scholarly journals Assessing ecological patterns in Wellington south coast's nearshore rocky-reef communities for resource conservation and management

2021 ◽  
Author(s):  
◽  
Tamsen Byfield

<p>Many coastal marine communities are increasingly affected by terrestrial and maritime human activities and growing coastal populations. Protection of coastal assets and the sustainable use of coastal resources requires knowledge of nearshore benthic community status; the environmental processes that structure and connect them; the quality, abundance, and distribution of physical habitat; essential habitat for species requiring protective measures, and the spatio-temporal scales at which these patterns and processes occur. To assess the status of Wellington South Coast’s (WSC) rocky-reef assemblages prior to the enactment of the Taputeranga Marine Reserve in 2009, two annual baseline surveys were conducted during the austral summers of 2007/08 and 2008/09. These surveys evaluated the biotic and abiotic components of the assemblages in terms of diversity, abundance distribution, and size-class frequency patterns of key macroalgal and mobile macro-invertebrate species. These results were analysed to develop recommendations for best post-reserve monitoring practices, including the identification of “indicator” species for rapid yet representative field surveys to assess structural and status changes. In combination with patterns described by a previous pre-reserve baseline survey series (2000) that focussed on a reduced list of macro-algal and mobile macro-invertebrate species, this final pre-reserve survey forms the basis of a historical dataset for WSC rocky reefs that can be used for long-term monitoring of ecosystem shifts due to the new reserve and to possible changes caused by anthropogenic activity or altered natural processes.  These aims were addressed by collecting information directly at local/site scale and remotely, at the larger area scale. Dived baseline surveys quantified nearshore WSC rocky-reef epibenthic assemblages at 9 sites at depths ranging from 5-13.6m and at a mean distance from shore = 113m. A survey design that included three sites west of the pending marine reserve, three sites to the east, and three sites within the designated reserve was selected to permit later BACI analyses of post-reserve changes. Species surveyed were those commonly encountered during daylight on exposed surfaces and in accessible crevices and belonged to one of three epibenthic groups: macro-algae (48 species), mobile macro-invertebrates (36 species), and sessile macro-invertebrates (30 morphotypes). These surveys did not include epizoa or smaller, cryptic newly recruited macro-invertebrates. Sessile macro-invertebrate cover was only logged if >0.1%/m2. To gauge possible spatio-temporal patterns in primary productivity as a measure of ecosystem function, biomass and plant size were measured semiannually (winter, summer) for dominant kelp and fucoid species and for two key recreationally and commercially important mobile macro-invertebrate species (sea urchin and abalone). Predictive regression equations developed from wet weight and plant size can be used for future non-destructive estimates of local primary productivity and in trophic modelling.   [...]  This mapping data forms the basis of a legacy dataset that will assist with monitoring changes in the integrity of critical physical habitat and associated biotic cover. It has also demonstrated that representative descriptions of both biotic and abiotic benthic components can be achieved with a minimum of sampling points and by using the quicker semi-quantitative visual analysis of video. These data can also be used to ground-truth a recently-completed multi-beam acoustic survey of the area.  This work has used the approach of landscape ecology, which explains patterns in community structure, function, status and biophysical causes from a spatial perspective, to study biophysical patterns in WSC epibenthic rocky-reef communities. The work identified a high degree of spatial and temporal variation within the abiotic and biotic community within and outside of the reserve area and the limited availability of preferred habitat. The work also identified the need to include indicator species in monitoring to improve the chance of detecting impacted assemblages. These results, and the development of non-destructive sampling tools for assessing ecosystem status, are relevant locally and nationally for resource managers.</p>

2021 ◽  
Author(s):  
◽  
Tamsen Byfield

<p>Many coastal marine communities are increasingly affected by terrestrial and maritime human activities and growing coastal populations. Protection of coastal assets and the sustainable use of coastal resources requires knowledge of nearshore benthic community status; the environmental processes that structure and connect them; the quality, abundance, and distribution of physical habitat; essential habitat for species requiring protective measures, and the spatio-temporal scales at which these patterns and processes occur. To assess the status of Wellington South Coast’s (WSC) rocky-reef assemblages prior to the enactment of the Taputeranga Marine Reserve in 2009, two annual baseline surveys were conducted during the austral summers of 2007/08 and 2008/09. These surveys evaluated the biotic and abiotic components of the assemblages in terms of diversity, abundance distribution, and size-class frequency patterns of key macroalgal and mobile macro-invertebrate species. These results were analysed to develop recommendations for best post-reserve monitoring practices, including the identification of “indicator” species for rapid yet representative field surveys to assess structural and status changes. In combination with patterns described by a previous pre-reserve baseline survey series (2000) that focussed on a reduced list of macro-algal and mobile macro-invertebrate species, this final pre-reserve survey forms the basis of a historical dataset for WSC rocky reefs that can be used for long-term monitoring of ecosystem shifts due to the new reserve and to possible changes caused by anthropogenic activity or altered natural processes.  These aims were addressed by collecting information directly at local/site scale and remotely, at the larger area scale. Dived baseline surveys quantified nearshore WSC rocky-reef epibenthic assemblages at 9 sites at depths ranging from 5-13.6m and at a mean distance from shore = 113m. A survey design that included three sites west of the pending marine reserve, three sites to the east, and three sites within the designated reserve was selected to permit later BACI analyses of post-reserve changes. Species surveyed were those commonly encountered during daylight on exposed surfaces and in accessible crevices and belonged to one of three epibenthic groups: macro-algae (48 species), mobile macro-invertebrates (36 species), and sessile macro-invertebrates (30 morphotypes). These surveys did not include epizoa or smaller, cryptic newly recruited macro-invertebrates. Sessile macro-invertebrate cover was only logged if >0.1%/m2. To gauge possible spatio-temporal patterns in primary productivity as a measure of ecosystem function, biomass and plant size were measured semiannually (winter, summer) for dominant kelp and fucoid species and for two key recreationally and commercially important mobile macro-invertebrate species (sea urchin and abalone). Predictive regression equations developed from wet weight and plant size can be used for future non-destructive estimates of local primary productivity and in trophic modelling.   [...]  This mapping data forms the basis of a legacy dataset that will assist with monitoring changes in the integrity of critical physical habitat and associated biotic cover. It has also demonstrated that representative descriptions of both biotic and abiotic benthic components can be achieved with a minimum of sampling points and by using the quicker semi-quantitative visual analysis of video. These data can also be used to ground-truth a recently-completed multi-beam acoustic survey of the area.  This work has used the approach of landscape ecology, which explains patterns in community structure, function, status and biophysical causes from a spatial perspective, to study biophysical patterns in WSC epibenthic rocky-reef communities. The work identified a high degree of spatial and temporal variation within the abiotic and biotic community within and outside of the reserve area and the limited availability of preferred habitat. The work also identified the need to include indicator species in monitoring to improve the chance of detecting impacted assemblages. These results, and the development of non-destructive sampling tools for assessing ecosystem status, are relevant locally and nationally for resource managers.</p>


2007 ◽  
Vol 343 ◽  
pp. 77-85 ◽  
Author(s):  
JI Sonnenholzner ◽  
LB Ladah ◽  
KD Lafferty

2018 ◽  
Vol 69 (10) ◽  
pp. 1496
Author(s):  
David R. Schiel ◽  
Tony Ayling ◽  
Michael J. Kingsford ◽  
Christopher N. Battershill ◽  
J. Howard Choat ◽  
...  

Marine reserves exhibit increases in targeted fish species, but long-term effects on biodiversity are poorly understood. Factors other than reserve status may affect decadal changes, including environmental change. We examined the fish fauna at the iconic Poor Knights Islands over 4 decades (1974–2016) before and after implementation of a no-take marine reserve in 1998. We document a substantial increase in commercially and recreationally targeted Chrysophrys auratus, which was virtually absent before 1994 but by 2016 had reached up to 11 fish per 500m2 (220 per hectare). There were also large changes to the fish community, including the decline of subtropical and coastal wrasses, some species with no change and others that increased significantly. Many declines occurred >20 years before the arrival of abundant C. auratus, suggesting the changes do not represent a trophic cascade. Furthermore, this normally benthic-feeding fish has adopted a mid-water foraging behaviour targeting planktivorous fish. The increase in C. auratus appears to be linked both to reserve status and catch regulations in the wider region. Overall, the data point to long-term environmental fluctuations from the late 1970s having a negative effect on the abundance of more than half the reef fish species at these islands.


Ecology ◽  
2013 ◽  
Vol 94 (7) ◽  
pp. 1636-1646 ◽  
Author(s):  
Jarrett E. K. Byrnes ◽  
Bradley J. Cardinale ◽  
Daniel C. Reed

Zoosymposia ◽  
2011 ◽  
Vol 5 (1) ◽  
pp. 439-452
Author(s):  
ILDIKÓ SZIVÁK ◽  
ARNOLD MÓRA ◽  
JÚLIA KATALIN TÖRÖK

In 2006–2007 larval caddisfly assemblages of a semi-natural calcareous stream (Örvényesi Creek) were studied. Characteristic sections can be detected along the whole length of the stream, which passes through diverse types of vegetation, resulting in highly heterogeneous aquatic habitats. Based on an annual survey of different aquatic habitats, our aims were to give an overview of the spatio-temporal distribution of the larval caddisfly assemblages in the Örvényesi Creek and to find indicator species characterizing different sections of the stream. In order to show the spatio-temporal patterns, samples were collected at 7 locations with different streambed morphology, from spring to the mouth of the stream. Caddisfly larvae were collected in every 3rd week during a 1 year period using the “kick and sweep” method. Multivariate analyses were carried out to explore the spatio-temporal structure of caddisfly assemblages. The indicator value method was applied to detect indicator species for different sections of the stream. A rich caddisfly fauna (20 taxa) was found in the Örvényesi Creek. Fast-running and relatively cold-water hypocrenal sections were characterized by Beraea maurus and Apatania muliebris at high indicator value. Three Limnephilidae species (Limnephilus rhombicus, Limnephilus lunatus and Glyphotaelius pellucidus) were identified as significant indicator species for slow flowing, lentic habitats. Along the length of the stream, distinctive spatial and temporal changes were detected in the distribution of the caddisfly assemblages. These changes were mainly connected to variations in morphology of the streambed, phenology of individual taxa, extreme weather conditions and human impacts.


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