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Effects of salinity and flooding on post-hurricane regeneration potential in coastal wetland vegetation

PREMISE OF THE STUDY: The nature of regeneration dynamics after hurricane flooding and salinity intrusion may play an important role in shaping coastal vegetation patterns. METHODS: The regeneration potentials of coastal species, types and gradients (wetland types from seaward to landward) were studied on the Delmarva Peninsula after Hurricane Sandy using seed bank assays to examine responses to various water regimes (unflooded and flooded to 8 cm) and salinity levels (0, 1, and 5 ppt). Seed bank responses to treatments were compared using a generalized linear models approach. Species relationships to treatment and geographical variables were explored using nonmetric multidimensional scaling. KEY RESULTS: Flooding and salinity treatments affected species richness even at low salinity levels (1 and 5 ppt). Maritime forest was especially intolerant of salinity intrusion so that species richness was much higher in unflooded and low salinity conditions, despite the proximity of maritime forest to saltmarsh along the coastal gradient. Other vegetation types were also affected, with potential regeneration of these species affected in various ways by flooding and salinity, suggesting relationships to post-hurricane environment and geographic position. CONCLUSIONS: Seed germination and subsequent seedling growth in coastal wetlands may in some cases be affected by salinity intrusion events even at low salinity levels (1 and 5 ppt). These results indicate that the potential is great for hurricanes to shift vegetation type in sensitive wetland types (e.g., maritime forest) if post-hurricane environments do not support the regeneration of extent vegetation.

Delmarva Peninsula

Interactive effects of redox intensity and phosphate availability on growth and nutrient relations of Cladium jamaicense (Cyperaceae)

Expansion of Typha domingensis into areas previously dominated by Cladium jamaicense in the Florida Everglades has been linked to anthropogenic phosphorus (P) enrichment and increased hydroperiod. The principal stress factor for plants in flooded soils is biochemical reduction, the intensity of which is measured as redox potential (Eh). The objective of this study was to assess the growth response of C. jamaicense to Eh (−150, +150, and +600 mV) and P availability (10, 80, and 500 μg P/L). Plants were grown hydroponically in a factorial experiment using titanium (Ti 3+ ) citrate as an Eh buffer. Treatment effects on growth, biomass partitioning, and tissue nutrients were recorded. Growth approximately doubled in response to a 50‐fold increase in P availability. Low redox significantly reduced growth and tissue P concentration. While plant P concentrations increased 20‐fold between the 10 and 500 μg P/L treatments, P concentrations were 50–100% higher at +600 mV than at −150 mV within each phosphate level. At high Eh, C. jamaicense appears well adapted to low nutrient environments because of its low P requirement and high retention of acquired P. However, at low Eh the ability to acquire or conserve acquired P decreases and as a consequence, higher phosphate levels are required to sustain growth. Findings of this study indicate that young C. jamaicense exhibits low tolerance to strongly reducing conditions when phosphate is scarce.

Florida

Chromosome numbers and karyotype evolution in holoparasitic Orobanche (Orobanchaceae) and related genera

Chromosome numbers and karyotypes of species of Orobanche , Cistanche , and Diphelypaea (Orobanchaceae) were investigated, and 108 chromosome counts of 53 taxa, 19 counted for the first time, are presented with a thorough compilation of previously published data. Additionally, karyotypes of representatives of these genera, including Orobanche sects. Orobanche and Trionychon , are reported. Cistanche ( x = 20) has large meta- to submetacentric chromosomes, while those of Diphelypaea ( x = 19) are medium-sized submeta- to acrocentrics. Within three analyzed sections of Orobanche , sects. Myzorrhiza ( x = 24) and Trionychon ( x = 12) possess medium-sized submeta- to acrocentrics, while sect. Orobanche ( x = 19) has small, mostly meta- to submetacentric, chromosomes. Polyploidy is unevenly distributed in Orobanche and restricted to a few lineages, e.g., O . sect. Myzorrhiza or Orobanche gracilis and its relatives (sect. Orobanche ). The distribution of basic chromosome numbers supports the groups found by molecular phylogenetic analyses: Cistanche has x = 20, the Orobanche -group ( Orobanche sect. Orobanche , Diphelypaea ) has x = 19, and the Phelipanche -group ( Orobanche sects. Gymnocaulis , Myzorrhiza , Trionychon ) has x = 12, 24. A model of chromosome number evolution in Orobanche and related genera is presented: from two ancestral base numbers, x h = 5 and x h = 6, independent polyploidizations led to x = 20 ( Cistanche ) and (after dysploidization) x = 19 ( Orobanche -group) and to x = 12 and x = 24 ( Phelipanche -group), respectively.

American Journal of Botany

Timing of seed dispersal generates a bimodal seed bank depth distribution

The density of soil seed banks is normally highest at the soil surface and declines monotonically with depth. Sometimes, for a variety of reasons, peak density occurs below the surface but, except in severely disturbed soils, it is generally true that deeper seeds are older. In seasonally dry habitats that develop deep soil cracks during the dry season, it is possible that some seeds fall down cracks and rapidly become deeply buried. We investigated this possibility for three dominant clonal perennials ( Scirpus maritimus , S. litoralis , and Juncus subulatus ) in the Doñana salt marsh, a nontidal marsh with a Mediterranean climate located in southwest Spain. Two species, which shed most of their seed during the dry season and have seeds with low buoyancy, had bimodal viable seed depth distributions, with peak densities at the surface and at 16–20 cm. A third species, which shed most seeds after soil cracks had closed and had seeds with high buoyancy, had viable seeds only in surface soil. Bimodal seed bank depth distributions may be relatively common in seasonally dry habitats with fine-textured soils, but their ecological significance has not been investigated.

American Journal of Botany

Seed storage conditions change the germination pattern of clonal growth plants in Mediterranean salt marshes

The effect of salinity level and extended exposure to different salinity and flooding conditions on germination patterns of three salt‐marsh clonal growth plants ( Juncus subulatus , Scirpus litoralis , and S. maritimus ) was studied. Seed exposure to extended flooding and saline conditions significantly affected the outcome of the germination process in a different, though predictable, way for each species, after favorable conditions for germination were restored. Tolerance of the germination process was related to the average salinity level measured during the growth/germination season at sites where established individuals of each species dominated the species cover. No relationship was found between salinity tolerance of the germination process and seed response to extended exposure to flooding and salinity conditions. The salinity response was significantly related to the conditions prevailing in the habitats of the respective species during the unfavorable (nongrowth/nongermination) season. Our results indicate that changes in salinity and hydrology while seeds are dormant affect the outcome of the seed‐bank response, even when conditions at germination are identical. Because these environmental‐history‐dependent responses differentially affect seed germination, seedling density, and probably sexual recruitment in the studied and related species, these influences should be considered for wetland restoration and management.

Doñana National Park

Salt tolerance and osmotic adjustment of Spartina alterniflora (Poaceae) and the invasive M haplotype of Phragmites australis (Poaceae) along a salinity gradient

An invasive variety of Phragmites australis (Poaceae, common reed), the M haplotype, has been implicated in the spread of this species into North American salt marshes that are normally dominated by the salt marsh grass Spartina alterniflora (Poaceae, smooth cordgrass). In some European marshes, on the other hand, Spartina spp. derived from S. alterniflora have spread into brackish P. australis marshes. In both cases, the non-native grass is thought to degrade the habitat value of the marsh for wildlife, and it is important to understand the physiological processes that lead to these species replacements. We compared the growth, salt tolerance, and osmotic adjustment of M haplotype P. australis and S. alterniflora along a salinity gradient in greenhouse experiments. Spartina alterniflora produced new biomass up to 0.6 M NaCl, whereas P. australis did not grow well above 0.2 M NaCl. The greater salt tolerance of S. alterniflora compared with P. australis was due to its ability to use Na + for osmotic adjustment in the shoots. On the other hand, at low salinities P. australis produced more shoots per gram of rhizome tissue than did S. alterniflora . This study illustrates how ecophysiological differences can shift the competitive advantage from one species to another along a stress gradient. Phragmites australis is spreading into North American coastal marshes that are experiencing reduced salinities, while Spartina spp. are spreading into northern European brackish marshes that are experiencing increased salinities as land use patterns change on the two continents.

American Journal of Botany

Genotype, soil type, and locale effects on reciprocal transplant vigor, endophyte growth, and microbial functional diversity of a narrow sagebrush hybrid zone in Salt Creek Canyon, Utah

When addressing the nature of ecological adaptation and environmental factors limiting population ranges and contributing to speciation, it is important to consider not only the plant's genotype and its response to the environment, but also any close interactions that it has with other organisms, specifically, symbiotic microorganisms. To investigate this, soils and seedlings were reciprocally transplanted into common gardens of the big sagebrush hybrid zone in Salt Creek Canyon, Utah, to determine location and edaphic effects on the fitness of parental and hybrid plants. Endophytic symbionts and functional microbial diversity of indigenous and transplanted soils and sagebrush plants were also examined. Strong selection occurred against the parental genotypes in the middle hybrid zone garden in middle hybrid zone soil; F1 hybrids had the highest fitness under these conditions. Neither of the parental genotypes had superior fitness in their indigenous soils and habitats; rather F1 hybrids with the nonindigenous maternal parent were superiorly fit. Significant garden-by-soil type interactions indicate adaptation of both plant and soil microorganisms to their indigenous soils and habitats, most notably in the middle hybrid zone garden in middle hybrid zone soil. Contrasting performances of F1 hybrids suggest asymmetrical gene flow with mountain, rather than basin, big sagebrush acting as the maternal parent. We showed that the microbial community impacted the performance of parental and hybrid plants in different soils, likely limiting the ranges of the different genotypes.

Utah

Genotypic and phenotypic variability of Zostera marina on the west coast of North America

The relation between environmental factors and leaf morphology of Zostera marina L. have long been unclear, primarily because the species is intrinsically variable. The common-garden method was used to determine the genetic, environmental, and interaction components of leaf size variation. Zostera marina consists of several ecotypes with a wide range of phenotypic plasticity. Variation in the morphology of Z . marina was of three types: genetic, accounting for 14% across the localities studied; environmental (phenotypic plasticity along temporal and spatial gradients), accounting for 32%; and interaction between genotype and environmental, acounting for 35%. Five ecotypes were described for the North American Pacific coast: Z . marina L. var. izembekensis Backman, Z . marina L. var. typica Setchell, Z . marina L. var. phillipsii Backman, Z . marina L. var. latifolia Morong, Z . marina L. var. atàm Backman. Temporal variation was due to seasonal phenotypic changes in ecotypes. Zostera marina var. izembekensis showed little seasonal morphological changes; Z . marina var. typica demonstrated minor increase in leaf size in spring and summer. Zostera marina var. phillipsii and Z . marina var. latifolia behaved similarly in that leaf size of both increased markedly in spring through early summer. Zostera marina var. phillipsii is adapted to Hood Canal and Puget Sound while Z . marina var. latifolia occupies the outer coast. Zostera marina var. atàm exhibits sexual reproduction exclusively and is specifically adapted to the Gulf of California.

Canadian Journal of Botany

Replacement of native oak and hickory tree species by the introduced American chestnut (Castanea dentata) in southwestern Wisconsin

American chestnut was introduced at West Salem, Wisconsin, about 1880 and had begun to replace native tree species in adjacent oak-hickory woodland before 1930. Chestnut is now an important canopy species over about 20 ha of forested ridge extending north and south of the original plantation. A smaller area of less than 5 ha is dominated by chestnut in both the canopy and understory. Chestnut seedlings and small saplings are more numerous along woodland edges and in recently disturbed soil, they are rare in the interior of ungrazed pasture and entirely absent from intensively grazed areas adjacent to chestnut-dominated woodland. Random sampling of recently established seedlings indicates that from 1 to 5 seedlings/(year ∙ ha) became established in undisturbed woodland between 1986 and 1988. The general pattern of chestnut distribution indicates the importance of woodland edges in chestnut propagation and the effects of livestock grazing in excluding chestnut. Replacement of native species by chestnut appears to have occurred in two steps: isolated groups of trees became established at favorable locations, after which many additional chestnut stems became established in the understory. The recent discovery and treatment of blight indicates that the West Salem site may not be available for study of blight-free chestnut in the future.

Wisconsin