growth during the course of storage. In order to meet these objectives, a model was formulated that represents the microbiology of the deterioration process and the transport of oxygen and heat through the silage. The geometry of the system was exploited to ensure that the model is computationally tractable. The model was used to evaluate the effect of silage pH and puncture size on the risk of Listeria contamination. Although the hazardous fraction was seen to be relatively insensitive to the initial pH of the silage, it increased rapidly with puncture size. However, a small puncture can result in the 'loss' of a considerable fraction of the bale because of the relatively long time scale over which bales are stored.     

A simulation model of the microbiological and chemical changes accompanying the initial stage of aerobic deterioration of silage

A mathematical model is presented that predicts the time-course of aerobic deterioration in grass and whole-crop maize silages. The model predicts the stability of the silage taking into account the buffering capacity of the silage, the initial contents of organic acids and ethanol, pH, the initial temperature and the initial populations of the microorganisms. The specific processes simulated include the growth of yeast and acetic acid bacteria, the oxidation of fermentation products, the consumption of oxygen and the production of carbon dioxide, the rise in temperature. and the increase in pH.
The deterioration of silage is seen to be initiated by acetic acid bacteria or by yeast, or by both groups together. The factors that determine which groups will prevail are the dry matter contents and the chemical composition of the silage. The output of the model is validated by comparison of the simulated data with data from published work on the deterioration of silage.     

The aerobic stability of silage: key findings and recent developments

When silage is exposed to air on opening the silo, or after its removal from the silo, fermentation acids and other substrates are oxidized by aerobic bacteria, yeasts and moulds. The aerobic stability of silage is a key factor in ensuring that silage provides well‐preserved nutrients to the animal with minimal amounts of mould spores and toxins. In this paper, key findings and recent developments are reviewed, and findings of recent research are integrated in terms of four themes: (i) the most significant biochemical and microbiological factors, (ii) physical and management factors, (iii) type of additive and (iv) silo sealing. The development of yeasts and moulds during plant growth, and during field wilting or storage, and the concentration of undissociated acetic acid in silage are important microbiological and biochemical factors affecting aerobic stability. Silage density and porosity are key physical factors that affect the rate of ingress of oxygen into the silage mass during the feed‐out period. A target for potential silage aerobic stability is 7 d including time in the feed trough. To achieve this target, speed of harvest should be coordinated with packing tractor weight to achieve a minimum silage density by the time of feed‐out of 210 kg DM m^?3, maximum proportional porosity of 0·4 and a rate of silage removal, which matches or exceeds the depth of air penetration into the silo. The use of additives to increase aerobic stability is advisable when there is the risk of these objectives not being met. Novel microbial approaches to solving the problem of silage aerobic deterioration are needed.     

Effects of different additives on fermentation quality and aerobic stability of Leymus chinensis silage

This study investigated the effects of different additives on fermentation quality and aerobic stability of Leymus chinensis silage. Treatments included (i) no additive, (ii) 3 mL kg^?1 formic acid (FA), (iii) 6 mL kg^?1 FA, (iv) 5 mL kg^?1 acetic acid (AA), (v) 10 mL kg^?1 AA, (vi) 2 mL kg^?1 propionic acid (PA), (vii) 4 mL kg^?1 PA, (viii) 5 mL kg^?1 butyric acid (BA), (ix) 10 mL kg^?1 BA, (x) 1.0 g kg^?1 potassium sorbate (PS), (xi) 1.0 g kg^?1 sodium benzoate (SB), (xii) 1 × 10⁸ colony‐forming units (cfu) kg^?1 Lactobacillus (Lb) plantarum LP (LP), (xiii) 1 × 10⁸ cfu kg^?1 Lb. brevis LB (LB) and (xiv) 1 × 10⁸ cfu kg^?1 Lb. buchneri NCIMB40788 (Fresh). Each additive treatment was based on fresh matter (FM). Results showed that all additives decreased pH values. All additives except Fresh decreased ammonia‐N content (p < .001). Both LP and LB increased lactic acid content (p < .001). Butyric acid content increased with FA (3 mL kg^?1) and BA, but decreased with PA, PS, SB, FA (6 mL kg^?1), AA, LP, LB (p < .001). FA (3 mL kg^?1), AA (10 mL kg^?1), PA, BA, PS, SB and Fresh improved aerobic stability (p < .001). After 8 days exposure to air, the pH value and yeast count were lower in FA (3 mL kg^?1), BA (10 mL kg^?1), SB treatments than in other treatments. Overall, AA outperformed all other additives in improving fermentation quality. Sodium benzoate and AA could be used as an effective additive to improve aerobic stability of L. chinensis silage.     

A meta‐analysis comparing standard polyethylene and oxygen barrier film in terms of losses during storage and aerobic stability of silage

A meta‐analysis was undertaken of 51 comparisons of standard polyethylene film with oxygen barrier (OB) film in covering systems for bunker silos, unwalled clamp silos and bales. Mean losses of DM or OM during storage from the top 10 to 60 cm of bunker and clamp silos were 195 g kg^?1 for standard film and 114 g kg^?1 for OB film systems (41 sets of data, P < 0·001), while mean total losses of DM from baled silage were 76·8 g kg^?1 for standard film and 45·6 g kg^?1 for OB film systems (10 sets of data, P < 0·001). Top surface silage judged subjectively to be inedible was 107 and 29·6 g kg^?1 for standard film and OB film systems respectively (5 sets of data, P = 0·02). Aerobic stability was 75 h for silage stored under standard film system and 135 h for silage stored under OB film system (11 sets of data, P = 0·001). It is concluded that the OB film system reduces losses from the outer layers of silos and from bales and increases the aerobic stability of silage in the outer layers of silos.     

Separating the effects of forage source and field microbiota on silage fermentation quality and aerobic stability

This study attempted to separate the effects of forage source and field microbiota on silage fermentation quality and aerobic stability. Single samples of grass, red clover and maize were used. Field microbiota was obtained by centrifugation of microbial suspensions of the three samples. The intact forages were dried and sterilized by heating at 60°C for 3 h + 103°C for 15 h, inoculated in a 3 (forage) × 3 (inoculum) design and reconstituted to a dry‐matter level of 400 g kg^?1 before ensiling. After ensiling for 71 d, subsamples were subjected to an 8‐d aerobic stability test, which included temperature and pH measurements. Bacterial community analysis was performed on samples before and after ensiling by 16S rRNA gene amplicon sequencing. Forage source had a marked effect on the levels of lactic acid, acetic acid, ammonia‐N and 2,3‐butanediol, but microbiota source only affected the acetic acid concentration. The forage and microbiota as well as their interactions affected silage stability variables. The maize microbiota improved silage stability, whereas silages made from the maize forage had the poorest stability. Bacterial community analysis revealed higher abundance of lactic acid bacteria on the maize forage, with Lactococcus and Leuconostoc being the dominant genera. These preliminary results suggested that fermentation quality is mainly affected by forage source, whereas the aerobic stability is affected by both forage and field microbiota.     

Lactic acid bacteria strains for enhancing the fermentation quality and aerobic stability of Leymus chinensis silage

Leymus chinensis is an important grass in China and Russia. Six lactic acid bacteria (LAB) strains (LB, LPL1, LPL2, LPL3, LCL and WH) from L. chinensis silage were screened and identified and their effects on fermentation quality were investigated. All six strains were grown at 6·5% NaCl and pH 4·00. Strains LPL1, LPL2 and LPL3 were identified as Lactobacillus plantarum, and LB, WH and LCL were classified as Lactobacillus brevis, Weissella hellenica and Lactobacillus casei respectively. The six isolated strains and a commercial inoculant (Lactobacillus buchneri) were added to L. chinensis for ensiling at densities of 500 and 600 kg m^?3. The control was sprayed with the same volume of distilled water. The effects of the strains on fermentation quality after 45 d ensiling and aerobic stability during 8 d of exposure to air were evaluated. The 600 kg m^?3 silage had lower pH, butyric acid, ammonia nitrogen content and coliform bacteria counts than the 500 kg m^?3 density silage (P < 0·05). The six isolated strains decreased pH, butyric acid content and increased lactic acid content, and all inoculants increased L. chinensis silage aerobic stability except LCL (P < 0·05). The fermentation quality of L. chinensis silage increased with higher ensiling density. The LAB strains improved the fermentation quality, and high‐quality silage could be obtained at low ensiling density with the addition of the LAB strains. The strains improved the aerobic stability; Lb. buchneri and Lb. brevis showed the best performance.     

Effect of Lactobacillus buchneri 40788 on the fermentation,aerobic stability and nutritive value of maize silage

The effect of adding Lactobacillus buchneri 40788, a heterofermentative lactobacilli, to whole‐plant maize and its effect on fermentation and aerobic stability of the resulting silage were evaluated. Whole‐plant maize (380 g DM kg^–1 fresh weight) was ensiled in laboratory silos after the following treatments: untreated, L. buchneri 40788 at 1 × 10⁵, 2·5 × 10⁵, 5 × 10⁵, and 1 × 10⁶ colony forming units g^–1 of fresh forage or, a commercial inoculant containing homolactic acid bacteria, a single species of propionibacteria and enzymes. Addition of L. buchneri 40788 resulted in a decrease in lactic acid concentration but increased the concentration of acetic acid in silage and markedly decreased the numbers of yeasts present in the silage. All levels of L. buchneri 40788, increased the aerobic stability of silages but the effect was greatest for the two highest levels of inoculation. Treatment with the commercial inoculant had no effect on the fermentation or aerobic stability of silage. On‐farm treatment of maize silage with L. buchneri 40788, stored in a bag silo, resulted in changes in fermentation that were similar to those observed in laboratory silos. Treatment decreased the numbers of yeast in silage and increased aerobic stability (+25 h) of the silage when exposed to air. Treatment had no effect on the dry‐matter intake of silage fed to sheep. These results showed that treating silage with L. buchneri 40788 can increase the aerobic stability of maize silage in laboratory and farm silos.     

The effects of lactic acid bacteria on the fermentation,aerobic stability and nutritive value of maize silage

Maize was harvested at one‐third milk line (297 g kg^?1 DM) stage. All inoculants were applied at 1 × 10⁶ cfu g^?1 of fresh forage. After treatment, the chopped forages were ensiled in 1·5‐L anaerobic jars. Three jars per treatment were sampled on days 2, 4, 7, 12 and 90 after ensiling, for chemical and microbiological analysis. Homofermentative LAB‐inoculated silages had lower pH and higher lactate:acetate ratio (except for Lactobacillus plantarum/Pediococcus cerevisiae and L. plantarum/Propionibacterium acidipropionici) than the control and both heterofermentative LAB‐inoculated silages. Both L. buchneri inhibited yeast growth and CO₂ production during exposure of silage to air. The L. plantarum/P. cerevisiae, L. plantarum (Ecosyl) and L. plantarum/Enterococcus faecium‐inoculated silages had higher dry‐matter digestibility than the control and L. buchneri‐inoculated silages. Inoculants did not affect digestibility of neutral detergent fibre, except for L. buchneri (Biotal), organic matter nor ME content of silages. The LAB silage inoculants generally had a positive effect on maize silage characteristics in terms of lower pH and shifting fermentation toward lactate with homofermentative LAB or toward acetate with L. buchneri. The use of L. buchneri can improve the aerobic stability of maize silages by the inhibition of yeast activity.     

Nitrate in silage

Due to intensive Fertilizer application most silage crops contain appreciable amounts of nitrate. During silage fermentation the nitrate is completely or partially degraded. End-products are ammonia and nitrous oxide with nitrite and nitric oxide occurring as intermediates. Factors that influence nitrate degradation and the levels of end products and intermediates found in silages are reviewed. The role of plant nitrate reductase and of enterobacteria, Clostridia and lactobacilli in nitrate catabolism and the significance for silage quality are discussed. Attention is paid to silo-filler's disease, an illness of farm workers that is caused by inhalation of oxides of nitrogen, and to the occurrence of nitrosamines in silages.     

Effects of potassium sorbate and sodium benzoate at two application rates on fermentation and aerobic stability of maize silage

This study evaluated two potassium sorbate (PS) and sodium benzoate (SB) application rates in improving the aerobic stability of maize silage. Treatments included no additive, the addition of PS at 1 and 2 g kg^?1 fresh matter (FM) and the addition of SB at 1 and 2 g kg^?1 FM. Four replicates of each treatment were ensiled in 15‐L plastic jars. The silages were analysed for their fermentative characteristics and were subjected to an aerobic stability test with pH and yeast and mould count measurements. Considering fermentation quality and aerobic stability, both additives were effective. The PS was more active against yeasts during aerobic exposure. When the additives were applied at 2 g kg^?1, the silages were more stable (256 h, on average) than those with 1 g kg^?1 (119 h, on average) and control (61 h). Aerobic deterioration was more pronounced in the controls than in the treated silages. Silages treated at 2 g kg^?1 had consistent effects on pH values and yeast counts over 288 h of aerobiosis. Overall, PS and SB applied at 2 g kg^?1 were more effective in improving aerobic stability.     

Effects of Lactobacillus buchneri isolated from tropical maize silage on fermentation and aerobic stability of maize and sugarcane silages

This study was aimed to perform a screening of Lactobacillus buchneri strains from maize silage and use them as inoculant in maize and sugarcane silages. In all, 151 lactic acid bacteria (LAB) strains were isolated from whole‐plant maize silage, and their identification was based on the sequence analysis of 16S rDNA. In total, 15 strains were categorized to the L. buchneri group and eight of these were selected based on growth rate and fermentation pattern. The selected strains were evaluated on fermentation and aerobic stability of maize and sugarcane silages. For maize, the inoculated silages had lower pH and higher LAB population, but lower acetic acid concentration in comparison with the untreated control silage. For sugarcane silage, the strains 56.1, 56.4 and 40788 resulted in highest dry‐matter (DM) content and lowest DM losses. However, only the strain 40788 showed lowest counts of yeasts and moulds. Sugarcane silages inoculated with the strains 56.9, 56.26 and the untreated control silage showed highest concentrations of lactic acid and ethanol, besides the great DM losses. Even so, for both crops, the aerobic stability was not affected by inoculation. After air exposure, all silages increased temperature and had high population of yeast and moulds. Nevertheless, the strains 56.1 and 56.4 are promising for use as a silage inoculant.     

Impact of field fungal contamination of barley on ensiling properties,nutritional quality and the microbiome of barley silage

Barley varieties of differing fungal disease resistance were grown in triplicate plots at Lacombe and Lethbridge, Alberta with the disease resistant variety (FR) sprayed with a foliar fungicide to maximize differences in field fungal disease. Both varieties were harvested at soft dough and ensiled in minisilos to assess differences in fungal contamination on ensiling properties, nutritional quality, aerobic stability and associated bacterial and fungal microbiomes. Data were analysed as repeated measures with the effect of treatment × time (duration of ensiling or aerobic exposure) included in the model. The percentage leaf area diseased by net form net blotch was higher (p < 0.05) in the untreated barley cv. Sundre (UN, 59.1% leaf area affected at Lacombe and 25.2% at Lethbridge) than in the FR barley cv. Chigwell (0.7% leaf area affected at Lacombe and 0.1% at Lethbridge). Fungal resistant barley had a lower (p < 0.01) acid and neutral detergent fibre content. Relative abundance of Xanthomonadales was higher (p = 0.02) for FR than UN, while Lactobacillales dominated the bacterial microbiome after 60 day of ensiling in both silages. Bacillales dominated both FR and UN after 21 day of aerobic exposure. Fungal resistant fresh barley forage had a tendency (p = 0.10) for a greater relative abundance of Pleosporales, while UN had higher (p < 0.01) Hypocreales. Mould counts were lower (p = 0.01) for FR than UN after 7 day of ensiling. Fungal resistant barley had minimal influence on the fungal community that contributed to the aerobic deterioration of barley silage.     

A new sterilization and inoculation method in silage research

The study aimed at evaluating an effective sterilization–inoculation technique to facilitate silage research on the effect of forage microflora on fermentation variables. The sterilization effect of heating at 60°C for 3 h + 103°C for 15 h was tested on samples of grass, grass–clover, white clover and maize, pre‐dried at 60°C to a dry‐matter (DM) content >900 g kg^?1. The ensilability of treated samples, reconstituted to original DM concentration (250–390 g kg^?1), was assessed by inoculation with microfloras extracted from the original samples. Microfloral inoculants were obtained by a combination of centrifugation (15 500  g for 40 min) and filtration (0·45 and 0·22 μm pore sizes) of the supernatant. The sterilization treatment effectively sterilized the forage samples but decreased water soluble carbohydrates by 49% and N buffer solubility by 22% and increased the acid detergent insoluble N proportion of total N by 53% (P < 0·05). The reconstituted silages had 18% less lactic acid, 20% less ethanol and 37% less ammonia‐N (P < 0·05), but volatile fatty acids and 2,3‐butanediol did not differ from the untreated silages (P > 0·05). Counts of lactic acid bacteria, enterobacteria, clostridia, yeasts and moulds in the two silage treatments were also similar (P > 0·05). It is concluded that, despite causing chemical and physical alterations, the sterilization–inoculation technique evaluated could be a useful tool for future studies on the effects of microflora on ensiling results.     

Causes for soil sickness affecting early plant growth in aerobic rice

In aerobic rice, adapted varieties are grown in non-flooded and non-saturated soil. In the Philippines, occasional poor crop growth and yield failures have been reported. To investigate the underlying causes, we conducted 3 pot experiments using the aerobic rice variety Apo and so-called “sick soil” from a field where aerobic rice failed in four successive dry seasons. The (experimental) aerobic rice crop replaced the farmer's practice of wet-season lowland rice and dry season sweet potato cropping. We hypothesized that abiotic factors, especially the inter-relationship between high soil pH and impaired micronutrient uptake, restrict plant growth, and that ammonium sulfate has an ameliorating effect. Experiment 1 used “sick soil” collected from around yellowing and dying plants in a field experiment with aerobic rice yield failure, and “healthy soil” collected from around well-growing plants in the same field. We used three N fertilizer treatments (ammonium sulfate, urea, no application) and two soil water conditions (well drained and water-logged). In experiment 2, the treatments were a combination of sick and healthy soil, N fertilizer, soil acidification, and foliar application of Fe. Experiment 3 compared the irrigation water used at the experimental field site with reverse-osmosis water. Irrigation with water from the field site increased soil pH, impaired plant growth, and induced chlorosis. The application of ammonium sulfate reduced soil pH to values below 6 and increased plant micronutrient (Fe, Mn and Zn) contents and plant growth. In early vegetative plant growth, the high soil pH appeared to be the key determinant of “sick soil”, while root knot nematodes were most likely secondary causes for poor plant growth.     

Effect of compaction,delayed sealing and aerobic exposure on maize silage quality and on formation of volatile organic compounds

Physical and management factors, such as compaction and sealing, greatly influence the outcome of forage conservation. This study aimed to determine the effects of compaction, delayed sealing and aerobic exposure after ensiling on maize silage quality and on formation of volatile organic compounds. Whole‐crop maize (277 g/kg dry matter [DM]) in 120‐L plastic silos was compacted at either high or low density, and sealed immediately or with delay at 2 days or 4 days post‐filling (six replicates each). After ensiling for at least 175 days, the silages were exposed to air for 6‐day intervals and sampled at 2‐day intervals. A delay in sealing caused an increase in yeast counts and a decline of up to 65% in water‐soluble carbohydrates before ensiling. Sealing the silos after 4 days caused DM losses of up to 11%. Delayed sealing promoted the formation of ethyl esters at silo opening. A 4‐day delay in sealing resulted in the lowest aerobic stability. Aerobic exposure led to considerable changes in silage composition, a loss in feed value and, finally, spoilage. This study indicates that maize silage quality is adversely affected by low compaction, delayed sealing and aerobic exposure.     

Grass silage as a basic feed for store lambs. 2. Effect of harvesting system and chop length of grass silage on silage intake and performance of store lambs

A perennial ryegrass sward was cut at a leafy stage of growth and harvested with different harvesters to produce silages differing in chop length to evaluate the effect of silage chop length on silage intake and on the performance of store Iambs when silage was fed as the sole diet. The silage was harvested in late May either as long silage (L), single-chopped (S). double-chopped (D). long precision-chopped (LP) or medium precision-chopped (MP) silage with (he appropriate machinery. The silages were treated with formic acid at 2.5 1 t^?1. were well preserved (pH 3.7–3.8) and were of high dry-matter digestibility [749–810 g DMD kg^?1 dry-matter (DM)]. The silages were fed ad libitum as the sole diet to Suffolk crossbred store lambs over a period of 11 weeks. Silage intake and lamb performance progressively increased as silage chop length declined from 32.4 cm (L) to 6.8 cm (MP). Silage intakes were 572, 661, 750, 893 and 1129 (± 21) g DM d^?1 for silages L, S, D, LP and MP respectively. The corresponding daily liveweight gains were -3, 40, 53, 85 and 151 (± 7.6) g d^?l. Similar increases in empty body weight gain and carcass weight gain were obtained as silage chop length declined. Rumen retention time (RRT), estimated from the rumen contents of the lambs at slaughter and their silage intake in the week before slaughter, was much shorter for silages LP and MP compared with silages L or S. Silage intake was negatively related to RRT(b= -24.5 ± 6.1 gDM h^?l RRT). The results of this study showed that high intakes of grass silage and liveweight gains were achieved when grass was cut at a leafy stage of growth and harvested with a precision-chop harvester set to produce a moderate chop length (7 cm). The feeding of long or flail-chopped silages resulted in lower intakes and lower liveweight gains.     

Effects of formic acid and potassium diformate on the fermentation quality,chemical composition and aerobic stability of alfalfa silage

The objective of this study was to evaluate the efficacy of potassium diformate (KDF) as a potential additive for alfalfa silage. Fresh alfalfa was untreated or treated with formic acid (4 g/kg fresh weight, FW) or three concentrations of KDF (4, 5.5 or 7 g/kg FW). After 60 days of ensiling, the addition of formic acid and greater levels of KDF (5.5 and 7 g/kg) effectively reduced silage pH and inhibited the undesirable bacteria, indicated by lower butyric acid, ethanol, ammonia N concentrations and microbial populations (including enterobacteria, yeasts, moulds and clostridia). Additives decreased the dry‐matter loss, and more water‐soluble carbohydrates were preserved in the silages with formic acid or potassium diformate than in the control. Alfalfa silages treated with formic acid at 4 g/kg FW or potassium diformate at 5.5 or 7 g/kg FW were classified as the highest quality silage based on the higher Flieg's point (above 70) and remained stable for more than 9 days during aerobic exposure. Potassium diformate is recommended as an effective additive for alfalfa silages at a level of 5.5 or 7 g/kg FW under the humid and hot conditions of southern China.     

Fermentation characteristics and aerobic stability of grass silage inoculated with Lactobacillus buchneri, with or without homofermentative lactic acid bacteria

Aerobic spoilage by yeasts and moulds is a major cause of reduced nutritional value of silage and increases the risk of potential pathogenic microorganisms. Recent studies have shown that inoculation with Lactobacillus buchneri inhibits yeast growth and reduces the susceptibility to aerobic spoilage of various ensiled forages. The aim of this study was to determine whether these effects are retained when L. buchneri is added in combination with homofermentative lactic acid bacteria. In three experiments, silages were produced from perennial ryegrass [240–421 g kg⁻¹ dry matter (DM)] inoculated with L. buchneri or L. buchneri plus a mixture of Pediococcus pentosaceus and Lactobacillus plantarum (inoculant PL). Uninoculated silage and silage inoculated with PL alone served as controls. Silages were examined for pH and DM loss in the course of ensilage and chemical and microbiological composition and aerobic stability after 3–4 months. L. buchneri plus PL and PL alone increased the initial rate of pH decline. L. buchneri alone and L. buchneri plus PL enhanced aerobic stability and, in general, reduced yeast and mould counts. In addition, these inoculants increased the final pH and DM loss and the concentrations of acetic acid and 1,2-propanediol (or propionic acid and 1-propanol instead of 1,2-propanediol), and decreased the concentration of lactic acid. The effects of L. buchneri on fermentation products increased with decreasing DM content. In silages of less than 270 g kg⁻¹ DM, L. buchneri increased the ammonia-N concentration. It is suggested that this was associated with the relatively high final pH resulting from the high metabolic activity of L. buchneri in these silages.