3.1. Article of S. Garthe, O. Hüppop [2]
Main provisions of the article. To one extent or another, this publication marked the beginning of a number of works on estimating the vulnerability of seabirds to the impact of wind farms. As far as the vulnerability index
WSI (wind farm sensitivity index) is concerned, it was based upon publications [
26,
29] (we have considered the first in [
1]).
Article [
2] presents the index of sensitivity
to wind farms (see
Table 2—Formula (3)) for 26 species of seabirds. The index is applied to compute seasonal (winter, spring, summer, autumn) and annual maps of the vulnerability of the exclusive economic zone of Germany in the North Sea with a grid of 6′ latitudes× 10′ longitudes each (total area~120 km
2). The final maps provided three levels of concern about the localisation of wind farms depending on percentile
WSI. The
WSI value is defined by the sum of the products of the natural logarithm of density of each bird species and its species-specific sensitivity index
SSIsp (sensitivity index). Bird density data were taken from ship observations with some adjustments or correction factor 1.3, based on the Baltic Sea data. Bird databases were also involved. Density in a grid cell for each species was obtained by dividing the sum of bird individuals, registered on a transect, by the total transect area, covered by cruises.
To calculate the sensitivity index SSIsp, the authors take nine factors into account. Each was rated on a 5–score scale of 1 (low vulnerability of seabirds) to 5 (high vulnerability). Five of these factors are based on real data about birds (factors b, c, f, g, h), though factor f is partially estimated based on observations. The remaining four (a, d, e, i) can be assessed only based on subjective judgements, also accounting for the experience of observation at sea. Experts corrected all primary estimates independently. The authors organized the nine vulnerability factors into three groups, comprising (A) flight behaviour (factors a–d), (B) general behaviour (factors e–f) and (C) status (factors g–i). For each group, an average score of the respective factors was calculated. These average scores were subsequently multiplied by each other to give the species-specific sensitivity index (SSI) for each species.
Let us note factors b, c, g, and h, with underlying quantitative data, which is necessary for further analysis.
Flight altitude (b): 5–score scale to account for the bird flight altitude is converted from six altitude classes (allowing for 50 and 90 percentiles) with ranges: 1 class—0–5 m; 2, 5–10 m; 3, 10–20 m; 4, 20–50 m; 5, 50–100 m; 6, >100 m. In all likelihood, this is a percentage of birds of a given species, flying within the specified altitude ranges. Flight time percent (c) or percentage of birds of a given species, flying over a given area, was assumed in the following ranges: 1 score—0–20%; 2, 21–40%; 3, 41–60%; 4, 61–80% and 5, 81–100%. Biogeographic size of populations (g): score 1 is assigned to the population containing more than 3 mln. bird individuals; 2, 1–3 mln.; 3, 500,000–1 mln.; 4, 100,000–500,000 and 5 for less than 100,000 bird individuals. Survival rate (h) for various species of birds: score 1, if h < 0.75; 2, h > 0.75–0.80; 3, h > 0.80–0.85; 4, h > 0.85–0.90; 5, h > 0.90.
It is also worth noting that as compared to the further described works, factor i incorporates both the population threat status, and the status of birds’ conservation in Europe.
Analysis of particular provisions of the article. Let us verify whether the conclusions obtained in the examined article are invariant. Conclusions based on the results of computations on any scale must not change at any permissible transformation on this scale (see
Section 2). Thus, for example, all computations can be made in miles or feet, rather than kilometres, though these are permissible transformations on a ratio scale, and in this case, we always arrive at the same conclusions based on the results of computations, irrespective of utilised measurement units. Let us now proceed from values 1, 2, 3, 4, 5 to values, e.g., 1, 2, 3, 40, 500. Any monotonic transformation of the initial ordinal data can be used to check the obtained final results. After such transformation, the ranking of species
SSIsp will change radically. Thus, among the five most vulnerable species (Black-throated diver, Red-throated diver, Velvet scoter, Sandwich tern, and Great cormorant), one new—Red-necked grebe (third by the degree of vulnerability) instead of Velvet scoter (which will become the 16th) will appear. Species occupied 1 and 2 places (Black-throated diver and Red-throated diver), will switch places. Species at the end of the list will also change. If Northern fulmar previously closed the list, it is the 15th on the list now, and its place will be occupied by Black-legged kittiwake, who held second to last place together with Black-headed gull (24–25th place). Mew gull will become the 25th on the list, though previously it had the 20–21
st place, and Black-headed gull will not lose its 24th position. The list will change substantially! However, if the problem lies in evaluating the most vulnerable species, the list (variation series), in this case, of such five species depends on the monotonic transformation of initial data for computations and can both remain unchanged, and change by one or several species. Of importance is that the use of particular values of ordinal quantities for the initial data changes the position of certain species in the final ranking of vulnerability
SSIsp at monotonic transformations (since ordinal quantities—the marks of the values of variation series—are merely numbers, rather than values, with which arithmetic operations can be performed).
With the foregoing as the background, as to the computation of means in
Section 2.1, it can be stated that only the values of one of the factors in each group can be taken as the arithmetic means from Formula (3). If, e.g., we have four factors of group
A with values 1, 1, 1, 5, the “ordinary” arithmetic mean will be equal to (1 + 1+1 + 5)/4 = 2. However, with allowance for the median theorem requirements, the median is to be taken as the mean, i.e., 1. It two-fold differs from the first. This alone (the use of “ordinary” arithmetic means, rather than the median) in any case will change the final conclusions (vulnerability ratios between species).
Likewise, in view of the foregoing in
Section 2.2, it can be stated that since
SSIsp is a product of ordinal quantities, these
SSIsp values fail to correspond to the real situation, since many
SSIsp values are incorrect when being compared to one another. Let us note for further use: all mean quantities from Formula (4), with allowance for what has just been said, can be considered ordinal quantities.
Once again, we turn our attention to the replacement of real metric values with their corresponding ordinal quantities, involving the replacement of corresponding ranges as well. Thus, for factor
g—biogeographic population size—ratio max/min ≥30. Given that, for survival rate
h, this ratio is merely about 0.95/0.73 = 1.30. However, real variation ranges of all other factors are also transformed into the range of ordinal quantities 1–5 (max/min = 5/1 = 5). Clearly, the ratio between individual values of ranges for each factor, including a particular max/min ratio, significantly affects the final value of
SSIsp. Additionally, replacement of real and, most likely, different variation ranges of the employed parameters with one and the same range (in this case, range 1–5) seriously distorts the final result of computations, even if the operation of multiplying ordinal quantities was justified. Let us also note that for five factors
a,
d,
e,
f,
i, no ratio between real minimum and maximum values are known even approximately (in addition, on principle, we do not measure factor
i in its usual sense), however, for ordinal values, the ratio is taken as equal to 5 ( =5/1) (also see our first article [
1]).
Summing up parameters
b and
c (percent scores (percentages) of birds at a particular altitude + percent scores of flying birds in relation to the total number of birds in the area) can hardly be correct as well. It is clear by default that species vulnerability
SSIsp is proportional to the percentage of birds, flying at the height of turbine blades’ operation in relation to the total quantity of birds in a cell. Further, this percentage, in its turn, constitutes the product of the percentage of birds, flying at the height of blades’ operation (
b as decimal quantities) and the percentage of flying birds (
c as decimal quantities as well) relative to the total number of birds at the specific section (vulnerability~
b ×
c). Additionally, all the remaining factors should be taken into account for this specific percentage. This remark is also relevant to the following works [
5,
6,
7].
Thus, all the results in work [
2] are obtained based on arithmetic operations with ordinal quantities, which is unacceptable. With allowance for this, the conclusions are non-invariant in relation to the permissible monotonically increasing transformation of data—ranking of species by
SSIsp changes significantly. When computing
SSIsp, the arithmetic mean values are used, rather than the variation series values. Products of ordinal quantities provide certain incorrect (and unknown to a researcher) values. For all the factors, whole-number values within the 1–5 range are taken, which fails to correspond to the real ratio between the values of ranges for various factors. Accordingly, the maps of vulnerability, drawn based on such calculations, are also incorrect.
Of certain importance is the provision, referred to by S. Garthe and O. Hüppop [
2]: “Debate on the effects of human activities on wildlife necessitates risk and impact assessments [
30] even where the database might be poor [
31]”. Indeed, the database can be low-quality, incomplete, deficient, and erroneous. Nevertheless, with the methodology of dealing with any data, any database must be mathematically justified, appropriate, and consistent with generally recognised methodological requirements, and the measurement theory requirements as well.
3.2. Article of R. Furness et al. [5]
Main provisions of the article. The authors mostly follow the work [
2], also using the same data, considering revisions and alterations due to new research data. Vulnerability indices are computed for 38 species of birds, dwelling in Scottish waters. No mapping of vulnerability/sensitivity is performed. Calculations use ten factors (
Table 2), actually, these are the same factors as in the work [
2]. Four factors (
e,
f,
g,
h), incorporated in the risk of collision with blades of wind turbines
Collision risk score (
CRS) (Formula (5)), are linked to the bird flight agility and flight behaviour, and two factors (
i,
j) (Formula (6)), defining the
Disturbance/displacement score (
Dist/
DispS) index of birds,—to using specialisation of habitat by birds and their susceptibility to disturbances. Each of these formulas contains the
Conservation importance score (
CIS) index, as a multiplier. It is defined, using four factors (
Table 2, Formula (7)), rather than three as in [
2]. Two factors (
c and
d) instead of one (
i), proposed in [
2], were applied as the conservation status. All the factors, except for
e (percentage of birds, flying at the height of turbine blades’ operation), are estimated as ordinal quantities in the 1–5 whole-number value range as well. Moreover, as opposed to factor
g, where scores are attributed according to the population size of each bird species (as in [
2]), factor
a is used in the work, where scores are attributed to the percentage of the biogeographic population in the Scottish waters. The scores were estimated as follows: 1, <1%; 2, 1–4%; 3, 5–9%; 4, 10–19%; 5, ≥20% [
4]. Since this index can vary depending on the season, in computations, the authors used the maximum season-wise score for each species.
What is principally new and important in [
5] is the breakdown of a single index of vulnerability into two. The first—
Collision risk score (Formula (5))—for the risk of collisions with the blades of wind turbines. The second—
Disturbance/displacement score (Formula (6))—for the risk associated with avoidance/displacement of seabirds depending on the degree of disturbance on the part of wind turbines, ships, and helicopters, and habitat change.
For
CRS in (Formula (5)) as compared to (Formula (4)), factor
e is given a greater significance (a higher weight). This factor is taken out as an individual multiplier, assuming that this is the main risk factor of collision with wind turbines. Such an approach to employing the factor of “flight altitude” is more logical and justified, since the death of birds directly from wind turbines, first and foremost, depends on what percentage of the total number of birds fly at the height of operation of the turbines’ blades. Of note is that this factor is a metric quantity, varying from 1 to 35% [
5], though it can also take the zero value, which other factors lack. It can be further used in making vulnerability maps. Of importance in computing anthropogenic impact is also the use of the percentage of the biogeographic population in the mapped area, here, in Scottish waters, rather than the total size of the population of birds of each species, because the larger this percentage, the stronger the corresponding negative effect on the overall population.
Analysis of particular provisions of the article. Actually, this article contains all the flaws of the work [
2]. The principal ones include unacceptable arithmetic operations with ordinal quantities, and, as a result, the uncertainty of some results due to using the operation of multiplying such quantities, and the arithmetic means for them in computations.
As in the case with the analysis of the work [
2] results, constancy of conclusions at a permissible transformation of the initial data as to
CRS (see Formula (5) in
Table 2) can be estimated. As should be expected, the final ranking of species will depend on the type of transformation, i.e., it can both change, and remain unchanged.
Of additional note is that the article contains no rationale for the multiplication of parameters i (disturbance/habitat displacement) and j (habitat specialisation).
Overall, to date, it is unclear, how two indices CRS and Dist/DispS can be jointly used. Everything suggests that each species of bird can be exposed to such different influences simultaneously, though CRS and Dist/DispS indices are still calculated separately, due to insufficient knowledge and information about this problem, and they are in no way compared and combined (not summed up).
3.3. Article of G. Bradbury et al. [6]
Main provisions of the article. This work follows publications [
2,
5] to a great extent. The formulas from [
5] are used. The work objectives are to present the sensitivity index
SSI for 54 species of seabirds, dwelling in the English waters; map densities of seabirds for these waters; combine these two results for seabird sensitivity mapping (maps of general sensitivity index
WSIwindfarm distribution—
Table 2, Formulas (8)–(13)). SeaMaST GIS–package (Seabird Mapping and Sensitivity Tool) is used for mapping.
WSIwindfarm index is calculated for separate segments of 9 km
2 (3 km × 3 km) as a sum
WSI for all the accounted bird species (
Table 2, Formula (8)). Indices
SSIcoll and
SSIdisp are computed according to Formulas (9) and (10). Prior to being used in
WSIwindfarm, they are ranked: values
SSIcoll for 5 ranges—score 1 for values 0–42; 2, 67–187; 3, 200–400; 4, 420–817; 5, 960–1470;
SSIdisp values for 4 ranges: score 1 for values 1–5; 2, 6–8; 3, 10–18; 4, 22–32; maximum score—either
SSIcoll or
SSIdisp is selected for each species. To forecast the density of the species of seabirds (
dencsp), the authors used estimates of parameters, obtained in the DSM–model [
32]. Due to the inhomogeneity of data, bird density maps were made only for 32 species. Seasonal (summer and winter): (1) maps of sensitivity to the risk of collision with turbine blades, employing only
SSIcoll values (Formula (9)); (2) maps of sensitivity to bird habitat flexibility, employing
SSIdisp values (Formula (10)); and (3) general maps of sensitivity
WSIwindfarm (Formula (8)) were drawn. To compute
SSIcoll and
SSIdisp, ten factors are used (
Table 2), actually, these are the same factors as in the publication [
5], though accounting for coverage and including updated data.
Analysis of particular provisions of the article. Overall, all the remarks, given as to the two previously discussed publications, also relate to this work. However, there are several considerations on the presented algorithm in terms of comparing and summing up SSIcoll and SSIdisp.
The authors of the examined work draw attention to the fact that “the top rank ‘Very High Risk’ was not assigned for displacement concern, acknowledging the lower risk to populations compared to collision risks”. SSIcoll and SSIdisp values after computation by Formulas (9) and (10) are ranked (for SSIcoll—5 scores, for SSIdisp—4 scores), since, according to the authors, “the two resulting scales should not be compared in a quantitative way but only in terms of the species ranking within one scale”. Actually, the work contains a comparison between calculated score values (sub-ranges) SSIcoll and SSIdisp of two scales, which are then taken to one scale after repeated ranking. When two quantities are compared on any scale (the greater of two is found), it is actually a comparison of quantitative values: one value is higher than the other. If the values are compared on an ordinal scale, they are estimated in an expert way: one is strictly higher than the other, though on a metric scale (on one and the same ratio scale or an interval scale) the values of these two quantities can be unknown. Further, it is not excluded that comparing values are on different metric scales. Then, such comparison is not possible.
Indeed, SSIcoll and SSIdisp must be summed up, though not in this way: it is impossible in the context of the proposed model. These values should be estimated in terms of quantity and compared on one and the same scale. If this is possible, basically, such values for the impact of collisions and habitat change can be identical or very close: on one part, for the birds, flying at the height of blades’ operation, on another part, for the birds, flying beyond the area of their impact (if the impact estimates are made on various ratio scales, in any case, some kind of comparison between these impacts can be performed). Then, the computation, if made with such values, by Formulas (8)–(10), would provide an almost two-fold lowered value of WSIwindfarm, since one of the impacts would not be taken into account. This problem, as we see, must be solved in terms of a strictly metric approach, and, as it has been above-mentioned, at the moment, it is not solved, since there is not enough knowledge and information about mutual consideration of these impacts. Analysis of this problem is beyond the scope of the present work. If it is impossible to compare SSIcoll and SSIdisp on a single metric scale, two different maps of vulnerability need to be drawn: based on SSIcoll and SSIdisp.
3.4. Article of G. Certain et al. [7]
Main provisions of the article. The article, based on the development and enhancement of the approaches from works [
2,
5], suggests a more common, and, as the authors write, “universal approach” to vulnerability—to not only the impact of wind turbines at sea on birds but also, on the whole, to any anthropogenic impact on any biological components of the ecosystem. Bird vulnerability to wind turbines at sea in the Bay of Biscay and vulnerability of benthos in the Barents Sea to the impact of bottom trawling are evaluated. We shall further consider only the impact on seabirds since, for various biological objects, basic methodological approaches are almost the same. The algorithm, proposed in [
7], as has been said at the beginning of our article, is applied in the work [
10] to estimate the vulnerability of marine avifauna to oil.
Indices of sensitivity to the risk of collision and the risk of avoidance of wind turbines for 30 species of seabirds are computed in the model of G. Certain et al. [
7]. Final calculations in the form of maps were made for the 5 km × 5 km areas for winter and spring periods. Abundant species based on the results of winter aero- and ship observations in spring were taken into account with allowance for quantity
pij, proportional to the number
ith of species at the
jth segment. As a result, a diagnostic panel with four maps for the mapped region is presented: (1) vulnerability of seabird communities to collisions with wind turbines (Formula (15)), (2) vulnerability of seabird communities to a disturbance on the part of wind turbines (Formula (16)), (3) map, reflecting a certain extent, the relative number of birds in the mapped region based on the
Aij value, and (4) an integral (synthetic) map, reflecting this information in a combined manner.
Three groups of factors are considered for each bird species, when calculating their vulnerability, as in the work [
2]. The analysis of the Formula (4) for
SSIsp by G. Certain et al. [
7] enables substantiation of the equations for these groups of factors:
ci—the individual vulnerability of seabirds to collisions with wind turbines (Formula (17)),
di—the individual vulnerability to concern and disturbance of normal vital activity of birds due to wind turbines and habitat change (Formula (18)),
si—species sensitivity determined by relative indices of elements, that describe the species conservation status and their recoverability after the exposure (Formula (19)).
G. Certain et al. [
7] account for ten various factors (
Table 2). Six factors (
F1–F6), relating to
ci and
di, are almost identical to those in [
2]. Four factors (
F7–F10) are taken into consideration to estimate species sensitivity: three factors of conservation status (
F7–F9) instead of one
i (European threat and conservation status) as in [
2] and
F10—a survival rate of adult bird species, the same as in [
2], though there is no factor of the biogeographic population size. As compared to [
5,
6], factor
a (percentage of biogeographic population) is not used, and the third factor
F7 is added to the two conservation ones. All the factors are estimated within the range of whole-value numbers 1–5, as in the three previous works, but taken to the scale 0.2, 0.4, …, 1.0. The values of factors are actually the same as in works [
2,
5], though accounting for mapping area and with some alterations and updated data.
An essential provision of the considered article includes the breakdown of anthropogenic factors into primary (a), which directly define vulnerability or sensitivity, and aggravation (g), which can be inessential as autonomous, though increasing the already existing vulnerability or sensitivity. Formula (14), based on a hierarchy of factors, is proposed, which, according to the authors, can be clearly formulated.
Analysis of particular provisions of the article. The authors write that “As these factors are all expressed on the same scale, they can be mathematically combined together”. However, all of them are specified on an ordinal scale, and failure to take this into account leads to a number of problems and inconsistencies.
Compensation between factors and their hierarchy. G. Certain et al. [
7] combine factors somewhat differently than in the three previously discussed works, accounting for, as they write, their different interaction with one another. The authors consider two ways of their combining: averaging and multiplication, as was suggested in [
2] and further used to a certain extent in the works [
5,
6]. G. Certain et al. [
7] note that averaging allows for compensation between factors, namely, a high value of one factor can be compensated with a low value of another (what is suitable for the factors of various natures), and multiplication can be convenient (appropriate), when factors are interacting, or when they are conditional to each other.
Overall, all these statements as to the two specified operations and their relationship with compensation and hierarchy are not quite correct. One cannot fully agree with the statement of G. Certain et al. [
7], that averaging, or multiplication of factors does not admit (does not account for) any hierarchy between factors. One of the factors from the
product can have the exponent, which is greater or less than one, hence, the contribution of this factor will differ upward or downward from that of others, depending on whether the factor value is greater or less than one. In
summing up or averaging several factors, the most important factor can have a multiplier other than 1. Then, when summing the factors up (fundamentally different, though on one and the same scale), if one of them has multiplier 2, and others 1, it is clear that as the value of this factor increases, its contribution to the final result will grow two times faster than the contribution of the others (although, it is not necessarily that its contribution will be two times greater than of the others). However, in this case, such a multiplier has no relation to the remaining factors, i.e., when this factor changes, the change in the final quantity, which it affects, depends only on the change of this factor with multiplier 2.
For further analysis, let the approach [
7] be assumed and considered in terms of the permissibility of actions with the used quantities, i.e., conventionally taking them as a metric, rather than ordinal. It is essential to analyse general formulas of computing
ci,
di,
si (Formulas (14) and (17)–(19)).
Individual vulnerability (ci) to collisions with turbine blades. For this quantity (Formula (17)), the authors distinguish the factors in the context of their hierarchy. Factors Fi1 (percentage of time in flight) and Fi2 (percentage of time at the height of blades’ operation in relation to the total flight time) are deemed the key factors of collision with turbines’ blades and directly define vulnerability. Manoeuvrability (Fi3) and nocturnal activity (Fi4) are aggravating factors that can worsen the existing vulnerability.
Time spent by a bird at the height of the blades’ operation
Fi2, is considered depending (determined by) on
Fi1, hence, the authors use a multiplication ratio between them. Multiplication of
Fi1 and
Fi2 produces the percentage of all birds, flying at the height of turbines’ blades operation relative to all flying birds of the species in this section. Conversely, the authors assume that it is beyond reason to assume any relationship between manoeuvrability and nocturnal activity, at least, as related to their contribution to vulnerability to collision with wind farms. Additive ratios between
Fi3 and
Fi4 are therefore used [
7]. These two different quantities, of which the meaning and impact on the final result are not clearly described, are defined in an expert manner and summed up.
Moreover, at the value , i.e., when all the birds from a segment fly and all of them fly at the height of the blades’ operation, there is merely not any influence (aggravation) neither on the part of Fi3 nor Fi4 (if Formula (17) is followed): 1, in any case, remains unchanged, i.e., at any values Fi3 and/or Fi4, ci will remain to be 1. However, it is very weird! The same relates to Formulas (17) and (18). As to Formula (18): if Fi7, Fi8, Fi9 = 1 (out of values 0.2–1), which corresponds to a very high degree of conservation at all levels, then always si = 1 irrespective of Fi10. However, it appears that the proposed model is not quite functional on the whole (also see uncertainty in values Cj and Dj below).
Individual vulnerability (di) to concern and disturbance of normal vital activity of birds due to habitat change and disturbance of birds in relation to a wind farm, ship traffic, and helicopters, is computed by Formula (18). It is assumed that this is a combination of a primary factor—the intensity of behavioural response to anthropogenic activity (Fi5) and a factor of aggravation—flexibility in using habitat (Fi6). No influence of Fi6 on Fi5 at Fi5 = 1 has been reported in the foregoing. It implies that at the such maximum value of Fi5, various values of habitat flexibility (Fi6) affect in no way an individual vulnerability of species to disturbance and habitat displacement di. However, it is hardly correct as well.
Species sensitivity si depends on the combination of four factors, three of which are associated with regulatory conservation statuses of species at various levels, namely, international, European, and national—Fi7-Fi9, as primary factors, and the parameter of adult survival rate of species (Fi10), as aggravation factor. The value of si is computed by the Formula (19).
Uncertainties in some final values Cj and Dj. As has been shown above, all three parameters (ci, di, si), included in the denominator of Formulas (15) and (16) can take values equal to 1. Then, we will obtain Cj and Dj with an infinite value, which is unacceptable! Formulas (models) must be applied within the entire presented (permissible) range of variation in the initial data, which is not observed in the assumed model. Hence, this model cannot be regarded as correct and adequate.
Total bird vulnerability to the impact of wind farms. As in the previous works, the total vulnerability is not calculated. It does not allow for ultimately assessing the final vulnerability of such projects relative to seabirds.
General considerations on accounting for diurnal and nocturnal activity. This article, as the three above-mentioned, combines four parameters in one formula: flight time percentage, flight height, flight manoeuvrability, and nocturnal flight activity (Formulas (4), (5), (9) and (17)). Nevertheless, here, no assumptions are made, no rationale or proof is provided as related to the fact that the first three factors change somehow or remain unchanged during nocturnal flight. E.g., all three such factors change equally proportional to nocturnal activity. Or they, and vice versa, change variously: for some species, the values of some factors decrease, and for others—increase. However, any model is built based on proofs and rationale, or, at least, assumptions. Unfortunately, neither this article nor the other discussed above contain anything of these. The parameter of nocturnal activity and other factors (factor) are just summed up. However, it is incorrect, even if the fact is omitted that all these factors are ordinal quantities. In any case, the approach, proposed in the analysed works, to nocturnal activity, likewise to the other factors, as to ordinal quantities, is incorrect and leads, when used in calculations, to wrong final decisions.
In view of the conducted analysis of the article [
7], it can be stated that the conclusions and recommendations obtained therein for estimating the anthropogenic impact of offshore power plants on seabirds cannot be considered correct and justified. Hence, the proposed approach cannot be applied to estimate other anthropogenic impacts on the particular components of marine biota as well.
3.5. The Wildlife Sensitivity Mapping Manual [8]
Main provisions of the Manual. This Manual [
8] is a comprehensive compendium of the information necessary to develop wildlife sensitivity mapping approaches to inform renewable energy deployment. Such maps should be a standard precursor to all renewable energy plans and development. We focus only on the part of “Step-by-step approach to wildlife sensitivity mapping”, namely, on the assessments of the biological objects sensitivity for the developed maps. The Manual states that data relating to the Natura 2000 network, collected on the base of a 10 × 10 km grid, can provide a good basis for data generation.
We will give a brief summary of the basic, somewhat simplified, approach to assessing sensitivity for mapping a selected area (without classifying certain core features, such as protected areas, as no-go sites and less sensitive, secondary locations, as sites where development could prove problematic and where caution is advised). More complex mapping exercises assign sensitivity by weighing features in relation to known parameters that increase sensitivity [
8]. Taking into account the recommendations given in the Guidance, it is proposed to identify the types of renewable energy infrastructure and which biota species and their habitats are likely to be affected. Next, to compile distributional datasets on sensitive species, habitats, and other relevant factors. Then, to develop a sensitivity scoring system for the species presented in the area. On the basis of GIS, to generate corresponding maps and develop a system for interpreting data on these maps.
In terms of developing a sensitivity scoring system for wildlife, it is necessary to select the main factors that determine the sensitivity of the species in the mapped area. These factors are
species characteristics (species behaviour, species morphology and migratory behaviour);
habitat characteristics (habitat fragility, and habitat dependence);
population dynamics (proportion of global/regional/national population);
conservation status (global, EU, regional or national conservation status) [
8].
The Guidance notes that once a list of at-risk species and habitats has been created, these can be scored in terms of the level of their sensitivity. Such lists should be based on a thorough investigation of the scientific literature and through consultation with key experts [
8].
On a theoretical example, for four species of biota, scores are given for morphological, behavioural, and population dynamic characteristics, as well as for conservation status. The following scores are accepted for the first three characteristics: 1 (low), 2 (medium), 3 (high), 4 (very high sensitivity); and for conservation status: 0 (low), 2 (medium), 4 (high), 6 (very high). The following ranges of overall sensitively scores are accepted for the summed scores: Medium (3–8), High (9–14), and Very High (15–20). Besides, any species scoring 3 or 4 for morphology/behaviour/population dynamics is automatically in the High category [
8]. In other words, for the first species, the sum of the scores is 5, since according to the morphology parameter, it has a score of 3 (high sensitivity), then the result (sensitivity score) is assigned to the High range (9–14).
Next, in the general case, for each grid cell, the sensitivity scores of all presented species are summed up, if necessary, with weight coefficients, such as the number (density) of species or proportion of the global or regional population of each species present.
Analysis of particular provisions of the Manual. Analysis of calculations based on the use of ordinal quantities in arithmetic operations (which is used in this methodology), were held in the first work [
1]. It is shown that such calculations give uncertain and incorrect results: conclusions based on the results of simple summing of ordinal quantities are changing with permissible monotonous transformations on such scale. It is obvious that this conclusion does not depend on whether the weight coefficients are used (even specified on the ratio scale) or not. Summing and multiplication of ordinal quantities are unacceptable according to ([
21], and other references in [
1]). In addition, the range of changes of all values of sensitivity characteristics is identical (1–4), except for conservation status. It also aggravates the negative situation, since the ranges, in reality, are most likely different.
3.6. Some Considerations on Taking into Account the Factor of the Seabirds Flight Altitude and the Impact of Other Factors on It
As appears from the considered above works, many factors impact the bird vulnerability to offshore wind farms. At the same time, the bird flight altitude
hsp is a key influencing factor. In turn, other factors impact it as wind speed and direction, rain and precipitation, visibility and cloudiness, time of the day, season, foraging, migration, distance to coast, habitat type and spatial arrangement, offshore wind farms, fishing boats and ships, and the others [
33]. Therefore, initially, it is important to know the dependence of this key parameter on these factors. However, such consideration is absent in the analysed works. We very briefly dwell on the impact of different factors on
hsp since the main aim of our research is to show, based on provisions of mathematics with ordinal data, the incorrectness of conclusions in the analysed articles.
There are developed models (methods) for taking into account the dependence of
hsp on the series of influencing factors (for example, see [
34,
35]). They explain from about 10–67% till 95% of the
hsp variability. In an elementary case, the method of the research and calculation
hsp =
f(
factors) is brought to the following. For single species of birds, the measurements of their flight altitude (altitude range) and factors affecting
hsp are carried out for areas with wind farms and for areas where wind farms are absent. Different methods can be used for the detection the flight altitude, including visual observations, a laser rangefinder, a radar of sea observation [
34]. As we understand, data on
hsp as results of visual observations are hardly suitable for further analysis since they have a large inaccuracy. The value
hsp should be measured with sufficient accuracy for solving such issue. Detailed and accurate observations of the bird location relative to the position zone of wind farms area and blades of single installations are also important. The most suitable instrument, in this case, is radar. The 5 cm radar is ideal for bird detection [
36]. Military radars, due to use of several rays combined into one [
37], make it possible to obtain three target coordinates that, in this case, gives the opportunity to solve practically all issues of ornithological observations. Based on the result of the field research, an array of measurement results is formed. Then, using one or another mathematical tool, for example, the factor analysis, the most significant factors (
x1, x2, x3, …), which impact the birds’ flight altitude (
hsp), are detected. At the final stage, the corresponding regression equation
hsp = f(x1, x2, x3,
…) of the flight altitude dependence on most significant factors is calculated. Another method is presented in [
35].