Archaeological and ethnohistorical evidence reveals the importance of domesticated dogs in Mesoamerica as early as the Late Archaic period and all the way through the Contact era (Valadez Azúa et al. 2003; White et al. 2001, Valadez Azúa et al. 2013). Dog remains have been recovered at ceremonial and elite centers (Pendergast 1974; Masson and Peraza Lope 2013; Rosenswig 2007; Valadez Azúa 2003) and human burial sites throughout Mesoamerica (Hamblin 1984; Wing 2013). They were used as a steady source of meat, as tribute payments, for medicinal purposes, in rituals, in hunting, and for companionship (Emery et al. 2013: 412). Iconographic and ethnohistoric evidence indicates that dogs were symbolically important in Mesoamerican religion and were linked to death, destruction, earth, and fire. They were seen as messengers who prepared the way to the other world and as companions when crossing “the nine rivers to the land of the dead” (Sahagun 1974; Tozzer and Allen 1910: 360-362; Wing 2013: 44).
The prevalence of dogs in zooarchaeological assemblages is evident in investigations across the Maya world, especially considering that dogs were the only true domesticated animal before the introduction of the domestic turkey during the Late Postclassic (Emery 2004: 45, 2013: 411). Dog remains were most prominent during the Preclassic period (Emery 2004: 45; Cunningham-Smith et al. 2020: 167). They were an important source of food in Cuello (Clutton-Brock and Hammond 1994), as well as Colha and Cerros, where they were recovered from ceremonial and elite contexts (Carr 1985, 1986; Shaw 1991). Dog bones were also used in jewelry, as evidenced by the 299 molars and 79 long bones that were drilled to form beads and separators for anklets interred with a woman in a Late Preclassic burial site in Caracol (Teeter 2004: 188-189). Emery (2004: 48; Emery et al. 2013: 413) suggests that the abundance of dog remains during the Preclassic may be linked to political development, which also explains their association with administrative and ceremonial structures. Ritual feasting to solidify power during the Preclassic may be responsible for the prevalence of dog remains in such contexts (Shaw 1999: 94-95). The Classic period is defined by a decrease in the quantity of dog remains recovered, followed by a resurgence during the Postclassic period (Emery 2004: 47). As examples, the presence of dog remains alongside human bones in caches declined during the Early Classic at Tikal (Moholy-Nagy 2004: 198); and small quantities of dog remains have been recovered from the epicenter of Caracol in structures dating from the Late/Terminal Classic (Teeter 2001: 211-213, 2004: 185). A general trend in Petén sites indicates that dogs tend to prevail in Preclassic and Postclassic contexts with a significant decrease during the Late Classic (Pohl 1976). Similarly, dogs dominate Preclassic assemblages at Kamilajuyu and are reported in Early Classic tombs but not in Late Classic deposits (Emery et al. 2013: 411-412). Increasing frequencies of dog remains at Post-classic sites, such as Lamanai, support the idea that the demand for specific animals as tributes or sacrifices was of great importance to commercial relations during the Postclassic period (Emery 1999: 75). Emery (2004: 49) raises the possibility that an increase in the quantity of dog remains recovered during the Postclassic may be related to a proliferation of ritual and social feasting activities.
Their significance in ritual practices was portrayed in Postclassic Maya codices, which depict dogs being used as sacrificial offerings for yearly renewal ceremonies (Pohl 1983; Pohl and Feldman 1982). Fray Diego de Landa reports cases of dog sacrifices during the contact period. According to Landa (1941: 164), dogs stained with cacao spots were sacrificed in cacao rituals. Landa and others note that animals were fattened in anticipation of these events and their meat was usually consumed at feasts (Pohl and Feldman 1982: 302; Shaw 1991: 259). Isotopic signatures of dog remains recovered in feasting contexts at the Classic Maya site of Lagartero indicate that dogs preferentially ate maize (White et al. 2004: 156) but it is uncertain whether they got it from garbage and food scraps or were intentionally fed with it.
Moreover, investigations have shown that dogs were used in ceremonial and domestic structures in Mayapán, the last regional political capital of the Maya region. As one of the most prominent Late Postclassic sites, Mayapán offers the opportunity to study the importance and function of dogs during this period. In the following pages, I analyze dog samples recovered from architectural structures in different sectors of the city in terms of their frequency, skeletal distribution, osteometry, weight, and age. This study also explores the variability of skeletal representation and the possibility that different breeds of dogs were used in domestic and ceremonial structures in the monumental center and outlying ceremonial centers of Itzmal Ch’en.
Dog remains in the city of Mayapán
Mayapán is located on the Yucatán Peninsula in Mexico and was the political capital and largest urban center of the Postclassic Maya world from 1200-1450 AD. The nucleated urban zone is circumscribed by a wall with a circumference of 9.1 km and 12 formal gates (Masson and Peraza Lope 2014; Masson et al. 2016: 241). Dispersed houselots are located beyond the city wall to a distance of 500 m (Russell 2008). The monumental center of Mayapán features mostly religious architecture, civic and administrative buildings, and elite residences (Chase 1992: Fig. 8.4; Delgado Kú 2004: 11-13; Smith 1962: 265-266). Outlying ceremonial sites probably used for local celebrations in the style of those held in the monumental center (Peraza Lope and Masson 2014a) were erected within the city limits. Elaborate elite residences in Mayapán are located around the eastern and western margins of the site center while lower-class neighborhoods throughout the city were mostly occupied by commoners (Hare et al. 2014: 170, 190).
Dog remains have been found in Mayapán in a variety of architectural structures including shrines, elite residences, and dwellings occupied by artisans and commoners, and are especially prominent in temples, colonnaded halls, and cenotes. They are unusually concentrated in the Templo Redondo group, which includes Templo Redondo (Q-152), the Hall (Q-151), and associated structures (Q-152a, Q-152b and Q-152d) (see Masson and Peraza Lope 2013: table 7). The public and ceremonial character of these structures confirms the role of dogs as an important component in Postclassic Mayapán rituals. House structures from all strata account for just a small percentage of the dog remains found in the city (see Pollock and Ray 1957; Masson and Peraza Lope 2008, 2013).
Pollock and Ray (1957: 543) report an abundance of dog remains at Mayapán, second only to deer as the most common mammals recovered by the Carnegie Project. The Carnegie sample included single dog bones, teeth, and jaws from simple houses, elite dwellings, colonnaded halls, temples, and cenotes. The highest frequencies were recovered from cenote deposits and midden materials adjacent to a colonnaded hall and a temple (Pollock and Ray 1957: 543). Masson and Peraza Lope (2008, 2013, 2014) faunal studies include remains recovered by the INAH (Instituto Nacional de Antropología e Historia) and PEMY (Economic Foundations of Mayapán) projects in the monumental center and the outlying settlement zone. Dog remains in the INAH and PEMY faunal assemblages are substantial, following white-tailed deer, turkey, and iguana as the most common taxa in the monumental center. In the residential zone, dog remains were the fourth most abundant taxa, followed by white-tail deer, iguana, and turkey (Masson and Peraza Lope 2014: 401).
Sample contexts
In this paper, I analyze dog remains recovered during the 1997 and 1998 INAH Templo Redondo group (Q-152) excavations and restorations, and six structures (Q-39, Q-40a, Q-176a, H-15, H-17, I-55) excavated and restored during 2008 and 2009 by the PEMY archeological project (Figure 1). The Templo Redondo group was excavated with test pits and larger units of variable dimensions (see Peraza Lope et al. 1999; Delgado Kú 2004). All the structures excavated by PEMY were horizontally exposed with grids of 2×2 m and test pits in specific sectors of the architectural layout (Masson et al. 2012). The faunal assemblages from structure Q-152 have been analyzed and published by Masson and Peraza Lope (2008, 2013).
Structure Q-152, or Templo Redondo, is located in main plaza of the city’s monumental center. It consists of a rounded structure with four doors spaced evenly around the central core, vaulted interiors, and a reverse-batter cornice. Mural fragments in two niches have designs outlined in black paint with step frets, feathers, and rosettes (Delgado Kú 2004: 70; Milbrath and Peraza Lope 2003: 11-12).
Three of the houses studied here are in the vicinity of the monumental center: Houses Q-39, Q-40a and Q-176a, which were part of an artisanal neighborhood where surplus production was concentrated. House Q-40a is located inside the outer property walls of an elite house (the elaborate Q-41 residence), which suggests that elites supervised the pottery, effigy censer, copper, and figurine production at this dwelling (Masson et al. 2012, 2016). House Q-39 is adjacent to the elite residential Q-41 group but is contained by its own outer walls. An elaborate family tomb in House Q-39 suggests a family relationship with the residents of Q-41; the residents of Q-39 also made handicrafts such as clay figurines, shell ornaments, copper objects, obsidian, and high-quality chalcedony. House Q-176a, in contrast, was more independent insofar as it was not directly next to or inside an elite compound. The residents of this house produced pottery, obsidian blades, shell ornaments, and figurines (Masson and Peraza Lope 2014; Masson et al. 2012, 2016).
The outlying ceremonial center of Itzmal Ch’en is on the eastern side of the city. Three structures in this area have been included in this analysis: a temple, a colonnaded hall, and an affluent commoner’s house. Structure H-17, located almost 2 km from the site’s monumental center, is the second largest temple in Mayapán. It was decorated with sculptures depicting humans and other animals, mainly serpents. H-15 is one of the halls in the group. It was decorated with cut geometric stones in addition to animal and human sculptures including a dog effigy tenoned sculpture. A mass grave was identified in a platform next to H-15. The structure I-55a corresponds to a wealthy commoner’s house where obsidian and shell objects were manufactured (Hutchinson and Delgado Kú 2012; Peraza Lope and Masson 2014b: 119; Masson et al. 2016).
Methods
I assess the representation, age, and frequency of the skeletal remains of dogs found in the aforementioned seven architectural contexts. Skeletal identifications are based on comparisons with reference collections from the Maya zooarchaeological laboratory at the University at Albany-SUNY. Dog bones were classified according to element, portion, side, and other attributes such as cultural modification (for example, burning). All samples were quantified by bone count (NISP), minimum number of individuals (MNI) based on sided or unique elements of the body, and density (NISP per cubic meter). Structural comparisons are based on these frequencies.
R Software (R Core Team 2019) was used to perform Chi Square and Fisher exact tests on pairs of structures to compare the frequency of skeletal elements. The Fisher exact test was used in cases where the sample size was too small to implement Chi square. Furthermore, a correspondence analysis was employed as an ordination method to measure the abundance of skeletal remains in different structures, the precise location of which provides contextual data to interpret the roles of dogs in ritual and domestic activities in the houses, halls, and temples of Mayapán.
Osteometric analyses were conducted on the most complete elements or on those with observable attributes. Measurements were taken based on criteria established by Von Den Driesch (1976), including the maximum length and breadth of the proximal and distal ends of long bones and the length and breadth of first molars. Given the fragmentation of the sample, some measurements were impossible to document. Osteometric analyses of long bones and teeth were used for the comparison of Mayapán dogs to the documented metrics of dog breeds in Mesoamerica (Table 1), including the Mesoamerican common dog (Valadez 2000, 2003, Valadez et al. 2009), the hairless or xoloitzcuintli dog (Valadez 2009; Valadez et al. 2010), the short-nosed or Mayan dog (Valadez 2000), the tlalchichi (Valadez 2009; Valadez et al. 2011), and the wolf-dog hybrid (Valadez et al. 2001; Valadez et al. 2006).
Breed | Long bones (mm) | Archaeological site | Reference | |||
---|---|---|---|---|---|---|
Humerus lenght | Radius lenght | Femur lenght | Tibia lenght | |||
Mesoamerican commong dog | 130 | 115 | 136 | 136 | Reference collection | Valadez et al. 2011 |
122 | 120 | 133 | Modern specimen | Rodríguez et al. 2001 | ||
128 | 139 | 138 | Teotihuacán, State of Mexico | Valadez 2000 | ||
136 | 120 | 147 | 152 | Huixtoco, State of Mexico | Valadez et al. 2004 | |
130 | 148 | |||||
129 | 123 | 136 | 139 | Punta Pájaros, Quintana Roo | Blanco et al. 1999 | |
121 | 136 | 138 | ||||
130 | Tula, Hidalgo | |||||
135.5 | 144 | 149 | Tula, Hidalgo | Blanco et al. 2009 | ||
144.2 | 160 | 161 | Teopancazco, Teotihuacán | |||
Hairless Dog | 138 | 132 | 140 | 151 | Tula, Hidalgo | Valadez 2000 |
133 | 124 | 140 | Punta Pájaros, Quintana Roo | Blanco et al. 1999 | ||
140 | ||||||
134 | Teotihuacán, State of Mexico | Blanco et al. 2009 | ||||
134.81 | 149 | 136.35 | Guadalupe, Michoacán | Rodríguez et al. 2001 | ||
127.8 | 129.91 | 145.86 | Modern specimen | |||
Short-nosed Mayan dog | 121 | Punta Pájaros, Quintana Roo | Valadez 2000 | |||
105.5 | 109 | Cozumel, Quintana Roo | Hamblin 1984 | |||
109 | 135 | |||||
126 | 140 | Punta Pájaros, Quintana Roo | Blanco et al. 1999 | |||
Tlachichi dog | 97 | 86 | 114 | 114 | Tula, Hidalgo | Valadez et al. 2011 |
79 | 70 | 91 | 78 | San Blas, Mazatlán, Sinaloa | ||
88.6 | ||||||
81.3 | Teopancazco, Teotihuacán | |||||
78.5 | ||||||
83.7 | 90.6 | Santa Cruz Atizapán, State of Mexico | ||||
Wolf-dog hybrid | 189 | 192 | 200 | 210 | Tenochtitlán, Mexico City | Valadez et al. 2001 |
190 | 197.5 | 202.5 | 208 | |||
151.2 | Teotihuacán, State of Mexico | Valadez et al. 2006 |
Following Wing (1978: table 2.1) and Hamblin (1984: 100), an allometric formula was utilized to predict body weight in grams (g) from the measurement of mandible height (mm) at the middle of the first lower molar (carnassial). The following regression formula was used for that purpose: Log y= 2.2574(Log x)+ 1.164. According to Wing (1978: 31), this formula is more accurate than those based on the length of the premolar or molar tooth row since the crowding of the teeth could produce a misleading estimate. Differences in body weight could indicate differences in breeds as well as age (Hamblin 1984: 100). Determination of age categories is based on the observation of fused and non-fused epiphysis and dental eruption. Age was determined by consulting the age charts created by Sutton et al. (2018: table 11.3, table 11.7). It was not possible to determine the age of all elements because of the high fragmentation of the sample analyzed.
Results
The sample analyzed here includes the variety of structure types reported in previous studies (Masson and Peraza Lope 2008, 2013) and is consistent with their findings. The structures located in or in the vicinity of the monumental center of Mayapán (Q-152, Q-39, Q-40a, Q-176a) present higher total percentages and densities of dog remains than those located in the outlying ceremonial center of Itzmal Ch’en (I-55a, H-15, and H-17). The sample consists of 619 bones including head elements (skull, mandibles, teeth), axial elements (vertebrae), limbs (scapulae, humeri, radii, ulnae, femora, tibiae, fibulae), and feet (carpals, tarsals, metatarsals, metacarpals, phalanges). A total of 33 MNI were identified in the sample, of which 22 were found in Templo Redondo. These 22 individuals were identified by the presence of 22 right dentaries. The density values of the sample indicate that Templo Redondo (Q-152) and two houses in the monumental center (Q-40a, Q-176a) are the structures with the highest relative abundance of dog remains (Table 2).
Structure | Structure type | Area excavated (m3) | NISP | % | MNI | Density (NISP/m3) |
---|---|---|---|---|---|---|
H-15 | Hall | 126.4 | 20 | 3.2% | 2 | 0.16 |
H-17 | Temple | 328.2 | 9 | 1.5% | 1 | 0.03 |
I-55a | House | 47.3 | 8 | 1.3% | 1 | 0.17 |
Q-176a | House | 33.1 | 34 | 5.5% | 3 | 1.03 |
Q-39 | House | 34.2 | 12 | 1.9% | 2 | 0.35 |
Q-40a | House | 21.7 | 25 | 4.0% | 2 | 1.15 |
Q-152 | Templo Redondo | 282.0 | 511 | 82.6% | 22 | 1.81 |
Total | 872.9 | 619 | 100% | 33 | 4.70 |
Skeletal Elements Found
The distribution of skeletal elements per structure indicates that the sample is mainly front limb bones (18.6%) consisting of humeri, radii, and ulnae. Front limbs are followed by detached teeth (13.1%), vertebrae (12.9%) and crania bones (12%). Other elements account for less than 10% of the total sample (rear limb 9.9%, dentary 9.5%, metapodial/phalanges 9.4%, pelvis 5.3%, ribs 4.7%, scapulae 3.1%, calcaneous 1.0%, and astragalus 0.5%) (Table 3).
Q-152 | H-15 | H-17 | I-55a | Q-176a | Q-39 | Q-40a | |
---|---|---|---|---|---|---|---|
Crania | 13.5% | - | - | 12.5% | 5.9% | 8.3% | 4.0% |
Dentary | 9.8% | 15.0% | 22.2% | - | 2.9% | 8.3% | 8.0% |
Loose teeth | 12.7% | 10.0% | - | 37.5% | 11.8% | 25.0% | 16.0% |
Vertebrae | 13.7% | 10.0% | - | - | 17.6% | - | 8.0% |
Scapula | 3.1% | - | - | - | - | - | 12.0% |
Rib | 5.1% | - | - | - | 8.8% | - | - |
Pelvis | 6.1% | - | - | - | 5.9% | - | - |
Rear limb | 8.6% | 5.0% | 33.3% | 12.5% | 14.7% | 33.3% | 12.0% |
Front limb | 20.0% | 5.0% | 11.1% | 12.5% | 11.8% | - | 24.0% |
Metapodial/Phalanges | 6.1% | 55.0% | 22.2% | 25.0% | 20.6% | 8.3% | 16.0% |
Calcaneous | 1.0% | - | - | - | - | 8.3% | - |
Astragalus | 0.4% | - | 11.1% | - | - | - | - |
Limb | - | - | - | - | - | 8.3% | - |
Templo Redondo (Q-152) is the structure where the most complete array of skeletal elements were found. This temple is also the structure with the highest NISP (n=511) and relative density of dog remains. Artisans’ houses in the vicinity of the monumental center -Q-176a (n=34) and Q-40a (n=25)- were next in terms of NISP and the density of skeletal remains, including cranial and postcranial bones. In contrast, Q-39 has a smaller NISP (n=12) and rear limb bones predominate in its assemblage. Given that it is one of the smallest structures in this study, a relatively large number of dog bones was recovered from Q-40a (Table 2, Figure 4). Structures H-15 (n=20), H-17 (n=9), and I-55a (n=8) in the Itzmal Ch’en outlying ceremonial center have consistently smaller NISP, quantities, and densities of skeletal remains. H-15 (the Hall) has the highest numbers in this sector, which is coherent with previous observations indicating the high number of dog remains in halls (Pollock and Ray 1957; Masson and Peraza 2008, 2013).
Hall H-15 in the Itzmal Ch’en outlying ceremonial center is differentiated by higher concentrations of foot and toe bones. Crania elements are absent in both the Hall (H-15) and Temple (H-17). Most of the elements found at H-17 are limb bones, especially femurs. The wealthy commoner’s house (I-55a), also in the Itzmal Ch’en center, has a small number of elements but it is mostly characterized by the presence of detached teeth (Figure 2).
A series of Chi squares and Fisher exact tests were done to compare the pairs of structures analyzed (Table 4). The results indicate a significantly different distribution of skeletal elements in Templo Redondo (Q-152), an artisan’s house (Q-39), the Hall (H-15), and the Temple (H-17).
Structures | Hall H-15 | Temple H-17 | Temple Q-152 | House I-55 | House Q-176a | House Q-39 | House Q-40a |
---|---|---|---|---|---|---|---|
Hall H-15 | / | ||||||
Temple H-17 | No difference (p: .1137) | / | |||||
Temple Q-152 | Different (χ2: 67.45 p: 3.7216e-10) | Different (χ2: 33.92 p: .0003) | / | ||||
House I-55 | No difference (p: .133) | No difference (p: .2963) | No difference (χ2:11.63 p: .3923) | / | |||
House Q-176a | No difference (p: .1323) | No difference (p: .2092) | No difference (χ2:17.82 p: .08575) | No difference (p: .7545) | / | ||
House Q-39 | Different (p: .0093) | No difference (p: .5431) | Different (χ2:22.56 p: .0202) | No difference (p: .7896) | No difference (p: .1794) | / | |
House Q-40a | No difference (p: .0744) | No difference (p: .35) | No difference (χ2:15.02 p: .1812) | No difference (p: .7824) | No difference (p: .3136) | No difference (p: .2016) | / |
Note: tests based on comparisons of frequencies of crania bones, dentaries, all loose teeth, rear limbs, front limbs, metapodial/phalanges, vertebrae, astragalus, calcaneous, pelvis, ribs, and scapulae between fully-excavated structures, p = .05, df = 11, p-values >/= .05 reject the null of no difference. Chi square values were calculated for comparisons only with Q-152. Chi square values are only approximate because assumptions are violated.
A correspondence analysis for the distribution of skeletal elements in each structure indicates the relationship between structures and the number of skeletal elements recovered from them (Figure 3). The structures with similar distributions are represented by their proximity in the graph. The proximity of the structures to specific elements illustrates the relative frequency of said element in the structure. Two artisans’ houses (Q-40a and Q-176a) have similar compositions to I-55a and are close to Q-152. As mentioned above, Templo Redondo (Q-152) is the structure with the highest number of elements. The Hall (H-15) shows a particularly different composition with a larger number of metapodials and phalanges. The Temple (H-17) is the only structure apart from Templo Redondo where astragali were recovered. Similarly, the artisan’s house Q-39 is the only structure apart from Templo Redondo where calcanei were found.
Distribution of Dog Remains per Structure
The spatial distribution of skeletal elements in and outside the structures was analyzed for residential houses (Figure 4) and temples and halls (Figure 5). House I-55a corresponds to a wealthy artisan’s house located in the vicinity of the Itzmal Ch’en group (Masson et al. 2016). The majority of the dog remains found in this house were recovered from a midden outside the northeastern corner of the structure. A radius shaft, phalanges, metapodials, skull fragments, and detached teeth were deposited in this midden. The femur located at the southwestern corner of I-55a was in the structure’s construction fill.
Most of the dog bones found at artisan’s house Q-39 were found just outside the western side of the structure and possibly belong to domestic refuse. One of the femur shafts was found in the fill below the burial cist. Only two femur shafts were found inside the structure. At artisan’s house Q-40a, the majority of dog remains were found just outside the southwestern structure boundary. Based on the discovery of two left ulnae, it may be assumed that at least two individuals were left there. Dog remains at artisan’s house Q-176a were recovered from middens located at the western and southern outside edges of the structure. Most of the dog remains from this structure were found during the excavation of an infant burial site six meters north of the house structure. At least two dog specimens were recovered from the same level as the burial. The MNI is calculated by the presence of two left humeri and two right femur shafts. The size of slipped serving vessels found at these three houses suggest that festive meals could have been served there (Peraza Lope and Masson 2014b: 122). Dog remains were also used for ornamental purposes since two of the canine teeth from artisans’ houses Q-39 and Q-176a show holes drilled through the roots, suggesting their modification for use as personal ornaments that could have been used as status or lineage paraphernalia (Shaw 1991: 263). The use of dog teeth as jewelry has been widely documented throughout the Maya area (Clutton-Brock and Hammond 1994: 825; Hamblin 1984: 114; Teeter 2004: 188).
Most of the dog bones recovered from the colonnaded Hall H-15 were found at the west side of the structure. A staircase leading to the Itzmal Ch’en group platform was built at the northeast corner of H-15. Evidence of a mass human burial and a burning event were discovered at this locality. The human bones recovered from this area are disarticulated, highly fragmented, and present evidence of postmortem modifications such as direct exposure to fire, blows, and cut marks (Serafin et al. 2012: 242; Paris et al. 2017).
The presence of ritual ceramics such as effigy censers along with these human remains suggests that the local elites of Itzmal Ch’en were the victims of this mass killing (Masson et al. 2012: 18-19). Ritual pottery appeared in great quantities in the mass grave while very little was recovered from the hall, suggesting the removal of ritual pottery from the hall, and possibly other ceremonial buildings of Itzmal Ch’en, to be placed in the grave (Peraza Lope and Masson 2014b: 117). Most disarticulated dog remains were recovered at the mass burial site together with other common species in Mayapán such as iguana, white-tail deer, brocket deer, peccary, turkeys, rabbits, turtles, and various marine fish species. Animal bones found in the mass grave suggest a mixture of midden debris with human remains (Paris et al. 2017: 80). Metapodials and phalanges predominate in this sample, followed by dentary fragments, vertebrae and detached teeth. In addition to the two burned dog phalanges found in this sector, several human remains from the mass grave evidence burning (Paris et al. 2017: 73-74), suggesting that burning events at the mass grave site may also have altered the faunal remains deposited nearby. The rest of the dog bones reported from H-15 were recovered from the front steps of the colonnaded hall (phalanges, a molar tooth, and a femur shaft), which means that they too were disarticulated.
Dog remains were recovered from the upper levels of the western and eastern sides of Temple H-17. On the eastern side, the skeletal elements were a femur shaft, a tibia shaft, and radius as well as metapodials and astragalus. On the western side, two dentaries were found along with another femur shaft and phalanges. Itzmal Ch’en temple H-17 was an important place for rituals and administrative activities as evidenced by the great abundance of ritual pottery recovered there (Peraza and Masson 2014b: 118). Along with Temple Q-58 in the center of the city, H-17 is the second tallest temple in Mayapán (Masson et al. 2012: 10). The presence of serpent imagery in Itzmal Ch’en temple H-17 suggests that ceremonies dedicated to Kukulcan were important in this group (Chowning 1956; Masson et al. 2012: 10). Dog bones were found in association with other faunal remains and artifacts, including Ch’en Mul effigy censers (Cruz and Flores 2012).
Templo Redondo (Q-152) is where the majority of dog remains has been found and it presents the largest number of skeletal elements identified in this study. The remains are concentrated in specific areas of the Templo Redondo platform (Figure 4). Most of the dog remains in this group were found at the edges of the Templo Redondo platform and behind the colonnaded halls (Q-151) or the Hall of Chaac Masks and Q-152c or Huhí Nah. The materials recovered by the Carnegie Project at the Hall of Chaac Masks suggests ritual activities that included vessels associated with copal burning (Shook and Irving 1955: 148; Milbrath and Peraza 2003: 11). Some ceramic drums were recovered from Hall Q-152c but overall there are very few materials there (Peraza Lope and Masson 2014b: 113). Human skulls and disarticulated bones between Q-152 and Q-151, and between Q-152 and Q-152c, were reported by previous excavations (Milbrath and Peraza 2003: 11, 15). Masson and Peraza (2013: 271) also report large quantities of dog remains at Halls Q-87a and Q-87a/Q-88a, which are part of the Templo Redondo group. The concentration of dogs in this group, along with elite serving vessels, suggests that dogs were preferred and possibly included in activities such as sacrifices, feasts, and ceremonies held at Templo Redondo and its surrounding buildings (Masson and Peraza 2013: 271; Peraza and Masson 2014b: 111).
The concentration located at the western side of the platform between Hall Q-151 and Sanctuary Q-152a represents 89.2% of the dog bones recovered from the Templo Redondo group. A total of 20 right dentaries were recovered from this same location. The dog remains from Hall Q-152c were found in much smaller quantities (7.8%), and the other two right dentaries came from this hall. Other elements dispersed in Templo Redondo, its platform, and at the base of Altar Q-152d make up the remaining 3% of the total bones. It is important to mention that dog phalanges are absent in this sample and foot bones make up a small percentage of the skeletal elements reported (Table 3).
Osteometric Analysis
Osteometric analysis included measurements of maximum length and breadth of the dogs’ proximal and distal long bone ends. Given the fragmentation of the sample and the large number of unfused bones, measurements were only recorded for a sample of six complete limb bones (see Table 5) recovered at Templo Redondo, which were fused at both proximal and distal ends.
Humerus Meassurements (mm) | ||
---|---|---|
GL | Bd | Bp |
117.4 | 25.4 | 28.5 |
Radius Meassurements (mm) | ||
GL | Bd | Bp |
104.1 | 19 | 14 |
103 | 16 | 13.5 |
111.3 | 19.2 | 14 |
Femur Meassurements (mm) | ||
GL | Bd | Bp |
124.5 | 29 | 25 |
Tibia Meassurements (mm) | ||
GL | Bd | Bp |
124 | 19.4 | 27.6 |
Note: GL= Greatest length, Bd= Breath of the distal end, Bp= Breath of the proximal end (based on Von den Driesch 1976).
Metric data can be compared to information reported for the five breeds identified in Mesoamerica: the Mesoamerican common dog, the Mexican hairless dog or xoloitzcuintle, the short-nosed or Mayan dog, the tlalchichi dog, and a wolf-dog hybrid. The Mesoamerican common dog is the most widely identified dog breed in Mexico. It is characterized by a medium-sized body and dolichocephalic skull (Valadez 2000: 195; Valadez et al. 2013: 572). The Mexican hairless dog can be found in Central Mexican and Mayan settlements. Its most outstanding osteological characteristics are the absence of premolars, small teeth, and poorly formed incisors and molars (Valadez 2000: 197, Valadez et al. 2009, 2010). The short-nosed dog is limited to the Maya area. Its morphological characteristics are its complete dentition, comparatively short height, short nose, and brachycephalic skull (Valadez 2000: 200). Valadez (2000) and Valadez et al. (1999) argue that this type of dog corresponds to Allen’s (1920) short-nosed dog as well as to the specimens recovered by Hamblin (1984) on Cozumel Island.1 The tlalchichi, or short-legged dog, tends to be scarce in archaeological contexts but has been found in Central Mexico sites and at Chichén Itzá. It has full dentition and a dolicho-cephalic skull, but short limbs are this breed’s main characteristic (Valadez 2000: 198, Valadez et al. 2011). The wolf-dog hybrid presents a large robust head, thin face, permanent deciduous incisors and canines together, and larger dentition. Specimens of this hybrid breed have been identified in Teotihuacán and Tenochtitlan in Central Mexico, Cerro de las Minas in Oaxaca, and Xcambó in Yucatán (Valadez et al. 2006; Valadez et al. 2014).
Humerus, femur, radius and tibia length from the Mayapán specimens were compared to the measurements described in the literature as these are the most consistently reported measurements (Table 1). Figure 6 shows the comparison of humerus lengths with the only complete fused humerus from Mayapán. The Mayapán example falls below measurements reported for the Mesoamerican common dog, hairless dog, and wolf-dog hybrid and above those reported for the short-nosed and the tlalchichi dogs. Figure 7 indicates a similar comparison, as Mayapán radii measurements fall below those of the Mesoamerican common dog, hairless dog, and wolf-dog hybrid and above those of the tlalchichi dog. No measurements were available for the short-nosed or Mayan dog.
Figure 8 shows the comparison of Mayapán femurs with the aforementioned breeds. Although only one specimen of Mayapán dog is reported in this graph, this measurement is clearly below that of the Mesoamerican common dog, hairless dog, and wolf-dog hybrid and above that of the tlalchichi dog. Femur lengths from Mayapán are the same as those reported for the short-nosed dog femur. Tibia lengths are also very similar (Figure 9). The Mayapán dog’s tibia length falls below that of the Mesoamerican common dog, hairless dog, and wolf-dog hybrid and above that of the tlalchichi dog. This profile is a closer match to the short-nosed dog. It is important to mention that although the sample size is small, the comparison of different skeletal elements can still provide clues about the breeds of dogs from Mayapán. The sizes of the Mayapán’s dog limbs are uniformly smaller than those reported for the Mesoamerican common dog and Mexican hairless dog and seem to make a better match with the smaller breeds reported for Mesoamerica. A larger sample and skull measurements are needed for more conclusive data and to account for variations among Mayapán dogs.
Measurements of first molar tooth length and breadth were taken for 27 teeth, including detached teeth and teeth attached to maxillae and dentaries (Table 6). The measurements of the first lower and upper molar were compared to those given by Rodríguez et al. (2001), Valadez (2000), Valadez et al. (2004, 2009) and Blanco et al. (2009) for the same teeth in the Mesoamerican common dog, hairless dog, short-nosed dog, and wolf-dog hybrid (Figure 10). Measurements of both breath and length are not provided in the literature fortlalchichi breeds. Ranges of length for lower first molar were obtained from Allen (1920), Rodríguez et al. (2001), Valadez (2000), Valadez et al. (2004, 2009) in examples of the Mesoamerican common dog, Mexican hairless dog, short-nosed dog, tlalchichi dog, and wolf-dog hybrid. The lower first molar teeth from Mayapán have lengths of 17-18 mm. These lengths clearly fall within the range of the short-nosed dog (17.5-18.7 mm) and the Mexican hairless dog (17.1-19.9 mm).2 They are below the ranges reported for the Mesoamerican common dog (18.7-21.2 mm), tlalchichi (18.5 mm), and wolf-dog hybrid (25 mm). When measurements of both breath and length were given in the literature and compared to the Mayapán examples, it is clear that both lower and upper first molar dimensions fall below those given for the Mesoamerican common dog, hairless dog and wolf-dog hybrids. The reported measurement for the short-nosed or Mayan dog3 (Blanco et al. 2009: table 12-14) falls within the range of measurements for upper and lower molars of Mayapán. Further analysis of dentition and additional cranial and tooth measurements are needed to make better comparisons. For the moment, the dental information suggests two possibilities: (1) that there are strong similarities with smaller breeds of dogs, or (2) that there are hairless dogs within the sample which usually have atypical teeth.
Structure | Structure type | Tooth | Side | Measurements (mm) | |
L | B | ||||
Q-152 | Templo Redondo | m1 | L | 18.00 | 7.5 |
Q-152 | Templo Redondo | m1 | L | 17.5 | 7.4 |
Q-152 | Templo Redondo | m1 | L | 17.5 | 6.5 |
Q-152 | Templo Redondo | m1 | R | 17.0 | 7.5 |
Q-152 | Templo Redondo | m1 | R | 17.7 | 7.2 |
Q-152 | Templo Redondo | m1 | R | 17.8 | 7.4 |
Q-152 | Templo Redondo | m1 | L | 17.3 | 6.8 |
Q-152c | Hall | m1 | R | 17.5 | 7.5 |
Q-176a | Crafting house | m1 | R | 17.8 | 6.6 |
Q-39 | Crafting house | m1 | R | 17.8 | 7.2 |
Q-40a | Crafting house | m1 | L | 17.1 | 6.1 |
Q-152 | Templo Redondo | M1 | L | 11.5 | 14 |
Q-152 | Templo Redondo | M1 | R | 10.8 | 15.3 |
Q-152 | Templo Redondo | M1 | R | 10.7 | 13.5 |
Q-152 | Templo Redondo | M1 | R | 11 | 13.3 |
Q-152 | Templo Redondo | M1 | R | 10.5 | 13.2 |
Q-152 | Templo Redondo | M1 | R | 9.8 | 15 |
Q-151 | Templo Redondo | M1 | R | 9.5 | 13.2 |
Q-152 | Templo Redondo | M1 | L | 9.2 | 12.8 |
Q-152 | Templo Redondo | M1 | R | 10 | 14 |
Q-152c | Hall | M1 | R | 10 | 13 |
Q-152c | Hall | M1 | L | 11 | 13.2 |
Q-40a | Crafting house | M1 | L | 8.1 | 14.3 |
Q-40a | Crafting house | M1 | L | 10 | 17.5 |
Q-176a | Crafting house | M1 | L | 7 | 16.3 |
Q-176a | Crafting house | M1 | L | 8.4 | 15.1 |
Q-176a | Crafting house | M1 | L | 8.8 | 16.3 |
Note: m1= lower first molar, M1= upper first molar, L= Length, B= Breadth. Ranges for lower first molar length by breed: Mesoamerican common dog= 18.7-21.2 mm (Rodríguez et al. 2001; Valadez et al. 2004); mexican hairless Dog=17.1-19.9 mm (Rodríguez et al. 2001; Valadez et al. 2009); short-nosed Indian dog=17.5-18.7 (Allen 1920; Hamblin 1984; Valadez 2000); Tlachichi=18.5 mm (Valadez 2000); dog-wolf hybrid= 25 mm (Valadez et al. 2001).
Measurements of mandibular height at the lower first molar were used to calculate the body weight of specimens.4 Mayapán body weights range from 3,408 g to 10,841 g. Blanco et al. (1999: Figure 7 and Figure 9) report body weight calculations for different breeds, including examples of two common Mesoamerican dogs found at Chac-Mool with weights of 9,480 g and 9,420 g and a short-nosed or Mayan dog weighing 8,610 g; a common Mesoamerican dog from Teotihuacán with a weight of 9,420 g; examples from Tula include two common Mesoamerican dogs with weights of 11,265 g and 9,885 g, a hairless dog weighing 11,475 g and a tlalchichi with a weight of 10,485 g. Moreover, Valadez et al. (2001) report the following range of weights: common Mesoamerican and hairless dogs from 9,000 to 10,000 g, the short-nosed or Mayan dog 5,500 to 8,700 g, and the tlalchichi 9,500 g.
Body weight estimates indicate that the smallest specimen is found in artisan’s house Q-40a, weighing an estimated 3,408 g, while the largest is at Templo Redondo, with an estimated weight of 10,841 g (Table 7). Weights below 9,000 g are more common in the Mayapán sample (n=14, 70%), suggesting the presence of smaller breeds such as the short-nosed dog. These were found in all the structures analyzed. On the other hand, the few examples (n=6, 30%) with weights above 9,000 g were recovered from Templo Redondo, which suggests the presence of larger breeds in this context.
Structure | Structure type | Height Mandible (mm) | Body Weight (g) |
---|---|---|---|
Q-40a | Crafting house | 15.5 | 7,096.7 |
Q-40a | Crafting house | 11.2 | 3,408.0 |
Q-39 | Crafting house | 17.1 | 8,858.6 |
Q-176a | Crafting house | 15.3 | 6,891.6 |
Q-152c | Hall | 18.0 | 9,946.1 |
Q-152 | Templo Redondo | 17.5 | 9,333.3 |
Q-152 | Templo Redondo | 17.0 | 8,742.1 |
Q-152 | Templo Redondo | 17.2 | 8,976.0 |
Q-152 | Templo Redondo | 16.5 | 8,172.4 |
Q-152 | Templo Redondo | 14.8 | 6,393.7 |
Q-152 | Templo Redondo | 15.5 | 7,096.7 |
Q-152 | Templo Redondo | 17.3 | 9,094.2 |
Q-152 | Templo Redondo | 18.7 | 10,840.7 |
Q-152 | Templo Redondo | 17.8 | 9,698.4 |
Q-152 | Templo Redondo | 16.1 | 7,731.9 |
Q-152 | Templo Redondo | 16.8 | 8,511.6 |
Q-152 | Templo Redondo | 17.5 | 9,333.3 |
Q-152 | Templo Redondo | 15.0 | 6,590.4 |
Q-152 | Templo Redondo | 16.0 | 7,624.0 |
Q-152 | Templo Redondo | 17.0 | 8,742.1 |
Note: Estimation of weight according to mandibular height at m1 (Log y= 2.2574(Log x)+ 1.164)
x= mandibular height in m1 (Wing 1978: table 2.1).
Hamblin (1984: 100) cautions that body weight variation could be related to breeds or age. In the Mayapán sample, almost all (n=18, 90%) of the mandibles measured exhibited erupted teeth, which occurs when the animal is about seven months old (Sutton et al. 2018: Appendix). Two examples (10%) with unerupted third molars (with weights of 8,742 g and 9,333 g) in mandibles were recovered from Templo Redondo.
Age Distribution
Dog ages were calculated according to published epiphyseal fusion schedules (Sutton et al. 2018: table 11.3, table 11.7). The fragmentation of the sample made it impossible to determine ages for all specimens. A total of 51.9% (n=125) of the sample of limb bones and foot bones were sufficiently preserved to document epiphyseal fusion stages. Limb bones with fused proximal and distal ends (or both) comprise 68% of the sample, while 32% present unfused epiphyses.
Table 8 presents late-fusing long bones along with metapodials and calcanea, which fuse early. The majority of elements from Mayapán are fused, indicating that the growth and ossification stage had been completed. Unfused elements were not recovered in all of the structures investigated. The majority of unfused bones were found in the Templo Redondo group, followed by House Q-40a and Hall H-15. The remaining structures present only fully fused bones (Table 9), suggesting the presence of adult dogs.
Element | Fused | Unfused | ||
---|---|---|---|---|
Humerus (whole) | 1 | 50.0% | 1 | 50.0% |
Distal humerus | 15 | 88.2% | 2 | 11.8% |
Proximal humerus | 7 | 63.6% | 4 | 36.4% |
Radius (whole) | 3 | 42.9% | 4 | 57.1% |
Distal radius | 2 | 33.3% | 4 | 66.7% |
Proximal radius | 2 | 25.0% | 6 | 75.0% |
Proximal ulna | 5 | 71.4% | 2 | 28.6% |
Femur (whole) | 1 | 33.3% | 2 | 66.7% |
Distal femur | 2 | 33.3% | 4 | 66.7% |
Proximal femur | 3 | 42.9% | 4 | 57.1% |
Tibia (whole) | 1 | 33.3% | 2 | 66.7% |
Distal tibia | 5 | 100.0% | - | - |
Proximal tibia | 3 | 50.0% | 3 | 50.0% |
Distal calcaneus | - | - | 1 | 100.0% |
Calcanea (whole) | 2 | 100.0% | - | - |
Metapodials (whole) | 20 | 100.0% | - | - |
Proximal metapodial | 8 | 100.0% | - | - |
Distal metapodials | 5 | 83.3% | 1 | 16.7% |
Total | 35 | 68.0% | 40 | 32.0% |
Note: Distal humerus fuses at 6-10 mo., proximal humerus fuses at 10-15 mo., distal radius fuses at 10-12 mo., proximal radius at 7-10 mo., proximal ulna fuses at 7-10 mo., proximal and distal femur 9-12 mo., proximal tibia fuses at 10-12 mo., distal tibia fuses at 12-15 mo., in metapodials proximal MC1 fuses at 6-7 mo. and distal MC2-5 fuses at 6-7 mo. (Sutton et al. 2018: table 11.3, table 11.7).
Element | Templo Redondo Q-152 & Q-152c | Crafting House Q-39 | Crafting House Q-40a | Crafting House Q-176a | House I-55a | Hall H-15 | Temple H-17 | |||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Fused | Unfused | Fused | Unfused | Fused | Unfused | Fused | Unfused | Fused | Unfused | Fused | Unfused | Fused | Unfused | |
Humerus (whole) | 1 | 1 | - | - | - | - | - | - | - | - | - | - | - | - |
Distal humerus | 14 | - | - | - | - | 1 | 1 | - | - | - | - | 1 | - | - |
Proximal humerus | 7 | 4 | - | - | - | - | - | - | - | - | - | - | - | - |
Radius (whole) | 3 | 4 | - | - | - | - | - | - | - | - | - | - | - | - |
Distal radius | 2 | 4 | - | - | - | - | - | - | - | - | - | - | - | - |
Proximal radius | 6 | - | - | - | - | - | - | - | - | 1 | - | 1 | - | |
Proximal ulna | 5 | 1 | - | - | - | 1 | - | - | - | - | - | - | - | - |
Femur (whole) | 1 | 2 | - | - | - | - | - | - | - | - | - | - | - | - |
Distal femur | 2 | 4 | - | - | - | - | - | - | - | - | - | - | - | - |
Proximal femur | 3 | 4 | - | - | - | - | - | - | - | - | - | - | - | - |
Tibia (whole) | 1 | 1 | - | - | - | 1 | - | - | - | - | - | - | - | - |
Distal tibia | 5 | - | - | - | - | - | - | - | - | - | - | - | - | |
Proximal tibia | 2 | 3 | - | - | 1 | - | - | - | - | - | - | - | - | - |
Distal calcaneus | - | 1 | - | - | - | - | - | - | - | - | - | - | - | - |
Calcaneus (whole) | 1 | - | 1 | - | - | - | - | - | - | - | - | - | - | - |
Metapodials (whole) | 15 | - | - | - | 2 | - | 2 | - | - | - | 1 | - | - | - |
Proximal metapodial | 4 | - | - | - | 1 | - | - | - | 2 | - | 1 | - | - | - |
Distal metapodials | - | 1 | - | - | - | - | 2 | - | - | - | 3 | - | - | - |
Total | 66 | 36 | 1 | 0 | 4 | 3 | 5 | 0 | 2 | 0 | 6 | 1 | 1 | 0 |
% | 52.8% | 28.8% | 0.8% | 0.0% | 3.2% | 2.4% | 4.0% | 0.0% | 1.6% | 0.0% | 4.8% | 0.8% | 0.8% | 0.0% |
Note: Distal humerus fuses at 6-10 mo., proximal humerus fuses at 10-15 mo., distal radius fuses at 10-12 mo., proximal radius at 7-10 mo., proximal ulna fuses at 7-10 mo., proximal and distal femur 9-12 mo., proximal tibia fuses at 10-12 mo., distal tibia fuses at 12-15 mo., in metapodials proximal mc1 fuses at 6-7 mo. and distal MC2-5 fuses at 6-7 mo. (Sutton et al. 2018: table 11.3, table 11.7).
It is important to note that the sample from domestic contexts included in this analysis is very small and the majority of bones reported correspond to metapodials and calcanea, which are early-fusing elements.
Summary
This study provides further evidence of the utilization of dogs in different structures of the Postclassic city of Mayapán. It seeks to broaden our understanding of their use in domestic and ceremonial contexts, the spatial distribution of skeletal remains, their ages, estimated weights, and possible breeds of dogs raised in Mayapán.
Dogs were regarded as an important symbolic component of rituals, feasts, and ceremonies as indicated by their presence in temples and halls both at the site center and the Itzmal Ch’en ceremonial center. Templo Redondo (Q-152) presents the highest frequency and skeletal representation of dog remains, including an important number of unfused elements indicating the presence of juvenile dogs in the deposits. Diego de Landa (Tozzer 1941) reports the use of puppies in Maya ceremonies, which suggest a preference for juveniles in ritual contexts such as the case of Templo Redondo (Q-152), which also features the largest specimens in the sample based on body weight, which suggest the presence of larger and probably different breeds of dogs. Most remains are concentrated between Templo Redondo platform and the back of Chaak Masks Hall.
This study indicates that dogs were also integrated in the domestic and everyday economy of Mayapán. They were recovered from middens of both commoner’s and affluent houses. The important quantities of major limb bones in all artisans’ houses could indicate their preference for or access to certain portions of the skeleton. However, it is important to note that artisanal or differential discard may have affected the representation of skeletal elements. Mandibles recovered in artisans’ houses Q-40a, Q-39, and Q-176a indicate the presence of mostly smaller dogs based on estimated body weight.
House Q-176a presents a special context in which dog remains were concentrated and the skeleton was more complete than in other areas. This context is associated with the child burial at the north of the house structure. It is possible that dogs were buried to accompany the child. This is a significant burial practice that has been documented at sites such as Yaxuná (Götz and Stanton 2013) and Chac Mool (Blanco et al. 1999).
Dogs’ symbolic importance is reaffirmed by their interment with humans and in ritual contexts. They were also utilized as personal paraphernalia as evidenced by the presence of drilled dog canines. No other modification marks (cutting) were observed in the assemblage that could indicate defleshing, dismembering, or butchering. Two burned phalanges from H-15 may have been the result of burning events at the mass grave that also affected nearby deposits.
The osteometric data is preliminary and require verification using a larger sample, additional measurements of cranial elements, and analysis of dentition. The data examined here suggest the presence of smaller breeds of dogs, probably the short-nosed or Mayan dog, which has been already identified at other sites in the Maya region (Blanco Padilla et al. 1999; Hamblin 1984). Other larger breeds are suggested by body-weight estimates and are concentrated in the Templo Redondo group.
Age estimation based on epiphyseal fusion stages suggests the importance of adult specimens and indicates that, in most cases, dogs were allowed to grow to their full size, which is expected in domestication practices. Younger specimens based on fusion rates were found at Templo Redondo, Hall H-15 and artisan’s house Q-40a.
Conclusion
Previous studies have provided evidence of the predominance of dog remains at the monumental center of Mayapán and of their identification as a sacrificial animal (Masson and Peraza Lope 2008, 2013). At the regional level, the high frequency of dog remains during the Postclassic may be related to the increase in ritual and feasting activities (Emery 2004: 49). The fact that dogs can be raised and controlled but are still not found in high frequencies in domestic contexts may speak to the symbolic importance of this animal for Mayan societies. Fewer dog remains in domestic contexts in Mayapán follows the tendency documented at other inland sites such as Chichén Itzá, Dzibilchaltún, and Siho (Götz 2008) in what seems to be a trend in the Maya region during all periods (Cunningham-Smith et al. 2020: 172).
The mention of dogs in Postclassic codices and ethnohistorical accounts provide further evidence of their role in Maya communities. Diego de Landa wrote that dogs were viable substitutes for human sacrifice and they were commonly chosen for that purpose (Tozzer notes on Landa 1941: 114, Masson and Peraza Lope 2013: 272). His account of the Yax Cocah Mut sacrifice mentions an offering of virgin dogs, which suggests the selection of juveniles for this purpose, a case that could be related to the importance of subadults in rituals at Templo Redondo.
This study indicates that dogs were not solely used in elite and ceremonial contexts. The presence of dog remains in commoner’s houses in Mayapán suggests that their breeding and utilization was part of the everyday lives of the Postclassic Maya. Records from the sixteenth century indicate that dogs were raised and fattened for feasting events (Pohl and Feldman 1982: 302). They were used as gifts to reaffirm kin ties, to barter in the marketplace (Masson and Peraza Lope 2008: 181), and may have been offered to elites as a tribute (Shaw 1991: 261).
During a time of political integration and restructuration in Postclassic Mayapán, the manipulation of faunal resources in community and regional rituals may have helped to integrate and stabilize social relations (Masson 1999). Dogs formed part of rituals and economic activities that linked residents and governing officials as well as the broad economic network of the city.