The FRDBN classification model was adopted to classify wetland features based on Sentinel-2 multi-spectral remote sensing data covering the Yellow River Estuary Nature Reserve from 2015 to 2021 (included), the established classification system, and the interpretation signs for the protected wetlands. The distribution of feature types was recorded annually throughout the investigation period at the Dawenliu and Yiqianer management stations. Considering the limited data coverage in September 2015, our analysis focused on the spatial-temporal distribution characteristics, area changes, and land type conversion in the monitoring area for results obtained after 2016.
4.1. Analysis of Spatial Patterns of Land Cover Types
The pseudo-color composite image (R8, G4, and B2 bands) from Sentinel-2 remote sensing and the distribution map of land types in the Yellow River Estuary Wetland Reserve are presented in
Figure 9. The gray shading indicates the part with missing image data in the Dawenliu management station area in September 2015. It can be preliminarily observed that the types of land features in this reserve are intricate and diverse, with pronounced seasonal and temporal dynamics, and considerable interannual variations may occur [
41,
42].
The number of pixels was counted for each land type in the classification map of the monitoring area and then multiplied by the ground size represented by each pixel (spatial resolution 10 × 10 m), resulting in the total area for each type of land feature in different periods, as shown in
Table 5. It can be seen that the area of herbaceous salt marsh vegetation totals the combined areas of reed,
Suaeda salsa, and
Spartina alterniflora.
The percentage of each land type area in the reserve from October 2016 to September 2021 was calculated, as summarized in
Figure 10. The research area totals 16.09 × 10
4 hm
2, with the non-water features primarily located in the intertidal and supratidal zones. The dynamic range of these zones is 9.33–11.06 × 10
4 hm
2, accounting for 58–69% of the total area. Wetland vegetation mainly consists of herbaceous salt marsh. This type of vegetation is widespread and serves important ecological functions. The area changes in reeds, Suaeda salsa, and Spartina alterniflora range from 2.36 × 10
4 to 3.52 × 10
4 hm
2, representing 15–22% of the total.
The marshy and salt-tolerant reeds are the foundational plant species in the wetlands at the Yellow River mouth. They are widely distributed in the salt marsh vegetation of the reserve, primarily in the intertidal and supratidal zones of the estuary. These plants constitute a narrow, elongated growth belt stretching along the river course extending into the inland areas, covering 1.11 × 104–1.95 × 104 hm2, or 75–12% of the total monitoring area. Due to the dense reed bed, they occupy an absolute advantage over potential plant competitors within their habitats. This land type typically hosts a small variety of species, such as Suaeda salsa, Tamarix chinensis, cattail, and Miscanthus sacchariflorus, growing in close proximity.
Suaeda salsa is concentrated on the tidal flats on both sides of the Yellow River mouth. This area is affected by seawater immersion, and the soil is highly salinized. Despite a tendency for seaward expansion, the distribution of Suaeda salsa along the coastline is often sparse. The area change in this land type ranges from 0.21 × 104 to 1.49 × 104 hm2, accounting for 1–9% of the total.
Native to North America, Spartina alterniflora was introduced to the Yellow River Estuary Conservation Area in 1996 to preserve embankments and facilitate land reclamation programs. Due to its favorable tolerance to saline-alkali soils and tidal flooding, this species quickly adapted to the shallow beach and tidal flat environment in the Yellow River Estuary and proliferated. It is mainly distributed in the upper intertidal zone, covering 0.34 × 104–0.45 × 104 hm2, accounting for 2–3% of the total area in this reserve. The spread of Spartina alterniflora can improve the soil structure, prevent soil compaction, promote the growth of beach silt, consolidate the coast. It is helpful to purify the air and green the environment, increase the wetland area, its developed root system and salt tolerance characteristics make it have the function of sand suppression, wind prevention, and wave resistance. It can also be used as feed, fuel, food and chemical raw materials, with a wide range of applications. At the same time, its strong environmental adaptability and reproductive ability lead to the occupation of local vegetation space, inhibit the growth of local species, destroy the original ecological balance, governance difficulty and other potential environmental problems. In view of potential problems, the special prevention and control of China began in February 2023, striving to achieve centralized prevention and control and proper management.
Aside from waters, cultivated land and harvested cropland or bare land dominate, primarily in the supratidal zone and extending inland along river courses, exhibit a dense, blocky distribution pattern. It covers an area of 2.66 × 104 to 3.83 × 104 hm2, representing 17–24% of the total research area.
Bare tidal flats are prevalent in the monitoring area and are mainly found in the intertidal zone, where the majority are regularly flooded by seawater and exhibit large-scale patchy distribution. They are also present in the supratidal zone, along the riversides, and at the estuaries. Due to the influence of marine dynamics and tidal action, this area experiences dynamic changes with high tide flooding and low tide exposure, ranging from 1.07 × 104 to 2.60 × 104 hm2, accounting for 7–16% of the total.
Tamarix chinensis mixed growth refers to the combined area of Tamarix chinensis, reeds, and Suaeda salsa. This land type is concentrated in the upper-middle and upper intertidal zones, i.e., saline-alkali lands, covering 0.35 × 104 to 0.68 × 104 hm2 (2–4% of the total monitoring area). These zones have intricate terrains with numerous gullies, and the growth and distribution of plants exhibit complexity and diversity. Reeds and Suaeda salsa are dominant plant spices in the distribution area. In addition, a small number of herbaceous plants grow, such as Miscanthus sacchariflorus, Cynanchum chinense, bitter lettuce, Apocynum venetum, and Limonium sinense. Affected by changing seasons and the growth status of plants, the dominant populations vary. Despite such dynamics, Tamarisk chinensis consistently remains the primary species present in this area.
Pit ponds comprise various artificial wetlands, such as man-made reservoirs, aquaculture ponds, salt ponds, and paddy fields, with a limited presence of reeds growing along their edges. The distribution areas are uniform and relatively concentrated due to artificial planning, with an area of variations ranging from 1.05 × 104 to 1.66 × 104 hm2, or 7–10% of the total area of monitoring region.
Black locust forests are distributed in higher inland areas adjacent to cultivated land. These forests are home to a small abundance of herbaceous vegetation such as reeds. In addition, tree communities are relatively concentrated and expensive. The area of change ranges from 0.09 × 104 to 0.19 × 104 hm2, making up for 0.5–1.2% of the total monitoring area.
4.2. Analysis of Land Cover Type Conversion
As of September 2021, the total area of wetlands in the monitoring area increased by 0.85 × 104 hm2 (increased 8.55%) compared to October 2016 (10.79 × 104 hm2 vs. 9.94 × 104 hm2). Apart from factors such as climate and tidal changes, the continuous expansion of wetland areas is primarily attributed to the sediment deposition from the Yellow River’s runoff in the Dawenliu monitoring area, which forms tidal flats. In addition, the extensive proliferation and growth of the invasive species Spartina alterniflora on the seaward side are also responsible.
The shift in land types in the Yellow River Estuary Nature Reserve from mid-October 2016 to late September 2021 is shown in
Figure 11. It can be seen that the transition between some salt marsh vegetation (such as reeds,
Suaeda salsa, and
Tamarix chinensis mixed growth) and artificial wetlands (including pit ponds, cultivated land, and harvested cropland or bare land) is pronounced. Statistical analysis of the spatial distribution and land type transition in various regions is described as follows. Firstly, the transformation between reeds and pit ponds, cultivated land, harvested cropland or bare land is significant. A total of 4050.31 hm
2 of harvested cropland or bare lands was converted into reeds. The areas transitioned from cultivated lands and pit ponds to reeds were 1855.68 hm
2 and 942.14 hm
2, respectively. Conversely, 1350.53 hm
2 of reeds were converted into cultivated land, 1070.10 hm
2 into harvested cropland or bare land, and 1043.00 hm
2 into pit ponds. Secondly, we observe a significant transformation between
Suaeda salsa and bare tidal flats. Specifically, 6047.20 hm
2 of bare tidal flats converted into
Suaeda salsa, and 826.12 hm
2 of
Suaeda salsa transitioned into bare tidal flats. The conversion also occurs between reed and black locust forests, with 993.42 hm
2 area shifted to reeds. A total of 967.76 hm
2 of
Suaeda salsa transformed into
Tamarix chinensis mixed growth, whereas 815.70 hm
2 of
Tamarix chinensis mixed growth shifted into
Suaeda salsa. The additional
Spartina alterniflora area mainly arises from bare tidal flats (693.24 hm
2) and water areas (678.71 hm
2). This reflects the continuous expansion of Spartina alterniflora at the boundaries of bare tidal flats and water areas on the map.
In addition, the transition between non-saltmarsh vegetation types mainly occurs in harvested cropland or bare land, cultivated land, pit ponds, water areas, and bare tidal flats. Specifically, 9868.03 hm2 of harvested cropland or bare lands were converted into cultivated lands, 1291.44 hm2 of pit ponds shifted into harvested cropland or bare lands, 980.51 hm2 of harvested cropland or bare lands were restored to pit ponds, 8107.63 hm2 of water areas changed into bare tidal flats, while 696.28 hm2 of bare tidal flats converted into water areas.
The percentage of conversion regarding various land types in the monitoring area is listed in
Table 6. In 2016, 46.35% of reeds, 45.16% of
Suaeda salsa, 13% of
Spartina alterniflora, and 54.91% of
Tamarix chinensis mixed growth underwent transitions. Bare tidal flats, black locust forests, and harvested cropland or bare lands experienced area loss of 49.96%, 64.45%, and 85.09%, respectively.
The conversion between various natural wetlands (including reeds, Suaeda salsa, Spartina alterniflora, Tamarix chinensis mixed growth, and bare tidal flats) is also noticeable. Specifically, 9.99% of the reed areas were transformed into Tamarix chinensis mixed growth. Suaeda salsas were transformed into Tamarix chinensis mixed growth (12.36%) and bare tidal flats (22.62%). The Spartina alternifloras had 5.07% and 4.87% of areas lost to bare tidal flats and reeds, respectively. In addition, 19.07%, 10.59%, and 6.53% of Tamarix chinensis mixed growth were transformed into Suaeda salsas, reeds, and bare tidal flats, respectively. The transition areas from the bare tidal flats into reeds, Suaeda salsas, Spartina alternifloras, and Tamarix chinensis mixed growth were 1.24%, 35.83%, 3.77%, and 2.3%, respectively. Furthermore, 49.41% of the harvested cropland or bare lands in 2021 were converted into cultivated lands. The main reason is that mature crops were harvested in most of the cultivated areas by mid-October 2016, while the seedlings were in the vigorous growth period in early September 2021. Water areas are the largest type of land cover across the entire monitoring area, and 15.79% of the area was converted into bare tidal flats. This is mainly due to the sediment-laden waters of the Yellow River, which form estuarine tidal flats. The other reason is associated with the changes in tidal flats area caused by tidal, water level, and climatic conditions between the two imagery periods.