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1

Sommer, Bea. "Australian Saltmarsh Ecology." Pacific Conservation Biology 16, no. 1 (2010): 71. http://dx.doi.org/10.1071/pc100071.

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Australia, including its territorial islands, is surrounded by almost 60 000 km of coastline (Geoscience Australia, http://www.ga.gov.au/education/) and, according to Saintilan, coastal saltmarshes occupy some 16 000 km2. Saltmarshes provide valuable ecosystem services and are generally recognized as among the most productive ecosystems on Earth. This is considered to be ecologically important because excess detrital matter exported to marine waters sustains food webs, including important fisheries (i.e., Odum?s [1980] ?outwelling hypothesis?). Although physically and biologically similar to s
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2

Prahalad, Vishnu, Jamie B. Kirkpatrick, John Aalders, Scott Carver, Joanna Ellison, Violet Harrison-Day, Peter McQuillan, Brigid Morrison, Alastair Richardson, and Eric Woehler. "Conservation ecology of Tasmanian coastal saltmarshes, south-east Australia – a review." Pacific Conservation Biology 26, no. 2 (2020): 105. http://dx.doi.org/10.1071/pc19016.

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Temperate Australian saltmarshes, including those in the southern island state of Tasmania, are considered to be a threatened ecological community under Australian federal legislation. There is a need to improve our understanding of the ecological components, functional relationships and threatening processes of Tasmanian coastal saltmarshes and distil research priorities that could assist recovery actions. A semisystematic review of the literature on Tasmanian coastal saltmarshes supported by expert local knowledge identified 75 studies from 1947 to 2019. Existing understanding pertains to sa
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3

Woodell, S. R. J., and P. Adam. "Saltmarsh Ecology." Journal of Ecology 79, no. 1 (March 1991): 259. http://dx.doi.org/10.2307/2260796.

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4

Long, Steven P., Christopher F. Mason, and B. J. Tomalin. "Saltmarsh Ecology." South African Journal of Zoology 21, no. 4 (January 1986): 355. http://dx.doi.org/10.1080/02541858.1986.11448012.

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5

Wyatt, Tristram, and Paul Adam. "Saltmarsh Ecology." Journal of Animal Ecology 61, no. 3 (October 1992): 797. http://dx.doi.org/10.2307/5632.

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6

Willis, A. J. "Saltmarsh ecology." Trends in Ecology & Evolution 6, no. 6 (June 1991): 200. http://dx.doi.org/10.1016/0169-5347(91)90219-n.

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7

Gray, Alan. "Saltmarsh Ecology." Journal of Experimental Marine Biology and Ecology 182, no. 1 (September 1994): 145–47. http://dx.doi.org/10.1016/0022-0981(94)90219-4.

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8

Hikouei, Iman Salehi, Jason Christian, S. Sonny Kim, Lori A. Sutter, Stephan A. Durham, Jidong J. Yang, and Charles Gray Vickery. "Use of Random Forest Model to Identify the Relationships Among Vegetative Species, Salt Marsh Soil Properties, and Interstitial Water along the Atlantic Coast of Georgia." Infrastructures 6, no. 5 (May 3, 2021): 70. http://dx.doi.org/10.3390/infrastructures6050070.

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Saltmarshes, known to be ecologically sensitive areas, face disturbances such as vegetation dieback due to anthropogenic activities such as construction. The current construction specifications recommended by state highway agencies do not specifically require documenting or restoring any prior saltmarsh soil/interstitial water properties, nor do they require re-establishing saltmarsh vegetation; restoring the abiotic properties and appropriate vegetation would enhance the long-term functionality and ecology of a disturbed area. In order to have a successful restoration of disturbed saltmarshes
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9

Saintilan, Neil, and Kerrylee Rogers. "The significance and vulnerability of Australian saltmarshes: implications for management in a changing climate." Marine and Freshwater Research 64, no. 1 (2013): 66. http://dx.doi.org/10.1071/mf12212.

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We review the distribution, status and ecology of Australian saltmarshes and the mechanisms whereby enhanced atmospheric carbon dioxide and associated climate change have influenced and will influence the provision of ecosystem goods and services. Research in temperate and subtropical saltmarsh has demonstrated important trophic contributions to estuarine fisheries, mediated by the synchronised mass-spawning of crabs, which feed predominantly on the C4 saltmarsh grass Sporobolus virginicus and microphytobenthos. Saltmarshes also provide unique feeding and habitat opportunities for several spec
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10

FAIRWEATHER, PETER G. "Australian Saltmarsh Ecology." Austral Ecology 35, no. 5 (November 23, 2009): 595–96. http://dx.doi.org/10.1111/j.1442-9993.2010.02131.x.

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11

Mazumder, Debashish, Neil Saintilan, and Robert J. Williams. "Trophic relationships between itinerant fish and crab larvae in a temperate Australian saltmarsh." Marine and Freshwater Research 57, no. 2 (2006): 193. http://dx.doi.org/10.1071/mf05040.

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Comparisons of zooplankton inputs and outputs for a temperate Australian saltmarsh demonstrate a substantial contribution of crab larvae to the ebbing tide water, particularly during the cooler months. Few crab larvae were present in the incoming tide (mean abundance 4 m−3), whereas many crab larvae were present in the outgoing water (mean abundance 2124.63 m−3). Stomach content analysis of itinerant fish exiting the saltmarsh with the ebbing tide demonstrated extremely high proportions of crab larvae in the gut of glassfish (Ambassis jacksoniensis), as well as flat tail mullet (Liza argentea)
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12

Prahalad, Vishnu, Violet Harrison-Day, Peter McQuillan, and Colin Creighton. "Expanding fish productivity in Tasmanian saltmarsh wetlands through tidal reconnection and habitat repair." Marine and Freshwater Research 70, no. 1 (2019): 140. http://dx.doi.org/10.1071/mf17154.

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Fish use of coastal saltmarsh wetlands has been documented for many parts of Australia with the notable exception of Tasmania. An initial investigation to examine the diversity, density and patterns of fish use in the Circular Head coast saltmarshes of north-west Tasmania was undertaken. To aid decision making in repair strategies, the effect of saltmarsh condition on fish assemblages was studied using paired sites of predominantly unaltered and altered saltmarshes where levees were present. In all, 851 fish from 11 species were caught in 37 of the 48 pop nets. Three species, Aldrichetta forst
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13

Mann, Kenneth H. "Saltmarsh ecology (P. Adam)." Limnology and Oceanography 39, no. 2 (March 1994): 475–76. http://dx.doi.org/10.4319/lo.1994.39.2.0475a.

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14

Shriver, W. Gregory, Peter D. Vickery, Thomas P. Hodgman, and James P. Gibbs. "Flood Tides Affect Breeding Ecology of Two Sympatric Sharp-Tailed Sparrows." Auk 124, no. 2 (April 1, 2007): 552–60. http://dx.doi.org/10.1093/auk/124.2.552.

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AbstractBreeding synchrony with the lunar cycle has been reported for many marine organisms but is essentially unknown for birds. Most organisms shown to breed synchronously with the lunar cycle provide no parental care to young, and such explosive breeding assemblages are usually promiscuous. Saltmarsh Sharp-tailed Sparrows (Ammodramus caudacutus caudacutus) nest exclusively on salt marshes and are subjected to predictable, catastrophic flooding caused during flood tides every 28 days. Here, we show that Saltmarsh Sharp-tailed Sparrow males were nonterritorial and promiscuous and provided no
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15

Zedler, Joy B. "Saltmarsh Plant Ecology: A Global View?" Ecology 72, no. 6 (December 1991): 2298. http://dx.doi.org/10.2307/1941581.

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16

Finlayson, C. M. "N. Saintilan, (ed.) Australian Saltmarsh Ecology." Wetlands 30, no. 1 (January 12, 2010): 171–72. http://dx.doi.org/10.1007/s13157-009-0012-3.

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17

Lara, Rubén José. "N. Saintilan (ed.): Australian saltmarsh ecology." Wetlands Ecology and Management 18, no. 1 (June 25, 2009): 107–10. http://dx.doi.org/10.1007/s11273-009-9152-8.

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18

Prahalad, Vishnu N., Jamie B. Kirkpatrick, and Richard E. Mount. "Tasmanian coastal saltmarsh community transitions associated with climate change and relative sea level rise 1975 - 2009." Australian Journal of Botany 59, no. 8 (2011): 741. http://dx.doi.org/10.1071/bt11206.

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Coastal saltmarshes are reputed to be one of the most vulnerable communities to global warming, with widespread evidence of retreat and movement of lower marsh vegetation into areas previously occupied by upper marsh vegetation in response to rising sea levels, and potential changes in community composition from changes in rainfall, temperature and wind. We undertook an investigation of decades scale change in the distributions of saltmarsh communities defined by dominant species, using historic vegetation maps, remote sensing imagery and extensive field data collection. Our study area in sout
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19

Platell, Margaret E., and Peter Freewater. "Importance of saltmarsh to fish species of a large south-eastern Australian estuary during a spring tide cycle." Marine and Freshwater Research 60, no. 9 (2009): 936. http://dx.doi.org/10.1071/mf08164.

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The dietary compositions of fish species over saltmarsh in a large south-eastern Australian estuary (Brisbane Water) were explored to ascertain the importance of this habitat type to the fish community of that estuary. Following tidal inundation, 12 fish species (<120 mm total length) were obtained using fyke nets, with Ambassis jacksoniensis being particularly abundant. The stomachs of all fish contained undigested prey, implying that they fed while on the saltmarsh. Three species (A. jacksoniensis, Atherinosoma microstoma and Redigobius macrostoma) fed nearly exclusively on the crab zoeae
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20

Zhao, Z., L. Zhang, L. Yuan, and TJ Bouma. "Saltmarsh seeds in motion: the relative importance of dispersal units and abiotic conditions." Marine Ecology Progress Series 678 (November 11, 2021): 63–79. http://dx.doi.org/10.3354/meps13891.

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Propagule dispersal is fundamental to the colonization of new habitats, metapopulation connectivity, and gene flow and thus enables saltmarsh species to cope with global change. In this study, mesocosm and flume experiments were used to quantify the effects of different dispersal units (i.e. seed, spikelet, inflorescence, and plant fragment-containing seeds) and abiotic conditions on the dispersal processes of 4 globally distributed saltmarsh species: Salicornia europaea, Scirpus maritimus, Spartina anglica, and Elymus athericus. The results showed that (1) moving seawater has a species-specif
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21

SAINTILAN, NEIL. "Biogeography of Australian saltmarsh plants." Austral Ecology 34, no. 8 (December 2009): 929–37. http://dx.doi.org/10.1111/j.1442-9993.2009.02001.x.

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22

Duke, Norman C., Colin Field, Jock R. Mackenzie, Jan-Olaf Meynecke, and Apanie L. Wood. "Rainfall and its possible hysteresis effect on the proportional cover of tropical tidal-wetland mangroves and saltmarsh–saltpans." Marine and Freshwater Research 70, no. 8 (2019): 1047. http://dx.doi.org/10.1071/mf18321.

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Mangrove–saltmarsh tidal wetlands are highly dynamic ecosystems, responding and adapting to climate and physical conditions at all spatial and temporal scales. Knowledge of the large-scale ecosystem processes involved and how they might be influenced by climate variables is highly relevant today. For tidal-wetland sites well within the latitudinal range of the mostly tropical mangrove communities, we confirm that average annual rainfall influences vegetative cover, as well as species composition and biomass of tidal wetlands. On the basis of 205 largely unmodified, tropical and subtropical est
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23

Hughes, R. G. "Saltmarsh erosion and management of saltmarsh restoration; the effects of infaunal invertebrates." Aquatic Conservation: Marine and Freshwater Ecosystems 9, no. 1 (January 1999): 83–95. http://dx.doi.org/10.1002/(sici)1099-0755(199901/02)9:1<83::aid-aqc323>3.0.co;2-9.

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24

Gonsalves, Leroy, Susan Lamb, Cameron Webb, Bradley Law, and Vaughan Monamy. "Do mosquitoes influence bat activity in coastal habitats?" Wildlife Research 40, no. 1 (2013): 10. http://dx.doi.org/10.1071/wr12148.

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Context Conservation of insectivorous bat populations requires appropriate management of foraging habitats and the prey resources they sustain. Endangered coastal saltmarsh communities support a diverse range of aquatic and terrestrial arthropods, including the saltmarsh mosquito (Aedes vigilax Skuse), an important vector of mosquito-borne viruses and a potentially important prey resource for insectivorous bats. Prey detectability by bats is considered to be limited with low-frequency echolocation, particularly in cluttered habitats, that may render abundant Ae. vigilax populations unavailable
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25

Zhang, Jing, Yan Zhang, Huw Lloyd, Zhengwang Zhang, and Donglai Li. "Rapid Reclamation and Degradation of Suaeda salsa Saltmarsh along Coastal China’s Northern Yellow Sea." Land 10, no. 8 (August 9, 2021): 835. http://dx.doi.org/10.3390/land10080835.

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Suaeda salsa saltmarshes are an important coastal wetland habitat of China’s northern Yellow Sea, which plays a critical role in sequestering carbon (blue carbon), protecting shorelines, maintaining biodiversity, and has substantial economic value (e.g., ecotourism). However, the area of S. salsa has been rapidly declining due to several different threats from reclamation and invasive species that impact its natural succession. Here, we map the changes in the distribution of the S. salsa saltmarshes along the northern Yellow Sea of China (NYSC) at 5-year intervals by applying the supervised ma
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26

Cain, S., and PI Boon. "Cellular osmotica of plants in relation to sediment nitrogen and salt content in mangroves and saltmarshes at Western Port, Victoria." Marine and Freshwater Research 38, no. 6 (1987): 783. http://dx.doi.org/10.1071/mf9870783.

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Sediments from mangrove and saltmarsh areas at Yaringa, Western Port contained high concentrations of chloride (c. 330-2100 mmol per litre of interstitial water) and sodium (c. 320-1900 mmol 1-1). The concentrations recorded during the study were highest in March and lowest in July-August; salinity in the marsh during summer was considerably higher than that commonly reported for saltmarshes in other parts of the world. Sediment ammonium contents (c. 180-580 nmol per cm3 of fresh sediment) were variable across the marsh and throughout the sampling period, with there being little overall patter
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27

Saintilan, Neil, and Debashish Mazumder. "Fine-scale variability in the dietary sources of grazing invertebrates in a temperate Australian saltmarsh." Marine and Freshwater Research 61, no. 5 (2010): 615. http://dx.doi.org/10.1071/mf09187.

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Saltmarsh floristic diversity declines with increasing latitude on the Australian east coast, with the dominant tropical C4 grass Sporobolus virginicus being replaced progressively by a suite of mostly succulent C3 species. The temperate Towra Point saltmarsh consists of a mosaic of vegetation communities, including stands of the C4 saltmarsh grass Sporobolus virginicus, and the C3 succulents Suaeda australis and Sarcocornia quinqueflora. The contrasting stable isotope signatures of these plants provide an opportunity to determine the extent to which plant material is contributing to the diet
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28

Laegdsgaard, Pia. "Ecology, disturbance and restoration of coastal saltmarsh in Australia: a review." Wetlands Ecology and Management 14, no. 5 (October 2006): 379–99. http://dx.doi.org/10.1007/s11273-005-8827-z.

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29

Moyo, Sydney, Hayat Bennadji, Danielle Laguaite, Anna A. Pérez-Umphrey, Allison M. Snider, Andrea Bonisoli-Alquati, Jill A. Olin, et al. "Stable isotope analyses identify trophic niche partitioning between sympatric terrestrial vertebrates in coastal saltmarshes with differing oiling histories." PeerJ 9 (July 16, 2021): e11392. http://dx.doi.org/10.7717/peerj.11392.

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Bioindicator species are commonly used as proxies to help identify the ecological effects of oil spills and other stressors. However, the utility of taxa as bioindicators is dependent on understanding their trophic niche and life history characteristics, as these factors mediate their ecological responses. Seaside sparrows (Ammospiza maritima) and marsh rice rats (Oryzomys palustris) are two ubiquitous terrestrial vertebrates that are thought to be bioindicators of oil spills in saltmarsh ecosystems. To improve the utility of these omnivorous taxa as bioindicators, we used carbon and nitrogen
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30

Katrak, G., S. Dittmann, and L. Seuront. "Spatial variation in burrow morphology of the mud shore crab Helograpsus haswellianus (Brachyura, Grapsidae) in South Australian saltmarshes." Marine and Freshwater Research 59, no. 10 (2008): 902. http://dx.doi.org/10.1071/mf08044.

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Burrowing by crabs is an important component of their functional role in mangrove and saltmarsh habitats. The grapsid crab Helograpsus haswellianus (Whitelegge, 1889) is one of the more conspicuous burrowing organisms in the saltmarshes of southern Australia. To evaluate intraspecific differences in burrowing behaviour among saltmarshes on a regional scale, we compared vegetation cover, sediment composition and burrow morphology at four sites using resin casts. Six burrow morphology characters were measured (burrow depth, number, lengths and diameter of the shafts, ratio of the shafts, number
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31

Walker, Julie E., Christine Angelini, Ilgar Safak, Andrew H. Altieri, and Todd Z. Osborne. "Effects of Changing Vegetation Composition on Community Structure, Ecosystem Functioning, and Predator–Prey Interactions at the Saltmarsh-Mangrove Ecotone." Diversity 11, no. 11 (November 1, 2019): 208. http://dx.doi.org/10.3390/d11110208.

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Decreasing frequency of freeze events due to climate change is enabling the poleward range expansion of mangroves. As these tropical trees expand poleward, they are replacing herbaceous saltmarsh vegetation. Mangroves and saltmarsh vegetation are ecosystem engineers that are typically viewed as having similar ecosystem functions. However, few studies have investigated whether predation regimes, community structure, and ecosystem functions are shifting at the saltmarsh-mangrove ecotone. In this study, we manipulated predator access to marsh and mangrove creekside habitats to test their role in
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32

Wilson, J. Bastow, and Robert J. Whittaker. "Assembly Rules Demonstrated in a Saltmarsh Community." Journal of Ecology 83, no. 5 (October 1995): 801. http://dx.doi.org/10.2307/2261417.

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33

Tyrrell, Megan C., Michele Dionne, and Jessica A. Edgerly. "Physical factors mediate effects of grazing by a non-indigenous snail species on saltmarsh cordgrass (Spartina alterniflora) in New England marshes." ICES Journal of Marine Science 65, no. 5 (February 27, 2008): 746–52. http://dx.doi.org/10.1093/icesjms/fsn009.

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Abstract Tyrrell, M. C., Dionne, M., and Edgerly, J. A. 2008. Physical factors mediate effects of grazing by a non-indigenous snail species on saltmarsh cordgrass (Spartina alterniflora) in New England marshes. – ICES Journal of Marine Science, 65: 746–752. In the southeastern US, grazing by a common indigenous littorinid snail has caused large declines in the biomass of saltmarsh cordgrass (Spartina alterniflora). In northeastern marshes, a closely related but non-indigenous snail may also negatively affect production of this key marsh-building plant. We manipulated densities of the gastropod
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34

Gjerdrum, Carina, Chris S. Elphick, and Margaret Rubega. "Nest Site Selection and Nesting Success in Saltmarsh Breeding Sparrows: The Importance of Nest Habitat, Timing, and Study Site Differences." Condor 107, no. 4 (November 1, 2005): 849–62. http://dx.doi.org/10.1093/condor/107.4.849.

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Abstract We examined nest-site selection and nesting success in Saltmarsh Sharp-tailed (Ammodramus caudacutus) and Seaside Sparrows (A. maritimus), at seven sites in Connecticut. We found 160 Saltmarsh Sharp-tailed Sparrow nests and 23 Seaside Sparrow nests, and compared characteristics of their locations to each other and to random locations. We tracked success of all nests, quantified nest productivity and causes of nest losses, and tested for habitat differences between successful and unsuccessful nests. Saltmarsh Sharp-tailed Sparrows nested in higher than average locations, where the vege
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35

O'Callaghan, M. "The saltmarsh vegetation of Langebaan Lagoon." Bothalia 24, no. 2 (October 10, 1994): 217–22. http://dx.doi.org/10.4102/abc.v24i2.774.

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The saltmarshes of Langebaan Lagxn arc the most extensive in southern Africa. These marshes, as sampled along six transects, are described. A general marsh, consisting o f three species assemblages, was recognized and elevation above mean sea level (MSL) is discussed as a probable determinant of species distributions. However, minor variations in species distributions have been induced by changes in soil characteristics, the effects of wind on inundation depth and differences in water salinity.
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36

Tinsley, Matthew C., and Stephen D. Reilly. "Reproductive ecology of the saltmarsh-dwelling marine ectoparasite Paragnathia formica (Crustacea: Isopoda)." Journal of the Marine Biological Association of the United Kingdom 82, no. 1 (February 2002): 79–84. http://dx.doi.org/10.1017/s0025315402005192.

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Adults of the isopod Paragnathia formica inhabit burrows in saltmarsh banks from which they release larvae during autumn high tides. Larvae pass through three moult stages, each of which feeds ectoparasitically on estuarine fish (including Pomatoschistus microps), before a final moult to a non-feeding adult stage. The entire energetic reserves for survival and reproduction up to nine months (females) or 16 months (males) later are therefore acquired during these three brief periods of parasitism. Application of a plankton sampling technique showed larval density in the water to vary considerab
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37

Rowbottom, R., S. Carver, L. A. Barmuta, P. Weinstein, and G. R. Allen. "How do local differences in saltmarsh ecology influence disease vector mosquito populations?" Medical and Veterinary Entomology 34, no. 3 (February 20, 2020): 279–90. http://dx.doi.org/10.1111/mve.12433.

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38

Shriver, W. Gregory, James P. Gibbs, Peter D. Vickery, H. Lisle Gibbs, Thomas P. Hodgman, Peter T. Jones, and Christopher N. Jacques. "Concordance Between Morphological and Molecular Markers in Assessing Hybridization Between Sharp-Tailed Sparrows in New England." Auk 122, no. 1 (January 1, 2005): 94–107. http://dx.doi.org/10.1093/auk/122.1.94.

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Abstract Hybridization is pivotal in framing ideas about species concepts and has the potential to produce novel genotypes that may serve as starting points for new evolutionary trajectories. Presently, Nelson’s Sharp-tailed Sparrows (Ammodramus nelsoni subvirgatus) and Saltmarsh Sharp-tailed Sparrows (A. caudacutus caudacutus) are in contact in salt marshes of Maine, New Hampshire, and northern Massachusetts. These two species hybridize, but the extent and direction of introgression has not been determined. We assessed morphological and genetic variation of 123 sharp-tailed sparrows from 5 sa
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39

Maynard, Clare, John McManus, Robert M. M. Crawford, and David Paterson. "A comparison of short-term sediment deposition between natural and transplanted saltmarsh after saltmarsh restoration in the Eden Estuary (Scotland)." Plant Ecology & Diversity 4, no. 1 (March 2011): 103–13. http://dx.doi.org/10.1080/17550874.2011.560198.

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40

DiQuinzio, Deborah A., Peter W. C. Paton, William R. Eddleman, and J. Brawn. "Site Fidelity, Philopatry, and Survival of Promiscuous Saltmarsh Sharp-Tailed Sparrows in Rhode Island." Auk 118, no. 4 (October 1, 2001): 888–99. http://dx.doi.org/10.1093/auk/118.4.888.

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Abstract We investigated site fidelity and apparent survival in a promiscuous population of Saltmarsh Sharp-tailed Sparrows (Ammodramus caudacutus) in southern Rhode Island. Based on capture–recapture histories of 446 color-banded sparrows studied from 1993 to 1998 at our primary study site, Galilee, we observed significant variation in apparent survival rates among years, but not between sexes. Return rates of adult males (37.6%) and females (35.6%) were not significantly different during any year. Juveniles exhibited high return rates, ranging from 0 to 44%, with males (61% of returns) more
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41

DiQuinzio, Deborah A., Peter W. C. Paton, and William R. Eddleman. "Nesting ecology of Saltmarsh Sharp-tailed Sparrows in a tidally restricted salt marsh." Wetlands 22, no. 1 (March 2002): 179–85. http://dx.doi.org/10.1672/0277-5212(2002)022[0179:neosst]2.0.co;2.

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42

Hollingsworth, Anna, and Rod M. Connolly. "Feeding by fish visiting inundated subtropical saltmarsh." Journal of Experimental Marine Biology and Ecology 336, no. 1 (August 2006): 88–98. http://dx.doi.org/10.1016/j.jembe.2006.04.008.

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43

Brownstein, Gretchen, J. Bastow Wilson, and David J. Burritt. "Waterlogging tolerance on a New Zealand saltmarsh." Journal of Experimental Marine Biology and Ecology 446 (August 2013): 202–8. http://dx.doi.org/10.1016/j.jembe.2013.05.025.

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44

Stevens, PW, CL Montague, and KJ Sulak. "Fate of fish production in a seasonally flooded saltmarsh." Marine Ecology Progress Series 327 (December 7, 2006): 267–77. http://dx.doi.org/10.3354/meps327267.

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45

Pagès, Jordi F., Stuart R. Jenkins, Tjeerd J. Bouma, Elwyn Sharps, and Martin W. Skov. "Opposing Indirect Effects of Domestic Herbivores on Saltmarsh Erosion." Ecosystems 22, no. 5 (November 30, 2018): 1055–68. http://dx.doi.org/10.1007/s10021-018-0322-5.

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46

Domínguez-Valenzuela, José Alfredo, Ricardo Alcántara-de la Cruz, Candelario Palma-Bautista, José Guadalupe Vázquez-García, Hugo E. Cruz-Hipolito, and Rafael De Prado. "Non-Target Site Mechanisms Endow Resistance to Glyphosate in Saltmarsh Aster (Aster squamatus)." Plants 10, no. 9 (September 21, 2021): 1970. http://dx.doi.org/10.3390/plants10091970.

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Of the six-glyphosate resistant weed species reported in Mexico, five were found in citrus groves. Here, the glyphosate susceptibility level and resistance mechanisms were evaluated in saltmarsh aster (Aster squamatus), a weed that also occurs in Mexican citrus groves. The R population accumulated 4.5-fold less shikimic acid than S population. S plants hardly survived at 125 g ae ha−1 while most of the R plants that were treated with 1000 g ae ha−1, which suffered a strong growth arrest, showed a vigorous regrowth from the third week after treatment. Further, 5-enolpyruvylshikimate-3-phosphate
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47

Russell, TL, BH Kay, and GA Skilleter. "Environmental effects of mosquito insecticides on saltmarsh invertebrate fauna." Aquatic Biology 6 (June 2, 2009): 77–90. http://dx.doi.org/10.3354/ab00156.

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48

Foster, N. R., B. M. Gillanders, A. R. Jones, J. M. Young, and M. Waycott. "A muddy time capsule: using sediment environmental DNA for the long-term monitoring of coastal vegetated ecosystems." Marine and Freshwater Research 71, no. 8 (2020): 869. http://dx.doi.org/10.1071/mf19175.

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Seagrass, saltmarsh and mangrove habitats are declining around the world as anthropogenic activity and climate change intensify. To be able to effectively restore and maintain healthy coastal-vegetation communities, we must understand how and why they have changed in the past. Identifying shifts in vegetation communities, and the environmental or human drivers of these, can inform successful management and restoration strategies. Unfortunately, long-term data (i.e. decades to hundreds of years) on coastal vegetated ecosystems that can discern community-level changes are mostly non-existent in
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49

Baily, Brian, and Robert Inkpen. "Assessing historical saltmarsh change; an investigation into the reliability of historical saltmarsh mapping using contemporaneous aerial photography and cartographic data." Journal of Coastal Conservation 17, no. 3 (May 1, 2013): 503–14. http://dx.doi.org/10.1007/s11852-013-0250-7.

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50

Saintilan, Neil, and Robert J. Williams. "Mangrove transgression into saltmarsh environments in south-east Australia." Global Ecology and Biogeography 8, no. 2 (March 1999): 117–24. http://dx.doi.org/10.1046/j.1365-2699.1999.00133.x.

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