Introduction
The study of ancient parasites, known as paleoparasitology or archaeoparasitology (Dittmar et al., Reference Dittmar, Araújo, Reinhard and Grauer2012; Ferreira, Reference Ferreira, Ferreira, Reinhard and Araújo2014; Reinhard et al., Reference Reinhard, Slepchenko, Shin and Smith2018) can provide valuable information on the life of past populations (Le Bailly et al., Reference Le Bailly, Maicher, Roche and Dufour2021; Mitchell, Reference Mitchell2024). This discipline is based on the study of the phases of the parasitic dispersal of intestinal helminths, given their preservation in archaeological contexts (Ramírez et al., Reference Ramírez, Fabra, Xavier and Iñiguez2022; Saldanha et al., Reference Saldanha, Pucu, Chame and Leles2022). In this way, by finding geohelminth eggs (such as Ascaris sp. or Trichuris sp.), we can better understand hygiene and sanitary conditions in these populations (Dufour et al., Reference Dufour, Segard and Le Bailly2016; Ledger et al., Reference Ledger, Micarelli, Ward, Prowse, Carroll, Killgrove, Rice, Franconi, Tafuri, Manzi and Mitchell2021; Wang et al., Reference Wang, Cessford, Dittmar, Inskip, Jones and Mitchell2022), as well as the use of certain agricultural practices such as the use of human faecal matter to fertilize fields used for agriculture (Mitchell, Reference Mitchell2017a; López-Gijón et al., Reference López-Gijón, Camarós, Rubio-Salvador, Duras, Botella-López, Alemán-Aguilera, Rodríguez-Aguilera, Bustamante-Álvarez, Sánchez-Barba, Dufour and Le Bailly2023a). The discovery of the eggs of zoonotic parasites is also very useful for our understanding of the presence and/or consumption of certain animals, helping to explain animal–human interactions (Ledger and Mitchell, Reference Ledger and Mitchell2022; Wang and Mitchell, Reference Wang and Mitchell2022; López-Gijón et al., Reference López-Gijón, Carnicero, Botella-López and Camarós2023b).
Paleoparasitology is becoming increasingly important in archaeological research (Gaeta and Fornaciari, Reference Gaeta, Fornaciari and Bruschi2022; Mitchell, Reference Mitchell2023) and has developed novel techniques to search for evidence of parasites in ancient populations (Jaeger and Mayo-Iñiguez, Reference Jaeger and Mayo-Iñiguez2014; Côté and Le Bailly, Reference Côté and Le Bailly2018; Wood, Reference Wood2018). These technological improvements allow analysis to be performed on a wide range of materials. Among these, the investigations commonly focus on sanitation infrastructure in which human faecal material accumulates (Mitchell, Reference Mitchell2015a), such as latrines (Williams et al., Reference Williams, Arnold-Foster, Yeh, Ledger, Baeten, Poblome and Mitchell2017), cesspits (Wang et al., Reference Wang, Deforce, De Gryse, Eggermont, Vanoverbeke and Mitchell2024) sewer drains and wastewater channels (López-Gijón et al., Reference López-Gijón, Hernández-Robles, Duras, Celma, Curto, González-Ballesteros, Dufour, Le Bailly and Eiroa2025). Examination of their sediment tends to yield larger numbers of parasites eggs and parasitic species in comparison with sediment from the pelvis and sacrum of human burials (see Flammer et al., Reference Flammer, Ryan, Preston, Warren, Prichystalova, Weiss, Palmowski, Boschert, Fellgiebel, Jasch-Boley, Kairies, Rümmele, Rieger, Schmid, Reeves, Nicholson, Loe, Guy, Waldron, Machácek, Wahl, Pollard, Larson and Smith2020; Ryan et al., Reference Ryan, Flammer, Nicholson, Loe, Reeves, Allison, Guy, Doriga, Waldron, Walker, Kirchhelle, Larson and Smith2022; López-Gijón, Reference López-Gijón2023). For these reasons, these findings from sanitation infrastructure linked to faecal remains are especially useful for gaining a better understanding of the parasitic diversity of the population. This is even more helpful in arid and semi-arid geographical areas, where taphonomic issues often limit parasite egg survival (Morrow et al., Reference Morrow, Newby, Piombino-Mascali and Reinhard2016; Ramírez et al., Reference Ramírez, Fabra, Xavier and Iñiguez2022). In the case of the Iberian Peninsula, often only tough geohelminth eggs survive at archaeological sites (Cunha et al., Reference Cunha, Santos, Matias and Sianto2017; Knorr et al., Reference Knorr, Smith, Ledger, Peña-Chocarro, Pérez-Jordà, Clapés, Palma and Mitchell2019; López-Gijón et al., Reference López-Gijón, Duras, Botella-López, Sentí-Ribes, Dufour and Le Bailly2022, Reference López-Gijón, Duras, Sánchez Susí, González Recio, Rubio Salvador, Botella López and Cámara Serrano2024b).
In this paper, new paleoparasitological findings from the city of Granada in the 17th and 18th centuries are provided by studying two toilet structures. Our aim is to better understand the lives of the people who lived in the silk production district of Realejo 300–400 years ago by comparing our results with historical texts from Granada and past paleoparasitological findings from similar socioeconomic contexts.
Materials and methods
Archaeological site
The archaeological material derives from a 2023 excavation of Molinos Street no. 21 in Granada city (Figure 1). The stratigraphy of four excavation sites allows us to distinguish layers corresponding to modern, early modern, medieval and Roman periods (Suliman and Fernández-Romero, Reference Suliman and Fernández-Romero2025).

Figure 1. Location of Molinos Street in the Dalmau’s map of Granada (Spain), printed in 1796. Map from Archivo Municipal de Granada (https://www.Granada.Org/inet/wcartografia.Nsf/fa/B8B8A4DDC35D69CCC125760A0036A6DF).
The modern layer (19th–20th centuries) comprises the excavated building, closed wastewater channels, foundation wall remains and bags of rubbish. The early modern layer (16th–18th centuries) contains the remains of wastewater channels and walls (loadbearing and partition) as well as one cesspit constructed of stone bricks and another comprising an earthenware jar recycled for this purpose; the samples analysed for this study all come from this early modern layer. The medieval layer (11th–15th centuries) corresponds to the Bab Alfajjarin necropolis (maqbara Bāb al-Fajjārīn), the largest cemetery in the eastern part of the city. Finally, the Roman phase (approx. 1st century B.C.) reveals the remnants of an olive mill pool made of opus signinum (Roman concrete) that was reutilized as a tomb in medieval times.
Historical context
The excavation site is within an area (Realejo) that had been occupied by a large Muslim cemetery known as Maqbarat Bab al-Fajjarin, which was cleared in the early 16th century (Torres Balbás, Reference Torres Balbás1995). In 1513, Christians in the city petitioned for plots of land on the site (Campo del Principe) to build homes (Archivo municipal de Granada, lib. II, fol 67 rº.).
A unitary constructive model was followed in accordance with building norms of the time, creating standardized houses that opened on to a central square and were arranged in a regular geometric form (Acale Sánchez, Reference Acale Sánchez2005). Houses constructed in the southern part of the Campo del Principe in the 16th–18th centuries were typically Casas de Vecinos (Houses of Neighbors), characterized by multiple dwellings on different floors with open corridors looking over a central courtyard.
The Campo de Principe was in the Realejo neighbourhood, a centre of silk production since Islamic times. Many craftspeople were employed in this industry, and the first craft guild was established in Realejo in 1528. The quality of their work gained international renown (Garzón Pareja, Reference Garzón Pareja1972), and the Venetian ambassador Andrea de Navagero wrote that most of the Christians were silk merchants, praising the quality of their silk, ‘perhaps better than in Italy’ (Navagero, Reference Navagero1951). Family silk workshops abounded in the area, where some street names still reflect their activity (e.g. Plegadero means ‘place for folding’).
The excavation site was one of the main buildings on the south side of the Campo del Príncipe. It was constructed in the 16th century and may be the edifice described by Henríquez de Jorquera in the 17th century as offices for ‘the higher art of silk’ around the ‘large and spacious square’ Campo de Principe (Henríquez de Jorquera, Reference Henríquez de Jorquera1987). It may therefore have been used by members of the guild, and restructured as a house of corridors, with the front of the house opening onto the square (Campo de Principe), or it may also have been one of the Casas de Vecinos built in the area (Figure 2).

Figure 2. A) Detail of Ambrosio de Vico map printed in 1613 showing the study site. Map from Archivo Municipal de Granada (https://www.Granada.Org/inet/wcartografia.Nsf/fa/09696CD302334900C12573F0002EDE74); B) Intact earthenware jar used as cesspit found in Molinos street.
Method
Paleoparasitological analyses were conducted in sediment from the two cesspits found at the archaeological site. Samples were gathered immediately upon their opening to avoid deterioration (Fugassa, Reference Fugassa, Ferreira, Reinhard and Araújo2014), and researchers wore surgical masks and protective clothing (PPE), using new dust-free nitrile gloves (López-Gijón et al., Reference López-Gijón, Jiménez-Brobeil, Maroto-Benavides, Duras, Suliman, Fernández Romero, Botella López, Sánchez-Montes and Mitchell2024a) and plastic spoons for each sample to prevent cross-contamination (Mitchell, Reference Mitchell, Mitchell and Brickley2017b; Sianto et al., Reference Sianto, de Miranda Chaves, Teixeira-Santos, Pereira, Godinho, Gonçalves and Santos2018).
The sampling method published by Le Bailly et al. (Reference Le Bailly, Maicher, Roche and Dufour2021) was followed. Control samples were taken from the exterior of the analysed structures (Cesspit 1C.S. and Cesspit 2C.S.1), as well as from the limestone caps that closed both cesspits (1C.S.1, 1C.S.2 and 2C.S.2). Regarding the samples taken from the interior of the structures, given the uniformity of the contents, samples could not be taken based on colour change. Therefore, artificial stratigraphic units were used to obtain the samples from the top until the bottom of both structures (1S.U.1, 1S.U.2, 1S.U.3, 1S.U.4, 2S.U.1 and 2S.U.2). Between 50 and 70 grams of sediment were collected from each sample.
Each sample was placed within two sealed plastic bags, labelled with the site name, site area, cesspit number and stratigraphic unit, and was delivered to the Laboratory of Physical and Forensic Anthropology of the University of Granada (Spain) for storage in darkness under controlled temperature and humidity conditions. Laboratory analysis followed the Rehydration, Homogenization and Micro-sieving (RHM) approach (Dufour and Le Bailly, Reference Dufour and Le Bailly2013). Briefly, 5 g of sample was rehydrated for seven days in aqueous solution of 50% 0.5% trisodium phosphate (Na3PO4) and 50% 5% glycerol (C3H8O3) containing formaldehyde (CH2O) drops against fungal growth. Next, the material was crushed in a porcelain mortar, immersed in ultrasound bath for 1 min, and then passed through 315, 160, 50 and 25 μm micro-sieves under a constant stream of water. Material was taken from the 50 and 25 μm micro-sieves, and then studied under light microscopy (Olympus CX43 at 100×, 400× and 600× coupled to Olympus SC-50 camera). Twenty slides were analysed per sample (n = 220) and analysed with Olympus CellSens software. The size and morphology of eggs served to identify the parasites, using reference manuals (Thienpont et al., Reference Thienpont, Rochette and Vanparijs1986; Roberts and Janovy, Reference Roberts and Janovy2008).
The analysis of eggs per gram has not been carried out, given the actual egg numbers per gram will be impacted by the commingled nature of the faeces in this cesspit. Firstly, some users may have had few or no parasites while others may have had plenty, and so any eggs per gram calculation with at best be a mean of the values from the original users. Secondly, the amount of refuse discarded into the cesspit is unknown, and such refuse will dilute out the faecal material and so impact the eggs per gram calculations. Thirdly, the rate of destruction of parasite eggs over time, which will be dependent upon how waterlogged the cesspit sediment was and the type and number of decomposing organisms present, remains unknown. A more waterlogged site might preserve eggs better than a drier one, and the presence or more bacteria, fungi or insects that feed off such eggs will also affect egg survival.
Results
Control samples from around the cesspit and lime levels were all negative for parasite eggs, indicating that the environment surrounding the toilets was not contaminated by human faeces. In contrast, the samples from lower levels within the cesspits were positive for eggs of Ascaris sp., Trichuris sp., Fasciola sp., Capillaria sp. and Spirometra sp. (Table 1). Ascaris sp. (roundworm) eggs (n = 11) were found in samples from both cesspits, characterized by their mamillated shell (Figure 3A), oval morphology and dimensions (63.51 ± 2.26 × 47 ± 1.31 μm). There was also one decorticated Ascaris sp. egg, commonly described in paleoparasitological studies (López-Gijón et al., Reference López-Gijón, Jiménez-Brobeil, Maroto-Benavides, Duras, Suliman, Fernández Romero, Botella López, Sánchez-Montes and Mitchell2024a). Trichuris sp. (whipworm) eggs (n = 5) were found in samples from both cesspits, characterized by their thick shell, smooth surface, lemon-like morphology, bipolar protuberances (polar plugs) (Figure 3B) and dimensions (49.64 ± 1.04 × 24.98 ± 1.28 μm). One probable Fasciola sp. egg was found in cesspit 1, characterized by its thin shell, flask-shaped morphology (operculum at one end) (Figure 4A) and dimensions (149.4 × 89.8 μm). Capillaria sp. eggs (n = 5) were also found in samples from both cesspits (n = 5), characterized by their thick wall with radiating pores (minute rod-shaped structures), slightly protruding polar plugs, lemon shape (Figure 4B) and dimensions (54.93 ± 0.53 × 30.22 ± 0.06 μm). Probable Spirometra sp. eggs (n = 4), were found in cesspit 1 (Figure 4C), characterized by their flask-shaped morphology, operculum and dimensions which are smaller and slimmer than those of fish tapeworm (70.78 ± 0.78 × 35.85 ± 0.33 μm).

Figure 3. A) Ascaris sp. Egg with mamillated coat (65.2 × 50.5 μm); B) Trichuris sp. Egg (51.6 × 25 μm).

Figure 4. A) Fasciola sp. Egg with operculum lost (149.4 × 89.8 μm); B) Capillaria sp. Egg (55.7 × 30.4 μm); C) Spirometra sp. Egg with operculum lost (72.5 × 35.4 μm).
Table 1. Details of the parasite eggs found in Molinos street. C.S. Stands for control sample. S.U. Indicates sediment from within each toilet feature

Discussion
In this study we found the eggs of five different helminths in the two toilet features from a 17th–18th century building in Granada. We will now consider the implications of these findings, and how it improves our understanding of the lives of those who lived and worked in the silk production district of Realejo.
Ascaris sp. and Trichuris sp. are observed in a range of mammals. In humans, we find A. lumbricoides (roundworm) and T. trichiura (whipworm), in pigs A. suum and T. suis, while dogs and foxes have T. vulpis and mice have T. muris (Roberts and Janovy, Reference Roberts and Janovy2008; Betson et al., Reference Betson, Søe and Nejsum2015). It is difficult to differentiate morphologically (Leles et al., Reference Leles, Gardner, Reinhard, Iñiguez and Araújo2012) or genetically (Alves et al., Reference Alves, Conceição and Leles2016) among Ascaris sp. while morphologic differences allow T. vulpis to be differentiated from T. suis or T. trichiura but do not allow T. trichiura to be distinguished from T. suis (Betson et al., Reference Betson, Søe and Nejsum2015). To avoid confusion, these parasites are described simply as Ascaris sp. and Trichuris sp. in this article.
Eggs of Ascaris sp. and Trichuris sp. were detected in both cesspits under study. The faecal-oral life cycle of these geohelminths involves the intake of water or food contaminated with human faeces (Vaz Nery et al., Reference Vaz Nery, Pickering, Abate, Asmare, Barrett, Benjamin-Chung, Bundy, Clasen, Clements, Colford, Ercumen, Crowley, Cumming, Freeman, Haque, Mengistu, Oswald, Pullan, Oliveira, Owen, Walson, Youya and Brooker2019; Eslahi et al., Reference Eslahi, Olfatifar, Karim, AbuOdeh, Modirian and Houshmand2022) by the lack of hand washing and other limitations to hygiene and sanitation (Fung and Cairncross, Reference Fung and Cairncross2009). These parasites are frequently present in areas with poor sanitation and polluted drinking water (Jourdan et al., Reference Jourdan, Lamberton, Fenwick and Addiss2018). They produce a very large number of eggs, up to 200 000 per day by roundworm females and 3000–20 000 per day by whipworm females (Roberts and Janovy, Reference Roberts and Janovy2008). This volume of eggs and their highly resistant shells (Wharton, Reference Wharton1980) make these geohelminths the most frequently detected parasites in ancient European material (Anastasiou, Reference Anastasiou and Mitchell2015; Gaeta and Fornaciari, Reference Gaeta, Fornaciari and Bruschi2022). The health effects of these parasites are related to the number involved in the infection, so that some individuals are asymptomatic, but others have abdominal cramps, diarrhoea, anaemia and malnutrition, with a reduction in intelligence and stunting of growth during childhood; in addition, there is a risk of intestinal obstruction in severe cases of roundworm infection (Jourdan et al., Reference Jourdan, Lamberton, Fenwick and Addiss2018). Roundworm was described by the Spanish physicians Miguel de Agustín in the 17th century and by Lorenzo Hervás y Panduro in the 18th century (Cordero Del Campillo, Reference Cordero Del Campillo1980), but none of the other parasites detected are mentioned in contemporaneous Spanish writings.
It is also not possible to differentiate microscopically among the eggs of different Fasciola sp. (Mas-Coma et al., Reference Mas-Coma, Valero, Bargues, Toledo and Fried2019), although F. hepatica is much more frequently observed in Europe. Likewise, no attempt is made here to identify specific Capillaria and Spirometra species due to the absence of characteristic morphological features (Almeida et al., Reference Almeida, Coscarelli, Melo, Melo and Pinto2016; Borba et al., Reference Borba, Gurjão, Martin, Dufour, Le Bailly and Iñiguez2025).
An egg likely to represent liver fluke (Fasciola sp.) eggs was found in one cesspit. This zoonotic parasite infects the host biliary tract, usually in herbivores (e.g. ruminants). When infected herbivore liver is consumed by humans, the eggs can pass through the body without causing harm (false parasitism); hence, their presence in faeces does not indicate human infection. However, true infection can result from the consumption of water or plants contaminated by Fasciola metacercariae (Cwiklinski et al., Reference Cwiklinski, O’Neill, Donnelly and Dalton2016; Mas-Coma et al., Reference Mas-Coma, Valero, Bargues, Toledo and Fried2019). The fact that only one egg was recovered probably indicates false parasitism rather than true human infection, and so reflects the foods consumed by those using this toilet.
Eggs likely to represent Spirometra sp. were found in one cesspit. Certain species of Canidae and Felidae are the definitive hosts of this zoonotic parasite, but humans can also be accidental hosts, largely by consuming contaminated drinking water or inadequately cooked meat from intermediate hosts, including amphibians, reptiles, birds, or even mammals (e.g. pigs). Contact with an intermediate host can also allow plerocercoid larvae to directly enter the skin or mucosa, especially through an open wound (Pampiglione et al., Reference Pampiglione, Fioravanti and Rivasi2003). The recovery of the eggs of this parasite in the toilet sediment and the considerable presence of their definitive hosts in the city of Granada (cats and dogs) indicate a potential risk of humans infections. On the balance of probability, these eggs may indicate that faeces from companion animals such as pet dogs or cats could have been discarded into this toilet, resulting in their being mixed in with the human faecal material analysed.
Eggs of Capillaria sp. were found in both the cesspits. Rodents are most frequently the definitive hosts of these zoonotic parasites, but they are detected in numerous other mammals, including beavers, cats, chimpanzees, coyotes, dogs, foxes, monkeys, pigs and wolves (Pal and Gutama, Reference Pal and Gutama2024), with rare reports of human infection, mainly by C. philippinensis, C. aerophile, or C. hepatica. In Europe, the most commonly reported human infections are caused by Capillaria hepatica. Unlike some other Capillaria species, eggs are not typically found in the stool of humans infected with C. hepatica. However, eggs may appear in the stool during spurious infections (false parasitism), which occur when a person consumes the liver of an infected animal, allowing the eggs to pass through the digestive system and be excreted (Ledger and Mitchell, Reference Ledger and Mitchell2022).
In contrast to earlier time periods, limited data are available on the presence of parasites in cesspits, latrines, or sewer drains from the early modern period in Europe. Studies on 16th–19th century faecal material have been carried out on sites in the UK (Anastasiou et al., Reference Anastasiou, Mitchell, Jeffries, Mitchell and Buckberry2012; Ryan et al., Reference Ryan, Flammer, Nicholson, Loe, Reeves, Allison, Guy, Doriga, Waldron, Walker, Kirchhelle, Larson and Smith2022), Belgium (Fernandes et al., Reference Fernandes, Ferreira, Gonçalves, Bouchet, Klein, Iguchi, Sianto and Araújo2005; Rocha et al., Reference Rocha, Harter-Lailheugue, Le Bailly, Araújo, Ferreira, Serra-Freire and Bouchet2006; Graff et al., Reference Graff, Bennion-Pedley, Jones, Ledger, Deforce, Degraeve, Byl and Mitchell2020; Rabinow et al., Reference Rabinow, Deforce and Mitchell2023; Ledger et al., Reference Ledger, Poulain and Deforce2024), the Czech Republic (Bartošová et al., Reference Bartošová, Ditrich, Beneš, Frolík and Musil2011), and France (Bouchet et al., Reference Bouchet, Bentrad and Paicheler1998). These show that roundworm and whipworm infection dominated, but some zoonotic species of parasites were also present.
The presence of parasite eggs in the environment can be considerably increased when human waste is poorly managed or when it is employed to fertilize crops, which has been a common practice throughout history (Mitchell, Reference Mitchell2015b; Dufour et al., Reference Dufour, Segard and Le Bailly2016; Knorr et al., Reference Knorr, Smith, Ledger, Peña-Chocarro, Pérez-Jordà, Clapés, Palma and Mitchell2019). Alongside poor waste management and the use of channel waters by humans and animals, these factors would have favoured the outbreak of epidemics by intestinal micro-organisms. The most severe mortality crises in Granada during the 17th century were a bubonic plague epidemic in 1679 (Jimenez-Brobeil and Al Oumaoui, Reference Jimenez-Brobeil and Al Oumaoui2002), and an earlier faecal-oral transmitted epidemic of typhus in 1648, attributed in the mortality records of some Granada parishes on contaminated watercourses (Jiménez-Brobeil et al., Reference Jiménez-Brobeil, Benavides and González2020). The severity of the typhus epidemic, exacerbated by the use in houses and vegetable plots of dirty water from irrigation canals, led to the promulgation by Granada Council of Water Ordinances (Ordenanzas de las Aguas) in 1670. Accordingly, water conduits, wastewater canals and the river had to be cleaned in March and September every year, and it was forbidden to wash clothes or fish or throw human waste or dead animals (e.g. dogs, cats or chickens) into the waters (Granada Council, 1670). Water contamination is known to be a risk factor for parasitosis due to geohelminths (Bowman, Reference Bowman2021; WHO, 2023) and liver flukes (Sabourin et al., Reference Sabourin, Alda, Vázquez, Hurtrez-Boussès and Vittecoq2018). This work together with previous results (López-Gijón et al., Reference López-Gijón, Jiménez-Brobeil, Maroto-Benavides, Duras, Suliman, Fernández Romero, Botella López, Sánchez-Montes and Mitchell2024a) shows the widespread presence of contaminated water in different parts of the city, with the different water channels analysed to date being contaminated by these parasites.
Water for domestic and public use in the Campo del Principe came from two Muslim acequias (irrigation canals), called the alquebira and the alcadí, which both entered the neighbourhood from Abahul Hill. The alcadí, which has since disappeared, was created by Mu‘ammal, the Viziar under Zirí Badis (1038–1077) and ensured the supply of water to the neighbourhood of Antequeruela, which had been inhabited since 1410 and was higher than the square (González F, Reference González F1986). In April 1517, a public basin was constructed in the Campo del Príncipe to receive surplus waters from the Alhambra (Actas Capitulares), while houses received waters from the Cenes river divide (Actas Capitulares). However, these supplies were not always clean and were often mixed with wastewater, as reflected in the names of some streets in the area, such as Alcubilla (cistern) and Darrillo sucio (dirty darrillo). In addition, the structure of the azacayuelas (water channels) was weak, and they developed leaks that exacerbated the problem of contamination. These problems had a long history, given that Granada Council issued Ordinances in 1552 to regulate the use of wastewater and avoid its contact with clean water, based on awareness of the risks of irrigating vegetable plots or washing clothes with faeces-contaminated waters.
Regarding the site previously analysed by López-Gijón et al., (Reference López-Gijón, Jiménez-Brobeil, Maroto-Benavides, Duras, Suliman, Fernández Romero, Botella López, Sánchez-Montes and Mitchell2024a) on Ventanilla Street, we also found Ascaris sp., Trichuris sp. and Fasciola sp. on Molinos Street. This demonstrates the poor hygienic conditions of the population at the time, as well as water contamination. This is evident in Granada’s different socioeconomic sectors, comprising silk merchants in the case of Molinos, and new settlers primarily linked to agriculture in the area of city expansion in the 17th and 18th centuries in the case of Ventanilla. Thus, the paleoparasitological results suggest that both populations were equally exposed to parasites associated with poor hygiene and water contamination. Furthermore, two new species (probable Spirometra sp. and Capillaria sp.) were identified in Molinos, providing a new perspective on zoonotic parasites in Granada during the 17th and 18th centuries.
Limitations of the study
Although the detection of parasite eggs in cesspits suggests the presence of parasite infection in a population, eggs found in mixed faecal material cannot be related to specific individuals. A further study limitation is the possible non-detection of taxonomic groups that might cause parasitosis in humans, due to taphonomic processes (Ramírez et al., Reference Ramírez, Fabra, Xavier and Iñiguez2022). Parasite eggs are less well preserved in dry than wet conditions (Bouchet et al., Reference Bouchet, Guidon, Dittmar, Harter, Ferreira, Chaves, Reinhard and Araújo2003), and a larger number of parasite species have been detected in more humid parts of the Iberian Peninsula (Maicher et al., Reference Maicher, Hoffmann, Côté, Palomo Pérez, Saña Segui and Le Bailly2017; López-Gijón et al., Reference López-Gijón, Carnicero, Botella-López and Camarós2023b) than in more arid areas such as the present site (Sianto et al., Reference Sianto, de Miranda Chaves, Teixeira-Santos, Pereira, Godinho, Gonçalves and Santos2018; Knorr et al., Reference Knorr, Smith, Ledger, Peña-Chocarro, Pérez-Jordà, Clapés, Palma and Mitchell2019). The preservation of eggs is also compromised in Granada by the typically high fluctuations in temperature and rainfall, which may account for the small number of eggs found (Rodrigo et al., Reference Rodrigo, Esteban‐Parra, Pozo‐Vázquez and Castro‐Díez1999). In view of the limited number of eggs with the appearance of Fasciola, Capillaria and Spirometra, the diagnosis of these parasites seems the most likely option, but they should be considered provisional rather than conclusive.
Data availability statement
All data used in this study are available from the authors on request.
Acknowledgements
We would like to express our gratitude to Dr Roman Kuchta for sharing his expertise in the attribution of parasitic species.
Author contributions
RLG conceptualized the study and performed laboratory analyses and data interpretation. RLG, SD and PDM drafted the initial manuscript. PLFR, SJB and FSM participated in the data interpretation. PDM contributed to data interpretation, manuscript preparation and revision.
Financial support
This research received funding from the Research Project ‘Health and diet in populations in southeast of al-Andalus’ (PID2019-107654-GB-100) of the Spanish Ministerio de Ciencia e Innovación. The University of Granada/CBUA contributed towards OA fees.
Competing interests
The authors declare there are no conflicts of interest.
Ethical standards
Not applicable.





