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<strong>in</strong>terpret the history <strong>of</strong> the deposition <strong>of</strong><br />

lh('s(' <strong>clay</strong> lens('s. However. the<br />

nwgafossils comb<strong>in</strong>f>d with othf>r floristic<br />

rea turt's and sedimentary features provide<br />

data that can be applied to the history <strong>of</strong><br />

deposition <strong>of</strong> the <strong>clay</strong> lens under consideration.<br />

We suggest a model for this<br />

deposition here.<br />

The depositional model presented is<br />

based primarily upon the vertical relation<br />

<strong>of</strong> the <strong>clay</strong> lenses to one another. It also<br />

provides an explanation for the vertical<br />

variation observed <strong>in</strong> the pollen pr<strong>of</strong>iles <strong>of</strong><br />

these <strong>clay</strong> lenses. There are some changes<br />

<strong>in</strong> floristic composition, leaf morphology,<br />

and cuticular anatomy observed between<br />

<strong>deposits</strong>. Also the depositional history <strong>of</strong><br />

each <strong>clay</strong> lens can be traced through<br />

phases, which resulted <strong>in</strong> similar sedimentary<br />

sequences or parts <strong>of</strong> sequences for<br />

most <strong>clay</strong> lenses studied. Support for this<br />

model <strong>of</strong> the ancient flood-pla<strong>in</strong> sediments<br />

<strong>in</strong> western Tennessee is also provided by<br />

evolutionary trends <strong>of</strong> select leaf types.<br />

INTRODUCTION<br />

Clay lenses are commonly distributed<br />

along the sedimentary beds <strong>of</strong> the<br />

Mississippi Embayment that are exposed<br />

<strong>in</strong> a narrow zone runn<strong>in</strong>g northeast by<br />

southwest through western Kentucky and<br />

Tennessee. The age <strong>of</strong> these sediments<br />

ranges from Upper Cretaceous to middle<br />

Eocene. Follow<strong>in</strong>g the Embayment axis<br />

(northeast-southwestf the Cretaceous<br />

sediments are exposed along the extreme<br />

eastern marg<strong>in</strong> <strong>of</strong> this zone and the<br />

youngest sediments lie to the west. This<br />

report is concerned with those <strong>clay</strong> lenses<br />

<strong>in</strong> western Kentucky and Tennessee which<br />

are considered to be part <strong>of</strong> the Claiborne<br />

Formation deposited dur<strong>in</strong>g the middle<br />

Eocene (Figure 8.l1.<br />

We have exam<strong>in</strong>ed the sediments<br />

from numerous <strong>clay</strong> pill; <strong>in</strong> the area shown<br />

<strong>in</strong> Figure 8.2. Nearly 2S <strong>clay</strong> pits have<br />

yielded fossil leaves, fruits, seeds, wood,<br />

flowers. and pollen. Each <strong>clay</strong> body<br />

212<br />

represents an isolated depositional event<br />

<strong>in</strong> space; and the question to be addressed<br />

is, do these <strong>clay</strong> <strong>deposits</strong> also represent<br />

isolated events <strong>in</strong> time? And, if these<br />

depositional events do represent limited<br />

and different segments <strong>of</strong> middle Eocene<br />

time, can some orderly arrangement <strong>of</strong><br />

their sequence <strong>of</strong> deposition be<br />

discovered? This paper is an attempt to<br />

arrange these <strong>clay</strong> pits <strong>in</strong> a stratigraphic<br />

sequence. The evidence available is the<br />

preserved palynomorphs, megafossil<br />

material, and the geomorphology <strong>of</strong> the<br />

<strong>clay</strong> bodies. The work presented here is an<br />

attempt to establish a prelim<strong>in</strong>ary sequence<br />

as a work<strong>in</strong>g model to be ref<strong>in</strong>ed<br />

and affirmed or corrected by further and<br />

more detailed study. The importance <strong>of</strong><br />

establish<strong>in</strong>g such a sequence is that it<br />

allows the use <strong>of</strong> the Mississippi Embayment<br />

sediments as a <strong>biostratigraphic</strong> tool<br />

to f<strong>in</strong>ely divide and sort out <strong>in</strong><br />

chronological order vegetational changes<br />

<strong>of</strong> plant ecosystems and evolutionary<br />

modifications <strong>of</strong> plant fonn <strong>in</strong> the structurally<br />

preserved fruits, seeds, leaves,<br />

flowers, and wood common <strong>in</strong> these<br />

sediments.<br />

Many leaves, fruits, seeds, and<br />

flowers are restricted to particular <strong>clay</strong><br />

pits; a few fossil forms are common to<br />

nearly all pits. Palynomorphs, as well,<br />

may be restricted to particular <strong>clay</strong> pits or<br />

even to particular zones with<strong>in</strong> a <strong>clay</strong> pit<br />

(Potter, 1976). A careful comparative<br />

study <strong>of</strong> the pollen types <strong>of</strong> various <strong>clay</strong><br />

pits has not been done, but it would yield a<br />

great deal <strong>of</strong> useful data. Isolated pollen<br />

samples have been analyzed and<br />

numerous megafossils have been collected<br />

from these <strong>clay</strong> pits. The data available<br />

from these studies are used <strong>in</strong> this report.<br />

Recent pollen studies <strong>of</strong> the<br />

Mississippi Embayment region have been<br />

summarized by Elsik (1974); Elsik and<br />

Dilcher, (19741. Fairchild and Elsik<br />

(19691, Frederickson. (19691, Potter<br />

(19761 and Tschudy (l973a, b, 19751.


These <strong>in</strong>vestigators recognize the<br />

usefulness and importance <strong>of</strong> the pollen<br />

pr<strong>of</strong>iles <strong>of</strong> these isolated <strong>clay</strong> <strong>deposits</strong> and<br />

some establish particular zones based on<br />

the presence or absence and the abundance<br />

<strong>of</strong> various pollen types. Basic pollen<br />

types have been recognized for the Eocene<br />

sediments <strong>of</strong> the embayment area and<br />

Fairchild and Eisik (1969); Tschudy<br />

0973bi: and Elsik (974). present <strong>in</strong>dex<br />

palynomorphs for the Gull Coast (based<br />

on presence or absence and abundance <strong>of</strong><br />

pollen types) that allow an <strong>in</strong>vestigator to<br />

discrim<strong>in</strong>ate among lower, middle, and<br />

upper Eocene sediments. Tschudy charts<br />

the occurrences f the palynomorphs <strong>in</strong><br />

the Mississippi Embayment <strong>in</strong>dicat<strong>in</strong>g<br />

limited stratigraphic ranges <strong>of</strong> several<br />

with<strong>in</strong> the middle Eocene; Elsik also plots<br />

relative abundances <strong>of</strong> palynomorphs for<br />

the Claiborne sediments <strong>of</strong> the Texas Gulf<br />

Coast. These ata suggest that<br />

palynomorphs can be used to place these<br />

isolated <strong>clay</strong> lenses <strong>in</strong> the Wilcox,<br />

Claiborne, or Jackson (lower, middle, upper<br />

Eocene) formations and possibly also<br />

provide precise <strong>in</strong>formation as to subdivision<br />

<strong>of</strong> member age equivalent for middle<br />

Eocene time.<br />

The ability to subdivide Claiborne<br />

time us<strong>in</strong>g palynomorphs (Tschudy.<br />

1973b gave some hope that each <strong>of</strong> the<br />

numerous isolated <strong>clay</strong> lenses <strong>in</strong> estern<br />

Tennessee and Kentucky could be placed<br />

stratigraphically if pollen samples were<br />

analyzed. Before such a general project <strong>of</strong><br />

sampl<strong>in</strong>g was undertaken. however, we<br />

felt that it was critical to exam<strong>in</strong>e the<br />

nature <strong>of</strong> a s<strong>in</strong>gle <strong>clay</strong> lens <strong>in</strong> some detail.<br />

Therefore, the palynomorphs <strong>of</strong> the Miller<br />

<strong>clay</strong> pit were exam<strong>in</strong>ed from precisely<br />

located samples lvertically at 10-cm <strong>in</strong>tervals)<br />

from the base up to the top <strong>of</strong> a<br />

lOom-thick seam <strong>of</strong> <strong>clay</strong>-lignite-<strong>clay</strong><br />

exposed <strong>in</strong> open pit m<strong>in</strong><strong>in</strong>g. As a result <strong>of</strong><br />

this work. Potter (1976) found that the<br />

relative abundance <strong>of</strong> pollen types present<br />

varied as the lithology <strong>of</strong> the sediments<br />

214<br />

varied, <strong>in</strong>dicat<strong>in</strong>g a strong environmental<br />

control <strong>in</strong>fluenc<strong>in</strong>g this aspect <strong>of</strong> the<br />

pollen pr<strong>of</strong>ile. Potter questioned the<br />

stratigraphic usefulness <strong>of</strong> the abundance<br />

<strong>of</strong> palynomorphs and <strong>in</strong>dicated that some<br />

pollen types may be more important as environmental<br />

<strong>in</strong>dicators than as <strong>in</strong>dicators<br />

<strong>of</strong> the subdivision <strong>of</strong> Claiborne time.<br />

Detailed pollen pr<strong>of</strong>iles <strong>of</strong> several <strong>clay</strong> pits<br />

open <strong>in</strong> this area should be completed.<br />

Such studies will provide important data<br />

to test the model proposed here <strong>of</strong> the<br />

depositional history <strong>of</strong> these lenses.<br />

Early paleobotanical report<strong>in</strong>g was<br />

done by Berry (1916, 1930 Ion the floras <strong>of</strong><br />

over 200 Pal ogene plant-bear<strong>in</strong>g<br />

localities (many <strong>of</strong> which were from <strong>clay</strong><br />

<strong>deposits</strong>) <strong>in</strong> southeastern North America.<br />

He suggested a paleoenvironment for<br />

deposition <strong>of</strong> such plant-bear<strong>in</strong>g<br />

sediments generalized from a locality he<br />

exam<strong>in</strong>ed <strong>in</strong> Texas. He concluded that<br />

these <strong>clay</strong> <strong>deposits</strong> represent near-mar<strong>in</strong>e<br />

paleoenvironments with strand vegetation<br />

while some others represent drowned river<br />

valleys Berry (1916, 1930).<br />

Dilcher (1971) considered the orig<strong>in</strong><br />

<strong>of</strong> the <strong>clay</strong> lenses only <strong>in</strong> western Kentucky<br />

and Tennessee. The <strong>in</strong>formation applied<br />

to this question was derived from<br />

outl<strong>in</strong>e maps <strong>of</strong> known <strong>clay</strong> <strong>deposits</strong>, the<br />

form <strong>of</strong> their cross-section, and the<br />

nature <strong>of</strong> sediments underly<strong>in</strong>g the <strong>clay</strong>s.<br />

Potter (19761, concentrat<strong>in</strong>g upon a s<strong>in</strong>gle<br />

<strong>clay</strong> lens, carried this <strong>analysis</strong> further.<br />

The results <strong>of</strong> these studies demonstrate<br />

that the small <strong>clay</strong> lenses typica <strong>of</strong> Henry<br />

County, Tennessee, and nearby areas are<br />

narrow, L<strong>in</strong>ear-elongated, most <strong>of</strong>ten<br />

curved, river-channel shaped <strong>in</strong><br />

cross-section, surrounded on the sides<br />

and undersides by cross-bedded sands<br />

(occasionally f<strong>in</strong>e gravels), and consist <strong>of</strong><br />

uniform f<strong>in</strong>e <strong>clay</strong>s with an occasional<br />

Lignitic seam or cap. Primarily upon this<br />

<strong>in</strong>formation, we proposed that these<br />

smaU,curved, elongated <strong>clay</strong> lenses represent<br />

<strong>clay</strong> plugs <strong>in</strong> oxbow lakes on an an­


personal communication 1 an upper<br />

Claiborne (Cockfield Fm., and perhaps<br />

Cook Mt. Fm. or lower Cockfield Fm.1<br />

age for them.<br />

Local<br />

The mar<strong>in</strong>e transgressions <strong>of</strong> the<br />

Eocene (Figure 8.3l can not be identified<br />

<strong>in</strong> the Henry County area <strong>of</strong> western Tennessee<br />

(Parks, 19711. The more extensive<br />

transgressions such as those separat<strong>in</strong>g the<br />

Wilcox, Claiborne, and Jackson groups<br />

can be identified only <strong>in</strong> the southwestern<br />

corner <strong>of</strong> Tennessee (Stearns, 1957; Murray,<br />

19611. The Claiborne Formation <strong>in</strong><br />

Henry County, Tennessee, consists ma<strong>in</strong>ly<br />

<strong>of</strong> non-mar<strong>in</strong>e sands and isolated disjunct<br />

lenses <strong>of</strong> <strong>clay</strong>. As already discussed,<br />

there are numerous plant fossil-bear<strong>in</strong>g<br />

lenses <strong>of</strong> <strong>clay</strong> <strong>in</strong> this area. Data from a<br />

regional consideration <strong>of</strong> the pollen flora,<br />

where it can be tied <strong>in</strong>to mar<strong>in</strong>e sequences.<br />

<strong>in</strong>dicates that these lenses are<br />

best considered to be late-middle Eocene<br />

<strong>in</strong> age ICockfield Formation <strong>of</strong> the<br />

Claiborne Group) \Elsik. ]974; Elsik and<br />

Dilcher. 1974; Tschudy, personal communicationl.<br />

Differences <strong>in</strong> the floras <strong>of</strong><br />

particular <strong>clay</strong> pits <strong>in</strong> Henry County, Tenn<br />

.ssee. ano near-by areas are obvious by<br />

a comparison <strong>of</strong> the composition <strong>of</strong> the<br />

floras from each pit and by the specific<br />

nature <strong>of</strong> the epidermal cells, trichomes,<br />

and aspects <strong>of</strong> the overall leaf form <strong>of</strong><br />

several taxa. Two explanations for these<br />

differences are: ecological variability or<br />

evolutionary variability. It is important to<br />

attempt to reconstruct the paleoenvironments<br />

and relative ages <strong>of</strong> these <strong>clay</strong><br />

pits <strong>in</strong> order to understand the cause <strong>of</strong> the<br />

variations observed <strong>in</strong> the fossil record<br />

between these sites.<br />

The ecology <strong>of</strong> most <strong>deposits</strong> seems to<br />

have repeated a relatively similar history<br />

for each <strong>clay</strong> lens. As discussed earlier <strong>in</strong><br />

this paper and by Dilcher (19711 and Potter<br />

(1976), the nature <strong>of</strong> these sediments<br />

<strong>in</strong>dicates a typical oxbow-lake cleposi­<br />

21/<br />

tional system. Each <strong>clay</strong> lens repeats a<br />

similar environmental history with some<br />

variation <strong>in</strong> the extent <strong>of</strong> associated lignite<br />

and relative abundance <strong>of</strong> plant fos"ik<br />

Thus environmental factors most probably<br />

do not account for the differences<br />

observed <strong>in</strong> the plant fossils from <strong>clay</strong> pit<br />

to <strong>clay</strong> pit.<br />

The most logical explanation for the<br />

observed differences <strong>of</strong> the types, relative<br />

abundance, form, and anatomy <strong>of</strong> the<br />

plants at the various localities is that each<br />

locality represents a slightly dilferent segment<br />

<strong>of</strong> time. The time <strong>in</strong>terval <strong>of</strong> evolu­<br />

,ion preserved <strong>in</strong> each <strong>clay</strong> pit is very short<br />

1500 to 1500 yearsl because oxbow lakes<br />

on a flood pla<strong>in</strong> are recognized as shortterm<br />

events when viewed aga<strong>in</strong>st<br />

geological time (Crisman and Whitehead,<br />

1975). The tools available at the present,<br />

such as palynology and knowledge <strong>of</strong> the<br />

megafossils are probably not sufficient to<br />

rank order these <strong>in</strong>dividual <strong>clay</strong> pits<br />

with<strong>in</strong> Cockfield Formation time. The<br />

data provided below is presented <strong>in</strong> an attempt<br />

to establish a rank order for these<br />

<strong>clay</strong> pits with<strong>in</strong> late-middle Eocene time.<br />

DEPOSITION OF FOSSIL·<br />

BEARING SEDIMENTS<br />

The low-ly<strong>in</strong>g features <strong>of</strong> the<br />

Mississippi Embayment allowed for easy<br />

migration <strong>of</strong> river s}'stems across broad<br />

flood pla<strong>in</strong>s; as sediments brought <strong>in</strong> by<br />

the rivers accumulated. Deposition <strong>of</strong> lhe<br />

flood-pla<strong>in</strong> sediments. discussed <strong>in</strong> lhis<br />

paper. resulted from the meander<strong>in</strong>g <strong>of</strong><br />

the"Appalachian" River system enter<strong>in</strong>g<br />

the embayment <strong>in</strong> Kentucky and build<strong>in</strong>g<br />

a poorly def<strong>in</strong>ed delta <strong>in</strong> North Central<br />

Mississippi (Grim, 19361.<br />

Based upon field exam<strong>in</strong>ation; the<br />

<strong>clay</strong> pits can be differentiated <strong>in</strong>to two<br />

types. One lype ha!l relatively massive<br />

<strong>deposits</strong> <strong>of</strong> <strong>clay</strong> and some associated<br />

lignites. Often these lignite seams overlie<br />

the <strong>clay</strong>s, although <strong>in</strong> some localities the<br />

lignite is <strong>in</strong>terspersed with the <strong>clay</strong>s. No


good megafossils have been found <strong>in</strong> these<br />

<strong>clay</strong>s. The lignites arc sufficiently decomposed<br />

to obscure plant structure and <strong>in</strong><br />

some localities numerous root channels extend<br />

from the lignite <strong>in</strong>to the underly<strong>in</strong>g<br />

<strong>clay</strong>. These features suggest a low-ly<strong>in</strong>g<br />

area <strong>of</strong> shallow water receiv<strong>in</strong>g f<strong>in</strong>e-gra<strong>in</strong><br />

sediments <strong>in</strong>terspersed with some swamp<br />

environments with accumulation <strong>of</strong><br />

organic material.<br />

The second type <strong>of</strong> <strong>clay</strong> pit consists <strong>of</strong><br />

small isolated <strong>clay</strong> lenses, <strong>of</strong>ten accompanied<br />

by overly<strong>in</strong>g lignite seams.<br />

Generally, these lenses have 5 to 10 m <strong>of</strong><br />

light tan <strong>clay</strong> lack<strong>in</strong>g micro-and<br />

megafossils, overla<strong>in</strong> by dark brown to<br />

gray <strong>clay</strong> rich <strong>in</strong> plant fossils. The overly<strong>in</strong>g<br />

lignites consist <strong>of</strong> compacted "leaves,<br />

wood, fruits, and seeds; and occasionally<br />

above the lignites are scattered layers <strong>of</strong><br />

light tan, gray, to p<strong>in</strong>k <strong>clay</strong>s or sands. The<br />

<strong>clay</strong> <strong>deposits</strong> are underla<strong>in</strong> by crossbedded<br />

channel sands (as seen at the<br />

Puryear site) and unsorted pea-size<br />

stream gravels (the Warman sitel; and, <strong>in</strong><br />

outl<strong>in</strong>e and cross-section. they are<br />

characteristic <strong>of</strong> abandoned channels apparently<br />

represent<strong>in</strong>g meander cut<strong>of</strong>f<br />

sloughs, oxbow lakes, and stream reaches<br />

(Figure 8.41. Field exam<strong>in</strong>ation <strong>in</strong>dicates<br />

a common depositional history for most <strong>of</strong><br />

the lenses <strong>of</strong> <strong>clay</strong>. The fossil-bear<strong>in</strong>g <strong>clay</strong>s<br />

are a product <strong>of</strong> f<strong>in</strong>e sediments, which filled<br />

the oxbow lakes on the ancient flood<br />

pla<strong>in</strong>. The lignites accumulated as the<br />

lake was filled with <strong>clay</strong>, form<strong>in</strong>g a wet<br />

swampy environment. These events probably<br />

took about 500 to 1500 years.<br />

Several <strong>clay</strong> lenses conta<strong>in</strong> fossil<br />

assemblages represent<strong>in</strong>g both <strong>of</strong> the<br />

above paleoenvironments, some lack any<br />

evidence <strong>of</strong> lignite accumulation, but all<br />

represent short <strong>in</strong>dividual segments <strong>of</strong><br />

time.<br />

Sufficient sites are present <strong>in</strong> western<br />

Tennessee to permit comparison <strong>of</strong> vertical<br />

position as determ<strong>in</strong>ed from<br />

topographic maps and overburden ex­<br />

218<br />

posures observed <strong>in</strong> the field (Figure 8.41.<br />

Although not all sites align precisely, an<br />

<strong>in</strong>itial eastward meander<strong>in</strong>g-channel<br />

shift is suggested. Once reach<strong>in</strong>g the<br />

eastern marg<strong>in</strong> <strong>of</strong> the embayment. cont<strong>in</strong>ued<br />

deposition shifted the channel back<br />

toward the bas<strong>in</strong> axis. This resulted <strong>in</strong> a<br />

sequence <strong>of</strong> channel <strong>deposits</strong> ascend<strong>in</strong>g <strong>in</strong><br />

age, oldest near the base <strong>of</strong> the series along<br />

the west edge <strong>of</strong> the study area, the<br />

youngest also at the western edge but at a<br />

higher elevation (Figure 8.51. The eastern<br />

pits. e.g., Puryear, are <strong>of</strong> <strong>in</strong>termediate<br />

age. Thus the sequenc<strong>in</strong>g <strong>of</strong> the relative<br />

ages <strong>of</strong> the pits is based upon their relative<br />

geomorphic position <strong>in</strong> the flood pla<strong>in</strong>.<br />

The whole series <strong>of</strong> <strong>clay</strong> lenses represents a<br />

geologically short time span, the last<br />

sweep <strong>of</strong> the river hav<strong>in</strong>g occurred dur<strong>in</strong>g<br />

late-middle Eocene (Claiborne Group)<br />

deposition.<br />

The lithology <strong>of</strong> the two pit types provides<br />

support<strong>in</strong>g evidence, the basal <strong>clay</strong><br />

and lignite sites are believed to represent<br />

an almost flat lowland-swamp<br />

flood-pla<strong>in</strong> environment slop<strong>in</strong>g approximately<br />

three feet per mile southward<br />

(Figure 8.6a), These lowland, swampy<br />

areas were dissected and buried by the<br />

sediments <strong>of</strong> the shift<strong>in</strong>g river system that<br />

produced the ascend<strong>in</strong>g series <strong>of</strong> <strong>clay</strong><br />

plugs (Figure 8.6bl. The amount <strong>of</strong> silt<br />

and <strong>clay</strong> accumulation and organic content<br />

<strong>of</strong> these plugs depended on the<br />

degrees <strong>of</strong> isolation from the ma<strong>in</strong> channel<br />

as the river returned to its orig<strong>in</strong>al course<br />

(Figure 8.6c).<br />

This model provides a straightforward<br />

explanation for the data presently<br />

available regard<strong>in</strong>g the nature <strong>of</strong> the fossil<br />

plant record and sedimentology <strong>of</strong> these<br />

<strong>clay</strong> lenses. The fossil assemblages can be<br />

exam<strong>in</strong>ed for evolutionary changes and<br />

environmental <strong>in</strong>fluences <strong>in</strong>dependently <strong>of</strong><br />

their use to establish the time controls.<br />

Selected megafossil distribution<br />

among the <strong>clay</strong> <strong>deposits</strong> is presented <strong>in</strong><br />

Figure 8.7. This figure is presented to


--------<br />

FIGURE 8.6 Meander sweep <strong>of</strong> the Appalachian River system dur<strong>in</strong>g Late-Middle<br />

Claiborne time. a, <strong>in</strong>itial position; b, eastern extent <strong>of</strong> migration; c, end <strong>of</strong> migration cycle.<br />

22J


show that more data than is presently<br />

available is required <strong>in</strong> order to use<br />

megafossils as reliable <strong>in</strong>dicators for arrang<strong>in</strong>g<br />

these <strong>clay</strong> <strong>deposits</strong> <strong>in</strong> an ordered<br />

sequence. Much more work is needed to<br />

sort out ecological versus stratigraphical<br />

control over the occurence <strong>of</strong> megafossils.<br />

To relate the <strong>clay</strong>s to the regional<br />

stratigraphy <strong>of</strong> the embayment, the most<br />

reliable and useful fossil material <strong>in</strong> these<br />

terrestrial <strong>clay</strong> <strong>deposits</strong> is pollen. The<br />

megafossil material reflects local paleoenvironments.<br />

The variability observed <strong>in</strong><br />

angiosperm leaf cuticles provides<br />

recognizable differences between elements<br />

<strong>of</strong> the floras that otherwise are difficult to<br />

dist<strong>in</strong>guish. Pollen from paleoenvironmentally<br />

equivalent samples <strong>of</strong> the<br />

<strong>clay</strong> <strong>deposits</strong> discussed here have not been<br />

studied. Perhaps if this were done, pollen<br />

would be as useful for local as well as<br />

regional stratigraphy.<br />

SEQUENCE OF DEPOSITION<br />

The suggested sequence <strong>of</strong> deposition<br />

presented <strong>in</strong> Table 8.1 is primarily derived<br />

from the <strong>in</strong>formation provided <strong>in</strong> Figure<br />

8.5. The vertical distributions <strong>of</strong> these <strong>clay</strong><br />

<strong>deposits</strong> <strong>in</strong> western Tennessee all appear<br />

to be restricted to the upper-middle<br />

Eocene (Cook Mt. and Cockfield formations,<br />

Figure 8.3). Their preservation probably<br />

results from their burial by subsequent<br />

sediments laid down <strong>in</strong> the rather<br />

extensive transgression mark<strong>in</strong>g the boundary<br />

between the Claiborne and the<br />

Jackson groups (Figure 8.3). These <strong>clay</strong>s<br />

deposited <strong>in</strong> a flood-pla<strong>in</strong> environment<br />

avoided destruction until their f<strong>in</strong>al<br />

burial. Many <strong>of</strong> these <strong>clay</strong> <strong>deposits</strong> are<br />

similar <strong>in</strong> age, while those deposited<br />

deeper <strong>in</strong>to the flood-pla<strong>in</strong> sediments are<br />

most probably older. This depositional sequence<br />

is the first approximation <strong>of</strong> such<br />

events <strong>in</strong> the Mississippi Embayment and<br />

is proposed as a model for subsequent consideration<br />

.<br />

223<br />

POST DEPOSITIONAL HISTOR Y<br />

Individual <strong>clay</strong> lenses <strong>of</strong>ten consist <strong>of</strong><br />

<strong>clay</strong>s that range <strong>in</strong> color from dark gray.<br />

brown, tan, cream, white, p<strong>in</strong>k to red.<br />

Previously, some field geologists held the<br />

idea that the color <strong>of</strong> this <strong>clay</strong> could be used<br />

as a field guide to differentiate<br />

sediments <strong>of</strong> the Wilcox Group from those<br />

<strong>of</strong> the Claiborne Group. The palynology<br />

and the megafossils <strong>in</strong> the <strong>clay</strong>s<br />

demonstrate that each deposit is a s<strong>in</strong>gle<br />

unit <strong>of</strong> a s<strong>in</strong>gle age. The differences <strong>in</strong> color<br />

are <strong>of</strong> no value to mark one group or<br />

formation from another <strong>in</strong> these <strong>deposits</strong>.<br />

The variations <strong>in</strong> color represent differences<br />

<strong>of</strong> postdepositional history that<br />

each <strong>clay</strong> lens and each part <strong>of</strong> a <strong>clay</strong> lens<br />

has undergrone.<br />

The gray and brown colors are the<br />

result <strong>of</strong> unoxidized organic material; the<br />

lighter colors <strong>in</strong>dicate either a total lack <strong>of</strong><br />

organic materials or some degree <strong>of</strong> oxidation.<br />

Subsequent color<strong>in</strong>g by iron is common,<br />

produc<strong>in</strong>g p<strong>in</strong>k or red days. Once<br />

deposited, the organic matter <strong>in</strong> a <strong>clay</strong> lens<br />

will not oxidize unless the water table is<br />

lowered. If only the upper portion <strong>of</strong> the<br />

<strong>clay</strong> lens extends above the water table.<br />

only the upper portion will oxidize. If the<br />

entire lens is above the water table it will<br />

oxidize from the top, bottom, and sides,<br />

slowly discolor<strong>in</strong>g the organic-rich <strong>clay</strong>s.<br />

Oxidation <strong>of</strong> such a lens <strong>of</strong> <strong>clay</strong> will proceed<br />

unevenly and probably take a great<br />

deal <strong>of</strong> time to be completed. Often a wide<br />

(4-10 feet) band <strong>of</strong> gray or brown <strong>clay</strong> may<br />

zxtend through the central portion <strong>of</strong> a<br />

lens surrounded by tan and cream colored<br />

<strong>clay</strong>s as a result <strong>of</strong> depressed water tables.<br />

Changes <strong>in</strong> the water table surround<strong>in</strong>g<br />

the <strong>clay</strong> lenses <strong>in</strong> Tennessee are<br />

possibly an ancient phenomenon and may<br />

have been a seasonal evenl. Some oxidation<br />

<strong>of</strong> these <strong>clay</strong> lenses may be the result<br />

<strong>of</strong> Recent water-table fluxuations <strong>in</strong><br />

Henry County, Tennessee.


CONCLUSIONS<br />

The leaf floras, fruits and seeds,<br />

dispersed cuticle, and palynology <strong>of</strong> the<br />

<strong>clay</strong> <strong>deposits</strong> <strong>in</strong> Henry County, Tennessee<br />

<strong>in</strong>dicate a similar (but not identical) age<br />

and paleoecology for these sediments.<br />

These same fossils also demonstrate some<br />

unique differences among the <strong>in</strong>dividual<br />

<strong>clay</strong> <strong>deposits</strong>. Many <strong>of</strong> these differences<br />

can be related to the slightly different ages<br />

<strong>of</strong> the <strong>in</strong>dividual <strong>clay</strong> lenses. But very few<br />

<strong>of</strong> these differences are related to the<br />

paleoecology <strong>of</strong> <strong>in</strong>dividual lenses when<br />

similar sediments <strong>of</strong> two <strong>deposits</strong> are compared.<br />

Thus, while these differences can<br />

be recognized for each deposit, it is extremely<br />

difficult to use this data to order<br />

rank the <strong>clay</strong> <strong>deposits</strong> from oidest to<br />

youngest. In order to circumvent this problem<br />

and establish a work<strong>in</strong>g model <strong>of</strong> the<br />

relative ages <strong>of</strong> these <strong>clay</strong> <strong>deposits</strong> their<br />

ages have been correlated with their<br />

relative elevation <strong>of</strong> deposition upon a<br />

common ancient flood pla<strong>in</strong>.<br />

The follow<strong>in</strong>g conclusions have been<br />

discussed above.<br />

1. Many <strong>of</strong> the <strong>clay</strong> pits <strong>in</strong> Henry County,<br />

Tennessee, represent <strong>clay</strong> plugs <strong>in</strong> oxbow<br />

lakes on an ancient flood pla<strong>in</strong>.<br />

2. Probably the <strong>clay</strong> pits represent a last<br />

major sweep <strong>of</strong> the .. Appalachian"<br />

River system through its flood pla<strong>in</strong><br />

near the end <strong>of</strong> the middle Eocene.<br />

3. The bas<strong>in</strong> cont<strong>in</strong>ued to subside<br />

throughout middle and post middle<br />

Eocene time, bury<strong>in</strong>g the river-channel<br />

features by later transgressions <strong>of</strong><br />

the Embayment and thus effectively<br />

prevent<strong>in</strong>g their loss by further floodpla<strong>in</strong><br />

activity.<br />

4. The extent <strong>of</strong> the entire depositional<br />

events discussed here was conf<strong>in</strong>ed to a<br />

moderately short span <strong>of</strong> geologic time.<br />

<strong>of</strong> sufficient length however, to provide<br />

an excellent model for detailed evolutionary<br />

studies between <strong>in</strong>dividual<br />

localities.<br />

5. Each <strong>in</strong>dividual <strong>clay</strong> pit represents a<br />

224<br />

very-short-term event last<strong>in</strong>g approximately<br />

500 to 1500 years.<br />

6. The fossil plants preserved with<strong>in</strong> the<br />

<strong>clay</strong> lenses <strong>in</strong> Henry County, Tennessee,<br />

conta<strong>in</strong> a record <strong>of</strong><br />

predom<strong>in</strong>antly flood-pla<strong>in</strong> vegetation.<br />

7. Many <strong>clay</strong> pits represent more than one<br />

paleoenvironment (<strong>clay</strong> sediments<br />

represent open oxbow lakes and lignites<br />

closed swampy environments).<br />

8. The postdepositional history <strong>of</strong> these<br />

<strong>clay</strong> lenses reflects the <strong>in</strong>fluence <strong>of</strong><br />

changes <strong>in</strong> the water table allow<strong>in</strong>g oxidation<br />

<strong>of</strong> those <strong>clay</strong>s that conta<strong>in</strong><br />

organic material. The oxidized <strong>clay</strong>s<br />

are light <strong>in</strong> color; those rich <strong>in</strong> organic<br />

material are darker.<br />

9. Some floristic variations observed may<br />

be ecological while the variations<br />

observed <strong>in</strong> the leaf form and anatomy<br />

<strong>of</strong> the cuticle <strong>of</strong> similar plant fossils<br />

found <strong>in</strong> several <strong>clay</strong> pits probably<br />

represent evolutionary changes, illustrat<strong>in</strong>g<br />

differences <strong>in</strong> age <strong>of</strong> <strong>in</strong>dividual<br />

pits.<br />

REFERENCES<br />

Berry, E. W. 1916. The Lower Eocene<br />

floras <strong>of</strong> southeastern North America.<br />

U.S. Geol. Surv. Pr<strong>of</strong>. Paper 91, 481p.<br />

Berry, E. W. 1930. Revision <strong>of</strong> the Lower<br />

Eocene Wilcox flora <strong>of</strong> the southeastern<br />

United States. U.S. Geol. Surv. Pr<strong>of</strong>.<br />

Paper 156, 196p.<br />

Crisman. T.L., and D. R. Whitehead.<br />

1975. Environmental history <strong>of</strong> Hovey<br />

Lake, Southwestern Indiana. Am.<br />

Mid. Nat. 93: 198-205.<br />

Dilcher, D. L. 1971. A revision <strong>of</strong> the<br />

Eocene flora <strong>of</strong> southeastern North<br />

America. Palaeobotanist 20:7-18.<br />

Elsik, W. C. 1974. Characteristic Eocene<br />

palynomorphs <strong>in</strong> the Gulf Coast,<br />

U.S.A. Palaeotographica, B<br />

149:90-111.<br />

Elsik, W. C., and D. L. Dilcher, 1974.<br />

Palynology and age <strong>of</strong> <strong>clay</strong>s exposed <strong>in</strong><br />

Lawrence <strong>clay</strong> pit, Henry County, Ten­

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