4.1. Image Analysis
Figure 12 summarizes the evolution of the area covered by the vegetation of the different test beds. The percentage of change in the area covered between the months of study, namely between December 22
nd, 2021, and June 20
th, 2022, was marked with dark points. There was a generalized increase in the area covered by vegetation during the period when digital analysis was performed, with a global average of 19.55% and a maximum of 39.2% for test bed 10. An exception was observed for test bed five, which presented a negative coverage change.
In the northern part of test bed three, there was a small increase in the area covered but, in the southern zone, there was almost a doubling of the area covered with vegetation, which can be justified by the strong presence of
Trifolium angustifolium. This species showed a high capacity to reseed in the test beds where it was previously sowed, as, in the end of the period under analysis, it was present in all of them. Also, it showed the ability to colonize other test beds, since it spontaneously appeared in test beds 3, 4, 5 and 6. The high persistence of this species has already been documented previously by other authors, in similar climates, by comparison to other annual self-reseeding legumes [
26].
For test bed four, there has been an increase of 0.68 m
2 in vegetation and it was completely dominated by the annual climbing species
Lathyrus tingitanus. This is in accordance with the growth and development habits of this species, documented by other authors as having the greatest canopy heights and providing the most ground cover in comparative trials with other legume species [
27,
28].
Regarding test bed seven, there has been an increase of 0.48 m2 of vegetation, and, for test bed eight, as in most of the other test beds, an increase in the area of vegetation occurred for both areas. At the end of the study, the total increase in vegetation was 0.62 m2 for this test bed.
Concerning test bed nine, the values in
Table 2 indicate that there has been an increase of 0.92 m
2 of vegetation area. This was justified by the presence of specimens of
Trifolium arvense, which predominate in the test bed.
For test bed 10, on both sides of the test bed, there is an increase of 0.98 m2, and this increase is higher in the southern zone. This could have been caused by the existence and great development of Holcus lanatus specimens, which prevail in the southern zone of this test bed.
Regarding test bed 11, the area in the northern zone increased more than in the southern area. Thus, at the beginning of the study, the area of covered vegetation was 0.64 m2 and, at the end of the records, its area became 1.07 m2, which translates to an increase of 0.43 m2. This increase can be reflected by the large growth of Trifolium arvense, which began to develop during the month of April.
In test bed 12, there was an increase of 0.46 m2 in the area of vegetation, which may be a consequence of the presence of a high number of Trifolium arvense specimens in the southern part of the test bed, and, in the northern part by the existence of specimens of Vulpia myuros, which, in the meantime, have developed.
Trifolium arvense is referred by other authors as being relatively independent of dormancy habits, with the ability to germinate whenever soil moisture and temperature conditions are favorable, particularly in spring, and well adapted to low rainfall and extreme temperature environments [
29]. Specifically for green roofs, it is also referred as being drought tolerant and a dominant species [
30]. This corroborates the observed behavior of this species in the test beds, related to dominance and to the relatively easy adaptation to the conditions of the rooftop.
Some small sources of error could be identified and must be noted. In the spring months - the end of March until the end of June - some flowers began to appear, thus contributing to the increase of the vegetation area, but these were not in bloom throughout all these months, and some did not develop at all. Adding to these, there are also factors resulting from meteorological conditions, such as the wind that, in taller plants, can cause them to occupy a larger area momentarily because they are inclined.
As mentioned in section 2.3, test beds with an increase of 0.50 m2 or more were considered for further analysis (test beds two, four, eight, nine, and ten). For these, it was possible to see that the species that occupy a larger area are, for test bed two, the specimens of Teucrium scorodonia and Trifolium angustifolium, for test bed four, the specimen of Lathyrus tingitanus, for test bed eight, Dittrichia viscosa, Teucrium scorodonia, and Trifolium angustifolium. For test bed nine are Trifolium angustifolium, Trifolium arvense, Teucrium scorodonia, and Rosmarinus officinalis. Finally, for test bed ten, are specimens of Teucrium scorodonia, Trifolium angustifolium, Holcus lanatus, and Dittrichia viscosa.
Except for test bed number five, it is possible to conclude that, in general, the percentage of area covered by vegetation has an increasing trend during the study period.
Finally, it should also be noted that there are species that, despite not being relevant in contributing to the increase of vegetation cover, are present in most of the test beds, being the spontaneous species Geranium purpureum, Laphangium luteoalbum and Vulpia myuros and, sometimes, of those previously planted, Trifolium angustifolium.
4.2. Vegetation Analysis
Considering the data presented in section 3.2, it is possible to note that several plant species appeared spontaneously: Bromus madritensis, Centaurium grandiflorum, Dittrichia viscosa, Geranium purpureum, Holcus lanatus, Laphangium luteoalbum, Lathyrus tingitanus, Silene vulgaris, Trifolium arvense, and Vulpia myuros, being all native species, except for L. luteoalbum, which is a non-invasive exotic, and that some of the vegetation emerged from previous introductions: Lavandula stoechas, Rosmarinus officinalis, Brachypodium phoenicoides, Asphodelus fistulosus, Antirrhinum linkianum, Briza maxima, Centranthus ruber, Papaver rhoeas, Reichardia picroides, Stachys germanica, Teucrium scorodonia, Trifolium angustifolium, and Anagallis arvensis (
Table 4).
The Brachypodium phoenicoides specimens present in test beds six, seven, 11, and 12 may have arisen from the NativeScapeGR project in 2014, which planted them in test beds one, three, five, seven, and nine.
On the other hand, the existence of Antirrhinum linkianum in test beds three, seven, and 11 could be justified by its pre-planting in 2018, following the ApiWall project, in test beds one, two, three, four, eight, nine, and ten.
Regarding the Reichardia picroides specimens, they were installed in test beds two, three, four, eight, nine, and ten at the time of the ApiWall project, in 2018, and are currently unintentionally in test beds seven, 11, and 12.
The Stachys germanica specimens exist only in test bed seven, however, they were planted in test beds one, two, six, and eight, in 2018, by the ApiWall project, and, in 2020, they were installed in test beds six and seven according to the ApiMat project.
The spontaneous existence of Teucrium scorodonia specimens in test beds seven and nine, on the other hand, should be based on their previous sowing in test beds one, two, six, and eight in 2018, for the ApiWall project, and in test beds six and seven, at the time of planting for the ApiMat project.
The existence of Briza maxima specimens in test bed nine must be justified by their installation in 2018, for the ApiWall project, in test beds one, two, six, and eight, or else by their subsequent planting in test beds six and seven on behalf of the ApiMat project.
As for the Rosmarinus officinalis specimens in test bed nine, this must originate from their planting in 2014, by the NativeScapeGR project, which installed them in test beds one, five, six, and eight.
The existence of Centranthus ruber specimens in test bed ten may have come from the ApiWall project, which planted them in test beds one, two, three, four, five, seven, and eight.
Finally, it is possible to understand that, despite the plantations, the sowing, and the transplantations in certain test beds, the vegetation could propagate to other test beds, which means that, in a green roof, for these species and conditions, it is likely to expect such a behavior. As previously noted [
31], the colonization by spontaneous species in a green roof may not necessarily be considered a failure, as it is also an opportunity to improve the functioning of the system and to achieve a more balanced system, closer to natural conditions. In the present situation, not only the colonization by spontaneous species, but also that of neighbor test beds by introduced species, denote an approach to natural equilibrium of the green roofs mimicked in this study, as the better adapted species thrive and are able to install in new locations.
4.3. Responses obtained to the survey
Through the survey, it was possible to understand the preferences of the population, their willingness and availability to install a green cover, and how much information they have about the subject. The results indicate that the most chosen plants by the population were Lathyrus tingitanus, Rosmarinus officinalis, Lavandula stoechas, Papaver rhoeas, and Anagallis arvensis. That is, people chose the plants they are more familiar with and that bring more color - through larger flowers and, consequently, more visible - to the green roofs.
Regarding familiarity with the subject of green roofs, from the 220 respondents, only 157 said they were familiar with the subject, which indicates that there is still some lack of information on the subject among the population.
Finally, the third objective of this survey consisted in understanding the disposition of the respondents towards the possibility of installing green roofs in their residences and, from the total sample, 141 answered that they would install them without any kind of financial incentive from the government, 46 would only install them if they had access to support and 33 answered they would not install them, regardless of the existing support.
Given the answers, it can be concluded that the measures created, such as monetary incentives, allow more people to be willing to install green roofs, which end up having an impact on the common life of all citizens. These results also show that more research is needed on this topic to increase knowledge, and the variety of species available, and to find more attractive and equally favorable specimens for green roofs.