The Bahamas has alkaline, oolitic and calcareous soils that are derived from dissolved limestone which is primarily calcium carbonate (CaCO3). Soil pH is an excellent indicator of the relative availability of nutrients. Maximal availability of nutrients is seen in soils with a pH range of 6 to 7 (Taylor et al., 2017). Due to the alkalinity of soils in Long Island, nutrient bioavailability was reduced. The presence of carbonate ions affects the soil chemistry. Soils with a pH greater than 7.5 result in deficiencies in iron (Fe), phosphorus (P), and zinc (Zn). In addition, there is a nutrient imbalance of the cations calcium (Ca), magnesium (Mg), and potassium (K) (Msimbira & Smith, 2020). In this study, the addition of Sargassum sp. did not affect soil pH as a result of the strong pH buffer capacity of soils containing clay (Senbayram et al., 2019). The Sargassum treatments also decreased plant growth; conversely, data from other studies are contrasting (Table S4). However, there was an increase in SOM, nutrient concentration (nitrate nitrogen and phosphorus), and salinity levels. Similar results are seen in a study conducted by Izzati et al. (2019) as there was an increase in SOM, and nitrogen levels. Contrarily, the addition of the macroalgae reduced the pH to 7, thus increasing nutrient bioavailability. Additionally, Muarif et al. (2022) articulates that the addition of seaweed increases SOM, nitrogen, phosphorus, potassium, and sodium (when used in large quantities) levels.
Soil pH, organic matter content, nutrient concentrations and salinity levels have a significant role in plant growth and development. Alkalinity stress on crop plants such as tomatoes is similar to salt stress. Alkalinity stress results in stunted plant growth due to poor nutrient uptake as seen in most Sargassum sp. treatments of the 60-day pot trial when compared to the control groups (Fig. 1). Furthermore, tomatoes are classified as glycophytes: plants that are sensitive to salt and cannot tolerate salt stress despite their ability to adapt by developing protective measures (Safdar et al., 2019). Soil salinity levels become toxic for glycophytes between 50 and 100 mM NaCl (Guo et al., 2021). However, Tola et al. (2023) states that tomatoes have a salinity threshold of 1600 mg kg − 1. Although this salinity threshold was not obtained in any of the soils treated with Sargassum treatments, there were treatments within soil from Central Long Island that surpassed 1000 mg kg− 1 (Fig. 4). The incredibly high salinity concentration of soil collected from Central Long Island prior to the Sargassum treatments is attributable to the nearby brackish bodies of water. During previous hurricanes, this area has experienced storm surge and settlement of water. Wei et al. (2021) corroborates that nearby brackish water can induce an accumulation of salt in soil.
Salinity is an abiotic stress that affects the growth of tomato plants at all stages and ultimately restricts fruit production. It interferes with the uptake of nitrogen thus minimizing plant growth, development, and reproduction (Devkar et al., 2020). Salinity reduces plant uptake of phosphate as it causes phosphate ions to precipitate with calcium ions; thus, limiting water uptake (Shrivastava & Kumar, 2015). In addition, high soil sodium (Na) levels increase water lost as stomatal closure is affected (Msimbira & Smith, 2020). This aggregation of sodium imposes osmotic stress, ion toxicity, and nutrient deficiency (of N, P, K, Ca, Fe, and Zn). Oxidative stress, resulting in reactive oxygen species, is also a consequence of sodium accumulation within the plant (Shrivastava & Kumar, 2015).
Root and shoot weights are also affected by soil alkalinity and salinity. Carbohydrates produced during the process of photosynthesis are allocated by plants to support growth, maintenance, development, and reproduction (Hartmann et al., 2020). The dry biomass, including root and shoot dry weights, show carbon allocation. Leaf number assists in increasing shoot biomass. Therefore, the more leaves, the higher the shoot biomass. Increased numbers of leaves allow for a greater surface area for photosynthesis to occur. Plants can detect changes in resources in the soil and respond accordingly by optimizing growth, development, and biomass allocation (Kudoyarova et al., 2015). In addition, carbon allocation to the roots is done in response to shortage of nutrients including nitrate and phosphorus (Kudoyarova et al., 2015). Larger shoot biomass, as compared to root biomass, is an indication that water and nutrients are readily available and more carbon is allocated to the shoot to allow for growth and development of leaves, fruits, etc. There are variations in the dry root to shoot biomass for the treatments of this study (Table 1). Increased salinity levels reduce root growth and development and result in a decline in the shoot biomass (Tang et al., 2021). Moreover, alkaline soils reduce root development by impairing the water supply to the plant (Msimbira & Smith, 2020).
Consequently, the macroalgae treatments negatively impacted the growth performance parameters of the cherry tomato plants as the control groups produced plants with greater changes in plant height and number of leaves (from day 1 to day 60) and reduced their total biomass (Figs. 2 and 3; Table 1). Additionally, the first plants to start reproducing were those in the control groups. Although the addition of Sargassum increased nutrient content, the bioavailability of the nutrients did not increase due to the alkalinity of the soil. As a result of stress from soil salinity and alkalinity, the survivability rate for tomato plants varied among treatments (Table S5).
To conclude, all the aims and objectives of this study were met. The soil quality of Long Island is poor as the soils lack sufficient concentrations of the basic macronutrients (nitrogen, phosphorus, and potassium). Sargassum sp. can be used as a biofertilizer for soils in Long Island with specific recommendations such as waiting on the soil to age, allowing decomposition and release of nutrients. Sargassum sp. has a positive effect on soil health and fertility as it increases nutrient concentration and organic matter; however, with the application rates used, it did not enhance growth performance. Lastly, based on results obtained, none of the application rates are ideal for tomato cultivation.
If this research was to be repeated, it is recommended that another species of algae be used, categorically a freshwater species, to prevent the increase in soil salinity, TDS and EC. However, if Sargassum sp. is used, the soil should be allowed to age so that nutrients can be released upon decomposition of the macroalgae and become more bio-readily available. Additionally, if time is limited, a halophyte can be used as these plants are tolerant to salt. Other recommendations include composting or bio-digesting the Sargassum, using different application rates, and conducting a field experiment instead of utilizing a pot trial method to limit the ‘pot effect.’