Academic literature on the topic 'Hauraki Gulf'

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Journal articles on the topic "Hauraki Gulf"

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Booth, Webber E., and Morten S⊘ndergaard. "Picophytoplankton in the Hauraki Gulf, New Zealand." New Zealand Journal of Marine and Freshwater Research 23, no. 1 (March 1989): 69–78. http://dx.doi.org/10.1080/00288330.1989.9516342.

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Greig, Malcolm J. "Circulation in the Hauraki Gulf, New Zealand." New Zealand Journal of Marine and Freshwater Research 24, no. 1 (March 1990): 141–50. http://dx.doi.org/10.1080/00288330.1990.9516409.

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Manighetti, B., and L. Carter. "Across-shelf sediment dispersal, Hauraki Gulf, New Zealand." Marine Geology 160, no. 3-4 (September 1999): 271–300. http://dx.doi.org/10.1016/s0025-3227(99)00024-9.

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Kendrick, Terese H., and Malcolm P. Francis. "Fish assemblages in the Hauraki Gulf, New Zealand." New Zealand Journal of Marine and Freshwater Research 36, no. 4 (December 2002): 699–717. http://dx.doi.org/10.1080/00288330.2002.9517124.

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Greig, Malcolm J., and Roger Proctor. "A numerical model of the Hauraki Gulf, New Zealand." New Zealand Journal of Marine and Freshwater Research 22, no. 3 (September 1988): 379–90. http://dx.doi.org/10.1080/00288330.1988.9516309.

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Boxberg, Florian, Brice Blossier, Willem P. de Lange, Bethany Fox, and Dierk Hebbeln. "Sediment deposition in the central Hauraki Gulf, New Zealand." Geo-Marine Letters 40, no. 2 (August 10, 2019): 227–41. http://dx.doi.org/10.1007/s00367-019-00583-1.

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Bassett, Imogen, Jeff Cook, Finlay Buchanan, and James Russell. "Treasure Islands: biosecurity in the Hauraki Gulf Marine Park." New Zealand Journal of Ecology 40, no. 2 (2016): 250–66. http://dx.doi.org/10.20417/nzjecol.40.28.

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Zeldis, John R., John Oldman, Sira L. Ballara, and Laura A. Richards. "Physical fluxes, pelagic ecosystem structure, and larval fish survival in Hauraki Gulf, New Zealand." Canadian Journal of Fisheries and Aquatic Sciences 62, no. 3 (March 1, 2005): 593–610. http://dx.doi.org/10.1139/f04-209.

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The ecosystem supporting snapper (Pagrus auratus) larvae was studied during three spring–summer (November–January 1985–1988) spawning seasons in Hauraki Gulf, New Zealand. Upwelling-favourable winds caused more incursion of shelf water into the Gulf in 1985–1986 and 1986–1987 than in 1987–1988, but in the first two seasons, the winds were relatively weak. Stronger winds in 1987–1988 drove greater vertical diffusivity and correlated with greater mixed-layer primary biomass and productivity. Effects of vertical mixing appeared to dominate horizontal incursion of upwelled shelf water in supporting upper water column productivity. The more productive 1987–1988 season had greater abundances of nauplii, copepodites, adult copepods, cladocerans, chaetognaths, hydromedusae, decapod larvae, and numerous larval fish taxa (including snapper). There was much higher survival of snapper between the late-stage egg and post-first-feeding larval stages in 1987–1988, which correlated spatially and temporally with high larval prey densities. Neither higher egg production, fewer predators, nor less horizontal advection accounted for these strong larval snapper cohorts. We hypothesize that larval competence improved within the superior larval feeding environment, reducing predatory losses. The ecosystem response to wind mixing may partially explain the correlation of sea temperatures with recruitment, previously observed for the Hauraki Gulf snapper stock.
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Francis, MP, and RICC Francis. "Growth rate estimates for New Zealand Rig (Mustelus lenticulatus)." Marine and Freshwater Research 43, no. 5 (1992): 1157. http://dx.doi.org/10.1071/mf9921157.

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Growth rate estimates were obtained for New Zealand rig (Mustelus lenticulatus) by analysing length frequency and tag-recapture data. Rig (0+) sampled by set-net in Porirua and Pauatahanui Inlets grew from about 25-30 cm total length at birth to 46-49 cm at age of about 6 months. Samples of juvenile and adult rig trawled in Pegasus Bay and Hauraki Gulf suffered from under-representation of large adults, probably because of escapement. Growth curves derived from length-frequency analysis indicated that Pegasus Bay males matured at 5.0 years and had a minimum longevity of 12 years. Hauraki Gulf males and females matured at 3.7 and 4.7 years, respectively. Growth rates and ages at maturity fell within the ranges reported for other Mustelus species. Tagging data for South Island rig suggested that females grew faster than males. However, growth rate estimates from length-frequency analysis were 2.7-3.3 times greater than estimates from tagging data, probably because the latter were biased by the combined effects of tagging on growth and set-net mesh selectivity.
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Wong, KL Clara, and Steve O'Shea. "Sediment macrobenthos off eastern Waiheke Island, Hauraki Gulf, New Zealand." New Zealand Journal of Marine and Freshwater Research 44, no. 3 (September 2010): 149–65. http://dx.doi.org/10.1080/00288330.2010.498088.

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Dissertations / Theses on the topic "Hauraki Gulf"

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Morrison, Mark Andrew. "Population dynamics of the scallop Pecten novaezelandiae in the Hauraki Gulf." Thesis, University of Auckland, 1999. http://hdl.handle.net/2292/1706.

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The population biology and ecology of scallops in Greater Omaha Bay (a semi-oceanic bay) and Kawau Bay (a estuarine bay) was quantified by observation and experiment. Information was collected to extend the knowledge base on northern New Zealand scallop population dynamics, and for application to potential scallop enhancement in the region. Contagious scallop population organisation was found at all spatial scales examined, ranging from bay wide through to individual bed patchiness, down to the scale of inter-animal distances. Such clumping has strong implications for a range of population processes, including fishing susceptibility and fertilisation success. Monitoring of adults found two main spawning events to occur; in late October and in mid January. Changes in the gonado-somatic index (GSI) were well synchronised between individuals within populations. Subsequent monitoring of spat-fall in artificial collectors documented two main recruitment events, probably the outcomes of the two local spawning events. These spat-fall events occurred on collectors separated by 1Os of km. However, substantial density variations occurred between sites, indicating that local hydrodynamics may have played a significant role in modifying local spat-fall intensities. Smaller spat-fall events were also present between the two major events. The number of spat collected at a number of combinations of site and time were sufficient to support commercial spat catching operations, although problems were encountered with spat detaching at sizes too small to be retained by the collectors. In the 1993/94 summer a large algal bloom event completely eliminated scallop recruitment to collectors for the first three months of that season. Mass mortality events were a major contributor to overall benthic scallop population mortality. Probable causes included intensive scallop harvesting (commercial and recreational), a major storm episode, and a large algal bloom. These effectively eliminated scallop populations from Greater Omaha Bay. The adjacent Kawau Bay was not affected by any of these particular events, but populations there did not survive long after reaching adult sizes. Estimates of M (natural mortality) were higher for all scallop populations than have been previously documented in New Zealand studies. Growth trajectories were reasonably consistent in waters shallower than 19 m, but a progressive decline occurred in both maximal size reached and average growth rates with increasing depth after this point. Food limitation may have been the mechanism involved, which is likely to vary significantly for other locations depending on local environmental conditions. Average time to recruitment to the fishery (100 mm shell width) was three years for the shallower populations. A slight reduction in average size of adults at higher densities was found for some populations, indicating a possible density-dependent effect. Examination of a high density scallop bed found animals to display distinctive substratum preferences over small spatial scales, with higher abundances occurring on coarser materials such as shell gravel, marl and grit. Mud was not favoured as a habitat type. Movements of tagged animals at this location were spatially limited to within the particular habitat patch in which an individual was tagged and released, i.e. at a scale of 1s to 1Os of metres. No animals moved between adjacent patches of similar habitat (100 m scale). A B.A.C.I type experiment was undertaken to assess incidental mortality effects of commercial scallop dredging on undersize scallops, at the spatial scale of beds. Significant negative effects were quantified, with the number of undersize animals killed per legal animal harvested estimated at 1.7 and 2.8 : 1, depending on the size frequency structure of the fished bed. Modelling of likely improvements in the number of animals surviving at the end of fishing, given a reduction in the minimum legal size from 100 to 90 mm, indicated improvements of 20 to 41% of the original population remaining after fishing, depending on animal size and assumed dredge efficiencies, A 90 mm MLS has subsequently been adopted by the Coromandel Scallop Fishery. The results from this work provide detailed population based estimates of parameters required for successful management and optimal harvesting strategies of Hauraki Gulf scallop populations. The large variability in parameters such as mortality, and strong abundance correlations with habitat type, has strong implications for such activities. This work also provides essential information for the undertaking of locally based enhancement operations, such as the spatial and temporal magnitude and variability of spat-fall events, and growth rates with respect to habitat features (i.e. depth).
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Francis, Malcolm 1954. "Population dynamics of juvenile snapper (Pagrus auratus) in the Hauraki Gulf." Thesis, University of Auckland, 1992. http://hdl.handle.net/2292/1976.

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The population dynamics of juvenile snapper, Pagrus auratus, were investigated in the Hauraki Gulf, north-eastern New Zealand, between 1982 and 1990. Attention focused on age and growth, temporal and spatial variation in abundance, and recruitment. Daily increment formation was validated in the sagittae of snapper up to about 160 days old. Increment width varied with time of year, and snapper age, and increments were not resolvable with a light microscope during winter. Increment counts inside a prominent metamorphic mark showed that larval duration was 18-32 days, and was inversely related to water temperature. Spawning dates were back-calculated from increment counts in settled juveniles, and ranged from September to March with a peak in November-January. The onset of spawning was temperature dependent. Fast-growing snapper had smaller sagittae than slow-growing snapper, indicating an uncoupling of otolith and somatic growth. Snapper gonads differentiated first as ovaries during the second year of life, and then some juveniles changed sex to become males during their third year. Sex change occurred before maturity, so snapper are functionally gonochoristic. Growth was slow during the larval phase, but increased rapidly after metamorphosis to about 0.6-0.9 mm.day-1. From the first winter, growth followed a well-defined annual cycle, with little or no growth during winter, and linear growth of 0.16-0.43 mm.day-1 during spring-autumn for 0+/1+ and 1+/2+ snapper. Snapper grew faster at higher temperatures. Trawl catch rates were affected by numerous gear and environmental factors, but probably provided reasonable estimates of snapper relative abundance. Recommendations are made for improving snapper trawl survey procedures. There was a strong annual abundance cycle in the Kawau region, peaking in spring, and declining to a minimum in winter. Snapper were patchily distributed at a spatial scale of 1-2 km, probably because of preference for specific micro-habitats. Year class strength of 1+ snapper varied 17-fold over seven years, and was strongly positively correlated with autumn sea surface temperature during the 0+ year. The strengths of the 1991 and 1992 year classes are predicted to be below average, and extremely weak, respectively.
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Wong, Clara. "The effects of green shelled mussel mariculture on benthic communities in Hauraki Gulf." Click here to access this resource online, 2009. http://hdl.handle.net/10292/663.

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Sea-bed benthic-invertebrate assemblages of species within and proximal to an existing mussel farm off Taniwhanui Point, eastern Waiheke Island, are reported. Substratum type, whether predominantly mud, gravels or an admixture of the two, mud/gravels, is shown to influence infaunal species assemblage composition; the bivalve Theora lubrica, ostracods, amphipods and polychaetes characterise muddy substrata; polychaetes, particularly spionids and syllids, ostracods, amphipods, bivalves and ophiuroids characterise mud/gravel substrata; and diverse assemblages of polychaetes, bivalves, pagurid crabs, gastropods, ostracods, ophiuroids and nemertean worms characterise gravel substrata. Significant differences in sea-bed assemblages are reported along one transect inside and outside the farm over the three seasons during which surveys were conducted, summer, autumn, winter of 2008. Along the northern side of the mussel farm those sediments beneath the farm are characterised by greater abundances of polychaetes and crustaceans (Malacostraca), whereas sediments outside the farm are characterised by greater abundances of bivalves and ostracods. Sediments both inside and outside the north-eastern border of the farm during summer are characterised by similar abundances of polychaetes, bivalves and ostracods. Similarly, those sediments within and outside the farm along its southern border during summer are characterised by abundances of polychaetes, bivalves, crustaceans (Malacostraca) and gastropods. Measures of relative abundance, rarity and species richness are applied to sea-bed assemblages off eastern Waiheke Island to enable an appraisal of the spatial distribution of each within and outside the farm, and throughout the eastern Waiheke Island region. One of these measures, relative abundance, is then compared with other, albeit limited abundance data from previous soft-sediment surveys conducted throughout Hauraki Gulf. The most species rich and abundant sites off eastern Waiheke Island occur in gravelly substrata between Waiheke Island and Pakatoa Island, and between Rotoroa and Ponui Islands, in addition to beneath the southern portion of the existing mussel farm. Gravel-based substrata are recognised to be the most species rich and densely populated with invertebrates for this sediment type in Hauraki Gulf. Similarly, the muddy substrata off eastern Waiheke Island region appear to host more individuals and species than any other reported muddy substratum in Hauraki Gulf. The existing mussel farm is shown to significantly affect sea-bed communities, but in a manner that has not been previously reported in New Zealand. Species richness and abundance are greater beneath the farm, as are the proportions of very rare and uncommon taxa to more common and ubiquitous taxa. Sediments beneath the farm are not characterised by elevated abundances and richness of opportunistic species; and no obvious difference in sediment grain size is apparent along a transect extending from 20 m inside the farm to at least 110 m outside it. The biological footprint of the farm is limited, appearing to extend no further than 20 metres from the northern physical boundary of the farm; the gross sedimentary characteristics (grain size) do not differ significantly within and outside the farm. Within and immediately outside the farm species richness and abundance tend to increase during colder seasons; beneath the farm, species richness (d), abundance (N), Shannon index (H’) and Simpson index (1-λ’) were higher during May (autumn) and August (winter) than during February (summer); diversity values outside the farm were similar during summer and autumn, but species richness (d), evenness (J’), Shannon index (H’) and Simpson index (1-λ’) were all greater during winter. No opportunistic taxa are considered to be appropriate indicators of organically enriched environments, at least enrichment that can be intuitively linked to any direct effect of the existing mussel farm. One species, the heart urchin Echinocardium cordatum, only rarely occurs inside the physical farm boundary, so its relative abundance renders it an appropriate indicator species of mussel-farm impacts.
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Wiseman, Nicky. "Genetic identity and ecology of Bryde's whales in the Hauraki Gulf, New Zealand." Thesis, University of Auckland, 2008. http://hdl.handle.net/2292/2612.

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Little long-term research has been conducted in the Hauraki Gulf on Bryde’s whales; the least studied baleen whale. This thesis investigates this population using photoidentification and sighting records obtained from boat-based opportunistic surveys and genetic analyses of samples from living and `stranded’ whales. Samples from `stranded’ Bryde’s whales have been collected since 1994 from the North Island of New Zealand. In addition, biopsy samples were collected from whales in the Hauraki Gulf. Fifty-two samples from `stranded’ and biopsied Bryde’s whales identified 49 unique individuals using 12 polymorphic microsatellites. The sex ratio for both sample collection types were equal with 22 males : 23 females (the sex of four could not be determined). MtDNA D-loop analysis (~800 bp) identified the samples as being consistent with Balaenoptera brydei with 11 haplotypes defined by 16 variable sites. Comparisons with published sequences (373 bp) revealed three shared haplotypes between the North Pacific and Indian Oceans. However, an AMOVA (FST and ΦST) showed high levels of differentiation between these oceans, likely resulting from ancestral gene flow. Between March 2001 and February 2006, 1,102 boat-based surveys were conducted during which there were 1,059 sightings over 521 days of Bryde’s whales (including two birth-length calves) in the Gulf. Since whales with calves, were observed during all months this suggests that the Hauraki Gulf is an important area for breeding whales. The seasonal change in `trip encounter rate’ indicated that some whales leave the Gulf for part of the year. Whales in the Gulf were observed in shallower (12.1 to 59.8 m) and cooler (12 to 24.5oC) water than has generally been reported elsewhere. Balaenoptera brydei corresponds to the form described in the offshore waters of the western North Pacific. In contrast, their habitat use in the Hauraki Gulf was more consistent with the `inshore’ form from the coasts off South Africa.
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Boxberg, Florian [Verfasser], Dierk [Akademischer Betreuer] Hebbeln, Dierk [Gutachter] Hebbeln, and Anne [Gutachter] Bernhardt. "Anthropogenic input of heavy metals to near-coastal sediment depocenters in the eastern North Sea and the Hauraki Gulf in historical times / Florian Boxberg ; Gutachter: Dierk Hebbeln, Anne Bernhardt ; Betreuer: Dierk Hebbeln." Bremen : Staats- und Universitätsbibliothek Bremen, 2018. http://d-nb.info/1153540932/34.

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Dewas, Severine E. A. "Benthic-invertebrate diversity of Tucetona laticostata (Mollusca: Bivalvia) biogenic substrata in Hauraki Gulf a thesis submitted through the Earth & Oceanic Sciences Research Institute, Auckland University of Technology, in partial fulfilment of the requirements for the degree of Master of Applied Science (MAppSc), 2008 /." Click here to access this resource online, 2008. http://hdl.handle.net/10292/454.

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Denny, Kirsty Marie. "The diet of moreporks (Ninox novaeseelandiae) in relation to prey availability, and their roost site characteristics and breeding success on Ponui Island, Hauraki Gulf, New Zealand : a thesis presented in fulfilment of the requirements for the degree of Master of Science in Ecology at Massey University, Albany, New Zealand." Massey University, 2009. http://hdl.handle.net/10179/1213.

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The ecological importance of introduced mammalian predators is well acknowledged in New Zealand, however, little research has focused on the ecology of native avian predators and their role in communities. This study investigated the ecology of moreporks (Ninox novaeseelandiae) on Ponui Island, Hauraki Gulf, New Zealand between August 2007 and April 2008. The primary aim was to investigate the functional response of moreporks to availability of their prey. The contents of regurgitated morepork pellets were compared with relative abundance of prey taxa (invertebrates, small birds and rodents) over the study period. The diet consisted primarily of a range of invertebrate prey, particularly weta (Anostostomatidae and Raphidophoridae) and beetles (Coleoptera). Small numbers of vertebrate prey were recorded including rodents and birds. A positive relationship between the percentage contribution to pellet samples of certain taxa and their relative availability was found, and there were peaks in the occurrence of seasonally abundant taxa including cicadas (Cicadidae), and huhu beetles (Prionoplus reticularis). The tendency of moreporks to prey on abundant taxa indicates that they are unlikely to depress prey populations to low levels, and may have some degree of stabilising influence. A significant increase in the rodent component of the diet in April indicated that the risk to moreporks of secondary poisoning during mammalian pest control operations may vary considerably with the time of year. The secondary aims were to collect data on roost site characteristics and breeding success. Moreporks roosted at a mean height of 4m, and foliar cover at the 4-6m height tier appeared to be the most important characteristic of roost sites when compared with control sites. These findings suggested that moreporks were selecting roost sites with high overhead cover. Possible reasons for this include predator avoidance, avoidance of mobbing passerines, and the microclimate provided. None of three established pairs and two other birds were observed to establish a nest or breed successfully. Additionally, only three juvenile moreporks were sighted or heard across the 90ha study area suggesting low breeding success in 2007-08. This may have been influenced by a range of factors including 1), predation by the high densities of ship rats on Ponui, or other predators 2), a lack of suitable nest sites such as tree hollows in some areas or 3), competition for invertebrate prey with high densities of ship rats and North Island brown kiwi (Apteryx mantelli).
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Cavendish, Tabbatha A. "Amino Acid Analysis of Marine Sediments, Hauraki Gulf, New Zealand." 2008. http://trace.tennessee.edu/utk_gradthes/342.

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Amino acid compositions, bulk organic carbon, total nitrogen, and total organic matter were measured for eight sediment samples from the Hauraki Gulf, New Zealand, in order to assess the source and fate of organic matter in a shallow marine environment. Samples were collected from near-shore and off-shore shore sites, as well as from a site receiving freshwater input from multiple rivers. A comparison of carbon, nitrogen, and amino acid compositions of samples between 1 cm depth (Uhle 2004) and 5 cm depth was used to assess changes in organic matter composition through time. Amino acid analyses in particular should be effective in deciphering organic decomposition through both the presence and abundance of amino acids. C:N values, which range from 6.5-9.3, are typical for marine sediments and indicate that the primary source for organic matter is marine despite potential terrigenous input from the surrounding environment. This interpretation is supported by carbon isotopes (-20‰ and -22‰ for most sites) which is typical for marine-derived organic materials. C:N ratios do not appreciably vary from 1-5 cm depth, suggesting that there has not been significant depletion of organic matter in these young deposits. Furthermore, both D- and L-amino acids are present at 5 cm depth, supporting minimal organic matter decomposition. However, concentrations of amino acid decreases with depth, and the presence of D-alanine, D-aspartic acid, D-glutamic acid, glycine, and non-protein amino acids, at 5 cm depth, suggests at least a small contribution to the organic carbon source from bacteria. A decrease in δ15N with depth further suggests the possibility of bacterial reworking under anoxic conditions. Combined, these results support hypotheses of microbial reworking of organic matter through time, but are not clearly diagnostic of this process.
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Peters, Murray Hamaka. "The confiscation of Pare Hauraki the impact of Te Ao Pākeha on the iwi of Pare Hauraki Māori, on the whenua of Pare Hauraki, 1835-1997, and the Foreshore and Seabed Act 2004 = Te raupatutanga o Pare Hauraki." 2007. http://adt.waikato.ac.nz./public/adt-uow20070321.101430.

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Dewas, Severine Emmanuelle Alexandra. "Benthic-invertebrate diversity of Tucetona laticostata (Mollusca: Bivalvia) biogenic substrata in Hauraki Gulf." 2008. http://hdl.handle.net/10292/454.

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Marine ecosystems are increasingly being subject to human impact from diverse recreational and commercial activities, not necessarily restricted to those of a marine nature. This has significant implications for biodiversity. The large dog cockle, Tucetona laticostata, once occurred live in Rangitoto Channel, Hauraki Gulf, although this species no longer appears to occur there, most likely as a consequence of repeated dredging and channel excavation and continued siltation. Tucetona laticostata still occurs in a few isolated pockets of sea bed throughout Hauraki Gulf, particularly off Otata Island, part of the Noises complex of islands, where it resides partially buried in shell and rock gravels in shallow water (to 15 metres depth). The shells of T. laticostata collect in large post-mortem deposits in an area ramping from the sea bed off southwestern Otata Island. These mounds differ significantly in structural complexity from those of adjacent, extensively fragmented shell and rock gravels. Using the mounds of T. laticostata shell as a proxy for structural complexity, in order to appraise the effect of complexity on benthic-invertebrate diversity, the sea bed off southwestern Otata Island was sampled quarterly at two depths and in both T. laticostata shell mounds and adjacent extensively fragmented shell and rock gravels. These data were complemented with those from additional surveys around Otata Island, and off eastern Motutapu Island to determine the distribution and composition of benthic-invertebrate community assemblages throughout the region, and from concurrent surveys throughout the Waitemata Harbour and inner Hauraki Gulf to determine the current distribution of T. laticostata in this region. The number of benthic invertebrate species and individuals within T. laticostata habitat almost always was higher than that occurring within extensively fragmented shell- and rock gravel habitat, with densities to 142,385 individuals m-2 encountered. Temporal and spatial variations in benthic community structure also are reported for the two habitats, T. laticostata-based shells and extensively fragmented shell- and rock gravels. The numbers of species were higher amongst samples collected off the southwestern and eastern sides of Otata Island than elsewhere around this island, or of eastern Motutapu Island. Of the 351 species reported from all Otata and Motutapu Island samples combined, 73% of them occurred off southwestern Otata Island, 30% of which were found exclusively within T. laticostata shell habitat, and 10.5% within extensively fragmented shell and rock gravel habitat. The sea bed off southwestern Otata Island is regularly, seasonally dredged by recreational scallop fishers, in addition to being a popular small-vessel anchorage site. Both of these activities, dredging and anchorage, stand to reduce substratum complexity by fragmentation and dispersal of the valves of T. laticostata. Given the unique benthic invertebrates reported from T. laticostata shell deposits reported from southwestern Otata Island, any activity that damages the shells of this species, regardless of whether they are live or dead, is likely to result in loss of biodiversity. Admittedly, many of species identified as major contributors to differences in benthic invertebrate assemblages between T. laticostata shell-based habitats and those of extensively fragmented shell and rock gravels are not particularly charismatic or large, but each likely plays a role in local food webs and/or sediment and water column chemistry. It was not the intention of this research to determine the effects of anthropogenic disturbances like dredging or vessel anchorage on benthic-invertebrate communities off southwestern Otata Island. However, given the reported differences in species diversity within the structurally complex substratum provided by T. laticostata, conservation of biogenic reef-forming species like it might be a prudent, precautionary measure to take.
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Books on the topic "Hauraki Gulf"

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Tribunal, New Zealand Waitangi. The Hauraki Gulf Marine Park report. Wellington, N.Z: Legislation Direct, 2001.

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Bercusson, Linda. Exploring the Hauraki Gulf: From Bream Head to the Coromandel. Nelson, N.Z: Craig Potton, 2008.

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Bercusson, Linda. Exploring the Hauraki Gulf: From Bream Head to the Coromandel. Nelson, N.Z: Craig Potton, 2008.

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Baker, A. N. Bryde's whales (Balaenoptera cf. brydei Olsen 1913) in the Hauraki Gulf and northeastern New Zealand waters. Wellington, N.Z: Science & Technical Pub., Dept. of Conservation, 2007.

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1940-, Wilcox Michael David, and Auckland Botanical Society, eds. Natural history of Rangitoto Island, Hauraki Gulf, Auckland, New Zealand. Auckland, N.Z: Auckland Botanical Society, 2007.

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Conference papers on the topic "Hauraki Gulf"

1

Corney, Paul, Colin Christian, Ross Vennell, and Alastair Barnett. "America's Cup 2000 — 3D Tidal Model of the Hauraki Gulf." In 27th International Conference on Coastal Engineering (ICCE). Reston, VA: American Society of Civil Engineers, 2001. http://dx.doi.org/10.1061/40549(276)293.

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Bell, Robert G., John W. Oldman, and Scott A. Stephens. "Recent Applications of 3D Wind-Driven Circulation Modeling to a Semi-Enclosed Sea: Hauraki Gulf, New Zealand." In Eighth International Conference on Estuarine and Coastal Modeling. Reston, VA: American Society of Civil Engineers, 2004. http://dx.doi.org/10.1061/40734(145)19.

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