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Article

AI in Biodiversity Education: The Bias in Endangered Species Information and Its Implications

by
Luis de Pedro Noriega
1,
Javier Bobo-Pinilla
2,*,
Jaime Delgado-Iglesias
2,
Roberto Reinoso-Tapia
2,
Ana María Gallego
2 and
Susana Quirós-Alpera
2
1
Facultad de Educación de Palencia, Universidad de Valladolid, 34004 Palencia, Spain
2
Facultad de Educación y Trabajo Social, Universidad de Valladolid, 47011 Valladolid, Spain
*
Author to whom correspondence should be addressed.
Sustainability 2025, 17(14), 6554; https://doi.org/10.3390/su17146554
Submission received: 21 May 2025 / Revised: 15 July 2025 / Accepted: 16 July 2025 / Published: 18 July 2025
(This article belongs to the Special Issue Sustainable Education in the Age of Artificial Intelligence (AI))

Abstract

The use of AI-generated content in education is significantly increasing, but its reliability for teaching natural sciences and, more specifically, biodiversity-related contents still remains understudied. The need to address this question is substantial, considering the relevance that biodiversity conservation has on human sustainability, and the recurrent presence of these topics in the educational curriculum, at least in Spain. The present article tests the existence of biases in some of the most widely used AI tools (ChatGPT-4.5, DeepSeek-V3, Gemini) when asked a relevant and objective research question related to biodiversity. The results revealed both taxonomic and geographic biases in all the lists of endangered species provided by these tools when compared to IUCN Red List data. These imbalances may contribute to the perpetuation of plant blindness, zoocentrism, and Western centrism in classrooms, especially at levels where educators lack specialized training. In summary, the present study highlights the potential harmful impact that AI’s cultural and social biases may have on biodiversity education and Sustainable Development Goals-aligned learning and appeals to an urgent need for model refinement (using scientific datasets) and teacher AI literacy to mitigate misinformation.

1. Introduction

1.1. Artificial Intelligence and Education

The genesis of artificial intelligence (AI) can be traced back to the mid-20th century, when pioneering figures such as Alan Turing introduced the concept of machines capable of performing cognitive tasks [1]. The term “artificial intelligence” was officially coined in 1956, marking the establishment of AI as a distinct field of study [2]. In recent decades, significant advancements in machine learning algorithms, deep learning techniques, and access to extensive datasets have contributed to the rapid progress of the field [3]. The sophistication of AI has reached unprecedented levels, as evidenced by applications such as ChatGPT, Gemini and, more recently, DeepSeek ([4]; among many others). These systems exhibit advanced capabilities in human-like interaction, complex reasoning, and content creation. They are enabled by sophisticated language models that have been trained on extensive datasets, thereby facilitating a wide range of capabilities, including text processing, multimedia generation, and the resolution of complex challenges such as medical diagnostics, autonomous vehicle navigation, and personalized services [5,6].
In the field of education, the integration of AI has led to significant advancements in the realm of learning solutions. These solutions are characterized by their personalized approach and accessibility, spanning diverse academic domains [7,8]. These tools can function as virtual tutors, delivering tailored explanations based on individual student needs [9,10]. Ref. [11] posit that AI-powered education facilitates personalized learning, thereby enhancing knowledge retention and student engagement. AI applications also support educators by automating administrative tasks such as grading assessments and generating instructional materials, thereby allowing teachers to allocate more time to direct student interaction [12]. Furthermore, these tools have the potential to democratize access to high-quality education, particularly in regions facing resource constraints. In this regard, ref. [13] have asserted that AI has the capacity to bridge educational gaps by providing real-time tutoring through chatbots, thereby mitigating geographic and economic barriers.
Nevertheless, the integration of AI into education is not without challenges [14,15]. A significant concern pertains to the potential overreliance on technology, which may impede the cultivation of critical cognitive abilities such as independent thinking and problem-solving [16,17]. Ethical concerns also arise, particularly regarding data privacy, bias in algorithmic decision-making, and the risk of diminishing the role of educators in the learning process [18,19,20,21]. Consequently, as Ref. [16] contends, the key to effective AI integration in education is its role as a complementary instrument, not a substitute for teachers and human interaction.

1.2. AI in Natural Sciences Education and Research

In the domain of the natural sciences, which encompasses disciplines such as biology, physics, chemistry, and earth sciences, the application of AI is facilitating the emergence of novel pedagogical and research opportunities. These tools have the capacity to enhance the learning experience by providing innovative resources, including customized explanations, interactive simulations, and conceptual diagrams to elucidate complex scientific phenomena. Furthermore, AI facilitates the creation of thematic questions and exercises, thereby enhancing classroom engagement [22,23]. In addition, AI can also serve as an instrumental tool in incorporating research methodologies into educational settings [24].
Additionally, and in line with the abovementioned limitations of AI, its indiscriminate use in scientific education also brings significant concerns. A primary risk is that students may employ AI primarily as a problem-solving or text-generation tool rather than as a means of fostering deeper analytical engagement with scientific concepts. This reliance may pose a challenge to the development of critical thinking and scientific literacy [25,26]. Furthermore, it is imperative to assess whether the information generated by AI aligns with current scientific knowledge [27,28]. A crucial question remains: Do widely used AI applications provide scientifically accurate and unbiased information, or do they introduce distortions that could mislead both educators and students?

1.3. Biodiversity Education and Sustainable Development

Biodiversity is a critical subject in education and plays a fundamental role in advancing the Sustainable Development Goals (SDGs) outlined in the United Nations’ 2030 Agenda. The significance of biodiversity stems from its function as the foundation of life on Earth and its interconnectedness with social, economic, and environmental sustainability [29,30]. Integrating biodiversity education into curricula has been demonstrated to foster environmental awareness from an early age. Students are able to gain insights into the interdependence of ecosystems and the consequences of human actions on the environment [31,32]. According to [33], environmental education is essential for cultivating responsible global citizens committed to sustainability. Moreover, biodiversity loss is recognized as one of the most pressing environmental challenges of the 21st century [34]. Education in this domain provides students with the knowledge and skills necessary to address critical issues such as climate change, deforestation, and species extinction [35].
Biodiversity is closely linked to several SDGs, as it is vital for human well-being and ecological balance. Specifically, it aligns with SDG 13 (Climate Action), given that biodiverse ecosystems—such as forests and oceans—serve as carbon sinks, thereby mitigating climate change. The importance of education in promoting the conservation of these ecosystems to reduce greenhouse gas emissions is also emphasized [36]. Furthermore, biodiversity is intricately linked to both SDG 14 (Life Below Water) and SDG 15 (Life on Land), underscoring the necessity for biodiversity conservation and the mitigation of desertification [37]. Moreover, within the educational context, biodiversity is integral to SDG 4 (Quality Education) as it constitutes a cross-disciplinary theme that interlinks biology, geography, and social sciences [33]. The integration of biodiversity education within curricula is a key strategy that fosters a holistic educational approach, one which is aligned with the principles of sustainability [33].
In Spain, the treatment of environmental education in general and biodiversity in particular is recurrent throughout the educational curriculum, but with obvious differences between the different educational stages. In Early Childhood Education (aimed at children up to 6 years of age), the legislation establishes objectives related to the observation and respect for the environment, without going into more detail due to the young age of the learners [38]. As students progress through the educational system, the curriculum becomes more intricate. In Primary Education (ages 6–12), two key competences, STEM and Citizenship, are introduced. These competences emphasize the importance of preserving the environment and living beings, as well as adopting sustainable lifestyles to contribute to biodiversity conservation. This term is first mentioned in educational legislation. In the section of basic knowledge entitled “Life on our planet”, the study of living beings, their classification, their relationships within ecosystems, and the importance of preserving their diversity is proposed; and in other sections such as “Sustainable development and environmental ethics”, the conservation of biodiversity is addressed as an eco-social problem to be solved [39]. Secondary education is arguably the one in which the treatment of biodiversity and its conservation is most intensified. This phenomenon is exemplified by the operational descriptor CC4 of the Citizenship Competence, which states that students should “begin to adopt sustainable lifestyles, to contribute to the conservation of biodiversity” [40]. Furthermore, various sections of basic knowledge refer to this issue and its eco-social relevance, particularly in the subjects of “Biology and Geology” and the first three courses [40]. Finally, in the Baccalaureate stage (16–18 years; non-compulsory), the subjects “Biology, Geology and Environmental Sciences” and “General Sciences” also address aspects such as sustainable development, the loss of biodiversity as a socio-environmental problem and the causes and consequences of this phenomenon [41].
According to this background, the present study investigates the accuracy and reliability of AI-generated information in the framework of biodiversity education, specifically aiming to determine if AI applications provide scientifically valid data on endangered species or exhibit biases that could misinform both educators and students.

2. Materials and Methods

To formulate an objective research question that would allow us to determine whether AI-generated responses exhibit bias, it was essential to pose a straightforward query while avoiding explanations that students or educators would be unlikely to request. Specifically, the initial question presented to AI applications was the following: “Generate a list of 100 living species that are endangered”. In total, 100 species were requested since higher numbers generate a volume of data that future teachers are unlikely to analyze for educational purposes, and lower numbers limit, taking into account the high number of species in real danger, the capacity to perform an efficient analysis; moreover, the question aimed to assess whether the responses provided by AI systems align with scientific data or whether they reflect societal biases, geographical biases, or preferential biases. For this study, three of the most relevant AI-based text generation tools to date were selected: ChatGPT-4.5 (based on GPT-4-turbo, OpenAI), DeepSeek-V3-chat (DeepSeek AI), and Gemini 1.5 Flash (Google), all accessed in February 2025. As an initial approach, to avoid influencing the chatbots’ responses, three runs were performed for each AI bot, and fresh accounts were used.
The species obtained were categorized by two biodiversity experts into taxonomic groups (predominantly at the class level but, in some cases, at the kingdom level, e.g., plants) and geographic region; in order to analyze the taxonomic bias (uneven phylum coverage and over/underrepresentation of specific taxa) and geographic bias, respectively. The findings were expressed as percentages to enable comparison with real-world extinction risk percentages reported by the International Union for Conservation of Nature (IUCN) and descriptive analyses, including mean and standard deviation, were conducted using R statistical software (version 4.4.0). To minimize potential biases in the comparison, IUCN values were adjusted based on the proportion of evaluated species relative to the total estimated species count (the IUCN estimates that there may be approximately 8 million species of which only 169,410 have been evaluated and of these 47,187 are in danger of extinction), and this adjustment accounts for discrepancies in assessment coverage across taxa (e.g., 84% of mammal species have been evaluated compared to only 1.2% of insect species).
The data of the geographic distribution of the species was also obtained from the IUCN (https://www.iucnredlist.org/es/statistics, accessed on 4 February 2025). The data of the absolute number of endangered species is variable along time, but the percentages are quite stable; to establish clear geographical entities, 8 areas were defined, with some of them being created by combining several IUCN areas (“Caribbean Islands” and “Mesoamerica” in Central America; “East Asia”, “North Asia”, “West and Central Asia” and “South and Southeast Asia” in Asia; “North Africa” and “Sub-Saharan Africa” in Africa) while others were obtained directly (“Europe”, “North America”, “South America”, “Oceania” and “Antarctica”).
To assess the consistency and magnitude of systematic error in the results, two complementary indicators were calculated using R statistical software (version 4.4.0): the taxonomic and geographic Bias Ratio and the Magnitude Error Bias. The Bias Ratio was computed as the mean of the signed differences between the values generated by the AI chatbots and the reference values (IUCN dataset), divided by the standard deviation of those differences; this ratio provides an indication of the directional consistency of the bias (higher absolute values indicate stronger and/or systematic bias, while values close to zero indicate either accuracy or random errors); when the standard deviation of the bias was zero (same percentage values for the three runs) the Bias Ratio was undetermined and noted as “na”; the Magnitude Error Bias is calculated as the mean of the absolute bias values.
Furthermore, considering that the differences between the actual IUCN data and the AI responses could be due to sampling error (this would be the case if the AI performed random sampling among the IUCN databases), three random samplings were performed on the IUCN database to calculate the mean and standard deviation values for both the taxonomic groups and the geographical areas.

3. Results

In the case of ChatGPT, the responses included 43.3 mammals (SD = 1.5), 15 birds (SD = 4.6), 6.7 plants (SD = 6.1), 10 reptiles (SD = 1.5), 6.3 amphibians (SD = 2.1), 6.7 fish (SD = 1.2), and 5.7 insects (SD = 1.5), as well as 1.7 mollusks (SD = 0.6), 1.3 arachnids (SD = 0.6), 1.3 cnidarians (SD = 1.2), one crustacean (SD = 1), and 0.7 fungus (SD = 1.2) (Appendix A and Table 1). Within its response, the AI tool explicitly stated “Below is a representative list of 100 species (including animals, plants, and other living organisms) that are classified as threatened or endangered according to various assessments (e.g., IUCN). It is important to note that conservation status may vary by region and that some species fall under categories such as Critically Endangered, Endangered, or Vulnerable. This list is illustrative and not exhaustive.”
Additionally, some of the responses did not refer to specific species (e.g., “orchids,” “crayfish,” “ferns,” or “certain species of beetles”).
About the ChatGPT taxonomic Bias Ratio, it showed a wide range (Table 2), from a minimum of −20.1 (insects) to a maximum of 28.2 (mammals). Notable underrepresentations include insects (−20.1), fungi (−9.7), and arachnids (−8.5), while mammals are strongly over-represented (28.2), followed by reptiles (6.5) and fish (5.0).
Regarding the geographical distribution of the mentioned species (Table 3), the region with the highest number of species listed was Asia (30.5), followed by Africa and South America (16.7 and 15.7%, respectively), Europe (10.2%), North America and Oceania (10.1 and 9.5%, respectively), Central America (6.9%), and finally, Antarctica (1%). It is important to note that some species were found in multiple regions, while others could not be precisely located due to the general nature of the response (e.g., “orchids”).
The geographic Bias Ratio showed the highest positive bias towards Europe (4.2) and Asia (3.3), followed by North America (2.3) and Antarctica (0.9). Negative biases were observed for Africa (−2.6) and Central America (−2.3), with smaller deviations for South America (−0.5) and Oceania (−0.4).
In the case of DeepSeek, the first response included a total of 120 items (including both species and subspecies, Appendix A and Table 1). Among them, 100 were mammals, of which 46 were subspecies of the insular grey fox (Urocyon littoralis); of these 46, only 7 different subspecies were listed, 4 of them being listed multiple times. Additionally, the tool listed 10 plant species and 10 coral species. The second and third run included 100 species each; considering the three runs together, the results included 53.1% of mammals (SD = 26.2), 15.3% of birds (SD = 13.3), 7.7% of reptiles (SD = 6.8), 6.1% of plants (SD = 1.9), 5.7% of amphibians (SD = 5.5), 4.1% of cnidarians (SD = 3.6), 2.7% of insects and fish, both with a SD = 2.5, 1% of arachnids and mollusks (SD = 1), and 0.7 crustaceans (SD = 1.2). The application also provided the following statement: “Here is a list of endangered living organisms. This list includes animals, plants, and other organisms facing serious threats to their survival. Some of these species are critically endangered, while others are classified as vulnerable or endangered according to the International Union for Conservation of Nature (IUCN) and other sources. This list is only a sample of the many species currently at risk of extinction worldwide.”
The DeepSeek chatbot showed a comparatively narrower taxonomic Bias Ratio range, with bias ratios ranging from −13.4 (insects) to 2.0 (mammals). It demonstrated underrepresentation in plants (−12.3), and mild over-representation in birds (1.1) and reptiles (1.1).
Regarding distribution, 26,6% of the mentioned species were from Asia and 26.0 were from North America, 13.1% were from Africa, 9.5% from South America, 9.2% from Central America, 7.5% from Europe, 7.2% from Oceania, and 1% from Antarctica (Table 3).
The geographic Bias Ratio presented the narrowest range of geographic bias, with values spanning from −3.1 in South America to 0.9 in Antarctica. It showed near-neutral bias for most regions (e.g., Asia: 0.0, Europe: 0.2, North America: 0.8), although some underrepresentation appeared for Africa (−3.0) and South America (−3.1).
The Gemini chatbot mentioned 100 species in each query: 23.8 mammals (SD = 5.5) and 20 bird species (SD = 0), 12.3 species of plants (SD = 2.5), 10.7 species of fishes (SD = 1.2), 10.3 species of reptiles (SD = 0.6), 7.3 species of amphibians (SD = 2.5), 4.7 species of fungus (SD = 4.7), and a few species of invertebrates (4.5 insects (0.6), 2 mollusks (SD = 1), 2.7 crustaceans (0.6), 1 arachnid (SD = 0), and 0.7 cnidarians (SD = 0.6)) (Appendix A and Table 1). Gemini also provided the following statement: “It’s important to remember that this list is just a sample, and there are many more species in danger of extinction around the world. Biodiversity conservation is crucial to the balance of our planet.”
In this case, the taxonomic Bias Ratio showed the most extreme bias overall, with a minimum of −55.5 (insects) and a maximum of 17.2 (reptiles). Underrepresentation was also observed in plants (−6.9), mollusks (−2.3), and amphibians (−2.7), while mammals (4.2) and fish (8.4) were over-represented. Data for arachnids and birds were undetermined (na).
Geographically, these species are distributed as follows: 21.8% of the species were native to Asia, 17.4% to Africa, 16.1% to South America, 14.8% to Oceania, 12,5% to North America and Europe, and 4.6% to Central America.
Regarding the geographic Bias Ratio, Gemini exhibited the most extreme geographic bias overall, ranging from −6.0 in Central America to 13.3 in North America. Other regions showing positive bias include Europe (1.8), Oceania (0.9), and Antarctica (0.4), while negative values were found for Africa (−3.3), Asia (−1.4), and South America (−0.7).
Regarding the data obtained from the International Union for Conservation of Nature (IUCN), the estimated percentages of endangered species vary significantly by taxonomic group, ranging from 36.37% of the total for insects to 0.23% for birds (detailed values can be found in Table 1).
Regarding geographical distribution, the total number of assessed species in each of the regions considered was also obtained from the IUCN, and the corresponding percentage of endangered species in each area was calculated (Table 3); the values ranged from 26.17% of endangered species found in Asia to 4.17% of the endangered species found in North America.
The results for the taxonomic Magnitude Error Ratio ranged from 11.3 (Gemini) to 13.9 (DeepSeek), and an intermediate value for ChatGPT (13.0). Geographic Magnitude Error Ratio: Given the Geographic Magnitude Error Ratio, DeepSeek also showed the highest value, with 7.7, while Gemini had a moderate Geographic Magnitude Error Ratio (5.0), and ChatGPT showed the lowest value (4.0).
The results of the random selection of species from the IUCN endangered species database showed taxonomic values of 63.3% (SD = 3.1) for plants, 7.7% (SD = 1.2) for fish, 7.3% (SD = 2.5) for amphibians, 5.7% (SD = 1.2) for insects, 5.3% (SD = 4.2) for mollusks, 3.3% (SD = 0.6) for reptiles, 2.7% (SD = 1.2) for mammals, 2% (SD = 1.4) for arachnids, 1.5% (SD = 0.7) for birds, 1.3% (SD = 0.6) for crustaceans, 0.7% (SD = 1.2) for the Other category, and 0.3% (SD = 0.6) for fungi. The cnidarian group was not represented. Regarding the geographical results, values of 30.3% (SD = 4.9) were obtained for Asia, 23.7% (SD = 2.1) for Africa, 18.7% (SD = 4) for South America, 10.7% (SD = 3.2) for Central America, 9% (SD = 1) for Oceania, 4.7% (SD = 2.3) for Europe and 2.7% (SD = 1.5) for North America, Antarctica did not obtain results. It is important to note that these results are based on the IUCN Endangered Species Database, and these values do not take into account the percentage of species assessed in each group.

4. Discussion

4.1. Bias in the Results of the AI

At present, AI applications are ubiquitous in both daily life and educational environments ([42], among many others); however, despite their numerous benefits and utilities, the results of this study suggest that caution should be exercised when using them, since the problems of their use are not limited to ethics, as is often highlighted. Both taxonomic and geographic bias have the potential to generate significant issues with teaching effectiveness and the self-taught capacity of students. In both instances, the absence of fundamental technical training can serve as a catalyst for the emergence of these biases (e.g., plant blindness) and perpetuate the associated challenges. This phenomenon has been previously observed in several domains [43].

4.1.1. Taxonomic Bias

With regard to the field of biology and the study of biodiversity, the human predilection for animals over other groups of living organisms, such as plants, fungi, and microorganisms, is a well-documented phenomenon [44]. This tendency, termed “zoocentrism,” signifies a cultural and psychological predisposition to assign greater value to animals than other forms of life. This bias influences not only daily interactions but also scientific research, environmental legislation (which tends to prioritize conservation efforts disproportionately on animals—particularly on charismatic species such as mammals and birds [45,46,47]), and education [27,48]. The findings of this study demonstrate that artificial intelligence applications also exhibit this phenomenon, which, as would be expected, reflect societal tendencies.
Furthermore, it is imperative to consider factors other than zoocentrism. As demonstrated in the results, both AI applications manifest a marked bias, not only towards animals but specifically towards mammals [47]. This bias becomes even more apparent when compared to objective data from the IUCN, which indicates that mammals represent a relatively small taxonomic group, especially among species classified as endangered. This phenomenon is also part of a well-documented cognitive bias known as Plant Blindness, or more recently, Plant Awareness Disparity [49]. This term describes the human tendency to overlook or undervalue the ecological significance of plants [50]. One contributing factor is the perception of plants as static, silent, and less interactive than animals [51]. Intriguingly, a juxtaposition of the IUCN data with the findings derived from AI applications reveals that plants do not constitute the most underrepresented group. As other authors have stated in similar studies, fungi, insects, and arachnids are even more significantly overlooked [52]. Despite the assertions of AI models that their lists encompass a broad taxonomic range, the outcomes evidently do not align with scientific reality. The paucity of species mentioned in the article makes the breakdown of the data impractical.
Regarding the exclusion of fungi, this is most likely a consequence of the ambiguity surrounding their classification. Fungi do not conform easily to the conventional categories of “animal” or “plant”. This has resulted in a lack of recognition concerning their ecological importance, including their role in decomposition, as well as their significance in medicine and food production [52]. Given that no fungal species were included in one of the three AI-generated lists (and in GTP-4.5 the mean value is 0.7%) and considering that fungi are rarely considered in discussions of endangered species, it is unsurprising that this bias remains largely unchallenged.
As for insects, despite the similarities between the AI results (specifically with ChatGPT) and the random selection, their underrepresentation is particularly concerning. This group exhibits the highest negative taxonomic Bias Ratio, which means a great underrepresentation in comparison with the IUCN data. This is especially shocking considering that they represent the most diverse group within the animal kingdom [53] and the fact that invertebrates—and insects in particular—exhibit higher rates of extinction and threatened species than more well-known taxa [54]. Furthermore, insects are recognized as being of paramount importance to human survival, given their pivotal role in agriculture, human health, and natural resources, among other aspects [55]. The observed underrepresentation may be attributed to society’s negative perception of this group, evoking responses such as fear or disgust more than other types of animals [56,57]. This is probably due to factors such as their unpredictable movements, their non-human morphology, or their ability, in some cases, of biting, stinging, and transmitting infection or disease [58,59].

4.1.2. Geographic Bias

In addition to the taxonomic classification of organisms, their geographical origin was also taken into account in order to study the potential existence of bias. In the case of ChatGPT, an underestimation (as a representation of taxa lower than their % of endangered species compared to the world total data) of Africa and Central America has been observed, while other continents such as Asia, North America and, especially, Europe show a notable overestimation. This phenomenon can be attributed to the historical and cultural influence of Western civilization [60], particularly in North America, which is also the geographical origin of the company developing ChatGPT. Indeed, other studies conducted with ChatGPT in various fields (e.g., education, culture) have demonstrated similar biases [61,62]. A similar trend was observed for Gemini, also of North American origin, with its list underestimating areas such as Asia, Africa, and Central America, and significantly overestimating Europe, North America, and Oceania. The findings obtained by these two tools also appear to suggest an influence of societal tendencies on the geographical variable. In the case of DeepSeek, a clear underrepresentation of Africa and South America can be mentioned. The variation in the different runs performed makes it difficult to decide if the representation in the other areas is fair or not. Moreover, the results are difficult to explain in terms of taxonomy and origin and are completely conditioned by the presence of seven subspecies (repeated 46 times in the first run performed with DeepSeek) of the same North American fox species (Urocyon littoralis). This finding appears to lack practical relevance, as the prompts provided were unambiguous in requesting the specified taxonomic category (species), and it is impractical to include subspecies within an extensive list such as that of endangered living beings. The most plausible explanation for this occurrence is the lack of internal mechanisms to ensure uniqueness unless explicitly requested; models do not always have the memory to remove duplicates, especially with long lists (>20 items) [63,64].

4.1.3. Biases and AI Applications

The statistical analyses conducted in this study have shown that the widest ranges for both taxonomic and geographic Bias Ratio were observed in Gemini, with broad differences between the most over- and underrepresented groups and areas, respectively. However, globally (i.e., for the whole set of taxonomic groups and/or geographic areas) the greatest bias, measured through the Magnitude Error Ratio, was observed for DeepSeek both from a taxonomic and geographic perspective, making it “the most biased” AI application in our study.
In any case, the results obtained, although simple, clearly show that the answers generated by generative artificial intelligence systems can reflect and amplify pre-existing biases (in this case both geographic and taxonomic) in the data they have been trained on (e.g., [65,66]), this situation was already detected in searches on regular search engines before the appearance of artificial intelligence chats [27]. The AI models rely on massive databases harvested mostly from the internet, which includes both academic sources and a large amount of unverified, popular, or socially biased content [67,68,69]. Since the majority of the corpus comes from data available online until 2024, there is a real risk that the models not only reproduce stereotypes, inequalities, and/or taxonomic/geographic bias, but reinforce them through a cumulative effect each time the system generates similar content based on previous interactions [70,71].
Added to this is the mechanism of user reinforcement, whereby popular or most accepted answers tend to be prioritized by the system, further reinforcing dominant biases [72]. Although the user can explicitly influence content through the use of prompts, these can also induce biased responses if they contain implicit assumptions or if the AI fails to recognize taxonomic, geographic, or social ambiguities [73].
Furthermore, each AI system implements its own filters, alignment models, and architectures, resulting in differences in the type and degree of bias across platforms. In this regard, probably the best known AI chatbot is ChatGPT, whose training process consists of four well-known steps [74]; it starts by training the model on large amounts of unlabeled data from different internet databases, thus allowing the learning of general patterns and data relations; after that, the pre-trained model is fine-tuned by using a small dataset, linked to a specific task, thus becoming more efficient and appropriate for it. This step is mainly performed by human AI trainers, who also assess the accuracy and quality of responses in the following step by assigning scores to each pair of “prompt-response”, prior to the final optimization process. The fact that the GPT model is pre-trained on presumably non-cleaned/refined data, together with the human dependency for fine-tuning and model training, increases the risk of obtaining wrong, biased, or inaccurate responses by this tool [74]. In the case of Gemini, a comparative study with ChatGPT was conducted by [75], who concluded that the model type of Gemini (Multimodal Language Model), together with its particular architecture (which, for example, includes Retrieval-Augmented Generation (RAG)) and the use of datasets curated by Google allow the production of more precise and informative responses. However, these features also seem to limit the creativity and conversational flow of the outputs and are not capable of avoiding the biased responses which derive from the human-conditioned training data mentioned for ChatGPT. Our results reveal the same weakness for the case of DeepSeek-V3, even though it has been found to be a high-performance tool that offers accurate responses at lower input costs than other chatbots [76]. The same study also concluded that the efficiency of this and other AI tools (including ChatGPT and Gemini) depends on the specific task requested by the user, which strongly limits the conclusions we can draw in our particular work where, as we mentioned before, DeepSeek offered the highest bias levels.
Taking into account the complexity of the models and the different architectures, understanding how these models are trained, how they prioritize responses, and what data they rely on is key to critically evaluating their use in educational, scientific, or social contexts.

4.2. AI Implications for Biodiversity Education

The findings of this study hint the challenges associated with the utilization of AI applications for self-directed learning and for non-specialist teachers. Educators who rely on these tools for classroom instruction may also encounter difficulties due to their inherent biases [44,77]. While AI applications offer significant benefits, they may also reinforce existing biases, particularly the disproportionate emphasis on mammals, rather than contributing to their correction. Consequently, these technologies still do not seem to be an optimal way to meet the biodiversity-related challenges outlined in the previously mentioned Sustainable Development Goals (SDGs), particularly regarding the conservation of endangered species, where biases may be maintained, both geographical and taxonomic. This is particularly salient in the context of Spain, where the recurrent presence of biodiversity in the educational curriculum has been previously highlighted [38,39,40,41]. A particularly problematic scenario emerges in the context of Primary Education, as educators at this level are not equipped with specialized training in scientific disciplines. This may result in a heightened inclination to rely on AI tools for the preparation of their lessons.
During Primary Education, complex content is already addressed, such as the identification and classification of living beings, the human relationship with ecosystems, the relevance of biodiversity, eco-social responsibility, or climate change. This can pose a challenge for those teachers less familiar with these topics. This problem is hypothesized to be less acute in the Early Childhood Education stage, due to the greater simplicity of its content, and in the Secondary and Baccalaureate stages, where teachers are expected to have specific training to access their job position. However, studies have revealed an increasing inclination towards AI among teachers at these levels [78], and the greater autonomy afforded to students in completing their tasks may also influence their utilization of AI. The findings of this study suggest that these trends could potentially contribute to the perpetuation of social trends concerning biodiversity, particularly with regard to species at risk of extinction, from both taxonomic and geographical perspectives. There is a lack of studies applied to these groups in which the teachers themselves are the focus; it is necessary to analyze the variations in the biases present to identify the depth of the problem and propose possible solutions.

5. Conclusions and Limitations

To summarize, the findings of this study demonstrate that AI applications not only replicate ethical biases, but also taxonomic and geographical biases, which have the potential to impede educational effectiveness and self-directed learning. The dearth of rudimentary technical training among pedagogues and pupils can intensify these biases, perpetuating issues such as zoocentrism and plant blindness. The prevailing cultural inclination towards the preference for animals, particularly mammals, at the expense of other organisms such as plants, fungi, insects, and microorganisms, is a salient concern. This bias is perpetuated by the predominance of artificial intelligence in various fields, despite the ecological significance of these other organisms. This imbalance is incongruent with scientific reality, as evidenced by IUCN data, and contributes to a distorted perspective of biodiversity in education and conservation. Furthermore, the geographical bias is indicative of the influence of sociocultural trends and the geographic origin of the developing companies, thereby limiting a balanced global perspective.
The integration of AI in educational settings, particularly at primary school levels where educators may not possess specialized scientific training, can perpetuate stereotypes rather than rectifying them. This hinders the achievement of the Sustainable Development Goals (SDGs) related to biodiversity and perpetuates a biased view of endangered species. To mitigate these biases, it is crucial to enhance the training of AI models with rigorous scientific data and to promote critical teacher training that encourages the responsible use of these tools.
Further research is required to develop solutions that have a tangible impact on teachers at these levels. It is also necessary to evaluate how learning models correct these biases, in the event that such progress occurs, and how other (and new) models reflect them.

Author Contributions

Conceptualization, J.B.-P. and L.d.P.N.; methodology, J.B.-P. and L.d.P.N.; formal analysis, J.B.-P., L.d.P.N., and S.Q.-A.; investigation, J.B.-P. and L.d.P.N.; data curation, J.B.-P., L.d.P.N., and A.M.G.; writing—original draft preparation, J.B.-P. and L.d.P.N.; writing—review and editing, all the authors; visualization, J.B.-P. and L.d.P.N.; supervision, J.D.-I. and R.R.-T. All authors have read and agreed to the published version of the manuscript.

Funding

This study has been developed within the framework of the research project TED2021-130300B-C21 funded by the Ministry of Science and Innovation.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Data are contained within the article.

Acknowledgments

Taking into account that it forms the basis for this study, the authors have used IA tools to obtain data (see text). The authors have reviewed and edited the output and take full responsibility for the content of this publication.

Conflicts of Interest

The authors declare no conflicts of interest.

Abbreviations

The following abbreviations are used in this manuscript:
AIArtificial Intelligence
SDGSustainable Development Goals
IUCNInternational Union for Conservation of Nature

Appendix A

Table A1. Example of the full list of the species provided by the IA chatbots (first run).
Table A1. Example of the full list of the species provided by the IA chatbots (first run).
GPT-4.5DeepSeek-V3Gemini (v.2025)
1Harlequin FrogSumatran tigerPolar Bear
2Panama Golden FrogMountain gorillaXerocomellus porosporus
3Central American Glass FrogBornean orangutanAsian Elephant
4Darwin’s FrogSumatran OrangutanWestern Chimpanzee
5Woodland SalamanderJavan rhinocerosDarwin’s Fox
6European Woodland SalamanderBlack rhinocerosNorth Atlantic Right Whale
7Tiger SalamanderSumatran ElephantMexican Fishing Bat
8Scorpion Endemic to Certain IslandsSnow leopardIberian Lynx
9Antarctic AlbatrossIberian lynxBrown-headed Spider Monkey
10Laysan AlbatrossPolar bearTibetan Bear
11Black StiltGiant pandaIrrawaddy River Dolphin
12Philippine Blue-winged CockatooChinese pangolinJavan Rhinoceros
13Moluccan CockatooSunda PangolinOmiltemi Rabbit
14California CondorVaquitaVenezuelan Red Siskin
15Cock-of-the-RockNorth Atlantic Right WhaleKakapo
16Spix’s MacawBlue WhaleCalifornia Condor
17Northern Bald IbisLeatherback Sea TurtleNorthern Bald Ibis
18KakapoHawksbill Sea TurtleIvory-billed Albatross
19Okarito KiwiGreen Sea TurtleAmsterdam Albatross
20Storm PetrelCalifornia CondorHelmeted Hornbill
21Darwin’s FinchPhilippine EagleSpix’s Macaw
22Bannerman’s TuracoHyacinth MacawNorth Island Brown Kiwi
23CrayfishScarlet MacawAmur Leopard
24Franklin’s BumblebeeTanimbar CockatooGalapagos Penguin
25Stag BeetleNorthern White RhinocerosBearded Vulture
26Blue Butterfly MorphoSumatran rhinocerosRed-cockaded Woodpecker
27Karner butterflyMalayan tapirBalearic Shearwater
28Monarch butterflyMountain tapirAlbert’s Lyrebird
29AxolotlBaird’s tapirCapercaillie
30Blue whaleAmazonian tapirNicobar Pigeon
31North Atlantic right whaleJaguarMauritius Parakeet
32European bisonRed panda bearBlack-bellied Sandgrouse
33BonoboSpectacled bearShoebill
34Common chimpanzeeSun bearMountain Gorilla
35Amazon river dolphinSloth bearFloreana Thrush
36African forest elephantRed wolfHawksbill Turtle
37Asian elephantMexican Grey wolfMalagasy Tortoise
38GharialNorthern lynxOrinoco Crocodile
39Mountain gorillaCanadian lynxTuatara
40IndriEurasian lynxRound Island Python
41Greater bamboo lemurAfrican lionVietnamese Box Turtle
42Bamboo lemurAsiatic lionTarzan’s Chameleon
43Mantilla lemurCheetahAnegada Iguana
44Crowned skull lemurAsiatic cheetahSan Francisco Garter Snake
45Gray mouse lemurStriped hyenaSumatran Tiger
46Ruffed lemurBrown hyenaHowe Island Giant Gecko
47Sand lemurSpotted hyenaAxolotl
48Asiatic lionDarwin’s FoxGolden Poison Frog
49Amur leopardSierra Nevada red FoxCarriqui Harlequin Toad
50Snow leopardArctic FoxManduriacu glass frog
51Iberian lynxArgentine Grey FoxChinese giant salamander
52Ethiopian wolfPatagonian Grey FoxEl Tambor marsupial frog
53Mexican wolfPampas Grey FoxBetic midwife toad
54Barbary macaqueIsland Grey FoxSagalla caecilians
55Northeastern howler monkeyChannel Islands Grey FoxTable Mountain ghost frog
56Bornean orangutanSan Miguel Islands Grey FoxChinese pangolin
57Sumatran orangutanSanta Rosa Islands Grey FoxApennine fire-bellied toad
58Giant pandaSanta Cruz Islands Grey FoxChinese sturgeon
59PangolinSan Clemente Islands Grey FoxFreshwater sawfish
60Palm PangolinSan Nicolas Islands Grey FoxGiant grouper
61African Wild DogSan Miguel Islands Grey FoxGreat white shark
62Javan RhinocerosSanta Catalina Islands Grey FoxAtlantic bluefin tuna
63Sumatran RhinocerosSan Clemente Islands Grey FoxAustralian lungfish
64Black RhinocerosSan Nicolas Islands Grey FoxEuropean eel
65SaolaSan Miguel Islands Grey FoxMekong giant catfish
66Verreaux’s SifakaSanta Catalina Islands Grey FoxDanube salmon
67Malayan TapirSan Clemente Islands Grey FoxBlue-eyed black lemur
68Bengal TigerSan Nicolas Islands Grey FoxBaxter Springs trout
69Sumatran TigerSan Miguel Islands Grey FoxLord Howe Island land snail
70Red UakariSanta Catalina Islands Grey FoxSwellendam crayfish
71VaquitaSan Clemente Islands Grey FoxQueen Alexandra birdwing butterfly
72Chinook (Pacific Salmon)San Nicolas Islands Grey FoxGiant Wallace’s bee
73Atlantic SturgeonSan Miguel Islands Grey FoxStag beetle Kempsey
74Giant Manta RaySanta Catalina Islands Grey FoxMaratus elephans peacock spider
75Asian CatfishSan Clemente Islands Grey FoxStaghorn coral
76Mekong CatfishSan Nicolas Islands Grey FoxGulf Coast freshwater mussel
77Napoleon WrasseSan Miguel Islands Grey FoxMurray freshwater lobster
78Fraser FirSanta Catalina Islands Grey FoxSaola
79Widdringtonia CedarSan Clemente Islands Grey FoxLord Howe Island tree cricket
80Cedar of LebanonSan Nicolas Islands Grey FoxCoast redwood
81Cyanea micronesicaSan Miguel Islands Grey FoxWollemia
82Socotra Dragon TreeSanta Catalina Islands Grey FoxLord Howe pine
83Tree Fern of Certain RainforestsSan Clemente Islands Grey FoxJellyfish tree
84European ElmSan Nicolas Islands Grey FoxVictoria giant water lily
85Wild OrchidSan Miguel Islands Grey FoxRafflesia arnoldii
86Madagascar PalmSanta Catalina Islands Grey FoxVenus flytrap
87PuyarRaimondiiSan Clemente Islands Grey FoxJade tree
88Rafflesia arnoldiiSan Nicolas Islands Grey FoxGhost orchid
89Wollemia Cuban alligatorSan Miguel Islands Grey FoxTapanuli orangutan
90Orinoco alligatorSanta Catalina Islands Grey FoxChilean pine
91Philippine crocodileSan Clemente Islands Grey FoxAmanita liquii
92Komodo dragonSan Nicolas Islands Grey FoxBoletus regineus
93Ricord’s iguanaSan Miguel Islands Grey FoxClavaria zollingeri
94Caribbean iguanaSanta Catalina Islands Grey FoxGeastrum britannicum
95Hawksbill turtleSan Clemente Islands Grey FoxHygrophorus erubescens
96Mekong river turtleSan Nicolas Islands Grey FoxMycena interrupta
97Leatherback turtleSan Miguel Islands Grey FoxRamaria Botrytis
98OryctesSanta Catalina Islands Grey FoxSarcosoma globosum
99Northeastern howler monkeySan Clemente Islands Grey FoxTricholoma caligatum
100Some Beetle speciesSan Nicolas Islands Grey FoxVaquita
101 Ghost orchid
102 Hawaiian passionflower
103 Copal resin tree
104 Wollemi Pine
105 Giant sequoia
106 Redwood
107 Cinchona tree
108 Cinnamon tree
109 Tree Vanilla
110 Nutmeg tree
111 Elkhorn coral
112 Brain coral
113 Star coral
114 Fire coral
115 Mushroom coral
116 Finger coral
117 Table coral
118 Column coral
119 Pillar coral
120 Brain coral

References

  1. Turing, A.M. Computing machinery and intelligence. Mind 1950, 236, 433–460. [Google Scholar] [CrossRef]
  2. McCarthy, J.; Minsky, M.L.; Rochester, N.; Shannon, C.E. A proposal for the Dartmouth summer research project on artificial intelligence. AI Mag. 2006, 27, 12. [Google Scholar]
  3. Lecun, Y.; Bengio, Y.; Hinton, G. Deep learning. Nature 2015, 521, 436–444. [Google Scholar] [CrossRef] [PubMed]
  4. Aydın, Ö.; Karaarslan, E. Is ChatGPT Leading Generative AI? What is Beyond Expectations? Acad. Platf. J. Eng. Smart Syst. 2023, 11, 118–134. [Google Scholar] [CrossRef]
  5. Russell, S.; Norvig, P. Artificial Intelligence: A Modern Approach, 4th ed.; Pearson: London, UK, 2021. [Google Scholar]
  6. Brown, T.B.; Mann, B.; Ryder, N.; Subbiah, M.; Kaplan, J.; Dhariwal, P.; Neelakantan, A.; Shyam, P.; Sastry, G.; Askell, A.; et al. Language models are few-shot learners. Adv. Neural Inf. Process. Syst. 2020, 33, 1877–1901. [Google Scholar]
  7. Díaz-Lara, C.; de la Calle Carracedo, M. Inteligencia Artificial en la formación del profesorado de Ciencias Sociales. In Proceedings of the Conference EDUNOVATIC 2024; REDINE, Ed.; Adaya Press: Madrid, Spain, 2024; pp. 70–71. [Google Scholar]
  8. Chiu, T.K.F.; Xia, Q.; Zhou, X.; Chai, C.S.; Cheng, M. Systematic literature review on opportunities, challenges, and future research recommendations of artificial intelligence in education. Comput. Educ. Artif. Intell. 2023, 4, 100118. [Google Scholar] [CrossRef]
  9. Porter, B.; Grippa, F. A platform for AI-enabled real-time feedback to promote digital collaboration. Sustainability 2020, 12, 10243. [Google Scholar] [CrossRef]
  10. Vieriu, A.M.; Petrea, G. The Impact of Artificial Intelligence (AI) on Students’ Academic Development. Educ. Sci. 2025, 15, 343. [Google Scholar] [CrossRef]
  11. Holmes, W.; Maya, B.; Fadel, C. Artificial Intelligence In Education: Promises and Implications for Teaching; Holmes, W., Maya, B., Fadel, C., Eds.; Center for Curriculum Redesign: Boston, MA, USA, 2019; ISBN 9781794293700. [Google Scholar]
  12. Luckin, R.; Holmes, W.; Griffiths, M.; Forcier, L.B. Intelligence-Unleashed: An argument for AI in Education; Luckin, R., Holmes, W., Griffiths, M., Forcier, L.B., Eds.; Pearson: London, UK, 2016; ISBN 9780992424886. [Google Scholar]
  13. Zawacki-Richter, O.; Marín, V.I.; Bond, M.; Gouverneur, F. Systematic review of research on artificial intelligence applications in higher education—Where are the educators? Int. J. Educ. Technol. High. Educ. 2019, 16, 39. [Google Scholar] [CrossRef]
  14. Ayuso del Puerto, D.; Gutiérrez Esteban, P. La Inteligencia Artificial como recurso educativo durante la formación inicial del profesorado. RIED-Rev. Iberoam. Educ. A Distancia 2022, 25, 347–362. [Google Scholar] [CrossRef]
  15. Moreno Padilla, R.D. La llegada de la inteligencia artificial a la educación. Rev. Investig. Tecnol. Inf. 2019, 7, 260–270. [Google Scholar] [CrossRef]
  16. Selwyn, N. Should Robots Replace Teachers? AI and the Future of Education; Polity Press: Cambridge, MA, USA, 2019. [Google Scholar]
  17. Berendt, B.; Littlejohn, A.; Blakemore, M. AI in education: Learner choice and fundamental rights. Learn. Media Technol. 2020, 45, 312–324. [Google Scholar] [CrossRef]
  18. Akgun, S.; Greenhow, C. Artificial intelligence in education: Addressing ethical challenges in K-12 settings. AI Ethics 2022, 2, 431–440. [Google Scholar] [CrossRef] [PubMed]
  19. Chen, J.J.; Lin, J.C. Artificial intelligence as a double-edged sword: Wielding the POWER principles to maximize its positive effects and minimize its negative effects. Contemp. Issues Early Child. 2024, 25, 146–153. [Google Scholar] [CrossRef]
  20. Huang, L. Ethics of Artificial Intelligence in Education: Student Privacy and Data Protection. Sci. Insights Educ. Front. 2023, 16, 2577–2587. [Google Scholar] [CrossRef]
  21. Sanusi, I.T.; Oyelere, S.S.; Omidiora, J.O. Exploring teachers’ preconceptions of teaching machine learning in high school: A preliminary insight from Africa. Comput. Educ. Open 2022, 3, 100072. [Google Scholar] [CrossRef]
  22. Almasri, F. Exploring the Impact of Artificial Intelligence in Teaching and Learning of Science: A Systematic Review of Empirical Research. Res. Sci. Educ. 2024, 54, 977–997. [Google Scholar] [CrossRef]
  23. Kumar, J.A.; Zhuang, M.; Thomas, S. ChatGPT for natural sciences course design: Insights from a strengths, weaknesses, opportunities, and threats analysis. Nat. Sci. Educ. 2024, 53, e70003. [Google Scholar] [CrossRef]
  24. Valderrama, D.A.; Numpaque, D.S.; Mariño, D.A.; Pinilla, A.Y. Artificial Intelligence in the Teaching of Natural Sciences on the Threshold of the Fifth Industrial Revolution. In Explainable AI for Education: Recent Trends and Challenges; Singh, T., Dutta, S., Vyas, S., Rocha, A., Eds.; Springer: Berlin/Heidelberg, Germany, 2024; pp. 147–168. ISBN 978-3-031-72410-7. [Google Scholar]
  25. Black, R.W.; Tomlinson, B. University students describe how they adopt AI for writing and research in a general education course. Sci. Rep. 2025, 15, 8799. [Google Scholar] [CrossRef] [PubMed]
  26. Wang, J.; Fan, W. The effect of ChatGPT on students’ learning performance, learning perception, and higher-order thinking: Insights from a meta-analysis. Humanit. Soc. Sci. Commun. 2025, 12, 621. [Google Scholar] [CrossRef]
  27. Bobo-Pinilla, J.; Marcos-Walias, J.; Delgado Iglesias, J.; Reinoso Tapia, R. Overcoming plant blindness: Are the future teachers ready? J. Biol. Educ. 2023, 58, 1466–1480. [Google Scholar] [CrossRef]
  28. Chan, C.K.Y.; Colloton, T. Generative AI in Higher Education: The ChatGPT Effect; Routledge: New York, NY, USA, 2024. [Google Scholar]
  29. Niesenbaum, R.A. The integration of conservation, biodiversity, and sustainability. Sustainability 2019, 11, 4676. [Google Scholar] [CrossRef]
  30. Kopnina, H.; Zhang, S.R.; Anthony, S.; Hassan, A.; Maroun, W. The inclusion of biodiversity into Environmental, Social, and Governance (ESG) framework: A strategic integration of ecocentric extinction accounting. J. Environ. Manag. 2024, 351, 119808. [Google Scholar] [CrossRef] [PubMed]
  31. Børresen, S.T.; Ulimboka, R.; Nyahongo, J.; Ranke, P.S.; Skjaervø, G.R.; Røskaft, E. The role of education in biodiversity conservation: Can knowledge and understanding alter locals’ views and attitudes towards ecosystem services? Environ. Educ. Res. 2023, 29, 148–163. [Google Scholar] [CrossRef]
  32. Kilinc, A.; Yeşiltaş, N.K.; Kartal, T.; Demiral, Ü.; Eroğlu, B. School Students’ Conceptions about Biodiversity Loss: Definitions, Reasons, Results and Solutions. Res. Sci. Educ. 2013, 43, 2277–2307. [Google Scholar] [CrossRef]
  33. UNESCO. Education for Sustainable Development Goals: Learning Objectives. 2017. Available online: https://unesdoc.unesco.org/ark:/48223/pf0000252423 (accessed on 1 February 2025).
  34. Cardinale, B.J.; Duffy, J.E.; Gonzalez, A.; Hooper, D.U.; Perrings, C.; Venail, P.; Narwani, A.; Mace, G.M.; Tilman, D.; Wardle, D.A.; et al. Biodiversity loss and its impact on humanity. Nature 2012, 486, 59–67. [Google Scholar] [CrossRef] [PubMed]
  35. Castro, P.; Azeiteiro, U.M.; Nicolau, P.B.; Filho, W.L.; Azul, A.M. Biodiversity and Education for Sustainable Development; Springer: Cham, Switzerland, 2020. [Google Scholar]
  36. IPCC. Special Report on Climate Change and Land. 2019. Available online: https://www.ipcc.ch/srccl/download/ (accessed on 1 February 2025).
  37. United Nations. Transformar nuestro mundo: La Agenda 2030 para el Desarrollo Sostenible. 2015. Available online: https://sdgs.un.org/publications/transforming-our-world-2030-agenda-sustainable-development-17981 (accessed on 1 February 2025).
  38. Ministerio de Educación y Formación Profesional. Real Decreto 95/2022, de 1 de febrero, por el que se establece la ordenación y las enseñanzas mínimas de la Educación Infantil. Boletín Of. Del Estado 2022, 28, 1–33. [Google Scholar]
  39. Ministerio de Educación y Formación Profesional. Real Decreto 157/2022, de 1 de marzo, por el que se establecen la ordenación y las enseñanzas mínimas de la Educación Primaria. Boletín Of. Del Estado 2022, 2014, 1–109. [Google Scholar]
  40. Ministerio de Educación y Formación Profesional. Real Decreto 217/2022, de 29 de marzo, por el que se establece la ordenación y las enseñanzas mínimas de la Educación Secundaria Obligatoria. Boletín Of. Del Estado 2022, 76, 1–198. [Google Scholar]
  41. Ministerio de Educación y Formación Profesional. Real Decreto 243/2022, de 5 de abril, por el que se establecen la ordenación y las enseñanzas mínimas del Bachillerato. Boletín Of. Del Estado 2022, 82, 1–325. [Google Scholar]
  42. Labadze, L.; Grigolia, M.; Machaidze, L. Role of AI chatbots in education: Systematic literature review. Int. J. Educ. Technol. High. Educ. 2023, 20, 56. [Google Scholar] [CrossRef]
  43. Crompton, H.; Burke, D. Artificial intelligence in higher education: The state of the field. Int. J. Educ. Technol. High. Educ. 2023, 20, 22. [Google Scholar] [CrossRef]
  44. Hershey, D.R. Plant Content in the National Science Education Standards. Available online: https://files.eric.ed.gov/fulltext/ED501357.pdf (accessed on 1 February 2025).
  45. Martín-López, B.; García-Llorente, M.; Palomo, I.; Montes, C. The conservation against development paradigm in protected areas: Valuation of ecosystem services in the Doñana social-ecological system (southwestern Spain). Ecol. Econ. 2011, 70, 1481–1491. [Google Scholar] [CrossRef]
  46. Bennett, J.W. The fungi that ate my house. Science 2015, 349, 1018. [Google Scholar] [CrossRef] [PubMed]
  47. Havens, K.; Kramer, A.T.; Guerrant, E.O. Getting plant conservation right (or not): The case of the United States. Int. J. Plant Sci. 2014, 175, 3–10. [Google Scholar] [CrossRef]
  48. Marcos-Walias, J.; Bobo-Pinilla, J.; Iglesias, J.D.; Tapia, R.R. Plant awareness disparity among students of different educational levels in Spain. Eur. J. Sci. Math. Educ. 2023, 11, 234–248. [Google Scholar] [CrossRef] [PubMed]
  49. Parsley, K.M. Plant awareness disparity: A case for renaming plant blindness. Plants People Planet 2020, 2, 598–601. [Google Scholar] [CrossRef]
  50. Wandersee, J.H.; Schussler, E.E. Toward a Theory of Plant Blindness. Plant Sci. Bull. 2001, 47, 2–9. [Google Scholar]
  51. Sanders, D.L. Standing in the shadows of plants. Plants People Planet 2019, 1, 130–138. [Google Scholar] [CrossRef]
  52. Talbot, N.J. A cure for ‘fungus blindness’. Nat. Plants 2020, 6, 1068–1069. [Google Scholar] [CrossRef]
  53. Misof, B.; Liu, S.; Meusemann, K.; Peters, R.S.; Donath, A.; Mayer, C.; Frandsen, P.B.; Ware, J.; Flouri, T.; Beutel, R.G.; et al. Phylogenomics resolves the timing and pattern of insect evolution. Science 2014, 346, 763–767. [Google Scholar] [CrossRef] [PubMed]
  54. Cardoso, P.; Erwin, T.L.; Borges, P.A.V.; New, T.R. The seven impediments in invertebrate conservation and how to overcome them. Biol. Conserv. 2011, 144, 2647–2655. [Google Scholar] [CrossRef]
  55. Scudder, G.G.E. The Importance of Insects. In Insect Biodiversity: Science and Society; Foottit, R.G., Adler, P.H., Eds.; John Wiley & Sons, Ltd.: Hoboken, NJ, USA, 2017; Volume I, pp. 9–43. [Google Scholar]
  56. Davey, G.C.L. Self-reported fears to common indigenous animals in an adult UK population: The role of disgust sensitivity. Br. J. Psychol. 1994, 85, 541–554. [Google Scholar] [CrossRef] [PubMed]
  57. Fukano, Y.; Soga, M. Why do so many modern people hate insects? The urbanization–disgust hypothesis. Sci. Total Environ. 2021, 777, 146229. [Google Scholar] [CrossRef]
  58. Lockwood, J.A. The Infested Mind: Why Humans Fear, Loathe, and Love Insects; Oxford University Press: Oxford, UK, 2013; ISBN 9780199930197. [Google Scholar]
  59. Borgi, M.; Cirulli, F. Attitudes toward Animals among kindergarten children: Species preferences. Anthrozoos 2015, 28, 45–59. [Google Scholar] [CrossRef]
  60. Allen, R.C. The rise of the West. In Global Economic History: A Very Short Introduction; Allen, R.C., Ed.; Oxford University Press: Oxford, UK, 2011; pp. 14–26. [Google Scholar]
  61. Qu, Y.; Wang, J. Performance and biases of Large Language Models in public opinion simulation. Humanit. Soc. Sci. Commun. 2024, 11, 1095. [Google Scholar] [CrossRef]
  62. Tao, Y.; Viberg, O.; Baker, R.S.; Kizilcec, R.F. Cultural bias and cultural alignment of large language models. PNAS Nexus 2024, 3, 346. [Google Scholar] [CrossRef] [PubMed]
  63. Sileo, D. Attention Overflow: Language Model Input Blur during Long-Context Missing Items Recommendation. arXiv 2024, arXiv:2407.13481. [Google Scholar]
  64. Lee, K.; Ippolito, D.; Nystrom, A.; Zhang, C.; Eck, D.; Callison-Burch, C.; Carlini, N. Deduplicating Training Data Makes Language Models Better. In Proceedings of the Annual Meeting of the Association for Computational Linguistics, Dublin, Ireland, 22–27 May 2022; Volume 1, pp. 8424–8445. [Google Scholar]
  65. Ferrara, E. Should ChatGPT be biased? Challenges and risks of bias in large language models. arXiv 2023, arXiv:2304.03738. [Google Scholar]
  66. Xue, J.; Wang, Y.-C.; Wei, C.; Liu, X.; Woo, J.; Kuo, C.-C.J. Bias and Fairness in Chatbots: An Overview. APSIPA Trans. Signal Inf. Process. 2024, 13, 1–26. [Google Scholar] [CrossRef]
  67. Alser, M.; Waisberg, E. Concerns with the Usage of ChatGPT in Academia and Medicine: A Viewpoint. Am. J. Med. Open 2023, 9, 100036. [Google Scholar] [CrossRef] [PubMed]
  68. Caspi, R.; Karp, P.D. An evaluation of ChatGPT and Bard (Gemini) in the context of biological knowledge retrieval. Access Microbiol. 2024, 6, 000790.v3. [Google Scholar] [CrossRef] [PubMed]
  69. Hu, T.; Kyrychenko, Y.; Rathje, S.; Collier, N.; van der Linden, S.; Roozenbeek, J. Generative language models exhibit social identity biases. Nat. Comput. Sci. 2024, 5, 65–75. [Google Scholar] [CrossRef] [PubMed]
  70. Caliskan, A.; Bryson, J.J.; Narayanan, A. Semantics derived automatically from language corpora contain human-like moral choices. Science 2017, 356, 183–186. [Google Scholar] [CrossRef] [PubMed]
  71. Glickman, M.; Sharot, T. How human—AI feedback loops alter human perceptual, emotional and social judgements. Nat. Hum. Behav. 2025, 9, 345–359. [Google Scholar] [CrossRef] [PubMed]
  72. Nazi, Z.A.; Peng, W. Large Language Models in Healthcare and Medical Domain: A Review. Informatics 2024, 11, 57. [Google Scholar] [CrossRef]
  73. Suresh, H.; Guttag, J. A Framework for Understanding Sources of Harm throughout the Machine Learning Life Cycle. In Proceedings of the Equity and Access in Algorithms, Mechanisms, and Optimization (EAAMO ’21), New York, NY, USA, 5–9 October 2021; ACM: New York, NY, USA, 2021; p. 9. [Google Scholar]
  74. Naik, I.; Naik, D.; Naik, N. ChatGPT Is All You Need: Untangling Its Underlying AI Models, Architecture, Training Procedure, Capabilities, Limitations And Applications. TechRxiv 2024. [Google Scholar] [CrossRef] [PubMed]
  75. Rane, N.; Choudhary, S.; Rane, J. Gemini versus ChatGPT: Applications, performance, architecture, capabilities, and implementation. J. Appl. Artif. Intell. 2024, 5, 69–93. [Google Scholar] [CrossRef]
  76. Aydin, Ö.; Karaarslan, E.; Erenay, F.S.; Džakula, N.B. Generative AI in Academic Writing: A Comparison of DeepSeek, Qwen, ChatGPT, Gemini, Llama, Mistral, and Gemma. arXiv 2025, arXiv:2503.04765. [Google Scholar]
  77. Köklükaya, A.N.; Demirhan, E.; Beşoluk, Ş. The Prospective Science Teachers’ Perceptions of Biodiversity. Procedia—Soc. Behav. Sci. 2014, 116, 1562–1567. [Google Scholar] [CrossRef]
  78. Pérez, J.Q.; Daradoumis, T.; Puig, J.M.M. Rediscovering the use of chatbots in education: A systematic literature review. Comput. Appl. Eng. Educ. 2020, 28, 1549–1565. [Google Scholar] [CrossRef]
Table 1. Values of endangered species obtained by taxonomy for the three IA applications. The data are segregated by the main taxonomic groups and are expressed in percentage and standard deviation (between parenthesis). The random values were obtained from the current IUCN database. The Endangered % data are extrapolated from the IUCN database giving the size of the taxonomic group, the species evaluated, and the percentage of species evaluated endangered (see text).
Table 1. Values of endangered species obtained by taxonomy for the three IA applications. The data are segregated by the main taxonomic groups and are expressed in percentage and standard deviation (between parenthesis). The random values were obtained from the current IUCN database. The Endangered % data are extrapolated from the IUCN database giving the size of the taxonomic group, the species evaluated, and the percentage of species evaluated endangered (see text).
GPT-4.5% (SD)DeepSeek-V3% (SD)Gemini % (SD)Random Selection from IUCN; % (SD)Endangered % (Extrapolated from IUCN)
Insect5.7 (1.5)2.7 (2.5)4.5 (0.6)5.7 (1.2)36.37
Plant6.7 (6.1)6.1 (1.9)12.3 (2.5)63.3 (3.1)29.6
Fungus0.7 (1.2)04.7 (4.7)0.3 (0.6)11.9
Arachnid1.3 (0.6)1 (1)1 (0)2 (1.4)6.26
Mollusk1.7 (0.6)1 (1)2 (1)5.3 (4.2)4.26
Crustacean1 (1)0.7 (1.2)2.7 (0.6)1.3 (0.6)3.84
Fish6.7 (1.2)2.7 (2.5)10.7 (1.2)7.7 (1.2)0.95
Amphibian6.3 (2.1)5.7 (5.5)7.3 (2.5)0.7 (1.2)0.57
Reptile10.3 (1.5)7.7 (6.8)10.3 (0.6)3.3 (0.6)0.39
Cnidarian1.3 (1.2)4.1 (3.6)0.7 (0.6)00.37
Mammal43.3 (1.5)53.1 (26.2)23.8 (5.5)2.7 (1.2)0.27
Bird15 (4.6)15.3 (13.3)20 (0)1.5 (0.7)0.23
Other0000.7 (1.2)15.87
Table 2. Taxonomic and geographic Bias Ratio values. Positive values indicate over-representation; negative values indicate underrepresentation.
Table 2. Taxonomic and geographic Bias Ratio values. Positive values indicate over-representation; negative values indicate underrepresentation.
Taxonomic Bias Ratio
GPT-4.5GeminiDeepSeek-V3
Insect −20.1−55.5−13.4
Plant −3.8−6.9−12.3
Fungus −9.7−1.5na
Arachnid −8.5na−5.3
Mollusk −4.5−2.3−3.3
Crustacean −2.8−2.0−2.7
Fish 5.08.40.7
Amphibian 2.82.70.9
Reptile 6.517.21.1
Cnidarian 0.80.51.0
Mammal 28.24.22.0
Bird 3.2na1.1
Geographic Bias Ratio
GPT-4.5GeminiDeepSeek-V3
Asia 3.3−1.40.0
Africa −2.6−3.3−3.0
South America −0.5−0.7−3.1
Central America −2.3−6.0−0.4
Oceania −0.40.9−0.5
Europe 4.21.80.2
North America 2.313.30.8
Antarctica 0.90.40.9
“na” values represent undetermined Bias Ratio.
Table 3. Values of endangered species obtained by regions for the three IA applications. The data are segregated by geographic area and expressed in percentages. The random values were obtained from the current IUCN database.
Table 3. Values of endangered species obtained by regions for the three IA applications. The data are segregated by geographic area and expressed in percentages. The random values were obtained from the current IUCN database.
GPT-4.5% (SD)DeepSeek-V3% (SD)Gemini % (SD)Random Selection from IUCN; % (SD)Endangered % (IUCN)
Asia30.5 (1.3)26.6 (9.5)21.8 (3.2)30.3 (4.9)26.17
Africa16.7 (2.6)13.1 (3.4)17.4 (1.8)23.7 (2.1)23.32
South America15.7 (5.4)9.5 (2.8)16.1 (3.2)18.7 (4)18.39
Central America6.9 (2)9.2 (6.5)4.6 (1.2)10.7 (3.2)11.56
Oceania9.5 (1.3)7.2 (5.4)14.8 (5.6)9 (1)9.97
Europe10.2 (0.9)7.5 (5.4)12.5 (3.5)4.7 (2.3)6.31
North America10.1 (2.6)26.0 (26.5)12.5 (0.6)2.7 (1.5)4.17
Antarctica1 (1)1 (1)0.4 (0.6)00.11
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de Pedro Noriega, L.; Bobo-Pinilla, J.; Delgado-Iglesias, J.; Reinoso-Tapia, R.; Gallego, A.M.; Quirós-Alpera, S. AI in Biodiversity Education: The Bias in Endangered Species Information and Its Implications. Sustainability 2025, 17, 6554. https://doi.org/10.3390/su17146554

AMA Style

de Pedro Noriega L, Bobo-Pinilla J, Delgado-Iglesias J, Reinoso-Tapia R, Gallego AM, Quirós-Alpera S. AI in Biodiversity Education: The Bias in Endangered Species Information and Its Implications. Sustainability. 2025; 17(14):6554. https://doi.org/10.3390/su17146554

Chicago/Turabian Style

de Pedro Noriega, Luis, Javier Bobo-Pinilla, Jaime Delgado-Iglesias, Roberto Reinoso-Tapia, Ana María Gallego, and Susana Quirós-Alpera. 2025. "AI in Biodiversity Education: The Bias in Endangered Species Information and Its Implications" Sustainability 17, no. 14: 6554. https://doi.org/10.3390/su17146554

APA Style

de Pedro Noriega, L., Bobo-Pinilla, J., Delgado-Iglesias, J., Reinoso-Tapia, R., Gallego, A. M., & Quirós-Alpera, S. (2025). AI in Biodiversity Education: The Bias in Endangered Species Information and Its Implications. Sustainability, 17(14), 6554. https://doi.org/10.3390/su17146554

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