The moth that makes an elephant cry

The moth that makes an elephant cry

Hypochrosis baenzigeri • Photo by budak (CC BY-NC-ND 2.0)

Originally published 7 August 1995

A pho­to­graph in the book review sec­tion of the jour­nal Nature shows three moths drink­ing from a trick­le of liq­uid that flows from a huge glis­ten­ing eye.

The cap­tion says, “…the Asian moth Hypochro­sis baen­zigeri makes an ele­phant cry and then drinks its tears.”

I have no idea how moths pro­voke an ele­phan­t’s tears, why the tears are more to be desired by the moths than nec­tar or plain water, or what ben­e­fit, if any, accrues to the elephant.

But the cap­tion has stuck in my mind, lin­ger­ing some­where between ecol­o­gy and poet­ry. It’s the sort of thing that might have evoked a long med­i­ta­tion by the poet Mar­i­anne Moore.

First, there’s the con­trast in scale between the two crea­tures: The ele­phan­t’s eye is twice the size of the moth, a great dark pool from which a riv­er flows. Sec­ond, the poet­ic ten­sion between sad­ness and nour­ish­ment: The moths refresh them­selves on the ele­phan­t’s tears.

But more than poet­ry, it is the inter­de­pen­dence of moth and ele­phant that I can’t get out of my mind, the sad and beau­ti­ful evo­ca­tion of sym­bi­ot­ic life on Dar­win’s “tan­gled bank.”

The word “sym­bio­sis” (two or more dif­fer­ent organ­isms liv­ing togeth­er in close asso­ci­a­tion) was coined over a cen­tu­ry ago, in an 1877 sci­en­tif­ic paper on lichen anatomy.

Lichens con­sist of a cohab­it­ing alga and fun­gus. The alga is able to pho­to­syn­the­size car­bo­hy­drates, upon which the fun­gus feeds. The fun­gus sup­plies the alga with min­er­als that it extracts from the envi­ron­ment. Nei­ther organ­ism is capa­ble of exist­ing inde­pen­dent­ly unless sup­plied with the prop­er nutri­ents; togeth­er, they are hardy enough to sur­vive where no sin­gle crea­ture could exist alone.

Sym­bio­sis is one of the dri­ving forces of evolution.

Biol­o­gist Lynn Mar­gulis of the Uni­ver­si­ty of Mass­a­chu­setts was the first to sug­gest that the many-com­part­ment­ed eukary­ot­ic cell — of which all mul­ti-celled crea­tures con­sist — was a prod­uct of sym­bio­sis. For exam­ple, the oxy­gen-respir­ing units of eukary­ot­ic cells, called mito­chon­dria, result­ed when respir­ing bac­te­ria were incor­po­rat­ed sym­bi­ot­i­cal­ly into larg­er microor­gan­isms that lacked the abil­i­ty to respire.

Sim­i­lar­ly, the hair-like appendages on eukary­ot­ic cells called fla­gel­la, which give cells motil­i­ty, may have orig­i­nat­ed as thin undu­lat­ing bac­te­ria that latched onto larg­er cells for feed­ing, found the arrange­ment sat­is­fac­to­ry, and nev­er let go.

Dit­to for the pho­to­syn­the­siz­ing units called chloroplasts.

What began as sym­bio­sis became uni­ty. The alliance of three or four sim­pler microor­gan­isms for mutu­al ben­e­fit cre­at­ed a super­cell that swept all before it.

In The Lives of a Cell, Lewis Thomas wrote: “If it is in the nature of liv­ing things to pool resources, to fuse when pos­si­ble, we would have a new way of account­ing for the pro­gres­sive enrich­ment and com­plex­i­ty of form in liv­ing things.”

It is not yet clear how much of this ten­den­cy to pool resources is in the nature of liv­ing things and how much is just use­ful evo­lu­tion­ary acci­dent. Nowhere is the ques­tion more vig­or­ous­ly con­test­ed than in the debate about Gaia.

The Gaia the­o­ry (named for the Earth god­dess of the Greeks) pro­pos­es an ulti­mate sym­bio­sis, embrac­ing all crea­tures great and small, from great blue whales to bac­te­ria, togeth­er with rocks, air, and oceans, mutu­al­ly reg­u­lat­ing the plan­e­tary envi­ron­ment so as to make it opti­mal for life. Gaia is a super organ­ism, as large and as old as the Earth itself, of which we are all a part, as cells are parts of our own bodies.

The Gaia hypoth­e­sis is close­ly asso­ci­at­ed with the British sci­en­tist James Love­lock and (again) Lynn Margulis.

Many sci­en­tists con­sid­er the Gaia the­o­ry far-fetched, based more on wish­ful think­ing than obser­va­tion, and with­out a mech­a­nism to make it work. Oth­ers see Gaia as a pow­er­ful new metaphor to replace the “world as machine” metaphor that has guid­ed sci­ence for most of the past 400 years.

All think­ing is metaphor­i­cal. In both poet­ry and sci­ence, we under­stand by mak­ing analo­gies. Sci­ence is always on the look­out for the anal­o­gy that most effec­tive­ly unites our experience.

Is the Earth a clock­work tick­ing accord­ing to the laws of mechan­ics, or is it a liv­ing organ­ism? Is the world best under­stood by break­ing it into its com­po­nent parts, or must we see the world as an unfrag­ment­ed unity?

The terms of the ques­tions are not nec­es­sar­i­ly mutu­al­ly exclu­sive. Nev­er­the­less, an emerg­ing pop­u­lar­i­ty of the organ­ic metaphor has begun to change the way we per­ceive and under­stand the world.

For the moment, the world-as-machine metaphor remains the dom­i­nant way of doing sci­ence. But what is appeal­ing about the “world as organ­ism” is the way it draws us into a poet­ic alliance with the objects of our study.

As when we read, “…the Asian moth Hypochro­sis baen­zigeri makes an ele­phant cry and then drinks its tears.”

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