Abstract
A biogenic agricultural compound enables pasture to synthesise more soluble sugars and delivers benefits attributable to bioactive molecules: phenylpropanoids. Phenylpropanoids are plant secondary compounds that help plants overcome biotic and abiotic stress to increase pasture quality and yield. When consumed by ruminants, phenylpropanoids improve the conversion efficiency of pasture protein to milk and meat. The effect of this compound, trademarked Biozest™, on pasture and ruminant efficiency was evaluated via split block trials followed by full scale, full life cycle, on-farm trials. Aspects measured include pasture resilience, quality and productivity, livestock productivity and urea excretion. Biozest™ improved pasture resilience, quality, and yield by over 75%. Soluble sugar content of the pasture increased (18%). When livestock grazed Biozest™ treated pasture, urea excretion was reduced (20–48%), and milk and meat production increased (30%). The pasture, livestock productivity and urea benefits of Biozest™ have been established. Trial results support the following inferences. First, the fermentation of the increased soluble carbohydrates in Biozest treated pasture would result in increased propionates and less acetoclastic methanogenesis. Second, the reduction in urea excretion and increase in livestock productivity would result from a reduction in the proportion of dietary protein digested to ammonia and reduced deamination of some of the ammonia to urea. Further, due to the reduced deamination, fewer carbonyls and hydride moieties would be available for methylotrophic and hydrogenotrophic methanogenesis. Future work may include quantification or modelling of increased carbon dioxide sequestration and quantification of the reduction in nitrous oxide and methane emissions.
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Introduction
Energy lost as methane (CH4) and feed protein wasted as urea are two significant inefficiencies inherent in ruminant production systems (Eckard et al. 2010). Addressing these inefficiencies can reduce environmental liabilities and increase productivity (Leng 1991).
On average, ruminants convert 24.7% of feed nitrogen (N) into milk or meat (Hristov and Jouany 2005). Seventy five per cent (75%) of feed N is wasted as urine or dung urea (Hristov and Jouany 2005). In addition, cattle typically lose 6% of their ingested energy as eructated CH4 (Johnson and Johnson 1995). Therefore, ruminant metabolic inefficiency significantly impacts farm productivity and the emission of CH4 and nitrous oxide (N2O), both of which are greenhouse gases (GHGs).
GHGs are gases in the atmosphere such as water vapour, carbon dioxide, CH4 and N2O that can absorb infrared radiation, trapping heat in the atmosphere. This process, known as the greenhouse effect, means that emissions of GHGs due to human activity contribute to global warming (IPCC 2019). N2O and CH4 have 265 and 28 times, respectively (with the inclusion of climate–carbon feedbacks) the global warming potential of carbon dioxide over 100 years (IPCC 2014). Therefore, a small reduction in urea excretion and CH4 eructation can significantly decrease farm GHG liabilities.
A small increase in the percentage of feed protein converted to milk or meat can deliver a substantial increase in farm productivity. For example, a feed protein conversion increase of 2.5% (from 25% to 27.5%) can deliver a 10% increase in farm productivity. In addition, increasing the conversion efficiency of pasture protein into milk or meat results in less waste as urea and CH4, thus increasing productivity while reducing environmental impacts and GHG emissions.
There are two probable processes for reducing methanogenesis during ruminant fermentation. One strategy is to increase the relative amount of soluble carbohydrates in pasture (Theodorou et al. 2006). The fermentation of these soluble carbohydrates is less methanogenic than the fermentation of cell wall carbohydrates (Moe et al. 1979; Wang et al. 2018). The second strategy for improving feed conversion efficiency in ruminants is to reduce urea excretion by reducing the amount of pasture protein converted into ammonia (NH3) in the rumen (Theodorou et al. 2006).
Phenylpropanoids are compounds with a chain of 3 carbons bound to an aromatic ring of 6 carbons (Calsamiglia et al. 2007). Plants produce a range of phenylpropanoids, including anthocyanins, flavonoids, isoflavonoids, flavones, lignin, suberin and coumestrol (Dixon and Paiva 1995). Phenylpropanoids have several roles in plant health and growth. Isoflavonoids, for example, strengthen the defence system against pest and disease damage (Chinnusamy et al. 2003), thus improving plant health. Scientific evidence also substantiates farmers’ assertions that phenylpropanoids improve animal health (Theodorou et al. 2006).
Phenylpropanoids can improve pasture productivity by reducing pest, disease and environmental (drought, waterlogging, wind, cold, salinity and light) stress (Dixon and Paiva 1995). Phenylpropanoids also signal soil microbes involved in nutrient procurement (Harrison and Baldwin 2004). For example, phenylpropanoids secreted by plant roots act as signals to attract N fixing bacteria (Hassan and Mathesius 2012). Phenylpropanoids also promote the development of mycorrhizal fungi that are crucial for phosphate uptake and enhance nutrient availability through chelation and mineralisation of soil calcium, iron and phosphates (Harrison and Baldwin 2004).
Phenylpropanoids in plants and pasture have beneficial effects on rumen fermentation, microbial populations, meat and milk production, feed conversion efficiency and CH4 inhibition (Patra 2011). In addition, an increased phenylpropanoid content in pasture increases the content of conjugated linoleic acids, the health promoting fatty acids found in milk and meat produced by pasture fed ruminants (Patra 2011). A higher content of phenylpropanoids in pasture can shift the type of N excreted in urine and dung from a soluble form to an insoluble form of N (Patra 2011), which has a beneficial effect on N cycling and the reduction of leaching.
Plants have membrane anchored molecular pattern recognition receptors (Panstruga et al. 2009). These receptors monitor extracellular biotic stress messenger molecules and abiotic stress sensory messages. One of the mechanisms of response to both abiotic and biotic stress signalling molecules is the induction and upregulation of the phenylpropanoid metabolic pathway in plants (Dixon and Paiva 1995; Sharma et al. 2019).
Knowledge of the presence of such receptors and the mechanisms by which microorganisms, plants and animals respond to each other (Harrison and Baldwin 2004), the environment (Chinnusamy et al. 2003), and defend against pathogens and pests (Nürnberger et al. 2004) enabled the development of a novel agricultural compound, Biozest™.
Biozest™ is a molecular pattern recognition receptor (MPR) signalling agricultural compound. The application of Biozest™ on crops and pasture delivers the range of phenomena attributable to phenylpropanoid cascades (Indigo Limited, unpublished reports). The full mechanism of the observed biological response has yet to be determined. However, field observations and data from several crops support the hypothesis that the membrane bound receptors on plants recognise and react to Biozest™ applications: inducing and sustaining the innate production of phenylpropanoid cascades.
This study examined the effect of Biozest™ on pasture productivity, milk and meat production and consequent impacts on urea excretion in pastoral farming systems. We hypothesised that the application of this compound on pasture would increase the availability of soluble carbohydrates and induce and sustain the production of phenylpropanoids. This pasture response might improve the feed conversion efficiency of ruminants that consume the treated pasture, leading to increased milk/meat production and reduced urea excretion and emissions of N2O and CH4.
Method
Biozest™ is a gene mediated technology and engages ecologically through multitrophic interactions. This complexity, combined with the number of benefits delivered, makes conventional replicated small plot evaluations highly variable and underpowered. A systems biology approach was employed to account for complex, multilevel interactions. The experimental design selected enabled the assessment of plant and ruminant responses in their natural or typical setting (Fang and Casadevall 2011). Trials were thus carried out in ‘real world conditions’ (Merfield and Johnson 2013) on commercial farms to establish the effect of Biozest™ pasture treatments and the consequent commercial benefits such as increased pasture productivity, milk production and quality and animal liveweight.
When assessing emissions mitigation strategies, the whole-farm impact must be examined (Eckard et al. 2010). This supported the decision to use large-scale trials for the assessment of Biozest™. Whole-farm system modelling and life-cycle assessments were employed to ensure production, quality and overall farm productivity were accounted for.
Pasture productivity and palatability
Pasture dry matter (DM) was measured using a statistically verified, industry standard method (Litherland et al. 2008). Rising plate pasture meters were used to measure the standard compression height of the sward, which was then converted to DM ha-1 via the standardised industry measurement and DM calculation protocol.
Pasture growth and DM production
Two (2) paddocks (paddocks 40 and 42) were selected and split into two on a New Zealand dairy farm in Taranaki. Two (2) sprays of Biozest™ were applied at a rate of 1 L ha−1 to one half of each paddock. The first spray was applied on 11 June 2009. The second spray was applied 7 days later. Pasture growth (measured as DM production) was measured across both paddocks on 30 June 2009 (19 days after the first Biozest™ treatment).
Pasture growth and DM consumption (palatability)
A trial to assess productivity and palatability was conducted on a dairy farm in Northland, New Zealand. Half of the paddock was treated with Biozest™ at the recommended rate of 1 L ha−1. The sprays were applied on 03 September and 07 September 2009. In this paddock, the DM measurements were taken before grazing (on 15 October 2009) and after grazing (on 19 October 2009).
Pasture productivity: cut baleage
A baleage harvest trial was conducted on two dairy farms located on the Hauraki Plains, Waikato, New Zealand. The two farms, owned and managed by one family, were located side by side and received similar management. Two (2) sets of paddocks on each farm were set aside for baleage production (Set A and Set B). One (1) farm was treated with Biozest™ twice (on 26 and 30 June 2017) as per the label directions, while the control farm received no Biozest™ treatments. Due to wet conditions, Set A paddocks were not grazed post treatment. Set A was cut on 21 November 2017. Set B paddocks were grazed, and a 3rd Biozest™ treatment was applied 3 days after grazing on 13 September 2017. Set B was cut on 24 November 2017. The number of bales per paddock was recorded and converted to bale production ha−1. The yield from the Biozest™ treated farm was compared to the untreated control farm.
Environmental stress tolerance
Stress tolerance trials were carried out on a dairy farm in Northland, New Zealand. Three paddocks were selected to provide a range of environmental conditions, pasture compositions and management variations within the farm. The paddocks were split into two, and the recommended Biozest™ treatment programme was applied to the treated half: 1 L Biozest™ in 500 L water ha-1. Two (2) applications 5 days apart were applied, followed by a 3rd application 3 to 5 days after grazing. DM production was measured using a rising plate meter before and after grazing. The trials were carried out in 2010.
Drought and frost tolerance
A paddock was selected with assistance from the farmer for the assessment of drought and frost tolerance. In 2010 this region experienced drought (January-April) and frosts in June–August, unusual for this northern region (NIWA 2011). The drought was described by the National Institute of Water and Atmospheric Research as the worst in the Northland region in 60 years when just 253 mm of rain fell between November 2009 and April 2010 (Tait 2011).
On drought tolerant pasture
A mixed pasture paddock: 60% ryegrass and 40% Kikuyu (Pennisetum clandestinum) was selected. Kikuyu has been shown to perform well compared to other common forage species (including ryegrass) in drought or low rainfall conditions (Neal et al. 2009).
Soil and water stress
On the same Northland farm, Biozest™ treatments were applied to a swampy/waterlogged paddock. The farmer identified that soil/water stress conditions typically occurred in this paddock in winter/spring when the soil becomes waterlogged and again in summer when the shallow rooted pasture is stressed and dries off early in the season.
Stock condition and weight gain (Angus stud bulls)
In 2011 on a farm in Oparau, Waikato, New Zealand, a herd of 40 Angus stud bulls was divided into two. Twenty (20) bulls grazed on 20 ha of untreated pasture while 20 bulls grazed on 20 ha of Biozest™ treated pasture throughout the 10-week finishing period. Two (2) Biozest™ treatments were applied by helicopter one week apart at a rate of 1 L ha-1. The bulls then grazed the pasture for 68 days. The bulls were weighed at the start and the end of the finishing period. The bulls were then sent to a sales auction, where the price achieved for each bull was recorded.
Soluble carbohydrate assessment
A split block/paddock experimental design was applied on a dairy goat farm in Pukeatua, Waikato, New Zealand. Biozest™ was applied to half the paddock at a rate of 1 L ha-1. Two (2) initial applications were made close together (5 days apart). Follow on treatments were applied 3 to 5 days after grazing throughout the season. The pasture was tested for soluble solids using a hand-held digital refractometer every 7 days for 28 days following the method recommended by Novel Technologies (Balsom and Lynch 2008). Sampling was undertaken on a clear day when the pasture was dry. The pasture samples were rolled by hand for 60 seconds, and juice exuding from the sample was squeezed directly onto a refractometer. Values were expressed in °Brix.
The same assessment methodology was applied on a sheep farm in Auckland, New Zealand. A paddock was split in half and received 3 applications of Biozest™ at a rate of 1 L ha−1. Seven (7) days after the 3rd application, samples were alternately taken from the treated and control side of the paddock. Six (6) samples were taken from each side.
Milk production and quality
Dairy goats on a farm in Pukeatua, Waikato, New Zealand, were fed pasture from paddocks treated with Biozest™ and control paddocks in cycles. Biozest™ treatments were applied at the rate of 1 L Biozest™ in 500 L water ha-1. Two (2) initial applications were made close together (5 days apart). Follow on treatments were applied 3 to 5 days after grazing throughout the season. The results reported were extracted from the supply and quality report data from Dairy Goat Co-operative Ltd.
A milk production trial was carried out on a dairy farm on the Hauraki Plains, Waikato, New Zealand. Biozest™ treatments were applied, beginning in late summer 2012, at the rate of 1 L Biozest™ in 500 L water ha−1. Two (2) initial applications were made close together (5 days apart). Follow on treatments were applied 3 to 5 days after grazing throughout the season. Gestating cows grazed Biozest™ treated pasture and untreated pasture in cycles of approximately 8 to 10 days from 02 February to 20 April. The milk production results were extracted from the cooperative milk processor’s supply and quality analysis report.
Urea discharge
Urine samples were taken from the herd described previously in the dairy goat trial in Pukeatua. Five (5) goats were selected at random, and urine samples were collected. Samples were collected during each feeding cycle on Biozest™ treated or untreated control pasture. Each round of sample collection was carried out 2 to 3 days before the stock were shifted onto Biozest™ treated or control pasture feed. The urine urea and creatinine levels in the urine were determined by an independent laboratory, Gribbles Veterinary, using an automated analyser (Hitachi Modular, Roche Diagnostics Corporation, Indianapolis, IN, United States of America) with kits supplied by Roche Diagnostics Corporation.
Urine samples from 5 randomly selected cows were collected from a dairy farm on the Hauraki Plains, Waikato, New Zealand. Samples were collected during each cycle of grazing on either Biozest™ treated or untreated control pasture. Each round of sample collection was carried out 2 to 3 days before the stock were shifted onto Biozest™ treated or control pasture.
Case study: sheep and cattle farm
Alpha testing of the technology was carried out on 2 sheep and cattle farms that have been farmed by the same family for several generations. The two farms are Mangapapa (309 ha), the control farm, and Haumai (201.7 ha), the Biozest™ treated farm. In previous years, the productivity of both farms was in the upper quartile for the Waikato region. The Biozest™ treatment was applied by helicopter at a rate of 1 L Biozest™ in 50 L water ha-1. Two (2) initial applications were made close together (3 to 5 days apart) in winter 2016, followed by 1 X 1 L ha-1 applied in spring, summer, autumn and winter. Pasture production and stock liveweight were monitored. The FARMAX (Farmax Ltd 2013) farm modelling tool was used to model the complexity and variables in the farm system and predict the biological and financial outcomes.
Statistical analysis
T-tests for statistical significance are reported for each trial. Two-tailed unpaired homoscedastic t-tests were used for the urea trial results. Two-tailed paired homoscedastic t-tests were used for the other trials. Measurement variables are approximately normally distributed, and other assumptions are consistent with the t-test.
Results
Pasture productivity
Pasture growth and DM production
Nineteen (19) days after the first Biozest™ treatment, pasture DM production in the treated halves of paddock 40 and paddock 42 had increased by 89% and 127%, respectively, compared to the control half of each paddock (p = 0.03) (Table 1).
Pasture growth and DM production (palatability)
The results (Table 2) confirm that pasture DM production on this Northland dairy farm was 23% greater in the Biozest™ treated area, and the cows consumed 21% more DM from the treated part of the paddock compared to the control. The cows preferentially grazed the treated pasture, consumed more DM and grazed the pasture evenly and closer to the ground in the treated area compared to the control area.
Pasture productivity: cut baleage
In set A, Baleage production ha−1 in the Biozest™ treated paddocks was 117% greater than the production in the control set of paddocks (p = 0.005) (Table 3). In Set B, baleage production ha−1 in the Biozest™ treated paddocks was 115% greater than the production in the control paddocks (p = 0.02) (Table 3).
Environmental stress tolerance
During the drought period, DM consumed ha−1 was much higher (121% higher in January, 260% higher in April) on the Biozest™ treated portions of the split paddocks compared to the control (p = 0.001) (Fig. 1a). During the frost period, DM consumed ha−1 was 85% higher in June, and 107% higher in August on the Biozest™ treated portions of the split paddocks compared to the control portions (Fig. 1a).
In the mixed pasture (60% ryegrass and 40% drought tolerant Kikuyu (Pennisetum clandestinum)), the stock consumed 85% more DM in the Biozest™ treated area than the control area across all seasons (p = 0.004) (Fig. 1b).
In a paddock prone to drying in late summer and waterlogging in winter, DM consumption in the Biozest™ treated area was 489% greater in February and 51% greater in August compared to the untreated area (p = 0.001) (Fig. 1c).
Stock condition and weight gain (Angus stud bulls)
The 20 bulls that grazed on 20 ha of treated pasture gained an extra 22% (p = 0.008) in liveweight during the 68-day finishing period compared to the control bulls. Bulls that grazed Biozest™ treated pasture realised higher bids than those that grazed the untreated area at auction. The net return ha−1 increased by NZ$1,645 (Table 4).
Soluble carbohydrate assessment
Samples taken every 7 days over a 28-day testing period on the Pukeatua dairy goat farm showed Brix levels ranged from 2 to 5 o in both the treated and untreated pasture. Brix levels in the treated pasture were generally 1° higher in the Biozest™ treated area compared to the control. On an Auckland sheep farm, where multiple samples were taken alternately from treated and untreated paddocks, Brix levels were 1.97 oBrix, or 18% higher, in the treated area than in the control area (p = 0.005).
Milk production and quality
The total milking season production data for the year the dairy goats were fed in cycles of treated/untreated feed (2011/2012) was compared to the previous season (2010/2011). The data obtained from the Dairy Goat Cooperative showed that the combined milk solids production in the 2011/2012 season was 43864 kg: an increase of 33% compared to the previous season (33027 kg). The total milk volume production for the 2011/2012 season was 377848L: a 31% increase compared to the previous season (2010/2011).
In dairy cows on the Hauraki Plains, the results directly from the cooperative milk processor’s supply and quality analysis report showed cows grazing on Biozest™ treated pasture produced 8.5% more milk solids, 3.3% more milk protein and 12.2% more fat L−1 compared to when they were feeding on control (untreated) pasture.
Urea discharge
Urine tests from the Pukeatua dairy goat farm where goats were fed treated and control pasture in rotation showed less urea was discharged when dairy goats consumed Biozest™ treated pasture and the urea discharge increased when they consumed control pasture (Fig. 2). The average difference in the ratio is 26% (p = 0.03).
Data from the South Island dairy farm confirmed that when dairy cows were grazing on treated pasture, 36% less urea was discharged compared to when the same herd was grazing untreated control pasture (p = 0.138).
On the two dairy farms on the Hauraki Plains, urea testing results from the 1st cycle of pasture grazing showed a reduction of 25% in one farm (p = 0.035) and 24% (p = 0.012) in the other during the treated pasture grazing period compared to the control pasture grazing period.
Case study: sheep and cattle farm
The alpha marketing test data from 2 sheep and cattle farms located in Waikato, New Zealand, shows that in a whole farm scale, controlled, comparative trial, Biozest™ applications on pasture can improve productivity by over 30% compared to the control farm (Table 5). The expected productivity gain is 215 kg ha−1 with a net gain (financial gain, less cost of Biozest™ and application costs) of NZ$650 ha−1 (over $130,000 for the 200 ha farm).
Discussion
The application of Biozest™ on crops and pasture delivers the range of phenomena attributable to phenylpropanoid cascades (Indigo Limited, unpublished reports). The full mechanism of the observed biological response has yet to be determined. However, field observations and data from several crops and pasture types support the hypothesis that membrane bound receptors on plant surfaces recognise and react to Biozest™ applications; inducing and sustaining the innate production of phenylpropanoid cascades and delivering the expected range of benefits, including improved growth and yield, improved pest and disease resilience and repair, reduced physiological issues, and improved quality and flavour (Indigo Limited, unpublished reports).
Increase in DM productivity and palatability
Plants sense physical and extrinsic molecular patterns and signals, such as pest, disease and environmental changes, and transmit this information throughout the plant to immediately activate repair growth and defence responses in undamaged parts (Toyota et al. 2018). Trial results suggest Biozest™ elicits a similar reaction when applied on pasture. The treated pasture is more resilient to environmental stresses, heathier and more productive. For example, 2 split paddocks on a Taranaki dairy farm treated with Biozest™ in winter (June) resulted in an increase of 89% and 127% in DM productivity 19 days after treatment (Table 1).
Farmers observed that livestock preferentially grazed treated pasture. This preference was confirmed when an almost equal amount of pasture was offered for grazing in a split block trial on a Northland dairy farm. The dairy cows grazed 21% more DM from the Biozest™ treated area compared to the control (Table 2). Preferential grazing supports the hypothesis that the application of Biozest™ increases phenylpropanoids, including the flavour compound group: flavonoids (Panche et al. 2016). The higher content of flavonoids and the bouquet from aromatic flavonoids could have enabled the livestock to sort and preferentially graze Biozest™ treated pasture. In addition, Brix testing on an Auckland sheep farm confirmed that Biozest™ treatment improves soluble sugars in pasture by 18%. The improved content of soluble sugars could also have encouraged preferential grazing.
Increase in baleage yield
Full growth cycle results (Table 3) from 2 Hauraki Plains dairy farms show the baleage yield ha−1 from Biozest™ treated farm paddocks increased by 117% compared to the control farm. In addition, treated paddocks that were grazed and then retreated with Biozest™ produced 115% more bales than the untreated, control farm confirming the increase in production is sustainable (Table 3).
Field observations revealed larger leaf and wider spread of grass and clover crowns, confirming the mode of action of Biozest™ is different to fertilisers or hormones. N fertilisers generally suppress white clover (Harris et al. 1996). Applications of hormones such as gibberellic acid result in morphological changes and repeat applications produce negative responses (Bryant et al. 2016). Biozest™ treatment produces denser pasture cover. This increased ground cover maximises the utilisation of water, land and fertiliser resources and can therefore reduce leaching.
The substantial increase in pasture (baleage) production (117% and 115%) had no negative impact on feed quality and dry matter production (Zest Biotech, unpublished reports). Applying Biozest™, rather than the common practice of applying N fertilisers to meet feed budget demands, avoids the negative impact of excess N on livestock productivity. In addition, applying Biozest™ avoids the environmental impacts of N fertiliser application and the excretion of urine containing high concentrations of N (Pacheco and Waghorn 2008). The ability to produce more feed on-farm avoids the environmental cost of feed importation as well as the economic cost, which can be significant (FAO and GDP 2018).
Pasture productivity under stress conditions
Split block trials carried out on a farm in Northland, New Zealand, during the 2010 drought showed that, throughout the drought period, cows grazed more than double the amount of pasture ha−1 from the Biozest™ treated area compared to the control. In winter, the district had an unusual series of frosts. During this cold stress period, the cows grazed more than double the amount of pasture out of the Biozest™ treated area compared to the control.
In a mixed pasture paddock (ryegrass 60% and 40% drought tolerant Kikuyu (Pennisetum clandestinum)), the stock consumed more dry matter in the Biozest™ treated areas across all seasons. Even in the C4 Pennisetum pasture species, which are naturally drought tolerant, Biozest™ treatment improved productivity.
Controlled trials on a swampy/waterlogged paddock show that Biozest™ treatment enabled the pasture to overcome soil/water stress conditions during summer when shallow rooted pasture dries out and in winter/spring when the soil becomes waterlogged. The dairy cows consumed more than twice as much pasture from the Biozest™ treated area during the stress periods.
Biozest™ treatment in this series of trials resulted in climate resilient pasture, tolerant to drought, waterlogging and frost.
The ability of Biozest™ treated pasture to overcome abiotic stress and be more productive is supported by the results obtained from the use of another formulation from the same technology platform, trademarked Agrizest™. Agrizest™ application enabled treated plants to overcome abiotic stress from salinity, herbicide contaminated soils, frost, and overcropping, and biotic stress from pest, disease and physiological damage. Reducing abiotic and biotic stress resulted in healthier and more productive trees and vines (Indigo Limited, unpublished reports). In addition, the flavour and colour of treated crops improved (Indigo Limited, unpublished reports). These benefits are attributable to phenylpropanoids (Sharma et al. 2019; Dixon and Paiva 1995).
The hypothesis that application of Biozest™ upregulates the biosynthesis of phenylpropanoids is supported by established science. The Slack, Roughan discovery of how plants desaturate fatty acid to linoleate (a precursor to omega oils) when subjected to chilling and other stresses, such as darkness or high hydrogen atmosphere (Slack et al. 1978), led to the inception of the Octadeconoid Pathway (Schaller 2001). When subjected to stress, plants swiftly upregulate the octadecanoid pathway. Membrane bound fatty acids are desaturated to linolenic acid. The signalling hormones jasmonic acid and ethylene accumulate and reach a threshold, upregulating the next level of defence reactions, resulting in the production of phenylpropanoid cascades. This knowledge of the biosynthesis of phenylpropanoids in response to stress and the role of phenylpropanoids in resistance to and recovery from abiotic and biotic stress supports the hypothesis that Biozest™ elicits phenylpropanoid biosynthesis, which results in healthier and more productive pasture.
Full life cycle productivity assessment and financial returns
The FARMAX™ farm modelling tool was used to predict farming and financial outcomes in a full life cycle, commercial scale sheep and cattle farm trial. The model predicted Biozest applications on pasture would improve productivity by over 30%. If the meat schedule price was NZ$4 kg−1, this increase in production would result in NZ$650 increased net revenue ha−1.
The scale of the productivity improvement affirms the consensus among scientists that animal productivity can be increased by 30% by improving farm efficiencies (FAO 2019; Knapp et al. 2014).
Pasture productivity is increased when Biozest™ is applied due to the efficient utilisation of land and resources. For example, when Biozest is applied, no additional water or fertilisers are required to sustainably increase pasture productivity Ha−1. Additionally, when ruminants graze Biozest™ treated pasture, the feed conversion efficiency improves. The result is a substantial increase in farm net revenue.
Milk and meat productivity and links to environmental liabilities (CH4, N2O and urea)
Increasing milk solids and meat production may reduce feed waste in the form of CH4 and urea (Edouard et al. 2016; Castillo et al. 2000). This study demonstrated that grazing ruminants on Biozest™ treated pasture substantially increased milk and meat production. When 20 Angus breed stud bulls grazed on 20 ha of treated pasture, they gained an extra 22% in weight during the 68-day finishing period compared to the control bulls. Bulls that grazed Biozest™ treated pasture realised higher bids at auction due to improved body condition. The net return ha−1 increased by NZ$1,645. In the dairy goat full production trial, Biozest™ treated pasture was cut and fed to dairy goats. The volume of feed was the same as the previous year, as was the herd size. However, the combined milk volume increased by 31%, and the total milk solid production increased by 33% compared to the previous season. Biozest™, therefore, improved both the quantity and quality of milk.
The productivity improvements are due to the efficient conversion of pasture protein to milk and meat. The higher content of phenylpropanoids in Biozest™ treated pasture forms conjugates with protein (Lee 2014) and therefore is indigestible in the rumen and, instead, undergoes intestinal digestion to amino acids which the livestock convert directly to milk and meat protein. The higher content of phenylpropanoids in pasture can shift the type of N excreted in urine and dung from a soluble form to an insoluble form of N (Patra 2011). This beneficial effect on N cycling and reduction of leaching has not been examined in this study. However, a key finding from the dairy goat full production trial was that urine urea excretion was reduced in the range of 20% to 40%. Short term trials on dairy cow farms confirmed that when cows graze Biozest™ treated pasture, milk solid production increases and urea excretion is reduced. Similar results were reported by Castillo et al. (2000), reflecting the known relationship between ruminant productivity and urea excretion.
Of further interest is the relationship between urea excretion and methane emissions. In all animals (including ruminants), the intestinal digestive system catabolises protein to amino acids. In the ruminant digestive system, the protein is digested further. Amino acids from digested protein are deaminated to NH3, carbonyl and hydride. Bacteria in the rumen can only use NH3 to synthesise protein. However, the rumen bacteria are unable to utilise NH3 at the rate it is produced. Therefore, the liver removes the excess and converts it to urea and, via the kidneys, discharges it in the urine. The residual carbonyls and hydride moieties undergo methylotrophic and hydrogenotrophic methanogenesis and are released as CH4. Therefore, there is a direct relationship between urea production and CH4 emission in ruminant digestion (Carmona-Flores et al. 2020).
The relationship between urea production and CH4 emissions may be positively exploited by using phenylpropanoids. The benefits of phenylpropanoids on ruminant efficiency and GHG production are well established. When fed as a supplement, specific phenylpropanoids or a mix of phenylpropanoids directly inhibit methanogens and likely act as hydride sinks via the cleavage of ring structures (Patra 2011) and reductive dihydroxylation. However, researchers have so far been unsuccessful in producing sustained effects without side effects. Elaborate on this. Biozest™ can overcome these constraints because the phenylpropanoids are not used as antibiotics. The mode of action of Biozest instead relies on the pasture de novo synthesised phenylpropanoids complexing with pasture proteins and protecting protein from digestion in the rumen (Lee 2014). When ruminant livestock consume Biozest™ treated pasture, the higher content of phenylpropanoids can complex with more of the pasture protein. The resulting conjugates are protected from digestion and deamination in the rumen. Instead, they are digested more efficiently in the intestine to amino acids and utilised in milk and meat protein production. As a result of the reduced digestion of protein in the rumen, less deamination occurs, and, therefore, less protein is wasted as urea and CH4. Because of the reduction in urea excretion as measured in trials, we deduce that deamination has likely been reduced. Therefore, CH4 production would also have been reduced in livestock consuming Biozest™ treated pasture.
A second strategy that may be employed to reduce CH4 emissions is to increase the relative amount of soluble carbohydrates in pasture. Higher soluble sugar content in pasture favours the production of more propionic acid relative to acetic acid, resulting in less CH4 production. We have not measured the CH4 reduction, but the data shows soluble sugars are higher in Biozest™ treated pasture than in untreated pasture. Therefore, we deduce that Biozest™ treatment of pasture has an added benefit in reducing CH4 production during carbohydrate digestion in the ruminant.
To summarise, the results support several inferences. First, when dairy cows and goats consume Biozest™ treated pasture, urea excretion is reduced between 20 and 48%. Therefore N2O production from excreta will be reduced. The reduction in urea excretion is a result of a reduction in deamination. The generation of carbonyls and hydride during the deamination process is also reduced, resulting in less methylotrophic and hydrogenotrophic methanogenesis. Secondly, during carbohydrate digestion, the higher content of soluble sugars (18% on an Auckland sheep farm) in treated pasture favours the production of propionate rather than acetate and butyrate. Therefore, acetoclastic methanogenesis is reduced.
New Zealand pasture contains more N than ruminants can utilise. However, farmers often apply N fertilisers to achieve the required feed budgets. While N fertilisers increase pasture growth, excess N negatively impacts animal and environmental welfare (Pacheco and Waghorn 2008). Unlike N, the previously described results from a range of farm types demonstrate that Biozest™ can sustainably double pasture productivity and when ruminants consume Biozest™ treated pasture, milk and meat production increases, and less urea is excreted. Based on the direct link between soluble sugar content and CH4 production and urea excretion and CH4 production, and potential avoidance of the direct application of urea to pasture for pasture growth, we deduce that Biozest will substantially reduce environmental liabilities.
Conclusion
Biozest can enable pastoral farmers to reduce environmental impact and increase food security. When ruminants graze Biozest treated pasture, milk and meat productivity increases and less pasture is wasted in the form of urea excreted in urine. The urea reduction suggests less deamination of pasture protein and methanogenesis can occur. Because less urea is excreted, it follows, less N2O is produced. The results presented are further evidence of the link between increased productivity and reduction in urea excretion. However, in this study, the plausible reduction in N2O and CH4 emissions that likely follows a reduction in deamination and urea excretion has not been quantified.
Carbon sequestration is a crucial area that requires further investigation via direct measurement or modelling. By doubling pasture productivity, every ha of Biozest™ treated pasture could double DM production and therefore possibly double the sequestration of atmospheric CO2 compared to untreated paddocks or sequester 3 times the C that forestry is capable of. Quantification of the increased C sequestered would enable farmers to earn carbon credits.
Stock graze Biozest™ treated paddocks more evenly. Therefore, the liability of post-grazing residual pasture decomposition and resulting emissions of CH4 and CO2 are reduced. In addition, the denser pasture growth covers more land, maximising resource utilisation which could further reduce environmental impact by reducing the leaching of nutrients.
Further work should be carried out on the type and quantity of urea excreted to land and consequent impacts on nitrate leaching using both the collection of urea from grazing animals in field-based trials and a model, such as GLEAM, to quantify GHGs and environmental footprint. Results may then guide livestock management and stocking rates and will result in meticulous climate change management and food security policy decisions. Observations from trial work and made by farmers, such as soil firmness even in wet conditions, thicker animal dung, easier calving/lambing, less incidence of mastitis, indicate that there may be wider benefits in terms of soil and animal health that are yet to be explored. Work into the influence of phenylpropanoids on the proliferation of microflora that convert fertiliser and soil minerals to plant available forms may reveal additional opportunities to reduce leaching and water pollution.
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The authors would like to thank those farmers and dairy companies who allowed us to conduct this research and assisted with the collection and provision of data.
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Both authors contributed to the design of the study and data interpretation and drafted and edited the manuscript.
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Both Nathan Balasingham and Usha Amaranathan are employees and directors of Zest Biotech, owner of the Biozest™ technology. All trial work has been carried out independently with data and samples collected and supplied by farmers or reported by dairy companies.
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Amaranathan, U., Balasingham, N. Cell signalling compound improves pasture and livestock productivity and the environment. Nutr Cycl Agroecosyst 123, 19–33 (2022). https://doi.org/10.1007/s10705-022-10194-5
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DOI: https://doi.org/10.1007/s10705-022-10194-5