Next Article in Journal
Value Management: Enterprises’ Interest in Stakeholders and Its Impact on Creating Sustainable Relationships with Suppliers and Buyers
Previous Article in Journal
Is More Always Better? Government Attention and Environmental Governance Efficiency: Empirical Evidence from China
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Analysis of Plastic Ingestion by Juvenile Loggerhead Sea Turtles (Caretta caretta) Stranded from Tenerife, Canary Islands

by
Marina Tortosa
1,*,
Juan Jesús Bellido
1,2 and
José Carlos Báez
3,4
1
Department of Animal Biology, University of Málaga, 29016 Málaga, Spain
2
Aula del Mar Mediterranean Foundation, 29004 Málaga, Spain
3
Oceanographic Center of Malaga, Spanish Institute of Oceanography (CSIC), 29640 Málaga, Spain
4
Ibero-American Institute for Sustainable Development, Universidad Autónoma de Chile, Temuco 4810101, Chile
*
Author to whom correspondence should be addressed.
Sustainability 2024, 16(16), 7147; https://doi.org/10.3390/su16167147
Submission received: 11 July 2024 / Revised: 9 August 2024 / Accepted: 17 August 2024 / Published: 20 August 2024
(This article belongs to the Section Sustainability, Biodiversity and Conservation)

Abstract

:
The exponential rise in plastic debris in oceans poses a severe threat to marine biodiversity, including loggerhead sea turtles (Caretta caretta) due to their widespread distribution and feeding habits. The present study aimed to assess plastic ingestion in juvenile loggerhead sea turtles stranded in Tenerife, Canary Islands. Among the 312 turtles admitted to the Wildlife Recovery Center “La Tahonilla” from July 2018 to November 2020, bycatch (20.8%) and entanglement (15.4%) were the primary admission causes, with significantly higher strandings in the island’s western region. Of these, 37 turtles (11.9%) had ingested plastic debris, totaling 546 pieces (average 14.59 ± 26.57 per turtle). Predominantly, filaments (44%), sheets (34%), and fragments (23%) were identified, with most being macroplastics (67%) in white or transparent colors. These findings, consistent with similar studies, underscore loggerhead sea turtles’ role as bioindicators of sea water pollution. They also highlight the urgent need for sustainable practices to mitigate plastic pollution in marine environments, preserve marine biodiversity, and achieve global sustainability goals.

1. Introduction

According to the Organization for Economic Co-operation and Development [1], an estimated 13.8 million tons of plastic enter the oceans annually, accounting for 80% of total marine debris [2]. Plastic presents a significant environmental threat due to its prolonged biodegradation, lasting potentially hundreds of years [3,4]. This persistence presents grave dangers to numerous organisms, as they may ingest or become entangled in plastic debris, especially those unable to distinguish it from food [5], such as various species of sea turtles [6,7,8]. The incidence of marine debris, especially plastics, and its high potential to cause damage to the marine environment has led to its recognition as a global problem, and it is currently included among the main threats affecting marine biodiversity [9].
Sea turtles are among the most impacted wildlife groups by marine debris [6]. Plastic ingestion has been documented across all seven sea turtle species [5,7,10,11,12]. Various characteristics make them susceptible to ingesting substantial quantities of marine litter or becoming entangled in items such as fishing gear [5,13]: they have an extensive distribution in European waters, including the Atlantic and Mediterranean [14,15,16,17,18,19]; inhabit diverse habitats and exhibit varied feeding behaviors throughout their life cycles [20,21]; often dwell within the upper layers of the water column, where plastic debris accumulates [22,23,24]; and are indiscriminate feeders [25]. This vulnerability positions them as valuable bio-indicators for assessing the impacts of marine debris in European waters [26].
Six species can be seen in Canary Islands waters, which are, in order of abundance of sightings: loggerhead turtle (Caretta caretta), green turtle (Chelonia mydas), leatherback turtle (Dermochelys coriacea), hawksbill turtle (Eretmochelys imbricata), olive ridley turtle (Lepidochelys olivacea), and Kemp’s ridley turtle (Lepidochelys kempii), with the last two being rare sightings [27,28]. The loggerhead turtle, the most commonly observed species in the Macaronesian region and in the Canary Islands [29], frequents this region in search of food during its oceanic juvenile stage [22,30]. This stage occurs from 7 to 11.5 years approximately for loggerhead turtles, when they reach an approximately size of 46–64 cm curved carapace length [22,31]. However, carapace length is not a precise measure of age, sexual maturity and feeding strategy [20].
Genetic studies on loggerhead turtle juveniles located in the Azores [32] and Madeira [33] suggest that these juveniles primarily originate from the eastern coast of the USA. In the Canary Islands, genetic analyses show the presence of juveniles from breeding populations in Florida, Mexico, and Cape Verde [34,35]. Historical nesting records exist for the island of Fuerteventura [36], although it does not currently nest naturally in the Canary Islands [29]. Currently, the loggerhead turtle is classified as “Endangered” on the Red List of Threatened Species by the International Union for Conservation of Nature (IUCN, www.iucnredlist.org/species/3897/119333622, accessed on 8 July 2024). Although global extinction of the species is improbable in the short to medium term, it is considered vulnerable due to the status of some of the subpopulations, which should be assessed independently [37]. In the Canary Islands, at least three subpopulations are found: Northwest Atlantic and Mediterranean subpopulations, listed as “Least Concern”, and the Northeast Atlantic subpopulation, listed as “Endangered”.
Recent studies have shown a correlation between plastic accumulation on Tenerife’s beaches and the surrounding currents, with debris from the North Atlantic Ocean gyre being carried towards the north and northeast of the island [38,39]. The eastern coast of Tenerife, influenced by strong currents, waves, and wind [38,39,40], has the highest levels of plastic pollution, with more than 1200 items (all of them between 1–5 mm) per square meter [39,41,42,43].
The first aim of this study was to determine the frequency of plastic ingestion by juvenile loggerhead sea turtles in Tenerife, Canary Islands by quantifying the presence of plastics in both the gastrointestinal tracts of deceased turtles and the feces of live specimens. The second aim was to characterize the plastics in terms of type, size, and color. Additionally, the study examined the relationship between the frequency of plastic ingestion and factors such as the body condition index (BCI) of the turtles, the stranding location, and the cause of stranding. This case study provides valuable insights into the impact of plastic pollution on the conservation and biology of sea turtles in the Canary Islands.

2. Materials and Methods

2.1. Area of Study and Sample Collection

All turtles sampled in this study belong to loggerhead turtles and were found on the coasts of the island of Tenerife, from July 2018 to November 2020, stranded on the beach, floating adrift, entangled or accidentally captured by fishing gear. They were taken to the Wildlife Recovery Center (WRC) “La Tahonilla” (Tenerife) and received an identification number and an individual record documenting the municipality of location, date and presumptive diagnosis upon admission. Biometric data, such as weight and carapace length measurements, were also recorded (see Appendix A, Table A1).
During their stay and recovery at the center, the turtles were kept in individual tanks, and they were fed three times a week with sardines, anchovies, and crustaceans. The daily food amount for each turtle was calculated in relation to the size of the animal and corresponded to approximately 5% of its weight. Tank water was changed every two to three days depending on turtles’ condition.
Sample collection was carried out following the INDICIT protocol [44]. INDICIT is a project funded by the European Union committed to support the implementation of the Marine Strategy Framework Directive (MSFD) [45] by developing a set of standardized tools for monitoring the impacts of litter on sea turtles. This protocol proposes a specific methodology for assessing ingested marine litter, including its composition and abundance, evaluating its impact on marine environments and establishing threshold values for its presence in turtles [44,45].
Following this protocol, sampling can be performed both in live and dead individuals. For live turtles, fecal samples were collected and the tank water was visually inspected for the presence of plastics. For deceased turtles, necropsies were performed, and the contents of the esophagus, stomach, and intestines—key areas for the presence and accumulation of marine debris—were analyzed. The minimum size of debris considered part of the “Garbage ingested by sea turtles” indicator was set at 1 mm [44,45].

2.2. Plastic Analysis and Identification

Similarly to the sampling process, the analysis and classification of marine debris followed the protocols outlined in the INDICIT project [44]. Turtle stomach contents were separated and prepared for measuring (maximum length, within 0.1 cm using a Tesa Digico 12 caliper) and weighing (dry mass, within 0.001 g using a Precisa 125A microbalance) (see Appendix A, Figure A1, Figure A2 and Figure A3). Plastics were described in as much detail as possible, also following the MSFD guide for monitoring marine debris in European seas [46]. They were classified into “item”, representing individual plastic units, and “pieces”, denoting fragments of an item.
Plastics were classified into nine categories Table 1 [44,46]: industrial plastic (IND PLA), sheet type (USE SHE), filament (USE THR), foam (USE FOA), fragments (USE FRAG), other plastics (USE OTH), non-plastic garbage (OTHER), natural food (FOO), and natural remains not identified as diet (NFO). Table 1 describes each category.
Finally, all plastics found were classified according to colour and size as microplastics (1–5 mm), mesoplastics (5–25 mm), and macroplastics (>25 mm) [44].
All plastic material is documented in Appendix A, Table A2.

2.3. Statistical Analysis

All analyses were performed using R Statistical Software v4.1.2 [47]. The percentage of turtles affected by ingestion of marine debris and plastic was estimated.
The average weight and total number of plastics found in each turtle were calculated and presented as mean ± standard error of the mean. The most abundant plastic category (lamella/SHE, fragment/FRAG, filiform/THR, foam/FOAM, and others/OTHER) and the predominant size (macro, meso, and micro) were calculated. Plastic items were also classified into the 12 observed color categories (black, blue, green, grey, red, pink, orange, purple, red, yellow, white and transparent). Items with more than one color were categorized as “multiple” [44,45].
Before conducting analyses, the Kolmogorov–Smirnov normality test assessed the normal distribution of all variables [48]. For those variables exhibiting non-normal distributions, logarithmic transformations were applied. Non-parametric tests were employed for variables that remained non-normally distributed after transformations [49].
To explore the relationship between plastic ingestion and turtle size, a Pearson correlation coefficient [50] was calculated, using the curved carapace length (CCL) as the independent variable and the total number of pieces per turtle as the dependent variable, with statistical significance set at 0.05.
The chi-square statistical test [51] was used to determine if there was any predominant type, size, or color of plastic, as well as any predominant stranding zone or cause of admission, with a statistical significance set at 0.05. Post hoc analysis, incorporating adjusted residuals and the Bonferroni correction, was conducted to identify specific groups exhibiting significant differences.
The body condition index (BCI) is a metric used to assess the overall health and physical state of a sea turtle based on its body size and weight. It provides insights into the animal’s nutritional status and helps determine whether a turtle is in good or poor physical condition. BCI can be established subjectively by assessing the physical appearance of the animal on a scale of 1–5, where 1 corresponds to an emaciated appearance characterized by sunken eyes and loss of musculature and 5 represents an obese turtle. A BCI value of 3 is considered normal [52]. Additionally, it can be calculated objectively according to the mass and length of the animal, using the formula:
B C I = w e i g h t k g L R C 3 c m 3 × 10000 ,
where LRC is the straight carapace length [52]. This formula was applied to compute the variable “BCI”.
To investigate distribution of the variable BCI between the two groups (turtles with and without plastics), the non-parametric Mann–Whitney U test [53] was employed. To specifically examine the correlation between BCI and the number of plastics ingested, the Pearson correlation test was used.
The Dunn–Bonferroni multiple comparisons test was used to identify significant differences between the plastics found in different zones sampled on the island, adjusting for the increased risk of Type I errors from multiple pairwise comparisons [54].

3. Results

During the study period, 312 sea turtles entered the WRC “La Tahonilla” (Tenerife) (Figure 1); 39 presented marine debris, of which 37 (11.9%) contained some plastic element. The two remaining turtles contained metal hooks with their respective nylon threads (Appendix A: Table A1 and Table A2). Of these 37 specimens (all loggerhead turtles), one was dead, three died at the center during the recovery process, and the rest were released. In total, 43,402 g of marine debris was collected, consisting of 546 pieces (Table 2).
The largest turtle (51 kg and 67.1 cm CCL; ID 10808) presented the highest number of plastics (140 pieces: 26 sheets (USE SHE), 11 filaments (USE THR), and 103 fragments (USE FRAG). The maximum weight of plastics was 7.29 g, found in a 9.9 kg, 45 cm CCL turtle (ID 12555). There are large differences in the ingestion of marine debris among the turtles sampled.
Considering the data obtained for the types of plastics found in marine debris ingested by loggerheads (Appendix A: Table A2), the most abundant plastic category was filiform plastics (USE THR), with 250 pieces (46%); followed by plastic in sheet form (USE SHE), with 187 pieces (34%); and fragments (USE FRAG), with 104 pieces (19%). The remaining types, foam plastics (USE FOAM) and other plastics (USE OTHER), were found in clearly smaller quantities (Figure 2). The chi-square test did not reveal any significant predominance within any category.
The predominant plastic size observed was macroplastic, constituting 66% of the total pieces, followed by mesoplastics at 29%, and microplastics at 4% (Figure 2). The chi-square test did not reveal any significant predominance within any size.
Among all plastic collected, white (31%) and transparent (20%) were the main colors ingested by sea turtles. Green (17%), blue (13%), and black (10%) were also quite abundant, and the remaining colors do not exceed 5% frequency. The chi-square test did not reveal any significant predominance within any color.
The linear regression correlating the ingestion of garbage with the turtle’s body size (logarithmic transformation of the variables “pieces” and “CCL” to comply with data normality) yields a Pearson correlation coefficient of p = 0.1243. Despite the p-value of 0.46, which is above the significance level of 0.05, indicating that there is not enough evidence to reject the null hypothesis of no correlation, the confidence interval includes both positive and negative values. The relationship is rather weak and is not considered statistically significant. Plastic was found in turtles of all size ranges (Figure 3).
The body condition indices of all turtles in this study varied between 0.175 and 2.963. The non-parametric Mann-Whitney U test resulted in a W coefficient of 5686.50 and a p-value greater than 0.05 (p = 0.24), indicating no significant difference between the groups (normal distribution of the data could not be achieved). The BCI of turtles with plastics is distributed in a tight range between 0.943 and 1.688 (Figure 4; Appendix A: Table A1). The average and standard deviation of the BCI for turtles with plastic were 1.218 ± 0.165. For the overall sample of turtles, the BCI was 1.183 ± 0.284.
The Pearson correlation test, conducted after logarithmic transformation of the “bci” and “pieces” variables, resulted in a coefficient value of −0.00289, indicating a weak negative very close to zero correlation between both variables. Moreover, the p-value exceeds 0.05 (p = 0.98), suggesting that there is no statistically significant correlation between the variables “pieces” and “bci”.
The strandings of the overall turtle population occur across the entire island, with a higher number observed in the southwest. In the specific case of turtles with plastics, strandings predominantly take place in the south and west, with almost no occurrences in the north. In both scenarios, strandings in the western part of the island are statistically and significantly higher than in the other regions, as indicated by the chi-square statistical test.
A compilation of studies on the presence of plastic debris (larger than 1 mm) on Tenerife’s beaches from 2016 and 2022 revealed a significant spatial variability in plastic concentrations. Samples were collected from beaches in the north (three beaches), south (four beaches), east (four beaches), and west (two beaches) zones. The findings indicate that Playa Grande in the east consistently shows high plastic concentrations across all studies. The Dunn-Bonferroni multiple comparisons test revealed significant differences between the eastern zone and the other zones.
When examining the cause of admission for all turtles, interaction with fishing gear, commonly known as “bycatch”, is the most prevalent cause, affecting 20.8% of the turtles, followed by entanglement, which affects 15.4% (excluding turtles with indeterminate causes of admission). In the specific analysis of turtles with plastic, it is observed that the majority, 29.7%, enter the center due to entanglement (Figure 5). The results of the chi-square test revealed statistically significant differences between the mentioned admission causes and the others for each group of turtles.

4. Discussion

The present study provides evidence and a comprehensive characterization of plastic debris found in the digestive systems of stranded loggerhead sea turtles in Tenerife, Canary Islands. The acquired data not only improve the current knowledge about plastic ingestion by loggerheads in the eastern North Atlantic but also highlights the importance of loggerhead turtles as key focal points in the research and conservation management of marine environmental challenges.
Other studies conducted in the Atlantic Ocean report incidences of 25% [55], 59% [12], and 83% [56]. In some cases, frequency of plastic ingestion may be underestimated, as only the stomach content was considered on dead turtles [55], and the intestines, where marine debris is often more abundant [56], were not examined. The significant variation in frequencies between studies could be attributed to various factors such as seasonality, life cycle stages (juveniles or adults) and status of the turtles sampled (alive or dead) and differences in sampling methodologies [7,10,56]. Nevertheless, results of this study should be taken into account when comparing with others, especially those using the INDICIT project protocol for sampling and analysis of live turtles.
The range of CCL of the turtles was very wide (17.5–67.1 cm), and plastic ingestion was not significantly related to age ranges, which was consistent with similar studies [57,58]. Some studies categorize turtles based of CCL to analyze plastic impact due to variations in feeding behavior [58,59]. The precise range and size limits of neritic–oceanic transitions remain undefined in the Northeast Atlantic [20,31], Northwest Atlantic [22,60], and Mediterranean [61,62]. This suggests that loggerhead turtles use adaptive ecological niches and demonstrates that carapace length is not conclusive for determining feeding strategy [20]. In this study, all turtles are treated as juveniles without habitat-based distinctions.
In our study, we treated all examined turtles as juveniles without distinguishing between their habitats, reflecting the undefined transitions mentioned earlier. Consequently, we deduce that plastic ingestion occurs across the different feeding strategies of juvenile turtles, given the broad size range analyzed. The presence of plastics across such a wide range of sizes indicates that the ingestion is not confined to a specific size class or feeding habitat. This underscores the pervasive nature of plastic pollution and its impact on sea turtles irrespective of their size or ecological niche. Therefore, our findings help us to understand the impact of plastics in the conservation and biology of sea turtle from Canary Islands and emphasize the need to reach comprehensive conservation strategies that address plastic pollution’s impacts to reach the sustainability and conservation of sea turtles.
The direct responsibility of waste ingestion for the death of marine turtles is rarely reported [63,64]. Although attributing a turtle’s death to plastic ingestion is complex, debris ingestion was not identified as a direct cause of death for most sampled individuals. Nearly all turtles in this study were successfully rehabilitated and released, with only two cases raising suspicions that ingested debris significantly contributed to their deaths:
(a)
In November 2020, a live loggerhead turtle (ID 13278) was admitted with signs of drowning, eye infection, and general weakness. Despite various treatments, it died after 11 days. Necropsy revealed a piece of soft white plastic (140 × 84 mm, 0.595 g) between the stomach and the intestine, obstructing the digestive tract along with severe inflammation and infection in the lungs, liver, and intestines. It was inferred that this obstruction played a significant role in its death, triggering infections in other organs.
(b)
In April 2019, a decomposed turtle was found in south Tenerife (ID 10808). Necropsy revealed 140 pieces: 103 filaments (thr), 11 fragments (frag), and 26 laminates (she). In total, 6.5 g of plastics, most of them macroplastics, including easily recognizable items such as two earbud sticks, a round washer over 3 cm in diameter, and food wrappers.
Studies on dead turtles often find significant plastic presence in the intestines, indicating their capacity to excrete most ingested debris [12,26,56]. The low mortality rate and effective waste excretion suggest turtles are robust bioindicators for assessing marine debris impact [5,8]. However, its known that it probably increases the risk of death due to sublethal effects that are more frequent and harder to detect [7,11].
The results showed differences between plastic types, although they were not statistically significant. The most frequent type of plastic was de filiforms—the same as in other studies [65,66]—followed by sheets and fragments. The high incidence of threads could be linked to interactions with fishing lines and materials related to fisheries [67]. This aligns with the primary stranding cause identified in this study, interaction with fishing gear, commonly referred to as “bycatch”, affecting 20.8% of turtles. This primary cause aligns with findings from other similar studies [12]. On the other hand, white and transparent plastic items are the most commonly ingested colors—the same as in other studies [26,56,58,63,65,66,68]—although they were not statistically significant. This finding corresponds with the predominant colors employed in the packaging industry in recent years [69]. Furthermore, these results align with the color findings of studies conducted on plastic debris on Tenerife beaches, where white and transparent were the most frequently observed colors [39,42]. The ingestion of light-colored debris may be attributed to its reduced visibility in the water, potentially leading to mistaken ingestion [70], or to its resemblance to jellyfish, a common prey item [5,11].
The decision to exclude particles smaller than 1 mm is based on MSFD Technical Sub-group guidelines, which set this as the minimum size for litter items [44,45]. However, this exclusion may lead to an underestimation of ingested debris, as smaller microplastics can still be harmful to sea turtles. This limitation should be noted, and future studies should consider including particles smaller than 1 mm for a more complete assessment of marine debris impacts on sea turtles.
The present study, the first in Tenerife analyzing and categorizing plastic ingestion by loggerhead turtles, increased the available data on the ingestion of plastics by this species. The findings not only highlight the threats faced by this species in the Northeast Atlantic subpopulation but also support the potential usage of live specimens of loggerhead turtles as indicator species for monitoring plastic debris in the marine environment.
This research underscores the urgent need for standardized procedures to accurately quantify ingested debris and calls for further extensive studies to evaluate the true impact of plastic ingestion on the health and survival of sea turtles. Moreover, the findings emphasize the critical importance of developing and implementing effective strategies to combat plastic pollution. By addressing these issues, we contribute to broader sustainability goals, including the preservation of marine biodiversity and the creation of science-based solutions for environmental protection.

Author Contributions

Conceptualization, J.C.B.; Formal analysis, M.T.; Investigation, M.T. and J.J.B.; Writing—original draft, M.T.; Writing—review & editing, J.J.B. and J.C.B.; Supervision, J.J.B. and J.C.B. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Ethical review and approval were waived for this study because no marine turtles were handled by the researchers to obtain the plastic samples. The samples were collected by the trained specialist staff of the Wildlife Recovery Center.

Data Availability Statement

The original contributions presented in the study are included in the article, further inquiries can be directed to the corresponding author.

Acknowledgments

Authors would like to thank to the dedicated staff at La Tahonilla Rescue Center for their invaluable support and tireless efforts in the collection and rehabilitation of hundreds of stranded sea turtles in Tenerife each year. Additionally, we extend our sincere gratitude to ADS Biodiversidad for their guidance and support in directing and supervising the master’s final thesis that laid the groundwork for this article.

Conflicts of Interest

The authors declare no conflict of interest.

Appendix A

Figure A1. Photographs of material defecated by 3 different study specimens.
Figure A1. Photographs of material defecated by 3 different study specimens.
Sustainability 16 07147 g0a1
Figure A2. Photographs of material defecated by 3 different study specimens.
Figure A2. Photographs of material defecated by 3 different study specimens.
Sustainability 16 07147 g0a2
Figure A3. Photographs of material defecated by 3 different study specimens.
Figure A3. Photographs of material defecated by 3 different study specimens.
Sustainability 16 07147 g0a3
Table A1. Information on the turtles and samples collected at the WRC “La Tahonilla” corresponding to the 37 turtles (Caretta caretta) affected by marine debris.
Table A1. Information on the turtles and samples collected at the WRC “La Tahonilla” corresponding to the 37 turtles (Caretta caretta) affected by marine debris.
IDCCL (cm)Turtle Weight (kg)PiecesPieces Weight (g)Body Condition Index (bci)Stranding CauseStranding Zone/Code
1044626.02.00250.3181.132226IndeterminatePuerto Colón4
1045240.09.2530.031.445313Symptoms of illnessPuerto Colón4
1050626.02.0040.0071.126536EntanglementPunta de Teno4
1051930.04.3810.0141.622222CollisionPuerto Colón4
1080867.151.001406.501.688117IndeterminatePlaya de Los Surfistas2
1081450.013.9071.0031.112000CollisionPuerto de Los Cristianos2
1090440.07.70511.8531.203125Symptoms of illnessPuerto Colón4
1158739.06.35803.6821.070483IndeterminatePuerto Colón4
1160432.03.6514.8121.113892EntanglementPuerto Colón4
1188637.06.1010.041.206246IndeterminatePuerto Colón4
1197946.013.2010.0011.356127EntanglementPlayas de Fañabé4
1198437.07.1020.4021.401694Symptoms of illnessCosta Adeje2
1198640.08.8030.1981.375000Symptoms of illnessPuerto Colón4
1198842.09.00180.3141.214772IndeterminatePuerto Colón4
1200252.518.00405.591.243926Symptoms of illnessPuerto Colón4
1200433.04.4580.7991.238556EntanglementPuerto Santiago4
1201764.034.7570.0291.325607BycatchPlaya de San Juan4
1207649.015.30131.821.300479IndeterminatePuerto Colón4
1208328.02.4510.0011.116071BycatchPuerto Colón4
1208960.023.6521.511.094907IndeterminatePuerto Colón4
1210622.81.48220.7721.248697Symptoms of illnessPuerto Colón4
1212130.23.6010.0041.307018BycatchPuerto Colón4
1212431.03.0520.0561.023799EntanglementPuerto Colón4
1212530.03.5041.1501.296296IndeterminatePuerto Colón4
1214330.03.3510.0731.240741Symptoms of illnessPuerto Colón4
1215763.530.0020.2091.171656BycatchLos Gigantes4
1229251.514.1530.1911.035940EntanglementPunta del Hidalgo1
1231126.01.9450.2241.103778EntanglementEl Poris3
1241526.02.06100.1041.172039EntanglementPunta del Hidalgo1
1245729.02.75120.2471.127558Healthy caughtPuerto Colón4
1254141.06.50230.670.943109EntanglementEl Poris3
1255545.09.90337.2941.086420EntanglementMuelle de Santa Cruz3
1294117.50.8040.2871.492711BycatchPuerto Colón4
1305642.08.9060.1751.201274EntanglementLos Gigantes4
1321654.018.0020.6371.143118IndeterminatePlaya de Fañabe4
1327857.018.5510.5951.001658Symptoms of illnessMalpaís3
1328033.03.8061.7941.057406BycatchLos Gigantes4
Stranding zone code: (1) North. (2) South. (3) East (4) West. (CCL) Curved length of the shell.
Table A2. Information on the turtles and samples collected at the WRC “La Tahonilla” corresponding to the 37 turtles (Caretta caretta) affected by marine debris.
Table A2. Information on the turtles and samples collected at the WRC “La Tahonilla” corresponding to the 37 turtles (Caretta caretta) affected by marine debris.
IDTypeSize
SheFragThrFoaOtherIndMacroMesoMicro
1044681160003148
10452201000210
10506004000130
10519001000100
108082611103000119210
10814520000520
109041463000037130
115875172400050302
11604000010100
11886001000100
11979001000100
11984101000200
11986210000120
1198820160001710
12002316300028120
12004710000350
12017106000610
120769310001030
12083001000010
12089200000200
1210630190002200
12121100000010
12124101000200
12125000400220
12143100000100
12157200000110
12292030000030
12311014000410
12415055000343
124570120000075
1254114180001940
1255542810006234
12941400000400
13056213000420
13216020000020
13278100000100
13280600000402

References

  1. OECD. Global Plastics Outlook: Economic Drivers, Environmental Impacts and Policy Options; OECD Publishing: Paris, France, 2022. [Google Scholar]
  2. Morales-Caselles, C.; Viejo, J.; Martí, E.; González-Fernández, D.; Pragnell-Raasch, H.; González-Gordillo, J.I.; Montero, E.; Arroyo, G.M.; Hanke, G.; Salvo, V.S.; et al. An inshore–offshore sorting system revealed from global classification of ocean litter. Nat. Sustain. 2021, 4, 484–493. [Google Scholar] [CrossRef]
  3. Hildebrandt, L.; Von der Au, M.; Zimmermann, T.; Reese, A.; Ludwig, J.; Pröfrock, D. A metrologically traceable protocol for the quantification of trace metals in different types of microplastic. PLoS ONE 2020, 15, e0236120. [Google Scholar] [CrossRef] [PubMed]
  4. Andrady, A.L.; Koongolla, B. Degradation and Fragmentation of Microplastics. In Plastics and the Ocean: Origin, Characterization, Fate, and Impacts; Wiley: Hoboken, NJ, USA, 2022; pp. 227–268. [Google Scholar] [CrossRef]
  5. Schuyler, Q.A.; Wilcox, C.; Townsend, K.A.; Wedemeyer-Strombel, K.R.; Balazs, G.; Van Sebille, E.; Hardesty, B.D. Plastic debris ingestion by marine turtles: An updated review and conservation implications. Front. Mar. Sci. 2016, 3, 73. [Google Scholar] [CrossRef]
  6. Gall, S.C.; Thompson, R.C. The impact of debris on marine life. Mar. Pollut. Bull. 2015, 92, 170–179. [Google Scholar] [CrossRef] [PubMed]
  7. Nelms, S.E.; Duncan, E.M.; Broderick, A.C.; Galloway, T.S.; Godfrey, M.H.; Hamann, M.; Lindeque, P.K.; Godley, B.J. Plastic and marine turtles: A review and call for research. ICES J. Mar. Sci. 2016, 73, 165–181. [Google Scholar] [CrossRef]
  8. Wilcox, C.; Puckridge, M.; Schuyler, Q.A.; Townsend, K.; Hardesty, B.D. A quantitative analysis linking sea turtle mortality and plastic debris ingestion. Sci. Rep. 2018, 8, 12536. [Google Scholar] [CrossRef] [PubMed]
  9. Tekman, M.B.; Walther, B.; Peter, C.; Gutow, L.; Bergmann, M. Impacts of Plastic Pollution in the Oceans on Marine Species, Biodiversity and Ecosystems; WWF Germany: Berlin, Germany, 2022. [Google Scholar] [CrossRef]
  10. Blais, N.; Wells, P.G. The leatherback turtle (Dermochelys coriacea) and plastics in the Northwest Atlantic ocean: A hazard assessment. Heliyon 2022, 8, e12427. [Google Scholar] [CrossRef]
  11. Hoarau, L.; Ainley, L.; Jean, C.; Ciccione, S. Ingestion and defecation of marine debris by loggerhead sea turtles, Caretta caretta, from by-catches in the South-West Indian Ocean. Mar. Pollut. Bull. 2014, 84, 90–96. [Google Scholar] [CrossRef]
  12. Nicolau, L.; Ferreira, M.; Santos, J.; Araújo, H.; Sequeira, M.; Vingada, J.; Marçalo, A. Sea turtle strandings along the Portuguese mainland coast: Spatio-temporal occurrence and main threats. Mar. Biol. 2016, 163, 21. [Google Scholar] [CrossRef]
  13. Duncan, E.M.; Broderick, A.C.; Fuller, W.J.; Galloway, T.S.; Godfrey, M.H.; Hamann, M.; Godley, B.J. Microplastic ingestion ubiquitous in marine turtles. Glob. Chang. Biol. 2019, 25, 744–752. [Google Scholar] [CrossRef]
  14. Bellido López, J.J.; Torreblanca, E.; Báez, J.C.; Camiñas, J.A. Sea turtles in the eastern margin of the North Atlantic: The northern Ibero-Moroccan Gulf as an important neritic area for sea turtles. Mediterr. Mar. Sci. 2018, 19, 662–672. [Google Scholar] [CrossRef]
  15. Camiñas, J.A.; Báez, J.C.; Ayllón, E.; Marco, A.; Hernández-Sastre, L.; López-Pérez, I.; Moreno-Colera, H.; Macías, D.; Cardona, L.; Belda, E.J.; et al. Estado de conservación de las tortugas marinas en España (revisión del periodo 2013–2018). An. Biol. 2021, 43, 175–198. [Google Scholar] [CrossRef]
  16. Casale, P.; Mariani, P. The first ‘lost year’ of Mediterranean sea turtles: Dispersal patterns indicate subregional management units for conservation. Mar. Ecol. Prog. Ser. 2014, 498, 263–274. [Google Scholar] [CrossRef]
  17. Castro, J.; Hughes, A.P.; Cid, A.; Patrício, A.R.; Laborde, M.I.; Matos, F.L. First long-term study of live observations of loggerhead and leatherback turtles in southern Portugal with relevance for conservation. Aquat. Conserv. Mar. Freshw. Ecosyst. 2023, 33, 1154–1160. [Google Scholar] [CrossRef]
  18. Orós, J.; Camacho, M.; Calabuig, P.; Rial-Berriel, C.; Montesdeoca, N.; Déniz, S.; Luzardo, O.P. Postmortem investigations on leatherback sea turtles (Dermochelys coriacea) stranded in the Canary Islands (Spain) (1998–2017): Evidence of anthropogenic impacts. Mar. Pollut. Bull. 2021, 167, 112340. [Google Scholar] [CrossRef]
  19. Varo-Cruz, N.; Cejudo, D.; Calabuig, P.; Herrera, R.; Urioste, J.; Monzón-Argüello, C. Records of the Hawksbill Sea Turtle (Eretmochelys imbricata) in the Canary Islands. Mar. Turt. Newsl. 2017, 154, 1–6. [Google Scholar]
  20. Cameron, S.J.K.; Baltazar-Soares, M.; Stiebens, V.A.; Reischig, T.; Correia, S.M.; Harrod, C.; Eizaguirre, C. Diversity of feeding strategies in loggerhead sea turtles from the Cape Verde archipelago. Mar. Biol. 2019, 166, 130. [Google Scholar] [CrossRef]
  21. Mansfield, K.L.; Wyneken, J.; Porter, W.P.; Luo, J. First satellite tracks of neonate sea turtles redefine the ‘lost years’ oceanic niche. Proc. R. Soc. B 2014, 281, 20133039. [Google Scholar] [CrossRef]
  22. Bolten, A.B. Active swimmers—Passive drifters: The oceanic juvenile stage of loggerheads in the Atlantic system. In Loggerhead Sea Turtles; Bolten, A.B., Witherington, B.E., Eds.; Smithsonian Institution Press: Washington, DC, USA, 2003; pp. 63–78. [Google Scholar]
  23. Lamont, M.M.; Fujisaki, I.; Stephens, B.S.; Hackett, C. Home range and habitat use of juvenile green turtles (Chelonia mydas) in the northern Gulf of Mexico. Anim. Biotelemetry 2015, 3, 53. [Google Scholar] [CrossRef]
  24. Patel, S.H.; Dodge, K.L.; Haas, H.L.; Smolowitz, R.J. Videography reveals in-water behavior of loggerhead turtles (Caretta caretta) at a foraging ground. Front. Mar. Sci. 2016, 3, 254. [Google Scholar] [CrossRef]
  25. Troëng, S. Migraciones de las tortugas marinas. Rev. Cienc. Ambient. 2019, 28, 20–30. [Google Scholar] [CrossRef]
  26. Matiddi, M.; Hochsheid, S.; Camedda, A.; Baini, M.; Cocumelli, C.; Serena, F.; Tomassetti, P.; Travaglini, A.; Marra, S.; Campani, T.; et al. Loggerhead sea turtles (Caretta caretta): A target species for monitoring litter ingested by marine organisms in the Mediterranean Sea. Environ. Pollut. 2017, 230, 199–209. [Google Scholar] [CrossRef]
  27. Camiñas, J.; Kaska, Y.; Hochscheid, S.; Casale, P.; Panagopoulou, A.; Báez, J.; Otero, M.M.; Numa, C.; Alcázar, E. Conservation of Marine Turtles in the Mediterranean Sea [Brochure]; IUCN: Málaga, Spain, 2020. [Google Scholar] [CrossRef]
  28. Monzón-Argüello, C.; Varo-Cruz, P. Canary Islands (Spain). Sea Turtles in the West Africa/East Atlantic Region. In MTSG Annual Regional Report 2020; Marine Turtle Specialist Group, International Union for Conservation of Nature (IUCN): Gland, Switzerland, 2020; pp. 112–128. [Google Scholar]
  29. Observatorio Ambiental Granadilla (OAG). Estado de Conservación de la Tortuga Boba (Caretta caretta) en las Islas Canarias, 2012–2017; Observatorio Ambiental Granadilla: Santa Cruz de Tenerife, Spain, 2018. [Google Scholar]
  30. Dellinger, T.; Zekovic, V.; Radeta, M. Long-Term Monitoring of In-Water Abundance of Juvenile Pelagic Loggerhead Sea Turtles (Caretta caretta): Population Trends in Relation to North Atlantic Oscillation and Nesting. Front. Mar. Sci. 2022, 9, 877636. [Google Scholar] [CrossRef]
  31. Bjorndal, K.A.; Bolten, A.B.; Martins, H.R. Somatic growth model of juvenile loggerhead sea turtles Caretta caretta: Duration of pelagic stage. Mar. Ecol. Prog. Ser. 2000, 202, 265–272. [Google Scholar] [CrossRef]
  32. Bolten, A.B.; Bjorndal, K.A.; Martins, H.R.; Dellinger, T.; Biscoito, M.J.; Encalada, S.E.; Bowen, B.W. Transatlantic developmental migrations of loggerhead sea turtles demonstrated by mtDNA sequence analysis. Ecol. Appl. 1998, 8, 1–7. [Google Scholar] [CrossRef]
  33. Dellinger, T. Comportamiento ecológico y conservación de las tortugas marinas en estado oceánico. In Recovery of Extinct Populations; López-Jurado, L.F., Liria Loza, A., Eds.; Instituto Canario de Ciencias Marinas: Las Palmas, Spain, 2007. [Google Scholar]
  34. LaCasella, E.L.; Epperly, S.P.; Jensen, M.P.; Stokes, L.; Dutton, P.H. Genetic stock composition of loggerhead turtles Caretta caretta bycaught in the pelagic waters of the North Atlantic. Endanger. Species Res. 2013, 22, 73–84. [Google Scholar] [CrossRef]
  35. Monzón-Argüello, C.; Rico, C.; Carreras, C.; Calabuig, P.; Marco, A.; López Jurado, L.F. Variation in spatial distribution of juvenile loggerhead turtles in the Eastern Atlantic and Western Mediterranean Sea. J. Exp. Mar. Biol. Ecol. 2009, 373, 79–86. [Google Scholar] [CrossRef]
  36. López-Jurado, L.F. Historical review of the archipelagos of macaronesia and the marine turtles. In Marine Turtles: Recovery of Extinct Populations; López-Jurado, L.F., Liria-Loza, A., Eds.; Instituto Canario de Ciencias Marinas: Las Palmas, Spain, 2007; pp. 53–76. [Google Scholar]
  37. Casale, P.; Tucker, A.D. Caretta caretta (amended version of 2015 assessment). In The IUCN Red List of Threatened Species; International Union for Conservation of Nature (IUCN): Gland, Switzerland, 2017. [Google Scholar] [CrossRef]
  38. Herrera, A.; Raymond, E.; Martínez, I.; Álvarez, S.; Canning-Clode, J.; Gestoso, I.; Gómez, M. First evaluation of neustonic microplastics in the Macaronesian region, NE Atlantic. Mar. Pollut. Bull. 2020, 153, 110999. [Google Scholar] [CrossRef]
  39. Reinold, S.; Herrera, A.; Hernández-González, C.; Gómez, M. Plastic pollution on eight beaches of Tenerife (Canary Islands, Spain): An annual study. Mar. Pollut. Bull. 2020, 151, 110847. [Google Scholar] [CrossRef]
  40. Guerra-Medina, D.; Rodríguez, G. Spatiotemporal variability of extreme wave storms in a beach tourism destination area. Geosciences 2021, 11, 237. [Google Scholar] [CrossRef]
  41. Álvarez-Hernández, C.; Cairós, C.; López-Darias, J.; Mazzetti, E.; Hernández-Sánchez, C.; González-Sálamo, J.; Hernández-Borges, J. Microplastic debris in beaches of Tenerife (Canary Islands, Spain). Mar. Pollut. Bull. 2019, 146, 26–32. [Google Scholar] [CrossRef]
  42. Domínguez-Hernández, C.; Villanova-Solano, C.; Sevillano-González, M.; Hernández-Sánchez, C.; González-Sálamo, J.; Ortega-Zamora, C.; Hernández-Borges, J. Plastitar: A new threat for coastal environments. Sci. Total Environ. 2022, 839, 156261. [Google Scholar] [CrossRef] [PubMed]
  43. González-Hernández, M.; Hernández-Sánchez, C.; González-Sálamo, J.; López-Darias, J.; Hernández-Borges, J. Monitoring of meso and microplastic debris in Playa Grande beach (Tenerife, Canary Islands, Spain) during a moon cycle. Mar. Pollut. Bull. 2020, 150, 110757. [Google Scholar] [CrossRef] [PubMed]
  44. INDICIT Consortium. Monitorización del Impacto de la Basura en Tortugas Marinas. Protocolo para la Colecta de datos en Ingestión y Enmallamiento de Tortugas Marinas (Caretta caretta Linnaeus, 1758); INDICIT Consortium: Bruxelles, Belgium, 2018. [Google Scholar]
  45. Matiddi, M.; De Lucia, G.A.; Silvestri, C.; Darmon, G.; Tomás, J.; Pham, C.K.; Camedda, A.; Vandeperre, F.; Claro, F.; Kaska, Y.; et al. Data Collection on Marine Litter Ingestion in Sea Turtles and Thresholds for Good Environmental Status. J. Vis. Exp. 2019, 147, e59148. [Google Scholar] [CrossRef]
  46. Galgani, F.; Hanke, G.; Werner, S.; De Vrees, L. Marine litter within the European Marine Strategy Framework Directive. ICES J. Mar. Sci. 2013, 70, 1055–1064. [Google Scholar] [CrossRef]
  47. R Core Team. R: A Language and Environment for Statistical Computing; R Foundation for Statistical Computing, Vienna, Austria. 2021. Available online: https://www.R-project.org/ (accessed on 8 July 2024).
  48. Mishra, P.; Pandey, C.M.; Singh, U.; Gupta, A.; Sahu, C.; Keshri, A. Descriptive statistics and normality tests for statistical data. Ann. Card. Anaesth. 2019, 22, 67–72. [Google Scholar] [CrossRef] [PubMed]
  49. Asmare, E.; Begashaw, A. Review on parametric and nonparametric methods of efficiency analysis. Biostat. Bioinforma. 2018, 2, 1–7. [Google Scholar] [CrossRef]
  50. Obilor, E.I.; Amadi, E.C. Test for significance of Pearson’s correlation coefficient. Int. J. Innov. Math. Stat. Energy Policies 2018, 6, 11–23. [Google Scholar]
  51. Connelly, L. Chi-square test. Medsurg Nurs. 2019, 28, 127. [Google Scholar]
  52. Norton, T.; Wyneken, J. Body Condition Scoring the Sea Turtle; Georgia Sea Turtle Center: Jekyll Island, GA, USA, 2015. [Google Scholar]
  53. Wall Emerson, R. Mann-Whitney U test and t-test. J. Vis. Impair. Blind. 2023, 117, 99–100. [Google Scholar] [CrossRef]
  54. Lee, S.; Lee, D.K. What is the proper way to apply the multiple comparison test? Korean J. Anesthesiol. 2018, 71, 353. [Google Scholar] [CrossRef] [PubMed]
  55. Frick, M.G.; Williams, K.L.; Bolten, A.B.; Bjorndal, K.B.; Martins, H.R. Foraging ecology of oceanic-stage loggerhead turtles Caretta caretta. Endanger. Species Res. 2009, 9, 91–97. [Google Scholar] [CrossRef]
  56. Pham, C.K.; Rodríguez, Y.; Dauphin, A.; Carriço, R.; Frias, J.P.G.L.; Vandeperre, F.; Otero, V.; Santos, M.R.; Martins, H.R.; Bolten, A.B.; et al. Plastic ingestion in oceanic-stage loggerhead sea turtles (Caretta caretta) off the North Atlantic subtropical gyre. Mar. Pollut. Bull. 2017, 121, 222–229. [Google Scholar] [CrossRef]
  57. Bugoni, L.; Krause, L.; Petry, M.V. Marine debris and human impacts on sea turtles in southern Brazil. Mar. Pollut. Bull. 2001, 42, 1330–1334. [Google Scholar] [CrossRef] [PubMed]
  58. Solomando, A.; Pujol, F.; Sureda, A.; Pinya, S. Ingestion and characterization of plastic debris by loggerhead sea turtle, Caretta caretta, in the Balearic Islands. Sci. Total Environ. 2022, 826, 154159. [Google Scholar] [CrossRef] [PubMed]
  59. Casale, P.; Abbate, G.; Freggi, D.; Conte, N.; Oliverio, M.; Argano, R. Foraging ecology of loggerhead sea turtles Caretta caretta in the central Mediterranean Sea: Evidence for a relaxed life history model. Mar. Ecol. Prog. Ser. 2008, 372, 265–276. [Google Scholar] [CrossRef]
  60. Avens, L.; Snover, M.L. Age and age estimation in sea turtles. Biol. Sea Turt. 2013, 3, 97–134. [Google Scholar] [CrossRef]
  61. Casale, P.; Mazaris, A.D.; Freggi, D. Estimation of age at maturity of loggerhead sea turtles Caretta caretta in the Mediterranean using length-frequency data. Endanger. Species Res. 2011, 13, 123–129. [Google Scholar] [CrossRef]
  62. Margaritoulis, D.; Argano, R.; Baran, I.; Bentivegna, F.; Bradai, M.; Camiñas, J.; Casale, P.; Metrio, G.; Demetropoulos, A.; Gerosa, G. Loggerhead turtles in the Mediterranean Sea: Present knowledge and conservation perspectives. Loggerhead Sea Turt. 2003, 11, 175–198. [Google Scholar]
  63. Casale, P.; Freggi, D.; Paduano, V.; Oliverio, M. Biases and best approaches for assessing debris ingestion in sea turtles, with a case study in the Mediterranean. Mar. Pollut. Bull. 2016, 110, 238–249. [Google Scholar] [CrossRef]
  64. Clukey, K.E.; Lepczyk, C.A.; Balazs, G.H.; Work, T.M.; Lynch, J.M. Investigation of plastic debris ingestion by four species of sea turtles collected as bycatch in pelagic Pacific longline fisheries. Mar. Pollut. Bull. 2017, 120, 117–125. [Google Scholar] [CrossRef]
  65. Biagi, S.; Dalla Via, G.; Rampazzo, F.; Gabai, G.; Gion, C. Impact of Plastic Debris on the Gut Microbiota of Caretta caretta from Northwestern Adriatic Sea. Front. Mar. Sci. 2021, 8, 637030. [Google Scholar] [CrossRef]
  66. Digka, N.; Bray, L.; Tsangaris, C.; Andreanidou, K.; Kasimati, E.; Kofidou, E.; Komnenou, A.; Kaberi, H. Evidence of ingested plastics in stranded loggerhead sea turtles along the Greek coastline, East Mediterranean Sea. Environ. Pollut. 2020, 263, 114596. [Google Scholar] [CrossRef]
  67. Parker, D.M.; Cooke, W.J.; Balazs, G.H. Diet of oceanic loggerhead sea turtles (Caretta caretta) in the central North Pacific. Fish. Bull. 2005, 103, 142–152. [Google Scholar]
  68. Duncan, E.M.; Broderick, A.C.; Critchell, K.; Galloway, T.S.; Hamann, M.; Limpus, C.J.; Godley, B.J. Plastic pollution and small juvenile marine turtles: A potential evolutionary trap. Front. Mar. Sci. 2021, 8, 699521. [Google Scholar] [CrossRef]
  69. PlasticsEurope. Plastics—The Facts 2020. An Analysis of European Plastics Production, Demand and Waste Data. Available online: https://plasticseurope.org/wp-content/uploads/2021/09/Plastics_the_facts-WEB-2020_versionJun21_final.pdf (accessed on 2 July 2024).
  70. Santos, R.G.; Andrades, R.; Boldrini, M.A.; Martins, A.S. Debris ingestion by juvenile marine turtles: An underestimated problem. Mar. Pollut. Bull. 2015, 93, 37–43. [Google Scholar] [CrossRef]
Figure 1. Map of the strandings of all turtles. The numbers within the dots refer to the number of stranded turtles.
Figure 1. Map of the strandings of all turtles. The numbers within the dots refer to the number of stranded turtles.
Sustainability 16 07147 g001
Figure 2. Number of plastics depending on type and size.
Figure 2. Number of plastics depending on type and size.
Sustainability 16 07147 g002
Figure 3. Size of the turtles and presence/absence of plastics.
Figure 3. Size of the turtles and presence/absence of plastics.
Sustainability 16 07147 g003
Figure 4. Body condition index (BCI) of all turtles and presence/absence of plastics.
Figure 4. Body condition index (BCI) of all turtles and presence/absence of plastics.
Sustainability 16 07147 g004
Figure 5. Causes of admission of the total turtle population (left) and turtles with plastics (right).
Figure 5. Causes of admission of the total turtle population (left) and turtles with plastics (right).
Sustainability 16 07147 g005
Table 1. Classification of marine debris items found in turtles, following the MSFD guidance [46].
Table 1. Classification of marine debris items found in turtles, following the MSFD guidance [46].
TypeCodeDescription
Industrial plasticIND PLAIndustrial plastic granules, usually cylindrical but also sometimes oval spherical or cubical shapes, or suspected industrial item, used for the tiny spheres (glassy, milky, etc.)
SheetSHERemains of sheet (e.g., bags, cling-foil, agricultural sheets, rubbish bags, etc.)
FilamentTHRThreadlike materials (e.g., nylon wire, net-fragments, woven clothing, etc.)
FoamFOAAll foamed plastics (polystyrene foam, foamed soft rubber, etc.)
FragmentFRAGFragments, broken pieces of thicker type plastics, flexible but not like sheet.
OtherOTHOther type of marine debris different from plastics
Table 2. Summary of results.
Table 2. Summary of results.
TotalAverage ± Standard DeviationMinimumMaximum
Turtle CCL (cm)-39.68 ± 12.6817.5067.10
Turtle weight (kg)-10.14 ± 10.610.8051.00
Plastics (items)54614.59 ± 26.571.00140.00
Plastic dry mass (g)43.401.17 ± 1.900.017.29
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Tortosa, M.; Bellido, J.J.; Báez, J.C. Analysis of Plastic Ingestion by Juvenile Loggerhead Sea Turtles (Caretta caretta) Stranded from Tenerife, Canary Islands. Sustainability 2024, 16, 7147. https://doi.org/10.3390/su16167147

AMA Style

Tortosa M, Bellido JJ, Báez JC. Analysis of Plastic Ingestion by Juvenile Loggerhead Sea Turtles (Caretta caretta) Stranded from Tenerife, Canary Islands. Sustainability. 2024; 16(16):7147. https://doi.org/10.3390/su16167147

Chicago/Turabian Style

Tortosa, Marina, Juan Jesús Bellido, and José Carlos Báez. 2024. "Analysis of Plastic Ingestion by Juvenile Loggerhead Sea Turtles (Caretta caretta) Stranded from Tenerife, Canary Islands" Sustainability 16, no. 16: 7147. https://doi.org/10.3390/su16167147

APA Style

Tortosa, M., Bellido, J. J., & Báez, J. C. (2024). Analysis of Plastic Ingestion by Juvenile Loggerhead Sea Turtles (Caretta caretta) Stranded from Tenerife, Canary Islands. Sustainability, 16(16), 7147. https://doi.org/10.3390/su16167147

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop