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A functional definition to distinguish ponds from lakes and wetlands

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Current scientific definitions of ponds

We compiled existing scientific definitions of ponds by conducting a backwards and forwards search of papers referenced in or subsequently referencing three seminal pond papers8,17,18 (see “Methods”). We ultimately compiled 54 pond definitions from scientific literature (data available19). The variables most often included in definitions were surface area (91% of definitions), depth (48%), permanence (48%), origin (i.e., natural or human-made; 33%), and standing water (33%; Fig. 2a). When surface area or depth were included in definitions, they were often mentioned qualitatively (e.g., “small” and “shallow”). Of the 61% of definitions that included a maximum pond surface area, the range was 0.1 to 100 ha, the median was 2 ha, and all but two definitions were ≤ 10 ha (Fig. 2b). For depth, only 17% of studies provided a maximum depth cutoff, which ranged 2 to 8 m (Fig. 2c). Of the 26 definitions mentioning permanence, 22 stated that ponds could be temporary or permanent and only three indicated that ponds are exclusively permanent waterbodies. Of the 18 definitions mentioning origin, 17 mentioned that ponds could be natural or human-made with the remaining study indicating ponds can have diverse origins.

Figure 2

Summary of “pond” definitions from scientific literature including (a) presence of various morphological, biological, and physical characteristics in the definition as blue bars (n = 54 definitions total). Bold black lines indicate the number of definitions with surface area and depth values. Histograms of the upper limits from “pond” definitions for (b) surface area and (c) maximum depth.

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Other important factors included in definitions related to morphometry. For example, 30% of definitions mentioned the potential for plants to colonize the entire basin, which relates to high light penetration (mentioned in 11% of definitions) and/or shallow depths. For example, Wetzel11 defines ponds as having enough light penetration that macrophyte photosynthesis can occur over the entire waterbody. As such, these conditions may be comparable to the littoral region of lakes (11% of definitions). Lastly, 7% of pond definitions mentioned mixing versus stratification, whereby ponds mix more than lakes20 yet less than shallow lakes due to a smaller fetch16.

To assess if there was agreement in pond definitions among papers, we examined the number of times each definition was cited. Across the 54 definitions, there were 89 citations of 48 unique papers. Ultimately, most papers (75%) were only cited only once, indicating no consensus in pond definition. The most cited paper was Biggs et al.21, which accounted for 15% of citations. The next two most cited papers were Oertli et al.17 and Sondergaard et al.18, which were seminal papers included in our backwards-forwards search, and each comprised 8% of citations.

International definitions

At an international level, there is no consensus on how to discriminate among ponds, lakes, and wetlands. In North America, wetlands are generally considered to be shallow: < 2 m in Canada22 and < 2.5 m in the US23, which differentiates them from lakes. Some nations, such as Australia, South Korea, and Uganda, explicitly include ponds and lakes in federal wetland definitions24 (see also22). The inclusion of ponds and some lakes within wetland definitions often stems from the Ramsar Convention, an international body interested in global wetland conservation that has been signed by 172 countries representing 6 continents as of 202125. The Ramsar Convention defined wetlands as “areas of marsh, fen, peatland, or water” across marine, brackish, and freshwater with varying degrees of permanence and natural or artificial states with a maximum depth of 6 m26, which overlaps depths found in many definitions of ponds and shallow lakes. In other countries, ponds are included in lake definitions under federal conservation laws. For example, in the Danish “nature protection” law §3, lakes are defined as waterbodies with a surface area of > 100 m2. As 98% of Danish ‘lakes’ are smaller than 1 ha27, this law protects many small waterbodies that may be considered ponds elsewhere. Still other agencies have only qualitative pond definitions: the European Commission simply defines ponds as “relatively shallow” and may also be called “pool, tarn, mere, or small lake,” a definition also used by the International Union for Conservation of Nature28,29. These examples underscore that waterbody definitions vary globally, are generally qualitative, and are rarely based on scientific evidence relating to ecosystem structure or function. The definitions possibly derive from different management, protection, and monitoring strategies; for instance, the European Union’s Water Framework Directive excludes waterbodies < 50 ha (0.5 km2) in size from monitoring30.

Current U.S. Federal and State definitions

In the US, waterbody definitions vary among federal agencies, with implications for both legal protection and monitoring. The US Environmental Protection Agency (EPA) and the US Army Corps of Engineers (ACE) define wetlands based on saturated soils and hydrophytic vegetation, which has the potential to include ponds within the category of wetlands. Conversely, the US Fish and Wildlife Service (USFWS) distinguishes among wetlands and lakes based on surface area, depth, and emergent vegetation31. Lakes are ≥ 8 ha or if smaller, they must be ≥ 2.5 m in maximum depth. In contrast, wetlands are are dominated by > 30% emergent plant cover; if there is less, the site may still be a wetland if < 2.5 m deep and < 8 ha in size. Therefore, ponds are often considered by USFWS to be wetlands, but this is not always the case: ponds have been used as an example of a waterbody that can be classified as lake, wetland, or both32. The lack of an explicit, unified, and scientifically based pond definitions across three federal agencies (EPA, ACE, USFWS) is confusing and contributes to ponds being underrepresented in US aquatic waterbody monitoring relative to their numerical dominance on the landscape3,8. For example, US EPA monitoring programs include ponds in both the National Wetland Condition Assessment and the National Lake Assessment; however, “ponds” represent a small number of waterbodies in each of these surveys (< 12% classified qualitatively as “pond” in 2011 wetland survey; 13% of waterbodies were < 5 ha in 2012 lake survey).

Reflecting political and geographic variability at the national scale, most US states have their own waterbody protections33. We surveyed US state agencies to examine state definitions of ponds, lakes, and wetlands (see “Methods”). Our survey responses included 42 of 50 (84%) states (Fig. 3). Only one state (Michigan) explicitly defined ponds, 11 states defined lakes (26%), and 30 states defined wetlands (71%). While only one state defined ponds, half of the surveyed states used the term “pond” in their legislation. Specifically, ponds were referenced as state waters (e.g., Vermont) or were included in state definitions for lakes (e.g., Kansas) or wetlands (e.g., Rhode Island). It is unclear how these definitions impact monitoring and protection or why the distinctions were originally made. For instance, many states monitor lakes based on minimum size thresholds, which vary widely from < 1 ha in Arizona and Alaska, 2–4 ha in many northeastern states, and up to 8 ha in Washington and Nebraska. The variety of definitions and monitoring size cutoffs do not appear to be scientifically based, but may stem from arbitrary decisions, historic references, mapping capabilities from decades ago, and resource limitations for monitoring; the same rationale for definitions likely apply to local, regional, and international organizations around the globe.

Figure 3

US state responses to surveys indicating if the state has a definition of wetland, lake, or pond and if the state used the term “pond” in their legislation. NR = no response.

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Comparing lake, pond, and wetlands characteristics from literature

We compared biological, physical, and chemical characteristics of waterbodies that scientists called lakes, ponds, or wetlands in published studies. To obtain data for the pond characteristics, we used the same literature search summarized above for pond definitions (also, see “Methods”). From the 519 papers that we examined, we extracted data on sites the authors called “ponds” and other variants (e.g., ‘small ponds’, ‘fish ponds’, but NOT ‘lakes’). We filtered waterbodies that were ≤ 20 ha surface area and ≤ 9 m depth (global distribution; n = 1327) to include waterbodies slightly greater than the maximum depth and maximum surface area used to define ponds in prior studies34,35. To compare ponds to lakes and wetlands, we used existing lake (US and Europe; n = 55,173) and wetland (US; n = 400) databases; waterbodies were classified as lake or wetland by the scientists or managers who published the database. Wetlands were classified as < 1 m in depth with no defined surface area and lakes were all > 0.02 ha with no defined depth (see “Methods” for details).

From the waterbodies that scientists called “ponds,” hydroperiod and origin varied over a large range of characteristics. Of the 608 ponds with hydroperiod data, permanent ponds accounted for 74% (n = 450) and temporary ponds for 26% (n = 158). Out of 648 ponds with known origins, 65% (n = 418) were constructed or manipulated and 35% (n = 230) were natural. Therefore, scientists consider ponds to be inclusive of both permanent and temporary hydroperiod and have natural or human-made origins.

When examining water chemistry, nutrients, and biotic data across different waterbody types, as defined by publishing scientists and managers, we found that ponds were distinct from lakes and wetlands in two metrics (TN, pH), similar to wetlands in one metric (TP), and similar to lakes in one metric (chl a; Fig. 4; Tables S1, S2). For example, ponds had distinctly high TN concentrations, which were greater than either lakes or wetlands (Fig. 4b; Table S2). Ponds and wetlands had similarly high TP concentrations, which were significantly greater than lakes; ponds were also most variable in TP (Fig. 4a; Table S2). Lastly, ponds chlorophyll (chl) a concentrations were similar to lakes, with wetlands being most variable but lower, on average (Fig. 4d; Table S2).

Figure 4

Comparison of various chemical and biological parameters across wetlands, ponds, and lakes, with waterbody category based on the term used by publishing scientists and managers (Table S2). Violin plots indicate distributions of waterbody characteristics, the white box indicates 25th to 75th percentile with median in the middle, whiskers indicate 1.5 × interquartile range, and outliers are black closed circles. Letters inside the plot indicate significant differences in means (LSD, alpha = 0.05). Note all x-axes have logarithmic scales.

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Does ecosystem structure and function distinguish ponds from lakes and wetlands?

We evaluated the relationship between key metrics of ecosystem structure or function with three quantitative variables that often showed up in pond, lake, or wetland definitions: surface area, maximum depth (hereafter depth), and emergent vegetation cover. Our metrics of ecosystem structure or function include nutrients (total phosphorus (TP), total nitrogen (TN)), water chemistry (pH), primary producer biomass (chl a), metabolism (gross primary production—GPP, respiration—R, net ecosystem production—NEP), and heat and gas distributions and movement (diel temperature ranges—DTR, methane fluxes, gas transfer velocities). The data was collated from global surveys of literature and federal or international databases (see “Methods”) with ultimately ten comparisons for surface area, six comparisons for depth, and four comparisons for emergent vegetation cover with a range of sample sizes for each comparison (n = 67 to 7931, see Tables S3, S5, S7). We assessed each relationship for four different patterns in increasing order of complexity: null, linear, segmented (nonlinear), and logistic (nonlinear) patterns and selected the best fit and most parsimonious relationship.

Ecosystem structure and function were mostly nonlinearly related to surface area (n = 9/10 variables), depth (n = 5/6 variables), and emergent vegetation cover (n = 3/4 variables) with both segmented and logistic relationships occurring (Figs. 5, 6, 7; Tables S3–S8). For surface area, six variables had logistic relationships: TP (Fig. 5b), methane fluxes (Fig. 5d), chl a (Fig. 5f), diel temperature range (Fig. 5h), gas exchange rates (k600; Fig. 5i), and pH (not pictured). The inflection occurred at 0.8 ha for TP, 1.1 ha for methane fluxes, 1.5 ha for chl a, 1.7 ha for pH, 4.6 ha for diel temperature range, and 17.5 ha for gas exchange rates (Table S3). NEP (Fig. 5c), R (Fig. 5e), and TN (Fig. 5g) all had segmented linear relationships where smaller systems had steeper slopes than larger systems (Table S4). The breakpoint in surface area was 1.0 ha for NEP, 1.2 ha for R, and 3.8 ha for TN (Table S3). For depth, two variables had logistic relationships: diel temperature range (Fig. 6e) and chlorophyll a (Fig. 6f), with the inflection occurring at 5.9 m and 14.9 m, respectively (Table S5). pH (Fig. 6b), TP (Fig. 6c), and TN (Fig. 6d) all had segmented linear relationships where smaller systems had steeper slopes than larger systems (Table S6) with breakpoints occurring at 1.0, 2.1, and 5.2 m, respectively (Table S5). For emergent vegetation cover, TN (Fig. 7b), TP (Fig. 7c), and pH (Fig. 7d) all had segmented linear relationships where systems with more emergent vegetation had steeper slopes than more open systems (Table S8). The breakpoint in emergent vegetation cover was 6.0% for TN, 8.2% for TP, and 26.0% for pH (Table S7).

Figure 5

Relationships between lentic waterbody size (excluding wetlands) and ecosystem structure and function metrics: (a) gross primary production (GPP), (b) total phosphorus concentrations (TP), (c) net ecosystem production (NEP), (d) methane fluxes (CH4 flux), (e) respiration (R), (f) chlorophyll a concentrations (Chl a), (g) total nitrogen concentrations (TN), (h) diel temperature ranges (DTR), and (i) gas transfer piston velocity (k600). Optimal model fits from null, linear, segmented, and logistic curves in bold foreground lines. For nonlinear segmented and logistic models (bi), plots are ordered by boundaries between ponds and lakes, as defined by model breakpoints or inflection points (vertical background lines).

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Figure 6

Relationships between lentic waterbody maximum depth (Max depth) and various ecosystem structure and function metrics: (a) methane fluxes (CH4 flux), (b) pH, (c) total phosphorus concentrations (TP), (d) total nitrogen concentrations (TN), (e) diel temperature ranges (DTR), and (f) chlorophyll a concentrations (Chl a) from literature data extraction with optimal model fits from null, linear or null, segmented linear, and logistic curves in bold foreground lines. For nonlinear segmented and logistic models (bf), plots are ordered by model breakpoints or inflection points (vertical background lines), indicative of boundaries between ponds and lakes.

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Figure 7

Relationships between lentic waterbody emergent vegetation cover (Emergent veg.) and various ecosystem structure and function metrics: (a) chlorophyll a concentrations (Chl a), (b) total nitrogen concentrations (TN), (c) total phosphorus concentrations (TP), (d) pH from literature data extraction with optimal model fits from null, linear or null, segmented linear, and logistic curves in bold foreground lines. For nonlinear segmented and logistic models (bd), plots are ordered by model breakpoints or inflection points (vertical background lines), indicative of boundaries between ponds and wetlands.

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To summarize across all three metrics (surface area, depth, and emergent vegetation cover), we evaluated where the boundaries of nonlinear relationships generally occurred, which informs boundaries between ponds, lakes, and wetlands (Table 1). For surface area, the boundary was 3.7 ± 1.8 ha (mean ± standard error) and the median was 1.5 ha, consistent with the median of 2 ha from scientific definitions (Fig. 2b). The depth boundary was 5.8 ± 2.5 m (mean ± standard error) and the median was 5.2 m, within the range of scientific definitions (Fig. 2c). The emergent vegetation cover boundary was 13.4 ± 6.3% (mean ± standard error) and the median was 8.2%, both of which were lower than the previously identified wetland lower bound of 30%31.

Table 1 Nonlinear boundary values, parameter estimate ± standard error (SE), from comparisons between surface area, maximum (max.) depth, and emergent vegetation (veg.) cover and ecosystem structure/function metrics including gross primary production (GPP), total phosphorus concentrations (TP), methane fluxes (CH4 flux), respiration (R), net ecosystem production (NEP), chlorophyll a concentrations (Chl a), pH, total nitrogen concentrations (TN), diel temperature ranges (DTR), and gas transfer piston velocity (k600).
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Pond morphology (e.g., size and depth) creates fundamentally distinct conditions that govern ecosystem structure and function. Specifically, ponds experience less wind-driven turbulence than larger waterbodies due to small fetch and sheltering from the landscape36. We found that gas exchange rates (k600) decreased at ~ 18 ha, presumably due to reduced wind shear (Fig. 5i; also supported by37) and altered thermal dynamics. For instance, ponds and shallow lakes can warm dramatically during the day, inducing stratification, and cool off and mix completely overnight38. We found higher diel temperature ranges were more common in waterbodies < 5 ha (Fig. 5h) and < 6 m (Fig. 6e; see also39). Such differences in temperature and mixing can promote internal nutrient loading40 and ecosystem respiration41, which may explain the higher TN (Figs. 4b, 5g), TP (Figs. 4a, 5b) and ecosystem respiration (Fig. 5e) found in ponds. Lastly, differences in water column mixing, increased nutrients, and higher respiration can all contribute to the higher greenhouse gas emissions found in ponds relative to lakes (Fig. 5d)4,42.

Metrics of phytoplankton biomass (chl a) and total ecosystem production in the water (GPP) exhibited weak or inconsistent relationships with surface area and depth, likely due to differences in the location and types of primary production across waterbody types. While total primary production in deep lakes is often dominated by phytoplankton43, shallow waterbodies can shift toward non-planktonic primary production like benthic algae or floating, emergent, or submerged macrophytes44. Ponds have pelagic phytoplankton, benthic algae (i.e., periphyton), and sediment rooted-submerged or floating macrophytes. In contrast, wetland productivity often predominantly occurs above the air–water interface45. Where emergent vegetation dominates, they may limit light and reduce water column nutrients, both of which are needed by phytoplankton and periphyton. Macrophytes can also modify water column and sediment geochemistry by providing autotrophic organic carbon and oxygen to rooting systems in the sediments46. Consequently, these opposing drivers can explain the high variability in primary production we observed (Fig. 5f, Table S2). Distinguishing ponds from wetlands will ultimately be aided by additional ecosystem measurements of metabolism, greenhouse gas production, and additional metrics (e.g., carbon burial) across shallow waterbodies with a range of emergent vegetation cover.

A functional pond definition

Our review of existing pond definitions highlights that surface area and depth are the most common variables used to define ponds; yet how small and how shallow a waterbody must be to classify as a pond is unclear, with definitions ranging by orders of magnitude. Emergent vegetation is a third variable useful in distinguishing wetlands from ponds, but the threshold value, > 30% emergent vegetation coverage for wetlands established at the US federal level, is not based on documented changes in ecosystem function. Comparing characteristics among waterbodies that scientists self-categorized into lakes, ponds, or wetlands, ponds were sometimes distinct from lakes and wetlands (pH, TN), sometimes similar to wetlands (TP), and sometimes similar to lakes (chl a), suggesting ponds are an ecologically distinct type of ecosystem. Lastly, we found clear nonlinear relationships when we examined relationships between ecosystem structure or function and surface area, depth, and emergent vegetation cover; these boundaries help to quantitatively define ponds.

Specifically, we found that across available ecosystem metrics, ecosystems shift in structure and function at average (± SE) values of 3.7 (± 1.8) ha in size, 5.8 (± 2.5) m in depth, and 13.4 (± 6.3) % emergent vegetation cover (Table 1). For surface area, all but one ecosystem metric (k600) was below 5 ha in surface area, which fits well within the range of most existing definitions (≤ 10 ha; Fig. 2), and we suggest may be used to distinguish ponds from lakes. For maximum depth, all but one ecosystem metric (chl. a) was below a 6 m depth threshold, which also fits well within the range of depths reported in pond definitions (Fig. 2), and matches the published threshold of 5 m maximum depth for shallow lakes44. Our depth analysis was less robust than surface area because we had less depth data, a common challenge in lentic studies47; we therefore advise further studies in waterbodies to explicitly evaluate this threshold. Until further work is done, we recommend using 5 m as a maximum depth threshold for ponds as it is close to both threshold shifts in ecosystem function and matches with the shallow lake literature44,48. We had the fewest ecosystem metric comparisons for emergent vegetative cover, and observed three nonlinear boundaries ranging from 6 to 26% cover. The mean (13.4%), though smaller, is not statistically different than the 30% emergent vegetation cover (one sample t-test, t2 = − 2.6, p = 0.12) proposed by Cowardin et al.31 to separate wetlands from lakes. We recommend separating ponds and wetlands using the 30% coverage in emergent vegetation threshold for now, but recognize that the Cowardin et al.31 metric is not data driven and our analysis was limited by existing data. Future studies must examine how ecosystem structure and function shifts across a gradient of emergent vegetation cover to better functionally distinguish wetlands from ponds and could ultimately lower that boundary.

Our review of data from the literature showed scientists and managers view ponds as permanent or temporary and natural or human made in origin. Therefore, we felt it necessary to provide the inclusivity of these concepts in a pond definition. Other definitions also link depth to light availability, where light penetrates to the sediments across the pond (e.g.,11). However, light availability is not only mediated by depth; even in the shallowest systems light can be limiting due to turbidity, dissolved organic matter, and submerged or floating plants (e.g.,49,50). For example, floating duckweed can cover most of a pond’s surface area and reduce light penetration to < 1% relative to the light above the water’s surface49, and dramatically change the ecology of shallow systems51.

As our analyses indicate that ponds are functionally distinct from lakes and wetlands, we propose the following scientifically informed pond definition (Fig. 8):

Ponds are small and shallow waterbodies with a maximum surface area of 5 ha, a maximum depth of 5 m, and < 30% coverage of emergent vegetation. Ponds will have light penetration to the sediments if water clarity permits and can be permanent or temporary and natural or human-made.

Figure 8

Conceptual model to define lentic waterbodies based on three different criteria (depth, surface area, and emergent vegetation). Boundaries for all three axes come from our analysis and are informed by existing pond, lake, and wetland definitions. Figure by Visualizing Science.

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Our proposed definition is based on the current state of the science; we anticipate that future research will further resolve differences among these five categories. For example, we call for future research to examine how ecosystem structure and function shift across our proposed boundaries, particularly for depth and emergent vegetation, which had smaller sample sizes and fewer ecosystem metrics than surface area. Additional variables such as basin geometry (e.g., area:volume ratios), sheltering from wind, water residence time, water clarity, and geographic location, may also affect a waterbody’s ecosystem structure and function, creating some overlap between classifications especially along the upper and lower bounds of our pond definition. For instance, a landscape with little wind sheltering increases water column mixing that could cause a waterbody the size of a pond to function more like a shallow lake. We therefore advocate for additional sampling of lentic waterbodies, especially in locations where lentic waterbodies are understudied or being rapidly constructed like tropical and subtropical regions52, to help resolve boundaries among waterbody types and further refine the pond definition.


Source: Ecology - nature.com

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