説明
The dataset includes measurements of key environmental parameters such as temperature, salinity, dissolved oxygen, and nutrient concentrations, together with data on phytoplankton composition and abundance. These data can be used to evaluate the influence of aquaculture activities on water quality and phytoplankton dynamics in coastal Mediterranean ecosystems.
データ レコード
この sampling event リソース内のデータは、1 つまたは複数のデータ テーブルとして生物多様性データを共有するための標準化された形式であるダーウィン コア アーカイブ (DwC-A) として公開されています。 コア データ テーブルには、64 レコードが含まれています。
拡張データ テーブルは2 件存在しています。拡張レコードは、コアのレコードについての追加情報を提供するものです。 各拡張データ テーブル内のレコード数を以下に示します。
この IPT はデータをアーカイブし、データ リポジトリとして機能します。データとリソースのメタデータは、 ダウンロード セクションからダウンロードできます。 バージョン テーブルから公開可能な他のバージョンを閲覧でき、リソースに加えられた変更を知ることができます。
バージョン
次の表は、公にアクセス可能な公開バージョンのリソースのみ表示しています。
引用方法
研究者はこの研究内容を以下のように引用する必要があります。:
Challouf R, Medhioub W, Rallis I, Medhioub M N (2026). Patterns of phytoplankton community structure and diversity at finfish offshore cage in the Mediterranean Sea (Bay of Monastir, Tunisia). University of Carthage, National Institute of Marine Sciences and Technologies (INSTM), Salammbô, Tunisia.
権利
研究者は権利に関する下記ステートメントを尊重する必要があります。:
パブリッシャーとライセンス保持者権利者は Hellenic Center for Marine Research。 This work is licensed under a Creative Commons Attribution (CC-BY 4.0) License.
GBIF登録
このリソースをはGBIF と登録されており GBIF UUID: 7d70a250-4507-4a60-b5c6-ef778ed38fa2が割り当てられています。 Ocean Biodiversity Information System によって承認されたデータ パブリッシャーとして GBIF に登録されているHellenic Center for Marine Research が、このリソースをパブリッシュしました。
キーワード
Samplingevent; Phytoplankton; Diversity; Species composition; Toxic microalgae; Aquaculture; Mediterranean Sea
連絡先
- メタデータ提供者 ●
- 最初のデータ採集者 ●
- 連絡先
- 最初のデータ採集者 ●
- 連絡先
- 最初のデータ採集者
- Custodiansteward(保管者)
- Custodiansteward(保管者)
地理的範囲
Sampling took place in the Bay of Monastir (Mediterranean Sea, Tunisia)
| 座標(緯度経度) | 南 西 [35.617, 10.803], 北 東 [35.826, 11.121] |
|---|
生物分類学的範囲
All phytoplankton were identified to genus or species, including dinoflagellates, diatoms, cyanobacteria, and euglenophytes. Silicoflagellates, foraminifera, and ciliates were identified to genus. Zooplankton and bivalve larvae were recorded as broad taxonomic categories.
時間的範囲
| 開始日 / 終了日 | 2018-02-20 / 2018-10-26 |
|---|
プロジェクトデータ
Investigating the potential for mussel aquaculture off the coast of Monastir, including assessment of environmental conditions, growth potential, and sustainable farming practices for Mytilus galloprovincialis and Perna perna.
| タイトル | Study on the possibilities for exploitation and farming of mussels (Mytilus galloprovincialis and Perna perna) off the coast of Monastir (Tunisia) |
|---|---|
| ファンデイング | This work was supported by the National Institute of Marine Sciences and Technologies (INSTM) |
| Study Area Description | Mediterranean Sea |
| 研究の意図、目的、背景など(デザイン) | The research tasks within this project were carried out by researchers from the National Institute of Marine Sciences and Technologies (INSTM). The team was responsible for field sampling, environmental monitoring, phytoplankton identification, and data analysis. Activities included the collection of plankton samples, laboratory identification of phytoplankton taxa, and the evaluation of environmental conditions related to the potential farming of the mussels Mytilus galloprovincialis and Perna perna off the coast of Monastir (Tunisia). |
収集方法
This study was conducted at a sea bream and sea bass aquaculture farm (35°45.902′ N, 10°55.548′ E) located in Monastir Bay near the Monastir-Kuriates Islands, approximately 15 km from the Tunisian Mediterranean coast, at a water depth of 28 m. The farm has been in operation since 2008. Sampling was carried out at four stations in the offshore waters of Monastir (Tunisia, Mediterranean Sea). Stations S1, S2, and S3 were located within the aquaculture farm, whereas station S4 was situated outside the farm and served as a control site. Sampling was conducted seasonally from February to October 2018. Seawater samples were collected using a 5-L Niskin bottle at three depths (0 m, 15 m, and 25 m). The collected samples were preserved and transported to the laboratory for phytoplankton identification and physicochemical analyses.
| Study Extent | The study was conducted in the offshore fish farm in Monastir, Tunisia (Mediterranean Sea) from February to October 2018. The project focused on phytoplankton taxa .Water samples were collected with a 5-L Niskin bottle. |
|---|---|
| Quality Control | Water samples (1 L) to be used for phytoplankton enumeration were preserved with formol solution (3‰) and stored in the dark at 4 °C.Water samples for nutrient analyses (60 mL) were collected and preserved immediately at − 20 °C in the dark. Water samples for suspended matter analysis were filtered by vacuum filtration through Whatman GF/C glass fiber filters, and the filters were immediately stored at − 20 °C. |
Method step description:
- Seawater temperature and dissolved oxygen (DO) were measured directly in situ using an electronic thermometer (LUTRON®BC-4308) and a DO meter (PCE®-WO2 10), respectively. To determine the concentration of SM, 1.5 liters of seawater was collected and filtered on pre-weighed GF/C 0.45 µm filters (WHATMAN®). Subsequently, filters were dried in an oven at 100 ◦C for 24 h and total SM weight (mg L-1) was estimated according to the differential weighing method of Aminot and Chaussepied (1983). Transparency of the water (in meters) was measured using a Secchi Disk as described by Testa et al. (2019). Nutrients (i.e., NO2−, NO3−, NH4+, PO43−, and Si(OH)4) were analyzed with a Bran+Luebbe type 3 auto-analyzer and concentrations were determined colorimetrically, using a UV-visible (6400/6405) spectrophotometer. For Chlorophyll a (Chl a), two liters of seawater were filtered, through 200–250 µm pore size membrane filters to remove large particulate matter and zooplankton. The eluate was filtrated on GF/C 0.45 µm filters (WHATMAN®). Chl a was extracted with 10 ml of acetone 90% for 24 hours at 4 ◦C then the absorbance at two wavelengths (665 µm and 750 µm) were determined before and after acidification using 100 µl of HCL 0.3 M according to Aminot and Chaussepied, (1983). The identification and enumeration of phytoplankton (including dinoflagellate cysts) and the estimate of abundance of the different algal groups were made using an inverse phase microscope based on the Utermohl (1931) and Sournia (1987) methods. The identification of the various phytoplankton taxa was achieved through the determination keys of Trégouboff and Rose (1957), Huber-Pestalozzi (1968) and Balech (1988). Phytoplankton density (expressed in cells l-1) is determined using the following formula: N = (n*1000)/V N: Total number of phytoplankton cells contained in one liter n: number of cells V: Volume of sedimentation cuve (ml)
書誌情報の引用
- Medhioub, W., Challouf, R., Laabir, M., Limayem, Y., Bchir, S., Slimeni, W., ... & Azaza, M. S. (2023). Potential to produce brown mussel integrated to a net-cage fish farm in a Mediterranean bay. Aquaculture Reports, 31, 101674. https://doi.org/10.1016/j.aqrep.2023.101674
追加のメタデータ
| 代替識別子 | 10.25607/7asluk |
|---|---|
| 10.25607/tzbgyk | |
| 7d70a250-4507-4a60-b5c6-ef778ed38fa2 | |
| https://ipt.medobis.eu/resource?r=phytomonastirbay2018 |