Analysis of the relationships between Spartina maritima and nutrient enrichment in North Adriatic salt marshes

Salt marshes are coastal ecosystem in the upper intertidal zone between internal water and sea and are widely spread throughout Italy, from Friuli Venezia Giulia, in the North, to Sicily, in the South. These delicate environments are threatened by eutrophication, habitat conversion (for land reclaiming or agriculture) and climate change impacts such as sea level rise. The objectives of my thesis were to: 1) analyse the distribution and biomass of the perennial native cordgrass Spartina maritima (one of the most relevant foundation species in the low intertidal saltmarsh vegetation in the study region) at 7 sites along the Northern Adriatic coast and relate it to critical environmental parameters and 2) to carry out a nutrient manipulation experiment to detect nutrient enrichment effects on S. maritima biomass and vegetation characteristics. The survey showed significant differences among sites in biological response variables - i.e., live belowground, live aboveground biomass, above:belowground (R:S) biomass ratio, % cover, average height and stem density – which were mainly related to differences in nitrate, nitrite and phosphate contents in surface water. Preliminary results from the experiment (which is still ongoing) showed so far no significant effects of nutrient enrichment on live aboveground and belowground biomass, R:S ratio, leaf %Carbon, average height, stem density and random shoot height; however, a significantly higher (P=0.018) increase in leaf %Nitrogen content in treated plots indicated that nutrient uptake had occurred.

Comparing Zostera and Spartina environments in relation to carbon burial: a sedimentary and geochemical approach from Ria Formosa

Dissertação de mestrado, Biologia Marinha, Faculdade de Ciências e Tecnologia, Universidade do Algarve, 2015

Influência da superfície sedimentar na dinâmica das macroalgas verdes e da sua macroepifauna associada na Ria Formosa

O sistema lagunar, conhecido vulgarmente por Ria Formosa, desenvolve-se na costa meridional Portuguesa, desde o Ancão a ocidente até Cacela a oriente. Com extensão, de aproximadamente 55 km, apresenta a sua maior largura, de 6 km, no sector Norte-Sul entre Faro e o Cabo de Santa Maria. Este sistema é um conjunto de ilhas-barreira que proteje a zona lagunar adjacente à plataforma litoral algarvia, da invasão marinha. A área total do Parque Natural da Ria Formosa é aproximadamente de 163 km2, sendo 48 km2 cobertos por sapal e 32 km2 ocupados por canais, esteiros e baixios (Teixeira & Alvim, 1978). Durante as marés vivas, as áreas intertidais expostas são de aproximadamente 50 km2. Estas áreas são predominantemente cobertas por plantas de sapal (Spartina maritima), angiospérmicas marinhas (Zostera e Cymodocea) e mantos de macroalgas (Entermorpha, Ulva e Fucus). 20 km2 do sistema são ocupados por salinas e aquaculturas (CCRA, 1984).

Contributo da geoquímica e da sedimentologia na caracterização de influências antropogénicas em ambientes estuarinos

Tese de doutoramento, Geologia (Geoquímica), Universidade de Lisboa, Faculdade de Ciências, 2016

Microbial community composition and mercury cycling in sediments of tagus estuary

Tese de doutoramento, Farmácia (Toxicologia), Universidade de Lisboa, Faculdade de Farmácia, 2016

Potencial de plantas estuarinas na remediação de produtos farmacêuticos e de cuidado pessoal

Dissertação para obtenção do Grau de Mestre em Engenharia do Ambiente, Perfil de Engenharia de Sistemas Ambientais

Effects of flooding on coastal vegetation and salt marshes

This thesis examines the effects of flooding on coastal and salt marsh vegetation. I conducted a field experiment in Bellocchio Lagoon to test the effects of different inundation periods (Level 1 = 0.468 or 11.23 hours; Level 2 = 0.351 or 8.42 hours; Level 3 = 0.263 or 6.312 hours; Level 4 = 0.155 or 3.72 hours; Level 5 = 0.082 or 1.963 hours; Level 6 = 0.04 or 0.96 hours) on the growth responses and survival of the salt marsh grass Spartina maritima in summer 2011 and 2012. S. maritima grew better at intermediate inundation times (0,351 hours; 0,263 hours, 0,115 hours; 0,082 hours), while growth and survival were reduced at greater inundation periods (0,468 hours). The differences between the 2011 and 2012 experiment were mainly related to differences in the initial number of shoots (1 and 5, respectively in 2011 and 2012). In the 2011 experiment a significant lower number of plants was present in the levels 1 and 6, the rhizomes reached the max pick in level 4, weights was major in level 4, spike length reached the pick in level 3 while leaf length in level 2. In the 2012 experiment the plants in level 6 all died, the rhizomes were more present in level 3, weights was major in level 3, spike length reached the pick in level 3, as well as leaf length. I also conducted a laboratory experiment which was designed to test the effects of 5 different inundation periods (0 control, 8, 24, 48, 96 hours) on the survival of three coastal vegetation species Agrostis stolonifera, Trifolium repens and Hippopae rhamnoides in summer 2012. The same laboratory experiment was repeated in the Netherlands. In Italy, H. rhamnoides showed a great survival in the controls, a variable performance in the other treatments and a clear decrease in treatment 4. Conversely T. repens and A. stolonifera only survive in the control. In the Netherlands experiment there was a greater variability responses for each species, still at the end of the experiment survival was significantly smaller in treatment 4 (96 h of seawater inundation) for all the three species. The results suggest that increased flooding can affect negatively the survival of both saltmarsh and coastal plants, limiting root system extension and leaf growth. Flooding effect could lead to further decline and fragmentation of the saltmarshes and coastal vegetation, thereby reducing recovery (and thus resilience) of these systems once disturbed. These effects could be amplified by interactions with other co-occurring human impacts in these systems, and it is therefore necessary to identify management options that increase the resilience of these systems.

Table 1: Soil chemical properties of the analysed depth profiles in the Venice lagoon

Visual traces of iron reduction and oxidation are linked to the redox status of soils and have been used to characterise the quality of agricultural soils.We tested whether this feature could also be used to explain the spatial pattern of the natural vegetation of tidal habitats. If so, an easy assessment of the effect of rising sea level on tidal ecosystems would be possible. Our study was conducted at the salt marshes of the northern lagoon of Venice, which are strongly threatened by erosion and rising sea level and are part of the world heritage 'Venice and its lagoon'. We analysed the abundance of plant species at 255 sampling points along a land-sea gradient. In addition, we surveyed the redox morphology (presence/absence of red iron oxide mottles in the greyish topsoil horizons) of the soils and the presence of disturbances. We used indicator species analysis, correlation trees and multivariate regression trees to analyse relations between soil properties and plant species distribution. Plant species with known sensitivity to anaerobic conditions (e.g. Halimione portulacoides) were identified as indicators for oxic soils (showing iron oxide mottles within a greyish soil matrix). Plant species that tolerate a low redox potential (e.g. Spartina maritima) were identified as indicators for anoxic soils (greyish matrix without oxide mottles). Correlation trees and multivariate regression trees indicate the dominant role of the redox morphology of the soils in plant species distribution. In addition, the distance from the mainland and the presence of disturbances were identified as tree-splitting variables. The small-scale variation of oxygen availability plays a key role for the biodiversity of salt marsh ecosystems. Our results suggest that the redox morphology of salt marsh soils indicates the plant availability of oxygen. Thus, the consideration of this indicator may enable an understanding of the heterogeneity of biological processes in oxygen-limited systems and may be a sensitive and easy-to-use tool to assess human impacts on salt marsh ecosystems.

Serviços dos ecossistemas prestados pelos estuários : especiação e capacidade de retenção do fósforo

O fator nutricional presente nos sapais não é só importante para os organismos que nele habitam como também apresenta uma importância ecológica a uma maior escala. Exemplifica-se este fato com a capacidade de retenção do Fósforo (P) por parte das plantas podendo estas competir como produto químicos para sua imobilização através da incorporação da sua fração biodisponível para cumprimento dos mecanismos básicos de sobrevivência. O rizosedimento dessas plantas é uma importante fonte de nutrientes necessários para garantia básica da perpetuação de todos os serviços (regulação, provisão, cultural) gerados pelo ambiente. A perda de áreas de sapal foi o motivo principal para a elaboração desta tese visto a preocupação em relação aos impactes que a perda de serviços associados à área de estudo escolhida, o sistema lagunar da Ria de Aveiro, poderá vir sofrer caso aconteçam alterações hídricas (naturais ou antrópicas) mais acentuadas no futuro. Essa tese assume como compromisso chamar a atenção para essa questão como também investigar os mecanismos do ciclo do P este importante nutriente considerado essencial para a manutenção da vida em nosso planeta. Para este estudo foram escolhidas 3 espécies de plantas halófitas representantes do sapal amostral, são elas: Bolbochenous maritimus, Spartina maritima e de Juncus maritimus. As questões levantadas buscam compreender o papel do P nas transformações que ocorrem no rizosedimento das halófitas em 3 diferentes contextos: (i) quando comparados os valores da biomassa de P associado às halófitas estudadas (estudo realizado nos sapais povoados por Spartina maritima e Juncus maritimus) em toda extensão da Ria de Aveiro (ii) quando da disponibilidade de P perante a presença de poluentes inorgânicos no Largo do Laranjo, que corresponde a uma zona historicamente contaminada por metais (estudo realizado no rizosedimento das espécies Bolbochenous maritimus e Juncus maritimus) e (iii) quanto à intrusão superficial da água salgada da laguna (estudo focado na avaliação da perda do P próximo às raízes das halófitas que habitam a zona externa do dique do Baixo Vouga Lagunar (BVL) que corresponde à zona de confluência do Rio Vouga com a Ria de Aveiro). Por meio da análise do rizosedimento e da biomassa das diferentes halófitas predominantes do sapal foi possível verificar que, em relação à carga nutritiva fosfática, de Norte (Canal de São Jacinto/Ovar) a Sul (Canal de Mira) da Ria de Aveiro, a cota do sapal é mais importante do que a natureza espacial do sistema. Esta informação é primordial para a assertividade de futuras medidas de criação e reabilitação das áreas de sapal na Ria de Aveiro. Os estudos realizados nas áreas impactadas (Largo do Laranjo e BVL) incidiram na análise do perfil vertical rizosedimentar das halófitas pertencentes ao sapal médio-alto. Estes estudos revelaram que o rizosedimento dessas halófitas possui características peculiares que definem a dinâmica do ciclo do P de forma bastante característica. O rizosedimento das halófitas presentes no Largo do Laranjo apresentaram teores biodisponíveis de P equivalentes àqueles presentes no rizosedimento de área mais afastada da fonte pontual de contaminação para as mesmas espécies. Numa visão otimista, os resultados revelam que ambos sapais, Largo de Laranjo e Cais do Bico, apresentam condições equiparável para perpetuação dos serviços por eles gerados, que nesse caso se tornam ainda mais valiosos devido a garantia da fitoestabilização dos contaminantes (prevenção da entrada de contaminantes na coluna d’água e na cadeia alimentar). No Baixo Vouga Lagunar a análise espacial do sapal na zona exterior ao dique revelou a perda da diversidade das espécies bem como o aumento da área de vasa e consequentemente a perda dos teores de P associados ao rizosedimento das halófitas mais expostas aos efeitos da compressão costeira intensificados pelas ações naturais e antrópicas a que a Ria está sujeita. Em geral, a degradação dessa área de sapal devido aos fenômenos de assoreamento ou de erosão não pode ser separada dos processos sedimentares na área envolvente, principalmente no caso da Ria de Aveiro que tem sofrido constantes mudanças para atender às necessidades das atividades humanas. Essa tendência provavelmente não mudará no futuro próximo. Consequentemente, a evolução da laguna será principalmente dependente do resultado direto das ações humanas que deverão sempre encontrar formas de compensar os danos causados no âmbito de intervenções de reabilitação do sistema hídrico. A recriação de áreas de sapal pode ter lugar como medida mitigadora no âmbito de intervenções de reabilitação de áreas degradadas e ainda poderá servir como forma de captura de P para programas de utilização de fertilizantes naturais (componente desejável para a agricultura moderna o que é particularmente importante para as regiões altamente dependentes do mercado de importação). Deste modo, recomenda-se que a recuperação das áreas de sapal seja enquadrada no âmbito de intervenções mais amplas de valorização dos sistemas estuarinos e lagunares.

Non-target Impacts to Eelgrass from Treatments to Control Spartina in Willapa Bay, Washington

Four methods to control the smooth cordgrass Spartina (Spartina alterniflora) and the footwear worn by treatment personnelat several sites in Willapa Bay, Washington were evaluatedto determine the non-target impacts to eelgrass (Zostera japonica). Clone-sized infestations of Spartina were treated bymowing or a single hand-spray application of Rodeo® formulatedat 480 g L-1acid equivalence (ae) of the isopropylaminesalt of glyphosate (Monsanto Agricultural Co., St. Louis, MO;currently Dow AgroSciences, Indianapolis, IN) with the nonionic surfactant LI 700® (2% v/v) or a combination of mowing and hand spraying. An aerial application of Rodeo® with X-77 Spreader® (0.13% v/v) to a 2-ha meadow was also investigated. Monitoring consisted of measuring eelgrass shoot densities and percent cover pre-treatment and 1-yr post-treatment. Impacts to eelgrass adjacent to treated clones were determined 1 m from the clones and compared to a control 5-m away. Impacts from footwear were assessed at 5 equidistant intervals along a 10-m transect on mudflat and an untreated control transect at each of the three clone treatment sites. Impacts from the aerial application were determined by comparing shoot densities and percent cover 1, 3 and 10 m from the edge of the treated Spartina meadow to that at comparable distances from an untreated meadow. Methods utilized to control Spartina clones did not impact surrounding eelgrass at two of three sites. Decreases in shoot densities observed at the third site were consistent across treatments. Most impacts to eelgrass from the footwear worn by treatment personnel were negligible and those that were significant were limited to soft mud substrate. The aerial application of the herbicide was associated with reductions in eelgrass (shoot density and percent cover) at two of the three sampling distances, but reductions on the control plot were greater. We conclude that the unchecked spread of Spartina is a far greater threat to the survival and health of eelgrass than that from any of the control measures we studied. The basis for evaluating control measures for Spartina should be efficacy and logistical constraints and not impacts to eelgrass. PDF is 7 pages.

Mellum Island (southern North Sea): dynamic processes and sedimentary structures. I. Southern tidal flat, transition zone and high-surface.[p.72 (Blasensand) only][Translation from: Senckenbergiana Maritima 11, 59-113, 1979]

This partial translation of a longer article describes the phenomenon of ”Blasensand”. Blasensand is formed when sedimentation of dried out sand is suddenly flooded from above. A more detailed explanation of Blasensand is given in this translated part of the paper.

Technology and success in restoration, creation, and enhancement of Spartina afferniflora marshes in the United States. Vol. 1: Executive Summary and Annotated Bibliography

Extensive losses of coastal wetlands in the United States caused by sea-level rise, land subsidence, erosion, and coastal development have increased hterest in the creation of salt marshes within estuaries. Smooth cordgrass Spartina altemiflora is the species utilized most for salt marsh creation and restoration throughout the Atlantic and Gulf coasts of the U.S., while S. foliosa and Salicomia virginica are often used in California. Salt marshes have many valuable functions such as protecting shorelines from erosion, stabilizing deposits of dredged material, dampening flood effects, trapping water-born sediments, serving as nutrient reservoirs, acting as tertiary water treatment systems to rid coastal waters of contaminants, serving as nurseries for many juvenile fish and shellfish species, and serving as habitat for various wildlife species (Kusler and Kentula 1989). The establishment of vegetation in itself is generally sufficient to provide the functions of erosion control, substrate stabilization, and sediment trapping. The development of other salt marsh functions, however, is more difficult to assess. For example, natural estuarine salt marshes support a wide variety of fish and shellfish, and the abundance of coastal marshes has been correlated with fisheries landings (Turner 1977, Boesch and Turner 1984). Marshes function for aquatic species by providing breeding areas, refuges from predation, and rich feeding grounds (Zimmerman and Minello 1984, Boesch and Turner 1984, Kneib 1984, 1987, Minello and Zimmerman 1991). However, the relative value of created marshes versus that of natural marshes for estuarine animals has been questioned (Carnmen 1976, Race and Christie 1982, Broome 1989, Pacific Estuarine Research Laboratory 1990, LaSalle et al. 1991, Minello and Zimmerman 1992, Zedler 1993). Restoration of all salt marsh functions is necessary to prevent habitat creation and restoration activities from having a negative impact on coastal ecosystems.