ect of changes in rainfall on the response of the water table to a major alley farming experiment

The effect of changes in rainfall on the response of the water table to a major alley farming experiment S. L. Noorduijn, K. R. J. Smettem, R. Vogwill, and A. Ghadouani Aquatic Ecology and Ecosystem Studies, School of Environmental Systems Engineering, The University of Western Australia, 35 Stirling Highway, Crawley, Western Australia, 6009, Australia Center for Ecohydrology, School of Environmental Systems Engineering, The University of Western Australia, 35 Stirling Highway, Crawley, Western Australia, 6009, Australia Department of Environment and Conservation, Locked Bag 104, Bentley Delivery Centre, Bentley, Western Australia, 6983, Australia Received: 3 June 2009 – Accepted: 3 June 2009 – Published: 23 June 2009 Correspondence to: A. Ghadouani (anas.ghadouani@uwa.edu.au) Published by Copernicus Publications on behalf of the European Geosciences Union.

Simple hydrograph analysis did not identify any treatment effects on the water table response.Subsequent statistical analysis revealed that 20-30% of the variability in the water table data over the 12 year period was attributable to the alley farming experiment.It was hypothesized that a climate trend (reducing annual rainfall over time) may be obscuring the effect of the experiment.To further investigate the effect of the experiment on groundwater response, further hydrograph analysis was conducted to compare the trends in the control piezometers in relation to those located within the belts.A difference of 0.9 m was observed between the mean groundwater levels in the control piezometers and the mean levels in the perennial belt piezometers.For a mean specific yield of 0.03 m 3 m −3 this equates to a small additional water use of 27 mm yr −1 by the perennial agroforestry system.It is concluded that declining annual rainfall is the principal control on hydrograph response at the site.Perennial biomass development and perennial root development (both laterally and vertically) exert only a small influence on water table depth.The implications of this study indicate that alley farming has

Introduction
Secondary dryland salinity is a result of the combined effects of groundwater rise and mobilisation of soil profile salt stores (Scott and Sudmeyer, 1993;Nulsen and Baxter, 1986;Asseng et al., 2001a, b).This form of land degradation affects a global area of more than 33 million ha (FAO-AGL, 2000).The causal mechanism is the different water use regimes and shallower rooting depths of introduced agricultural crops compared to native species (Clarke et al., 2002;Ferdowsian et al., 1996).Seasonal water use by annual agricultural crops and reduced ability to utilise water from deeper in the soil profile leads to an increase in recharge (Scott and Sudmeyer, 1993;Asseng et al., 2001b;Eastham and Gregory, 2000).The development and successful implementation of natural resource management str ategies to improve ecosystem health and remediation of degraded land relies on a quantitative understanding of these changes to the water cycle (Kareiva and Marvier, 2003).
The reintroduction of native woody perennial species is one management option for controlling groundwater rise by increasing evapotranspiration (Bari et al., 1996;Langford, 1976;Ruprecht and Stoneman, 1993) and re-establishing a more ecologically sustainable hydrology at catchment scale (Cramer and Hobbs, 2002;Hatton et al., 2003).The proportion of land required for perennial revegetation and the location within the catchment to achieve recharge control is still not entirely resolved.Estimates range up to 80% of the catchment area (George et al., 1997;Bell and Froend, 1990).Recommendations for more targeted local planting originally focused on the zone of recharge (Nulsen, 1984) but recent recommendations have encompassed the entire catchment area (Clarke et al., 1999;George et al., 1991;Salama et al., 1991).The large area of perennial revegetation required to control groundwater recharge implies a loss of agricultural land and this is of economic concern to the farming community.Therefore, agroforestry techniques have generated interest because they can potentially reduce recharge whilst minimising the area of revegetation (Clarke et al., 2002).The practise of alley farming, or runoff agroforestry, has been promoted as a management option because the system retains agricultural output by planting trees in rows/belts interspersed with conventional food crops (Lefroy and Stirzaker, 1999;Ogunlana et al., 2006;Kang et al., 1984;Droppelmann and Berliner, 2003).Originally initiated to eliminate fallow periods in the African agricultural areas (Kang et al., 1984;Ogunlana et al., 2006), alley farming has been extensively trialled in the rain-fed agricultural regions of Australia.Alley farming has demonstrated positive environmental outcomes, for example disease and pest control, food sources and habitat for native fauna (Bird et al., 1992;Lefroy et al., 2005;Mooris and Johnson, 1967).The economic potential of perennial alley systems may also be enhanced if they can be developed as greenhouse sinks and sources of biofuel (Harper et al., 2007;Bartle et al., 2007).Research has focused on understanding the hydrological functioning of hillslope alley systems (Ellis et al., 2006;Oliver et al., 2005;White et al., 2002;Wildy and Pate, 2002) and the water requirements for successful production in dryland environments (Cooper et al., 2005).
In an attempt to identify the most effective alley farming design for reducing groundwater levels at a lowland valley site, a large replicated experiment was established in 1995.The objective of this experiment was to test the hypothesis that water tables will be lowest under alley farming designs with the greatest biomass per unit area (and hence the greatest leaf area and transpiration).Transects of piezometers were installed across the site to monitor the water table response over a 12 year period after establishment.Simple piezometer hydrograph analysis of the 12 year data did not identify any treatment effects on the water table height.Using a more complex spatial statistical analysis it was possible to attribute 20 to 30% of the variability in the water table data set, after the climatic signature was removed, to the impacts of the alley farming experiment (Noorduijn et al., in press).It was concluded that the impacts of the experiment were being masked by broad scale temporal and spatial trends which account for the remaining 60% of the variability.The absence of a strong water table response to the treatments indicates that the biomass attained by the alley belts may be insufficient to significantly lower the groundwater under the treatments.
In this study, we further investigate the effects of climate on piezometer hydrograph levels and their response to the alley farming experiment.The objective is to determine the relative contributions of climate change and alley transpiration on the observed changes in the water table depth.This will help to develop a more complete understanding of the impacts of both rainfall and perennial plant development on groundwater levels under the alley farming experiment.

Site description
The Toolibin Alley Farming Trial (TAFT) comprises of two field sites (Davenport and Nepowie) within the Natural Diversity Recovery Catchment of Lake Toolibin.The site under investigation is located 8 km north of Toolibin Lake, Western Australia (Davenport, 32 • 50 36 South, 117 • 38 65 East).The site has a Mediterranean climate with the majority of rainfall during the winter months (May-August, 60%), the remaining months remain comparatively dry and receive between 23-44% of the annual rainfall.Average pan evaporation is 1800 mm yr −1 and potential evaporation usually greatly exceeds rainfall from September to April.The average maximum and minimum temperatures for the study site range from 32 • C to 9 • C during the summer months (November-April) and 20 • C to 5 • C during the winter month (May-October) (Bureau of Meteorology, Australia).Water influx to the site from groundwater is comparatively minor due low hydraulic conductivity of the soils and very low hydraulic gradients (George, 1992).Figures

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Experimental design
The study was designed to investigate three independent variables: revegetation density (belt width/alley width), belt width (m), and tree species.Seven different treatment designs (A-F) were applied to the sites in a randomised complete block design (Fig. 1).Each design comprised five tree species, of which the three keys species were Eucalyptus vegrandis, E. occidentalis and Casuarina obesa; for this study only E. vegrandis is considered due to lack of consistent sampling for the remaining two species.Piezometers were installed in each plot on transects orientated perpendicular to the tree belt (within E. vegrandis).They were installed to a depth of 3.7 m with slotted casing for the bottom 2 m.A minimum of two piezometers were installed in each plot, running from the centre of the perennial tree belt to the centre of the alley (Table 1).Two control piezometers were installed on the site, to assess the water table response in the adjacent paddock under annual grass.Water table depth was monitored every one to two months for the first three years.Subsequent measurements were sporadic, with a frequency of once or twice a year.From April 2007 to January 2008 monthly measurements were made.

Data collection and analysis
The water table data set was initially recorded as static water level (s.w.l.) depths in meters below ground level (m b.g.l.) and consisted of 74 piezometers monitored on 39 dates (over the period October 1995 to January 2008).Piezometers were excluded where monitoring had been infrequent and the remaining 69 piezometers were surveyed to obtain elevations above Australian height datum (m a.h.d.) using a local datum.Daily rainfall and meteorological data were obtained for the meteorological station at Corrigin (32.33 • South, 117.87 • East) from the Bureau of Meteorology.
An extensive biomass survey was conducted at the site to assess the growth of the perennial species at 12 years of age.Destructive sampling was conducted for the different belt widths in the experiment; the samples were dried and weighed.The Introduction

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Full Screen / Esc Printer-friendly Version Interactive Discussion density of surviving stems was comparable between the different belt widths preventing biased results in the above-ground biomass results.57 individual E. vegrandis trees were sampled for above ground biomass from the different belt width.An allometric correlation was established between stem basal area at 10 cm and the above-ground biomass for those samples (r 2 =0.81), the results of the calculated biomass show a high correlation with the observed values (r 2 =0.86).At the site, basal area was recorded for 332 individual E. vegrandis trees from which biomass were estimated using the allometric correlation.This enabled good estimates of standing biomass per m 2 to be undertaken.

Regional climate trends
A significant decrease in both winter and total annual rainfall has been observed in the region over the last century.The observed decline since 1969 is 21%, compared to the period from 1907-1968 (Smith et al., 2000).This decline is shown in Fig. 2 for the Corrigin rainfall data, where the mean monthly rainfall remains equal to or above the mean monthly average from 1910 to 1950 after which the mean monthly rainfall falls below the monthly average for the period of 1910 to 2008 resulting in the observed decline.Over the period of the experiment (1996-2007) the average annual rainfall was 367 mm (SD±77 mm).The highest annual rainfall for this period occurred in 2006 (537 mm) and contained a contribution from one large (149 mm) out of season rainfall event in January of that year.
The control piezometers can be assumed to reflect the annual climatic effects on water table depth at the site.The departure of the experimental water table depths from the control piezometers provides a measure of the treatment effect.For most years, the summer water table depth integrates the effects of the season on water piezometer measurements and this is reflected in the water table rise in this summer.

Water table fluctuations
Groundwater levels have declined over the study period.In 1996 the water table was between 0.05-1.82m b.g.l. and in 2007 between 0.68-4.15m b.g.l.In 1996 the average height of the seasonal fluctuation in water level across the site was 1.24 m b.g.l.
(SD±0.13 m).In 2007 this had increased to 1.45 m b.g.l.(SD±0.31m), which has a possible association to the impacts of vegetation and to the variability in treatment types.A general overview of the water table response at the site is shown in Fig. 3.A comparison is made between the winter minimum and summer maximum groundwater depths for all the experimental data with the average summer minima for the control piezometers.The trend observed can be divided into two periods, between 1996-2000 a continued rise in the water table heights are observed followed by a subsequent drop from 2000-2002 after which it appears to remain at a constant depth of approximately 2.5 m b.g.l.(Fig. 3).After 2000 the summer minimum water table depths in the experiment were consistently lower than the control piezometers.
Combining all the experimental data and comparing the mean water table level to the mean from the control piezometers shows that the water table in the trail piezometers (post 2000) was on average, 0.9 m deeper than in the control piezometers (Fig. 4).This applies to every year, irrespective of the control piezometer level, as shown by the trend line in Fig. 4. Given a site average specific yield of 0.03, the 0.9 m drop in groundwater level corresponds to 27 mm of additional water use by the perennial tree belts compared to the control.Given the variability of both the specific yields (0.01-0.07, with a mean of 0.03) observed at the site and the range observed in Fig. 4 (0.3-1.5 m b.g.l.), the value attributed to perennial water use will vary considerably across the site (Table 2).
Modelling results for the control plot showed that after 1996 bare soil evaporation was practically equal to rainfall for every year of the experiment ( groundwater by the perennial vegetation was constrained by poor water quality and by periodic saturation of the root zone.The observed post 2000 decline and stabilisation of the water table height for piezometers within perennial tree belts (B belt ) and those in the centre of the alley (B alley ) are shown in Fig. 5.A t-test identified a significant difference in the means of the two locations for January 2001 only (t=2.97, p=0.0046).A Levene's test for homogeneity of variance of the normalised water table data (m b.g.l.) organised by piezometer location (belt or centre of the alley) indicates a significant difference in the variance of the two locations (F =7.4,p <0.007) (Levene, 1960) The trend in the average water table depth for B belt and B alley for both high and low biomass plots shows that for both locations and treatment design the water tables for the low biomass treatments remained equal to or higher than the water table within the high biomass treatment design.This corresponds well with the water table responses observed for B alley .The difference in average water table depths for B alley for treatment design A (low biomass) and F (high biomass) were relatively high at the start of 2000 (Fig. 5), this difference decreases through time; as opposed to the water table trends in B belt where this difference appears to increases through time.

Biomass production
The biomass data for Eucalyptus vegrandis across the experiment showed that as belt width narrows the biomass increases (Table 4).Biomass increased with belt width from 38 to 4 m, the difference in biomass t between a belt of 38 m and 138 m are minor (approximately 2 kg m −2 ) at the site.The data displayed a non-linear trend (r 2 =0.98) which stabilises at mean biomass per m 2 of approximately 0.06 kg m −2 .In terms of maximum biomass production, a double row of trees measuring 4 m wide would pro-Introduction

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Full Screen / Esc Printer-friendly Version Interactive Discussion duce the highest above ground biomass whereas block planting (138 m width) would produce the least.

Regional climate trends
The south west of Western Australia is experiencing a decrease in annual rainfall and an increase in summer rainfall events (Hennessy et al., 1999;Yu and Neil, 1993).Intense summer rainfall events can be harmful to the environment, and have been linked to an increase in flood frequency, soil erosion, inundation of lowland areas and episodic aquifer recharge (Suppiah and Hennessay, 1998).As a result, recharge events may occur episodically, strongly influenced by rainfall depth and duration.The impacts of such high rainfall events are evident in the groundwater response to the peak summer rainfall event in 2006.Such out of season events will also negatively impact agricultural production due to soil erosion and loss of soil structure.The redistribution of annual rainfall will reduce agricultural yields and encourage a move towards more sustainable perennial plant options (Connor, 2004;John et al., 2005).

Water table fluctuations
The observed increase in depth to water table has been shown to be driven primarily by rainfall decline rather than by perennial biomass production and hence, plant transpiration; the trend in the control piezometers mimics that of piezometers within belts (Fig. 3), but overall the experiment has lowered the water table by an additional 0.9 m.
Division of the data into piezometers within the perennial belts and those in the centre of the alley (regardless of distance) for the period subsequent to 2000 showed no statistically significant difference in the mean; however the variance was approximately twice as much for piezometers located in the perennial belt (Fig. 5).This difference in Introduction

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Full the variance of the two locations can be attributed to the effects of lateral root extension from the tree belt.Lateral root extension has been recorded at up 20 m from the trunk (Ellis et al., 2005;Zohar, 1985).For treatments with wide alleys (<30 m) lateral root extension from the belt was observed within piezometers up to 15 m from the belt edge.This suggests that the response in the water table between B belt and B alley within treatment F (4 m belt, 17.5 m alley, see Fig. 5) would be very similar.This is not observed within the data, site variability such as soil structure may be responsible for this limited response.Site conditions prior to 2000 would have proven detrimental to growth due to the shallow water table promoting water logged conditions that could delay the response in root growth (Barrett-Lennard, 2002, 2003).The quality of the groundwater at the site (pH ranged 3-5 and electrical conductivity between 22.1-45.9mS cm −1 ) suggests that it would restrict the growth of vertical tap roots.Under such conditions, perennial plant growth rates would be low (Greenwood et al., 1985) and this is reflected in the low biomass recorded at the site.During drought or stress, groundwater may have been accessed as a potential source by perennial vegetation but fresher rainfall derived recharge would be a preferred water source (Archibald et al., 2006).
The average water table depth beneath high (treatment design F) and low biomass (treatment design G) perennial showed some deviation (Fig. 5) after more than 6 years growth.On average, the water table depths beneath the low biomass belt were shallower than beneath a high biomass belt.However, this difference is marginal in terms of additional water use.

Biomass production
The observed response in the perennial above-ground biomass for the various belt widths was in agreement with observations by Ritson (2004); who showed a similar decline in above-ground biomass production for Pinus pinaster as belt width increased.An increase in competition between individual trees for resources (water, sunlight and nutrients) reduces biomass production and in extreme cases causes plant death.greater the number of rows of perennial trees in the belts, the greater the competition.This reduction in growth due to competition is greatest in the 100% revegetation plots at the site (belt width=138 m).All of the 100% revegetation plots had large numbers of tree deaths, implying severe drought stress.Previous studies have shown that block planting can increase water table depth in areas of good quality groundwater (Harper et al., 2005;Sudmeyer and Goodreid, 2007).Those plots with only 2 rows of trees within the belts produce the highest amount of above-ground biomass.Trees placed on the edge of the belt have a greater opportunity to take advantage of resources from within the alley, providing a biophysical yield advantage over trees planted within the belt (Kho, 2000).Therefore, the above-ground biomass production for treatment design F (belt width of 4 m, a double row of trees) was highest because both tree rows have the capacity to access resources from within the alley.

Conclusions
This work and another concurrent study (Noorduijn et al., 2009) have shown that the effects of this large scale alley farming experiment contributed to the water table response, and accounted for half of the effect of the regional climate trend.A decline in rainfall over recent years may explain a large proportion of the decline in groundwater levels (approximately 60% of the variance), however the presence of vegetation has contributed approximately 30% to the variability.This study has established that the relative contribution of the experiment, in terms of additional water used, is an additional average of 27 mm per annum by the perennial tree belts.Lateral root growth by the perennial belt into the alley can account for this additional availability of water.To optimise this water use by the perennial tree belts at the site, a large proportion of land would need to be converted to perennial belts.A narrow perennial belt (approximately 4 m) would achieve this and produce the largest biomass providing potential economic returns.depth beneath belt (white) and centre of the alley (solid) which produced the largest biomass (triangles, treatment design F) and lowest biomass (square, treatment design G for the belt and A for the alley) are also indicated.The star identifies dates on which there was a statistically significant difference in the means of the water table depth between the belt and the alley.

Fig. 1 .Fig. 2 .Fig. 3 .Fig. 4 .Fig. 5 .
Fig. 1.(a) Location and (b) layout of Davenports experiment site.The location of a surface water drain and paddock boundaries have been identified.(c) shows the conceptual layout of each of the treatment types; the black boxes identify the locations of the experiment plots and the black circles show the locations of the individual piezometers within the plots in the form of a transect.

table drawdown .
However, in 2006 the large summer storm immediately preceded the Introduction

Table 3 )
. The observation that ET from the site was only marginally enhanced may indicate that transpiration of Figures . There is a high correlation between water table depth at B belt and B alley from February 2000 until June 2002 with an ad- The Figures

Table 1 .
The conceptual model of alley farming, i.e. deep rooted perennial vegetation create Figures greater unsaturated zone storage buffer for future large rainfall events (or wet years) and greater store of freshwater, has only marginal relevance at this site due to shallow groundwater having poor quality and restricting vertical root development.This restriction to vertical tap root development and use of groundwater also contributes to the low biomass produced across the site.Introduction Detailed of Toolibin Alley Farming Experiment at Davenport's site. a

Table 2 .
Range of perennial belt water use (WU) values, where Sy is the specific yield, P Dev is the perennial belt deviation from the control bores (generated from Fig.4), and WU is the depth of water transpired by the perennial belt.MIN, MAX, and AV represent the minimum, maximum, and average values for that variable.

Table 3 .
Evaporation loss values generated using a one-dimensional soil water balance model from 1996 to 2007.

Table 4 .
Estimates above-ground biomass for 12 year old E. vegrandis for 5 different belt widths.