Medieval Aquatic Systems Impact
Medieval Aquatic Systems Impact
1000–1350
183
1
Readers who recall Hoffmann, “Economic development and aquatic ecosystems” will at
first see in this chapter extensive carry-over from that article. But decades of evolving
environmental understandings and continued research into medieval conditions have
shown that humans alone, even in the newest Anthropocene, are neither the sole
drivers nor determinants of environmental interaction. Despite the silent opacity of
most written sources, scholars must now concede that natural and cultural forces had
become well entwined long before synthetic treatment of late medieval marine fisheries
becomes possible. This must not deter efforts to trace environmental changes of
whatever origin.
2
In Regier et al., “Rehabilitation,” 87–88 (and see works there cited), fisheries ecologists
argued that “conventional exploitative development” damages aquatic ecosystems through
a sequence and synergy of excessive harvests, damming, destructive cultural practices,
organic and toxic pollution, and urbanization without regard for environmental effects.
Their ecosystem model comes primarily from comparative study of more or less modified
river systems in the late twentieth century. A longer temporal perspective on changes
humans have caused in New World marine coastal environments is laid out in Jackson,
“Historical Overfishing.” The deeper historical record here sketched generally confirms
these models, but suggests greater nuance and different specific processes. Whether in
marine or freshwater systems, the fishes first or most affected will be those ‘ecological
guilds’ with the most vulnerable habitat requirements (see Chapter 1, p. 49 above). Further
discussion of habitat issues appears in Supplement 5.1.
3
Darby, “Clearing the woodland,” is a classic and so, too, Wickham, “European forests”;
Hoffmann, Environmental History, 119–136, attempts an update.
4
Writing about 1300, a Colmar Dominican compared his own times with the less-
developed Alsace his fellow friars had entered a century before, including “Torrentes et
flumina non ita magna tunc sicut nunc fuerunt, quia radices arborum fluxum nivium et imbrium
per tempus in montibus retinuerunt.” (Jaffé, ed., “De rebus Alsaticis,” 236).
5
Fumagalli, Landscapes, 110–121. Dunin-Wąsowicz, “Natural environment and human
settlement,” 94–95 and 102, refers to “great changes in the hydrographic balance [viz. of
Central Europe], which reached proportions of a natural disaster during the course of the
13th century.”
6
Compare Hynes, Ecology, 327–332, and the different habits of “white fish” and “grey fish”
in Regier et al., “Rehabilitation,” 93–96.
7
A point emphasized in both Vogt, “Aspects of historical soil erosion,” 86–88, and Bell,
“Archaeology under alluvium,” 272. For a global perspective see Hoffmann et al.,
“Human impact … during the Holocene.”
8
Nitz, “Feudal woodland colonization,” 178; Hoffmann et al., “Trends and controls of
Holocene floodplain sedimentation.” A more general view of the process is in Wickham,
“European forests,” 534, and works there cited.
9
Lambrick, “Alluvial archaeology,” 222; Williamson, Shaping Medieval Landscapes,
169–173; and with such regional studies synthesized in Lewin, “Medieval
environmental impacts,” 277–280 and 294–299. Note the temporal coincidence of
these destructive impacts on English rivers with the so-called fish event horizon there
(Chapters 2 and 4).
10
Colardelle and Verdel, eds., Chevaliers-Paysans, 31–32, and Colardelle and Verdel, eds.,
Les habitants, 57–60. Pollen analysis finds cultivated plants and field weeds in the new
sediments. Bertrand and Bertrand, “Pour une histoire écologique,” 74–80, think this a
common phenomenon in France during central medieval centuries.
11
Bravard, “Des versants aux cours d’eau”; Bork, Bodenerosion und Umwelt; Bork et al.,
Landschaftsentwicklung, 221–226 and 237–249; and Bork and Schmidtchen, “Böden:
Entwicklung, Zerstörung.”
12
TeBrake, Medieval Frontier, 70 and 147–148; Filuk, “Biologiczno-rybacka
charakterystyka ichtiofauny,” 146–148.
13
Large areas in peninsular Italy and other parts of the classical Mediterranean had,
however, already suffered enduring damage from deforestation, overgrazing, and
erosion followed by coastal deposition in Roman times (Hughes, Pan’s Travail, 90 and
190; Hughes, Mediterranean, 39–44 and 54–57), so further changes during the Middle
Ages (as for instance at the mouth of the Tiber) were less dramatic there. Nevertheless
Ortolani and Pagliuca, “Cyclical climatic-environmental changes,” summarize local
For some fish species, this could mean loss of important migratory,
spawning, and juvenile habitats. Heavy silt loads make water more often
turbid, reduce light penetration, and can smother fish or prey species
adapted to live in weed or gravel beds. Like the more dramatic alterna-
tion of floods and low water, the effects favour certain species relative to
others. A tenth-century monastic chronicler at Novaliense in the Italian
Piedmont was well aware that clear mountain water held lots of fish and a
muddy stream few.14 Soils from unstable cleared lands in tenth–twelfth-
century Sicily went down local rivers to trigger shifts in their fish
populations.15
To process the new grain supplies a little-used late antique invention,
the watermill, surged across the medieval landscape. From perhaps a
couple hundred in King Alfred’s England, they multiplied to 5,624 in the
Domesday Book of 1085. In Poitou, Berry, Languedoc, Burgundy, and
Lorraine mills proliferated from the tenth century through the twelfth.
On the Aube, where fourteen mills are recorded in the eleventh century,
sixty-two may be counted in the twelfth century, and almost two hundred
in the early thirteenth. Then and later their construction became a
normal part of rural development in the Egerland and in central Silesia.
Late thirteenth-century Milanese writer Bonvesin de la Riva estimated
the territory of his city held 900 mills running about 3,000 wheels.16 One
historian of technology summed it up this way:
By the close of the Middle Ages watermills were in use on streams of every type.
They dammed up the rivers of medieval man; they were on the banks of his
brooks and creeks, in the middle of his rivers, under his bridges, and along his
coastlines. They impeded navigation and created streams (in the form of mill
races and power canals) and lakes (in the form of storage reservoirs behind
waterpower dams) where none had existed before.17
17
Reynolds, Stronger Than a Hundred Men, 69. Compare Lewin, “Medieval environmental
impacts and feedbacks,” 291–293.
18
For technical particulars and their implications, see Lucas, Wind, Water, Work, whose
focus is industrial applications of milling power, and the essays in Walton, ed., Wind and
Water, whose contributors have more social interests. Langdon, Mills, 70–107, shows
breast and overshot designs dominating England by the late twelfth century and Benoit
and Rouillard, “Medieval hydraulics in France,” 203–208, the same for northern
France, although undershot wheels were there more common in flat terrain and
horizontal wheels remained a tradition in certain Mediterranean areas and also Ireland
(Rynne, “Waterpower in medieval Ireland,” 9–40). Nevertheless, Chiappa Mauri,
I mulini a acqua nel Milanese, 152–175, emphasizes an early medieval replacement of
horizontal with vertical wheels, and Sicard, Moulins de Toulouse, 38–43, documents a
shift from mills on anchored rafts to land-based mills with dams or weirs.
19
Brykala, “Watermills’ functioning.”
20
Clay, “A Norman mill dam,” and works there cited. Compare Bagniewski and Kubów,
“Średniowieczny młyn wody,” and other medieval Polish mills described in Dembińska,
Przetwórstwo zbożowe, 90–135.
21
Fossier, La terre et les hommes en Picardie, 366–368, 380–389, and 395–397. Compare
findings by Walter and Merrits, “Natural streams and the legacy of water-powered
mills,” of extensive siltation behind preindustrial mill dams in eastern North America.
22
Pertz, ed., “Vita Iohannis,” MGH, SS, 4: 362, “cum molendinis fluminibus causa piscium
obcludendis”; Beyer, Cistercienser-Stift und Kloster Alt-Zelle, charter nos. 216, 510, and 518.
23
Perez-Embid Wamba, El Cister en Castilla y Leon, 137–138 and 178–179; Mousnier,
L’Abbaye de Grandselve, 189–190; Sicard, Moulins, 118–128; Derveeghe, Domaine du Val
Saint-Lambert, 63–66; Luttrell Psalter, fol. 181r.
24
Stolz, Geschichtskunde der Gewässer, 346.
25
Hoffmann, “Salmo salar in late medieval Scotland,” 362–363, and sources there cited.
The so-called Assizes of King William, art. 10, described the requisite opening as “so
large that a well-fed three-year-old pig could turn about without touching its snout or its
tail” (in tantum quo unus porcus trium annorum bene pastus est longus, ita quod neque grunnus
porci appropinquet sepi nec cauda . English counterparts occur in Wright, Sources, 91, and
Winchester, Landscape and Society, 111.
26
Fleta, III, 110–114. Those mills and mill leets on the Garonne at Toulouse also damaged
the fishing (Mousnier, La Gascogne Toulousan, 115). On the other hand, as in the early
modern Elbe, flood events could break downstream barriers and allow the return of
salmon to upriver fisheries where they had long been rare or absent (Wolter, “Historic
catches”).
27
Lenders et al., “Historical rise of waterpower”; Boddeke, Vissen, 169–176.
28
See discussion in Jungwirth et al., “Re-establishing and assessing ecological integrity”
and the comparative survey of French river systems in Merg et al., “Modeling
diadromous fish loss.”
29
Schalk, “Structure,” 222–224. For extended discussion of anadromous issues see
Supplement 5.1.1.
30
Grewe, “Wasserversorgung,” 75, cites nineteenth-century calculations of an annual
preindustrial per capita output of 34 kg of feces and 428 kg of urine, totaling 462 kg of
nitrogen-rich excrement. The daily adult output estimated by Leguay, L’eau dans la ville,
123, totals 47.5 kg of human fecal matter and 360–550 kg of urine per year.
31
“Descriptio … Claraevallensis.” Monastic effluents are left untreated in Lillich’s classic
“Cleanliness with godliness” and by Magnusson, Water Technology, 98–101, but get
more attention from Kosch, “Wasserbaueinrichtungen in hochmittelalterlichen
Konventenanlagen,” notably pp. 96, 110–112, and 134–135, and Benoît and Wabont,
“Wasserversorgung in Frankreich,” especially pp. 195, 204, and 207–216, which include
orders besides Cistercians.
32
Grewe, “Wasserversorgung,” 74–75; Benoît and Rouillard, “Medieval hydraulics in
France,” 180–187.
33
Grewe, “Wasserversorgung,” 75–80; Dirlmeier, “Die kommunalpolitischen
Zuständigkeiten und Leistungen”; Frieser, “Abwasserkanäle und heimlichen
Gemächer Nürnbergs”; Lachmann, “Die Gewässer und ihre Nutzung,” 311–315; La
Casva, Ingiene e Sanità di Milano, 64–66; Guillerme, Age of Water, 105–107; Leguay,
L’eau, 247–275; Leguay, Pollution, 16–32. Crouzet Pavan, “Les eaux noires,” details the
doubted the wisdom of eating fish from waters polluted with urban
effluent.34 But Robert Guillerme has argued that organic acid- and
alkaline-based processes used by early medieval textile and leather crafts
caused “the precipitation of solid organic materials in water which river
currents carried beyond city limits.”35
And what was downstream? One introductory fish tale has already told
of Constance’s pollution of its lakeshore with urban wastes. Along what
was London’s little river Fleet, sediments from a human generation or
two of the mid fourteenth century show loss of molluscs requiring clean
water and appearance of diatoms typical in dirty water.36 Excavations in
the bed of the Pegnitz below medieval Nürnberg recovered late medieval
butchery waste and household refuse, findings which corroborate the
stream’s foul repute when each summer’s low water left it long
unflushed. By the early 1400s Parisian effluent was likewise making the
Seine below town “infectée et corrumpue” every summer.37 All are
symptoms of aquatic ecosystems under stress.
Nor, despite Guillerme’s optimism, did medieval industry merely add
nutrients. More immediate toxic effects came from crafts such as slaugh-
tering livestock, tanning, or extracting fibers from flax and hemp by wet
decomposition (‘retting’). When the latter activity killed fish near Douai
in 1452, holders of fishing rights sued a clothier for damages.38 Brewers,
fishers, and ordinary consumers at Colchester in 1425 complained that
the tanners and tawers caused the “impayring and corrupcion” of the
river Coln and “destruction of the ffysche therynne.”39
problems Venetian authorities faced in expelling human waste from urban waters into
the lagoon.
34
Nada Patrone, Il cibo, 339–340. Species and stable isotopes found in fish remains from
sites near Basel suggest increased nutrient loads and contamination in the fourteenth-
century Rhine (Häberle et al., “Carbon and nitrogen isotopic ratios”).
35
Guillerme, Age of Water, 97–100.
36
Schofield and Vince, Medieval Towns, 213. Regier, “Rehabilitation,” 88, specifies the
latter botanical phenomenon as characteristic of an aquatic ecosystem under stress.
Where current speed and substrate prevent establishment of rooted aquatic vegetation,
larger nitrate loads encourage suspended algae to grow and increase turbidity. Jørgensen,
“Local government responses,” highlights authorities’ efforts to mitigate contamination
in rivers.
37
Frieser, “Abwasserkanäle,” 194–195. The Seine was so pungently described in a royal
ordinance against waste disposal from 1415 (Isambert et al., eds., Recueil général des
anciennes lois, vol. 8, p. 565, cap. 683).
38
“Et ont esté si puantes et infectés que les puissons qui estoient es yauwes de mesdis seigneurs sont
aulcuns et en grant nombre mors et les autres espars au loings en estranges yauwes,” Leguay,
L’eau, 292, citing Plouchard, “La Scarpe et les gens de rivière,” 850–851. Amacher,
Zürcher Fischerei, 96, reports a similar fish kill in 1466.
39
Gimpel, Medieval Machine, 86, quotes from Page and Round, eds., Victoria History of
Essex, vol. 2, p. 459, and further mentions thirteenth-century archival regulations against
letting any tanning waste flow into Marseilles harbor. More fish kills occur in Guillerme,
Age of Water, 152; and Heine, “Umweltbesogenes Recht,” 123. Sawmill waste harming
fish was an object of 1504 legislation in Tyrol (Stolz, Geschichtskunde der Gewässer,
381–383).
40
Passmore and Macklin, “Geoarchaeology of the Tyne”; Hudson-Edwards et al.,
“Mediaeval lead pollution”; Macklin et al., “Pollution from historic metal mining.”
41
Goldenberg, “Frühe Umweltbelastungen”; Diecke, “Findings.” Mining and smelting
waste in the Valle d’Aosta are in Di Gangi, L’attivita mineraria, 81–92, and Tumiati,
“Ancient mines of Servette.” Claustres, “Mining legacy in French Pyrenees,” reported
lakes with lead concentrations in medieval layers greater than those of the
nineteenth century.
42
Jaworowski et al., “Heavy metals in human and animal bones”; Rasmussen et al.,
“Comparison of mercury and lead levels”; Agricola, De Re Metallica, 5 (tr. Hoover,
p. 8).
43
Guillerme, Age of Water, 47–50 and 118–131.
44
Lambert et al., Making of the Broads; Borger, “Draining–digging–dredging,” 153–157;
Dam, “Sinking peat bogs,” and Dam, Vissen in veenmeren, 58–81.
45
Reynolds, Stronger, 69–97; Benoît and Rouillard, “Medieval hydraulics in France,”
208–214.
46
A general comparative point made in Regier, “Rehabilitation,” 88–89.
47
Lelek, “Rhine River”; Cioc, The Rhine, 21–75 and 145–171. Or are modern historians as
well as biologists susceptible to a form of shifting baseline syndrome?
48
Materné, “Beroeps- en vrijetijdsvisserij,” 142–144. Subsequently Van Neer and
Ervynck, “New data on fish remains,” 225, argued that the relatively greater reliance
on marine fish in the diets of late medieval Belgian towns as compared to rural castles
and monasteries marks the reduction of fish populations near those urban
concentrations
49
Cum omnia et singula flumina necnon et riparie magne et parve regni nostri per maliciam
piscatorum seu excogitata ingenia sint hodie absque fructu, ac per eos impediantur pisces crescere
usque ad statum debitum, nec sint alicujus valloris quando ab eis capiuntur, nec etiam prosint
humano usui ad vescendum, immo pocius obsint, et inde accidit quod sint multo plus solito
cariores, quod cedit in dampnum non modicum tam divitum quam pauperum regni nostri …
Duplés-Agier, “Ordonnances inédites,” 49. Jeulin, “L’élaboration par la monarchie,”
observes how these themes became a commonplace of French legislation. Further
discussion in Rouillard, “La législation royale.”
50
Freudlsperger, “Kurze Fischereigeschichte,” 100.
Diagnosing overfishing from evidence of fishing and fish shortages does betray aspects
of circular reasoning, but the assertion in Jäger, Einführung, 192, of no evidence for
decline in numbers of aquatic organisms before the 1500s rests on the unrealistic
assumption that only governmental records of catches constitute “scientific” and hence
credible data.
51
Wright, Sources, 91, cites an unpublished Plea and Memoranda roll of 1386; Given-
Wilson et al., eds., PROME, Henry V, 1416 March 16, membrane V, 33, X (Rotuli
Parliamentorum II temp. Hen. V, vol. 4, 79).
52
Rombai, “Le acque interne … Maremma,” 38–42; Echevarria Alonso, La actividad
comercial, 40–48 and 92. Supplement 5.1.2 offers more governmental worries
about overfishing.
53
Susłowska and Urbanowicz, “Szczątki kostne ryb,” 53–65. Early medieval remains of fish
distinctly larger than later norms for the same species are also remarked by Kozikowska,
“Ryby w pokarmie średniowiecznych (X–XIV w.) mieszkańców Wrocławia,” 3–14; Paul,
“Knochenfunde,” 59–60; and Driesch, “Fischreste aus Hitzacker,” 420–421.
54
Clavel, L’Animal, 146–149: European flounder and plaice are not easily distinguished
archaeologically, for they share many skeletal elements and the same benthic habitat. At
Abbeville especially the largest specimens (over 45 cm) had vanished by 1300, became
fairly common again around 1400, and were disappearing by 1500. The average size of
plaice landed by Dutch coastal fishers also began to fall from the fifteenth century (Dam,
“Feestvissen en vastenvissen,” 491–492).
100%
90%
80%
percentage of fish remains
70%
60%
50%
40%
30%
20%
10%
0%
10th 11th 12th 13th 14th18th
banquets, even well away from the sea.55 As salmonid remains preserve
poorly in archaeological contexts56 it is worth observing the presence of
salmon bones in excavations from Anglo-Saxon Wraysbury in Berkshire,
the local Slavic prince’s dwelling at high medieval Hitzacker on the Elbe,
twelfth-century castles along the lower Rhine, the neighbourhood of the
late medieval Louvre palace, and a contemporary house of canons at
Saarbrucken.57
55
Association of salmon with “the very proud and rich” in the Cluny customal was
remarked in Chapter 2 above (Bruce, Silence and Sign Language, 177). Some other
systems used the same sign for sturgeon. See further, for example: Anthimus De
observatione ciborum, ed. Lichtenhan, pp. 18–20, or tr. Grant, §41 (pp. 66–67); Jacques
de Vitry, Exempla, ed. Greven, p. 26; Dyer, “Household accounts,” 116; Serjeantson
and Woolgar, “Fish consumption,” 104 and 124; Serrano Larráyoz, La mesa del rey,
200–203; Piekosiński and Szujski, Najstarsze księgi, 271–286 passim; Santucci,
“Nourritures et symbols.”
56
Heinrich and Heidermanns, “Lachs.”
57
Coy, “Fish bones,” 118; Driesch, “Fischreste,” 401; Reichstein, Untersuchungen an
Tierknochen von der Isenburg; Desse and Desse-Berset, “Pêches locales, côtières ou
lointaines”; Huster-Plogmann, “Fische.”
58
Lampen, Fischerei und Fischhandel, 208.
59
Page, ed., Three Early Assize Rolls, 103; London TNA, Plea Rolls: KB 27/509 11R2,
m1d; Wright, Sources, 91; Williams, Welsh Cistercians, 75–76; Kowaleski, “Seasonality,”
132–133. The second statute of Westminster (1285) ordered protection of smolts. Mid-
fourteenth-century financial accounts kept for the Counts of Namur indicate the collapse
of a functional salmon fishery in middle reaches of the Meuse (Balon, “La pêche,”
28–31).
60
Halard, “Peche du saumon,” 175–177. On the best-known river, catches in 1423 were
less than a third those of the early 1300s, though the price per fish rose by a factor of
twelve. Less grain-centred agrarian regimes and rivers unsuited to be spanned by mill
dams help explain strong survival of Irish and Scottish salmon stocks (Hoffmann, “Salmo
salar in late medieval Scotland,” 64–65).
61
Volk, Wirtschaft und Gesellschaft, 350–367. Lenders et al., “Historical rise of
waterpower,” would generalize this medieval decline across the entire lower
Rhine catchment.
62
As seen in Laurière et al., Ordonnances des roys, vol. 2 (1729), 578–582; Puñal-
Fernandez, Mercado en Madrid, 169–175; Martens, Mittelalterlichen Gartensiedlungen,
154–156; Benecke, “Beiträge,” 308–309 and 314–315; Sarnowsky, Wirtschaftsführung
des Deutschen Ordens, 130–131; Martens, De zalmvissers van de Biesbosch, 41–54,
114–135, and 211–219.
5.2 Beneficiaries?
A schedule of tolls taken around 1275 by seigneurs of Audenarde
(Oudenaarde) at their bridge over the Scheldt en route to Ghent speci-
fied only four fish taxa: salmon and sturgeon paid per specimen, two and
four denier respectively; eel and herring turned over a hundred fish per
los (“Last”), a measure of quantity, probably 12,000, so weighing about a
metric ton.64 Different fiscal assessments reflect some of the previous two
or three centuries of change in the status of fish stocks and consumption
demand, contrasting the traditional elite favourites from threatened
anadromous species with smaller more numerous varieties, possibly
more resilient, for a broader range of consumers. Variant critical adapta-
tions and regional ecologies across western Christendom help explain
especially large increases since around 1000 CE in consumption of eel
and herring, and also the territorial spread of common carp, three fishes
and fisheries then on trajectories opposite to those of salmon and stur-
geon. In subtle ways all had gained from socio-economic developments
typical of high medieval Europe.
5.2.1 Eel
Eel are as migratory as salmon but travel in reverse directions
(catadromy). Unlike the sensitive eggs and young of salmon, subadult
eels enjoy broad ecological tolerances and omnivorous habits during
their long maturation in estuaries and waters far inland. With well-
chosen techniques people could catch eels throughout their freshwater
phase and when the sexually mature adults migrated downstream to
spawn at sea. Despite cultural antipathies to its snake-like morphology
63
Desse and Desse-Berset, “Pêches locales, côtières ou lointaines,” 125–126; Sternberg,
“L’approvisionnement de Paris en poisson”; Ervynck and Van Neer, “De
voodselvoorziening,” 425–426.
64
Verriest, ed., Le polyptyque illustré, fol. 12r. Unless specific sources indicate otherwise, the
last as a quantity (rather than a volume) counted ten “long thousands” of 1,200
items each.
65
See views transmitted by Anthimus, De Observatione Ciborum (Lichetenhan, ed, p. 19:
Grant tr., p. 65); Hildegard of Bingen, Physica, lib. 5, §33 (Hildebrandt and Gloning,
eds., vol. 1, pp. 283–284); Albertus, De Animalibus, lib. 24, §3; and legends of a saintly
bishop expelling eels from Lake Lausanne (Chène, “Une sainteté exemplaire”).
66
Harland et al., “Fishing and fish trade,” 174–186, and Reynolds, “Social complexities,”
215–218. Dietary primacy at St. Augustine’s abbey, Canterbury, shifted from eel to
herring at about the same time as York (Nicholson, “Fish remains”). While eel remains
at Lyminge outnumbered those of herring by ten to one, in the contemporary coastal site
of Bishopstone on the east Sussex coast, eel provided only 20% of remains and herring
26%. Orton et al., “Catch per unit research effort,” 15 and fig. 9, find a high medieval
rise of eel consumption in London.
67
Hardy et al., Ælfric’s Abbey, 356–359 and 395–396. Also at Wraysbury on the Thames,
eel comprised 82% of fish remains from the late ninth century through early twelfth
(Coy, “Fish bones”). Holmes, Animals, 51–53, table 3.3, found eel at the largest share of
Late Saxon and Saxo-Norman sites with fish remains.
68
Clavel, L’animal, 101–102; IJzereef and Laarman, “Animal remains from Deventer,”
435–436.
69
Clavel and Cloquier, “Pratiques halieutiques fluviales,” 207–208; Cloquier, “Pêches et
pêcheries”; Ervynck and van Neer, “De voodselvoorziening,” table 2 and p. 430
(although in the latter case remains of indeterminate cyprinids and flatfishes were both
still more numerous).
70
Audoin-Rouzeau, Ossements animaux, 147. For more French eel consumption see
Supplement 5.2.1.
71
Dam, Vissen in veenmeren, 103–121, and “Eel fishing in Holland”; Van Neer and
Ervynck, “Apport de la archéologie.”
72
Makowiecki, Historia, 145. Dembińska, Konsumpcja żywnościowa, 52, observes rising
verbal references to eel from twelfth–fourteenth-century northern Poland (Pomerania),
but the archaeological record is sparse.
73
Stouff, Ravitaillement, 201–203; Amargier, “La pêche en Petite Camargue,” 331–336;
Weiss, Versorgung des päpstlichen Hofes, 394–397; Berman, “Reeling in the eels.”
74
Compare, for instance, Grove and Rackham, Nature of Mediterranean Europe, 290–311;
Bresc, “La pêche … dans la Sicile,” 167–169, Un monde méditerranéen, 261; and “La
pêche dans l’espace normand,” 280–282; Vendittelli, “La pesca nelle acque interne,”
116–123, and “Diritti ed impianti,” 409–422; Lanconelli, “Gli Statuta pescivendulorum
urbis,” 94–102; Vincenti, “La tutela ambientale”; Rombai, “Le acque interne in
Toscana,” 30–42; Spicciani, “Il Padule di Fucecchio,” 64; Balletto, Genova nel
duecento, 189–192; Onori, L’abbazia di San Salvatore, 55–56; and Martin, “Citta’ e
campagna,” 333–334.
75
Lanconelli, “I lavori alla peschiera”; Biganti, “La pesca nel lago Trasimeno,” 795–797.
76
Clark et al., “Food refuse … Tarquinia,” 240–242.
77
For more context on herring history and historiography see Supplement 5.2.2.
78
For relevant biology see Fish Base, sub Clupea harengus; Hodgson, The Herring, 15–24;
Klinkhardt, Der Hering; Bailey and Steele, “North Sea herring”; Krovnin and Rodionov,
“Atlanto-Scandian herring,” with a useful summary from a historical Anglocentric
perspective in Locker, Role of Stored Fish, 31–44.
night. Writing about 1200, Danish chronicler Saxo bragged that the fish
along the Scanian coast were so abundant that they blocked shipping and
could be caught by hand.79 But these oily creatures spoil in a day unless
promptly dusted with salt, smoked, or packed in simple salt brine. Such
light cures make herring – ‘powdered,’ ‘red,’ or ‘pickled’ – an inexpensive
portable food, palatable enough for several months, especially during the
cold season after the autumn spawning. By the mid-twelfth century
coastal artisans from Picardy to Pomerania were tapping the silvery
billions to feed themselves, their neighbours, and nearby inland popula-
tions, especially in fast-growing towns.
The booming twelfth-century herring industry had emerged from a
historically obscure century and more of parallel development by fishers
with access to local consumers and local fish. Early medieval coast-
dwellers from Sussex to Sweden ate herring they, their neighbours, or
79
Saxo, Gesta danorum, preface 2:4 (Olrik and Ræder, ed., vol. 1, p. 6):
Ab huius ortivo latere occasivum Scaniae media pelagi dissicit interruptio, opimam praedae
magnitudinem quotannis piscantium retibus adigere soliti. Tanta siquidem sinus omnis piscium
frequentia repleri consuevit, ut interdum impacta navigia vix remigii conamen eripiat nec iam
praeda artis instrumento, sed simplici manus officio capiatur.
Also tr. Fisher, History of the Danes, vol. 1, p. 7. Albert, De animalibus, 24:2, observed
the abundance of these tasty little fish in waters off France, Britain, Germany, and
Denmark (“allec piscis est maximae multitudinis in Occeano quod partes Galliae et Angliae
et Teutoniae et Daciae attingit”).
80
Kowaleski, “Early documentary evidence,” 23–24; Loveluck, Northwest Europe, 198–200
and 211; Reynolds, “Social complexities”; Enghoff, “Herring and cod,” 137; Barré,
“Droit maritime médiéval,” 524–525; Makowiecki et al., “Cod and herring,” 118–119;
and in many of the references to follow.
81
But not meaningfully earlier. For credible indicators of the absence of herring-eating
inland, see Supplement 5.2.2.
82
Van Neer and Ervynck, “Rise of sea-fish consumption,” 159–164; Enghoff, “Baltic
region,” 48, 56–58, et passim; Enghoff, “Denmark,” 177 and 142–143; Lepiksaar and
Heinrich, Fischresten aus Haithabu, 119; Heinrich, “Temporal changes,”151–156. As
Locker (Role of Stored Fish, 114–168) argues, when archaeologists have carefully sieved,
individual herring are so small that their share of fish flesh consumed was much less than
their proportion of all bones recovered.
83
Barrett et al., “Dark Age economics” and Barrett et al., “Origins of intensive marine
fishing,” more fully shown in Orton et al., “Fish for the city,” 517, and Harland et al.,
“Medieval York,” 175–193. For herring at least this was a more widespread, if plainly
incremental, phenomenon.
84
Leciejewicz, “Z denara” and “Zum frühmittelalterlichen Heringshandel”; Rulewicz,
Rybołówstwo Gdańska, 68–88 and 342–347; Makowiecki, “About the history of
fishing,” 120; Makowiecki, “Catalogue”; Makowiecki et al., “Cod and herring,”
118–123; Chełkowski and Filipiak, “Cognitive potential,” 45; Kozikowska, “Ryby”;
88
Lovelock, Northwest Europe, 207; Hardy et al., Aelfric’s Abbey, 379–381. Fishing for
nearshore migratory herring schools in the Firth of Forth is documented in the twelfth
century, supported by salteries in the immediate area (Oram, “Estuarine environments,”
366–367).
89
Harland et al., “Fishing and fish trade,” 189–190, makes clear that the herring consumed
at eleventh–early fourteenth-century York had not been processed for packaging in
barrels, so had to be consumed fresh or shipped dry-salted. Those reaching Bourges
about 1100 by way of boats on the Loire paid toll by count (Querrien, “Pêche et
consummation,” 428–429) and so did the herring entering Flanders as late as 1252
(Lampen, Fischerei und Fischhandel, 186, citing Hansische Urkundenbuch, vol. 1, no. 432).
90
Alanus, De planctu, Prose 1, tr. Sheridan, 94–98.
91
Clavel, L’Animal, 154–160; Jarecki, Signa Loquendi, 122–124 (Ulrich of Cluny) and
252–253 (Fleury); Bernard and Bruel, eds., Recueil des chartes, #4132, p. 481;
Sternberg, “Une spécificité de la cuisine monastique,” 93–94, points out absence of all
marine fish from abundant sieved kitchen remains at eleventh–thirteenth-century
Tournus on the Saône and at La Charité-sur-Loire.
but tepid confirmation from rare finds in slightly later urban latrines at
Basel.92 In Bavaria no herring bones are reported in a survey of fish
remains from six castles and four urban contexts predating 120093 nor
do they leave any trace in either the Iberian or Italian peninsulas. Further
east in the Baltic than Viking-Age Birka in Sweden, herring likewise
occur only after 1200.94
Expanding eel fisheries at (western) European scale met growing
medieval demand for fish by exploiting a species whose habitat itself
was then growing in unintended consequence of human activities.
Herring, however, epitomize intensified human use in northwestern
coastal areas of an existing fish stock under conditions where larger
cultural and demographic demand pressures confronted limited and
probably dwindling supply from hitherto preferred varieties taken in fresh
water. In a third emerging case during the same tenth through thirteenth
centuries, the westward spread and human use of common carp repli-
cated some features of the two previous, but reached across the extensive
upper Danube basin into neighbouring waters then little affected by
intensified consumption of eel or herring.
92
Ekkehard of St. Gallen, Benedictiones (ed. Egli, 285–289); Heinricus Laureshamensis,
Summarium Heinrici, lib III, c. xvi (pp. 156–160); Jarecki, ed., Signa loquendi, 165–168
(William of Hirsau); Hildegard, Physica, lib. 5, cap. 22 (Hildebrandt and Gloning, eds.,
vol. 1, pp. 278–279; tr. Throop, p. 71); Hüster-Plogmann, “… der Mensch lebt nicht
von Brot allein,” 193–197; Deschler-Erb et al., “Tierknochen aus St. Arnoul,” 529–532.
93
Pasda, Tierknochen als Spiegel, 106–110. Remains of other small-boned fishes
were recovered.
94
Lõugas, “Fishing and fish trade,” 111–112.
95
A systematic survey and interpretation of the material and verbal evidence summarized
in Map 5.1 is Hoffmann, “Remains and verbal evidence,” later slightly revised and
augmented in Hoffmann, “Environmental change and the culture of common carp.”
Subsequently Enghoff, “Fishing in the Baltic Region” and Enghoff, “Fishing in the
southern North Sea,” confirm these findings, both generally and in the discussion
pp. 100–107, as does Makowiecki, “Catalogue.” I remain unconvinced by single
isolated finds of alleged early carp bones found at waterside sites many hundreds of
years and kilometers away from other contemporary evidence and in regions where the
fish is a well-known later introduction – as, for example, Dobney et al., Of Butchers and
Breeds, with a single purportedly third-century carp bone from Lincoln. More
confidence-inspiring recent evidence is mentioned below.
96
Balon, “The common carp,” 1–55. Indeed in this same region, the last remnant
population of wild, not feral, common carp, survived into the 1960s, when they were
so identified by the late biologist Eugene Balon. For the hydrological barrier see Balon
and Holčik, “Gabčíkovo river barrage system,” 2–4. As opposed to carp consumption in
the Roman Balkans, Balon’s assertions of Roman domestication of carp, as reiterated in
his Domestication; “Origin and domestication,” 21–32, and “About the oldest
domesticates,” 6–10, and set in the inland delta area or elsewhere, are in continued
absence of supportive material or written evidence to be construed as wishful thinking.
Carp remains at Roman and early medieval Austrian sites show a size distribution typical
of wild populations; only from the fifteenth century do carp of uniform size indicate a
farmed population (Galik et al., “Fish remains,” 349–350). For much of what follows,
Leonhardt, Der Karpfen, 12–15 and 49–54, embedded seminal ideas in much
historical error.
97
Cassiodorus, Variarum libri dvodecim, 12:4 (Fridh, ed., p. 467). Other fishes there meant
to impress visitors were to come from the Rhine, Sicily, and southernmost Italy. Carpa is
reputedly one of only two Gothic words Cassiodorus ever wrote (O’Donnell,
Cassiodorus, 94).
98
De Grossi Mazzarin, “I resti archeozoologici,” 56–57; Gabriel, “Fish assemblages,”
126–128.
99
Ruodlieb, Fragment X, ll. 36–48 (Haug and Vollmann eds., 2:1, pp. 136–137; Vollmann,
ed. and tr., pp. 494–495; Ford tr., p. 74). This identification is undisputed, as are most of
the other distinctively middle European/Danubian fishes in the list, but some of the
English names used in Ford, tr., p. 74, are entirely implausible.
basin, or did he recall eating this fish during his youth at Regensburg on
the Danube? Might William signify carp’s movement across water-
sheds?100 If so, this is corroborated by recent finds of carp remains from
tenth-/early eleventh-century layers at Sulzbach castle, seat of the Count
of Nordgau, in a zone of interlaced Danube and Rhine tributaries and
then, barely a decade after William’s death, by a bilingual lexicographer
at Lorsch abbey in the northern Black Forest who glossed a fish called in
Latin carabus with the German charpho.101 Carp remains of late eleventh-
and early twelfth-century date at Nürnberg castle and a house of canons
at Saarbrücken further fit this scenario.102
Five centuries from Bratislava to the Rhine; less than two from there to
Paris? Mention by Hildegard of Bingen in her Physica (c. 1160) confirms
the establishment of carp (carpo) in the middle Rhine. The abbess likely
learned from abbey fishers how the species fed on bottom organisms and
vegetation in swampy and clear water and something of its spawning
habits, while herself assessing its value as food and, suitably prepared, a
cure for fever.103 No remains or verbal mentions from before 1200 sug-
gest carp culture or artificial fishponds. These were wild fish.
Further west the written and archaeozoological records seem to lag,104
and then suddenly blossom in the mid-thirteenth century. Does this
100
Jarecki, Signa loquendi, 165–168. For William’s Bavarian background and subsequent
experience at Cluny, whence his model for the sign language, see Jakobs, Die Hirsauer,
8–30.
101
Pasda, “Tierhaltung als Spiegel,” 106–109, and “Tierknochen auf Sulzbach,” 254;
Heinricus, Summarium Heinrici, lib. III: cap. xvi (ed. Hildebrandt, 159–160). Latin
carabus was used by Pliny (Historia naturalis IX:LI) for a kind of crab, but in present-day
scientific nomenclature refers to a family of beetles.
102
Boessneck and von den Driesch-Karpf, “Tierknochenfunde Nürnberg,” 70–72;
Huster-Plogmann, “Fische,” 529–532, and Deschler-Erb et al., “Tierknochen aus St.
Arnoul,” 529–532, and personal correspondence with Heide Huster-Plogmann,
15 April 2014. Outer limits to carp’s range before the twelfth century are well
established. See Supplement 5.2.3.
103
Hildegard, Physica, lib. 5, cap. 5, cap. 11 (Hildebrandt and Gloning, eds., vol. 1,
pp. 273–274; Throop, tr., p. 168). More recent finds by Dutch and Swiss experts in
ichthyoarchaeology have better confirmed the presence of carp in the Rhine around
Hildegard’s time: twelfth- and early thirteenth–century remains from Utrecht are
independently attested in Buitenhuis and Brinkhuizen, “Faunaresten,” and
Beerenhout, “Het Huis te Vleuten,” while van Dijk and Beerenhout, “Het
botmateriaal,” 40–41, encountered carp bone at thirteenth-century Hoorn, on what
was then a still freshwater Zuider Zee. Closer to the top of the watershed the carp
remains from latrines in Schaffhausen suggested in Hüster-Plogmann and Rehazek,
“Historical record versus archaeological data,” to come from the twelfth century have
now been redated by the same scholars to the later Middle Ages (see Hoffmann “Der
Karpfen”).
104
Carp are conspicuously absent from late twelfth- and early thirteenth-century works by
writers associated with Parisian schools and evidently interested in fishes: Gui of
Bazoches, Epistolae 23 (Adolfsson, ed., pp. 89–99); Alexander Neckham, De naturis
108
Clavel, L’Animal, 133; Ervynck and Van Damme, “Archeozoölogisch onderzoek”; Van
Neer and Ervynck, Archeologie en Vis. Benoît, “La carpe,” provides an overview of
French records.
109
Boretius and Krause, eds., Capitularia Regum Francorum, #32, c. 21 and 65 (pp. 85 and
89). Exemplary such vivaria in lay and religious possession appear in the Carolingian
Brevium exempla (ibid., #128, pp. 250–256) and a mid-ninth-century survey of imperial
properties in what is now easternmost Switzerland and western Austria (Häberle and
Marti-Grädel, “Teichwirtschaft,” 150–151). Earlier structures were built at St. Denis
(“Chronique” 1987, 179–181) and documented in Burgundy (Bouchard, Flavigny, #3).
110
Galik, Private correspondence, “Fischresten aus … Lanzenkirchen”; Pertz, ed., “Vita
Iohannis,” 362; Pichot and Marguerie, “Sur l’aménagement,” 119–124. Elsewhere
across the territory where carp moved westwards see mills and ponds on estates in
lower Bavaria as described in eleventh–twelfth-century charters (Krausen, ed.,
Urkunden … Raitenhaslach, nos. 1, 2, 3, and 29), in Franconia (Cnopf, Entwicklung
der Teichwirtschaft, 10–12, and Mück, “Beginn der Teichwirtschaft”), and in Burgundy
(Bouchard, St-Marcel-lès-Chalon, #12).
111
Generally for French ponds see Benoit and Wabont, “Mittelalterliche
Wasserversorgung,” 189–196; Gislain, “Le role des étangs,” 89; and Benoît and
Rouillard, “Medieval hydraulics,” 177–180. Local cases appear in Delatouche, “Le
poisson d’eau douce,” 174–175; Sanfaçon, Défrichements, 26 and 85–90; Blary, Le
domaine de Châalis, 31–40; Richard, “Le commerce du poisson,” 181–197; and
Grand and Delatouche, L’Agriculture, 544. See also Holt, “Medieval England’s water-
related technologies,” 65–66 and 83–88, and Aston, ed., Medieval Fish, passim.
112
Longnon, Documents, 3:1–7; Roberts, “Bishop of Winchester’s fishponds,” 130–135.
Belliard et al., “Increasing establishment of non-native fish species,” rightly consider
carp the first known invasive fish species in France.
Table 5.1 Predominant fish taxa in large bone assemblages from selected high medieval sites
dated to number of Rank % Rank Rank Rank Rank Rank % Rank Rank Rank Rank All
identified Clupeids % % % % Eel Salmonids % Pike % % % other
fish remains Gadids Flat- Smelt Perch Cyprinids Carp taxa
fishes
blank cell indicates taxon not found ◌ taxon present * includes a few carp † includes a few cod
Sources: York Coppergate: Harland et al., “Fishing and fish trade,” table 15.4, pp. 182–183, namely the column labeled 1200–
late 1200s, with proportions calculated by R. Hoffmann. When all Gadidae (haddock, cod, and other species) are totaled, they
come to 24%, so still not half of the herring. Flatfishes and pike (the leading resident freshwater taxon) trail at 3% and 2%.
https://doi.org/10.1017/9781108955898.007 Published online by Cambridge University Press
Paris Louvre, Cour Carrée: Clavel, L’Animal, table IV, p. 13. The context was a trash-filled ditch beside the palace. While the
author calculated percentages on all bones, I have recalculated them based on identified remains, lumping the six carp bones with
the other cyprinids. In the remaining 11% of bones from Cour Carrée, no taxon or grouping exceeded 3%. No salmon or
sturgeon; gadids came to 2%, mostly whiting.
Charité-sur-Loire, monastic (Cluniac) priory kitchen and refectory: Audoin, Ossements animaux, 146–147, enumerates no
individual elements or taxa, though mentioning abundant bream among the cyprinids in early phases and barbel and ide in
the fourteenth century. Carp appear only from the fifteenth century and marine species are absent.
Mechelen/Malines, Het Steen: Troubleyn et al., “Consumption patterns … inside Het Steen,” tables 7–9, pp. 32–36. Context was
two very large cesspits in a structure then the municipal prison. Archaeologists agree that inmates at Het Steen represented a
cross-section of town society and ate mainly food supplied by their own households or purchased from outside.
Bremen Altmarkt: Galik and Küchelmann, “Fischreste,” 215–218, notably table 2, with proportions recalculated on base of the
identified bones. No carp are reported and only 1% each of eel and gadids. A smaller (104 identified bones) trash pit of similar
date nearby has a similar pattern, although the particulars had not yet been analyzed for ibid., 219.
Lekno monastic (Cistercian) kitchen: Makowiecki, Historia, Aneks 2, p. 188, item 203; Wywra and Makowiecki, “Fish in the
menu of Cistercians,” 65. Lekno is about 30 km south of Poznań. There are traces of sturgeon and catfish but few diadromous
species and no marine other than herring. Here listed are only the well-dated and sieved finds from the 2001 excavations, not
those earlier (item 202) at this site, which provide no additional taxa.
Five lowland Austrian sites, all located between Vienna and Linz: Galik et al., “Fish remains as a source,” table 1, pp. 344–345,
with composite calculations by R. Hoffmann. Sturgeon remains, mainly of beluga, came to 3%. Present were one bone each of
herring and a flatfish, with no sign of cods, mackerel, or any other marine organisms.
5 Aquatic Systems under Stress, c. 1000–1350 215
114
In Regier’s evocative terms (“Rehabilitation,” 93–96), sensitive ‘white fish’ were losing
habitat and yielding their prior importance in human catches and consumption to more
broadly tolerant guilds of ‘grey fish’ and ‘black fish’, whose favoured conditions were
less damaged and which, in certain regions and localities, were thus becoming more
common. Although in contrast to post-industrial impacts, preindustrial development
more affected lotic components of aquatic systems, the general ecological outcome was
closely similar as “through their greater flexibility [grey fish] come to dominate within
modified ecosystems.”
115
While early medieval Europeans likely consumed relatively more predatory freshwater
fishes (pike, pike-perch, trout) than did their heirs in 1200 or 1300, and eel, carp, and
small cyprinids are closer to the base of the freshwater food webs, evidence now
available shows no clear sign of a trophic cascade, where smaller, short-lived
organisms explode in numbers and biomass as a result of fishers selectively removing
large predators. Eel may have occupied and expanded a niche in part left available by
diminished sturgeon, whose possible earlier keystone role in large river and estuarine
ecosystems simply vanished. Was this a regime shift from one relatively stable ecosystem
to another? In contrast, the salmon actually participant in freshwater ecosystems are and
were not the adults, which do not feed in fresh water, but the young, which there
interact with other small salmonids and fishes of comparable size, habits, and habitats.
Unlike the Pacific salmons (Genus Oncorhyncus), Atlantic salmon adults do not in
temperate Europe transport in their dying bodies ocean-gathered nutrients essential
to life in infertile waters where their young must survive. European fresh waters are just
more nutrient-rich and diverse, even when the salmon are removed.
other inland areas neither eel nor herring could provide actual catches
nor then more than rare and occasional exotic food, so heavier use was
made of native cyprinids, perch, and some whitefishes, while some
people intervened more actively in the distribution and life cycle of carp.
Herring and to a lesser degree eel provided protein to a larger, less
wealthy, consumer base than had the traditional fisheries or the emerging
ones for carp or codfishes.
But for all the reasonable likelihood that forces and activities of medi-
eval Europeans both purposely and inadvertently drove significant alter-
ations to the subcontinents’s aquatic ecosystems and fish stocks, humans
were not the only probable post-millennial engines of change. The sparse
and lacunae-ridden record of the ninth through early fourteenth centur-
ies contains signs of naturally driven environmental fluctuations affecting
biodiversity and interactions among regional fish communities of interest
to human fishers and consumers.
1.5
1
Medieval Climate Anomaly
L I t t l e I c e A g e
0.5
0.5
1
1.5
2
850 900 950 1000 1050 1100 1150 1200 1250 1300 1350 1400 1450 1500 1550
Year
Area-weighted June-July-August mean temperature anomalies relative to Europe means, 1961-1990, as reconstructed from nine annually
resolved tree-ring width (TRW), tree-ring maximum latewood density (MXD) and documentary records in Luterbacher et al., “European
Summer Temperatures.” Data set and permission from J. Luterbacher. Graphed for R. Hoffmann by K. Hoffmann
averages are less relevant than the regional conditions wherein humans
and other organisms experience the impact of climatic anomalies.116
Energy flowing from the sun (solar irradiance) and terrestrial volcan-
ism principally drove the earth’s premodern climate, with regional fea-
tures a result of global oceanic and atmospheric circulation.117 The
MCA coincided with high solar activity, especially during 1080–1280,
and flow of energy to the earth. Only one solar minimum during
1040–1080 (the Oort) took place during the MCA, which came to an
end with the Wolf minimum, 1280–1350. The ensuing LIA, a period of
cooler global climates, coincided with three more minima in rapid suc-
cession.118 Volcanic eruptions introduce aerosols and dust into the
atmosphere. These reduce arrival of solar energy to the Earth’s surface
116
Quotation from Diaz et al., “Medieval warm period redux,” 32. Christiansen and
Ljungqvist. “Northern Hemisphere temperature,” 277, confirm a greater geographic
variability during the MCA than the LIA. See also Glaser and Riemann, “Thousand-
year record of temperature,” 446; Luterbacher et al., “European summer
temperatures.” Discovery of this variability led climatologists to replace the term
‘medieval warm period’ with MCA and calls into question scientific or scholarly
explanations which assume unbroken or year-round heat at this time.
117
Steinhilber and Beer, “Solar activity.”
118
The Spörer minimum dated to 1460–1550, Maunder to 1645–1715, and Dalton to
1790–1820. For reconstruction across the MCA and LIA see Luterbacher et al,
“European summer temperatures,” as here replicated in Figure 5.3.
119
Goosse et al., “Origin of the European ‘Medieval Warm Period’,” 105–110; Trouet
et al. “Persistent positive North Atlantic Oscillation”; Seager and Burgman, “Medieval
hydroclimate revisited,” 11–12; Ortega et al., “Model-tested North Atlantic Oscillation
reconstruction”; and Franke et al., “North Atlantic circulation.” Christiansen and
Ljungqvist, “Northern Hemisphere temperature,” 765, conclude “The two-millennia
long reconstruction shows a well defined Medieval Warm Period, with a peak warming
c. 950–1050 AD reaching 0.6 C relative to the reference period 1880–1960 AD.”
European averages were probably higher, but still below those of the late
twentieth century.
120
Ljungqvist et al., “Northern Hemisphere hydroclimate variability.”
121
Campbell and Ludlow, “Climate, disease and society,” figure 1 and appendix 5,
construct for western Europe an “Index of Environmental Instability” to help
contextualize late medieval crises.
122
Mensing et al., “2700 years of Mediterranean environmental change,” and Mensing
et al., “Human and climatically induced environmental change,” 54–57.
123
Seager and Burgman, “Medieval hydroclimate revisited,” 12; Ortolani and Pagliuca,
“Cyclical climatic–environmental changes”; Moreno et al., “Hydrological pattern.”
Written proxy sources (Camuffo and Bertolin, “Climate in the Mediterranean,”
figure 1, p. 127) indicate colder Italian winters set in about 1270 to 1360.
124
Vigne et al., “Sensibilité des microvertébrés.”
125
Glaser and Riemann, “Thousand-year record of temperature,” 444–447; Christiansen
and Ljungqvist, “Extra-tropical Northern Hemisphere temperature.”
126
Seager and Burgmann, “Medieval hydroclimate revisited”; Amann et al., “Warm
season precipitation”; Büntgen et al., “2500 years of European climatic variability”;
Büntgen and Tegel, “European tree-ring data and the Medieval Climate Anomaly”;
McCarroll et al., “A 1200-year multiproxy record of tree growth and summer
temperature.”
127
Vinther, “Medieval climate anomaly in Greenland”; Campbell, Great Transition, 45–47
and 200–201; Cunningham et al., “Reconstructions of surface ocean conditions,”
929 and appendix 1.
128
See for example Menant, Campagnes lombardes, 59 and 176; Fumagalli, Landscapes,
104–105; Pinto, “Incolti, fiumi, paludi,” 1–7; Bravard, “Des versants aux cours d’eau”;
Levy, “Tant va la cruche à l’eau”; Rossiaud, La Rhône, 93–155; Molkenthin, “Der
Rhein,” 49–53.
129
Lewin, “Medieval environmental impacts and feedbacks,” 277–278. Lewin (p. 297)
stresses that natural physical forces drove changes in channel morphology, while human
activity more resulted in floodplain wetness and sedimentation, although the scale and
form of the latter also depended on local soil types.
130
Molkenthin, “Der Rhein,” 50; Trusen, “Insula in flumine nata.”
131
Berger and Brochier, “Rapports de la géoarchéologie”; Calvet et al., “Les cours d’eau
des Pyrénées orientales,” 286–287. Flood records from other French rivers, the Arno,
Po, and those of Germany share this general chronology (Grove and Rackham, Nature
of Mediterranean Europe, 133–136; Leguay, L’eau dans la ville, 399–406; Fumagalli,
Landscapes, 88–89, 110–112, and 117–121; Camuffo and Enzi, “Two bi-millenary
series”; and Bork et al., Landschaftsentwicklung, 237–249). But a very long-term study
of sediments dated by 14C found riverine flooding in coastal Iberia, southern France,
and Italy most frequent during the sixth/seventh, tenth, and late fifteenth centuries,
while the thirteenth and sixteenth were drier (Benito et al., “Holocene flooding,”
21–23).
132
Bravard et al., “La diversité spatiale des enregistrements morphosédimentaires”;
Rossiaud, Le Rhône, 128–137.
133
Bartolus wrote in his 1355 Tractatus de fluminibus “Travelling towards a certain villa
situated near Perugia above the Tiber, I began to contemplate … the changes of the
137
Grupe et al., “A brackish water aquatic foodweb”; Becker and Grupe, “Archaeometry
meets archaeozoology.” Likewise at the northern tip of Jutland deposition of eroded
sand closed the Limfjord in the twelfth century, shifting its waters from a marine to a
freshwater or brackish habitat (Hybel and Poulsen, Danish Resources, 48–49).
138
Besides formation of the Zuiderzee, other well-known counter-examples to what
happened at the mouth of the Wisła occurred during the transition from the MCA to
the LIA. Large losses of human lives, arable, and villages along the North Frisian coast
from ‘de grote mandrenke’ (the great human drowning) of 17 January 1362, and similar
marine incursions recreated extensive areas of tidal flats and marshlands, productive
aquatic environments of the Wadden Sea (Meier, “From nature to culture,” 95–102,
attends to the losses). More cases are in Supplement 5.4.1.
139
James Galloway provides much local detail in his “Storm flooding”; “London and the
Thames estuary,” 130–135; “Storms, economic and environmental change,” 388–391;
and “Expansion or eclipse?”. Bailey, “Per impetum maris,” describes coastal inundations
elsewhere in eastern England but not their effect on local fisheries.
140
Clavel, “Restes osseux animaux,” 200–202; Clavel and Cloquier, “Sources
documentaires et archéologiques,” 207–208; Abel, “Defining a new coast”; Bourin-
Derruau et al., “Le littoral languedocien au Moyen Âge,” 349–357; Carozza et al.,
“Lower Mediterranean plain accelerated evolution.” Provensal et al, “Geomorphic
changes,” explores the evolving Rhône delta.
141
Adult carp, however, tolerate even very cold conditions. Kottelat and Freyhof,
Handbook, 147–148; www.fishbase.org/summary/Cyprinus-carpio.html (consulted 20
December 2016).
142
What follows summarizes Van Damme et al., “Introduction of the bitterling,” with
added biological information from fishbase.sub Rhodeus-amarus (consulted
20 December 2016) and Kottelat and Freyhof, Handbook, 82–84. Some authorities
consider European Rhodeus amarus synonymous with R. seriecus, which has a widely
separate Asian distribution. The little fish drew attention for the ‘farting’ sound it makes
when handled and for the long tubular ovipositor the female deploys to insert her eggs
into freshwater mussels, where the larvae live as parasites. Recent debates are over the
bitterling’s indigenous status in western Europe and thus its qualification for special
protection under EU water regulations.
143
Dirk Heinrich explored in several articles probable connections between climatic
conditions and the discontinuous range in northwestern European watersheds of
another thermophilic species, catfish: “Fischreste als Quellengattung,” 176–178;
“Bemerkungen zur nordwestlichen Verbreitung des Welses”; “Information … from
tales,” 19–20; and “Methodological considerations,” 163–165.
Medieval evolution of herring and cod fisheries inside the Baltic may
owe more to natural variability than to human enterprise or impacts. To
recapitulate and anticipate: herring were abundant in the central and
southwestern Baltic (Bornholm, Pomerania, the Schlei) from the fifth/
sixth centuries into the thirteenth and by the latter date also in the Danish
straits (of which much more in Chapter 8). Cod were certainly present in
the Baltic during the Neolithic and again from the fourteenth century,
while during early and high medieval times this species is virtually absent
from the written and archaeozoological record there.144 The traditional
explanation is that Slavic peoples had no taste for cod but immigrants
from Germany did. Stable isotope and other studies of the cod bones
themselves, however, identify the oldest medieval cod remains found at
Haithabu and in the eastern Baltic as imports from the North Sea or
Norway, that is, as imported stockfish. Yet by the end of the Middle Ages
people in this region did plainly fish locally for cod.
More recent suggestions observe that known low salinity and hypoxic
(low oxygen) conditions in deep water basins of the medieval Baltic could
have suppressed cod populations. In the Baltic today strong hypoxic
conditions thought to arise from a westerly flow of wind and waters from
the Atlantic, a warming climate, and eutrophication from nutrient-rich
runoff place a cap of warmed fresh water on top of colder saltier waters
where no mixing occurs. This situation drives many free-floating eggs of
cod into the deepest basins where lack of oxygen prevents larval develop-
ment and so threatens cod recruitment.145 Baltic herring, however, like
their North Sea kin, breed in relatively warm, biologically productive, and
often brackish surface layers. Sediment cores demonstrate that hypoxia in
the Baltic is not just a modern but rather a recurring phenomenon, present
144
Heinrich, “Fang und Konsum” and “Fishing and consumption of cod”; Makowiecki,
“Studies on the evolution,” 176–179, “Catalog,” table 2, and “Usefulness of
archaeozoological research,” 109–110; Lõugas, “Fishing during the Viking Age” and
“Fishing and fish trade,” 111–112 and 114–115; Holm, “Commercial sea fisheries,”
18–19. Absence of cod remains from the early Viking Age site of Truso and from pre-
1200 Gdańsk, as well as the Atlantic origin of cod bones at Haithabu suggest that even
the Norse found few of the species in the early medieval Baltic (Makowiecki, “Janów
Pomorski”; Rulewicz, Rybołówstwo Gdańska, 61; Lepiksaar and Heinrich, Fischresten aus
Haithabu, 119; Schmölcke and Heinrich, “Tierknochen aus dem Hafen,” 220–233).
145
The analysis here proposed applies to evident medieval fluctuations in Baltic hydrology
and fish ecologies the observed late twentieth-century environmental and regime shifts
there as set out in detail by Hammer et al., “Fish stock development under hydrographic
and hydrochemical aspects,” 557–564, and briefly by Alheit and Pörtner, “Sensitivity of
marine ecosystems to climate and regime shifts,” 168. These refer to work by Mackenzie
et al., “Quantifying environmental heterogeneity”;MacKenzie et al., “Ecological
hypotheses,” 177–190; Köster et al., “Baltic cod recruitment”; Zillen et al., “Past
occurrences of hypoxia in the Baltic”; van der Lingen et al., “Trophic dynamics,”
135 and 145; and Brander, “Impacts of climate change on fisheries,” 393.
both during the early Holocene (c. 9000–c. 5000 ybp) and roughly
between 550 CE and 1200 50 years. Thereafter bottom waters became
better oxygenated and remained so into the nineteenth century.146
Long-term changes in the state of the Baltic, termed a ‘regime shift’ by
recent ecologists, have been linked to climate variations. The earlier
medieval and the most recent condition of deep water hypoxia beneath
a warm surface layer of low salinity result from a positive NAO charac-
teristic of both the MCA and modern warming. Predominant westerlies
then push salt water in from the North Sea and raise precipitation levels
across the Baltic watersheds. Temperature and salinity differences
encourage stratification. Near-surface temperatures and biological prod-
uctivity are high. Fading of the MCA from around 1200 tended to bring
more negative NAO, with lower salinity but also lower temperatures and
nutrient levels. More balanced salinity and temperature allowed greater
mixing, so conveying more oxygen to the deep basins. Distinctive onset
of the LIA by around 1500 strengthened a negative NAO, produced drier
and colder conditions in central European lands, and prolonged the no
longer new marine trophic regime for another three centuries.
In the present-day Baltic abundant cod are the principal predator on
herring, which controls the herring population. Under modern conditions
of intensive fisheries, removal of predators results in superabundant prey
populations, a typical form of trophic cascade. With few cod present, early
medieval herring stocks could explode until limited by some other eco-
logical factor.147 Very recent ecological field work and theories even
suggest that, as herring will themselves predate on planktonic cod eggs
and larvae, the large medieval schools could (further?) have suppressed a
Baltic cod stock already under stress from low oxygen in the habitats
critical for its reproductive life stage. Both the abundance of adult cod
and cod recruitment show negative correlation with herring biomass.148
146
Zillén et al., “Past occurrences of hypoxia in the Baltic,” 87; Kuijpers et al., “Baltic Sea
inflow regime”; Weckström et al., “Palaeoenvironmental history of the Baltic”; and
Franke et al., “North Atlantic circulation.” During the LIA, in contrast, east-central
Europe experienced dry conditions and an unstable hydroclimate (Tylmann and
Grosjean, “Climate variability in Central and Eastern Europe”). For the conceptual
framework of ‘regime shifts’ used here return to Chapter 1, note 34.
147
Sparholt, “Fish species interactions”; Köster et al., “Baltic cod recruitment”; and
Heikinheimo, “Interactions between cod, herring and sprat.” Corten, Herring and
Climate, demonstrates the positive response of herring to warmer waters.
148
Fauchald, “Predator–prey reversal”; Van Denderen and Van Kooten, “Size-based
species interactions,” 3; and Sánchez-Garduño et al., “Role reversal.” On the
negative relationship in the twentieth-century North Sea see Engelhard et al., “ICES
meets marine historical ecology,” 1391–1394,” and works there cited. Auber et al.,
“Regime shift in an exploited fish community,” suggest synergy between exploitation
and climate change in driving regime shifts involving small pelagic species.
149
None of the essays in Buti et al., eds., Moissonner la mer (2018), or Tønnes Bekker-
Nielsen and Gertwagen, eds., The Inland Seas: Towards an Ecohistory of the
Mediterranean and the Black Sea (2016), or Mylona and Nicholson, eds., The Bountiful
Sea (2016) show any interest in Camuffo, “Freezing of Venetian lagoon,” 54; Camuffo
At local and regional scale aquatic systems of high medieval Europe were
subject to multiple pressures and constraints across the interplay of nat-
ural and cultural forces. Relevant drivers and effects varied from one
socio-natural site to another. A widely evident rise in human environ-
mental impact had negative consequences for fishes with strict habitat
requirements, while favouring varieties more tolerant of heat, low oxygen,
and high nutrient levels. Changes of natural origin, a warmer climate and
more, also created, destroyed, or shifted equilibria among fish species,
with at least some effect on human use. Contemporary Europeans may
have been oblivious to some such variations or lacked the perspective to
see them in the longer term, but people plainly did become aware of
certain changes. Some traditional fisheries seemed less productive
(scarce) and other local stocks to offer fishers opportunities to respond
to greater demand for fish. Neither resource destruction and depletion nor
the dilemmas of allocation and conservation are peculiar to present-day
fisheries crises. The next chapter turns to responses in medieval commu-
nities to perceptions of limits, declines, and shortages in fishes Europeans
had long liked to eat, so exploring Europeans’ own cultural resilience and
adaptability. Reciprocal and reiterative interactions among medieval
European natures and cultures drove the larger narrative of fisheries to
be apprehended as collectivities of myriad socio-natural sites.
and Bertolin, “Climate in the Mediterranean,” 127; Benito et al., “Holocene flooding”;
Luterbacher et al., “Review of palaeoclimatic evidence”; or even the tight correlation of
Mediterranean clupeids (sprat, sardine, anchovy) with eastern Atlantic species driven
by the Atlantic Multidecadal Oscillation as shown in Alheit et al., “Atlantic
Multidecadal Oscillation (AMO) modulates dynamics.” But see Županović, Ribarstvo
Dalmacije, 37–131, notably 58–64, 90–98, and 145–158, despite its necessary
dependence on what are now obsolete weather reconstructions.