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Approximately 3.1 Mha (22%) of the agricultural area of south-eastern Australia can be classified as native pasture. There is the assumption that, owing to the widespread occurrence of low-fertility soils in Australia, native grass species do not respond to increased phosphorus (P) fertility. Currently, there are no industry recommendations of target soil-test P values for native-grass-based pastures. This paper reviews the responses of perennial native pasture species endemic to south-eastern Australia to P application in controlled environments, surveys, replicated experiments and paired-paddock trials. Eighty-seven site-years of trial data where different levels of P were applied, conducted over the last two decades, on native-based pastures in south-eastern Australia are reviewed. Data indicate that application of P fertilisers to native grass pastures can increase dry matter (DM) production and maintain pasture stability. However, minimum targets for herbage mass (800 kg DM/ha) and groundcover (80%) are required to ensure persistence of perennial native grasses. Stocking rates also need to match carrying capacity of the pasture. Based on previous research, we recommend target soil-test (Olsen; 0–10 cm) P levels for fertility-tolerant native grass pastures, based on Microlaena stipoides, Rytidosperma caespitosum, R. fulvum, R. richardsonii, R. duttonianum and R. racemosum, of 10–13 mg/kg, whereas for pastures based on fertility-intolerant species such as Themeda triandra, lower levels of

Temperate pastures that leak water below the root zone have been linked to an increase in dryland salinity in southern Australia through their conservative use of stored water. An experiment was conducted at Hamilton in south-western Victoria to test the hypothesis that deep-rooted, summer-active perennial pasture species can substantially reduce leakage. On topographic crests the experiment compared lucerne and chicory with a traditional perennial ryegrass variety with low summer activity, whereas on the poorly drained valleys the comparison was between tall fescue, kikuyu and a perennial ryegrass variety with high summer activity. Lucerne developed a buffer of dry soil to a depth of at least 5 m. An empirical relationship with June–September rainfall indicated that with this dry buffer, leakage below the root zone would not occur even in the wettest of years. Chicory developed a dry buffer to the depth of measurement (3 m), but plant density gradually declined and leakage started to occur 5 years after sowing. The perennial ryegrass with low summer activity had leakage nearly every year. On the valleys kikuyu was initially the most effective at drying the soil in summer, but its density declined at the expense of annuals and 3 years after sowing it became wetter than the other treatments. None of the pasture options on the valley fully controlled leakage, but both the summer-active perennial ryegrass and tall fescue were persistent and there was little difference in their capacity to extract summer moisture. This study showed that four characteristics were associated with a pasture that controlled leakage – summer activity, persistence, adequate density and deep rootedness. Of the species tested only lucerne satisfied all these criteria.

The present paper covers reproductive performance in an artificial-insemination (AI) program of the Sheep CRC Information Nucleus with 24 699 lambs born at eight locations in southern Australia across five lambings between 2007 and 2011. Results from AI with frozen semen compared well with industry standards for natural mating. Conception rates averaged 72%, and 1.45 lambs were born per ewe pregnant for Merino ewes and 1.67 for crossbreds. Lamb deaths averaged 21% for Merino ewes and 15% for crossbreds and 19%, 22% and 20% for lambs from ewes that were mated to terminal, Merino and maternal sire types, respectively. Net reproductive rates were 82% for Merino ewes and 102% for crossbreds. From 3198 necropsies across 4 years, dystocia and starvation-mismothering accounted for 72% of lamb deaths within 5 days of lambing. Major risk factors for lamb mortality were birth type (single, twin or higher order), birthweight and dam breed. Losses were higher for twin and triplet lambs than for singles and there was greater mortality at relatively lighter and heavier birthweights. We conclude that reproductive rate in this AI program compared favourably with natural mating. Lamb birthweight for optimum survival was in the 4–8-kg range. Crossbred ewes had greater reproductive efficiency than did Merinos.

Achieving higher lamb weaning percentages by reducing lamb mortality can improve the profitability of sheep enterprises. In this paper we estimated the financial benefits from providing shelter to reduce the mortality of twin lambs in self-replacing Merino or dual-purpose Merino flock enterprises in south-west Victoria. A whole-farm bio-economic model (MIDAS) was initially used to estimate the increase in profit from reducing mortality of twin lambs and a second analysis included the costs of using perennial grass hedges to provide the shelter during lambing. The economic value of providing shelter was tested at three rates of twinning (10, 30 and 50%), three rates of mortality without shelter (70, 50 and 30%) and two levels of reduction in lamb mortality by providing shelter (25 and 50% reduction). A sensitivity analysis to wool and lamb prices, costs of establishing the grass hedges and stocking rates in the shelter area were also tested. Overall, more than 2500 scenarios were tested. Across the range of twinning rates and levels of twin mortality tested, at standard wool and meat prices, providing shelter to the dual-purpose Merino ewe flock was always profitable ($0.05 to 11.35/ewe) and the profits from providing shelter to the self-replacing Merino ewe flock were generally lower ($0.15 to $6.35/ewe). The impacts of changing wool and lamb prices depended on enterprise type, whereas the costs of establishment of the hedges or stocking rate of ewes in the hedge area during lambing had little impact on profitability. The main factor that determined the economic return from shelter was the reduction in mortality provided by the shelter but the proportion of twin-bearing ewes in the flock and the base rate of lamb mortality without shelter was also important. Overall, based on the assumptions used, we conclude that the profitability of many sheep enterprises lambing during frequent high chill weather conditions in temperate areas of south-eastern Australia could be improved by providing low cost shelter for twin-bearing Merino ewes lambing from July to September.

Improved dryland pastures for sheep and beef cattle production in south-western Victoria are typically based on summer-dormant cultivars of perennial ryegrass (Lolium perenne L.) or phalaris (Phalaris aquatica L.). These are highly productive in spring but exhibit low accumulation rates over summer–autumn. Summer-active perennial pasture species could potentially alleviate this summer–autumn feed gap. Three pasture systems that used different pastures on each of the three landscape classes (crest, slope, and valley floor) were compared over 4 years. The perennial ryegrass system (henceforth Ryegrass) had a different ryegrass cultivar on each landscape class. The Triple system used lucerne (Medicago sativa L.) (crest), perennial ryegrass (slope), and summer-active tall fescue (Lolium arundinaceum (Schreb) Darbysh.) (valley floor). The Novel system used chicory (Cichorium intybus L.) (crest), Italian ryegrass (Lolium multiflorum Lam.) or hybrid ryegrass (L. × boucheanum Kunth.) (slope), and kikuyu (Pennisetum clandestinum Hochst. ex Chiov.) (valley floor). The pastures were grazed by either one (in the case of the Novel system) or three (in the case of the Ryegrass and Triple systems) animal systems that varied over the life of the experiment. Total annual herbage accumulation of the Ryegrass and Triple systems did not differ. The Novel system consistently had lower total annual dry matter accumulation than the other two systems. Lucerne pastures generally had the highest accumulation rates over summer, followed by the chicory pastures. The kikuyu pastures responded well to summer rainfall but otherwise had similar accumulation rates to the perennial ryegrass and tall fescue pastures over summer. Tall fescue pastures grew well in autumn following wet summers. In spring the perennial ryegrass pastures based on Fitzroy or Avalon were highly productive but seldom grew faster than other pastures. The results support the hypothesis that incorporating deep-rooted, summer-active perennial species will increase pasture production over summer–autumn compared with conventional pasture systems but not at the expense of winter–spring production.

Climate change projections for Australia predict increasing temperatures, changes to rainfall patterns, and elevated atmospheric carbon dioxide (CO2) concentrations. The aims of this study were to predict plant production responses to elevated CO2 concentrations using the SGS Pasture Model and DairyMod, and then to quantify the effects of climate change scenarios for 2030 and 2070 on predicted pasture growth, species composition, and soil moisture conditions of 5 existing pasture systems in climates ranging from cool temperate to subtropical, relative to a historical baseline. Three future climate scenarios were created for each site by adjusting historical climate data according to temperature and rainfall change projections for 2030, 2070 mid-and 2070 high-emission scenarios, using output from the CSIRO Mark 3 global climate model. In the absence of other climate changes, mean annual pasture production at an elevated CO2 concentration of 550 ppm was predicted to be 24-29% higher than at 380 ppm CO2 in temperate (C-3) species-dominant pastures in southern Australia, with lower mean responses in a mixed C-3/C-4 pasture at Barraba in northern New South Wales (17%) and in a C-4 pasture at Mutdapilly in south-eastern Queensland (9%). In the future climate scenarios at the Barraba and Mutdapilly sites in subtropical and subhumid climates, respectively, where climate projections indicated warming of up to 4.4 degrees C, with little change in annual rainfall, modelling predicted increased pasture production and a shift towards C-4 species dominance. In Mediterranean, temperate, and cool temperate climates, climate change projections indicated warming of up to 3.3 degrees C, with annual rainfall reduced by up to 28%. Under future climate scenarios at Wagga Wagga, NSW, and Ellinbank, Victoria, our study predicted increased winter and early spring pasture growth rates, but this was counteracted by a predicted shorter spring growing season, with annual pasture production higher than the baseline under the 2030 climate scenario, but reduced by up to 19% under the 2070 high scenario. In a cool temperate environment at Elliott, Tasmania, annual production was higher than the baseline in all 3 future climate scenarios, but highest in the 2070 mid scenario. At the Wagga Wagga, Ellinbank, and Elliott sites the effect of rainfall declines on pasture production was moderated by a predicted reduction in drainage below the root zone and, at Ellinbank, the use of deeper rooted plant systems was shown to be an effective adaptation to mitigate some of the effect of lower rainfall.

The effects of combinations of different fertiliser rates and grazing methods applied to phalaris-based pastures on an acid, saline, yellow sodosol on the Dundas Tablelands of western Victoria (mean annual rainfall 623�mm) were measured from 1997 to 2000. The objective was to help identify management systems that improve phalaris growth and persistence, water use, and animal production, and thereby the productivity and sustainability of grazing systems. Pastures were either set stocked with low [mean 6.4 kg phosphorus (P)/ha.year] or high (mean 25 kg P/ha.year) fertiliser rates, or rotationally grazed with high fertiliser (mean 25 kg P/ha.year). Rotational grazing was implemented as either a simple '4-paddock' system (fixed rotation length), or a more intensive system where rotation length varied with pasture growth rate. Unreplicated paddocks of volunteer pasture (dominated by onion grass and annual grass weeds) receiving an average of 8 kg P/ha.year were also monitored. All treatments were stocked with spring-lambing Merino ewes. Stocking rate was an emergent property of each treatment, and was driven by pasture quality and availability. Total pasture herbage accumulation ranged from 7150 to 9750 kg DM/ha.year and was significantly lower on the set-stocked, low-fertility treatment than on all other treatments. A significant treatment.day effect in the spline analysis of herbage mass was explained by a trend toward higher pasture mass in the rotationally grazed treatments than set-stocked treatments from the break of season until mid-spring. Rotational grazing led to significantly higher phalaris herbage accumulation than set stocking (mean 3680 v. 2120 kg DM/ha.year), but significantly lower subterranean clover herbage accumulation (1440 v. 2490 kg DM/ha.year). Despite the stronger growth of deep-rooted phalaris in the rotationally grazed treatments, maximum soil water deficits at the end of summer differed only slightly between treatments, with the difference between driest and wettest treatments amounting to only 14 mm. Summer growth of phalaris was apparently insufficient to generate significant differences in soil water extraction at depth, even when phalaris content was increased by rotational grazing, and re-wetting of the soil profile occurred at a similar rate for all treatments. Rotationally grazed treatments supported higher stocking rates than set-stocked treatments at high fertiliser rates (mean 14.9 v. 13.7 ewes/ha), but apparent losses in pasture feeding value due to lower legume content under rotational grazing meant that there were few significant differences between treatments in lamb production per hectare. The experiment showed that grazing method can have a substantial and rapid effect on pasture botanical composition. There are clear opportunities for producers to use temporal and spatial combinations of set stocking and rotational grazing to manipulate herbage mass and pasture composition within broad target ranges for achieving both animal production (e.g. high per-head animal performance) and sustainability (e.g. persistence of perennial grasses) objectives. Rigid application of either set stocking or rotational grazing imposes limitations on both pasture and animal production, and neither grazing method will optimise system performance under all conditions. The experiment also demonstrated that management and land-use changes that have much greater potential to increase water use than those examined here will be needed to ensure the sustainability of pasture systems in the high rainfall zone of western Victoria.

Changes in soil pH from a long-term experiment at Hamilton, Vic., associated with time, fertiliser application, and stocking rate were assessed. The pH was measured in a 1 :5 suspension of soil in water (pHW) from 1980 onwards and in a 1:5 suspension of soil in 0.01 M CaCl2 (pHCa) from 1984 onwards. Topsoils (0–10 cm) were sampled regularly from 1980 to 1999, and the soil profile to a depth of 80 cm in 1994. The site was sown to perennial ryegrass, phalaris, and subterranean clover in 1977. Treatments fertilised with different amounts of superphosphate were grazed by sheep at stocking rates of 7–19 dry sheep equivalents (DSE)/ha. Average applications of phosphorus (P) ranged from 0.5 to 38.7 kg P/ha.year. The pHCa of the topsoil in 1984 was 4.9. It decreased at an average rate of 0.005 pHCa or 0.008 pHW units/year, with little variation due to fertiliser or stocking rate. Measurements in 1994 revealed subtle but statistically significant (P < 0.01) trends in soil pHCa that were associated with grazing pressure, inputs of fertiliser, and whether or not areas sampled were used by the sheep for camping. The top 0–5 cm of soil was slightly less acidic (+0.07 pHCa units) in the camp areas compared with non-camp areas. Below 5 cm to a depth of 80 cm, camp areas were more acidic (–0.19 pHCa units). At the highest stocking rates, heavier applications of superphosphate were associated with greater subsoil acidity: –0.06 pHCa units per 100 kg phosphorus (P) applied. There was no relationship at medium stocking rates. At low stocking rates, higher P applications were associated with more alkaline subsoils. Net removal of product from 1979 to 1994 (wool and meat removed from plots and excreta transferred to camps) was estimated to be equivalent to 140–380 kg/ha of lime over this 15-year period. The organic carbon (OC) content of the topsoil did not change over 20 years of records from 1979, and was unaffected by inputs of P. In 1994, the OC content of the 0–5 cm layer of topsoil was greater than the 5–10 cm layer (mean values 5.5% and 3.8% respectively; P < 0.001). The OC content of camp areas was higher than that of non-camp areas, this difference being more pronounced in the 0–5 cm layer (P < 0.01). It was concluded that the rate of change of pH was slow because of the high pH buffering capacity of the soil, the small amount of alkalinity removed in product, and the generally high perennial grass content of the pastures. Soils shown to be at greatest risk of acidification from this study were those under camp areas, and where high fertiliser rates were applied to pastures with a low perennial grass content. Rotational grazing should diminish these problems by reducing the concentration of excreta in camp areas, and favouring perennials over annuals in both camp and non-camp areas. Inputs of lime may eventually be needed to compensate for the acidifying effect of product removal.

Relationships between amounts of superphosphate applied to pasture and stocking rate on available nutrient status were assessed from 1979 to 2000 on a chromosol derived from basalt at Hamilton, Victoria. The pastures were stocked with sheep at low, medium, or high grazing pressures in factorial combination with 6 levels of superphosphate. Overall annual amounts of single superphosphate (8.8% P, 11% S, 19% Ca) applied ranged from 0.4 to 36 kg P/ha. Potassium chloride (KCl) was applied to all plots periodically. Average stocking rates ranged from 7 to 19 dry sheep equivalents (DSE)/ha. The nutrient status of plots was monitored by sampling the soil to a depth of 10 cm, avoiding the areas used by the sheep for camping. In 1994, samples of topsoil (0–5 cm and 5–10 cm) were taken from the camp areas and non-camp areas in each plot in order to assess 'plant-available' P, S, and extractable cations. Changes in P and S with depth to 80 cm in high and low grazing pressure treatments were also assessed. The influence of cumulative P applied on Olsen P varied with time and grazing pressure. During the first 12–15 years, the Olsen P of high grazing pressure plots was greater than that of low grazing pressure plots, but subsequently the reverse has been the case. Plant-available S also increased where more superphosphate had been applied. Levels were greater than 7 mg S/kg soil except at the lowest level of superphosphate, indicating that forms of P fertiliser with less S could be used here. After initial applications of KCl, this fertiliser was not applied for 8 years. During this time the K status fell from 270 to 120 mg K/kg soil, just above where plant responses to K are likely, emphasising the need to monitor the K status of productive pastures on these soils. Levels of exchangeable Mg2+ fell as more superphosphate was used, whereas levels of Ca2+ rose. The Olsen P of soil deeper than 10 cm was always less than 5 mg P/kg soil. P supply to deep-rooted pasture plants may thus be limiting when the topsoil is dry. These results, together with published assessments of animal production at this site, show that for pastures fertilised annually, the Olsen P associated with the most profit varied from 7 mg P/kg soil at 7 ewes/ha (10.5 DSE/ha), to 14 mg P/kg soil at 18 ewes/ha.

A nutrient audit was conducted on a long-term grazed fertiliser experiment at Hamilton in south-western Victoria to determine the fate of applied phosphorus (P) and sulfur (S). Single superphosphate had been applied at rates averaging between 1 and 33 kg P/ha.year since the start of the experiment in 1977. Soil samples were taken in 1994 by coring to a depth of 80 cm, and analysed for total soil nutrient concentration. Most (80%) applied P was in the top 43 cm of the soil profile. A further 6.5% had been transferred to sheep camp areas and 6.5% had been exported as product. It was estimated that

Three methods were compared for providing data to accompany a daily rainfall record: (i) a seasonal mean calculated from smooth curves; (ii) a seasonal mean modified by rainday effects; and (iii) actual data with missing observations filled in by method (ii). Existing plant growth models developed for the Australian tropics were used to compare the three data generation methods. These models were used to predict the number of growth days (a measure of how much plant growth would be expected in a season), green days (a measure of the duration of weight gain by rangeland cattle), runoff, and germination days. Three stations were used, one each from the monsoonal tropics, the coastal dry tropics, and the coastal subtropics. Comparatively little bias was introduced from methods (i) and (ii). Differences were greater for episodic events such as runoff and germination, than for more continuous events such as growth. There were no significant effects of generation method on calculated growth days or green days. Runoff calculated from method (i) averaged 7% lower than when actual data were used, compared with only a 3% underestimate from method (ii). The number of germination days were underestimated by between 4 and 17% when method (i) was used, compared with between a 3% underestimate and a 6% overestimate with method (ii). It was concluded that method (ii) should be used in preference to the seasonal mean alone, because of the more accurate model predictions from method (ii). A stochastic weather generator would however be required where events such as frosting would be important in risk analyses.