Introduction

Named after its colors, Chinese blue-and-white porcelain was one of the most popular trade products in Southeast Asia and beyond between the fifteenth and eighteenth centuries. The ware came mostly from **gdezhen, the city of porcelain, and was manufactured in folk kilns while orders for the imperial court were fulfilled by official kilns [1]. For the latter, textual evidence indicates that the production organization was based on the division of labor with a strictly controlled and highly compartmentalized structure which contributed to maintaining a high level of constancy and quality [2, 3]. In contrast, and despite scant documentation, numerous archaeological findings from terrestrial and submerged sites point to a lot more variability among the ware for overseas markets produced in folk kilns, as for example color differences. The so-called blue-and-white porcelain is indeed not always blue and white, and the ‘blue’ decor could be gray or even black whereas the ‘white’ area could look grayish or beige. Besides, it can be noted that these atypical hues are not an issue for native speakers since the Chinese term for the products, Qinghua, meaning patterns with qing color, refers to a broad spectrum, ranging from green to black [4, 5]. In relation to this problem, color differences and glaze opacity could be repeatedly observed on the blue-and-white porcelain cargo of the Santa Cruz, one of the best-preserved shipwrecks in Southeast Asia [6], which raise questions about the origin of such notable features for ceramics in these contexts.

The Santa Cruz, a 25 m long junk, was found at a depth of 32 m about 10 km off the Zambales coast in the northern part of Luzon Island, the Philippines. Among its abundant cargo, there were more than 15,000 ceramics of various origins, including China, Vietnam, Siam, and Myanmar, reflecting a complex maritime trading network [7]. Chinese ware, mainly blue-and-white porcelain and celadon, accounted for as much as 86% of the ceramic discoveries and piles of the former were found in the bulkheads as loaded and almost intact, while pieces placed in the upper part of the boat were scattered around the wreck [8,9,10,11,12] (Fig. 1). Based on stylistic analysis, the blue-and-white porcelain was produced in **gdezhen during the Hongzhi period (1488–1505 CE) of the Ming Dynasty [13,14,15,16]. The prevalence of Chinese ware in the Santa Cruz, also observed for the Lena and Brunei wrecks, two other contemporary sunken junks found along the east side of the South China Sea, was considered exceptional since Chinese overseas activities declined between c. 1380–1580 due to the maritime ban from the Ming Court and Southeast Asian ceramics dominated the market [16,17,18,19,20,21]. Scholars have suggested that such high proportions of Chinese ware could be evidence of illicit trade [11] or a lessening of the ban [22].

Fig. 1
figure 1

Map of East and Southeast Asia with the location of the Santa Cruz Wreck (left) and images taken during the underwater excavation (right)

Beyond these historical considerations, the Chinese blue-and-white porcelain in the Santa Cruz is of particular significance since records of representative pieces from the late fifteenth century are relatively few and indeed, mostly from shipwrecks. Moreover, as the ware loaded in a specific vessel was most likely from the same workshop, and hence considered relatively homogeneous, the occurrence of peculiar features makes it an interesting case to investigate factors and causes responsible for color variations and defects like glaze opacity.

Deterioration of glass and high-fired ceramic glazes: a brief overview

From a materials viewpoint, at first glance, the alteration of high-fired ceramic glazes (Ca-rich) and associated pigments in decorative patterns can be paralleled with the degradation (corrosion) of glass in general, and more specifically with colored, stained, and/or enameled glass, in particular the potash-lime-silica type commonly found in medieval stained-glass windows. The corrosion of glass is a multifaceted phenomenon primarily controlled by the chemical composition of the glass (e.g., soda-based glasses have much better durability than potash equivalents [23]) and the characteristics of the corrosion medium (composition, pH, temperature, etc.) as well as numerous other environmental, physical and biological factors [24,25,26,27,28] and references therein. The main process is best described by an ion-exchange mechanism where protonic species from the surrounding solution diffuse into the glass and replace network modifier cations which are leached out of the silicate matrix resulting in a cation-depleted silica-rich surface layer with lower density [29,30,31]. This basic mechanism is however associated with (or followed by) various complex reactions occurring in or at the surface of the modified layer, such as network depolymerization, interfacial dissolution-reprecipitation, secondary crystallizations and microcracks formation, which are essentially controlled by the pH of the solution as well as other microenvironmental parameters. Only recently has a clearer picture of the overall transformation process emerged owing to high-resolution analyses of ancient glass samples and model glass altered in natural or controlled conditions [26, 32,33,34,35,36]. Yet, the typology and micromorphology of the corrosion layer remain dependent on the complex interaction of many factors and hence, on the historical and/or archaeological context.

For example, medieval stained-glass windows and model analogs weathered in atmospheric conditions and different environments show an alteration crust with neoformed amorphous and/or crystalline phases, the latter usually composed of salts from the leached cations [33, 37,38,39]. Moreover, when crystallizations create a network of microcracks under the influence of cyclic climate variations, it can induce scaling at the surface of the glass and increase the alteration rate [40]. On sixteenth-to-twentieth-century enameled stained-glass windows, pronounced flaking of the glassy paint layer could be observed with a partial loss of the decorations and was correlated with an insufficient degree of vitrification of the enamel and/or a high concentration of K and low content of Ca and Pb [41]. The latter result is consistent with the known behavior of these elements, which can be easily leached out and contribute to the formation of the alteration layer while, for Ca and Pb, also increase the stability of the glass phase when present in higher concentrations [24, 42,43,44].

On the other hand, the weathering of glass in soils or underwater is characterized by a stratified alteration layer composed of iridescent laminated structures which can evolve in parallel, hemispherical or more complex patterns [35, 36, 45,46,47,48,49,50]. A comparative analysis of Roman glass buried in soil and seabed sediments has indeed shown that silica-rich laminations form in both environments, but in addition, an opaque and heterogeneous white crust of similar composition was only observed on submerged colorless glass, while in soils, the laminated structures contain Mn-rich (+Fe) phases, also found together with Ca and P inside cavities developed along microcracks, pointing to a probable external (soil) origin [48]. Likewise, the presence of Mn (and Fe) was identified in the laminated structures of archaeological fragments from stained-glass windows [51]. Manganese was associated with a darkening of the glass induced by the oxidation of Mn(II) ions and the precipitation of insoluble, black-colored Mn(IV)-rich phases. This reaction is of particular relevance here as darker, sometimes blackish, hues of the decorations on blue-and-white ceramics have been attributed to the oxidation of Mn (and Fe) associated with the Co-based pigment [52, 53].

Besides such differences, it seems that the two environments have a rather similar impact apart maybe from the faster corrosion kinetics in underwater contexts, possibly favored by the continuous replenishment of the contact solution, which often translates into thicker corrosion crusts [48, 54]. Conversely, the underwater artefact-environment interface shows considerable variability, even at the scale of a wreck site [55], and the alteration rate can be significantly reduced in confined conditions [56] or when bio-colonization protects the glass surface [57].

Although observed in the alteration layer of tin glazes [58], the characteristic laminated structures have not been reported for Ca-rich glaze in high-fired ceramics, neither from land-based nor underwater archaeological contexts [59,60,61,62], and in general, this type of glaze is less prone to degradation. On excavated fragments of Jun porcelain (Song Dynasty), there was no alteration layer per se, and corrosion features were constrained to areas where wollastonite, a calcium silicate, had crystallized during firing and was partially ‘dissolved’ leaving dendritic or columnar pits and craters on the surface of the glaze [59]. Similar corrosion patterns, associated with a pronounced loss of transparency, were observed on the glazes of land-excavated Ru ware (Northern Song Dynasty) and underwater Longquan celadons (Dalian Island shipwreck, Yuan Dynasty) with a preferential dissolution of the Ca-rich component in the phase-separated glassy matrix within (or close to) the anorthite clusters [61, 62]. A shard from a black-glazed porcelain bowl (Southern Song Dynasty) buried in acidic soil and excavated at the Tushan kiln site (Chongqing, SW China) only showed a thin (~ 10 μm) amorphous silica-rich alteration layer and some thicker crust-like protrusions with heterogeneous micro-morphology and composition [60].

The corrosion resistance of high-fired ceramic glazes can be linked to their chemical composition. In comparison to potash-lime-silica glass, they contain less K and often less Ca (though still high), but critically, more Al (and Si) which contributes to increasing the stability of the glaze [63, 64]. Whenever such ware shows significant degradation, it appears that the corrosion patterns are connected to defects and heterogeneities in the glaze, notably the presence of wollastonite or anorthite crystals resulting from the devitrification during the firing process. Interestingly, these phases are absent in Vietnamese underglazed ceramics and celadons, and the ware, from both land and underwater contexts, is relatively well-preserved [65]. Moreover, the various shades of blue observed on blue-and-white sherds from the Chu Ðâu-My Xa kiln site and Cù Lao Chàm shipwreck (but produced at the same kiln site) seem uncorrelated with the archaeological context and are more likely associated with the composition of the pigments used for the decorations [66]. However, the frosted appearance and loss of gloss on some sherds from the shipwreck indicate that chemical corrosion was active; an observation confirmed by the higher hydration state of the glaze surface detected with Raman microspectroscopy compared to a sherd from the kiln site [67]. Similar corrosion features have been observed on sherds from the blue-and-white cargo of several Portuguese shipwrecks while some sherds have kept their gloss, notably those from Kraak ware [68].

The deterioration of ancient glass and ceramic glazes has been analyzed with various spectroscopic, spectrometric and imaging techniques [54, 69,70,71,72,73,74,75]. Of particular interest are portable non-invasive techniques such as portable X-ray fluorescence (pXRF) and Raman spectroscopy which have been used for the in-situ analysis of glass, glazes and pigments [76,77,78,79,80,81,82]. In this paper, variations in the color of the blue decorations and the aspect of the glaze, notably the loss of transparency, have been researched by combining detailed visual observations with pXRF and another non-invasive and portable technique: fiber optics reflectance spectroscopy (FORS); the latter providing the raw data for quantitative colorimetric analysis. Results from scientific investigations were further compared with other studies and contextualized into the development of **gdezhen at the turn of the sixteenth century.

Materials and methods

Blue-and-white porcelain

The selection of the blue-and-white ware was based on visual differences in color and aspect but constrained by both time and accessibility. Only a small part of the Santa Cruz cargo could be quickly surveyed in the storage room of the National Museum in Manila. Among the boxes which were open, all containing plates, one of the most common types in the assemblage, the color variability was impressive. For the purpose of this study, it was decided to focus on plates with atypical colors and peculiar features, and twelve plates were selected for analysis. In addition, a homogeneous set of objects with large flat surfaces was considered an advantage, particularly for the pXRF measurements. Originally, the porcelain plates were loaded in piles, mostly at the port side of the vessel, and distributed in bulkhead one, three, five, seven, and nine [8]. All of them are saucer-shaped and of similar size with a diameter of about 26 cm and a height of 4 cm, while their foot-ring diameter is about 13 cm. The interior blue decorations display casual-style motifs consisting of flowers, mainly chrysanthemums, and other plants as well as rocks, deer and pine trees (Fig. 2). All plates but one (SC-256) are also decorated on the exterior of the cavetto with floral patterns but dates or trademarks are absent at the bottom of the plates. Blue-and-white dishes with similar designs were found in other mid-Ming shipwrecks such as the Lena Shoal, the Brunei junk, Ko Samui and Laoniujiao N°1 [16, 18, 20, 83]. For example, the depiction of fallow deer, a symbol of Taoism, in association with the pine tree on SC-256 (a motif called ‘Song Lu Zhang Chun’ in Chinese, meaning long life and wealth) is almost identical to the decoration on a dish (BRU376) from the Brunei junk [84].

Fig. 2
figure 2

Photographs of the twelve blue-and-white porcelain dishes from the Santa Cruz shipwreck analyzed in this study

The primary motifs are outlined and filled with light colors, whereas the small leaf patterns were drawn directly with thicker pigments favoring the formation of darker spots after firing. The glaze was applied on the whole dish, and for several of them, it appears slightly opaque rather than transparent; it was apparently scraped off the foot ring leading to a somewhat angular rim where the clay body is visible though irregularly. The glaze often shows defects such as crazing, pinholes and Y-shaped dewetting patterns (Fig. 3a, b). The latter two seem to be more developed on the bottom of the dishes which could be related to the different degree of finishing of the clay body compared to the decorated areas. While all dishes were cleaned and desalinated after the excavation, some still show marine calcareous encrustations (Fig. 3c). The main characteristics of the selected blue-and-white dishes are summarized in Table 1.

Fig. 3
figure 3

Features on the bottom of three selected dishes. a Homogenous glaze with some defects (SC14679); b crazed glaze with pinholes and Y-shaped dewetting patterns (SC5135); c shell and worm-like encrustations (SC13671)

Table 1 Characteristics of the selected blue-and-white porcelain dishes

Methods

Portable X-ray fluorescence (pXRF)

Compositional data were obtained with a Thermo Niton XL3t GOLDD + handheld XRF spectrometer equipped with a silver anode tube and a large silicon drift detector (SDD) operating at a maximum voltage of 50 kV and current of 200 μA with a resolution better than 160 eV. Single pXRF measurements were carried out directly on the transparent glazed surface of the blue-decorated and ‘white’ areas with a standard spot diameter of about 6 mm, the built-in camera allowing precise positioning. Data were collected in both soil (blue and ‘white’) and mining (only ‘white’) modes with acquisition times set to 60 and 90 s, respectively. The two modes use different algorithms and proprietary calibrations for the conversion of counts into concentrations. From a practical viewpoint, the mining mode is better adapted for the analysis of major and minor elements while the soil mode is optimized for elements present at trace levels; typically, above 0.5–1% for the former and in the tenths to thousands ppm range for the latter, depending on the element. Measurements on the blue decoration (glaze + blue pigment) and the ‘white’ were taken on the flat surface of the plate’s interior while an additional ‘white’ was analyzed at the bottom. When the surface of the ‘white’ next to the blue on the interior was too small or inadequate, the ‘white’ was sometimes analyzed on the less decorated external side of the dishes. Additional information about the pXRF methodology and limitations of the technique can be found elsewhere [81] and references therein.

Fiber optics reflectance spectroscopy (FORS)

Reflectance spectra were acquired with a portable FieldSpec®3 spectrometer (ASD Inc., Malvern Panalytical) in the 350 to 2500 nm spectral range with a resolution varying from 2 to 10 nm. Spectral data are internally re-sampled by the instrument to 1 nm intervals, and each collected spectrum corresponds to the average of thirty scans. Reflectance was measured with a high-intensity contact probe equipped with a halogen light source giving a spot diameter of about 10 mm and was calibrated against a white Spectralon® standard. Measurements were taken on the blue decorated areas and on the ‘white’ at the bottom because there was often not enough space for the measuring probe between the blue decor. Colorimetric data (XYZ) were extracted from the reflectance spectra and converted into the CIELAB chromatic color space and HEX color codes (http://www.easyrgb.com/en/) for analysis and visualization.

Results and discussion

Chemical composition and production kilns

In agreement with the historical context and stylistic analysis, elemental data obtained with pXRF on the transparent glaze confirm a **gdezhen production for the blue-and-white plates based on the concentrations of some discriminative elements such as zirconium, thorium and titanium (Table 2). Values for these elements are close to the ones measured with pXRF and other techniques in previous studies despite the different time periods [81, 85,86,87,88,89]; such compositional similarities could correspond to a relative constancy in the procurement of raw materials and processing technologies from the middle to late-Ming period. However, variations in rubidium levels, i.e. the higher values reported in the present study, also found for the Guanyinge and other unspecified late-Ming kiln sites (Rb: 428 ± 78 ppm, [86]; Rb: 436 ± 84 ppm, [85]), compared to the lower averages measured on **gdezhen blue-and-white ware from the Nan’ao One shipwreck in China (Rb: ~ 270 ppm, [86]) and sherds from the Philippines and Indonesia (315 ± 40 ppm, [81]) dated to the late-Ming and early-Qing periods, might reflect some intra-site variability among the numerous folk kilns in **gdezhen.

Table 2 Elemental composition and absorptions in the visible spectral range of the selected blue-and-white porcelain dishes

As expected, the chemistry of the glaze analyzed in the ‘white’ area corresponds to an aluminosilicate glassy network containing calcium and potassium added as fluxing agents and network modifiers. The average amounts of Ca (CaO ~ 6.1 ± 0.9) and K (K2O ~ 4.3 ± 0.4) are higher and lower, respectively, than those obtained with pXRF on sherds from the Xuande and Chenghua periods [89] but still in the range of Ca values known to have significantly varied (from a few to more than twelve percent CaO) throughout the Ming (and Qing) dynasty [68, 81, 87, 88, 90,91,92,93]. It should also be mentioned that because of the X-rays emission depth for Ca and K (about a few tenths of micrometers in this type of matrix) [94, 95], these two elements could be underestimated if the glaze is corroded on the surface. On the other hand, Ca seems not related to the degree of translucency of the glaze, making it challenging to identify the origin of the opacity which could be linked to the firing process and/or underwater weathering. For a few dishes, the low calcium levels, if associated with lower firing temperatures, could indirectly contribute to opacify the glaze through a silica matt effect. However, translucency has probably a different origin as the correlation with calcium levels is far from systematic.

Also noticeable are some significant differences in the composition of the glaze applied to the bottom, which shows lower calcium and higher iron levels in comparison to the glaze in the ‘white’ areas. Although there are exceptions to this trend (SC-3245 for Ca and Fe, SC-1269 and SC-5135 for Fe), it could suggest the usage of a modified recipe for the glaze applied to the bottom, which also implies a two-step glazing process. However, a systematic study on a much larger number of plates would be needed to exclude other explanations and confirm this hypothesis.

Blue decorations: pigment characteristics

The comparative analysis of pXRF data from the blue decorated and ‘white’ areas shows that the cobalt-based pigment contains high levels of manganese, low iron and significant amounts of nickel as well as traces of copper (Table 2) which points toward an Asian source [52]. After subtracting the manganese and iron contribution from the transparent glaze (‘white’ area), normalized percentages of Mn, Co and Fe are similar to the blue pigment analyzed on other export blue-and-white porcelain produced in **gdezhen (Fig. 4, left). Although the heterogeneous distribution of the coloring elements and particles within the glaze, combined with the constraints on the probing depth, prevent a precise determination of the pigment’s chemical composition, this elemental profile and the average Mn/Co ratio (7.1 ± 1.7) are consistent with results of previous studies [81, 87, 93, 96, 97] and confirm the use of Mn-rich asbolane ores in folk kilns during the Hongzhi period of the Ming dynasty.

Fig. 4
figure 4

Ternary plot visualizing the blue pigment composition based on the relative proportions of Co, Mn and Fe; Santa Cruz data compared to a set of **gdezhen blue-and-white from [87] (left). FORS spectra with the main absorptions of Co(II) in the visible and water in the near-infrared obtained on decorated areas for three plates from the analyzed set (right)

Spectral profiles obtained with FORS on the blue decorated areas (Fig. 4, right) show the characteristic absorptions of Co(II) in tetrahedral coordination with the triplet located around 520, 583 and 672 nm [81, 98]. For some plates, darker colors translate in an overall lower reflectance in the visible, but the cobalt absorptions with variable relative intensities are always present (Table 2). The gray-greenish or blackish hue of the decoration is most likely correlated with the manganese and iron in the pigment, combined with redox firing and cooling conditions favoring the crystallization of Mn and Fe-rich oxide phases [52, 53, 93].

Similar dark colors were also observed on blue-and-white sherds from the late fifteenth to the early sixteenth centuries by Wang et al. [99] and Qu et al. [100]. More specifically, these colors have been connected with the crystallization of Mn(Fe)-rich spinels [101, 102] in dark spots which parallel the ‘iron spots’ observed on Yuan and early-Ming blue-and-white when imported Fe-rich Co-pigment was in use [53]; in fifteenth century Vietnamese blue-and-white, a dark-greenish blue tint was even obtained intentionally by adding iron [103]. In our FORS spectra, although the presence of Mn-rich phases might be associated with weak absorptions (only visible on 2nd derivative spectra) at ~ 420 nm Mn(II) and ~ 490 nm Mn(III), the correlation is not well-established despite a thorough study of the spectral profiles. The analysis is complicated by the probable contribution of various Fe(III) absorptions to the overall spectral profile below 500 nm [104, 105]. Further research is definitely needed, notably on reference materials, to make more solid interpretations using the potential of FORS.

Finally, in the near-infrared spectral range, some plates show an asymmetrical absorption of variable intensity around 1910 nm corresponding to the combination band OH + δHOH) of water which could be adsorbed in the glaze and/or in the body. The presence of water might be due to weathering and/or indirectly reflect a residual porosity in the body resulting from lower firing temperatures. Depending on its location, water could be a contributing factor to the opacity, a possibility that would require additional specific analysis.

Color, technology and weathering

Visual observations

The pictures in Fig. 2 clearly show variations and alterations in the appearance of both the glaze and the blue decorations. As described earlier, surface corrosion and abrasion on ceramic ware recovered from shipwrecks is not uncommon [62, 68] and the weathering induced by the immersion in seawater for hundreds of years has certainly contributed to some of the features observed here. It does not explain however why several dishes in the same environment still look almost pristine. Moreover, the striking differences between dishes excavated from the same grid (e.g., SC-2963 and SC-3245) indicate that location in the wreck is not a prime factor and point to other causes.

The glaze of most dishes is rather transparent but for a few it tends to be slightly opaque with sometimes a milky and/or frosted appearance. This translucency affects the visibility of the decoration underneath which shows significant differences in the hue and brightness of the Co-based pigment. The blue areas often look dull with the naked eye and have a greenish or grayish tint. Intriguingly, this color shift was also frequently observed on blue-and-white ware from contemporaneous shipwrecks such as the Lena and Brunei junks [16, 20, 84]. Occasionally, a brownish material can be observed on top of the dark blue areas, often in association with whitish spots marked by a network of needle-like crystals (Fig. 5) similar to the clusters of anorthite or wollastonite identified in the corroded areas on other types of high-fired glazed ceramics mentioned earlier [59, 61, 62]. Here, they are probably composed of anorthite (CaAl2Si2O8), which is the main crystalline phase found in traditional glazes [106] as well as in modern Al-rich glaze formulations when firing cycles include longer soaking times favoring devitrification [107]. Although the presence of anorthite in the glaze of blue-and-white porcelain has been reported in numerous studies, the crystals are usually located at the body-glaze interface in close association with the cobalt pigment [99, 100, 108,109,110,111]. They are rarely found throughout the whole thickness of the glaze or near the surface as observed for dish SC-14878.

Fig. 5
figure 5

Details of a dark blue decoration on the broken edge of dish SC-14878 showing the change to a brownish color (arrow) and the network of whitish minerals (right, top view)

Interestingly, a sherd from the Guthe collection (GU09, Fischer and Hsieh [81]) might provide some clues about the features observed on dish SC-14878 as it displays similar surface patterns (Fig. 6, left). Scanning electron micrographs in backscattered electron mode show indeed anorthite (confirmed with energy dispersive spectroscopy analysis) crystals at the surface of the glaze with a partial dissolution of the interstitial glass phase (Fig. 6, center) while the cross-section reveals insightful details about the glaze microstructure and anorthite distribution (Fig. 6, right). It is generally assumed that anorthite crystallizes at the glaze-body interface because of a change in the glaze composition near the interface resulting from the partial melting of the body and subsequent diffusion of aluminum [112]. Here though, anorthite crystals are not only visible at the interface but within the entire thickness of the glaze. Moreover, the pigmented layer with Co-rich particles embedded in the network of anorthite, usually found close to the body, is located near the surface, indicating that it was lifted in the molten glaze by further bottom-up crystallization and growth of anorthite which might be favored by longer soaking times at high temperature. Likewise, the formation, growth and migration of bubbles can have a similar effect (e.g., Pinto et al. [111], Fig. 7d). This mechanism not only explains the anorthite spots but also creates a (sub)surface heterogeneous microstructure particularly sensitive to dissolution and oxidation reactions that can affect the residual glassy matrix and elements originally associated with the pigment such as Mn, Fe and Ni, and possibly produce color changes. Less specifically, if the anorthite crystallization in the glaze is extensive, it can reduce the transparency by scattering the light and contribute to the surface mattness [107] which most likely explains the appearance of dishes SC-3245 and SC-7026.

Fig. 6
figure 6

Brownish spot on the sherd GU09 observed with a digital microscope (left) and a scanning electron microscope (NanoSEMTM230, FEI): same surface (center) and corresponding cross-section (right)

Fig. 7
figure 7

2D scatterplot of chromaticity values a* and b* with corresponding CIELAB colors. Reported data include measurements on the dishes from the Santa Cruz (SC), mid to late Ming blue-and-white sherds (TZ, Pinto et al. [111]) and various modern Co–Al blue pigments (CB). See text for additional information and refs

Another explanation for the presence of the Co-pigment + anorthite near the surface could be the two-layers glaze technology described for sherds of blue-and-white export ceramics from China as well as Vietnam [68, 113,114,115,116]. Contrary to the traditional underglaze blue-and-white, in the two-layers technology the body was glazed and fired twice with the blue decoration applied in between after the first firing. The presence of two glaze layers has been recognized through observations and analyses on cross-sections with optical (+digital) microscopy and scanning electron microscopy coupled with energy dispersive X-ray spectroscopy for elemental analysis (SEM–EDS). The two layers appear to have a different composition with notably higher Ca in the upper layer which imparts both a better chemical stability to the glaze and a lower melting point avoiding re-melting of the first glaze layer during the second firing. However, SEM images were often taken at too low magnification to clearly visualize the two layers and the spatial organization of the different phases in the colored glaze [114], or not shown at all while EDS spectra are plenty [68]. Furthermore, elemental data were preferentially collected in the colored glaze, where Ca-rich crystalline phases can potentially affect the Ca value (requiring precise analysis location frequently not indicated), and sometimes compared to only one measurement in the colorless glaze. In fact, Ca concentrations should be systematically measured in the inner and outer parts of the colorless glaze as well in order to confirm the existence of two glaze layers, as exemplified by Zhang’s EDS analysis, with two sherds showing such robust compositional evidence (114, Table 2, samples 1 and 10). Although beyond the research presented here, these experimental limitations and the importance of the topic certainly warrant further investigations. Finally, the sherds are all late-Ming productions, either from Fujian kilns [114, 115] or unspecified kiln sites [68], and only one is purportedly attributed to **gdezhen ([113], sample N2), calling into question whether the technology was ever implemented in **gdezhen, and all the more so during the mid-Ming period, making for now this alternative explanation unlikely.

All these observations and hypothesis suggest a critical role of pre-existing characteristics determined by the original quality and aspect of the ware in relation to manufacturing technology and raw materials composition, particularly of the Co-based pigment. In an attempt to explore further causal links and key parameters, color variations were investigated more systematically through a quantitative approach based on colorimetry.

Color analysis

Color variations between the different plates were analyzed after converting the XYZ colorimetric data obtained with FORS into the CIELAB color space (Table 3). Also referred to as L*a*b*, in this representation, L* corresponds to the brightness while a* indicates the red and green hues for positive and negative values, respectively, and for b* similarly the yellow and blue, with intensifying blue as negative values increase for the latter [117]. In Fig. 7, coordinates b* are plotted in function of a* using corresponding HEX color codes for the symbols. Data include the chromaticity values of the Santa Cruz dishes (SC) and for comparison, those of some mid to late Ming blue-and-white porcelain excavated from the Maojiawan archaeological site, Bei**g, but produced in **gdezhen (TZ, Pinto et al. [111]). Some modern cobalt aluminate blue pigments synthesized by various methods were also added as reference (CB) [118,119,120].

Table 3 Colorimetric data from FORS

For most Santa Cruz dishes, color parameters are characterized by negative a* and negative (or slightly positive) b* values not exceeding − 15 which is consistent with the overall weak blue tint. These chromatic values are similar to the ones of sherds dated to the mid-fifteenth to the early sixteenth centuries analyzed and classified by Pinto et al. [111] in groups B and C (− 16 < b* < 4; − 4.2 < a* < − 3). On the other hand, in the same study, sherds from the late Ming period (group A, TZ08-11) have a more pronounced blue tint, as shown by the higher b* negative values (b* ~ − 23). But these levels are still far from b* values obtained for modern Co–Al pigments synthesized through wet-chemistry processes [119, 120] or with oxide powder precursors [118] and calcinated at various temperatures (Table 4). The difference between CB-1a and CB-1b exemplifies the well-known role of the firing temperature on the blue color of cobalt aluminates [121, 122]. Interestingly, Llusar et al. [118] show how the mixing of the Co–Al pigment (CB-3a) with a porcelainized glaze results in a less intense blue tint which could be due to some dissolution of the Co–Al spinel in the molten glaze in addition to the lower cobalt concentration effect.

Table 4 Color parameter b* and calcination conditions for modern Co–Al blue pigments (CoAl2O4 spinel) prepared by various methods

However, a major difference is that the modern Co–Al pigments are ‘pure’ and do not contain Mn and/or Fe, which conversely could confirm the role of these elements in the development of darker grey-black or greenish hues for the blue decoration as argued by several authors, even if in the process the respective contribution of Mn and Fe-rich phases is still debated [99, 111]. The connection with color changes is not straightforward anyway because there is no direct correlation between decreasing b* values and higher manganese and/or iron levels. Multiple variables might be involved such as pigment particles’ composition, structure, density and size as well as the use of mixtures [110, 111], not to mention the upstream influence of cobalt ore processing and firing conditions.

From a historical viewpoint, it is worth mentioning that blue-and-white porcelain produced during the Hongzhi period is often described as unremarkable by art historians because associated with minor technological and stylistic innovations even if the porcelain ware equaled the outstanding achievements of the preceding Chenghua period (1464–87 CE). The latter though ended with unsustainable production costs for the imperial factory and thus, to avoid further straining the court’s finances, the Hongzhi emperor decided to almost halt the operation of official kilns entirely during his reign [123]. Moreover, the Chenghua period marked the transition from imported cobalt pigments to local asbolane ores, which were seemingly easier to grind resulting in a finer pigment but fired to a greyish shade of blue [124]. This color particularity was also noted by Valenstein [125] for blue-and-white ware produced during the following Zhengde period. Therefore, it can be argued that the apparent ‘predominance’ of greyish-blue hues during the Hongzhi and Zhengde periods was primarily due to a trial-and-error experimental approach in relation to the procurement and processing of cobalt-rich pigments from the newly exploited domestic sources. This could be supported by a mid-Ming blue-and-white porcelain bowl found at the Zhushan official kiln site (Fig. 8). The distinct colors of the numbered decorative motifs show that this ware was used to evaluate various cobalt-based pigments, possibly from different sources and refining methods and/or applied in mixtures.

Fig. 8
figure 8

Blue-and-white porcelain bowl from the Ming dynasty apparently used for the evaluation of different types or formulations of Co-based pigments (Museum of Official Kiln, **gdezhen)

Additionally, the ware attributes from folk kilns fluctuated much more compared to official kiln productions, most likely because of looser quality controls inherent to the large volumes manufactured for overseas markets and more variability in the pigment raw materials. In this context, blue color standardization might not have been a primary concern for the traders on the Santa Cruz, knowing for example that Southeast Asian customers had used greyish ware from Vietnam and Siam for decades [126]. Although less frequent, quality differences also occurred later when trade expanded further if one refers to the notes by Italian Jesuit Matteo Ricci (1552–1610 CE) mentioning that skilled craftsmen did not seek perfection since buyers were satisfied with less finished goods [127].

Conclusion

This research has investigated variations in the appearance and color of blue-and-white porcelain recovered from the late fifteenth-century Santa Cruz shipwreck, with a particular focus on the aspect of the glaze and the peculiar hues of the blue decorations. In agreement with stylistic studies and historical data, compositional analysis has shown that the ware was produced in **gdezhen, and the pigment for the ‘blue’ decorations was processed from Co-Mn-Ni-rich domestic asbolane ores.

Based on visual observations and microtextural comparisons, the origin of the opacity of the glaze was linked to the extensive crystallization of anorthite and its distribution in the glaze layer. In the blue-decorated areas of some plates, the anorthite laths associated with pigment particles reached the surface of the glaze, probably during prolonged soaking times, and subsequently formed white-brownish spots enhanced by weathering-induced dissolution and oxidation reactions. Chromaticity analysis has confirmed the visual perception of a grey-greenish, occasionally even blackish color of the ‘blue’ decorations, which contrasts with the brighter and lighter, sometimes deeper blues characteristic of the Yuan, early Ming and, to a lesser extent, late Ming periods.

While atypical hues and attributes variability have been known throughout the production history of Chinese blue-and-white porcelain, it is suggested here that their widespread occurrence in folk kiln ware of the Hongzhi and Zhengde periods reflects a phase of experimentation prompted by the transition from imported to domestic cobalt pigments. The blue-and-white cargo of the Santa Cruz and other junks of the same period thus indirectly reveal some of the changes that happened in the capital of porcelain at the turn of the sixteenth century when production in folk kilns ramped up significantly to satisfy the demand from abroad. It also shows that the line of causality extends well beyond the sunken history of the ware, back to its manufacture and, more specifically, to the characteristics and processing of the pigment raw materials. On the other hand, it raises essential questions about the difficulties faced by potters and other craftsmen, from technological challenges and organizational constraints to the intricate concept of quality, and hence value, especially when comparing production in folk and official kilns, questions of which our limited understanding calls for further research.