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Sep 6, 2013 - Jailbreak: a fishway releases the endangered Macquarie perch from confinement below an anthropogenic barrier. B. T. Broadhurst. A,B,E.
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Marine and Freshwater Research, 2013, 64, 900–908 http://dx.doi.org/10.1071/MF12245

Jailbreak: a fishway releases the endangered Macquarie perch from confinement below an anthropogenic barrier B. T. Broadhurst A,B,E, B. C. Ebner B,C, M. Lintermans A,B, J. D. Thiem A,D and R. C. Clear A,B A

Parks, Conservation & Lands, Territory & Municipal Services, GPO Box 158, Canberra, ACT 2601, Australia. B Present address: Institute for Applied Ecology, University of Canberra, Bruce, ACT 2601, Australia. C Present address: Tropical Landscapes Joint Venture, CSIRO Ecosystem Sciences & TropWATER, PO Box 780, 47 Maunds Road, Atherton, Qld 4883, Australia. D Present address: Fish Ecology and Conservation Physiology Laboratory, Department of Biology, Carleton University, 1125 Colonel Bay Drive, Ottawa, Ontario K1S 5B6, Canada. E Corresponding author. Email: [email protected]

Abstract. Management interventions are often needed to facilitate the recovery of ecosystems affected as a result of human alteration. Population-level monitoring is often central to evaluating the effectiveness of specific on-ground actions. In the present study, we assessed the response of a remnant population of the endangered Macquarie perch (Macquaria australasica) to the construction of a rock ramp fishway on the Cotter River, Australia, over a 7-year period. Prior to fishway construction, this obligate riverine spawner had been previously confined to Cotter Reservoir and six kilometres of stream by a raised road-crossing. Surveys conducted in the 2 years following fishway completion failed to detect Macquarie perch upstream of the fishway. Subsequent surveys (6–7 years post-fishway completion) detected Macquarie perch up to 12 km upstream of the fishway. The number and distribution of smaller-sized individuals (0þ (,100-mm total length (TL) and 1þ (100- to .150-mm TL)) suggests that individuals found upstream of the fishway are resident stream fish and not fish that have migrated from known downstream spawning areas. The success of the fishway has been timely because enlargement of a downstream reservoir will inundate four kilometres of river and destroy the majority of spawning sites of this species downstream of the fishway in the Cotter River. Additional keywords: distribution, fish passage, long-term assessment, Macquaria, Percichthyidae, rock-ramp fishway. Received 6 September 2012, accepted 24 June 2013, published online 6 September 2013

Introduction Connectivity refers to the degree to which the landscape enables biota to move among habitats (Henein and Merriam 1990; Tischendorf and Fahrig 2000). For instance, individuals may need to move among feeding, breeding, nursery and refuge habitats either on daily, seasonal or annual timeframes. Populations can also intermix or have the capacity to recolonise areas after local disturbances, and the temporal nature of such connections operate across a multitude of scales and frequencies. Natural connections of habitats may be intermittent (e.g. glacier formation, seasonal ice formation, the cover of night) and in undisturbed ecosystems provide drivers of ecosystem and evolutionary structure and function. Importantly, this connectivity is a function of landscape features and the dispersal ability of species (Tischendorf and Fahrig 2000). Fragmentation occurs when connectivity is discontinued and can be a basis for speciation and species extinction (Darwin 1859). Anthropogenic disturbances leading to fragmentation of Journal compilation Ó CSIRO 2013

landscapes and populations represent a major threat to many ecosystems (Lord and Norton 1990; Saunders et al. 1991). Fragmentation can reduce the probability that critical habitats are available (Dunning et al. 1992) and increase isolation of populations, rendering them more susceptible to stochastic events, leading to population and species extinction (Fahrig 1997; Hilderbrand and Kershner 2000b). Riverine ecosystems are easily fragmented because of their linear nature (riverscapes) and the relative inability of in-stream biota (e.g. fish) to pass barriers (Fausch et al. 2002; Fullerton et al. 2010), and are commonly disrupted because water is a valuable human resource. A variety of anthropogenic structures result in fragmentation of river ecosystems, with dams, weirs and road crossings being the most common (Warren Jr and Pardew 1998; Verreault et al. 2004; Sheer and Steel 2006; Williams et al. 2012). Fragmentation of river habitats can have negative effects on fish populations, especially those of migratory species (Laine et al. 2002; Wofford et al. 2005). Fishways are a common www.publish.csiro.au/journals/mfr

Fishway releases the endangered Macquarie perch

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Cotter Reservoir A B

Vanitys fishway C

E

Co tter

Riv er

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Flo w

and effective management tool for increasing connectivity of river habitats for fish (Jungwirth 1998; Stuart et al. 2008; Williams et al. 2012) and have been used for more than 300 years to facilitate fish movement past barriers (Nemenyi 1941). Many of Australia’s freshwater fish species are migratory, at least to some degree (Harris et al. 1998) and barriers to fish passage have long been recognised as a contributing factor to freshwater fish declines in Australia (Mallen-Cooper 1999). The majority of anthropogenic barriers to fish passage occur in the Murray–Darling Basin in south-eastern Australia (some 4000), where human occupation and agriculture are concentrated (Harris and Mallen-Cooper 1994; Lintermans 2007; Koehn and Lintermans 2012). Consequently, fishways have a history in Australia spanning at least a century, although some earlier fishways were ineffective for Australian fish species (Harris and Mallen-Cooper 1994; Barrett and Mallen-Cooper 2006). Recent and ongoing research on the swimming abilities of native fish has provided more detailed parameters for fishway design specifically targeted at Australian fishes (Harris and MallenCooper 1994; Mallen-Cooper 1994; Starrs et al. 2011). At low level weirs (,1.5 m) and road crossings, rock-ramp (or naturelike) fishways are being increasingly used as a relatively inexpensive and effective means of providing fish passage (Harris et al. 1998; Beatty et al. 2007; Calles and Greenberg 2009; Steffensen et al. 2013). Furthermore, rock-ramp fishways adopt a design philosophy which is ecologically based and aims to mimic natural river segments (Katopodis et al. 2001) and offer a relatively efficient means of passage (Bunt et al. 2012). Macquarie perch, Macquaria australasica Cuvier, 1830, has reduced in distribution and in abundance since the early 1980s, so much so that the species was declared nationally endangered (Ingram et al. 2000; Lintermans 2007). Barriers to passage, sedimentation, alien fish species and overfishing are commonly associated with the decline of Macquarie perch (Lintermans 2007). Macquarie perch is a medium-sized deep-bodied Percichthyid that attains a maximum size of 3.5 kg and 550 mm in total length (TL), although individuals larger than 1 kg and 350-mm TL are uncommon (Ingram et al. 2000; Lintermans 2007; Lintermans and Ebner 2010). Sexual maturity is reached at 2 years (150–200-mm TL) for males and 3 years (,300-mm TL) for females, although this can vary based on whether a fish matures in a river or reservoir (Appleford et al. 1998; Lintermans 2007). The species is highly fecund (50 000– 100 000 eggs per female) and long-lived (commonly 10–15 years, maximum of 26 years) (Cadwallader and Rogan 1977; Cadwallader 1984; Ingram et al. 1994; Lintermans and Ebner 2010). Macquarie perch requires access to riverine habitats for spawning (Cadwallader and Rogan 1977; Tonkin et al. 2010). Adult Macquarie perch that inhabit reservoirs have been found to migrate only a few kilometres from the reservoir into the river to spawn (Cadwallader and Rogan 1977; Tonkin et al. 2010). Translocated populations have established in several catchments, although time between translocation and detection of a population can be delayed (Lintermans 2013c). In the current study, we aimed to determine whether the installation of a rockramp fishway facilitated upstream expansion of a Macquarie perch population immediately post-installation, and over a longer period (.5 years) after installation. It was predicted that the fishway would allow upstream access for Macquarie perch,

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F Bendora Reservoir

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0

2

4 km N

Fig. 1. Location of Macquarie perch sampling sites (A–F) and Vanitys Crossing fishway on the Cotter River between Bendora Dam and Cotter Dam (inset location of study area within Australia).

increasing its distribution and providing access to potential spawning areas upstream. Materials and methods Study site The study was undertaken in the Cotter River, an upland stream that flows north along the western edge of the Australian Capital Territory (ACT), Australia (Fig. 1). The Cotter River, located within the Murray–Darling Basin, is a highly regulated upland stream interrupted by numerous road crossings and the following three dams: Cotter Dam (500 m above sea level (asl), 358190 1000 S, 1488560 1900 E), Bendora Dam (778 m asl, 358260 4800 S, 1488490 4300 E) and Corin Dam (955 m asl, 358320 0700 S, 1488500 1300 E) (Nichols et al. 2006). The Cotter River has a total catchment area of 480 km2 and serves as the main domestic water supply for the city of Canberra. Two nationally endangered fishes, Macquarie perch and trout cod, Maccullochella macquariensis Cuvier, 1829, and one locally threatened fish, two-spined blackfish, Gadopsis bispinosus Sanger, 1984, as well as introduced rainbow trout, Oncorhynchus mykiss Walbaum, 1792, brown trout Salmo trutta Linnaeus, 1758, goldfish Carassius auratus Linnaeus, 1758, oriental weatherloach, Misgurnus anguillicaudatus Cantor, 1842, and eastern Gambusia, Gambusia holbrooki Girard, 1859, currently reside in the Cotter River (Lintermans 2007, 2012).

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In 2001, a rock-ramp fishway was installed on a road crossing (Vanitys Crossing 358200 4600 S, 1488530 2300 E, approximately 6 km upstream of Cotter Reservoir, see Fig. 1); this was constructed to provide access for Macquarie perch to 22 km of upstream river habitat (Ebner and Lintermans 2007). Previous sampling in the 1980s and 1990s using a variety of methods (fyke netting, backpack electro-fishing) had not detected Macquarie perch upstream of the road crossing and it was believed that this species was extinct from this reach of the Cotter River (M. Lintermans, unpubl. data). However, ad hoc observations and sampling had demonstrated that the species was present up to the pool immediately downstream of the road crossing (M. Lintermans, unpubl. data). The crossing was not believed to be a barrier to either of the salmonid species, because both were encountered frequently both upstream and downstream of the crossing, and both are capable of surmounting in-stream obstacles by jumping (M. Lintermans, unpubl. data). The current study was undertaken along the 27-km river reach, from immediately upstream of Cotter Reservoir to immediately downstream of Bendora Dam (Fig. 1). Full supply level of the recently completed enlarged Cotter Dam will move the extent of the impounded waters upstream to within 1.5 km of the Vanitys Crossing fishway (Lintermans 2012; Site B, Fig. 1). Vanitys Crossing fishway Vanitys Crossing is a concrete ford ,45 m in length that was constructed in the 1970s and acted as a barrier preventing upstream migration of Macquarie perch (Fig. 2a; Lintermans 1991). A partial-width rock-ramp fishway with a random-ridge rock and reverse-leg design was installed here because the stream is relatively narrow (,20 m), this fishway design requires minimal maintenance and the fishway only needed to operate over a small range of flows (Fig. 2b). Biological characteristics of Macquarie perch were incorporated into specific design elements of the fishway. The fishway was designed with a lower than customary gradient (1 : 30 rather than 1 : 25), specifically to accommodate the perceived poor swimming performance of adult Macquarie perch (actual performance unknown at the time of sampling). Velocities in the fishway ranged from 0 to .1.0 m s1, although they were typically ,0.5 m s1, on the basis of three random transects (Ebner and Lintermans 2007). The fishway was also designed with a ‘v’ profile (deeper in middle) to accommodate the depth requirement of large adult Macquarie perch. Capping was installed on the downstream side of the road crossing to raise the water depth of the fishway exit over the existing roadway. Fish collection Sampling of riverine subreaches (Fig. 1, Table 1) was conducted over two periods; in the 2 years after installation of the fishway at Vanitys Crossing (2001–2002) and 6–7 years later (2007–2008), to determine whether Macquarie perch had used the fishway to access the river upstream. Riverine reaches were sampled between September and May (spring to autumn) in 2001–2002 and between January and April (summer to autumn) in 2007–2008. Cotter Reservoir was sampled year-round in 2001–2002 and between January and March (summer to autumn) in 2007–2008. Cotter River was in the middle of a

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(a)

(b)

Fig. 2. Vanitys Crossing (a) before and (b) after installation of the rockramp fishway.

Table 1. Summary of fyke net effort used per site for the 2001]2002 and 2007]2008 surveys of the Cotter Reservoir and Cotter River DNS ¼ did not sample Reach

Cotter Reservoir Site A Site B Site C Site D Site E Site F

Distance upstream of Cotter Reservoir (km)

2001–2002

Net nights 2007–2008

0 1 5 9 14 18 27

227 70 40 24 16 13 DNS

24 24 24 24 24 24 24

decade-long drought throughout the entire period (Fig. 3). Cotter Reservoir was also sampled to provide an indication of the status of the reservoir population. Sampling effort (number of net nights and the number of sites sampled) differed between the two sampling periods (Table 1). Abundances of Macquarie perch captured at each site were standardised by dividing the number of fish caught by the number of net nights per site. Fish were captured using single-winged fyke nets (wing 5 m; 20-mm stretched mesh in 2001–2002 and 13-mm stretched mesh in 2007–2008) set from shore. For pools, three or four fyke nets

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16 000

Mean daily flow (ML day⫺1)

14 000 12 000 10 000 8000 6000 4000 2000 0 1988

1990

1992

1994

1996

1998

2000

2002

2004

2006

2008

2010

2012

Year Fig. 3. Mean daily flow (ML day1) of the Cotter River at Vanitys Crossing from 1988 to 2012 (ACTEW Water, unpubl. data).

Results Distribution Macquarie perch was not recorded upstream of the fishway in 2001–2002, whereas in 2007–2008, it was detected at the first and second sites upstream of the fishway (Sites C and D, Fig. 4). Note that an individual was captured by backpack electro-fishing at Site E in 2008 (B. T. Broadhurst, unpubl. data). The recorded distribution of Macquarie perch increased from 1 km upstream of Cotter Reservoir in 2001–2002 (when it was found only in the Cotter Reservoir and Site A) to 16 km in 2007–2008 (when it was found at every site up to and including Site D, Fig. 4).

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Data analyses To test for differences in abundance, a repeated-measures ANOVA was undertaken, with location (downstream and upstream of the fishway) as a fixed factor, year as a withinsubject factor and site nested within location and treated as subjects in the analysis. The data were non-normally distributed and PERMANOVA analysis was also employed (Anderson 2001). The results of the PERMANOVA were almost identical to the repeated-measures ANOVA, so the latter was retained for interpretation. To complement the abundance analysis, we looked at proportional occurrence between the sites and dates as an indicator of fish abundance at a site. A log-linear analysis was employed to compare proportions of nets with fish (number of net nights divided by the number of net nights with fish present) between years and sites. The analysis was followed by pair-wise tests between years within sites to tease out interaction effects. Statistical significance was set at a ¼ 0.05. Data analysis was performed using SAS (v9.1, SAS Institute, Cary, North Carolina, USA). Data is reported as mean  standard error (s.e.), unless otherwise specified.

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Abundance (individuals/net night)

were set per pool, and 10–12 were set from a boat around the perimeter of the reservoir. Fyke nets were set for ,16 h (typically from 1530 hours to 0730 hours). Total length of captured Macquarie perch was recorded to the nearest millimetre, with fish then released unharmed at the site of capture.

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0 Cotter Res.

A

B

C

D

Site Fig. 4. Abundance (mean individuals per net night  s.e.) of Macquarie perch in the lower Cotter River and Cotter Reservoir in 2001–2002 (black bars) and 2007–2008 (grey bars).

Abundance There was a greater relative abundance of Macquarie perch captured at all riverine sites in 2007–2008 than in 2001–2002 (Fig. 4). Of the riverine sites, Site A was the only site where Macquarie perch was captured in 2001–2002. At riverine sites in 2007–2008, the highest abundance of Macquarie perch was at Site C, followed by Sites A, B and D (Fig. 4). In both 2001–2002 and 2007–2008, Cotter Reservoir had higher abundances of Macquarie perch than did the riverine sites (Fig. 4). There was no significant effect of year, location (i.e. upstream vs downstream of the fishway) or the interaction between year and location on the relative abundance of Macquarie perch (Table 2). However, there was a significance difference among sites and the interaction between site and year in the relative

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Table 2. Results of repeated-measures ANOVA on the relative abundance of Macquarie perch between years, locations and sites in the Cotter River Source Site (location) Year Year  Site (location) Year  Location Location

d.f.

F-value

P.F

2 1 2 1 1

10.53 2.40 7.54 0.25 0.20

,0.0001 0.2616 0.0007 0.6642 0.6989

abundance of Macquarie perch (Table 2). Analysis of the proportion of nets that contained Macquarie perch detected a significant difference in year (x2¼ 10.76, d.f. ¼ 1, P ¼ 0.001), site (x2 ¼ 100.62, d.f. ¼ 3, P , 0.0001) and a significant interaction between year and site (x2 ¼ 15.55, d.f. ¼ 3, P ¼ 0.0014). There was significantly higher proportion of nets containing Macquarie perch in 2007–2008 than in 2001–2002 for Sites B (x2 ¼ 25.6282, d.f. ¼ 1, P , 0.0001) and C (x2 ¼ 27.8693, d.f. ¼ 1, P , 0.0001), but no difference at Site A (x2 ¼ 3.4888, d.f. ¼ 1, P ¼ 0.0618) or Site D (analysis void because more than 50% of 225 nets contained fewer than five). Population structure Macquarie perch individuals captured in Cotter Reservoir in 2001–2002 were predominantly fish that were 0þ and 1þ years of age (TL ranging from 51 to 150 mm, Fig. 5a). Similarly, the majority of individuals captured in the river downstream of the fishway (Sites A and B) comprised small Macquarie perch individuals with a higher proportion of 1þ age fish (101–150-mm TL) than in the Cotter Reservoir (Fig. 5a–c). In 2007–2008, at both Cotter Reservoir and the two river sites downstream of the fishway (Sites A and B), the dominant size of Macquarie perch caught was between 101 and 150 mm in TL (Fig. 5a–c). Over 80% of Macquarie perch individuals caught upstream of the fishway (Sites C and D) in 2007–2008 were 0þ individuals of less than 50-mm TL (Fig. 5d). Site C contained fish from at least four different size classes, likely corresponding to different annual cohorts (Fig. 5d; cf. Cadwallader 1984). Discussion Fragmentation of aquatic habitats is a major issue worldwide (Nilsson et al. 2005; Dudgeon et al. 2006), and restoration of fish passage has become a priority recovery activity both internationally (e.g. Calles and Greenberg 2007; Kemp and O’Hanley 2010; Gough et al. 2012) and in Australia (Barrett 2008; Lintermans 2013a, 2013b). Although many fishways are now commonly designed to pass a range of species and sizes (e.g. Stuart et al. 2008; Thiem et al. 2013), the targeting of fishpassage remediation at a single species or species group still occurs, particularly for highly valued sportfish (e.g. salmonids) or, increasingly, threatened species (e.g. Morgan and Beatty 2006), and the Vanitys Crossing fishway is an example of this. Macquarie perch is now largely confined to upland streams in south-eastern Australia (Douglas 2002; Lintermans 2007; Tonkin et al. 2010), and this is where many impoundments are also located, altering downstream flow regimes and potentially

creating or exacerbating low-flow barriers. The success of the fishway in establishing a population of Macquarie perch in upstream reaches validates the fishway design parameters, and provides a useful template for providing fish passage for this species in other locations. The present study has illustrated the benefit of long-term (.5 years) assessment following management intervention aimed at conservation of an endangered species. In the present situation, short-term assessment in the first year following installation of a rock-ramp fishway did not detect any positive effects in the form of upstream colonisation by Macquarie perch. However, a considerably longer duration of assessment has revealed a significant benefit of the fishway installation, with Macquarie perch making its way past the road crossing and establishing a significant population in upstream reaches. The delayed result highlights the need for funding for longer-term monitoring after interventions, to ensure adequate assessment of their success can be made. The depth and water velocities in the Vanitys Crossing fishway are passable by Macquarie perch on the basis of laboratory flume-tank trials of swimming performance of adults and subadults (Starrs et al. 2011). Fishways, including those of the rock-ramp design in the present study, have been shown to be passable by many Australian fish species (e.g. Harris et al. 1998; Stuart and Berghuis 2002; Beatty et al. 2007). Our result may be explained by the fact that the majority of Macquarie perch resided in Cotter Reservoir rather than the river in 2001 and 2002, and rarely encountered the fishway during short-term movements (Ebner et al. 2011). Macquarie perch are a moderately long-lived species (Cadwallader 1984; Lintermans and Ebner 2010) and, on the basis of the results of the present study, can be slow dispersers and colonisers. As well as slow dispersal, the species may also take a prolonged period to commence recruitment in new reaches, with no recruitment detected in 5 years of monitoring following a translocation of adult fish in the Queanbeyan River (Lintermans 2013c). It is also possible that low numbers of Macquarie perch used the fishway in the Cotter River immediately following its installation, but remained at undetectable levels for the first few years, similar to that found for a translocated population of Macquarie perch in the Queanbeyan River (Lintermans 2013c). Fishway efficiency, a key determinant of the success of a fish passage structure (Bunt et al. 2012), has yet to be quantified for different fishway types for Macquarie perch and is still an important knowledge gap for management of this structure and the facilitation of movement by this species. Range expansion of this isolated remnant population of Macquarie perch is of significant conservation benefit. It is also fortuitous in its timing; a decade-long drought in southern Australia has affected the Cotter Catchment (Fig. 3) and led to the enlargement of the existing Cotter Reservoir for water supply to the city of Canberra. This in turn will inundate the Cotter River by a further 4.5 km, flooding the river to within ,1.5 km of the fishway at Vanitys Crossing (Lintermans 2012). Without a functioning fishway (or translocation) and the establishment of a self-sustaining subpopulation upstream of the fishway, the resident Macquarie perch population faced local extinction as a result of loss of riffle-run-pool habitat critical for spawning and nursery functions (Cadwallader and Rogan 1977), akin to what occurred in Googong Reservoir

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2001/2002

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n ⫽ 193

n ⫽ 129

n ⫽ 49

n⫽0

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0 80

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0 0

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Total length (mm) Fig. 5. Length frequency distribution (expressed as a percentage of catch for each site) of Macquarie perch captured in 2001–2002 and 2007–2008. (a) Cotter Reservoir, (b) Site A, (c) Site B and (d ) Site C.

following damming of the nearby Queanbeyan River (Lintermans 2013c). The expanded spatial extent of the population from 5.5 km of river to at least 17.5 km and the establishment of a riverine subpopulation is a welcome result for Cotter River Macquarie perch. The increase in connectivity of both habitats and

subpopulations will render the Cotter population less vulnerable to stochastic demographic and localised environmental events (Fahrig 1997; Hilderbrand and Kershner 2000a; Fullerton et al. 2010). To this end, we recommend developing quantitative relationships among factors (e.g. flow requirements, invasive species) affecting Macquarie perch spawning

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and recruitment and support the commitment to improvements to fish passage on road crossings upstream of Vanitys Crossing in the Cotter River (see also Ebner et al. 2008; Lintermans et al. 2010). Young-of-the-year was the most abundant cohort in the population of Macquarie perch upstream of the fishway. This suggests that spawning and recruitment (at least to juvenile stage) has been successful upstream of the fishway. Larvae and juvenile Macquarie perch were observed via snorkelling up to 9 km upstream of Cotter Reservoir (Broadhurst et al. 2012). The riverine extent of the young-of-the-year individuals detected in the current study and the distribution of larval and juvenile Macquarie perch found in Broadhurst et al. (2012) were threefold greater than the extent of breeding sites reported previously (usually ,3 km) from studies of reservoir populations of Macquarie perch (Cadwallader and Rogan 1977; Douglas 2002; Tonkin et al. 2010), and most likely reflect a recruiting riverine population upstream of the fishway. Furthermore, the presence in the current study of up to four Macquarie perch cohorts upstream of the fishway suggests establishment of a selfsustaining riverine subpopulation, which has important implications for the long-term survival of this species in the Cotter River (i.e. increasing the population resilience to stochastic events). The absence of larger adults (.350-mm TL) in the current study may reflect the true population structure of the newly established riverine subpopulation, or may simply reflect a sampling bias, because fyke nets are a poor method of capturing larger adults in both reservoir and riverine habitats (Ebner and Lintermans 2007). On the basis of the extent of spawning migrations from previous studies of ,1 km (Cadwallader and Rogan 1977; Douglas 2002; Tonkin et al. 2010), it is unlikely that the absence of large adults upstream of the fishway would be due to these adults returning to Cotter Reservoir before spawning. The number of adult fish that has contributed to the establishment of the riverine subpopulation is unknown. Other genetic studies on Macquarie perch subpopulations in the upper Murrumbidgee River catchment have revealed very small effective population sizes (Ne), often .10 (Farrington et al. 2009). Indeed, the Ne of the Cotter Reservoir Macquarie perch population has been estimated at only 17–79 (Farrington et al. 2009), with an Ne of 1000 individuals recommended for maintaining adaptive potential in the face of environmental change (Franklin and Frankham 1998; Weeks et al. 2011). Low Ne was estimated for the re-established Queanbeyan River Macquarie perch population, which although establishing and persisting for more than a decade, is now undetectable (Lintermans 2013c). The Ne of the Cotter River subpopulation upstream of the fishway should be investigated and appropriate management undertaken (i.e. translocation from the Cotter Reservoir) if it is significantly lower than that in Cotter Reservoir. In summary, the current study has demonstrated the value of a long-term commitment to conservation management in a river catchment. Specifically, the focus has been on understanding the effects of a successful management intervention, in this case, installing a fishway for an endangered species. Our success bodes well for planned additional Macquarie perch passage improvements upstream of the Vanitys Crossing fishway in the Cotter River. The success of the current fishway will inform future fish-passage designs for this species and has wider

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relevance in demonstrating the benefit of long-term assessment for evaluating effectiveness of in-stream interventions. Acknowledgements Thanks go to David Shorthouse for long-term support that made this study possible. Danswell Starrs, Mark Jekabsons and Simon Godschalx assisted with field work. The manuscript was improved through comments from Chris Fulton and discussion with Ivor Stuart along with two anonymous reviewers. Wayne Robinson (NSW DPI Fisheries) provided statistical advice. ACT Government provided funding for the construction of the rockramp fishway at Vanitys Crossing. Martin Mallen-Cooper designed the fishway. Thanks also go to the two anonymous reviewers who provided comments on this manuscript. This research was conducted with approval from the University of Canberra Animal Ethics Committee (Project numbers CEAE 01/05; CEAE 05/10). This research was funded by the Australian Federal Government under the National Action Plan for Salinity and Water Quality and Natural Heritage Trust funding schemes. Our research was conducted in Ngunnawal country.

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